Your new company You will be joining a well-established and expanding pharmaceutical manufacturer based in North Wales, operating within a highly regulated GMP environment. The site has recently undergone significant investment and continues to grow, supporting the production of complex drug substances within a collaborative and quality-driven setting. Your new role As a Pharmaceutical Process Technician, you will play a key role in supporting manufacturing operations across both upstream and downstream processes. This is a hands-on position within a cleanroom environment, working closely with production, quality, and engineering teams. Key responsibilities will include: Executing GMP manufacturing activities such as media preparation, component transfers, upstream/downstream processing, and equipment cleaning. Accurately completing batch records and GMP documentation in real time, ensuring full compliance with regulatory standards Operating process equipment in line with SOPs and validated procedures Supporting validation and qualification activities, including protocol execution and data recording Carrying out basic preventative maintenance and equipment checks to ensure operational efficiency Participating in environmental monitoring, sampling, and facility checks Contributing to deviation investigations, CAPAs, and continuous improvement initiatives Maintaining high standards of health & safety and GMP compliance at all times This is a shift-based role, requiring flexibility across early and late patterns, with occasional weekend work. What you'll need to succeed To be successful in this role, you will have: A degree in a Life Sciences discipline (e.g. Biotechnology, Chemistry, Biology) or equivalent hands-on experience Prior experience working in a GMP regulated environment, ideally within pharmaceutical or biopharmaceutical manufacturing Exposure to cleanroom environments and controlled processes A strong understanding of GMP principles, documentation, and compliance standards High attention to detail with a methodical and process-driven approach The ability to follow strict procedures and work effectively within a team-based manufacturing environment Desirable: Experience in bioprocessing (upstream/downstream) Exposure to validation, qualification, or environmental monitoring activities What you'll get in return Opportunity to gain experience within a growing pharmaceutical manufacturing site Exposure to regulated GMP processes and validation activities A collaborative working environment with strong technical teams Competitive contract offering with potential for extension beyond initial term Valuable experience to support progression into manufacturing, validation, or quality roles What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
Jun 30, 2026
Contractor
Your new company You will be joining a well-established and expanding pharmaceutical manufacturer based in North Wales, operating within a highly regulated GMP environment. The site has recently undergone significant investment and continues to grow, supporting the production of complex drug substances within a collaborative and quality-driven setting. Your new role As a Pharmaceutical Process Technician, you will play a key role in supporting manufacturing operations across both upstream and downstream processes. This is a hands-on position within a cleanroom environment, working closely with production, quality, and engineering teams. Key responsibilities will include: Executing GMP manufacturing activities such as media preparation, component transfers, upstream/downstream processing, and equipment cleaning. Accurately completing batch records and GMP documentation in real time, ensuring full compliance with regulatory standards Operating process equipment in line with SOPs and validated procedures Supporting validation and qualification activities, including protocol execution and data recording Carrying out basic preventative maintenance and equipment checks to ensure operational efficiency Participating in environmental monitoring, sampling, and facility checks Contributing to deviation investigations, CAPAs, and continuous improvement initiatives Maintaining high standards of health & safety and GMP compliance at all times This is a shift-based role, requiring flexibility across early and late patterns, with occasional weekend work. What you'll need to succeed To be successful in this role, you will have: A degree in a Life Sciences discipline (e.g. Biotechnology, Chemistry, Biology) or equivalent hands-on experience Prior experience working in a GMP regulated environment, ideally within pharmaceutical or biopharmaceutical manufacturing Exposure to cleanroom environments and controlled processes A strong understanding of GMP principles, documentation, and compliance standards High attention to detail with a methodical and process-driven approach The ability to follow strict procedures and work effectively within a team-based manufacturing environment Desirable: Experience in bioprocessing (upstream/downstream) Exposure to validation, qualification, or environmental monitoring activities What you'll get in return Opportunity to gain experience within a growing pharmaceutical manufacturing site Exposure to regulated GMP processes and validation activities A collaborative working environment with strong technical teams Competitive contract offering with potential for extension beyond initial term Valuable experience to support progression into manufacturing, validation, or quality roles What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
Dispensary Technician Based in Worthing, West Sussex Rolling days, 4 on 2 off 06:52 - 15:00 From 15.57 per hour to 17.30 per hour Our respected client is a global pharmaceutical company manufacturing a diverse range of products including medically critical sterile products, equipment and medicines that help to save the lives of millions of people worldwide. GSK are committed to moving Ahead Together and aim to have a positive impact on the health of 2.5 Billion people by the end of 2030. We are looking for candidates to join our team of exceptional individuals doing work that truly matters to the health of people worldwide. We are recruiting a Dispensary Technician to support the manufacturing operations by collating, dispensing and moving materials safely and accurately. You'll be based within the dispensary rooms/booths, dispensing powders for the manufacturing department, ensuring all activities meet GMP and regulatory standards. All work will be controlled through SAP and linked to the weighing system to ensure full traceability. Your responsibilities will consist of but are not limited to: Collate and dispense raw materials (including powders) for manufacturing areas. Complete all material movements and transactions accurately using SAP and the site weighing system. Ensure safe loading, unloading, stowing and internal transfer of materials using the correct manual handling equipment. Operate manual handling equipment in line with your licence/training (e.g., pallet trucks, reach truck ). Maintain dispensary areas to the required GMP standard, including: General housekeeping Daily checks/inspections Filter changes Strip and seal of floors (as required) Follow all SOPs and escalate any quality or safety concerns immediately. Work collaboratively with internal teams to deliver a high level of internal customer service The following are essential to the role: Reach Truck Licence required and previous experience Experience using SAP/MRP/ERP systems Previous experience within a warehouse, production or manufacturing environment Strong quality mindset and pride in delivering accurate work All roles are recruited on a temporary basis with the maximum tenure of 2 years. Why GSK? Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to ensuring that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. GSK is open to all talent and is an Equal Opportunity Employer. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class ( US only).' Should you require any support or assistance, please contact your local Gi Group office. Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, corperate members for Neurodiversity in business, Disability Confident committed members, Gold status for the Armed Forces Covenant, Bronze trail blazers for Racial Equality matters and Age Freindly Employer pledge members. Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role. We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.
Jun 29, 2026
Seasonal
Dispensary Technician Based in Worthing, West Sussex Rolling days, 4 on 2 off 06:52 - 15:00 From 15.57 per hour to 17.30 per hour Our respected client is a global pharmaceutical company manufacturing a diverse range of products including medically critical sterile products, equipment and medicines that help to save the lives of millions of people worldwide. GSK are committed to moving Ahead Together and aim to have a positive impact on the health of 2.5 Billion people by the end of 2030. We are looking for candidates to join our team of exceptional individuals doing work that truly matters to the health of people worldwide. We are recruiting a Dispensary Technician to support the manufacturing operations by collating, dispensing and moving materials safely and accurately. You'll be based within the dispensary rooms/booths, dispensing powders for the manufacturing department, ensuring all activities meet GMP and regulatory standards. All work will be controlled through SAP and linked to the weighing system to ensure full traceability. Your responsibilities will consist of but are not limited to: Collate and dispense raw materials (including powders) for manufacturing areas. Complete all material movements and transactions accurately using SAP and the site weighing system. Ensure safe loading, unloading, stowing and internal transfer of materials using the correct manual handling equipment. Operate manual handling equipment in line with your licence/training (e.g., pallet trucks, reach truck ). Maintain dispensary areas to the required GMP standard, including: General housekeeping Daily checks/inspections Filter changes Strip and seal of floors (as required) Follow all SOPs and escalate any quality or safety concerns immediately. Work collaboratively with internal teams to deliver a high level of internal customer service The following are essential to the role: Reach Truck Licence required and previous experience Experience using SAP/MRP/ERP systems Previous experience within a warehouse, production or manufacturing environment Strong quality mindset and pride in delivering accurate work All roles are recruited on a temporary basis with the maximum tenure of 2 years. Why GSK? Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to ensuring that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. GSK is open to all talent and is an Equal Opportunity Employer. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class ( US only).' Should you require any support or assistance, please contact your local Gi Group office. Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, corperate members for Neurodiversity in business, Disability Confident committed members, Gold status for the Armed Forces Covenant, Bronze trail blazers for Racial Equality matters and Age Freindly Employer pledge members. Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role. We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.
Senior Operator Technicians Pencoed Competitive salary Full-time Temporary Onsite Introduction Acorn by Synergie is recruiting experienced Senior Operator Technicians to join a client's Pencoed site. This role is key to managing the safe and efficient operations of machinery and equipment, requiring technical skills and knowledge of safety procedures. Key Duties Carry out testing and release of Immunodiagnostic products in accordance with controlled procedures. Ensure HSE requirements are adhered to within the immediate work environment. Perform manufacturing operations following cGMP and GLP, recording any anomalous observations and empowered to halt processes if necessary. Provide first-level supervision to operational teams, ensuring adherence to production plans. Prepare SOPs and associated documents for existing procedures. Operate production equipment or carry out manual operations. Conduct routine quality control tests, interpret results, and recommend appropriate actions. Maintain operational environments and control charts, understanding SPC principles. Supervise contract maintenance staff and ensure production equipment maintenance schedules are met. Participate in quality improvement initiatives, shopfloor workflow planning, and new production setups. Maintain personal and team training records, supporting the annual appraisal and unit training plans. On occasion, deputise for senior members, make hiring recommendations, plan work, train employees, and review work quality. Requirements 5 GCSEs including Maths and a relevant Science or HTEC. Relevant operational experience; science background preferred. Laboratory or production line experience desirable. Ability to communicate effectively with all operational team members. Team player with awareness of section activities. What We Offer Competitive salary. Temporary role with potential to become permanent. Supportive team environment with career development opportunities. Access to Employee Assistance Programme (EAP) and Acorn Rewards App. Interested? Apply today or contact Ceri at Acorn by Synergie Head Office, Newport, for more details. Acorn by Synergie acts as an employment business for the supply of temporary workers.
Jun 26, 2026
Seasonal
Senior Operator Technicians Pencoed Competitive salary Full-time Temporary Onsite Introduction Acorn by Synergie is recruiting experienced Senior Operator Technicians to join a client's Pencoed site. This role is key to managing the safe and efficient operations of machinery and equipment, requiring technical skills and knowledge of safety procedures. Key Duties Carry out testing and release of Immunodiagnostic products in accordance with controlled procedures. Ensure HSE requirements are adhered to within the immediate work environment. Perform manufacturing operations following cGMP and GLP, recording any anomalous observations and empowered to halt processes if necessary. Provide first-level supervision to operational teams, ensuring adherence to production plans. Prepare SOPs and associated documents for existing procedures. Operate production equipment or carry out manual operations. Conduct routine quality control tests, interpret results, and recommend appropriate actions. Maintain operational environments and control charts, understanding SPC principles. Supervise contract maintenance staff and ensure production equipment maintenance schedules are met. Participate in quality improvement initiatives, shopfloor workflow planning, and new production setups. Maintain personal and team training records, supporting the annual appraisal and unit training plans. On occasion, deputise for senior members, make hiring recommendations, plan work, train employees, and review work quality. Requirements 5 GCSEs including Maths and a relevant Science or HTEC. Relevant operational experience; science background preferred. Laboratory or production line experience desirable. Ability to communicate effectively with all operational team members. Team player with awareness of section activities. What We Offer Competitive salary. Temporary role with potential to become permanent. Supportive team environment with career development opportunities. Access to Employee Assistance Programme (EAP) and Acorn Rewards App. Interested? Apply today or contact Ceri at Acorn by Synergie Head Office, Newport, for more details. Acorn by Synergie acts as an employment business for the supply of temporary workers.
We have partnered with a valued client to assist their search for a number of Production Technicians. As the Production Technician of a designated process, you will operate processes such as Chromatography, Centrifugation or ultrafiltration and other fully automated processes, for which you will develop a full operational understanding. You will actively support an environment of continuous improvement ensuring that all quality and productivity targets are achieved through the optimum use of resources in a safe environment. You will use effective communication skills with all team members to ensure completion of the Production Manufacturing and filling plans. This is a fully on site role, operating on a 24/7 shift rotation. You will also require your own vehicle in order to access the facility. Key duties and responsibilities: The role of Production Technician will be hands on and varied. Here are some of the core responsibilities of the role: 1. Set up and operate automated and semi-automated manufacturing equipment as detailed within the department training matrix including Ultrafiltration, centrifuge and Chromatography processes as required. 2. Develop a full working knowledge in one or more of the processes in downstream processing. For example, having a sufficient understanding of chromatographic techniques in production in order to operate equipment in compliance unsupervised with the ability to solve problems. 3. To develop an understanding of the principles of gas and liquid filtration and be able to troubleshoot problems with filter testing and use. 4. Set up and operate automated and semi-automated manufacturing equipment. Carry out Process Formulations unsupervised and ensure that critical process samples are taken and submitted correctly in accordance with the procedure and relevant IMS. 5. Carry out sterile transfers of final product to the Aseptic filling suite in time to meet the scheduled filling plan. 6. To operate and trouble shoot Clean in Place systems for department specific static equipment. 7. pH and conductivity monitoring and testing. Skills and experience: 1. Prior manufacturing experience is essential, gained from pharmaceuticals, biopharmaceuticals, food, drink, brewing or similar highly regulated environments. 2. Experience of pH, conductivity and chromatography. 3. You will be expected to demonstrate excellent communication skills, excellent organisational skills and the ability to problem solve. 4. Any additional experience working in a clean room environment, or under GMP regulations would prove advantageous.
Jun 23, 2026
Full time
We have partnered with a valued client to assist their search for a number of Production Technicians. As the Production Technician of a designated process, you will operate processes such as Chromatography, Centrifugation or ultrafiltration and other fully automated processes, for which you will develop a full operational understanding. You will actively support an environment of continuous improvement ensuring that all quality and productivity targets are achieved through the optimum use of resources in a safe environment. You will use effective communication skills with all team members to ensure completion of the Production Manufacturing and filling plans. This is a fully on site role, operating on a 24/7 shift rotation. You will also require your own vehicle in order to access the facility. Key duties and responsibilities: The role of Production Technician will be hands on and varied. Here are some of the core responsibilities of the role: 1. Set up and operate automated and semi-automated manufacturing equipment as detailed within the department training matrix including Ultrafiltration, centrifuge and Chromatography processes as required. 2. Develop a full working knowledge in one or more of the processes in downstream processing. For example, having a sufficient understanding of chromatographic techniques in production in order to operate equipment in compliance unsupervised with the ability to solve problems. 3. To develop an understanding of the principles of gas and liquid filtration and be able to troubleshoot problems with filter testing and use. 4. Set up and operate automated and semi-automated manufacturing equipment. Carry out Process Formulations unsupervised and ensure that critical process samples are taken and submitted correctly in accordance with the procedure and relevant IMS. 5. Carry out sterile transfers of final product to the Aseptic filling suite in time to meet the scheduled filling plan. 6. To operate and trouble shoot Clean in Place systems for department specific static equipment. 7. pH and conductivity monitoring and testing. Skills and experience: 1. Prior manufacturing experience is essential, gained from pharmaceuticals, biopharmaceuticals, food, drink, brewing or similar highly regulated environments. 2. Experience of pH, conductivity and chromatography. 3. You will be expected to demonstrate excellent communication skills, excellent organisational skills and the ability to problem solve. 4. Any additional experience working in a clean room environment, or under GMP regulations would prove advantageous.
Line Leader Leyland, Lancashire Full-time, shift-based Shifts available: AM Shift 6:00am to 2:00pm - £24,297 PM Shift 2:00pm to 10:00pm - £25,369 The Role Lead a team of production operatives to achieve daily targets. Set up and operate production lines, working with technicians where required. Assign tasks, monitor performance, and ensure compliance with SOPs. Train, mentor, and support both permanent and temporary staff. Carry out quality checks and complete required production paperwork. Maintain equipment and ensure smooth running of the line. Monitor efficiency, identify issues, and implement improvements. Ensure compliance with Health & Safety, GMP, and company policies. Collaborate with other departments to meet production schedules. Maintain a safe, tidy, and efficient working environment. The Person Previous leadership/supervisory experience in a manufacturing environment. Strong communication and organisational skills. Attention to detail with a focus on quality and safety. Ability to motivate and coach a diverse team. Comfortable working under pressure in a fast-paced setting. Flexible approach to shifts and overtime. Positive, proactive, and adaptable to change. Our clients and their customers come from diverse backgrounds and so do we. We hire our people from various walks of life, each of whom make our company stronger with their talent, uniqueness, and expertise. This is what makes our company special; if you want to help us grow and take this ethos to our clients, then we cannot wait to collaborate with you! The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Although the closing date for applications was 30th Jun 2021, if you have not yet applied but believe that you would qualify under the EU Settlement Scheme, the Home Office have confirmed that they will consider late applications. For further information please see (url removed)> Many Thanks
Oct 09, 2025
Full time
Line Leader Leyland, Lancashire Full-time, shift-based Shifts available: AM Shift 6:00am to 2:00pm - £24,297 PM Shift 2:00pm to 10:00pm - £25,369 The Role Lead a team of production operatives to achieve daily targets. Set up and operate production lines, working with technicians where required. Assign tasks, monitor performance, and ensure compliance with SOPs. Train, mentor, and support both permanent and temporary staff. Carry out quality checks and complete required production paperwork. Maintain equipment and ensure smooth running of the line. Monitor efficiency, identify issues, and implement improvements. Ensure compliance with Health & Safety, GMP, and company policies. Collaborate with other departments to meet production schedules. Maintain a safe, tidy, and efficient working environment. The Person Previous leadership/supervisory experience in a manufacturing environment. Strong communication and organisational skills. Attention to detail with a focus on quality and safety. Ability to motivate and coach a diverse team. Comfortable working under pressure in a fast-paced setting. Flexible approach to shifts and overtime. Positive, proactive, and adaptable to change. Our clients and their customers come from diverse backgrounds and so do we. We hire our people from various walks of life, each of whom make our company stronger with their talent, uniqueness, and expertise. This is what makes our company special; if you want to help us grow and take this ethos to our clients, then we cannot wait to collaborate with you! The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Although the closing date for applications was 30th Jun 2021, if you have not yet applied but believe that you would qualify under the EU Settlement Scheme, the Home Office have confirmed that they will consider late applications. For further information please see (url removed)> Many Thanks
Hi, Are you looking for an immediate start? Are you an experienced lab technician? We have a great opportunity for laboratory technician who would like to be part of a large team working for a multinational global brand. Helping to produce medical devices at the BD plant in Plymouth you would get involved in all aspects of the production cycle from operating moulding machines to quality control to Continuous Improvement, honing your transferable skills in manufacturing. Job title : Lab Analyst 08:00-16:00 Standard Days Monday-Friday Pay rate: 12.38 Benefits : Access to Randstad 'Happi' benefits scheme which includes 100's of high street discounts, gym membership and much more! Employee Assistance Programme / Well being Support Flexible shift patterns Paid breaks Free soft drinks and hot drinks on site Free parking Internal training and development Weekly pay Access to permanent vacancies Responsibilities : Comply with safety standards and good laboratory practice standards (COSHH). Comply with all PPE, GMP requirements and manual handling regulations and training. Maintain the cleanliness of the microbiology laboratory and Sterility Suites and apparatus therein, wash and prepare glassware, discard waste and cultures following appropriate practices. Preparation and sterilisation (autoclaving) of microbiological growth media to carry out routine test functions. Assist in the preparation of routine environmental monitoring equipment and media. Document all work on corresponding controlled documents. Preparation, sterilisation and supply of multiple sterile stopper lubricants to production. Dispensing provisions into production and removal of expired provisions. Sanitisation of components used within the production process. Assist in process/product/non-conformance investigations as required. Carry out any reasonable request of the Senior Laboratory Technician, Sterility Assurance and Quality Systems Leader, Microbiologist and/or the Associate Director Quality Management. Communicate all relevant information to the Senior Laboratory Technician to ensure smooth running of the laboratory. Individuals have the authority to execute all responsibilities detailed within their job description and any procedures or processes in C2C or otherwise. Education and Experience: GCSE's in relevant subjects Experience working in a scientific laboratory desirable. Requirements : Applicants must be computer literate Applicants must be eligible to work in the UK and be able to provide proof of this Applicants must be over 18 years old If you'd like to be part of our success please apply with your up-to-date CV to be considered for the role.
Oct 07, 2025
Seasonal
Hi, Are you looking for an immediate start? Are you an experienced lab technician? We have a great opportunity for laboratory technician who would like to be part of a large team working for a multinational global brand. Helping to produce medical devices at the BD plant in Plymouth you would get involved in all aspects of the production cycle from operating moulding machines to quality control to Continuous Improvement, honing your transferable skills in manufacturing. Job title : Lab Analyst 08:00-16:00 Standard Days Monday-Friday Pay rate: 12.38 Benefits : Access to Randstad 'Happi' benefits scheme which includes 100's of high street discounts, gym membership and much more! Employee Assistance Programme / Well being Support Flexible shift patterns Paid breaks Free soft drinks and hot drinks on site Free parking Internal training and development Weekly pay Access to permanent vacancies Responsibilities : Comply with safety standards and good laboratory practice standards (COSHH). Comply with all PPE, GMP requirements and manual handling regulations and training. Maintain the cleanliness of the microbiology laboratory and Sterility Suites and apparatus therein, wash and prepare glassware, discard waste and cultures following appropriate practices. Preparation and sterilisation (autoclaving) of microbiological growth media to carry out routine test functions. Assist in the preparation of routine environmental monitoring equipment and media. Document all work on corresponding controlled documents. Preparation, sterilisation and supply of multiple sterile stopper lubricants to production. Dispensing provisions into production and removal of expired provisions. Sanitisation of components used within the production process. Assist in process/product/non-conformance investigations as required. Carry out any reasonable request of the Senior Laboratory Technician, Sterility Assurance and Quality Systems Leader, Microbiologist and/or the Associate Director Quality Management. Communicate all relevant information to the Senior Laboratory Technician to ensure smooth running of the laboratory. Individuals have the authority to execute all responsibilities detailed within their job description and any procedures or processes in C2C or otherwise. Education and Experience: GCSE's in relevant subjects Experience working in a scientific laboratory desirable. Requirements : Applicants must be computer literate Applicants must be eligible to work in the UK and be able to provide proof of this Applicants must be over 18 years old If you'd like to be part of our success please apply with your up-to-date CV to be considered for the role.
Premier Recruitment Group has the privilege to recruit on behalf of our very prestigious client based in Rainham, East London, Essex. We are recruiting for experienced and forward thinking Multi-Skilled Shift Engineer . This is full time and permanent position and working for very well established company. Very interesting and varied role with a scope for progression. We are currently seeking Multi-Skilled Shift Engineer. This is a very exciting time to join a growing company regarded as experts in their industry, with opportunities for employees to develop within their role. Attractive salary and benefits. Work Pattern: Shift pattern 39 - 42 hrs per week (rotating days and nights) Days: 6am - 6pm Nights: 6pm - 6am The role: Reporting to Engineering Team Leader Follow GMP, Safety, Quality, Operational and Engineering procedures. Support production prioritising Safety, Quality and Production Volume. Comply with legislative and statutory requirements. Key areas of responsibility: Ensure all work is documented through the computerised maintenance management system (CMMS), shift handovers and PM worksheets. Awareness of site performance and KPI's, and support others to achieve targets for safety, Identify and control spare stock holding and procurement linking into PM system and CMMS Identifying and planning of maintenance and corrective actions in area from CMMS Carry out continuous improvement tasks identified within the area. Providing Technical expertise within area to other Technicians and Operators. Assist and deliver basic training for Operators and Technicians on equipment function and Supervise and take responsibility for Contractors on site. Understand the Service Building and Site Maintenance, complete basic tasks in these areas. Control work through the Permit to Work system. Proactively drive continuous improvements within own area liaising with other departments Offer improvement ideas for production equipment and facilities Electrical and mechanical installation works. Qualifications/Experience required: Prefer Advanced Modern Apprenticeship trained Electrically/Mechanical qualified within the following range: (a) degree (b) HND/HNC( c) OND/ONC (d) BTEC 4 0R 3 NVQ level 3 or above Completed authorised or competent persons training Technically competent to safely operate, make safe and test systems or installations IT literate Experienced shift engineer with a proven track record Flexible to work days and nights. Multi Skilled (or electrical 18th edition) Workshop machines and power tools experience IOSH managing safely. Experience of working in confirmed spaces & working at height CI trained in manufacturing environment. Lone worker experience (preferred) Knowledge of BRC and HACCP food standards If you are interested please apply directly or call Tom Kurczab at Premier Recruitment Group INDTKJOBS
Oct 07, 2025
Full time
Premier Recruitment Group has the privilege to recruit on behalf of our very prestigious client based in Rainham, East London, Essex. We are recruiting for experienced and forward thinking Multi-Skilled Shift Engineer . This is full time and permanent position and working for very well established company. Very interesting and varied role with a scope for progression. We are currently seeking Multi-Skilled Shift Engineer. This is a very exciting time to join a growing company regarded as experts in their industry, with opportunities for employees to develop within their role. Attractive salary and benefits. Work Pattern: Shift pattern 39 - 42 hrs per week (rotating days and nights) Days: 6am - 6pm Nights: 6pm - 6am The role: Reporting to Engineering Team Leader Follow GMP, Safety, Quality, Operational and Engineering procedures. Support production prioritising Safety, Quality and Production Volume. Comply with legislative and statutory requirements. Key areas of responsibility: Ensure all work is documented through the computerised maintenance management system (CMMS), shift handovers and PM worksheets. Awareness of site performance and KPI's, and support others to achieve targets for safety, Identify and control spare stock holding and procurement linking into PM system and CMMS Identifying and planning of maintenance and corrective actions in area from CMMS Carry out continuous improvement tasks identified within the area. Providing Technical expertise within area to other Technicians and Operators. Assist and deliver basic training for Operators and Technicians on equipment function and Supervise and take responsibility for Contractors on site. Understand the Service Building and Site Maintenance, complete basic tasks in these areas. Control work through the Permit to Work system. Proactively drive continuous improvements within own area liaising with other departments Offer improvement ideas for production equipment and facilities Electrical and mechanical installation works. Qualifications/Experience required: Prefer Advanced Modern Apprenticeship trained Electrically/Mechanical qualified within the following range: (a) degree (b) HND/HNC( c) OND/ONC (d) BTEC 4 0R 3 NVQ level 3 or above Completed authorised or competent persons training Technically competent to safely operate, make safe and test systems or installations IT literate Experienced shift engineer with a proven track record Flexible to work days and nights. Multi Skilled (or electrical 18th edition) Workshop machines and power tools experience IOSH managing safely. Experience of working in confirmed spaces & working at height CI trained in manufacturing environment. Lone worker experience (preferred) Knowledge of BRC and HACCP food standards If you are interested please apply directly or call Tom Kurczab at Premier Recruitment Group INDTKJOBS
Our client, a pharmaceutical manufacturer is looking for a Mechanical Maintenance Technician to provide support in a sterile products facility which will include the maintenance of washing, filling, and sealing machines. You will also support production with current engineering procedures and compliance with GMP. This is a clean room working environment which will require the successful candidate to wear gowns and protective clothing and equipment. Shift rota basis - 4 on, 4 off, 12 hour days 7am to 7pm (no nights) You will need to be a qualified engineer, with a strong background and maintenance experience working on clean utility systems within a GMP regulated manufacturing environment such as food, pharmaceutical or some other clean room environment. Engineering experience with purified water, water for injection, clean steam, compressed gases, and HVAC systems is required. Recognised Engineering Apprenticeship (Multi-Skilled would be an advantage) Relevant experience working in a clean room, pharmaceutical, food, manufacturing or GMP environment is essential. Benefits Pension scheme 7% matched contribution Rewards platform discounts on shopping, restaurants, holidays and more Generous holiday allowance Salary sacrifice schemes Sports and Social club Subsidised canteen Free parking If this role is initially of any interest, please apply and I will be able to provide a full job description and further information.
Oct 07, 2025
Full time
Our client, a pharmaceutical manufacturer is looking for a Mechanical Maintenance Technician to provide support in a sterile products facility which will include the maintenance of washing, filling, and sealing machines. You will also support production with current engineering procedures and compliance with GMP. This is a clean room working environment which will require the successful candidate to wear gowns and protective clothing and equipment. Shift rota basis - 4 on, 4 off, 12 hour days 7am to 7pm (no nights) You will need to be a qualified engineer, with a strong background and maintenance experience working on clean utility systems within a GMP regulated manufacturing environment such as food, pharmaceutical or some other clean room environment. Engineering experience with purified water, water for injection, clean steam, compressed gases, and HVAC systems is required. Recognised Engineering Apprenticeship (Multi-Skilled would be an advantage) Relevant experience working in a clean room, pharmaceutical, food, manufacturing or GMP environment is essential. Benefits Pension scheme 7% matched contribution Rewards platform discounts on shopping, restaurants, holidays and more Generous holiday allowance Salary sacrifice schemes Sports and Social club Subsidised canteen Free parking If this role is initially of any interest, please apply and I will be able to provide a full job description and further information.
Job Title: Senior Instrument Engineer Job ID: 36854 Location: Seal Sands, Middlesbrough Salary: £60,000 to £65,000 (dependent on experience) Hours: 40 hours per week - flexible working hours core hours Monday to Friday 9:30am to 3:00pm Contract/Permanent: Permanent Site Based/Office/Remote: Site and Office based Start Date: ASAP Benefits: 28 days holiday plus bank holidays Pension is Salary sacrifice 6% and we match up to another 3% Incentive bonus at 2% per quarter Onsite Parking Overview As a key member of the EC&I Team, the Senior Instrument Engineer will be responsible for the design, development, installation, management of all instrumentation and systems across the site. Provide technical support to the maintenance technicians. The Senior Instrument Engineer will support the Manufacturing facilities in production. Contribute and deliver capital projects. Ensure regulatory compliance. Main Tasks and Responsibilities: The Senior Instrument Engineer will development and design of advanced instrumentation and control systems for both new and existing processes. Author and review detailed specifications and comprehensive design documentation for complex instrumentation systems. The Senior Instrument Engineer will supervise and coordinate the installation and commissioning of instrumentation and control system, managing installation contractors and ensuring adherence to project timelines. Conduct thorough site inspections and rigorous testing to verify proper installation and optimal functionality of instrumentation systems. Collaborate closely with multidisciplinary project teams to seamlessly integrate instrumentation systems into overall plant operations. Develop, implement, and oversee maintenance schedules for instrumentation and control systems, ensuring long-term reliability and performance. Diagnose, troubleshoot, and resolve complex issues with instrumentation and control systems, providing expert guidance and support. Lead and actively contribute to HAZOP (Hazard and Operability Study) and LOPA (Layer of Protection Analysis) meetings, ensuring safety and compliance. Maintain meticulous documentation and records in strict accordance with COMAH regulations, ensuring regulatory compliance. Ensure all instrumentation and control systems comply with ATEX directives, providing expert oversight and guidance. Select, install, and validate ATEX-certified equipment in hazardous areas, ensuring safety and compliance. Identify, evaluate, and implement opportunities for process improvements, driving innovation and efficiency within the instrumentation domain. Oversee functional safety activities, including the development of Safety Requirements Specifications (SRS), arranging Functional Safety Assessments (FSA), and performing verification calculations to ensure compliance with safety standards. SHEQ: Ensure that all Health, Safety and Environmental requirements are met including (but not limited to) workplace organization, work instructions, risk assessments, COSHH assessments, housekeeping standards in accordance with GLP and GMP Demonstrable evidence of understanding the importance of creating a safe environment Working in a safe manner Follow appropriate and relevant practices and procedures Team Building & Incentive: Assist in the generation, data collection and monitoring of key performance indicators (KPIs). Organize and deliver SHE related training modules for staff. Communication: Verbal and written communication within Engineering Team. Participate in interdepartmental communications. Communication: Verbal and written communication within Engineering Team. Participate in interdepartmental communications. Confidentiality: Follow company policies and procedures to keep confidentiality on sensitive information. Skills & Qualifications: Bachelor's degree in Electrical, Instrumentation & Control Systems Engineering, or a related field. Functional safety qualifications (desirable) CompEx Ex12 (Desirable) Strong knowledge of COMAH and ATEX regulations and safety standards. Proficiency in instrumentation and control system design, installation, and maintenance. Excellent problem-solving and analytical skills. Strong communication and teamwork abilities. Proficiency in AutoCAD for designing and drafting instrumentation and control systems. Experience with batch processing systems (Desirable) Familiarity with PLC, DCS, and SCADA systems particularly Siemens PCS7 (Desirable) You have been sent this vacancy list by EC&I Partners. By clicking "accept", we will call you to discuss your current circumstancesand process your application. If you choose to"reject", please add a comment to help us understand why the role isn't for you. If you would like to talk to one of our consultants before making a decision, our phone number is (phone number removed). Please note our office hours are 9am-4pm Monday-Friday.
Oct 03, 2025
Full time
Job Title: Senior Instrument Engineer Job ID: 36854 Location: Seal Sands, Middlesbrough Salary: £60,000 to £65,000 (dependent on experience) Hours: 40 hours per week - flexible working hours core hours Monday to Friday 9:30am to 3:00pm Contract/Permanent: Permanent Site Based/Office/Remote: Site and Office based Start Date: ASAP Benefits: 28 days holiday plus bank holidays Pension is Salary sacrifice 6% and we match up to another 3% Incentive bonus at 2% per quarter Onsite Parking Overview As a key member of the EC&I Team, the Senior Instrument Engineer will be responsible for the design, development, installation, management of all instrumentation and systems across the site. Provide technical support to the maintenance technicians. The Senior Instrument Engineer will support the Manufacturing facilities in production. Contribute and deliver capital projects. Ensure regulatory compliance. Main Tasks and Responsibilities: The Senior Instrument Engineer will development and design of advanced instrumentation and control systems for both new and existing processes. Author and review detailed specifications and comprehensive design documentation for complex instrumentation systems. The Senior Instrument Engineer will supervise and coordinate the installation and commissioning of instrumentation and control system, managing installation contractors and ensuring adherence to project timelines. Conduct thorough site inspections and rigorous testing to verify proper installation and optimal functionality of instrumentation systems. Collaborate closely with multidisciplinary project teams to seamlessly integrate instrumentation systems into overall plant operations. Develop, implement, and oversee maintenance schedules for instrumentation and control systems, ensuring long-term reliability and performance. Diagnose, troubleshoot, and resolve complex issues with instrumentation and control systems, providing expert guidance and support. Lead and actively contribute to HAZOP (Hazard and Operability Study) and LOPA (Layer of Protection Analysis) meetings, ensuring safety and compliance. Maintain meticulous documentation and records in strict accordance with COMAH regulations, ensuring regulatory compliance. Ensure all instrumentation and control systems comply with ATEX directives, providing expert oversight and guidance. Select, install, and validate ATEX-certified equipment in hazardous areas, ensuring safety and compliance. Identify, evaluate, and implement opportunities for process improvements, driving innovation and efficiency within the instrumentation domain. Oversee functional safety activities, including the development of Safety Requirements Specifications (SRS), arranging Functional Safety Assessments (FSA), and performing verification calculations to ensure compliance with safety standards. SHEQ: Ensure that all Health, Safety and Environmental requirements are met including (but not limited to) workplace organization, work instructions, risk assessments, COSHH assessments, housekeeping standards in accordance with GLP and GMP Demonstrable evidence of understanding the importance of creating a safe environment Working in a safe manner Follow appropriate and relevant practices and procedures Team Building & Incentive: Assist in the generation, data collection and monitoring of key performance indicators (KPIs). Organize and deliver SHE related training modules for staff. Communication: Verbal and written communication within Engineering Team. Participate in interdepartmental communications. Communication: Verbal and written communication within Engineering Team. Participate in interdepartmental communications. Confidentiality: Follow company policies and procedures to keep confidentiality on sensitive information. Skills & Qualifications: Bachelor's degree in Electrical, Instrumentation & Control Systems Engineering, or a related field. Functional safety qualifications (desirable) CompEx Ex12 (Desirable) Strong knowledge of COMAH and ATEX regulations and safety standards. Proficiency in instrumentation and control system design, installation, and maintenance. Excellent problem-solving and analytical skills. Strong communication and teamwork abilities. Proficiency in AutoCAD for designing and drafting instrumentation and control systems. Experience with batch processing systems (Desirable) Familiarity with PLC, DCS, and SCADA systems particularly Siemens PCS7 (Desirable) You have been sent this vacancy list by EC&I Partners. By clicking "accept", we will call you to discuss your current circumstancesand process your application. If you choose to"reject", please add a comment to help us understand why the role isn't for you. If you would like to talk to one of our consultants before making a decision, our phone number is (phone number removed). Please note our office hours are 9am-4pm Monday-Friday.
Walker Cole International is searching for a Process Technician to join a global pharmaceutical manufacturing business at their high-volume, GMP-regulated production site in Cambridgeshire. As the Process Technician, your responsibilities will include: Operating and monitoring pharmaceutical manufacturing equipment in compliance with GMP, safety, and environmental regulations. Carrying out raw material charging, basic equipment maintenance, and cleaning procedures to support batch production. Maintaining accurate production records and reporting any deviations or quality issues. Supporting investigations, process improvements, and updates to Standard Operating Procedures (SOPs). Collaborating with cross-functional teams and adapting to changing operational needs across multiple production areas. To be successful as the Process Technician, you will have: Experience in a GMP-regulated or manufacturing environment (pharmaceuticals or chemical manufacturing preferred). Strong attention to detail, communication, and observational skills. A proactive, team-oriented approach with the flexibility to work across different production zones. Willingness to learn and contribute to continuous improvement initiatives. A strong standard of written English and basic numeracy for documentation and reporting. Manufacturing Technician Process Operator GMP Pharmaceutical Production Cleanroom Regulated Manufacturing
Oct 03, 2025
Contractor
Walker Cole International is searching for a Process Technician to join a global pharmaceutical manufacturing business at their high-volume, GMP-regulated production site in Cambridgeshire. As the Process Technician, your responsibilities will include: Operating and monitoring pharmaceutical manufacturing equipment in compliance with GMP, safety, and environmental regulations. Carrying out raw material charging, basic equipment maintenance, and cleaning procedures to support batch production. Maintaining accurate production records and reporting any deviations or quality issues. Supporting investigations, process improvements, and updates to Standard Operating Procedures (SOPs). Collaborating with cross-functional teams and adapting to changing operational needs across multiple production areas. To be successful as the Process Technician, you will have: Experience in a GMP-regulated or manufacturing environment (pharmaceuticals or chemical manufacturing preferred). Strong attention to detail, communication, and observational skills. A proactive, team-oriented approach with the flexibility to work across different production zones. Willingness to learn and contribute to continuous improvement initiatives. A strong standard of written English and basic numeracy for documentation and reporting. Manufacturing Technician Process Operator GMP Pharmaceutical Production Cleanroom Regulated Manufacturing
We have partnered with a valued client to assist their search for a number of Production Technicians. As the Production Technician of a designated process, you will operate processes such as Chromatography, Centrifugation or ultrafiltration and other fully automated processes, for which you will develop a full operational understanding. You will actively support an environment of continuous improvement ensuring that all quality and productivity targets are achieved through the optimum use of resources in a safe environment. You will use effective communication skills with all team members to ensure completion of the Production Manufacturing and filling plans. This is a fully on site role, operating on a 24/7 shift rotation. You will also require your own vehicle in order to access the facility. Key duties and responsibilities: The role of Production Technician will be hands on and varied. Here are some of the core responsibilities of the role: 1. Set up and operate automated and semi-automated manufacturing equipment as detailed within the department training matrix including Ultrafiltration, centrifuge and Chromatography processes as required. 2. Develop a full working knowledge in one or more of the processes in downstream processing. For example, having a sufficient understanding of chromatographic techniques in production in order to operate equipment in compliance unsupervised with the ability to solve problems. 3. To develop an understanding of the principles of gas and liquid filtration and be able to troubleshoot problems with filter testing and use. 4. Set up and operate automated and semi-automated manufacturing equipment. Carry out Process Formulations unsupervised and ensure that critical process samples are taken and submitted correctly in accordance with the procedure and relevant IMS. 5. Carry out sterile transfers of final product to the Aseptic filling suite in time to meet the scheduled filling plan. 6. To operate and trouble shoot Clean in Place systems for department specific static equipment. 7. pH and conductivity monitoring and testing. Skills and experience: 1. Prior manufacturing experience is essential, gained from pharmaceuticals, biopharmaceuticals, food, drink, brewing or similar highly regulated environments. 2. Experience of pH, conductivity and chromatography. 3. You will be expected to demonstrate excellent communication skills, excellent organisational skills and the ability to problem solve. 4. Any additional experience working in a clean room environment, or under GMP regulations would prove advantageous.
Oct 01, 2025
Full time
We have partnered with a valued client to assist their search for a number of Production Technicians. As the Production Technician of a designated process, you will operate processes such as Chromatography, Centrifugation or ultrafiltration and other fully automated processes, for which you will develop a full operational understanding. You will actively support an environment of continuous improvement ensuring that all quality and productivity targets are achieved through the optimum use of resources in a safe environment. You will use effective communication skills with all team members to ensure completion of the Production Manufacturing and filling plans. This is a fully on site role, operating on a 24/7 shift rotation. You will also require your own vehicle in order to access the facility. Key duties and responsibilities: The role of Production Technician will be hands on and varied. Here are some of the core responsibilities of the role: 1. Set up and operate automated and semi-automated manufacturing equipment as detailed within the department training matrix including Ultrafiltration, centrifuge and Chromatography processes as required. 2. Develop a full working knowledge in one or more of the processes in downstream processing. For example, having a sufficient understanding of chromatographic techniques in production in order to operate equipment in compliance unsupervised with the ability to solve problems. 3. To develop an understanding of the principles of gas and liquid filtration and be able to troubleshoot problems with filter testing and use. 4. Set up and operate automated and semi-automated manufacturing equipment. Carry out Process Formulations unsupervised and ensure that critical process samples are taken and submitted correctly in accordance with the procedure and relevant IMS. 5. Carry out sterile transfers of final product to the Aseptic filling suite in time to meet the scheduled filling plan. 6. To operate and trouble shoot Clean in Place systems for department specific static equipment. 7. pH and conductivity monitoring and testing. Skills and experience: 1. Prior manufacturing experience is essential, gained from pharmaceuticals, biopharmaceuticals, food, drink, brewing or similar highly regulated environments. 2. Experience of pH, conductivity and chromatography. 3. You will be expected to demonstrate excellent communication skills, excellent organisational skills and the ability to problem solve. 4. Any additional experience working in a clean room environment, or under GMP regulations would prove advantageous.
Talent STEM is supporting a well-established organisation in Kent to recruit a Manufacturing Technician. This is a permanent, full-time role offering the opportunity to work in a modern, regulated manufacturing environment, supporting the production of high-quality products across a technical sector. Key Responsibilities - Carry out daily manufacturing activities within a controlled production environment - Operate, monitor, and maintain process equipment in line with SOPs - Complete accurate production records, ensuring compliance with documentation standards - Report and support resolution of process deviations and equipment issues - Assist with planned maintenance, troubleshooting, and improvement projects - Work closely with quality teams to maintain operational standards - Manage incoming materials and maintain stock levels Maintain a safe, clean, and compliant working environment - Contribute to initiatives to improve efficiency, quality, and productivity Experience, Skills & Qualifications Essential: - Strong attention to detail with excellent record-keeping skills - Ability to follow structured processes in a regulated environment - Physically capable of lifting and handling materials - Flexibility to work a shift rota (including weekends) Desirable: - Previous experience in manufacturing, production or technical operations - Familiarity with quality or compliance standards (ISO, GMP, or similar) Next Steps If you are looking to develop your career in technical manufacturing and want to join a forward-looking organisation, Talent STEM would like to hear from you.
Sep 25, 2025
Full time
Talent STEM is supporting a well-established organisation in Kent to recruit a Manufacturing Technician. This is a permanent, full-time role offering the opportunity to work in a modern, regulated manufacturing environment, supporting the production of high-quality products across a technical sector. Key Responsibilities - Carry out daily manufacturing activities within a controlled production environment - Operate, monitor, and maintain process equipment in line with SOPs - Complete accurate production records, ensuring compliance with documentation standards - Report and support resolution of process deviations and equipment issues - Assist with planned maintenance, troubleshooting, and improvement projects - Work closely with quality teams to maintain operational standards - Manage incoming materials and maintain stock levels Maintain a safe, clean, and compliant working environment - Contribute to initiatives to improve efficiency, quality, and productivity Experience, Skills & Qualifications Essential: - Strong attention to detail with excellent record-keeping skills - Ability to follow structured processes in a regulated environment - Physically capable of lifting and handling materials - Flexibility to work a shift rota (including weekends) Desirable: - Previous experience in manufacturing, production or technical operations - Familiarity with quality or compliance standards (ISO, GMP, or similar) Next Steps If you are looking to develop your career in technical manufacturing and want to join a forward-looking organisation, Talent STEM would like to hear from you.
Randstad Construction & Property
Swindon, Wiltshire
Title: Maintenance Technician (Night Shift) Location: Swindon Shifts: 10pm - 10am, 3 days on 3 days off Salary: Circa £45,000 - £50,000 (inclusive of shift allowance) + Benefits Package Are you a skilled engineer looking to make a real impact in the world of medical technology? We're looking for a skilled Maintenance Technician to join our team. This is a critical role where you'll be instrumental in ensuring the smooth operation of our manufacturing processes, helping us to advance the world of health. As a Maintenance Technician, you'll provide both electrical and mechanical support across all areas of production. This includes working in clean rooms and other controlled environments while adhering to strict Good Manufacturing Practice (GMP) standards. Your day-to-day work will involve performing scheduled maintenance, monitoring machine performance, and quickly responding to breakdowns to minimize downtime. Key Responsibilities: Achieve and maintain production output standards. Maintain and service production machinery. Plan and execute preventative maintenance programs using a Computerized Maintenance Management System (CMMS). Manage machine spare parts inventory. Provide technical expertise and advice on equipment issues. Contribute to continuous improvement initiatives. Rapidly respond to and troubleshoot machine breakdowns. Monitor and analyze machine performance data. Assist with training activities for other team members. Pre-plan maintenance activities to optimize efficiency. Analyze breakdown frequencies to identify root causes and implement solutions. Participate in training and risk assessment programs. Experience Required: We're looking for someone with a background in Electrical/Mechanical Engineering or Tooling/Plastics processing. This could be through a formal apprenticeship, HND, or university degree. The ideal candidate will have Experience in a medium to high-volume manufacturing environment. A strong understanding of high-speed automated assembly processes. Proven skills in problem-solving and fault-finding on manufacturing machines. The ability to work independently with minimal supervision. Excellent communication skills to collaborate effectively with colleagues at all levels. Proficiency with computers, including Microsoft Office. Benefits: 24 Days Holiday (25 after 5 years) Share Save Scheme (matched up to £150/month) Matched Contribution Pension Scheme (up to 10% of salary) Life Assurance and Critical Illness Cover Private Medical Insurance Reward and Recognition Program Employee Assistance Program Flexible Benefits Subsidized Canteen Free Car Parking Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Sep 23, 2025
Full time
Title: Maintenance Technician (Night Shift) Location: Swindon Shifts: 10pm - 10am, 3 days on 3 days off Salary: Circa £45,000 - £50,000 (inclusive of shift allowance) + Benefits Package Are you a skilled engineer looking to make a real impact in the world of medical technology? We're looking for a skilled Maintenance Technician to join our team. This is a critical role where you'll be instrumental in ensuring the smooth operation of our manufacturing processes, helping us to advance the world of health. As a Maintenance Technician, you'll provide both electrical and mechanical support across all areas of production. This includes working in clean rooms and other controlled environments while adhering to strict Good Manufacturing Practice (GMP) standards. Your day-to-day work will involve performing scheduled maintenance, monitoring machine performance, and quickly responding to breakdowns to minimize downtime. Key Responsibilities: Achieve and maintain production output standards. Maintain and service production machinery. Plan and execute preventative maintenance programs using a Computerized Maintenance Management System (CMMS). Manage machine spare parts inventory. Provide technical expertise and advice on equipment issues. Contribute to continuous improvement initiatives. Rapidly respond to and troubleshoot machine breakdowns. Monitor and analyze machine performance data. Assist with training activities for other team members. Pre-plan maintenance activities to optimize efficiency. Analyze breakdown frequencies to identify root causes and implement solutions. Participate in training and risk assessment programs. Experience Required: We're looking for someone with a background in Electrical/Mechanical Engineering or Tooling/Plastics processing. This could be through a formal apprenticeship, HND, or university degree. The ideal candidate will have Experience in a medium to high-volume manufacturing environment. A strong understanding of high-speed automated assembly processes. Proven skills in problem-solving and fault-finding on manufacturing machines. The ability to work independently with minimal supervision. Excellent communication skills to collaborate effectively with colleagues at all levels. Proficiency with computers, including Microsoft Office. Benefits: 24 Days Holiday (25 after 5 years) Share Save Scheme (matched up to £150/month) Matched Contribution Pension Scheme (up to 10% of salary) Life Assurance and Critical Illness Cover Private Medical Insurance Reward and Recognition Program Employee Assistance Program Flexible Benefits Subsidized Canteen Free Car Parking Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Finishing Operator Process Location : Liverpool Are you passionate about manufacturing excellence and operational safety? Join our team as an Finishing Operator Process and play a key role in the production of high-quality products. Key Responsibilities As an Finishing Operator Technician, you ll be responsible for: Production Operations : Following SOPs and cGMP standards, conducting process testing, and ensuring water sampling schedules are met. Maintenance : Performing planned and reactive maintenance to ensure equipment reliability and process continuity. Problem Solving : Diagnosing equipment and process issues, identifying root causes, and implementing corrective actions. Documentation : Accurately completing batch production records, requisitions, and work requests. Continuous Improvement : Supporting equipment upgrades and contributing to the development of operating procedures. Safety & Compliance : Operating safely, reporting EHS incidents, and participating in investigations and proactive monitoring. IT Systems : Using process control systems and business tools such as CMMS, SAP, and Outlook Express. Training & Development : Managing your Individual Training Plan and sharing specialist knowledge with the team. Qualifications & Experience Minimum of 5 GCSEs (A C) including Maths and English. At least 2 years of experience in a manufacturing environment. Strong understanding of GMP and safety standards. Good problem-solving and diagnostic skills. Comfortable using IT systems and process control tools. Valid in date FLT licence
Sep 23, 2025
Seasonal
Finishing Operator Process Location : Liverpool Are you passionate about manufacturing excellence and operational safety? Join our team as an Finishing Operator Process and play a key role in the production of high-quality products. Key Responsibilities As an Finishing Operator Technician, you ll be responsible for: Production Operations : Following SOPs and cGMP standards, conducting process testing, and ensuring water sampling schedules are met. Maintenance : Performing planned and reactive maintenance to ensure equipment reliability and process continuity. Problem Solving : Diagnosing equipment and process issues, identifying root causes, and implementing corrective actions. Documentation : Accurately completing batch production records, requisitions, and work requests. Continuous Improvement : Supporting equipment upgrades and contributing to the development of operating procedures. Safety & Compliance : Operating safely, reporting EHS incidents, and participating in investigations and proactive monitoring. IT Systems : Using process control systems and business tools such as CMMS, SAP, and Outlook Express. Training & Development : Managing your Individual Training Plan and sharing specialist knowledge with the team. Qualifications & Experience Minimum of 5 GCSEs (A C) including Maths and English. At least 2 years of experience in a manufacturing environment. Strong understanding of GMP and safety standards. Good problem-solving and diagnostic skills. Comfortable using IT systems and process control tools. Valid in date FLT licence
Multiskilled Engineer/ Technician, Pharmaceutical Manufacturer Location: Skipton, North Yorkshire Type: Permanent Salary: £44,000 Hours: Days - Rotational weeks: Week 1: Mon Thurs (06:15-16:30) Week 2: Mon Thurs (07:15-16:00), Friday (07:30-14:00) NB there may be a requirement for applicants to move onto 1 weeks of backshift (4-14.00) Mon Thurs with a 25% additional shift premium) Our client, a global medical device manufacturer is looking to recruit for an experienced Multi- Skilled Technician/ Engineer. The site is state of the art and there is potential to move onto shift too for one of the working weeks/rotational (25% uplift ), this is a perfect role for someone looking to move into a GMP facility (from a BRC/ FMCG background), for someone looking to move to days or for people looking to further their career working for an established medical devices company. The Role: Maintenance of Medical Device Manufacturing equipment and processes located within controlled manufacturing areas. Carry out planned maintenance, calibration, machine changeover/set-up, breakdown repair of mechanical, electrical and instrumentation, associated with process equipment. Support to site Facilities as required, ensure recording of all work activities within the Computerised Maintenance Management System (CMMS), adhering to Good Manufacturing Practices (GMP) to ensure compliance within a regulated industry. Respond quickly to Maintenance support on manufacturing equipment, to achieve production output standards. Support to environmental and utilities systems at our manufacturing facility. Delivery of excellent customer service resulting in asset uptime, first time fix and quality workmanship. Actively involved in the development of departmental processes, procedures. Lead maintenance activities in areas of responsibility, both breakdown support and improvement work. Proactive support of a continuous improvement culture that develops factory assets, procedures, processes and systems. Comply with planned maintenance / calibration regimes, ensure work is completed and recorded in a timely manner within the CMMS. Ensure effective communications with stakeholders regarding equipment status, during breakdown support and any engineering requirements within Operational areas. Comply with site Health Safety and Environmental procedures and standards; ensure safe working conditions are maintained. The Person: Will hold a HNC or equivalent in Mechanical or Electrical Engineering, NVQ 3, ONC/HNC equivalent or have sufficient experience working as a Main Technician/ Eng in a similar setting Experience working as a Maintenance Technician and/or Engineer in a Pharmaceutical, Chemical, FMCG, Food setting is essential. The ideal candidate will hold additional electrical qualifications (17th/ 18th edition etc) Strong fault finding and problem solving skills (electrical with some mechanical). Proficient in IT / Microsoft applications (Word, Excel, Outlook, PowerPoint etc). Good interpersonal skills, effective communication skills needed. Good team player and able to work independently when needed.
Sep 22, 2025
Contractor
Multiskilled Engineer/ Technician, Pharmaceutical Manufacturer Location: Skipton, North Yorkshire Type: Permanent Salary: £44,000 Hours: Days - Rotational weeks: Week 1: Mon Thurs (06:15-16:30) Week 2: Mon Thurs (07:15-16:00), Friday (07:30-14:00) NB there may be a requirement for applicants to move onto 1 weeks of backshift (4-14.00) Mon Thurs with a 25% additional shift premium) Our client, a global medical device manufacturer is looking to recruit for an experienced Multi- Skilled Technician/ Engineer. The site is state of the art and there is potential to move onto shift too for one of the working weeks/rotational (25% uplift ), this is a perfect role for someone looking to move into a GMP facility (from a BRC/ FMCG background), for someone looking to move to days or for people looking to further their career working for an established medical devices company. The Role: Maintenance of Medical Device Manufacturing equipment and processes located within controlled manufacturing areas. Carry out planned maintenance, calibration, machine changeover/set-up, breakdown repair of mechanical, electrical and instrumentation, associated with process equipment. Support to site Facilities as required, ensure recording of all work activities within the Computerised Maintenance Management System (CMMS), adhering to Good Manufacturing Practices (GMP) to ensure compliance within a regulated industry. Respond quickly to Maintenance support on manufacturing equipment, to achieve production output standards. Support to environmental and utilities systems at our manufacturing facility. Delivery of excellent customer service resulting in asset uptime, first time fix and quality workmanship. Actively involved in the development of departmental processes, procedures. Lead maintenance activities in areas of responsibility, both breakdown support and improvement work. Proactive support of a continuous improvement culture that develops factory assets, procedures, processes and systems. Comply with planned maintenance / calibration regimes, ensure work is completed and recorded in a timely manner within the CMMS. Ensure effective communications with stakeholders regarding equipment status, during breakdown support and any engineering requirements within Operational areas. Comply with site Health Safety and Environmental procedures and standards; ensure safe working conditions are maintained. The Person: Will hold a HNC or equivalent in Mechanical or Electrical Engineering, NVQ 3, ONC/HNC equivalent or have sufficient experience working as a Main Technician/ Eng in a similar setting Experience working as a Maintenance Technician and/or Engineer in a Pharmaceutical, Chemical, FMCG, Food setting is essential. The ideal candidate will hold additional electrical qualifications (17th/ 18th edition etc) Strong fault finding and problem solving skills (electrical with some mechanical). Proficient in IT / Microsoft applications (Word, Excel, Outlook, PowerPoint etc). Good interpersonal skills, effective communication skills needed. Good team player and able to work independently when needed.
