43 jobs found

QC Lab Technician (Weekend Days) Wigan Friday to Sunday 6am to 6pm £35,025 My client, who is a leading manufacturer withing polymers and synthetic resins, is seeking an experienced QC Lab Technician to join their team. QC Lab Technician The Role The main purpose of the QC Laboratory Technician is to ensure the quality of all goods entering or leaving the company. All aspects of site operations must be completed in a safe, timely and professional manner reporting any problems which arise. QC Lab Technician Responsibilities Ensure the timely completion of product testing in process and final analysis / specifications. Prepare pre-shipment samples and ensure accurate documentation Testing of incoming materials, as and when required Carry out project / development work when assigned Carry out procedures relevant to the test equipment calibration schedule Carry out test method training for operators and other assigned deputies Issue of accurate process adjustment instructions to production Complete inspection and test procedures, as specified in the product manufacturing instructions, and complete the respective quality documents in a timely manner Identify non - conforming material or process operations and take action to arrange for re-processing, usage under concession or safe disposal of non - conforming material / product and the completion of the corresponding quality records To inform the Senior QC Chemist or QC Lab Manager immediately of any abnormal situation which cannot be dealt with successfully To authorise changes in product specifications, formulas, and manufacturing instructions. (In the absence of Works QC Chemist Liaise with Senior QC Chemist, QC Lab Manager and/or Managing Director for technical matters and concessions Respond to non-conformance corrective and preventive actions (customer complaints, process failures) in a timely manner. Report to Senior QC Chemist or QC Lab Manager regarding such actions Immediately report any incident which the management need to address using the appropriate reporting systems in place Respond to required corrective and preventive action in a timely manner Ensure that all duties/activities associated within quality control department are carried out in compliance to Health, Safety, Environment and Quality management systems QC Lab Technician The Candidate Skills / Knowledge / Experience Essential Desirable Ability to follow chemistry testing techniques X Experience working in a busy industrial lab X Practical hands-on attitude X Strong verbal and written communication skills X Willingness to comply with safety and quality regulations, including wearing and maintaining PPE X A desire to work with team members to improve processes and product quality X Flexible approach to working X Excellent attention to detail including housekeeping X Calibration X Troubleshooting issues with Lab equipment and processes X Good understanding of sampling and product testing X Experience of working in a chemical / process type industry COMAH site experience would be advantageous X Familiar with management systems 9001, 14001 & 45001 X Ability to complete root cause analysis and contribute to investigation X Understanding of chemical processes X Qualifications Essential Desirable BTEC / HNC in Chemistry (or equivalent Level 4 qualification in chemistry) X Educated to Degree level in relevant subject X IOSH Managing Safely X First Aid training X Internal Auditor X QC Lab Technician Benefits 28 days - includes bank holiday entitlement Company Pension - Company contributes 3% and the employee contributes 5% Healthcare - Eligible for BUPA cover after 6 months probationary period QC Lab Technician Key Skills Quality Coordinator, Quality Lab Controller, Quality Lab Tester, Quality Lab Technician, Quality Laboratory Analyst, QC Laboratory Technician Please contact Marie Brisson at Winsearch UK for further information - (url removed) Winsearch acts as an employment agency for permanent staff. We recruit for roles based in Engineering & Manufacturing, Food & Drinks, Pharmaceutical, Supply Chain & Procurement and Professional Services. View our latest jobs today on our website(url removed) and follow us on LinkedIn. Manh INDWIN 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

Technical Sales Specialist Reading 32,000 - 41,000 Basic + Bonuses + Commission (OTE 48,000+) + Remote Working + Technical Training + Private Healthcare + Holidays + Career Progression + Industry-Leading Pension + Company Car / Car Allowance + Company Credit Card + Immediate Start Are you an Analytical Chemist or Laboratory Technician looking to take your career in a new direction? Do you have a chemistry background and want to break into a Technical Sales Specialist role with a global leader who will provide full product and sales training? Join an industry-leading manufacturer of scientific measuring and analytical equipment as a Technical Sales Specialist , where you'll use your technical knowledge to support customers across the pharmaceutical, chemical and laboratory sectors. You'll receive specialist training, build long-term customer relationships and earn an excellent package with realistic progression opportunities. Your Role As A Technical Sales Specialist Will Include: Technical Sales Specialist Role Managing Existing & New Customer Accounts Solution Selling Analytical & Laboratory Equipment Visiting Pharmaceutical, Chemical & Industrial Customers Remote Role - Covering The South Of England As A Technical Sales Specialist You Will Have: Degree or Equivalent Qualification In Chemistry Experience As An Analytical Chemist, QC Chemist or Laboratory Technician Looking To Move Into A Technical Sales Role Full UK Driving Licence Please Apply Or Call Charlie Auburn on (phone number removed)

Job Title: Laboratory Technician - Hair Care Location: Manchester Salary: 26,000 - 29,000 DOE Term: Fixed-Term Contract - 12 months Benefits: Join a global company with a dedicated UK-based suite of laboratories, working within a small, close-knit team on a wide range of products. Full training provided. SRG are working with an innovative, global company who specialise in the creation of speciality chemical ingredients for a range of markets. The are now looking for a Laboratory Technician to join their Hair Care team on a 12-month fixed-term contract. This is a great opportunity to build hands-on laboratory experience with a business that invests heavily in developing its people, working across the evaluation of hair dyes and hair care actives, applications chemistry and formulation of hair care products used and sold worldwide. Working Hours: Monday to Friday, 8.30am - 4.40pm (37.5 hours a week), 32 days holiday Role / Description Evaluation of hair dyes across a range of substrates and formulations, including wash and light fastness testing Assessing hair and scalp care actives to support their development and commercialisation Preparing samples, reagents, buffers and batch formulations for testing and analysis Recording experimental data accurately and preparing clear technical reports Maintaining and developing technical databases for the Hair Care team Keeping laboratory areas clean, organised and well-stocked, and maintaining lab equipment Preparing COSHH and risk assessments, working to company health, safety and quality procedures Supporting commercial and R&D project teams to help deliver new products to market Requirements Minimum degree (or equivalent) in Cosmetic Science, Chemistry, Formulation sciences or relevant scientific discipline Practical laboratory experience gained through industry, a placement year, internship or university Full right to work in the UK there is no sponsorship available for this role. SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV. For more information regarding this position or any others, please call Rhi on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

FINANCE ASSISTANT - Remote - One day a week in London Company: Stablepharma Ltd - Based in London & Madrid Location: Remote (UK-based) with travel to London 1 day per week Reporting to: Financial Controller Contract: Full-time (5 days per week) Must be able to work, or used to working autonomously. Role Overview This role supports the Financial Controller in managing the day-to-day finance operations of an early-stage pharmaceutical company. The Finance Assistant will take ownership of transactional and administrative finance activities, ensuring accurate records and timely processing, thereby enabling the Financial Controller to focus more on strategic, reporting, and commercial activities. Key Responsibilities Processing and posting supplier invoices in Xero, ensuring accurate coding Processing purchase orders and matching to invoices Preparing weekly/monthly payment runs for approval Administering employee expenses and ensuring compliance with company policy Performing bank and card reconciliation's Reconciliation of accounts, management accounts support Assistance with budget preparation Support VAT return preparation Maintaining organised financial records for audit and grant reporting purposes Liaising with outsourced bookkeepers, accountants and auditors (UK and Spain) on routine matters Responding to internal queries relating to invoices, expenses, and payments Skills and Experience Trainee bookkeeper, accounting technician, or equivalent experience Experience using ERP/accounting systems (Xero preferred) Experience or exposure to VAT returns desirable Strong Excel and Microsoft Word skills (essential) Strong attention to detail and accuracy Organised with ability to manage multiple tasks Comfortable working remotely with minimal supervision Good communication skills; comfortable working as part of a small, dynamic team Qualifications PART QUAL AAT or similar accounting qualification preferred, or QBE . - Qualified by experience. MINIMUM two years as finance assistant/assistant accountant Working Arrangements Remote-first role with requirement to attend London office approximately one day per week. Opportunity to gain broad exposure across finance in a high-growth start-up environment. Holiday - 28 days + Bank Holidays Benefits Medical and dental insurance with BUPA 3% pension contribution Share options after at least one year All office equipment and computer hardware provided. Start date: September 2026

FINANCE ASSISTANT - Remote - One day a week in London Company: Stablepharma Ltd - Based in London & Madrid Location: Remote (UK-based) with travel to London 1 day per week Reporting to: Financial Controller Contract: Full-time (5 days per week) Must be able to work, or used to working autonomously. Role Overview This role supports the Financial Controller in managing the day-to-day finance operations of an early-stage pharmaceutical company. The Finance Assistant will take ownership of transactional and administrative finance activities, ensuring accurate records and timely processing, thereby enabling the Financial Controller to focus more on strategic, reporting, and commercial activities. Key Responsibilities Processing and posting supplier invoices in Xero, ensuring accurate coding Processing purchase orders and matching to invoices Preparing weekly/monthly payment runs for approval Administering employee expenses and ensuring compliance with company policy Performing bank and card reconciliation's Reconciliation of accounts, management accounts support Assistance with budget preparation Support VAT return preparation Maintaining organised financial records for audit and grant reporting purposes Liaising with outsourced bookkeepers, accountants and auditors (UK and Spain) on routine matters Responding to internal queries relating to invoices, expenses, and payments Skills and Experience Trainee bookkeeper, accounting technician, or equivalent experience Experience using ERP/accounting systems (Xero preferred) Experience or exposure to VAT returns desirable Strong Excel and Microsoft Word skills (essential) Strong attention to detail and accuracy Organised with ability to manage multiple tasks Comfortable working remotely with minimal supervision Good communication skills; comfortable working as part of a small, dynamic team Qualifications PART QUAL AAT or similar accounting qualification preferred, or QBE . - Qualified by experience. MINIMUM two years as finance assistant/assistant accountant Working Arrangements Remote-first role with requirement to attend London office approximately one day per week. Opportunity to gain broad exposure across finance in a high-growth start-up environment. Holiday - 28 days + Bank Holidays Benefits Medical and dental insurance with BUPA 3% pension contribution Share options after at least one year All office equipment and computer hardware provided. Start date: September 2026

Contract Personnel are seeking an experienced Quality Control & Compliance Manager to join a renowed manufacturing business, and take lead of Quality Management System (QMS) and ensure the manufacture of safe, legal and high-quality products that consistently meet customer and regulatory requirements. Reporting to the Operations Manager, you will be responsible for Quality Control, Food Safety, Product Compliance and Continuous Improvement across the business. Working closely with Production, Purchasing, Warehouse and Sales, you will drive quality standards, support operational excellence and promote a strong culture of compliance. We are ideally looking for someone with strong experience in the food, food supplement, nutraceutical, or pharmaceutical manufacturing sector who is commercially aware, passionate about quality, and confident leading both people and systems. Key Responsibilities Lead and continuously improve the Quality Management System (QMS). Maintain compliance with BRCGS Food Safety, HACCP, GMP and relevant food legislation. Manage all quality control activities from raw material receipt through to finished product release. Lead internal and external audits, including BRCGS certification and customer audits. Investigate quality issues and customer complaints, implementing effective corrective and preventive actions. Manage supplier approval and quality assurance processes. Monitor quality performance, analyse trends and drive continuous improvement initiatives. Lead the Environmental Monitoring Programme and oversee product testing activities. Manage, coach and develop the Quality Control Technician. Provide technical guidance and support across the business. About You The successful candidate will have: Previous experience in a Quality or Technical Management role within food manufacturing. Strong working knowledge of BRCGS Food Safety, HACCP, GMP and food legislation. Experience managing audits and Quality Management Systems. Excellent problem-solving, analytical and organisational skills. Strong leadership, communication and stakeholder management abilities. A proactive approach with a passion for continuous improvement and maintaining the highest quality standards. If you are passionate about playing a pivotal role in driving a positive quality culture across the business you work for, this is for you. About Contract Personnel: Contract Personnel are one of East Anglia s longest-standing, leading independent recruitment agencies established in 1989. Offering Temporary and Permanent recruitment solutions, we keep you updated with the latest opportunities and support you throughout your job search. Contact Rosie or Hannah at Contract Personnel for more details today!

We are recruiting a Packaging Technician to join our clients packaging team within a manufacturing environment. You will work in line with Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP) to ensure products are packed safely, accurately, and to the required quality standards and output targets. Location: Worthing, East Sussex Salary: 14.48 per hour paying up yo 16.09 per hour Shift: Rotating Shift Pattern (Week 1 Early shift 07:00-14:30 - Week 2 - Late shift 14:15 - 22:00) 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. Key Responsibilities of a Packaging Technician: Operate as part of the packaging team, following relevant SOPs for the line/area Carry out packaging activities in line with GMP standards Deliver planned output while maintaining high quality standards Ensure products are produced to the required specification and within agreed time frames Follow all site safety requirements at all times Wear the correct PPE as required Keep training records up to date Maintain work areas to 5S standards (clean, organised, safe working environment) Adhere strictly to timekeeping (start/end of shift and breaks) Requirements for the ideal Packaging Technician: Previous experience in a packaging/manufacturing/production environment is desirable (training may be provided) Ability to follow procedures and work to quality and safety standards Reliable, punctual, and able to work as part of a team GCSE Maths & English (or equivalent) is preferable 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, corporate 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 Friendly 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.

PERMANENT JOB OPPORTUNITIES AVAILABLE - MACHINE OPERATOR Are you an experienced Machine Operator looking for stability in your next job role and are you happy working 4 on 4 off shifts (rotating days and nights)? We are proud to be working with a long-standing manufacturer in Telford (Shropshire) who are seeking a Machine Operator to join them on a straight permanent basis, the starting salary for these roles will range between £35,000 - £36,300 per annum and the working hours are 6am-6pm / 6pm - 6am (4 on 4 off shifts rotating days and nights). We are looking for people who live within a 25-mile radius of Telford (Shropshire), and the hiring manager is looking for people who have a minimum of 3 years experience within a similar role. People who have worked in similar job roles such as a Production Technician, Manufacturing Technician, Technical Operator, Process Operator, Conversion Operator, Rewind Operator, Core Rewinder, Skilled Machine Operator, Machine Setter or Skilled Machinist would be well received. The company conduct a 2 stage interview process, the first stage would involve you completing an on-line SHL assessment, with the view to you then being invited to the factory for an on site interview and full factory tour. What's on offer? Highly Competitive Salary: £35,000 £36,300 per annum. Shift Pattern: Consistent 4 on, 4 off (12-hour days and nights, 6-6) allowing for great work-life balance. Stability: A permanent position with a leading manufacturer that values long-term commitment. Growth: A clear path to develop your technical skills in a supportive, high-tech environment. The On-boarding Process: A brief on-line technical assessment to verify your core skills. An on-site interview and factory tour an opportunity for you to see the operation and meet the team. Your Role: As a core member of the production team, you will ensure our high-speed machinery operates at peak efficiency. You will: Set up and operate high-speed machinery with a focus on accuracy and speed. Troubleshoot and adjust machinery to minimize downtime and maximize productivity. Maintain quality standards by conducting regular checks and keeping precise production records. Collaborate with the wider team to exceed daily production targets. What You Bring: Experience: A minimum of 3 years in a similar role (e.g., Production Technician, Manufacturing Technician, Technical Operator, Rewind Operator, or Machine Setter). Industry Knowledge: Experience within the FMCG, Packaging, Food Manufacturing, Print, or Pharmaceutical sectors are highly desirable. Technical Aptitude: Confidence in making minor machine adjustments and performing routine maintenance. Reliability: You live within a 25-mile radius of Telford and are looking for a long-term career move. Ready to advance your career? Apply today with your latest CV. We are looking for people who take pride in their work and want to be part of a winning manufacturing culture. Your CV will be forwarded to Jonathan Lee Recruitment, a leading engineering and manufacturing recruitment consultancy established in 1978. The services advertised by Jonathan Lee Recruitment are those of an Employment Agency. In order for your CV to be processed effectively, please ensure your name, email address, phone number and location (post code OR town OR county, as a minimum) are included.

We are seeking a detail-oriented and experienced Manufacturing Technician to join our client's pharmaceutical production team. The successful candidate will be responsible for supporting manufacturing and quality control processes within a regulated laboratory environment. This role offers an excellent opportunity for someone who wants to expand experience within highly advanced pharmaceutical operation and is prepared to work in a cleanroom environment and ensure compliance with cGMP regulations at all times. The ideal candidate will therefore have a pharmaceutical background and have ideally gained experience within a cGMP, FDA and MHRA regulated environment. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience of pharmaceutical manufacturing or working in a cleanroom environment Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Be flexibile - to ensure production output and client demands Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Previous cGMP (current Good Manufacturing Practice) experience Good practical skills Demonstrates good literacy and numeracy skills Required: Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Please note: Only candidates with permanent Right to Work in the UK will be considered. Benefits Private Medical Insurance and Health Cash Plan with Bupa Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please email your CV or apply through this website.

Overview We are looking for detail-oriented, reliable and trustworthy Cleaner to join our client's Pharmaceutical Manufacturing team. The successful candidate will be responsible for all cleaning aspects within a cGMP regulated environment usually in a Clean Room. This role offers an excellent opportunity for someone who wants to have a higher purpose in the job and work for stable company with market-leading work benefits. The shift pattern is rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Perform routine and deep cleaning of cleanrooms, production areas, and equipment in line with cGMP standards Clean floors, walls, ceilings, equipment parts and exteriors, fixtures, and controlled surfaces using approved methods and materials Follow validated cleaning procedures and schedules strictly Use approved disinfectants and cleaning agents correctly, including rotation schedules cGMP & Compliance Adhere to cGMP, SOPs, and site-specific cleaning instructions at all times Complete all required cleaning logs, checklists, and documentation accurately and in real time Report any deviations, contamination risks, or damaged equipment immediately Comply with regulatory requirements (e.g. MHRA, FDA, EMA as applicable) Wear required PPE and cleanroom garments correctly at all times Follow gowning, hand hygiene, and entry/exit procedures for controlled areas Handle cleaning chemicals safely and in accordance with COSHH or equivalent regulations Maintain a safe and tidy working environment Operate and maintain cleaning equipment such as mops, vacuum systems, and scrubbers. Ensure cleaning tools are stored, labelled, and segregated correctly to prevent cross-contamination Previous Experience Previous cleaning experience in a regulated environment (pharmaceutical, medical device, food, or healthcare preferred) Strong attention to detail and ability to follow strict procedures Good understanding of hygiene and contamination control Ability to read and follow written SOPs and complete documentation Experience working in cGMP cleanroom environments would be an advantage Knowledge of pharmaceutical regulatory standards is a bonus Basic understanding of validation and audit processes would be helpful Computer literate to complete SOP's and Benefits Private Medical Insurance and Health Cash Plan Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking Discretionary annual bonus This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, good levels of physical fitness, willingness to work closely with manufacturing and QC teams, and the ability to follow detailed procedures meticulously. Please note: Only candidates with permanent Right to Work in the UK will be considered. Please apply through this website.

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.

Laboratory Technician - Pharmaceuticals Pharmaceuticals Supply Chain, tissues, bloods, samples, drugs Salary: £28,000k - £30,000k Type: Full time permanent site based - 1 week in 4 oncall 24/7 @ £220 allowance Location: Rochdale M62 / North West / Oldham Sector: Pharmaceuticals / Life science supply chain, warehouse, logistics & distribution This is an excellent opportunity to join a global pharmaceuticals organisation in a Laboratory & Facilities Technician appointment. You will work internally supporting site teams and managers that are responsible for several large blood, tissue, sample pharmaceuticals / NHS storage contracts, ensuring laboratories / site storage and logistics Quality Management Systems KPI s are achieved. Key Areas: - Laboratory Technician Managing Sample lifecycle - process quality and assurance Working to GMP ISO 9001 Quality System requirements experience and standards Planning and support of operations projects Working at negative temperatures / freezers / chillers / storage Administration and audit of pharmaceutical products The key responsibilities: - Laboratory Storage Operations: Receive, receipt, and physically check incoming samples against client documentation, ensuring accuracy of quantities, identification, and condition. Store and manage customer products within designated stability chambers and storage areas in accordance with approved protocols, SOPs, and GMP/GLP requirements. Remove samples at defined protocol time points and prepare samples for dispatch or testing, issuing associated documentation (e.g. certificates, receipt/return notes). Deliver services to the portfolio of customers from the life Science / pharma sector Able to work supportively as part of a team and with a friendly and approachable personality Support the Quality team and Auditors in maintaining: ISO 9001 Quality System requirements Liaising with clients and UK quality staff to ensure clients receive complete and accurate information concerning practical operation of the suite Leading and supervising the pharmaceutical administration team to ensure efficient and effective operation at all times Reporting capacity levels and issues in a timely and accurate fashion relevant stakeholders Ensuring GMP and IMB regulations are applied and adhered to at all times throughout the site Ensure integrity of customer products are maintained at all times. Qualifications / experience High attention to detail with strong organisational and record-keeping skills. Experience working in a regulated environment (GMP, GLP, GxP) desirable. Good written and verbal communication skills. A-levels in a Science, Maths, English or equivalent qualifications Previous laboratory storage or scientific services experience desirable.

Multi-Skilled Maintenance Engineer location: Wembley, North West London Salary: 55,000 + Benefits Shift Pattern: 4 On 4 Off (Days Only) Job Type: Permanent The Opportunity A well-established manufacturing business is seeking a Multi-Skilled Maintenance Engineer to join its engineering team at a modern production facility in North West London. This is an excellent opportunity for a Maintenance Engineer looking to work within a fast-paced, highly automated manufacturing environment where engineering excellence, equipment reliability, and continuous improvement are a core focus. The successful candidate will play a key role in maintaining production performance, reducing downtime, and driving operational efficiency across the site. The company has an outstanding reputation for investing in its people, promoting from within, and creating a positive working culture with low staff turnover. Engineers are empowered to take ownership of their areas, contribute to improvement projects, and develop their skills through ongoing training and support. Working on a 4 on 4 off days-only shift pattern , you will join a stable and growing engineering team within a business that continues to invest heavily in both its facilities and workforce. Responsibilities Carry out planned preventative maintenance (PPM) activities across manufacturing equipment Diagnose and repair electrical and mechanical faults Respond effectively to equipment breakdowns and minimise production disruption Support continuous improvement and reliability initiatives Conduct Root Cause Analysis (RCA) to eliminate recurring failures Maintain accurate maintenance records using a CMMS system Work closely with production teams to maximise equipment availability Support machinery upgrades, installations, and engineering projects Ensure all maintenance activities are completed in line with Health & Safety requirements Skills & Experience Completed Engineering Apprenticeship, NVQ Level 3, City & Guilds, HNC, or equivalent qualification Previous experience working as a Maintenance Engineer within FMCG, food manufacturing, beverage, packaging, pharmaceutical, logistics, or similar production environments Electrically biased engineer preferred, although strong multi-skilled engineers with a good balance of electrical and mechanical experience will also be considered Strong electrical and mechanical fault-finding skills Experience working with automated production equipment and PLC-controlled machinery Knowledge of conveyors, motors, drives, sensors, pumps, pneumatics, and automation systems Experience using SAP PM, Maximo, Pirana, Shire, CMMS, or similar maintenance management systems Ability to work effectively within a fast-paced manufacturing operation What's On Offer? 55,000 annual salary 4 On 4 Off Days-Only Shift Pattern Overtime opportunities available Pension scheme Ongoing training and development Clear career progression opportunities Stable and growing manufacturing business Modern production environment Strong investment in engineering and technology Excellent company culture with low staff turnover Apply Now If you're a Maintenance Engineer, Multi-Skilled Maintenance Engineer, Shift Engineer, Electrical Maintenance Engineer, Engineering Technician, or Multi-Skilled Engineer looking for your next challenge in North West London, we'd love to hear from you. For more information on this opportunity, please apply or contact: Xaviour Davids (phone number removed) (url removed) Proactive Global is committed to equality in the workplace and is an equal opportunity employer. Proactive Global is acting as an Employment Business in relation to this vacancy.

Critical Shift Engineer - Data Centre Maintenance Guildford, Surrey 52,000 + 10% Bonus + Outstanding Client-Side Benefits An exciting opportunity has arisen for a Critical Shift Engineer to join a leading owner and operator of critical infrastructure, delivering engineering maintenance within a state-of-the-art Data Centre Maintenance environment in Guildford, Surrey . Working a continental nights-only shift pattern (7:00pm-7:00am) , this Critical Shift Engineer will be responsible for the operation, maintenance and fault-finding of critical electrical and mechanical infrastructure, ensuring maximum uptime across a highly resilient facility. This is a rare opportunity to join a client-side organisation renowned for investing in its engineers through exceptional training, career progression and one of the strongest benefits packages in the industry. The successful Critical Shift Engineer will ideally have previous experience within Data Centre Maintenance or another critical environment such as healthcare, banking, pharmaceuticals, manufacturing or mission-critical commercial buildings. LVAP or HVAP experience would be highly advantageous. Requirements City & Guilds Level 3 (or equivalent) in Electrical or Mechanical Engineering Previous experience within Data Centre Maintenance or another critical environment preferred Strong fault-finding experience across critical M&E systems Knowledge of UPS, generators, transformers, LV distribution, BMS, CRAC/CRAH units and chilled water systems LVAP or HVAP experience desirable Experience producing or working to SOPs, EOPs and switching procedures Salary & Benefits 52,000 salary 10% annual bonus Overtime available 20 shift days annual leave Pension matched up to 5% Private medical insurance Life assurance (4x salary) Enhanced maternity & paternity pay Electric vehicle salary sacrifice scheme Subsidised gym membership Cycle to Work scheme Free parking Excellent training and career progression Shift Engineer Building Maintenance Mechanical & Electrical Engineering Data Centre Maintenance Shift Technician Critical Engineering Site Engineer Guildford, Surrey

Join a Growing, Innovative Online Pharmacy Founded in 1999, Clarity Pharma Ltd is one of the UK's leading pharmaceutical and healthcare distribution providers. We deliver bespoke end-to-end distribution solutions, combining industry expertise with the latest market insights and strategies. Working alongside a wide range of pharmaceutical manufacturers, we provide storage and distribution services to wholesalers, pharmacies, GP surgeries, and hospitals nationwide. Due to continued growth, we are looking for an experienced Accuracy Checking Technician to join our thriving private online pharmacy team. This is an exciting opportunity to play a vital role in ensuring patients across the UK receive their medication safely, accurately, and efficiently. If you are a GPhC-registered Pharmacy Technician with an accredited checking qualification and a passion for patient safety, we'd love to hear from you. The Role As an Accuracy Checking Technician, you will be responsible for carrying out the final accuracy check of dispensed prescriptions that have been clinically screened by a pharmacist. Working within a fast-paced online pharmacy environment, you will help ensure the highest standards of accuracy, compliance, and patient care. Key Responsibilities Complete final accuracy checks on dispensed medicines and associated items in line with SOPs, regulatory requirements, and professional standards. Ensure prescriptions are accurately assembled, labelled, packed, and ready for dispatch. Work closely with pharmacists, dispensers, and support staff to maintain efficient dispensary workflows. Identify, report, and escalate dispensing errors, discrepancies, and near misses through appropriate governance procedures. Support prescription processing, stock management, and workflow organisation within a high-volume digital pharmacy environment. Communicate professionally with colleagues, patients, and external partners via telephone, email, and digital systems where required. Maintain accurate records and ensure compliance with confidentiality, GDPR, and information governance requirements. Contribute to audits, continuous improvement initiatives, and safe working practices across the pharmacy. About You We're looking for a highly organised and detail-focused individual who thrives in a regulated environment and is committed to delivering exceptional patient care. Essential Skills & Experience GPhC-registered Pharmacy Technician with an accredited checking qualification. Previous experience working within a pharmacy dispensary environment. Excellent attention to detail with a strong focus on patient safety and accuracy. Ability to work effectively under pressure and manage competing priorities. Strong IT skills and confidence using pharmacy systems and digital workflows. Excellent communication, teamwork, and problem-solving abilities. Desirable Experience Experience within a private, online, mail-order, or hub-based pharmacy. Familiarity with automated or centralised dispensing processes. Experience supporting high-volume prescription workflows. Knowledge of medicines governance, stock control procedures, and audit processes. Why Join Clarity Pharma? 25 days annual leave plus our Birthday Club. On-site parking. Company social events. Opportunity to join a growing and ambitious healthcare organisation. Supportive and collaborative team environment. Career development opportunities within a rapidly expanding business. Working Environment This is a full-time onsite role in a busy private online pharmacy. You ll be working in a fast-paced, regulated environment where accuracy, efficiency, and confidentiality are essential. Apply Today If you're looking for your next challenge and want to be part of a forward-thinking pharmacy team that is transforming healthcare delivery across the UK, we'd love to hear from you. Apply now and become part of the Clarity Pharma team.

Join a Growing, Innovative Online Pharmacy Founded in 1999, Clarity Pharma Ltd is one of the UK's leading pharmaceutical and healthcare distribution providers. We deliver bespoke end-to-end distribution solutions, combining industry expertise with the latest market insights and strategies. Working alongside a wide range of pharmaceutical manufacturers, we provide storage and distribution services to wholesalers, pharmacies, GP surgeries, and hospitals nationwide. Due to continued growth, we are looking for a GPhC-registered Pharmacist to join our thriving private online pharmacy team based in Stansted. This is an exciting opportunity to play a key role in delivering safe, effective, and patient-focused healthcare services to patients across the UK. If you are a proactive pharmacist with strong clinical judgement and a passion for delivering exceptional patient care, we'd love to hear from you. The Role As a Pharmacist within our online pharmacy team, you will be responsible for ensuring the safe and appropriate supply of medicines, clinically reviewing prescriptions, supporting patient enquiries, and maintaining the highest standards of professional practice. Working in a fast-paced digital environment, you will collaborate closely with prescribers, pharmacy technicians, dispensers, and the wider pharmacy team to ensure a seamless patient experience. Key Responsibilities Clinically review and check prescriptions to ensure the safe and appropriate supply of medicines. Assess patient information and verify the suitability of treatments before supply. Provide professional advice and support to patients via telephone, email, and online communication channels. Liaise with prescribers and other healthcare professionals where additional information or clinical clarification is required. Support safe prescribing and dispensing processes in line with legal, regulatory, and professional standards. Ensure all medicine supplies are accurate, appropriate, and fully documented. Respond to patient and operational queries efficiently and professionally. Maintain the highest standards of patient safety, confidentiality, and GDPR compliance. Support stock management, ordering processes, and operational efficiency within the pharmacy. Contribute to the ongoing development and improvement of pharmacy services, systems, and patient care processes. About You We're looking for a motivated and patient-focused pharmacist who thrives in a collaborative and evolving healthcare environment. Essential Skills & Experience Registered Pharmacist with the General Pharmaceutical Council (GPhC). Strong clinical knowledge and sound professional judgement. Excellent written and verbal communication skills. Ability to work accurately and efficiently in a fast-paced environment. Strong organisational skills and attention to detail. Comfortable working with digital systems and online pharmacy workflows. Commitment to delivering outstanding patient care and maintaining safe practice. Desirable Experience Previous experience within a private, online, or distance-selling pharmacy. Familiarity with online consultation, prescribing, or dispensing platforms. Experience supporting high-volume prescription and medicine supply operations. Knowledge of medicines governance, regulatory compliance, and pharmacy quality systems. Why Join Clarity Pharma? Competitive salary, dependent on experience. 25 days annual leave plus our Birthday Club. On-site parking. Company social events. Ongoing training and professional development opportunities. Supportive and collaborative working environment. Opportunity to help shape and develop a growing online pharmacy service. Career progression opportunities within a rapidly expanding healthcare business. Working Environment This role is based onsite at our Stansted facility, with full-time and part-time opportunities available. You will be joining a busy, professional, and highly regulated online pharmacy environment where quality, accuracy, and patient care are at the heart of everything we do. Apply Today If you're looking for an opportunity to make a meaningful impact within a growing and innovative healthcare business, we'd love to hear from you. Apply now and become part of the Clarity Pharma team.

Job Role: Press Setter Salary: £39000 - £40000 per annum Holiday: 25 Days + Bank Holidays annually Our client is a global leader in the design and manufacture of closure liners and flexible packaging for food, beverage, pharmaceutical, health care, personal care, household and industrial applications. About the Position: Experienced Press Setter to set individual tooling correctly and to the required specification on the presses. Ensuring all pm sheets and safety checks are completed and legally compliant. Preferably worked on Bruderer, Invernizzi or Hydraulic Presses and is aware of Regulations for working on presses PUWER and LOLER The Position Responsibility; To always work in a safe manner ensuring the safety of yourself and your colleagues. To exchange Press Tooling as per Syteline instruction. To set individual tooling correctly and to required specification. To ensure the line is clear of all excess tooling and ancillaries (nuts/bolts etc). To ensure all guarding and e-stops are operating correctly during set up and the guard sheet is signed. To load the line and confirm good quality first off specifications are achieved prior to handing over to the operator. To ensure all work times on the press are recorded correctly on Rhombus. To maintain product quality throughout the run To assist within the department as and when required during your shift this could include acting as an operator/packer when required to do so by your supervisor. To maintain BRC levels of hygiene. To act as Material Handler ensuring all presses have materials available to run and to load when possible. To learn the universal grinding machine to complete duties. To always treat your fellow workers with respect and abide by the company Values. Education and Experience • Excellent communicator with a positive proactive approach. • Press setting experience desirable. • Basic computer skills. • Organized and tidy. Essential Skills and Characteristics Required • Press tooling knowledge or material knowledge desirable. • Manual press experience essential. • Knowledgeable of the legal requirement for press setting. Location and Relationships • Based in Slough • Reports to Shift Supervisor. • Works with machine operators, quality technicians and supervisors. • No direct reports. Hours of Work Monday to Friday (3 rotating shift): • 06 00 • 14 00 • 22 00

QC Microbiology Technician - Swindon Opportunity: This is a brand new position that has been created due to expansion. My client is a global pharmaceutical manufacturing company are looking to recruit an experienced Microbiologist where you will be carrying out high volume microbiology testing on finished drug products and raw materials to GMP and GLP standards. Duties and responsibilities include: Conducting QC Microbiology testing on raw materials and finished drug products. Providing technical support to the Scientists. Testing the microbiological properties of materials and products, to defined specifications, using defined methods and procedures in accordance with GLP and GMP. Receiving and reporting results on GLIMS. Collecting environmental monitoring and water samples. Conducting Growth Promotion testing of incoming goods. Testing of validation protocols. The hours of work are either Tuesday-Saturday 8.00 am to 4.00 pm or Sunday-Thursday 8.00 am 4.00 pm. This is a 12 months contract based in Swindon which will be reviewed for a possible extension or go permanent however this is all dependent on the candidate and business performance. The PAYE rate is £13.58 per hour. Skills: To apply for the role of QC Microbiology Technician you will have the following: Need to be clean shaven for this role. No make up or jewellery allowed in the clean rooms. Microbiologist qualification or similar. Ideally Microbiology experience within the pharmaceutical industry or another highly regulated environment. Good IT skills Word, Excel and Outlook. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.