Smart4Sciences

Smart4Sciences is supporting a leading manufacturing organisation in recruiting a QC Analyst to join their Quality Control team. This role offers an excellent opportunity to work within a laboratory environment, carrying out quality control testing to ensure raw materials and finished products meet both company and customer specifications. The Role Perform quality control testing of raw materials, finished goods, and other samples as required Prepare and analyse samples in accordance with established laboratory procedures Support the Quality Manager and Quality Control Manager with routine and ad hoc testing activities Follow Good Laboratory Practice (GLP), health and safety regulations, and maintain laboratory housekeeping standards Ensure the correct storage and disposal of retained production and laboratory samples Validate laboratory instruments in line with company procedures Manage laboratory consumables and solvent stock, carrying out regular stock checks and arranging replenishment where required Issue Certificates of Analysis (CoAs) and maintain accurate laboratory records and filing systems Support Production, Customer Service, Technical Service, Purchasing, R&D, and Commercial teams through timely and accurate testing Identify and implement process improvements to enhance laboratory performance and efficiency Utilise Microsoft Word, Excel, and internal systems including Epicor, BOS, COSHH databases, Torque databases, and email systems The Candidate Experience working within a laboratory environment Previous experience in a Quality Control role A Levels or equivalent qualifications in one or more scientific subjects Proficient in Microsoft Word and Excel Strong attention to detail and commitment to quality standards Ability to manage workloads effectively and work flexibly to meet business needs Excellent communication skills with the ability to build strong working relationships across departments Knowledge of laboratory health and safety practices and quality procedures If you're looking to develop your career within a quality-focused laboratory environment and contribute to the delivery of high-quality products, Smart4Sciences would love to hear from you.

Senior Automation Engineer - Pharmaceuticals I am currently recruiting for a Senior Automation Engineer for a leading pharmaceutical manufacturer based in the Yorkshire area. This will be a great opportunity for someone who has experience working on various SCADA, Simens, PLCs and DCS systems for a pharmaceutical manufacturer. Key responsibilities for the Senior Automation Engineer - Pharmaceuticals Lead the design, development, implementation, and optimisation of automation and control systems across manufacturing operations. Provide technical expertise for PLC, SCADA, HMI, and DCS systems, ensuring optimal system performance and reliability. Collaborate with internal department such as, Production, Engineering, Validation, Quality, and IT teams on continuous improvement initiatives. Troubleshoot automation and control system issues, implementing effective solutions to minimise production downtime. Manage external vendors and contractors to ensure successful project delivery. Support the delivery of capital projects, including system design, commissioning, qualification, and validation. Support and lead the junior automation Engineer for operational excellence within the team. Requirements for the Senior Automation Engineer - Pharmaceuticals Degree qualified in Automation, Electrical, Electronic or Controls Engineering or equivalent qualification. Strong knowledge of PLC programming (Siemens, Allen-Bradley, or similar), SCADA, HMI, and DCS platforms Strong communication and stakeholder management abilities. Experience with delivering automation projects from concept through to implementation. Benefits for the Senior Automation Engineer - Pharmaceuticals Good career development. Impacting life changing pharmaceutical manufacturing. Competitive salary To apply for the Senior Automation Engineer - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on (phone number removed) or email .

Operations Manager - Pharmaceuticals I am currently recruiting for an Operations Manager to work within the pharmaceutical industry, for a niche, yet established product, this is a great opportunity for a Production Manager to work standard hours and develop their skillset and work with an expanding business in the Nottinghamshire area Key responsibilities for the Operations Manager - Pharmaceuticals Lead the day-to-day operations of the manufacturing facility, ensuring production targets, quality standards, and customer commitments are consistently achieved. Drive a strong culture of safety, quality, compliance, and continuous improvement across all operational areas. Develop and implement operational strategies to improve efficiency, productivity, and overall equipment effectiveness (OEE). Ensure all manufacturing activities comply with GMP, regulatory requirements, and company quality standards. Lead, mentor, and develop cross-functional teams, fostering a high-performance and collaborative culture. Manage operational budgets, resource planning, and cost control initiatives to achieve business objectives. Work closely with Engineering, Quality, Supply Chain, Validation, and Maintenance teams to optimise manufacturing Requirements for the Operations Manager - Pharmaceuticals Degree qualified in Engineering, Science, Pharmacy, Manufacturing, Operations Management, or a related discipline. Proven experience in an Operations Manager, Manufacturing Manager, or Senior Production Manager role within the pharmaceutical, biotechnology, or other highly regulated manufacturing industry. Strong knowledge of GMP, pharmaceutical regulations, and quality management systems. Strong communication and stakeholder management abilities with the confidence to influence at all levels of the organisation. Benefits for the Operations Manager - Pharmaceuticals Good career development. Free Parking Desirable location Competitive salary To apply for the Operations Manager - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on (phone number removed) or email .

About the job Are you an experienced Quality Assurance professional looking to take the next step in your career? Smart4 Sciences is partnering with a growing pharmaceutical manufacturer in Sandwich, Kent , specialising in the production of Cannabidiol (CBD) Active Pharmaceutical Ingredients (APIs) and industrial hemp derivatives for the pharmaceutical and nutraceutical sectors. They are looking to recruit a QA Officer who will play a key role in maintaining and continuously improving the company's Quality Management System (QMS). Working closely with Production, Quality Control and the wider business, you'll ensure products are manufactured and released in accordance with GMP standards while supporting a culture of quality and continuous improvement. This is a varied, hands-on role offering exposure across the full Quality Assurance lifecycle, making it an excellent opportunity for someone looking to broaden their experience within a growing pharmaceutical business. Key Responsibilities: Maintain and continuously improve the Quality Management System (QMS) Review and approve batch manufacturing documentation prior to batch release Review and approve SOPs, controlled documents and quality records Manage Deviations, CAPAs, Change Controls, Complaints and Out of Specification (OOS) investigations Support internal, supplier and regulatory audits Assist with supplier qualification activities and Quality Agreements Support product recalls and quality investigations where required Maintain GMP training records and ensure compliance across the business Work collaboratively with Production, QC and other departments to drive continuous quality improvements Support validation activities and lead quality improvement initiatives where appropriate What We're Looking For: Minimum of 3 years' experience within a GMP pharmaceutical Quality Assurance environment Strong understanding of GMP and wider GxP regulations Experience managing QMS activities including CAPAs, Deviations, Change Controls and batch record review Experience supporting internal or supplier audits Strong investigation, root cause analysis and problem-solving skills Excellent technical writing and documentation skills Good working knowledge of Microsoft Office Strong organisational skills with the ability to manage multiple priorities Excellent communication skills and the confidence to work across multiple departments Desirable Experience: Validation activities Supplier Quality Management Training and mentoring colleagues Continuous Improvement projects Experience supporting regulatory inspections Personal Attributes: Highly organised with excellent attention to detail Proactive with a continuous improvement mindset Strong communicator and collaborative team player Able to take ownership and work independently Committed to maintaining the highest quality and compliance standards This is an excellent opportunity to join a growing pharmaceutical manufacturer where you'll gain broad exposure across the full Quality Assurance function, take ownership of key quality systems and contribute directly to the company's continued growth and success. If you're looking for a role where you can make a genuine impact while developing your career, we'd love to hear from you.

HVAC Engineer- Pharmaceuticals I am currently recruiting for a HVAC Engineer for a leading pharmaceutical manufacturer based in the Yorkshire area. This will be a great opportunity for someone who has experience with commonising, preventive and corrective engineering within a pharmaceutical HVAC operation. Key responsibilities for the HVAC Engineer- Pharmaceuticals Carry out planned preventative maintenance and reactive maintenance on HVAC and associated building services systems. Assist with HVAC upgrades, capital projects, commissioning, qualification, and validation activities. Ensure all work complies with GMP, health & safety, and pharmaceutical industry standards. Work closely with Production, Facilities, Validation, and Quality teams to ensure uninterrupted manufacturing operations. Work closely with Production, Facilities, Validation, and Quality teams to ensure uninterrupted manufacturing operations. Monitor system performance and recommend energy efficiency and continuous improvement initiatives. Requirements for the HVAC Engineer- Pharmaceuticals Relevant engineering qualification in Mechanical Engineering, Building Services, HVAC, or equivalent. 2 years minimum experience working within Pharmaceutical Manufacturing. Knowledge of GMP, regulatory compliance, and engineering best practices. Good fault-finding, problem-solving, and communication skills. Benefits for the HVAC Engineer- Pharmaceuticals Good career development. Impacting life changing pharmaceutical manufacturing. Competitive salary To apply for the HVAC Engineer- Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on (phone number removed) or email .

Production Manager - Pharmaceuticals I am currently recruiting for a Production Manager to work within the pharmaceutical industry, for a niche, yet established product, this is a great opportunity for a Production Manager to work standard hours and develop their skillset and work with an expanding business in the Nottinghamshire area Key responsibilities for the Production Manager - Pharmaceuticals Lead and manage day-to-day pharmaceutical manufacturing operations to ensure production schedules are achieved. Drive a culture of safety, quality, compliance, and continuous improvement across the production department. Ensure all manufacturing activities comply with GMP, company procedures, and regulatory requirements. Monitor production KPIs, identify performance trends, and implement improvements to maximise efficiency and reduce waste. Work closely with Engineering, Quality, Validation, Supply Chain, and Maintenance teams to optimise manufacturing performance. Drive Lean Manufacturing and continuous improvement initiatives to enhance operational performance. Manage departmental budgets, staffing levels, and resource planning to meet business objectives. Requirements for the Production Manager - Pharmaceuticals Degree qualified in Science, Engineering, Pharmacy, Manufacturing, or a related discipline. Strong knowledge of GMP, regulatory compliance, and pharmaceutical manufacturing processes. Experience in a Production Manager or Manufacturing Manager role within the pharmaceutical, biotechnology, or other highly regulated manufacturing industry. Benefits for the Production Manager - Pharmaceuticals Good career development. Free Parking Desirable location Competitive salary To apply for the Production Manager - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on (phone number removed) or email .

Smart4Sciences is recruiting for a QC Analyst to join a leading pharmaceutical manufacturer in Basildon . This is a fantastic opportunity to work within a GMP-regulated laboratory, supporting the testing of pharmaceutical products and ensuring compliance with quality standards. The Role Perform QC testing of raw materials and finished products Prepare samples, standards, and reagents for analysis Maintain accurate laboratory records in line with GMP and ALCOA+ requirements Operate and maintain laboratory equipment, including HPLC, GC, pH meters, and titrators Support OOS investigations, method validations, and method transfers Participate in audits, inspections, and continuous improvement activities Ensure laboratory housekeeping and compliance standards are maintained at all times The Candidate Experience working in a QC or laboratory environment Knowledge of analytical testing techniques, including HPLC and GC Strong attention to detail and data accuracy Good communication and organisational skills Proficient in Microsoft Office Degree in a Life Science discipline desirable Knowledge of GMP and pharmaceutical quality standards advantageous If you're looking to develop your career within pharmaceutical quality control, Smart4Sciences would love to hear from you

Smart4Sciences is recruiting for a Microbiologist to join a leading pharmaceutical manufacturer in Basildon . This is an excellent opportunity to join a Quality Control team, taking responsibility for microbiological testing and ensuring compliance with GMP and regulatory requirements. The Role Perform microbiological testing and accurately analyse and interpret results Organise and support the day-to-day activities of the microbiology laboratory Conduct OOS, out-of-trend investigations, and root cause analysis Prepare microbiology protocols and reports where required Maintain laboratory equipment, stock levels, and audit-ready standards Support self-inspections, audits, and regulatory inspections Ensure all testing activities comply with cGMP, pharmacopoeial requirements, and data integrity standards Assist with continuous improvement initiatives and KPI reporting The Candidate Previous microbiology laboratory experience within a pharmaceutical or regulated environment Experience investigating OOS and out-of-trend results Strong understanding of data integrity and GMP requirements Excellent attention to detail and organisational skills Strong communication skills and ability to work collaboratively Proficient in Microsoft Office Degree in Microbiology, Biology, Pharmacy, or a related Life Science discipline desirable Experience within a pharmaceutical manufacturing environment advantageous If you're looking to develop your career within pharmaceutical microbiology and join a company committed to quality and compliance, Smart4Sciences would love to hear from you.

Smart4 Sciences is partnering with a leading pharmaceutical manufacturer in St Albans to recruit a Senior QC Analyst who will play a key role in supporting Quality Control operations and ensuring products are tested to the highest GMP and regulatory standards. You'll be joining a collaborative QC team where you'll play a key role in ensuring raw materials, in-process samples and finished products meet the highest quality standards while supporting continuous improvement and regulatory compliance. The Role Your responsibilities will include: Performing analytical testing on raw materials, in-process samples and finished products Operating and troubleshooting HPLC , Karl Fischer Titration , Dissolution and other analytical equipment Carrying out physical testing of tablets, capsules and packaging materials Preparing, reviewing and checking analytical data prior to approval Peer reviewing laboratory documentation and analytical results Supporting the review and update of SOPs, specifications and analytical procedures Ensuring compliance with GMP, Data Integrity and Good Documentation Practices Maintaining laboratory equipment, reference standards and consumables Supporting investigations relating to analytical issues and implementing corrective actions Completing allocated training and maintaining competency across analytical techniques What we are looking for : Essential Degree, Diploma or Certificate in Chemistry, Analytical Science, Medical Laboratory Science or a related scientific discipline Previous experience working within a pharmaceutical QC laboratory Hands-on experience with HPLC analysis Experience using a range of laboratory instrumentation and analytical techniques Strong understanding of GMP , Data Integrity and Good Documentation Practices Excellent attention to detail and analytical skills Strong written and verbal communication skills Desirable Experience with Agilent HPLC systems and OpenLab software Experience with Karl Fischer Titration , Dissolution testing and physical testing of pharmaceutical dosage forms Experience reviewing analytical data and laboratory documentation Previous experience supporting SOP reviews and method improvements If you're an experienced QC Analyst looking for your next challenge in pharmaceutical manufacturing, we'd love to hear from you.

My client is looking for an experienced Synthetic Organic Chemist to join their production team. Previous experience working with large-scale reactors is highly desirable for this role. If you don't meet every requirement I strongly recommend you still apply - especially if you meet several of the Advanced Experience targets. Responsibilities Support the scale-up of research and development projects from laboratory concepts through to full production manufacturing Operate distillation equipment and support small-scale fine chemical manufacturing activities Provide technical troubleshooting and problem-solving support to Operations, Quality Control, and Research teams Maintain accurate technical documentation and ensure compliance with quality systems, SOPs, and operational procedures Record and manage production and development data within ERP and associated systems Maintain safe working practices when handling hazardous chemicals and process equipment Collaborate closely with Production, Quality, and R&D teams to support operational and development objectives Equipment experience desired Distillation Units Pilot-Scale and Production-Scale Reactors Gas Chromatography (GC) High Performance Liquid Chromatography (HPLC) Fourier Transform Infrared Spectroscopy (FTIR) Karl Fischer (KF) Skills Process development and scale-up Distillation Technical troubleshooting and problem solving Strong understanding of chemical process safety Ability to work effectively in a busy manufacturing environment Strong organisational and time management skills High attention to detail and documentation standards Proficiency with Microsoft Office, particularly Excel and Word Ability to work flexibly under changing priorities and deliver results in a timely manner Demonstrated Experience Successfully supported the scale-up of chemical processes from laboratory or pilot scale into manufacturing environments Operated distillation units and process equipment safely and effectively within a chemical production setting Worked with hazardous chemicals while maintaining high safety and compliance standards Contributed to the manufacture, optimisation, or development of fine chemicals, speciality chemicals, pharmaceutical intermediates, or related products Organometallic chemistry experience would be advantageous Applied scientific and technical expertise to resolve production, process, or quality-related issues Maintained accurate technical records, batch documentation, and quality system requirements Worked collaboratively with different functions to achieve project and operational objectives Demonstrated the ability to manage multiple priorities and deliver results in a timely manner Advanced Experience Led or played a significant role in process development, optimisation, or technology transfer projects that resulted in improved manufacturing performance Demonstrated expertise in organic chemistry within industrial manufacturing environments Experience operating or scaling processes using production-scale reactors (typically 5L+ and above) Resolved complex process, yield, quality, or operational issues through structured troubleshooting and root cause analysis Contributed to the safe introduction of new processes, products, or manufacturing technologies into production Supported continuous improvement initiatives that improved efficiency, quality, throughput, or process robustness Operated within fine chemical, speciality chemical, or pharmaceutical manufacturing environments and demonstrated an understanding of the associated technical and regulatory challenges Applied analytical techniques such as GC, HPLC, FTIR, KF, and titrations to support process development, manufacturing, or troubleshooting activities Provided technical leadership, mentoring, or specialist expertise to colleagues and cross-functional teams Holds a PhD, MChem, or equivalent advanced background in Chemistry, with demonstrated application of organic chemistry principles in an industrial setting

Shift Packaging Operator - St. Albans Are you a Packaging Operator looking to take on a new challenge? Do you want to join a company with great opportunities for progression? Then this opportunity with a Pharmaceutical manufacturer is looking for you! Responsibilities: Carry out packaging operations to meet daily and weekly production targets in line with company objectives and while working across rotating day and night shifts. Load and feed packaging materials into machinery to maintain continuous line operation. Ensure all products are packed in line with quality standards and regulatory requirements. Monitor production processes and promptly replace components or materials as required. This list is not exhaustive and you will be expected to carry out additional duties where reasonable. Requirements: Previous experience working in a manufacturing, production, or packaging environment. Technical or vocational qualification in manufacturing, engineering, or a related field (desirable). Familiarity with GMP or regulated environments (desirable). Experience operating automated or semi-automated machinery and performing quality checks and completing production documentation (desirable). NB - This is a shift role and requires flexibility according to business needs If you are interested in having a confidential chat regarding the role please reach out to Chad Petersen at Smart4 Sciences.

We are working with a well-established specialist chemical manufacturer to recruit a Lab / Operations Manager for their site in South East London. This is a fantastic opportunity for an experienced laboratory and operations professional to take ownership of quality, R&D, and manufacturing activities within a growing business supplying products to customers across global commercial and secure printing markets. Reporting directly to the Group Operations Manager, you will play a key role in driving operational performance, developing teams, and supporting the continued growth of the organisation. Key Responsibilities Lead the laboratory function, overseeing both Quality Control and Research & Development activities. Manage laboratory technicians and departmental managers, ensuring high levels of performance and accountability. Drive continuous improvement initiatives across laboratory, production, and operational processes. Ensure all products meet customer specifications, quality standards, and regulatory requirements. Support product development activities, working closely with technical and commercial teams. Monitor operational performance and implement improvements to increase efficiency, productivity, and quality. Manage departmental budgets and resources to achieve business objectives. Develop, coach, and mentor staff, building capability across the organisation. Ensure compliance with Health & Safety, Quality, and Environmental standards. Work closely with senior leadership to support business strategy and site development plans. Provide operational leadership across the wider manufacturing facility as responsibilities expand within the role. Requirements Minimum of 5 years' experience within a chemical laboratory environment. Previous management experience with responsibility for leading and developing people. Strong background in Quality Control, Research & Development, and manufacturing operations. Experience within inks, coatings, paints, pigments, resins, or other speciality chemical manufacturing environments. Ideally educated in Chemistry, Polymer Science, Colour Science, or a related scientific discipline. Strong understanding of laboratory operations, quality systems, and manufacturing processes. Commercial awareness and experience managing budgets and operational performance. Computer literate with strong organisational and administrative skills. Excellent leadership, communication, and problem-solving abilities. Personal Attributes Hands-on leader with a proactive and practical approach. Strong team player capable of building positive working relationships across all levels of the business. Results-driven with a focus on continual improvement and operational excellence. Able to balance technical, commercial, and operational priorities effectively. Ambitious individual looking to develop into a broader senior leadership role. What's on Offer Competitive salary (available upon application). Opportunity to join a successful and growing specialist manufacturer. Direct exposure to senior leadership and strategic business decisions. Varied role with responsibility across laboratory, quality, R&D, and operations functions. Long-term career progression with the opportunity to take on increasing responsibility. Collaborative and supportive working environment within a well-established family-owned business.

Drug Safety Executive - Wrexham - Hybrid I am currently working with a leading pharmaceutical manufacturer based in Wrexham, who operate an MHRA-approved sterile injectable facility. This is an excellent opportunity for an experienced pharmacovigilance professional to further develop their career within a well-established pharmaceutical business. Key responsibilities for the Drug Safety Executive Lead and conduct all aspects of signal management, from detection through to assessment. Chair product safety signalling meetings and contribute to process improvement initiatives. Evaluate complex and conflicting drug safety data to support decision-making. Ensure compliance with current pharmacovigilance legislation and internal procedures. Collaborate with cross-functional teams to maintain consistency and quality in safety processes. Provide input into continuous improvement activities across safety systems and documentation. Requirements for the Drug Safety Executive Degree in Pharmacy or Life Sciences. Strong background in pharmacovigilance, with specific expertise in signal management. In-depth knowledge of pharmacovigilance legislation and its application. Broad understanding of medical terminology and disease pathology. Excellent attention to detail, organisational skills, and communication abilities. Proficiency in pharmacovigilance safety databases and computer literacy. Benefits for the Drug Safety Executive 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 To apply for the Drug Safety Executive role or to hear more information, please contact Rezaune Koopman at Smart4Sciences on (phone number removed) or email at .

QC Technician Location: Northamptonshire Are you looking to build your career in Quality Control within a successful manufacturing business? We're recruiting for a QC Technician to join a well-established manufacturer supplying high-quality products to global consumer markets. This is an excellent opportunity for someone with a scientific background and laboratory experience who enjoys working in a fast-paced, quality-driven environment. The Opportunity As a QC Technician, you'll play a key role in ensuring raw materials, production batches and finished products consistently meet quality standards before release. Working closely with Production and other internal teams, you'll help maintain product quality while supporting the smooth running of manufacturing operations. Key Responsibilities Carry out Quality Control testing on raw materials, in-process and finished products Release materials and batches against agreed specifications Investigate and record non-conformances Support batch rework activities where required Maintain accurate laboratory records and quality documentation Update internal quality systems Liaise with internal departments to ensure products are released on time Maintain high laboratory housekeeping and Health & Safety standards We're looking for someone who has: A strong scientific background gained through education, vocational qualifications or hands-on laboratory experience Previous experience within a Quality Control, laboratory or manufacturing environment (preferred) Excellent attention to detail Strong organisational and problem-solving skills Good written and verbal communication skills The ability to work both independently and as part of a team Must be flexible to occasionally work either the 6:00am-2:00pm or 2:00pm-10:00pm shift to provide holiday cover and support the wider team. Experience within the chemical, homecare, household, fragrance, personal care or consumer products sectors would be advantageous, but is not essential. Please note that this position does not offer visa sponsorship . Applicants must already have the unrestricted right to work in the UK, as we are unable to support future sponsorship requirements. What's on Offer? Competitive salary Training and career development opportunities Supportive and collaborative team environment Stable, long-term opportunity with a well-established manufacturer If you're looking to take the next step in your laboratory or Quality Control career, we'd love to hear from you. Apply today or contact us for a confidential discussion.

Cosmetic Chemist - Liverpool - Personal care We're working with an industry leader in lash, brow, haircare, and skincare treatments to recruit a Cosmetic Formulation Chemist to join their Liverpool-based lab. This is an exciting opportunity to work on innovative professional-grade cosmetic treatment products with a focus on sustainability, efficacy, and stability. Key Requirements: Expertise in formulating for lash, brow, skincare, and haircare products Strong practical lab skills in formulation and stability testing Proven ability to develop sustainable carriers and bases Degree-qualified in Chemistry or Analytical Chemistry (or similar) Solid understanding of raw materials and performance testing Experience in developing and validating methods for new formulations and packaging compatibility Strong communication and data management skills Proactive, detail-driven, and self-motivated You'll play a pivotal role in driving innovation and ensuring high-quality standards for market-leading cosmetic treatments. If you're passionate about lab work, product development, and clean science in beauty, we'd love to hear from you. To apply or find out more, get in touch today.