Regulatory Affairs SpecialistLocation: Redditch (On-site) Are you an experienced Regulatory Affairs professional with strong CLP classification and SDS... Read more
Regulatory Affairs Specialist
Location: Redditch (On-site)
Are you an experienced Regulatory Affairs professional with strong CLP classification and SDS authoring expertise? Do you enjoy being the go-to regulatory expert within a business and influencing product compliance from concept through to market launch?
An established manufacturer supplying products across UK and international markets is seeking a Regulatory Affairs Specialist to join its growing technical team. This is a fantastic opportunity for someone who enjoys a varied role combining chemical regulations, product compliance, artwork approval, and regulatory support across multiple departments.
The Opportunity
Working closely with R&D, Quality, Commercial and Manufacturing teams, you will play a key role in ensuring products remain fully compliant with UK and European chemical regulations. You'll be responsible for providing practical regulatory guidance, managing product classifications, and supporting the business through regulatory changes and new product introductions.
Key Responsibilities:
Prepare, review and maintain Safety Data Sheets (SDS) for a diverse product portfolio.Classify products in accordance with CLP, GHS and UK regulatory requirements.Assess formulation changes and determine regulatory impact.Review supplier documentation and evaluate compliance implications.Approve product labels, packaging artwork and regulatory claims.Manage Poison Centre Notifications (PCNs) and UFI submissions.Ensure regulatory information remains consistent across labels, SDSs and technical documentation.Support internal teams with regulatory advice and compliance guidance.Monitor emerging legislation and communicate potential business impacts.Contribute to continuous improvement initiatives and regulatory best practice.To be successful, you will have:
Previous experience within a Regulatory Affairs position.Strong knowledge of CLP classification and chemical regulations.Experience authoring and maintaining Safety Data Sheets.Exposure to PCN submissions and UFI management.Excellent attention to detail and documentation skills.The ability to communicate complex regulatory requirements to non-technical stakeholders.Experience within chemicals, detergents, household products, industrial chemicals, manufacturing or a related sector.What's on Offer?
Opportunity to become the regulatory lead within a respected manufacturing business.Varied role with significant exposure across technical, commercial and operational functions.Long-term career development opportunities.Supportive and collaborative working environment.Competitive salary and benefits package.For a confidential discussion regarding this opportunity, please apply today.
Read lessWe are working with a leading global manufacturing organisation to recruit an Inspection Lead for their site in... Read more
We are working with a leading global manufacturing organisation to recruit an Inspection Lead for their site in Blackburn.
This is an excellent opportunity for an experienced quality professional to take ownership of a final inspection function within a highly regulated manufacturing environment. Reporting to the Quality Manager, you will lead a team of inspectors, drive performance improvements, support quality initiatives, and ensure products meet the highest standards before reaching customers.
Key Responsibilities* Lead the final inspection team, ensuring inspection activities are completed efficiently and in line with required quality standards.
* Manage day-to-day inspector resourcing, including holiday planning, absence management, and overtime requirements.
* Develop and maintain training plans and competency matrices for inspection personnel.
* Supervise inspection activities to ensure accurate data recording and timely completion of work.
* Monitor departmental KPIs and drive improvements across efficiency, quality, and health & safety performance.
* Escalate quality concerns and non-conformities to the wider Quality and Operations teams.
* Support root cause investigations and implement corrective actions relating to inspection activities.
* Manage team performance, ensuring adherence to company procedures, quality standards, and behavioural expectations.
* Support documentation reviews and continuous improvement of inspection processes and procedures.
* Contribute to the wider quality strategy and development plans across the manufacturing facility.
* Work closely with production and quality teams to ensure customer requirements are consistently met.
* HND or equivalent qualification in an Engineering, Manufacturing, Scientific, or related discipline.
* Previous experience within an inspection, quality assurance, or quality control environment.
* Proven experience supervising or managing teams within a manufacturing setting.
* Strong understanding of quality standards, inspection processes, and compliance requirements.
* Experience investigating non-conformities and supporting corrective action activities.
* Excellent communication skills, both written and verbal.
* Customer-focused approach with strong attention to detail.
* Well-organised with the ability to manage multiple priorities effectively.
* Comfortable working within a fast-paced manufacturing environment.
* Flexible and adaptable approach to work.
* Natural leader with the ability to motivate and develop teams.
* Strong problem-solver with a continuous improvement mindset.
* Results-driven with a focus on quality and operational excellence.
* Able to influence stakeholders positively across multiple departments.
* Highly organised with excellent planning and decision-making skills.
* Committed to maintaining the highest standards of quality and health and safety.
* Positive and professional team player who leads by example.
* Opportunity to join a successful and growing international manufacturing business.
* Leadership role with genuine influence over quality and inspection performance.
* Exposure to continuous improvement and operational excellence initiatives.
* Career development opportunities within a global organisation.
* Collaborative and supportive working environment.
* Competitive salary and benefits package.
Location: Blackburn
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Quality Audit Officer - BedfordAre you a detail‑driven quality professional with a passion for compliance and client engagement?... Read more
Are you a detail‑driven quality professional with a passion for compliance and client engagement? One of our leading pharmaceutical partners is seeking a Quality Audit Officer to join the Bedford team, where you'll play a pivotal role in hosting client audits and driving the self‑inspection programme across the business. This client‑facing role places you at the forefront of audit activities, ensuring compliance with ISO 9001, ISO 13485, and GDP regulations while building strong relationships with client quality teams.
Working alongside the Quality Integration Manager, you'll arrange and host audits, draft and submit audit responses, and act as the main point of contact for client queries. You'll also support regulatory inspections, lead self‑inspections, and contribute to continuous improvement initiatives that strengthen the company's Quality Management System.
Key ResponsibilitiesArrange, host, and respond to client audits at Bedford and other UK sites as required
Act as subject matter expert or provide backroom support during regulatory inspections
Organise, perform, and report on self‑inspections across the UK
Oversee supplier qualification and maintain the Approved Supplier List
Conduct detailed root cause analysis of non‑conformances/deviations and implement corrective actions
Perform and facilitate risk assessments on GxP and quality processes
Identify training needs and update quality training materials based on audit findings
Review and improve SOPs, work instructions, and forms to ensure compliance and consistency
Build strong client relationships and communicate clearly with external quality teams
What We're Looking ForMinimum 3 years' experience in a quality department certified to ISO 9001 or ISO 13485
Strong working knowledge of GDP guidelines and Quality Management Systems
Experience in quality auditing and supplier qualification programmes
Skilled in Microsoft Office packages (Excel, Word, Visio, PowerPoint, Outlook)
Ability to work independently and in a team, under pressure and to strict deadlines
Confident communicator with excellent organisational and problem‑solving skills
Desirable:
QMS Lead Auditor qualification
Certified training within GxP
QA Officer About the RoleSmart4 Sciences is partnering with a leading pharmaceutical company to recruit a QA Officer... Read more
Smart4 Sciences is partnering with a leading pharmaceutical company to recruit a QA Officer - Validation & Compliance. This is an excellent opportunity for someone with experience in pharmaceutical Quality Assurance who enjoys working across validation, compliance, technology transfer, and new product introduction activities.
Working within a GMP-regulated environment, you will play a key role in ensuring third-party manufacturers and laboratories remain compliant with regulatory requirements and registered dossiers while supporting the successful delivery of new product projects and ongoing quality initiatives.
Key ResponsibilitiesSupport new product development, technology transfers, and new product introductions from a Quality Assurance perspective.
Coordinate and participate in project meetings with internal stakeholders and external manufacturing and testing partners.
Review and approve analytical method validation, verification, and transfer protocols and reports.
Review manufacturing and packaging process validation protocols and reports.
Review Master Batch Manufacturing and Packaging Records, finished product specifications, methods of analysis, shelf-life specifications, and stability protocols.
Evaluate technical documentation provided by Contract Manufacturing Organisations (CMOs) and Contract Testing Laboratories (CTLs).
Assess Quality Management System documentation including Change Controls, Deviations, Out of Specification (OOS) investigations, CAPAs, and associated quality records.
Maintain and update the Validation Master Plan to ensure ongoing compliance.
Support investigations, market complaints, SOP updates, and continuous improvement activities.
Contribute to site KPIs, product quality objectives, and Health, Safety & Environmental (HSE) standards.
Build strong working relationships with internal departments including Regulatory Affairs, Supply Chain, Logistics, and Sales, as well as external CMOs and CTLs.
About YouWe're looking for someone who has:
Experience within Pharmaceutical Quality Assurance in a GMP-regulated environment.
Knowledge of validation principles, including analytical method validation and process validation.
Experience reviewing validation documentation, batch records, technical reports, and quality documentation.
Good understanding of Change Control, CAPA, Deviations, OOS investigations, and Quality Management Systems.
Familiarity with technology transfer and new product introduction activities would be advantageous.
Excellent attention to detail with strong document review skills.
Strong communication and stakeholder management skills.
The ability to manage multiple priorities while meeting project deadlines.
A degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Life Sciences, or a related scientific discipline is desirable.
What's on OfferOpportunity to work on exciting new product and technology transfer projects.
Exposure to cross-functional teams and external manufacturing partners.
Career development within a growing pharmaceutical quality function.
Supportive and collaborative working environment.
Competitive salary and benefits package.
If you're passionate about pharmaceutical quality, validation, and compliance and want to play a key role in delivering high-quality products to market, we'd love to hear from you. Apply today!
Read lessWe are working with a leading manufacturer within the construction materials sector to recruit a Technical Manager for... Read more
We are working with a leading manufacturer within the construction materials sector to recruit a Technical Manager for their site in Bolton.
This is an excellent opportunity for an experienced technical professional to take ownership of the company's entire technical function, leading product innovation, research and development, and the successful launch of new products to market. Working closely with senior leadership, you will drive the development of advanced insulation and membrane products while managing and developing a growing technical team.
Key Responsibilities* Lead the company's technical function, overseeing all Research & Development and New Product Development activities.
* Drive the development of innovative polymer-based products from concept through to commercial launch.
* Manage and develop the technical team, providing leadership, mentoring, and performance management.
* Identify opportunities for product improvements, innovation, and market differentiation.
* Oversee product formulation, testing, validation, and performance evaluation activities.
* Ensure new products meet relevant industry standards, regulatory requirements, and customer expectations.
* Collaborate with Manufacturing, Quality, Sales, and Commercial teams to support successful product launches.
* Degree educated in Chemistry, Polymer Science, Materials Science, or a related scientific discipline.
* Strong background within Research & Development or New Product Development environments.
* Proven experience working with polymer-based materials and products.
* Previous experience leading, managing, and developing technical teams.
* Strong understanding of product development processes from concept through to commercialisation.
* Experience within insulation products, construction materials, membranes, or related manufacturing sectors would be highly advantageous.
* Excellent project management and organisational skills.
* Strong analytical, problem-solving, and decision-making abilities.
* Excellent communication skills with the ability to influence stakeholders across all levels of the business.
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QC TechnicianLocation: Brixworth, NorthamptonshireSalary: Competitive + BenefitsAre you looking to build your career in Quality Control within a... Read more
Location: Brixworth, Northamptonshire
Salary: Competitive + Benefits
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 OpportunityAs 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 ResponsibilitiesCarry out Quality Control testing on raw materials, in-process and finished productsRelease materials and batches against agreed specificationsInvestigate and record non-conformancesSupport batch rework activities where requiredMaintain accurate laboratory records and quality documentationUpdate internal quality systemsLiaise with internal departments to ensure products are released on timeMaintain high laboratory housekeeping and Health & Safety standardsAbout YouWe're looking for someone who has:
A strong scientific background gained through education, vocational qualifications or hands-on laboratory experiencePrevious experience within a Quality Control, laboratory or manufacturing environment (preferred)Excellent attention to detailStrong organisational and problem-solving skillsGood written and verbal communication skillsThe ability to work both independently and as part of a teamExperience within the chemical, homecare, household, fragrance, personal care or consumer products sectors would be advantageous, but is not essential.
Important InformationThis position is based in Brixworth, Northamptonshire and starts at 6:00am.
Applicants must be able to reliably commute to Brixworth for a 6:00am start each working day. Candidates living locally or with access to their own transport will be best suited to this opportunity.
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 salaryTraining and career development opportunitiesSupportive and collaborative team environmentStable, long-term opportunity with a well-established manufacturerIf you're looking to take the next step in your laboratory or Quality Control career and can commit to a 6:00am start in Brixworth, we'd love to hear from you.
Apply today or contact us for a confidential discussion.
Read lessDrug Safety Executive - Wrexham - HybridI am currently working with a leading pharmaceutical manufacturer based in Wrexham,... Read more
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.
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.
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.
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 01925 239723 or email at .
Packaging Operator (Days) - St. AlbansAre you an Operator looking to take on a new challenge? Do you... Read more
Packaging Operator (Days) - St. Albans
Are you an 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.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).If you are interested in having a confidential chat regarding the role please reach out to Charlize Witbooi at Smart4 Sciences.
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We are working with a well-established specialist chemical manufacturer to recruit a Lab / Operations Manager for their... Read more
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.
* 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.
* 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.
* 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.
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We are working with a well-established specialist chemical manufacturer to recruit a Lab / Operations Manager for their... Read more
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.
* 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.
* 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.
* 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.
Read less
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