HSE Manager - Wigan Are you a HSE Lead looking for a new challenge? Are you familiar with... Read more
HSE Manager - Wigan
Are you a HSE Lead looking for a new challenge? Are you familiar with managing and completing risk assessments? Have you managed and lead scenario training or emergency drills? Do you want to join a company with great opportunities for progression? Then this opportunity with a Chemical manufacturer is looking for you!
Responsibilities:
Management, Implementation and Communication of the Management Systems (ISO 45001 & 14001).Acknowledge, Investigate, and resolve non-conformance.Organise all required HSE training programmes for relevant site personnel.Accident and incident investigations, report findings and Identify countermeasures to prevent recurrence by RCA and Risk Management; identification of hazard and planning of action to remove or reduce.
This list is not exhaustive and you will be expected to carry out additional duties where reasonable.
Requirements:
Degree or HNC/HND in relevant discipline.IOSH and NEBOSH certifications.Knowledge of ISO 45001 & 14001.Experience in a similar is advantageous.
If you are interested in having a confidential chat regarding the role please reach out to Chad Petersen at Smart4 Sciences.
Read lessWigan, England, United KingdomPermanent
Senior Quality EngineerWe are working with a leading global advanced materials manufacturer to recruit a Senior Quality Engineer... Read more
We are working with a leading global advanced materials manufacturer to recruit a Senior Quality Engineer for their manufacturing facility in Cambridgeshire.
This is an excellent opportunity for an experienced quality professional to play a key role in driving continuous improvement across a highly regulated manufacturing environment. Working closely with Production, Engineering, Customers, and Suppliers, you will support quality excellence through robust problem-solving, process improvement, and the ongoing development of quality systems.
Key Responsibilities* Support internal, external, and customer audits, ensuring compliance with quality management systems and customer requirements.
* Lead and support non-conformance investigations, corrective actions, and preventive improvement activities.
* Conduct root cause analysis and drive sustainable solutions to product and process quality issues.
* Interpret technical specifications and quality requirements to support manufacturing and quality decision-making.
* Partner with production and engineering teams to improve process performance, product quality, and operational efficiency.
* Monitor and analyse quality data and KPIs to identify trends, risks, and opportunities for improvement.
* Apply quality tools and methodologies to strengthen manufacturing processes and reduce defects.
* Produce and maintain PPAP documentation where required.
* Manage customer quality communications and support the resolution of customer concerns.
* Support supplier quality activities and audits.
* Contribute to the continual development and improvement of the Quality Management System.
Candidates should have experience within Quality Engineering, Manufacturing Engineering, Process Engineering, or a similar role within a manufacturing environment. Applications are welcomed from sectors such as aerospace, automotive, advanced manufacturing, industrial engineering, sheet metal fabrication, or other highly regulated industries.
RequirementsApplicants should be degree qualified in Engineering, Quality Management, or a related discipline, although equivalent industry experience will also be considered. A strong understanding of Quality Management Systems, manufacturing processes, root cause analysis, audits, and continuous improvement methodologies is essential, alongside excellent analytical and stakeholder management skills.
LocationCambridgeshire
ReferenceSenior Quality Engineer | Advanced Manufacturing & Quality Systems
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Cambridgeshire, United KingdomPermanent
QC Analyst | London | Pharmaceutical ManufacturingSmart4Sciences is partnering with a pharmaceutical manufacturer in London to recruit an... Read more
QC Analyst | London | Pharmaceutical Manufacturing
Smart4Sciences is partnering with a pharmaceutical manufacturer in London to recruit an experienced QC Analyst to join their Quality Control team.
This is an excellent opportunity for a detail-oriented analytical professional with experience in a GMP-regulated environment, who is passionate about laboratory testing, product quality and regulatory compliance.
Key Responsibilities:
Perform routine testing of raw materials and finished products using analytical techniques such as HPLC, GC, UV, FTIR and titration.
Conduct method validation, method transfer and method development in line with relevant regulatory guidelines.
Review analytical data, raw data and batch documentation to ensure compliance with cGMP requirements.
Support stability studies, OOS investigations, deviations and CAPA implementation.
Prepare, review and update SOPs, product specifications and controlled quality documentation.
Perform raw material sampling, visual inspections and material release activities.
Maintain laboratory equipment and support equipment qualification and routine maintenance.
Monitor environmental and microbial data, prepare trend reports and maintain accurate records.
Support change controls, supplier management, quality investigations and continuous improvement initiatives.
What We're Looking For:
Experience in a pharmaceutical or GMP-regulated laboratory environment.
Practical experience with analytical techniques such as HPLC, GC, UV, FTIR or titration.
Knowledge of cGMP and laboratory documentation requirements.
Experience in method validation, stability testing, OOS investigations and CAPA is advantageous.
Strong analytical skills, attention to detail and excellent documentation practices.
If you're looking for your next opportunity in pharmaceutical Quality Control, we'd love to hear from you!
Read lessLondon, England, United KingdomPermanent
Smart4 Sciences - specialists in pharmaceutical recruitment - are currently partnering with an established pharmaceutical organisation to recruit... Read more
Smart4 Sciences - specialists in pharmaceutical recruitment - are currently partnering with an established pharmaceutical organisation to recruit a Head of Quality to join their Site Leadership Team.
This is a senior leadership role with full responsibility for the QA and QC functions, driving the site's quality strategy and ensuring compliance across manufacturing, licensing and parallel import operations.
You will play a key role in maintaining an inspection-ready environment, leading regulatory audits and acting as the primary contact for the Medicines and Healthcare products Regulatory Agency.
Lead and develop the site Quality Management SystemOversee QA & QC teams and departmental performanceHost regulatory and customer inspectionsDrive continuous improvement and compliance with EU GMPOperate as a key member of the Site Leadership TeamWe're looking for a senior pharmaceutical quality leader with strong GMP knowledge, inspection experience, and a proven ability to lead quality teams in a regulated environment.
Please apply today or contact Gareth Gooley @Smart4 Sciences for a confidential discussion
Read lessManchester, England, United KingdomPermanent
Head of Quality - Manchester - On-Site I am currently working with an established parallel imports pharmaceutical organization... Read more
Head of Quality - Manchester - On-Site
I am currently working with an established parallel imports pharmaceutical organization in Manchester that operates across pharmaceutical manufacturing, licensing and medicines supply. This is an excellent opportunity for an experienced Quality leader to take ownership of site-wide Quality operations, drive continuous improvement initiatives, and ensure the highest standards of GMP compliance across the business.
Key Responsibilities:
Provide strategic and operational leadership for a fast-paced parallel import company, managing a department of QA and 7 in QC employees.Develop and implement site quality strategies aligned with business objectives and regulatory expectations.Act as the primary quality representative for internal stakeholders, customers and regulatory authorities.Lead regulatory, customer and internal inspections, ensuring inspection readiness at all times.Maintain and enhance Quality Management Systems in line with GMP and relevant pharmaceutical regulations.Oversee risk management processes, ensuring quality and compliance risks are proactively identified and controlled.Drive continuous improvement initiatives across quality systems, processes and site operations.Review and approve quality documentation, including SOPs, quality agreements, validation documentation and GMP records.Ensure robust deviation, CAPA, change control and complaint management processes are maintained and effective.Manage supplier qualification programmes, audit schedules and quality oversight of third-party partners.Provide leadership for validation activities, including process, equipment and computerised systems validation.Monitor quality metrics and KPIs, identifying trends and implementing improvements where required.Support the maintenance of manufacturing licences and regulatory commitments.Collaborate closely with operational teams to ensure compliance is embedded throughout the business.Lead, coach and develop Quality teams, fostering a high-performance and quality-focused culture.Manage departmental resource planning, succession planning and team development activities.Ensure ongoing awareness and implementation of emerging regulatory requirements and industry best practices.
Requirements:
Degree in a scientific discipline, ideally Pharmaceutical Science, Chemistry or a related field.Head of Quality experience within the pharmaceutical (parallel import) industry, alongside validation experience is highly advantageous.Significant experience within pharmaceutical Quality Assurance, Quality Control and Quality Systems.Strong knowledge of GMP regulations and pharmaceutical quality standards.Experience leading regulatory inspections and customer audits.Demonstrated leadership experience with responsibility for managing and developing teams.Strong understanding of Quality Management Systems, deviation management, CAPA and validation activities.Excellent communication, stakeholder management and influencing skills.Proven ability to drive continuous improvement and quality culture initiatives.Strong organisational, decision-making and problem-solving capabilities.Proficiency in quality reporting, performance metrics and compliance management.
To apply, please contact Rezaune Koopman at .
Read lessManchester, England, United KingdomPermanent
About the RoleAre you a detail-oriented quality professional looking to develop your career within the pharmaceutical industry?Smart4 Sciences... Read more
Are you a detail-oriented quality professional looking to develop your career within the pharmaceutical industry?
Smart4 Sciences is partnering with a pharmaceutical business seeking a proactive Senior QA Officer to join its Quality team. The role involves supporting pharmaceutical operations, maintaining robust quality systems, and ensuring compliance with GMP, GDP, and internal quality procedures.
This is an excellent opportunity for a scientifically qualified professional with strong organisational skills and an interest in Quality Assurance, quality systems, and regulatory compliance.
Key ResponsibilitiesReview finished batch records and GMP release documentation.
Maintain and manage Quality Management Systems (QMS), including CAPAs, deviations, change controls, and non-conformances.
Prepare, review, issue, and control SOPs, forms, and batch manufacturing records.
Investigate quality issues, customer complaints, deviations, and product recalls.
Maintain quality databases, documentation, master lists, and performance metrics.
Support regulatory licence approvals and ensure inspection readiness.
Liaise with suppliers to obtain quality and regulatory documentation.
Assist with internal and external audits and regulatory inspections.
Prepare quality reports, analyse data, and identify opportunities for improvement.
Collaborate with cross-functional teams to maintain compliance and drive continuous improvement.
RequirementsEssential:
A degree in a scientific discipline, preferably Pharmaceutical Sciences, Chemistry, or a related field.
Experience in an administrative or office-based role.
Excellent organisational, communication, and interpersonal skills.
Strong attention to detail and the ability to manage competing priorities.
Proficiency in Microsoft Word, Excel, and PowerPoint.
The ability to work independently and collaboratively while meeting strict deadlines.
A proactive, flexible, and quality-focused approach.
Desirable:
Previous experience within the pharmaceutical industry.
Experience with product release and batch documentation.
Knowledge of GMP guidelines and Regulatory Affairs.
Familiarity with QMS processes, CAPAs, deviations, and change controls.
Experience in problem-solving, investigations, and root cause analysis.
Why Apply?The opportunity to develop your career within a growing pharmaceutical group.
Exposure to a broad range of Quality Assurance and regulatory activities.
A collaborative and supportive working environment.
Ongoing training and professional development opportunities.
Interested in taking the next step in your Quality Assurance career? Apply today to find out more about this opportunity.
Read lessManchester, England, United KingdomPermanent
Quality Assurance Manager - UK - Onsite Working within the unique and highly regulated radiopharmaceutical industry, this role... Read more
Quality Assurance Manager - UK - Onsite
Working within the unique and highly regulated radiopharmaceutical industry, this role offers the opportunity to make a genuine impact on products that support vital diagnostic and treatment pathways. As Quality Assurance Manager, you'll lead site quality activities, oversee GMP compliance, and help drive a culture of quality excellence within a specialist manufacturing environment.
Key Responsibilities:
Act as the site Quality Assurance lead, providing quality oversight across manufacturing, testing, and operational activities.Lead and develop the QA team, managing performance, training, workload planning, and staff development initiatives.Ensure the site Quality Management System remains compliant with GMP requirements and industry best practices.Review and approve quality events including deviations, CAPAs, change controls, complaints, OOS and OOT investigations.Drive continuous improvement initiatives and support the implementation and enhancement of eQMS and LIMS platforms.Lead internal audit programmes and support supplier, contractor, client, and regulatory inspections.Maintain oversight of data integrity practices and ensure appropriate controls and assessments are implemented.Review and approve quality documentation including SOPs, risk assessments, validation documentation, and site quality records.Support product introductions, validation activities, and cross-functional projects from a QA perspective.Lead site inspection readiness activities and act as a key contact during MHRA and customer audits.Monitor regulatory developments and ensure quality systems remain aligned with evolving GMP requirements.Work closely with operational teams to ensure effective contamination control strategies and ongoing compliance across the site.Support quality defect investigations, recalls, and escalation of critical quality issues where required.Promote a strong quality culture through coaching, mentoring, and training across the wider business.
Requirements:
Degree in a scientific discipline or equivalent pharmaceutical industry experience.Minimum of 5 years' Quality Assurance experience within a GMP-regulated pharmaceutical environment.Previous leadership, supervisory, or people management experience as well as experience in an aseptic/sterile environment is imperative.Strong working knowledge of GMP, quality systems, and regulatory compliance requirements.Experience managing deviations, CAPAs, change controls, audits, and validation activities.Excellent communication and stakeholder management skills.Strong organisational skills with a proactive approach to problem solving and continuous improvement.Experience supporting regulatory inspections and customer audits.Proficiency in Microsoft Office applications and electronic quality management systems.Read less
Guildford, England, United KingdomPermanent
Chemistry & Technical Opportunities - Plastics & PolymersLocation: Greater ManchesterSalary: £35,000-£50,000, depending on experienceWe are recruiting for several... Read more
Key responsibilities may include:
Supporting laboratory testing, material development and technical investigations.
Working with polymers, thermoplastics, additives or masterbatch materials.
Assisting with product development, trials and scale-up activities.
Operating laboratory equipment and supporting practical processing activities.
Investigating technical issues and helping identify suitable solutions.
Contributing to project work and, where relevant, communicating technical information to customers.
What we're looking for:
A background in chemistry, polymer science, materials science or a related discipline, or relevant hands-on technical experience.
Exposure to plastics, polymers, thermoplastics, masterbatch, compounding or a closely related manufacturing environment.
Practical laboratory skills and an interest in material development or technical problem-solving.
The ability to work independently, manage priorities and contribute to a wider technical team.
Strong communication skills for positions involving technical support or customer interaction.
Greater Manchester, United KingdomPermanent
Laboratory TechnicianLocation: North WalesSalary: £27,000-£35,000 pa + shift allowanceWorking pattern: Monday to Friday, rotating shifts (after probation)We are... Read more
Key Responsibilities
Prepare samples and carry out laboratory testing.
Operate relevant equipment and machinery.
Record, review and document test results accurately.
Follow technical procedures and maintain high safety standards.
Support the wider team with testing and day-to-day laboratory activities.
What We're Looking For
Practical laboratory or materials-testing experience in an industrial or engineering environment.
Confidence working with equipment, machinery or test instruments.
Good attention to detail and the ability to follow technical procedures.
Strong record-keeping and basic computer skills.
A relevant technical qualification is advantageous.
Additional Information
Monday-to-Friday rotating shift pattern, involving shifts.
Occasional overtime may be required.
Applicants must meet the role's UK nationality or settled-status eligibility requirements.
Wrexham, Wales, United KingdomPermanent
Location: United Kingdom (Remote) | Hybrid options available in Leeds or London Job Type: Permanent, Full-Time Salary: £50,000-£75,000... Read more
Location: United Kingdom (Remote) | Hybrid options available in Leeds or London
Job Type: Permanent, Full-Time
Salary: £50,000-£75,000 DOE + Performance Bonus + Long-Term Incentive Scheme
Smart4Sciences are recruiting for a Technical Sales Manager to join a rapidly growing speciality ingredients and chemicals business as it expands its presence within the nutraceutical, food ingredient and speciality ingredient markets.
This is an exciting opportunity for a commercially minded individual with a strong scientific background and experience selling ingredients into food, nutraceutical, pharmaceutical or related sectors. The successful candidate will play a leading role in developing a growing business unit focused on speciality raw materials, antioxidants, supplements and performance ingredients supplied across UK and European markets.
This position offers a unique blend of technical sales, business development and commercial leadership. Working closely with senior leadership, you will be given significant autonomy to drive growth, develop customer relationships and help shape the future direction of the division.
Key ResponsibilitiesDrive business development and growth across nutraceutical, food ingredient and speciality ingredient markets.Identify, pursue and secure new business opportunities across the UK and Europe.Develop and maintain strong relationships with customers, distributors and supply partners.Manage the entire sales cycle from prospecting and technical discussions through to commercial negotiation and account management.Conduct market analysis to identify growth opportunities, industry trends and competitive activity.Produce and deliver technical and commercial presentations to prospective and existing customers.Work closely with technical and formulation teams to support customer projects and application requirements.Support the development and growth of the commercial team as the business expands.Monitor sales performance, pipeline activity and revenue forecasts.Manage profitability and contribute to budgeting and commercial planning activities.Represent the business at exhibitions, conferences and industry events.Continuously improve sales processes, tools and customer engagement strategies.Travel throughout the UK and EMEA region to support customers, suppliers and business development activities.Skills & Experience RequiredMinimum 3 years' experience within the nutraceutical, food ingredient, supplement or speciality ingredient sectors.Proven experience in technical B2B sales within chemicals, ingredients or related industries.Strong understanding of raw materials, ingredient applications and customer requirements.Degree qualified in Chemistry or a related scientific discipline.Strong business development experience with a proven track record of generating and growing revenue.Ability to remain hands-on in sales and customer engagement activities.Experience conducting market analysis and contributing to commercial strategy.Strong commercial awareness and negotiation skills.Excellent verbal and written communication skills.Experience developing customer presentations and delivering technical proposals.Experience using CRM and ERP systems.Ability to work independently within a remote working environment.Strong proficiency with Microsoft Office applications.Full UK driving licence and willingness to travel throughout the UK and EMEA.Desirable ExperienceExperience managing, mentoring or building commercial teams.Experience within speciality chemicals, antioxidants, food additives, nutraceutical ingredients or pharmaceutical ingredients.Additional management or leadership training.MSc or PhD in Chemistry or a related scientific discipline.What's On Offer£50,000-£75,000 basic salary depending on experience.Performance-related bonus scheme.Long-term incentive and share option scheme.Remote working with hybrid options available.Opportunity to build and grow a strategically important business unit.Significant autonomy and influence within a growing organisation.Exposure to UK and international markets.Long-term career progression opportunities.Entrepreneurial and fast-paced working environment.Opportunity to work closely with senior leadership and directly influence business growth.Apply TodayIf you are an experienced Technical Sales Manager, Business Development Manager, Ingredient Sales Manager, Commercial Manager or Account Manager with experience in nutraceuticals, food ingredients, supplements or speciality chemicals, we would be delighted to hear from you.
Submit your CV today for immediate consideration.
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London, England, United KingdomPermanentRemote
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