QC ChemistLocation: Manchester, UKDepartment: Quality Control & AnalyticsWorking Hours: Full-timeSalary: Competitive, dependent on experienceAre you an experienced Analytical... Read more
Location: Manchester, UK
Department: Quality Control & Analytics
Working Hours: Full-time
Salary: Competitive, dependent on experience
Are you an experienced Analytical Chemist with experience working within a GMP or ISO-regulated laboratory?
We are working with a pharmaceutical development and manufacturing organisation seeking a proactive and detail-oriented QC Chemist to join its Quality Control & Analytics team in Manchester.
This is an excellent opportunity to join a dynamic and collaborative environment, supporting manufacturing, research and development, and a diverse range of customer projects. You will play an important role in ensuring products meet the highest quality standards while contributing to scientific innovation and continuous improvement.
Key ResponsibilitiesConduct qualitative and quantitative chemical analysis of raw materials, intermediates and finished products.
Perform material sampling, sample preparation and analytical testing to support QC, Production and PR&D activities.
Carry out routine laboratory testing in accordance with GMP, ISO standards, SOPs and client requirements.
Support analytical method development and continuous improvement initiatives.
Maintain accurate, detailed and audit-ready laboratory records and project documentation.
Interpret, evaluate and communicate analytical results to internal teams, management and clients where required.
Manage multiple testing priorities and deadlines while maintaining accuracy and high analytical standards.
Support the QC Manager and QC Team Leader with day-to-day laboratory operations.
Promote and maintain Health & Safety, Quality and 5S standards within the laboratory.
Requirements & ExperienceExperience within a Quality Control laboratory operating under GMP and/or ISO-regulated standards.
A background in Analytical Chemistry or a related scientific discipline.
Practical experience with at least 1-2 of the following analytical techniques:
HPLC (preferred)
GC (preferred)
NMR (preferred)
LC-MS
ICP-OES
Strong practical laboratory and analytical chemistry skills.
Excellent attention to detail and the ability to produce accurate and reliable analytical results.
Strong organisational and time-management skills, with the ability to manage competing priorities.
Confident written and verbal communication skills.
Ability to work independently, including occasional lone working, as well as collaboratively within a team.
A proactive approach to troubleshooting, problem-solving and continuous improvement.
Why Consider This Opportunity?Exposure to a varied range of analytical projects and customer requirements.
Opportunity to develop your technical expertise within a collaborative laboratory environment.
Involvement in manufacturing, research and development, and continuous improvement activities.
Interested?
If you have a background in Analytical Chemistry and experience working within a GMP or ISO-regulated QC laboratory, we would love to hear from you.
Apply today or get in touch to find out more about this opportunity.
Read lessManchester, 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
We are working with a leading manufacturer of premium decorative coatings to recruit a QC / Technical Chemist... Read more
We are working with a leading manufacturer of premium decorative coatings to recruit a QC / Technical Chemist for their North West facility.
This is an excellent opportunity for a hands-on laboratory professional to join a well-established coatings manufacturer with a reputation for producing high-quality, technically advanced products. Reporting to the Lab R&D Manager, you will play a key role in quality control, technical problem-solving, batch release, and supporting manufacturing operations to ensure consistently high product standards.
Key Responsibilities* Carry out quality control testing on raw materials, colorants, in-process batches, and finished products against established specifications.
* Perform laboratory testing including viscosity, density, pH, opacity, gloss, colour, drying time, scrub resistance, adhesion, stability, and application assessments.
* Support batch approval and product release activities through accurate testing and result evaluation.
* Investigate quality, production, and customer-related technical issues, recommending corrective actions where required.
* Assist with colour matching, shade adjustment, tinting accuracy, and product consistency checks.
* Prepare laboratory samples, drawdowns, application panels, and performance trials.
* Maintain accurate quality records, specifications, test reports, and supporting documentation.
* Calibrate and maintain laboratory equipment to ensure reliable and consistent testing.
* Work closely with Production, Technical, and Procurement teams to support quality improvements and issue resolution.
* Assist with raw material evaluations, benchmarking activities, and formulation support projects.
Candidates should have previous experience within a QC, technical laboratory, or coatings testing environment, ideally within paints, coatings, chemicals, or a manufacturing setting. Experience carrying out laboratory testing, batch approval activities, and investigating quality issues would be highly beneficial.
RequirementsA scientific qualification such as a Degree, HNC, HND, or equivalent is desirable, although strong practical laboratory experience will also be considered. Applicants should possess excellent attention to detail, strong problem-solving skills, and a good understanding of quality control procedures and safe laboratory practices.
What's on Offer* Salary of £28,000 - £34,000 depending on experience.
* Opportunity to join a respected manufacturer with a strong reputation for premium products.
* Varied and hands-on technical role with responsibility across quality control and manufacturing support.
* Collaborative working environment with close interaction between laboratory and production teams.
* Ongoing training, development, and progression opportunities within the technical function.
Read less
Manchester, England, United KingdomPermanent
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