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A growing organisation within the molecular imaging space is seeking a Senior Quality Manager to lead oversight of EU and Rest-of-World (RoW) manufacturing partners and supply chain quality. This is a high-impact role focused on ensuring compliant, uninterrupted supply of specialised medicinal products across international markets. Key Responsibilities • Lead quality oversight of EU/RoW Contract Manufacturing Organisations (CMOs), • Manage manufacturing performance, investigations, and quality issue resolution, • Own and execute a risk-based audit programme, • Drive quality governance, including deviations, complaints, CAPAs, and change control, • Analyse performance data to identify risks and enable continuous improvement, • Support and enhance the Quality Management System (QMS), • Monitor regulatory developments and ensure ongoing compliance, • Collaborate cross-functionally to maintain a robust global supply chain Requirements • Strong experience within EU GMP environments (sterile and/or radiopharmaceuticals preferred), • Proven experience managing CMOs or external manufacturing partners, • Background in GxP inspections and auditing, • Solid understanding of QMS (deviation, CAPA, change control, risk management), • Ability to interpret and act on quality and operational data, • Willingness to travel (~30% across EU with occasional international travel) About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information: E:

A degree in Analytical Chemistry and relevant lab experience are essential. Momentive is seeking a QC Analytical Chemist to manage its analytical laboratory in Abingdon, UK.

A leading biotech company in Oxford is seeking a Senior Quality Assurance Officer to support manufacturing operations and ensure GMP compliance.

Berry Recruitment are NOW hiring for a committed and experienced Compression Operators (Pharma) to join a growing pharmaceutical company based in Oxford. Due to a significant period of expansion, we have multiple opportunities available. This is a hands-on manufacturing role focused on the production of medicinal products including tablets (pills), liquids, and gels within a regulated cleanroom environment. Candidates must have previous experience within pharmaceutical manufacturing, with a strong understanding of GMP standards and production processes. This role is commutable from Oxford, Woodstock, Bicester, and Witney. Role: Compression Operators (Pharma) Location: Oxford, Oxfordshire Hours: Full-time, 08:00 - 16:30 Key Responsibilities: Machine Setup Install punches and dies Set compression force, speed, and fill depth Ensure correct tooling for the product Material Handling Load granules or powder into the hopper Check material flow and prevent segregation Process Monitoring Monitor tablet weight, hardness, thickness, and appearance Adjust machine parameters in real time In-Process Quality Control (IPQC) Perform routine checks (e.g., every 15-30 minutes) Record data according to GMP documentation 5Troubleshooting Identify defects like: Capping Lamination Sticking/picking Adjust pressure, speed, or lubrication Cleaning & Maintenance Clean machine parts between batches Follow Good Manufacturing Practice (GMP) guidelines Report wear or damage to tooling About You: Essential: Previous experience within pharmaceutical manufacturing Experience working in regulated production environments (cleanroom experience desirable) Experience within a Compression Operator role is highly desirable. Strong understanding of GMP and compliance procedures High attention to detail and accuracy in documentation Proactive, reliable, and able to work effectively within a team No candidate will meet every single desired qualification listed. If your experience differs slightly but you believe you can bring value to this role, we would still love to hear from you. For more information and to apply, contact the Oxford branch of Berry Recruitment on (phone number removed) or click 'Apply Now' to submit your application. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job

Cleaning Operative - Oxford We have an urgent opportunity for a cleaner to join our team in the Oxford area. This role will involve working across multiple sites, so a full driving licence and access to transport are essential. You will be working 30-40 hours per week, starting as soon as possible. The role involves: Cleaning laboratories and GMP cleanroom facilities Some unsupervised work once full training has been completed Maintaining high standards of hygiene and compliance We're looking for someone reliable, proactive, and comfortable working in specialised environments. If you're interested and available to start quickly, please get in touch. TAGS:CLEANERS/CLEANING/CLEAN/DANIELOWEN/OXFORD/RECRUITMENT/JOBS/WORK/CLEAN/CLEANER/WELFARE

Sr Quality Control (QC) Microbiologist, 12 Months Maternity Cover Join Us in Changing Lives. At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful . We are currently recruiting for a Senior QC Microbiologist to cover a period of maternity within the Quality Control team. The purpose of this role is to be responsible fortheplanningand performance of environmental monitoring within the manufacturing facilities, and the testing and data analysis ofallmicrobiological testing to ensure that both the product and the cleanroom environments where they are made are in suitable biocontamination control. Your responsibilities in this role would be: Responsible for scheduling, planning,organisingtestingand ensuring the microbiology laboratory ismaintainedto GMP standards. Represent the microbiology laboratory in communications withother departments and supportandparticipateininternaland externalaudits. To write, update and reviewdepartmental documentationandbe competent inwritingand executingmethod suitability studies. Supervise and support a team of microbiologistsand be the first point of contact. Responsible fortraining ofnew staffas a trainer and provide scientific background information to trainees. Responsible for thetimely,accuratecompletionand reviewof assay paperworkand reporting of results,monthly trend meetings and trend report writing. Leadand implementcontinuous improvement initiatives to enhance working practices. Partake and lead investigationsand root cause analysis meetingsto helpidentifycontributory factors, assign root cause and corrective/preventative actions. We are looking for: Degree level qualified in Microbiology or related subjectand/orsignificantrelevantGMP microbiologicalexperience Relevanthigh levelof microbiological laboratory technicaland GMP/clean roomexperience. Good understanding and knowledge of practical and theoretical microbiology/aseptictechniques; Sterility testing on finished product, Bioburden and Endotoxin testing. Thorough understanding of GMP and cleanroom biocontamination control. Advanced understanding of laboratory health and safety requirements. Greater understanding of regulatory requirements e.g. GMP, and/or Validation and Quality Management systems. Computer literate (Word, Excel) andhigh levelof familiarity with Microsoft Office software. Flexibility to work shifts covering the hours from 07.00am to 03.00am Mon-Fri Why Join Us? Competitive total reward packages Wellbeing programmesthat support your mental and physical health Career development opportunitiesto help you grow and thrive Supportive, inclusive, and collaborative culture State-of-the-art labs and manufacturing facilities A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. At OXB, were future-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. TPBN1_UKTJ

Berry Recruitment are NOW hiring for a committed and experienced Pharmaceutical Manufacturing Technician to join a growing pharmaceutical company based in Kidlington. Due to a significant period of expansion, we have multiple opportunities available. This is a hands-on manufacturing role focused on the production of medicinal products including tablets (pills), liquids, and gels within a regulated cleanroom environment. Candidates must have previous experience within pharmaceutical manufacturing, with a strong understanding of GMP standards and production processes. This role is commutable from Oxford, Woodstock, Bicester and Witney. Role: Pharmaceutical Manufacturing Technician Location: Oxford, Oxfordshire Hours: Full-time, 08:00 - 16:30 Key Responsibilities: Manufacture pharmaceutical products including tablet, liquid, and gel formulations Operate production equipment in line with validated manufacturing processes Carry out batch manufacturing activities in accordance with GMP and SOPs Perform production and packaging procedures following approved documentation Complete and maintain accurate batch records to ensure full traceability Clean and sanitise processing equipment and production areas in line with procedures Monitor manufacturing processes and report any deviations, adverse events, or environmental abnormalities Promote and adhere strictly to CGMP standards and Health & Safety regulations Support Right First-Time manufacturing principles Assist across the Production Department as requiredAbout You: Essential: Previous experience within pharmaceutical manufacturing Experience working in regulated production environments (cleanroom experience desirable) Strong understanding of GMP and compliance procedures High attention to detail and accuracy in documentation Proactive, reliable, and able to work effectively within a team No candidate will meet every single desired qualification listed. If your experience differs slightly but you believe you can bring value to this role, we would still love to hear from you. For more information and to apply, contact the Oxford branch of Berry Recruitment on (phone number removed) or click 'Apply Now' to submit your application. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job

Production Technician, £26,000 - £28,000, Abingdon, Oxfordshire £26,000 - £28,000 depending on experience + pension + 25 days holiday Full-time, permanent position. Manufacturing role within a growing medical device company Are you a hands-on Production Technician, Assembly Operative or Development Technician with experience in a clean, regulated manufacturing environment? Your background as a Production Technician: Experience working with small components ideally in medical, electronics, or precision manufacturing Able to follow detailed written instructions and complete accurate production records Confident working under a microscope or with intricate components A methodical approach reliable, process-driven, and comfortable working to high quality standards Any experience with ISO 13485, GMP, or GLP is beneficial but not essential Good communication skills and a team-first attitude. Production Technician responsibilities: Assemble medical devices to precise specifications, following SOPs Carry out detailed production tasks under a microscope where required Record data clearly and accurately during manufacturing and product testing Maintain a clean and organised work area, ensuring equipment is cleaned, calibrated and ready for use Support product development by building prototypes and performing performance testing Assist with technical support for suppliers and internal teams Contribute to documentation, including work instructions and process records. This Production Technician job is commutable from Abingdon, Witney, Didcot, Wantage, Oxford, Oxfordshire and surrounding areas. To apply, please send your CV to Sam Hilton at Euro Projects Recruitment Ltd. Please note that if you are not contacted within ten working days, your application has not been successful. This vacancy is posted by Euro Projects Recruitment specialists in engineering and manufacturing careers TPBN1_UKTJ

Manufacturing Technician, £26,000 - £28,000, Abingdon, Oxfordshire £26,000 - £28,000 depending on experience + pension + 25 days holiday Full-time, permanent position. Manufacturing role within a growing medical device company Are you a hands-on Manufacturing, Production Technician, Assembly Technician or Development Technician with experience in a clean, regulated manufacturing environment? Your background as a Manufacturing Technician: Experience working with small components ideally in medical, electronics, or precision manufacturing Able to follow detailed written instructions and complete accurate production records Confident working under a microscope or with intricate components A methodical approach reliable, process-driven, and comfortable working to high quality standards Any experience with ISO 13485, GMP, or GLP is beneficial but not essential Good communication skills and a team-first attitude. Manufacturing Technician responsibilities: Assemble medical devices to precise specifications, following SOPs Carry out detailed production tasks under a microscope where required Record data clearly and accurately during manufacturing and product testing Maintain a clean and organised work area, ensuring equipment is cleaned, calibrated and ready for use Support product development by building prototypes and performing performance testing Assist with technical support for suppliers and internal teams Contribute to documentation, including work instructions and process records. This Manufacturing Technician job is commutable from Abingdon, Witney, Didcot, Wantage, Oxford, Oxfordshire and surrounding areas. To apply, please send your CV to Sam Hilton at Euro Projects Recruitment Ltd. Please note that if you are not contacted within ten working days, your application has not been successful. This vacancy is posted by Euro Projects Recruitment specialists in engineering and manufacturing careers TPBN1_UKTJ

Technical Manager Oxfordshire Competitive package Are you a driven technical leader ready to take ownership of food safety, quality and compliance in a fast-paced, multi-channel food environment? We're looking for an ambitious Technical Manager to lead from the front-ensuring audit excellence, driving continuous improvement, and supporting operations across production, travel and events. Lead and develop the technical function, coaching and mentoring your team to deliver exceptional standards across food safety, quality and compliance. Act as the technical authority across the business, supporting Production, NPD, Travel and Events teams to ensure operational excellence and full regulatory compliance. Own audit readiness and delivery, leading BRCGS and SALSA audits, customer visits and inspections with confidence and precision. Drive a culture of continuous improvement, working cross-functionally to enhance QMS, GMP standards and product integrity. Manage customer complaints end-to-end, leading root cause analysis and implementing robust corrective and preventative actions. Oversee food safety systems, including HACCP, environmental monitoring, swabbing programmes and shelf-life validation. Conduct internal audits and verification activities, ensuring systems are effective, compliant and consistently audit-ready. Champion food safety training and engagement, embedding best practice across all teams and creating a proactive compliance culture. What We're Looking For Proven experience in a Technical or Quality leadership role within food manufacturing (high care/high risk/RTE environments preferred) Strong knowledge of BRCGS, SALSA, HACCP and UK food safety legislation Demonstrated ability to lead, coach and develop high-performing technical teams Excellent problem-solving skills with experience in root cause analysis and continuous improvement Confident communicator with the ability to influence cross-functional stakeholders If you believe you have the skills and personality to fit these requirements please either apply via this advert or call Henderson Brown on (phone number removed) for more information

Berry Recruitment are NOW hiring for a committed and experienced Nutraceutical Operator to join our client based in Oxford. We are seeking a reliable and detail-focused Manufacturing Technician to join our nutraceutical production team. This is a hands-on role within a structured, GMP-aligned environment, supporting the manufacture of high-quality products including powders, capsules, and tablets. Role: Nutraceutical Operator Location: Oxford, Oxfordshire Hours: Full-time, 08:00 - 16:30 Key Responsibilities: Operate machinery including Pill presses, Capsule fillers and blending equipment Operate production equipment in line with validated manufacturing processes Carry out batch manufacturing activities in accordance with GMP and SOPs Perform production and packaging procedures following approved documentation Complete and maintain accurate batch records to ensure full traceability Clean and sanitise processing equipment and production areas in line with procedures Monitor manufacturing processes and report any deviations, adverse events, or environmental abnormalities Promote and adhere strictly to CGMP standards and Health & Safety regulations Support Right First-Time manufacturing principles Assist across the Production Department as requiredAbout You: Experience working in regulated production environments (cleanroom experience desirable) Strong understanding of GMP and compliance procedures High attention to detail and accuracy in documentation Proactive, reliable, and able to work effectively within a team No candidate will meet every single desired qualification listed. If your experience differs slightly but you believe you can bring value to this role, we would still love to hear from you. For more information and to apply, contact the Oxford branch of Berry Recruitment on (phone number removed) or click 'Apply Now' to submit your application. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job

ROLE OVERVIEW We are currently looking for a Senior Process Engineer to join a leading pharmaceutical company based in the Oxford area. As the Senior Process Engineer, you will be responsible for supporting the development of a robust, scalable manufacturing process. You will also support external engineering and manufacturing contractors to ensure delivery to specification and within both budget and timelines. Additionally, you will provide technical review and input into manufacturing processes and/or engineering designs for equipment and supervise the installation and qualification of an aseptic manufacturing line. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Pharmaceutical Process Engineer will be varied; however, the key duties and responsibilities are as follows: 1. Provide technical input into the design of GMP manufacturing processes and new equipment suitable for use in sterile operations., 2. Lead the commissioning and qualification of GMP equipment for clinical use., 3. Support the technology transfer., 4. Lead IMP packaging development to ensure suitability for sterile IMP clinical use. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Senior Pharmaceutical Process Engineer, we are looking to identify the following on your profile and past history: 1. MSc/MEng degree or higher in a relevant science/engineering field., 2. Extensive industry experience in process development and/or pharmaceutical engineering., 3. A working knowledge and practical experience with GMP equipment qualification and process development/industrialisation. Key Words: Senior Pharmaceutical Process Engineer/ Solid Dose / Tableting / Powder / GMP manufacturing / aseptic operations / process development / pharmaceutical engineering / clinical use / technology transfer / IMP packaging / regulatory submission / CDMO / sterile manufacture / #LI-DNI Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career

Civil Project Engineer - Contract Opportunity Your Next Challenge Awaits Join our client, a leading name in the FMCG sector, and contribute to innovative civil projects in Oxfordshire. As a Civil Project Engineer, you'll play an integral role in delivering key construction initiatives for a food manufacturing environment. If you're an all-rounder with a strong civil construction focus and adaptability in mechanical and electrical elements, this role is for you. With a 6-month contract (potential for extension), this is the perfect opportunity to showcase your expertise in project delivery and regulations compliance in a dynamic and highly skilled team. What You'll Bring to the Role Civil Construction Focus: Expertise in construction projects, including new buildings and service connections. Project Versatility: Ability to work across various phases of projects, from design to spades-in-the-ground execution. Regulations Knowledge: Experience with GMP and CDM regulations in a manufacturing environment. Well-Rounded Skills: Familiarity with mechanical and electrical aspects to effectively navigate multidisciplinary challenges. Role Details Location: On-site in Oxfordshire Contract Length: 6 months, with potential for extension Rate: £400 per day (Outside IR35) Schedule: 5 days on-site Ready to Apply? Don't miss this chance to make an impact in a thriving sector. Reach out to secure your place for a start in 6-8 weeks. Please click to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Progressive please visit Progressive Recruitment, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC(phone number removed) England and Wales

Join us in changing lives. At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful Were currently recruiting for a Senior Quality Assurance Officer to join our Quality Assurance team. In this role, you will provide expert QA support for OXB Manufacturing Operations, playing a key part in advancing our mission and making a real difference. Please note, this role will be 5 days a week onsite at our Cowley facility. Your responsibilities in this role would be: Reviewing and approving deviations, CAPAs and change controls within defined timelines. Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities. Reviewing batch documentation and support preparation for Qualified Person batch disposition. Participating in investigations, root cause analysis and risk assessments for quality events. Reviewing and approving SOPs, protocols, reports and other GMP documentation. Supporting implementation of new manufacturing processes for incoming client programs. Contributing to continuous improvement initiatives to strengthen quality systems and operational processes. We are looking for: Experience in a GMP-regulated pharmaceutical, biotechnology or similar manufacturing environment. Significant experience managing quality events such as deviations, CAPAs and change controls. Strong understanding of GMP regulations and regulatory expectations (FDA / EMA). Ability to work independently, make sound quality decisions and manage multiple priorities. Strong communication skills and the ability to collaborate closely with manufacturing and technical teams. About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXBs world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise. Why Join Us? Competitive total reward packages Wellbeing programmes that support your mental and physical health Career development opportunities to help you grow and thrive Supportive, inclusive, and collaborative culture State-of-the-art labs and manufacturing facilities A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. AtOXB,werefuture-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. TPBN1_UKTJ

Candidates should possess at least one year of experience in a GxP or GMP setup, along with strong communication skills and proficiency in Microsoft Office. A leading biotech company in Greater London is seeking a meticulous QC Materials Technician to support material inspection and release in a GMP

This senior technical position focuses on the delivery and cost control of capital projects in compliance with cGMP and EHS standards. The successful candidate will lead cross-functional teams, manage project proposals, and ensure adherence to GMP regulations.

Join Our Team as an Actuarial Consultant - GMP Equalisation and Project Work (Nationwide). Are you a talented and ambitious actuary with a strong background in GMP rectification and equalisation? At Mercer, we are excited to expand our dynamic team by welcoming skilled part-qualified or qualified ac

An established industry player is seeking a Quality Assurance Officer to join their dynamic team in Oxfordshire.This pivotal role involves ensuring the highest standards of quality and regulatory compliance in the biotechnology sector.You will manage batch reviews, oversee audits, and maintain Quali

The successful candidate will have at least 1 year of GMP manufacturing experience and a degree in Pharmaceutical production technology.

A European manufacturer of hygienic components based in West Yorkshire is seeking a Quality Technician to ensure product quality and compliance with internal standards.The role involves conducting inspections, managing quality concerns, and supporting continuous improvements.Candidates should have p

This role involves performing routine analytical testing in a GMP-regulated environment, supporting product release, and conducting stability studies.

Deep GMP experience not essential (you will be trained) but previous experience in GMP calculations at some level is. A fantastic role offering the opportunity to carve a career within the GMP space now and lots of opportunity thereafter!. Technical GMP Actuary or Specialist (Pensions).

Candidates should possess a strong understanding of GMP and HACCP, with excellent communication skills.

A pharmaceutical company in Greater London is seeking a Process Technician to support production operations within a GMP-regulated environment. Candidates should have experience in GMP or manufacturing environments, and strong attention to detail is essential.

A global healthcare company is seeking a Quality Lead for their manufacturing site in North East England.The role involves leading a team of QA Specialists, ensuring compliance with regulatory standards, and driving quality improvement initiatives.Ideal candidates will have experience in the pharmac

Successful candidates will have a relevant engineering qualification and experience in GMP environments.

Responsibilities include ensuring GMP compliance, training junior staff, and maintaining high standards of production.

Required: degree in engineering or a related field, extensive GMP experience, and significant leadership experience.

Candidates must have a degree in a relevant scientific discipline and prior experience in highly regulated environments such as cGMP or ISO.

Ideal candidates should have experience in radiopharmaceutical or aseptic production, work well in teams, and comply with GMP regulations.

The successful candidate will ensure GMP compliance, conduct laboratory experiments, and support project initiatives.

This role entails overseeing validation project activities while ensuring compliance with GMP guidelines.

You will manage projects from concept to completion, ensuring compliance with GMP standards while optimizing plant infrastructure.

A growing global pharmaceutical manufacturer in the UK is seeking a Microbiology Manager to lead microbiology activities ensuring compliance in a GMP-regulated environment.

A leading digital recruitment agency in the UK is seeking a senior professional with extensive experience in the Google Marketing Platform (GMP). Candidates must have at least 7 years of GMP experience and a strategic mindset to engage with senior clients successfully.

A leading digital marketing technology firm in Greater London is seeking a professional to develop and support its Google Marketing Platform clients.The role requires over 5 years of PPC experience and strong communication skills.You will manage client onboarding, provide technical support, and deli

LUNAR LABS LIMITED is seeking a Quality Management System (QMS) specialist to oversee and support the Quality Management System in compliance with GMP standards. A Bachelor's degree in Pharmaceutical Sciences or related field is required along with experience in a GMP-regulated environment.

You will oversee maintenance activities, manage technical documentation, and ensure compliance with GMP regulations. The ideal candidate has experience in GMP environments and relevant engineering education.

Applicants should have a pharmacist qualification, experience in GMP environments, and a passion for driving continuous improvement.

Integrating new capabilities for prototyping of tech solutions for both Assembly and GMP Clients. Be an evangelist to help our clients be at the top of their game by helping with their technical solutions of the GMP & GCP tools. Experienced throughout the GMP tech stack.

A UK-based innovation organization is seeking an experienced IT Director to lead their technology strategy.This role will enhance digital platforms and ensure compliance with cybersecurity regulations.Responsibilities include overseeing IT operations across multiple sites, leading a team, and aligni

The role involves running the packaging line, ensuring compliance with GMP, and maintaining quality standards while packaging pharmaceuticals.

This role requires a Bachelor's degree in science or engineering and 5-7 years of experience in GMP environments.

A global pharmaceutical leader is seeking a Packaging Operator to join their production team in England.This mid-senior level role involves operating packaging equipment and ensuring compliance with safety and quality standards.Ideal candidates will have experience in pharmaceuticals or similar regu

The ideal candidate will have at least 3 years of experience in a GMP environment, a university degree in pharmaceutical production technology, and strong communication skills.

A pharmaceutical manufacturing company is seeking a Multi Skilled Engineer for its Holmes Chapel site.This onsite, permanent role involves maintaining pharmaceutical production equipment and ensuring compliance with safety standards.Candidates should have at least 2 years of relevant experience and

NHS Blood and Transplant is seeking an Eye Services Technical Officer to support our Eye Bank team in maintaining high-quality services.This role includes preparing samples, maintaining equipment, and ensuring compliance with standards.The position offers a supportive work environment, flexible work

Deze rol vereist minimaal 2 jaar labervaring, een MLO opleiding, en kennis van GMP/GcLP.