1 to 25 of 47 Permanent GMP Jobs

change control, deviation, back up and archive, security, and other support processes for IT systems. • Participate in quality meetings keeping the group updated on initiatives within the QA owned GMP IT systems. Continuous Improvement & Strategy: • Identify areas for optimization in data flow, system integration, and validation strategies. • Champion initiatives in digital transformation, data contextualization, and visualization to enhance decision-making More ❯

required. About You Degree in a Life Science subject (or equivalent experience). At least 3 years' experience in QA/QC within pharmaceutical manufacturing. Strong working knowledge of GMP and QMS processes. Excellent attention to detail and strong organisational skills. A collaborative team player who can also work independently. What's On Offer Competitive salary plus shift allowance and More ❯

with diverse cultures Necessary legal status to work in the UK. Beneficial requirements: The closest relevant experience would be MES/EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers. Experience of different project delivery methodologies including waterfall and agile Experience of client account management Knowledge of Computer System Validation is an advantage. Key Responsibilities: Become an expert More ❯

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National Regulatory Authority (AIFA) and is compliant with the FDA More ❯

a scientific discipline (e.g., microbiology, biology, biomedical sciences) or equivalent. Proven experience in quality assurance within a regulated manufacturing or laboratory environment. Strong knowledge of quality systems, ISO standards, GMP/GDP principles, and regulatory compliance. Skilled in leading audits, managing CAPAs, and interpreting quality metrics. Excellent leadership, communication, and problem-solving abilities. Proficient in data analysis tools, LIMS, and More ❯

as QA Manager will take ownership of Quality Assurance. Duties Lead and manage the QA team across the Abattoir and Boning Hall. Be responsible for delivering high levels of GMP, food safety and integrity standards within the factory. Support in driving food safety, compliance, and quality improvements across site. Update and maintain the QMS, conduct audits and ensure any corrective More ❯

Participating in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Auditing compliance against Quality Management Systems, GMP and HACCP controls - raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participating in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Auditing compliance against Quality Management Systems, GMP and HACCP controls - raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

perform other functions as assigned. Top 3-5 skills, experience, or education required for this position: Fully bilingual in Spanish & English with written communication skills Knowledge of good manufacturing (GMP) and safety practices Basic knowledge in computer systems Available to learn and work Nice to have (but not required) skill, experience, education, or certification: POMS, SAP, Sample Management Type of More ❯

and embedded analytics for production KPIs. Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable. Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.). Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs. Ability to translate complex operational processes into streamlined SAP-enabled solutions. More ❯

cycle methodologies, 21 CFR Part 11, and GAMP. 4. Development of detailed specification, engineering documents, SOP and operating standards. 5. Ownership and administration of process control automation in a GMP regulated manufacturing setting. 6. Engage in, and process change control requests per established SOP and processes. 7. Lead technical root cause analysis, incident investigations, and troubleshooting on process control issues More ❯

policies and procedures Ensuring samples are collected for testing schedules and testing schedules are met Logging micro samples Accurate carrying out of positive release checks for all finished products GMP audits/Glass and plastic audits, including generation of improvement areas, completing database Ensure close outs of non-conformances Sampling and recording of finished product shelf life Carryout of routine More ❯

Factory Food Safety Inspections, Audits, Customer Complaint and Foreign Body handling. Working hours:4 days on, 4 days off. 6am-6pm Pay: £29,092 per annum Main Responsibilities Conduct GMP audits with production and address any issues. Verify traceability documents have been completed correctly and challenge any mistakes Log complaints and Foreign Bodies conduct investigations and work with production to More ❯

discipline or equivalent experience working in a laboratory environment Proven leadership capabilities with experience managing teams and driving performance Strong understanding of laboratory operations, scientific processes, and compliance within GMP-regulated environments Demonstrated knowledge of health, safety, and environmental standards in laboratory settings Proficiency in Microsoft Office 365 and familiarity with lean methodologies such as Kaizen and Tiered Daily Management More ❯

PharmaSuite implementation and integration For both positions: - Degree in Electrical, Chemical, Process Control, or related Engineering field - Experience with automation projects in life sciences or regulated industries - Familiarity with GMP, GAMP5, and 21 CFR Part 11 - Strong troubleshooting and collaboration skills - Business-fluent English Why apply? - Work on high-impact automation projects at one of the world’s most advanced More ❯

changes to the QA/Technical Manager promptly. Complete reasonable requests from QA/Technical Manager. Training & Support Support and train new QA team members as required. Auditing Conduct GMP audits and maintain audit schedules. Carry out fabrication audits to ensure compliance with standards. Skills & Knowledge Strong understanding of Quality Systems procedures and documentation. Self-motivated with effective time management More ❯

customer specifications are always achieved. A key member of the HACCP Team, attend and participate in all HACCP meetings. As part of the internal auditing team, you will conduct GMP, Glass, Hygiene and other internal audits to ensure the site meets the safety, quality and legality requirements Attend site meetings as required and prepare accordingly. Be the ERP specialist for More ❯

Carry out routine quality checks across raw materials, production processes, and finished products. Maintain accurate and compliant documentation in line with industry and company standards. Ensure adherence to HACCP, GMP, and site-specific quality procedures. Support internal and external audits through meticulous record-keeping and process compliance. Investigate non-conformances and assist in implementing corrective actions. Work closely with production More ❯

not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work locationKey Requirements and Technology Experience: Key Skills:Rockwell PLC, GAMP/GMP, Validation Testing. Rockwell PLC/DCS systems, Logix 5000, FT View, PlantPAx. GAMP 5 (V-Model) documentation. Verification test planning and execution. Cross-functional teamwork, coordination, and communication skills. Proficient More ❯

continuous improvement in patient outcomes. Your new role As QA Compliance Manager, you'll lead a team responsible for maintaining and improving the Quality Management System in line with GMP, ISO, and regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits. You'll also contribute to strategic quality … Qualified Person (QP) sponsorship for the right candidate. What you'll need to succeed A degree in a scientific discipline (e.g. Chemistry, Biology, or related field) Extensive experience in GMP-regulated environments (10+ years preferred) Strong leadership and people management skills In-depth knowledge of EU cGMP and ISO standards (9001, 13485) Experience supporting or conducting batch release under QP More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯