2 jobs found

Quality Assurance Officer (GMP/Cannabinoids) Sandwich Up to £40,000 + Company Bonus + Private Healthcare + Pension + Training Are you a Quality Assurance Officer or similar with GMP experience looking to join an innovative pharmaceutical manufacturer operating within one of the fastest-growing areas of the life sciences industry? Do you want to join a specialist pharmaceutical manufacturer backed by a globally recognised leader in its field, offering the opportunity to work on cutting-edge Active Pharmaceutical Ingredients (APIs), broaden your Quality Assurance experience and play a key role within a growing business? On offer is a fantastic opportunity to join an expanding pharmaceutical manufacturer producing specialist APIs for highly regulated pharmaceutical and nutraceutical markets. You'll gain exposure across the full Quality Assurance lifecycle, take ownership of key quality systems and contribute to the continued growth of a business operating in an exciting and evolving sector. This role would suit a Quality Assurance Officer or similar with GMP experience looking to broaden their technical expertise within a specialist pharmaceutical environment, where they'll have genuine responsibility, opportunities to influence quality systems and excellent prospects for long-term career development. In this role, the successful Quality Assurance Officer or similar will maintain and improve the Quality Management System, review batch manufacturing documentation prior to release, manage CAPAs, Deviations, Change Controls and investigations, support internal and supplier audits, and work closely with Production and Quality Control teams to ensure products are manufactured to the highest GMP standards. There will also be opportunities to become involved in validation activities, supplier quality and wider continuous improvement projects. The Role: Maintaining and improving the Quality Management System within a GMP pharmaceutical manufacturing environment Reviewing batch records, quality documentation and managing CAPAs, Deviations and Change Controls Supporting audits, validation activities and continuous improvement projects The Person: Quality Assurance Officer or similar GMP experience within pharmaceutical or another highly regulated manufacturing environment or similar Knowledge of QMS, CAPAs, Deviations, Change Controls and batch record review Looking to develop their career within a specialist pharmaceutical manufacturer Reference Number: BBBH26365 If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job is not quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C's, Privacy Policy and Disclaimers which can be found at our website.

QA Officer About the Role 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 Responsibilities Support 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 You We'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 Offer Opportunity 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!