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Piramal Pharma Solutions is seeking a QA Team Leader to play a pivotal role in shaping and governing the Pharmaceutical Quality System (PQS) at our Grangemouth site. This role goes beyond routine compliance — it’s about quality leadership, risk-based decision making, and continuous improvement in a fast-paced clinical manufacturing environment. You will provide quality oversight for Antibody–Drug Conjugate (ADC) and other bioconjugate drug substances/products in clinical activities, ensuring regulatory readiness while partnering with site functions to embed quality into day-to-day operations. This role is ideal for a QA leader who thrives in collaboration, governance, and proactive quality improvement. Responsibilities 🏛️ Quality Governance & Systems Leadership 🔹 Lead governance of key PQS elements including Quality Management Reviews, PQRs, Vendor Qualification, and Audits (self-inspections, vendor, and customer audits) 🔹 Act as site system owner for TrackWise, ensuring effective and compliant use of the electronic QMS 🔹 Maintain and manage site regulatory registrations, licenses, and certifications 🔹 Serve as a Single Point of Contact between site QA and Corporate Quality (as delegated by the QA Manager) 🧪 Clinical & GxP Quality Oversight 🔹 Ensure site and functional compliance with UK/EU/US GMP/GDP, ICH, and other applicable regional guidance 🔹 Provide QA leadership supporting clinical ADC manufacturing, focusing on risk-based quality decisions rather than checkbox compliance 🔹 Identify, analyse, and communicate GxP trends, supporting proactive risk management and mitigation plans 🔹 Track regulatory intelligence and inspection trends to support inspection readiness 📊 Continuous Improvement & Metrics 🔹 Coordinate and report Quality Compliance KPIs and metrics to key stakeholders 🔹 Drive site-wide initiatives to reduce out-of-compliance events and improve right-first-time performance 🔹 Support and lead quality system and compliance improvement projects 🧠 Investigations, Audits & Training 🔹 Support quality investigations and ensure development of robust, effective CAPAs 🔹 Lead and support pre-audit preparation, audit hosting, and post-audit follow-up for customers and regulators 🔹 Coordinate and oversee QMS and GxP training, ensuring regulatory alignment and site engagement 🔹 Lead Quality Management Review meetings, clearly highlighting risks, actions, and improvement opportunities ✅ What We’re Looking For ✔️ Strong QA leadership experience in clinical-stage GMP environments (ADC or sterile/biologics experience highly desirable) ✔️ Deep understanding of PQS, risk management, and quality governance ✔️ Proven ability to influence cross-functional teams and embed quality culture ✔️ Experience working with electronic QMS systems (TrackWise preferred) ✔️ Confident communicator who can balance compliance, pragmatism, and business needs ✔️ Passion for continuous improvement and modern quality thinking

Piramal Pharma Ltd in Falkirk is looking for a diligent QA Document Controller to provide document control support within the Quality Assurance department.

Logging and tracking of documents through QA department.

Piramal Pharma Limited is seeking a QA Document Controller in Falkirk, UK.

QA Document Controller page is loaded## QA Document Controllerremote type: Onsitelocations: Falkirktime type: Full timeposted on: Posted Todaytime left to apply: End Date: May 28, 2026 (29 days left to apply)job requisition id: R00000985DivisionPiramal Phar

The Opportunity We are working with a leading biopharmaceutical manufacturer who are seeking an MSAT Bioprocess Engineer to support the technology transfer of biologics processes from development into GMP manufacturing. This role is central to ensuring smooth scale‑up, robust documentation, and ongoing process improvements within a compliant Quality Management System. Key Responsibilities Lead the technology transfer of new and existing biologics processes into GMP manufacturing. Prepare, review, approve and issue GMP manufacturing documentation, including batch records. Define scale‑up criteria and develop process mass balances and flow diagrams. Specify large‑scale equipment and assess material suitability for GMP use. Generate quality documentation for raw materials and equipment. Work within the site Quality Management System, raising and managing change controls. Conduct and close investigations, deviations and CAPAs. Project manage the introduction of processes into manufacturing from end to end. Perform risk assessments aligned with ICH Q9 principles. Collaborate cross‑functionally with MSAT, Development, Manufacturing, QA, Supply Chain, Engineering and Project Management teams, as well as relevant external partners. Essential Qualifications & Experience BSc (Hons) or equivalent in a Science or Engineering discipline. Proven GMP biologics manufacturing or process development experience. Strong organisational and stakeholder influencing skills. Demonstrated project management capability and ability to meet deadlines. Experience in process scale‑up/transfer and providing manufacturing support. Effective communication across all levels. Experience evaluating materials for process suitability and writing GMP batch records. Desirable Experience Commercialisation and process validation. Process improvement and process mapping. Defining, sourcing and validating large‑scale bioprocessing equipment. Key Competencies Strong time‑management skills Effective team working Clear communication High attention to detail Strong problem‑solving Sound decision making Why Join You'll play a pivotal role linking development and GMP operations, directly influencing manufacturability, compliance and the successful delivery of biologics processes- while working within a collaborative, growth focused environment. The company also offer an extensive benefits package. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

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QA Engineer — £45k–£50k — Join the Fintech Powering Superyachts & Artists Worldwide.

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Throughout your learning journey, you are fully supported by your dedicated QA skills coach and your mentor at work.

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QA Engineer II - Data Discovery and Test.

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Quality Assurance Administrator, Skipton.A role where organisation meets purpose – and every detail matters.If you enjoy keeping things running smoothly, love a well‑organised system, and take pride in getting the details right, this position may feel like home.In this role you will become an es