Find jobs in pharmaceutical quality assurance (QA) and quality control. Includes jobs requiring GCP, GLP, GMP.
Quality Assurance jobs in Belgium (1), Bulgaria (1), Croatia (2), Cyprus (1), Denmark (5), France (5), Germany (5), Hungary (1), Ireland (2), Italy (2), Lithuania (1), Multiple Countries (1), Netherlands (5), Poland (1), Portugal (1), Romania (1), Spain (1), Switzerland (7) and United Kingdom (4).
This role is accountable for defining the vision, operating model, and multi-year strategy for internal QC to support Genmab’s evolving pipeline and transition to a fully integrated, commercial-stage biotechnology company. The role will shape future QC
You lead the site Quality organization and serve as the key authority for GMP compliance and quality strategy. In this executive leadership role, you shape the site’s quality culture while enabling the successful delivery of innovative therapies,
Lead, motivate and mentor your team to maximize their effectiveness by clearly communicating task details and goals to your team members, allowing them to work effectively. Foster a positive progressive culture within the lab that focuses on EED&I
Maximizes development of staff through guidance, coaching, training, and performance management. Provides leadership, direction and management to staff related to monitoring, enrollment and/or site management to ensure deliverables are met. Contributes to
In this role, you will oversee complex analytical projects, drive method development and validation activities, and ensure the highest standards of data integrity and regulatory compliance. You will collaborate closely with cross-functional partners -
The role assures that project output meets combination product regulatory requirements. This position assists in the development and implementation of site/Global QMS GMP policies and procedures. Additional responsibilities will ensure departmental
Ensures the contamination control and mibcrobiological quality control of the Sanofi-products in a complex environment and within the strongly regulated area of the production of active substances with the chosen quality strategy, the applied processes
Ensuring effective and efficient Quality Operations in compliance with legal requirements, standard operating procedures and evolving global regulatory expectations; Optimizing the global Quality Management System to deliver fit for purpose processes
This pivotal role is responsible for maintaining supply chain integrity and product quality across API, cosmetics, drugs, devices, components, and finished products. You will be central to ensuring operational excellence, regulatory compliance, and
Assess, review and approve quality records and release files/dossiers e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions, complaints, APR/PQRs, in line with current local SOPs. Act as QA contact for specific projects
Ensure compliance with all applicable cGMP directives, regulations, and guidelines to maintain the high quality of pharmaceutical products; Lead and oversee deviation investigations, ensuring compliance with Teva corporate procedures and local quality
In this role, you will provide expert support for clinical trial quality, ensure compliance with ICH-GCP and global regulatory expectations, and act as a key partner to internal teams and CROs. You will be responsible for quality oversight, process
A senior leadership role responsible for the technical strategy and process excellence of drug product manufacturing at an Oral Solid Dosage manufacturing site. This includes technical oversight for drug product intermediates control strategy from spray
Provide leadership for strategic site initiatives, and represent site SLT quality in local cross-functional teams representing site quality. Ensure overall compliance to cGMP during manufacturing, testing and distribution of drug products meeting Sandoz
Establish and Maintain collaborative relationships with CMO/CDMO manufacturing organization to ensure successful product manufacturing, process development, and scale-up activities. Assess the performance of external manufacturing partners, identify