Find jobs in pharmaceutical quality assurance (QA) and quality control. Includes jobs requiring GCP, GLP, GMP.
Quality Assurance jobs in Belgium (4), Bulgaria (1), Czech Republic (1), Denmark (1), France (1), Germany (4), Ireland (7), Italy (1), Multiple Countries (4), Netherlands (2), Poland (2), Spain (1), Sweden (1), Switzerland (18) and United Kingdom (8).
This is a senior leadership role with enterprise-wide authority and accountability for the governance, effectiveness, and continuous advancement of BioMarin’s global Supplier Quality Management framework across the external supply network for GMP/GDP
Develop and lead clinical biomarker strategies across Ipsen's oncology and rare disease portfolio to support critical development and portfolio decisions. Define biomarker plans to support target engagement, pharmacodynamic and mechanistic understanding,
You will be responsible for managing the required quality activities and documentation associated with the portfolio of CMOs, ensuring that the CMOs manufacture and deliver products in compliance with Sanofi’s requirements specifications and regulations
Ensure that all NPI and Commercial Products manufactured at AbbVie Biologics are in accordance with the relevant GMPs. Ownership and Accountability for the Management and oversight for effective product transfer of NPIs and transfer to commercial
Lead and ensure compliance of global CQA processes across multiple sites; Act as key Quality partner for cross-functional stakeholders (e.g. Clinical Trial Teams, Biometry, CROs); Drive continuous improvement initiatives and proactively identify risks and
The Senior GVP QA Manager is responsible for supporting the maintenance and continuous improvement of the global Pharmacovigilance (PV) System to ensure that Santhera fulfils its legal PV obligations as both a Marketing Authorisation Holder (MAH) and
The role is responsible for formulation design and process development across various modalities, with a focus on ADCs, within the Formulation Technology Research Laboratories (FTRL). Responsibilities include supporting the preparation of regulatory
Manage day-to-day QC lab operations, including raw materials, in-process, and final product testing; Lead analytical method qualification, validation, and transfer; Oversee analytical methods including flow cytometry, qPCR/ddPCR, and cell-based assays;
Fully accountable for planning execution of sterilization validation, cleaning validation, filter validation, shipping validation, temperature mapping and other validations. Manage investigations of complex validation deviations related to cleaning,
Drive continuous improvement initiatives, monitor quality performance metrics and identify opportunities to improve processes and team effectiveness. Ensure quality activities, including batch record review, quality event management and documentation, are
This role ensures compliant, efficient, and high-quality manufacturing execution through strong cross-functional collaboration, technical oversight, and proactive issue resolution. The position also leads team development and drives continuous improvement
In this role, you will be responsible for managing a team of Quality Assurance and Quality Control Specialists, oversee customer and regulatory audits, be QC named responsible person to maintain our MHRA license, overseeing batch release of GMP batches,
Ensure compliance with international quality standards and regulatory requirements. Participation in regulatory inspections and external audits. Support the planning and execution of internal audits. Support with document control activities, including