Få nye jobs på e-mail
- ...candidate holds a Master’s degree in Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences or similar with interest and knowledge of GMP and quality systems with a minimum of 10-year relevant QA experience. The perfect candidate has experience operating in the field...
- ...development and expansion of the company’s headquarters and production facilities. Ensure strong governance, compliance and performance : GMP compliance, risk management, sustainability initiatives and financial oversight of operational budgets and investments....
- ...culture. You will model exemplary behavior: building teamwork and mutual support, rigorously following Good Manufacturing Practices (GMP) to ensure product quality and safety, sustaining productivity across all shifts, maintaining efficient, focused workflows, and...
- ...Are you passionate about clinical trial supply management? Do you have experience within GMP/GDP-regulated environments and managing complex clinical trial supply chains? If so, now is your chance to join Ascendis Pharma as our new Clinical Trial Supply Manager. Ascendis...
- ...Do you have experience with secondary packaging in a GMP-regulated pharmaceutical environment, including development and lifecycle management? Can you strike the balance between adhering to a well-defined set of regulations, quality standards and execution with respect...
- ...security, and business continuity? Could you see yourself leading OPEX/CAPEX projects, building high-performing teams, and ensuring GMP-compliant excellence? Then we have an opening for you as our Director of Facility Management, Security & Business Continuity. The Role...
- ...improvements projects) Provide support to tech transfer programs and operations as equipment owner Responsible for driving and supporting GMP events related to equipment in scope such as deviations, change controls, events, inspections Participate in Operational board...
- ...collaboration with the site Quality function. Developing and executing the annual plan for periodic review, ensuring qualified status of GMP-classified systems and processes. Leading and participating in both customer-related and internal projects. Who we are looking...
- ...role, why now We are supporting a Nordic biotechnology scale-up operating within advanced cell therapy (ATMP). The company combines GMP-certified manufacturing with a dual-track model, where patient-funded clinical use runs in parallel with formal clinical development....
- ...huvudkontor ligger i Frösundavik i Solna. Vi söker en QA Specialist med 3–5 års erfarenhet som vill arbeta brett inom kvalitetsarbete, GMP och kvalitetssystem, med fokus på att säkerställa robusta processer, effektiva arbetssätt och hög regelefterlevnad. Rollen passar...