Senior Manager GQA Corporate Audits

Are you meticulous, curious, and interested in joining a team where your high integrity is trusted and valued?

If you have a strong background in pharmaceutical manufacturing and quality assurance, we invite you to join Ferring Pharmaceuticals as a Qualified Person (QP).

In this business-critical function, you will support our R&D CMC teams in development projects, delivering high-quality Investigational Medicinal Products to clinical trials across the world.

Procesoperatør til vores produktion

Som en del af vores team er du med til at gøre en forskel for mennesker, der lever med ledproblemer og/eller ønsker at opretholde en aktiv livsstil.

Dine arbejdsopgaver:

• Overvågning og styring af procesanlæg (SCADA)
• Prøveudtagning
• Håndtere råvarer, mellem og færdigvare

Director - Analytical Development, Methods & Characterisation

Do you find great professional fulfillment in empowering individuals to excel in their roles, and do you have experience managing a team of highly skilled scientists?

As Director of Analytical Development, Methods, and Characterization, you are encouraged to use a coaching leadership style to strategically strengthen the area of analytical method development, validation, and chemical characterization in the Ferring CMC organization.

Clinical Trial Manager – Empower progress in clinical studies

Do you thrive in a dynamic environment where your problem-solving skills and passion for optimizing workflows can truly shine?

NBCD is a world-leading CRO specializing in osteoarthritis and musculoskeletal diseases.

You will be at the forefront of driving the planning and execution: Lead the planning, implementation, management, and close-out of clinical trials, ensuring that each phase is executed with precision and care.

Toxicologist (Scientist)

In this role, you’ll contribute to meaningful work that ensures the safety of our innovative products. Your responsibilities will include:

• Providing toxicological insights, risk assessments, and advice on Novonesis products throughout their development phases.
• Designing and overseeing in vitro and in vivo toxicological and ecotoxicological studies conducted by contract research organizations (CROs).