3 jobannoncer matcher din søgning 3 jobannoncer fundet

Senior Technical Writer - Regulatory (CMC)

You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.

Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.

Clinical Site Manager

Are you looking to make a significant impact on ensuring oversight of our outsourced clinical studies in Ferring Pharmaceuticals? Do you thrive in a global role that requires cross-functional collaboration?

In this role you will solidify the implementation of the Clinical Site Manager role. This role was recently introduced as being responsible for providing sponsor oversight of clinical site monitoring (outsourced to a CRO) and establishing strong relationships with clinical sites to ensure delivery of high-quality and timely clinical trials.

In this role you will be working closely with counterparts in the US and stakeholders at our International PharmaScience Center (IPC) in Copenhagen.

Senior QA Specialist

As a member of our professional QA team, you'll be responsible for ensuring that our release and quality systems meet regulatory and industry standards. Working alongside a team of 8 QA Specialists and 2 student workers, you'll report directly to the QA Manager.

Your responsibilities will include:

• Reviewing and approving batch documentation, raw materials, process solutions, API intermediates, and final API
• Releasing materials and APIs