Kunne du tænke dig at arbejde med udvikling og optimering af farmaceutiske produkter i et dedikeret team af dygtige kolleger og har du erfaring med HPLC i en farmaceutisk kontekst?

Zealand is looking for an MD with significant experience in clinical safety and pharmacovigilance for the PV Director position, reporting to the Head of Patient Safety.

Novo Nordisk is on a mission to bring novel stem cell therapies out to people in disease areas with large unmet needs. We need you in our journey!

You will join the Non-Clinical Safety Team in the Non-Clinical Development & Bioanalysis Department with highly experienced scientists and report directly to the Senior Director of Non-Clinical Safety. You will be part of a team that consists of 5 highly skilled colleagues being responsible for several different projects. Your role will be to work cross functional focused on the cooperation with CMC. Ascendis Pharma is in Denmark, Germany and California and you will be in regular contact with employees at all three geographic locations.

In a biotech company focused on the discovery, design and development of innovative peptide-based medicines

In this exciting position, your quality competencies and experience will come into play as a Lead Auditor within the field of Pharmacovigilance. You will be responsible for performing pharmacovigilance audits of the ALK Headquarter, ALK affiliates, Service Providers and Distributors on your own or in close collaboration with other GVP, GDP and GCP Lead Auditors in ALK. In addition to the auditor role, you will act as Quality Business partner to the Global Pharmacovigilance organization including the QPPV office.

Lundbeck’s passion links to our purpose about restoring brain health so every person can be their best. We strive to make a real difference to patients. By developing innovative treatments, we improve the lives of people living with brain diseases. Your dedication is crucial. That is why you can expect us to be committed to your progress, so you can stay committed to ours.

Y-mAbs is now looking for a Regulatory Affairs CMC senior manager in a newly established position in Global Regulatory Affairs. You will become an important part of managing regulatory submissions and approvals in new markets and establishing LCM. You will report to the LCM Lead of Global Regulatory Affairs.

Best Talent is on behalf of Unilabs looking for a business oriented Project Manager to further strengthen the growth and help Unilabs develop the project model and upgrade their project tools and inspire, teach and motivate the other Project Managers.

For vores klient søger vi en International Product Manager der skal tage et helt nyt forretningsområde indenfor Urologi, fra start til lancering WW.

In ALK´s Global Quality function, you will become part of a dynamic team with about 10 dedicated employees working to optimize and simplify the quality management system and the corporate processes in close collaboration with global stakeholders. Your main role will be to the process expert and drive changes and improvements

You will act in a close collaboration with several external Contract Manufacturing Organizations (CMOs) and process- and QC SMEs internally at Ascendis Pharma. It is expected that you find solutions and that you can think out of the box within your area of responsibility. You go through different processes to drive the area most effectively for the team and the company. The team is characterized by high quality, result orientation and speedy realizations of the goals in an entrepreneurial environment.

The Clinical Trial Operations area of Genmab is growing and looking for a Sponsor Oversight Lead (SOL) to join the team in Copenhagen. As Sponsor Oversight Lead at Genmab you will be responsible for the planning, conducting and coordination of trial oversight activities together with internal and external stakeholders to ensure quality and integrity of the data.. The SOL works closely together with the Clinical Trial Managers with the oversight activities across Genmab clinical trials.

The Clinical Operations team is looking for an eTMF Manager, who will be part of an eTMF management team and work in close collaboration with the Clinical Trial Process Management (CTPM) team and the Clinical Management Teams (CMTs) ensuring that the eTMF is audit and inspection ready.

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients.