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23 jobannoncer matcher din søgning 23 jobannoncer fundet
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Manager Virus Production
Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?
Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.
Specialist, Regulatory Affairs (Temporary Position)
As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.
Further, your main responsibilities include to:
- Gather information and documentation for variation applications
- Update dossier sections
Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)
Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?
Your core responsibilities:
- Handling deviations for products manufactured at our factories.
- Handling of product quality related complaints.
- Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.
Department Manager for Molecular Pharmacology
Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.
Your tasks include
- Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
- Guide the team to accomplish department goals and objectives.
- Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.
Senior Application Specialist - Culinary
For the Culinary Design in Brabrand, we are seeking a Senior Application Specialist to assist us in servicing our external and internal customers.
Main Responsibilities:
- Servicing our European based customers within the Culinary solutions – from Globals to Start ups
- Execution of customer related tasks in close collaboration with colleagues in the group and across the entire organization
Project Coordinator
Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?
As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.
Scientist for In Vivo Sales in Boston
Are you passionate about discussing science, identifying opportunities for customer value creation and creating visible results? Do you have excellent analytical skills and a strong commercial mindset? Are you a natural communicator and thrive building relationships? If that is the case, we have a great career opportunity for you.
Your primary area of responsibility will be to partake in day-to-day sales operation, drive the forward-looking dialogues with key customers as well as identifying and following up on new business opportunities. Furthermore, you will be involved preparing sales presentations, market analyses, and marketing materials.
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.
GMP Material Scientist
Are you motivated by challenges and thrive in a fast-paced environment?
Delegated QP for QA Finished Goods Manufacturing
We are looking for an experienced delegated Qualified Person (QP) to join our successful QA team supporting Finished Goods Manufacturing (FGM).
Product Stability Scientist
Are you passionate about working with solid dose products and other emerging technologies?
Senior QMS Professional
Are you ready to make a difference for people living with diabetes and be part of the tablet production in Emerging Technologies (ET).
Adv QA Professional in Device Development
Are you looking for an exciting opportunity to advance your career in Quality Assurance?
QA Professional, Team Facility and Equipment
Are you eager to play an important role in ensuring the quality and safety of products for clinical trials?
Qualified Person Delegate - QPD
Are you a Qualified Persons Delegate (QPD) seeking a rewarding career opportunity in the pharmaceutical industry?
QA Assistent
Kunne du tænke dig at være med til at sikre kvaliteten af lægemiddelprodukter til kliniske forsøg?
Senior QA Professional
Are you an experienced Quality Assurance professional with a passion for ensuring high standards and compliance?
Associate Manager
Do you want to be part of Novo Nordisk’s journey towards developing and manufacturing new oral products for clinical trials?
Scientist - Mammalian Cell Cultivation
Do you have experience with mammalian cell cultivation at a pilot scale or motivated to learn?