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28 jobannoncer matcher din søgning 28 jobannoncer fundet
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Manufacturing Associate - Operator
We are looking for process operators, preferably with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.
We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.
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.
Associate Sensory scientist/Sensory Panel Lead - Arla Innovation Centre, Aarhus
We are looking for two new Sensory Panel Leads. One new collegue for a 1 year maternity cover and one for a 3 year project. For both positions we hope we will be able to prolong the employment or offer new challenges within Arla Foods.
Your key responsibilities will be:
- In close contact with stakeholders, guide and choose the proper test-setup to deliver the sensory results needed
- Panel training and development of panel competences within specific areas of interest
Regulatory Affairs Specialist
The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.
In this role, you will have the opportunity to:
- Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
- Ensure compliance with EU regulations.
- Generate STED files, international submissions & assess design changes.
- Plan and execute projects for new regulatory requirements.
Senior Regulatory Specialist
The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.
If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.
Regulatory Affairs Manager
The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.
This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:
- Ensure regulatory compliance to maintain market approvals
- Lead a team of skilled RA associates
- Ensure alignment with relevant stakeholders
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
Senior Engineer Device Manufacturing
Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?
Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.
QA Specialist
You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.
You will have the opportunity to:
- Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
- Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.
Senior Scientist - Enzyme Development - Animal Nutrition and Health
Would you like to be part of a world leading international team developing groundbreaking enzyme solutions for Animal Nutrition and Health?
You will join dedicated project teams and work with leading scientists from around the world on new enzyme-based products for major global companies. And you can apply world class industrial bioscience competencies to generate new sustainable solutions for Animal Nutrition and Health.
Continuous Improvement Partner
As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.
Your primary tasks will include but not be limited to:
- Develop and sustain CI systems and tools.
- Coach on ideal behaviour that drives a proactive improvement culture.
Medical Scientific Liaison Renal Acute
Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company.
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).
Manufacturing Project Supporter
We’re in search of our new team-mate for the role of Manufacturing Project Supporter, to join the Manufacturing Support Department in Hillerød!
Upstream Support Specialist
Would you like be responsible for providing technical assistance within process design and process documentation?
Microbiologist in Quality Control - Maternity Cover (12 months)
Are you eager to join a fast-growing pharmaceutical company?
Adv QA Professional in Device Development
Are you looking for an exciting opportunity to advance your career in Quality Assurance?
Project Senior QA professional
Do you possess a strong quality-oriented mindset and excellent interpersonal skills that can contribute to a significant impact on 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?