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Head of Division for the WMC division at DTU Wind and Energy Systems

You will take an important leadership position, which involves the responsibility of 80-100 highly qualified employees, including PhD students, researchers, professors, development engineers, technicians, and administrative staff.

You will have overall responsibility for the division's research, education, innovation, and commercial activities, as well as the operation of research facilities.

As Head of Division, you will also be part of the department's management group, which, in addition to the Head of Department, consists of three other Heads of Division and the Head of Administration.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.

Team Lead

For our Offshore Equipment Material Management department in Esbjerg, we are looking for an Equipment Center Team lead, Offshore Equipment Material Management department handle lifting, calibration, and maintenance activities.

Offshore Equipment Material Management is an internal service provider responsible for all equipment required for transporting, installing, and servicing of the wind turbines all over the world. The Material Management department is based in Denmark, United Kingdom, Taiwan and soon US.

Manufacturing Lean Leader

This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

As our new Lean Leader, you will lead the site’s Kaizen funnel, daily management system, coach colleagues and work on improving for a better tomorrow. You will lead and manage projects that positively impact operations.

You will be a key staff member of the site operations team, this role exercises a high level of operational judgment, and sets team priorities in alignment with the strategic imperatives of the manufacturing site.

Column Pack Operator

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us. We’re growing our locations, our capabilities, our teams and looking for passionate, mission-driven people who want to make a real difference in people’s lives.

We are currently looking for candidates to work within Drug Substance Manufacturing (DSM) Support and become part of a newly established team, responsible for preparation, packing and qualification of chromatography columns.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Senior QA Specialist

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.

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.

Project Manager – Test & Verification

You get the possibility to be a key person in Foss New Product Development projects by ensuring high quality and product compliance to our world class analytical solutions.

As a member of the R&D Hardware Test & Verification team, you will be one of three Project Managers responsible for overseeing all reliability, environmental, and legal testing of instruments used in analytical solutions. Additionally, you will plan and ensure that our team develops and integrates value-adding production tests, which are crucial for the seamless assembly of the instruments.

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.

Specialist in Organic Coating Processes and Chemicals, Materials & Processes Engineering Department, Terma Aerostructures A/S.

Your role involves overseeing all organic coating processes, ensuring compliance and quality of materials such as epoxy- and polyurethane-based paints. You will also manage the requirements for consumable chemicals, like solvents for surface cleaning.

The responsibility furthermore entails the overall responsibility for REACH surveillance and chemical substitution activities at our Grenå manufacturing site, in close collaboration with other process owners.

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 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.

Lean Manager

As Svendborg Brakes are facing great challenges going forward, we are looking for a competent person who is keen about improving, growing and developing smarter ways to work efficient.

The Lean Manager will be responsible for the development, implementation, and evolution of the business systems and tools, such as 6Sigma, 5S, Kaizen, value stream and other lean tools in our facilities. There will be a focus on driving growth through the lean philosophy and tools while collaborating with the facilities’ teams and management to drive a culture of continuous improvement.

Senior QA Specialist

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

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.

Packaging Technician

We are seeking a highly organized and detail-oriented Packaging Technician to join our energetic and innovative Global Packaging Team.

As a Packaging Technician in CO-RO, working closely together with a wide range of stakeholders globally, you will assist the Global Packaging Innovation and Strategy Director and Packaging Technologists in the delivery of their projects and initiatives, from concept to launch.

You will have the opportunity to work within a manufacturing plant and a technical department, within an exciting and innovative environment.