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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.

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

QHSE, Compliance & Improvement Responsible

We are looking for a colleague with a high drive, who is ready to ensure the right processes and compliance, especially with new regulations for DESMI to comply to – e.g. new legislation and other external requirements for Supply Chain, quality management and continuous improvements.

Your possibilities includes:

• Opportunity to work in globally recognized and growing company
• Professional and personal development as well as educational opportunities
• Freedom in the position and flexible working conditions with the possibility of occasionally working from home

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.

Global Director of Training

FairWind is a leading provider of one-stop solutions for installation and service of onshore and offshore wind turbines throughout the world. Some of your responsibilities will be to:

• Ensure EWA and all future FairWind Group training centres operate at best-in-class safety- and quality levels.
• Drive the global expansion of the FairWind Group training activities.

We offer stable employment with freedom under responsibility, and an agile company structure and short decision-making path.

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.

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.

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.