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Process Engineer

The Process Engineer will be responsible for process engineering and technical support of Tetra Pak capital projects, as well as specification of equipment and functional design within the given time and budgets.

You should be prepared to travel approximately 30% of your time to meet colleagues, customers and suppliers to fulfil the role (internationally, with extensive travel throughout North Europe & Benelux).

Maintenance Manager

As the Maintenance Manager, you will be a key member of the leadership team, collaborating closely with our other leaders from various departments.

Collaborating with the leadership team, you will be a part of driving the factory's success and contributing to the achievement of our business objectives. As maintenance manager, you will oversee our maintenance team and ensure the implementation of best practices to optimize the performance of our manufacturing equipment and facilities, ensuring alignment with our organizational goals and HSE principles.

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.

Group Lead

Help us to be ready to face the energy challenges of tomorrow and make a green footprint.

We are looking for someone who:

• Ensures adherence to defined manufacturing guidelines, processes and procedures.
• Supervises production activities according to established quality standards and EHS requirements.
• Contributes to production planning processes, and determines manufacturing priorities based on established weekly production schedules.

Biocompatibility Specialist

We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.

This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.

Senior Product Test Engineer - Medical Devices

Do you want to design safe and reliable medical devices, bringing our clients' life-changing solutions into the hands of patients and helping patients to get better treatment?

You will be an essential contributor in the development and designing optimal verification methods for requirement confirmation.

We seek to enable the best work environment that helps you and the business work together to produce superior results.

Surveyor

As a surveyor you will be involved in the blade production from beginning to end. Your will be in charge of inspection and optimalisation of the production equipment at the Aalborg plant.

Your responsibilities will include:

• Measuring, verification and quality control
• Optimization and implementing new projects
• Conducting quality control of the production equipment

You will be working in an international team, so good communication skills are a must. Good skills in written and spoken English are needed as well as working knowledge of MS Office.

Continuous Improvement Leader

You will cover a fundamental position within the EMEA Continuous Improvement team for Kimberly-Clark Professional. You will be responsible to provide leadership, vision, coordination and functional direction to the Mill leadership team for all elements to the development, introduction and sustainability of LEAN operating principles.

: we can offer a hybrid model (on remote 2 days/Koblenz Mill 3 days per week) for candidates already based in Koblenz Area.

Technical Writer to GE HealthCare Denmark

Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. 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.

Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.

QHSE Senior Manager

To support our mission to provide effective and quantifiable energy solutions in a safe and sustainable manner, Welltec is strengthening the QHSE organization and actively recruiting for a QHSE Senior Manager with a global role.

The QHSE Senior Manager owns and drives activities in alignment with the global QHSE direction and ensures that they are conducted in accordance with internal and external requirements, promoting safe, reliable and sustainable solutions. You will be responsible to effectively drive the implementation of QHSE processes globally.

QHSE Coordinator

To support our mission to provide effective and quantifiable energy solutions in a safe and sustainable manner, Welltec is strengthening the QHSE organization and actively recruiting for a QHSE Coordinator with a global role. This role will support our mission to provide effective and quantifiable energy solutions in a safe and sustainable manner.

The QHSE Coordinator provides continuous advice and support to ensure activities are conducted in accordance with internal and external requirements, promoting safe, reliable and sustainable solutions.

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.

Group Lead

På vores fabrik i Aalborg producerer vi vinger til vores offshore vindmøller, og her kommer du til at stå i spidsen for ca. 30 til 40 medarbejdere på enten Primo eller Ultimo skiftene. Der arbejdes 6 vagter af 12 timer fordelt på 14 dage.

Du har ansvaret for produktionen, og her er du den synlige leder og holdkammerat, der ude på gulvet sætter retningen for sine medarbejdere.