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Clinical Supply Manager

The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.

You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.

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.

QA Specialist

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.

Factory Manager Odense

You will be responsible for the factory and its production, where your most important task will be to support stakeholders – with focus on the Nordic market.

You will contribute with input for improvements that can strengthen Unilever's business and participate in meetings with your colleagues from other European Home Care factories, where learning is shared across the factories.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

Quality Manager

We are looking for a new hands-on Quality Manager who will continue the development of the Dancop Quality System.

Othe tasks will include internal auditing of our quality system and work processes, and training of employees in quality assurance.

You are offered an attractive workplace with good and skilled colleagues, and an international working environment with an informal and humorous tone.

QHSE Manager

We are seeking a QHSE Manager who is passionate about establishing a robust safety and quality culture and implementing best practices to join our dynamic team.

Responsibilities will include:

• Assisting the leadership team in developing, managing, and monitoring the company's QHSE performance
• Monitoring and advising on all QHSE matters to ensure compliance with statutory requirements, company and contractual requirements, and industry best practices

Health, Safety and Environment (HSE) Manager

Are you a seasoned Health & Safety professional seeking an opportunity to thrive in a supportive and dynamic environment?

We have an exciting opportunity to recruit a Health & Safety Manager, you will play a crucial role in maintaining and enhancing the safety standards at our facility. Your responsibilities will include designing training programs, conducting risk assessments, identifying, and controlling hazards.

Director, Quality

If you are a dynamic, results-driven leader with a passion for quality and a proven track record of driving excellence in engineering and manufacturing environments, join us in shaping the future of our business service the energy industry worldwide.

The Director of Quality for Subsea Production Systems (SPS) is a strategic role responsible for leading our global quality assurance and quality control initiatives. This individual will drive the quality agenda across all levels of the organization, ensuring the integrity, reliability, and performance of our products.

Downstream processing engineer – 12 months position

In this position you will be part of River Stone’s downstream processing (DSP) team, which is responsible for developing purification methods for our biological production processes for pharmaceutical ingredients.

The ideal candidate possesses:

• M.Sc. or Ph.D. degree in chemical engineering, food process engineering, chemistry, or similar
• Experience within down-stream purification processes, like solid-liquid separation, membrane filtration, crystallization and/or drying is a requirement
• Flair and motivation for hands-on laboratory work
• Ability to work in a fast-paced environment with deadlines and sometimes limited time for data analysis

Elbek & Vejrup søger konsulent til Graduate-stilling indenfor produktion

Brænder du for at dele din viden og for at optimere forretningsprocesser i produktionsvirksomheder?

Vi søger ny kollega med branchekendskab inden for produktion, der brænder for at prøve kræfter med rollen som konsulent og for arbejdet med at optimere vores gode kunders forretninger gennem IT.

Vi tilbyder personlig udvikling samt faglig kompetenceudvikling og en tilknyttet mentor samt en fleksibel arbejdsplads med frihed under ansvar og mulighed for at arbejde hjemme.

Project Manager, New Product Introduction

As a member of the New Product Introduction (NPI) team within the Production and Supply Chain (P&SC) department, you'll represent P&SC in strategic product development projects. Your responsibilities encompass overseeing manufacturing, quality control, warehouse, logistics, and sourcing & purchasing to ensure timely deliveries and high-quality outcomes.

You'll engage in the entire product lifecycle from conception to post-launch production refinement, setting ambitious goals to enhance FOSS' product development and production processes. Emphasizing a culture of collaboration and openness, you'll work closely with stakeholders across departments.

Technical Drawing Engineer

Would you like to play a critical role in implementing, overseeing and management of key deliverables, and manage the repository of approved technical and regulatory drawing at Bavarian Nordic?

You will establish corporate drawing standards, manage drafting updates carried out by 3rd parties, and oversee the administration of drawing management using multiple software systems.

Fødevarefaglig Quality Manager & Labeling Specialist

Interesserer du dig for det tekniske område inden for fødevarer, og trives du i specialistrollen, hvor du sidder med ansvar for områder som mærkning af fødevarer, egenkontrolprocedurer, kvalitetskontrol, importforordninger, fødevarelovgivning, m.m.?

Som Labeling Specialist & Quality Manager hos Janax vil du blive budt på en spændende og afvekslende hverdag. Det er vigtigt, at du motiveres af hele processen fra at dykke ned i lovgivning til at analysere, planlægge, koordinere og kommunikere, mens du holder det forkromede overblik.

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.

Senior Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.

Project Manager

Your primary responsibilities will include leading the project team, ensuring comprehensive customer communication, and coordinating activities and team members.

Engage in a diverse and challenging role within an international and innovative company and experience a strong team spirit and a dedication to sustainable solutions.

Erfaren akademiker til procesforbedringer

Vil du være med til at bekæmpe kræft? Brænder du for at lave forbedringer? Er du klar til at gøre en forskel for dine kolleger og forbedre produktionsfaciliteterne til gavn for Agilents kunder?

Stillingen er i Filling And Packaging (FAP), der er en del af produktionen i Agilent, Glostrup. FAP har to producerende afdelinger (Filling og Packaging) med i alt 25 operatører og et supportteam på 7 produktionssupportere. Vi fokuserer på at levere diagnostiske produkter af høj kvalitet til vores kunder. Du bliver en del af vores team af produktionssupportere, der skal understøtte og optimere produktionen i Filling og Packaging.