Business Supporter for product documentation in Human Health

Would you like to be part of a forward-thinking organization dedicated to advancing Human Health? The Global Business Support team is looking for a new colleague who will play a key role in the management of product documentation within Human Health.

You will be overseeing product documentation and you will have an important role in managing and maintaining documentation for new product implementations as well as for existing products. You will support daily product-related queries, optimize internal processes, and engage in stakeholder training.

Associate Director of Clinical Operations Management

Are you ready to take on a leadership role in driving change and building a strong and newly established, global Clinical Operations Management function?

Your role will be critical in optimizing the end-to-end execution of clinical trials and implementing a simplified new operational model set up to accelerate the trial startup phase, drive operational effectiveness, provide scalability, and ensure consistency in execution. You will be part of a workstream defining and ensuring roll out of the newly established COM function within GCO.

Clinical & Product Training Manager (EMEA/Asia) to GE HealthCare Denmark

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 global Clinical and Product training team consists of fifteen dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities.

We are a strong team that values collaboration, support, honesty, and respect. We are driven by making a difference and continually improving training activities across the globe.

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.

PhD scholarship in Clinical Assessments of Vestibular Balance Disorders and Rehabilitation – DTU Health Tech

Are you interested in combining clinical medicine and engineering to help create better healthcare for individuals suffering from vertigo?

This PhD project focuses on clinical assessments of patients with vertigo, with a focus on benign paroxysmal positional vertigo. The aim is to supplement existing diagnostic tools with more objective and valid estimates of balance assessment to improve decisions on relevant diagnostic pathways and treatment, as well as to facilitate more effective counselling and expectation management regarding balance rehabilitation.

Clinical Operations Manager

Do you want key operational responsibility in phase 1-4 clinical trials as part of a high performing team?

As Clinical Operations Manager you are indispensable in the trial, leading and executing all the operational aspects throughout the different trial stages. You work closely with the Clinical Project Manager who is responsible for the clinical and strategic deliverables.

Nanofabrication Technician to state of the art laboratory

We are looking for a Nanofabrication Technician for our client’s brand new, state of the art, semiconductor and fabrication laboratory in Copenhagen. The lab is among the largest in Europe and you get to work with cutting edge technology in a highly dynamic environment of scientist, researchers and engineers trying to push the boundaries of computing.

Material science and fabrication are the foundation and the enablers of qubit devices. In their research, our client deals with complex stacks of different materials, combined at the nanoscale, and require high repeatability of fabrication processes.

QA Device Senior Manager

Currently, we are looking for a new QA Device Senior Manager, who has experience with providing QA support to Drug/Combination Products development projects (early phase to Commercial).

You will be responsible for supporting our device development projects with setting direction for device quality in terms of internal and external requirements.

We bond as a result of our entrepreneurial culture where our people are encouraged to pursue their ideas and turn them into reality. We are curious about each other’s knowledge and expertise.

Senior Compliance Professional

Do you have a broad experience with compliance-related matters within root cause investigations and systematic problem-solving in a pharmaceutical Engineering or Manufacturing organization?

You will participate in improving our systematic problem-solving skills and systems to prevent recurrent deviations and deliver compliance support for the Utility-, Metrology-, Maintenance- and Automation- specialists.

You will be part of a team with a focus on well-being, and achieving our goals, and where there is room to have fun along the way.

Analytical Chemist at NCK A/S

Do you thrive in a dynamic work environment where you can take responsibility and contribute to patient safety? Are you ready to develop new analytical methods for new drug candidates?

As part of our competent QC team consisting of seven people (laboratory technicians and academics), you will develop and validate new analytical methods in accordance with the ICH guidelines and also perform laboratory work – both independently and in collaboration with other laboratory technician

QA Manager

Your success will depend on your ability to excel as an inspiring, supportive, and motivating leader, while effectively managing stakeholders in a complex and dynamic organization.

You will

• Provide leadership and inspire continuous development of the team members through coaching and dialogue.
• Lead the quality team and ensure high motivation and work-life balance.

Specialist til API-produktion i København - Vær med, når vi redder liv

Du vil lede root cause-analyser, koordinere kvalitetsopgaver, være ansvarlig for kvalificeringer/valideringer af procesændringer, følge op på produktionsdata samt overvåge processerne. Arbejdet foregår i tæt samarbejde med kvalitetsafdelingen og den tekniske afdeling. Du vil ligeledes opleve operatører, teknikere, specialister og API-ledelsen som vigtige interessenter.

I stillingen vil dit primære ansvar og dine opgaver være:

• teknisk sparring og processupport til produktionen
• håndtering af kvalitetssager

Area Sales Support Manager

As Area Sales Support Manager, you will be responsible for specific markets, building and maintaining relations with customers, negotiating sales and facilitating the growth potential in your markets for the sales of ice cream equipment.

We offer you a variety of exciting challenges with ample opportunities for development and training in a truly global landscape.

With growing volumes and increasing demand from our key markets, we need to further enhance our channel to market, therefore we offer this excellent opportunity.

Coop Trading A/S søger en teknisk ekspert til kosmetik og personlig pleje

Vil du gerne gøre en forskel for 27 millioner nordiske kunder? Går du op i, at kosmetiske – og personlige plejeprodukter er af den rette kvalitet, er sikre at anvende og overholder den gældende lovgivning?

I tæt samarbejde med leverandører og teamet skal du udvikle et attraktivt og konkurrencedygtigt sortiment indenfor personlig pleje og kosmetik for det nordiske private brand marked. Du skal sikre, at sortimentet overholder vores høje standarder indenfor sikkerhed, bæredygtighed, forbrugerinformation og kvalitet

Coop Trading is looking for a technical expert to handle cosmetics and personal care products

Do you have a technical background within chemistry or pharmacy, and are you curious by nature to learn more, e.g. about developing products for retail?

You will develop an attractive and competitive personal care and cosmetic product portfolio for the Nordic Private Brand market in close cooperation with the team and suppliers. You wil also quality assure that the portfolio complies with Coop's high standards within safety, sustainability, consumer information and quality.

Investment & Maintenance Specialist to Nordic Sugar

Would you like to work in a hugely automated process industry that produces several million tons of sugar and animal feed made from sugar beet?

As our new colleague, you will participate in key projects that support our business needs. Specifically, you will:

• Developing and supporting Go Green and I&M projects from planning to commissioning together with the plants or departments
• Managing projects incl. monitoring budgets

Analyst and Project Coordination In Life Science Consultancy

Would you like to work with data analysis and research of worldwide trends in the pharmaceutical and biotechnological industries?

You will get the responsibility of managing and coordinating the day-to-day operations needed to solve our projects and writing reports for our commercial unit.

An academic background in life science (pharmacy, biotechnology etc.), economics or similar is required.

Supporter til produktionsforbedringer og drift

Vil du være med til at bekæmpe kræft?

Brænder du for at lave forbedringer af processer og produktionsfaciliteter, samtidig med, at produktionen holdes kørende?

Dine opgaver vil være at stå for store og små procesforbedringer. Det kan være mindre tilretninger af SOP’er eller store forandringer som fundamentalt ændrer vores måde at arbejde på.

Vi tilbyder masser af ansvar og indflydelse på dine arbejdsopgaver.

Akademiker til daglig support og procesforbedringer

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

Dit hovedansvar vil være at sikre GMP-niveauet i produktionen. Du vil i den forbindelse skulle afklare GMP-spørgsmål samt udarbejde Non-Conformance Reports (NCRs).

Regulatory Affairs Specialist

We are on an exciting path of growth and are currently seeking a new specialist to join our team and play a crucial role in ensuring that our operations adhere to relevant regulations and industry standards.

A significant part of your role will be to take regulatory ownership of selected product areas, and ensure the required activities take place, to ensure we are following current regulatory standards for medical device development.