Senior Clinical Data Manager

Are you an experienced clinical data manager whom is ready for the next step in your career? Are you excited about taking on more responsibility for data management deliveries and a more oversight perspective to clinical trials?

Here you will be part of an environment driven by dedication and a positive mind-set, you will have the opportunity to make a difference and you will have the opportunity to broadening your skillset, being introduced to all clinical and non-clinical pre-market aspects of drug development in one place.

Senior LIMS Specialist for Global QC Development

In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.

Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.

Environmental Senior Specialist

Drives du af at være en nøglespiller i en EHS/ESG agenda, og har du erfaring med miljøgodkendelser, spildevand/affaldshåndtering, emissionsmåling samt rapportering, så er du måske vores nye kollega?

Du vil være ansvarlig for Palsgaards miljøaktiviteter, herunder miljøgodkendelser, miljøuheld, spildevands-, affalds- og kemikaliehåndtering i Danmark.

Som ny kollega kan vi tilbyde dig rig mulighed for personlig og faglig udvikling nationalt og globalt.

Senior Vice President, Global Chief Medical Office

We are seeking a highly experienced and dynamic medical executive to join our Global Research & Development organisation in a newly established senior leadership role as SVP, Global Chief Medical Office (GCMO).

In this role, you will act as scientific advisor to the EVP of R&D and the Global R&D leadership team, and your primary objective will be to ensure “one global medical voice” for ALK internally and represent the medical voice of ALK externally.

Distinguished Engineer for Large Scale Business Unit

Do you have extensive experience with the management of large technical projects in a complex pharmaceutical environment?

In this role you will assist in Antibody Drug Conjugates, process engineering and automation activities. You will ensure alignment on shared goals through collaboration with Holly Springs location, engaging with other sites and stakeholders as needed.

Bachelor's degree required in Electrical, Biochemical, Chemical, or other Engineering disciplines.

QA senior profesional/QA specialist

Do you want to help secure products for the market from our Production Facility? Are you motivated by a diverse everyday life characterized by new challenges and problem-solving?

We offer an inclusive and flexible workplace with a strong focus on personal and professional development, and we welcome people who are passionate for saving lives. If you are open-minded and have the willpower to succeed, we might just be a perfect fit.

Food Engineer/Digital and Capex Specialist

Are you passionate about capex execution, equipment specifications and implementing digital solutions in pilot plant? Now is your chance to show it. You will be part of a strong team, working daily with the development of new dairy products and technologies. It is our goal to be at the forefront of dairy product development and match the consumer needs worldwide.

As Pilot Plant Specialist you will be the prime responsible for rolling out digital solutions in our pilot plant where we run pilot scale trials for a wide range of dairy/plant-based products. You will work in close collaboration with pilot plant technicians and specialists from different teams.

Regulatory Affairs Senior Specialist

Convatec Infusion Care is expanding and currently looking for a new colleague to join our Regulatory Affairs Department.

The primary responsibilities of the position are to ensure regulatory compliance of a defined group of Convatec products, drive regulatory processes and activities (such as regulatory strategy, product registration, change control, review of marketing materials, etc) and continue to develop strong working relationships with internal and external customers.

Senior Laborant til LC-MS proteomik

Brænder du for at gøre en forskel i vores patienters liv med dine færdigheder?

Som vores nye laborant vil du i samarbejde med andre laboranter og kemikere i vores team have mange spændende opgaver på daglig basis.

Vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Product Experience Senior Researcher (Maternity Cover)

As Product Experience Researcher II in this team, you will be responsible to guide and drive sensory and consumer research activities and projects in alignment with business opportunities and corporate strategies.

Main responsibilities: Define, drive, and implement sensory and consumer research to support Global Innovations programs, always keeping in mind speed, quality, and differentiation as priorities.

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.

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.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

Site QEHS

Brænder du for at arbejder med QEHS, kan du godt lide at arbejde i et overskueligt team – så er du måske vores nye Site QEHS på vores site i Aabenraa? Du vil være tovholder på at implementere og opretholde kvalitets- og EHS standarder.

Dine ansvarsområder bliver udvikling og implementering af QEHS-strategier, -politikker og -mål i overensstemmelse med virksomhedens overordnede mål.

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.

Laborant til meget velfungerende peptidkemi laboratorie

Som laborant i vores peptid laboratorie er dit og kollegernes fokus at skabe grundlaget for udvikling af nye lægemidler. Du giver dit vigtige bidrag ved at bruge størstedelen af din tid med at arbejde hands-on i vores state-of-the-art laboratorie.

Du får et meget alsidigt job med ekstraordinært gode muligheder for at lære nyt og udvikle dig. Du kommer til at udføre alle typer af opgaver fra betjening af robotter og forskellige instrumenter til vedligehold og procesoptimering. Du kommer også til at arbejde med databehandling og dokumentation.

Quality & Compliance Manager

Are you passionate about quality and decency, and do you want to hold a key position in a growing sound international company focused on sustainability? Then you should read on.

You will be a part of the global supply chain organization in Middelfart and report to COO. The area of responsibility is material quality, compliance, and risk management, and you will be the driver of creating a culture of continual improvement by identifying opportunities for efficiency and innovation within the quality and compliance area with a focus on sustainability and the global ESG agenda.

Senior Research Technician

Do you want to work with data and HPLC analysis?

You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.

Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:

• Perform analytical method development in close collaboration with the responsible scientists
• Support formulation development studies with analyses