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Ferring Pharmaceuticals A/S

Senior Research Technician

Kastrup

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
Ferring Pharmaceuticals A/S
Ferring Pharmaceuticals A/S

Senior Research Technician

Kastrup

Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?

As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.

Ferring Pharmaceuticals A/S
Ferring Pharmaceuticals A/S

Clinical Project Manager

Kastrup

Do you want impact, freedom to perform, global perspective and super colleagues?

As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.

Ferring Pharmaceuticals A/S
Zealand Pharma A/S

(Senior) Drug Substance Specialist

Søborg

We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.

Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.

Zealand Pharma A/S
Sylvest+ recruiting on behalf of Pharmacosmos A/S
Gem
Sylvest+

Ambitious Project Manager to lead key strategic projects

Holbæk

Are you an experienced Project Manager motivated by making a difference? Then look no further – Pharmacosmos is looking for a Project Manager who can solve complex problems across our value chain and deliver impact to the organisation.

As Project Manager, you will become a key member of a small project management team in Pharmacosmos. You will be allocated to important strategic projects that you will lead and drive to completion to the satisfaction of all involved stakeholders using your existing toolbox and competencies for managing projects.

Evaxion Biotech A/S

Senior Scientist, Infectious Disease Vaccine Discovery and Research

Hørsholm

You will conduct various laboratory activities with the primary goal of producing reliable test results and optimizing lab procedures while adhering to correct procedures as well as health and safety guidelines. The role also includes documentation and reporting of results both in writing and in different forums.

You will work with dedicated colleagues in an inspiring and fast-moving environment with a collaborative and innovative spirit.

Evaxion Biotech A/S
Ferring Pharmaceuticals A/S

Kemiker til QC med GMP-erfaring

Hvidovre

Syntese A/S søger en erfaren kemiker med kompetencer og interesse for analytisk kemi og GMP. Stillingen er en udvidelse af nuværende team.

Dine primære opgaver er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne.

Ferring Pharmaceuticals A/S
Zealand Pharma A/S

Regulatory Affairs Clinical Specialist

Søborg

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Zealand Pharma A/S
Ferring Pharmaceuticals A/S

Senior Medical Writer

Kastrup

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Ferring Pharmaceuticals A/S
Gem
Gubra A/S

Department Manager for Molecular Pharmacology

Hørsholm

Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.

Your tasks include

  • Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
  • Guide the team to accomplish department goals and objectives.
  • Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.

Associate Manager in Oral Product Development

Måløv

Are you a strong people leader motivated by building the right team and making it thrive and perform?

Associate Manager, Cultivation Pilot Plants

Bagsværd

Are you a strong people leader motivated by building the right team and making it thrive and perform?

Senior Regulatory Affairs CMC Professional

Søborg

Do you have experience from either RA, CMC, QA, and/or QC – or any other relevant area?

Senior Regulatory Affairs Professional

Søborg

Do you want to play a key role in accelerating the development of our patient-focused products?

Trial Product Handling Professional

Måløv

Do you have a desire to support processes around Trial Product Handling at the clinical sites globally which is essential for the Novo Nordisk’s clinical trials?

Clinical Pharmacology Specialist

Søborg

Are you passionate about clinical pharmacology and drug development?

CRA- Cardiovascular Diseases

København S

We are looking for a CRA’s to join our team.

Regulatory Affairs Professional

Søborg

If you are passionate about drug development within Diabetes and Obesity and want to be a subject matter expert in a leading international...

Statistical Specialist

Søborg

Are you a highly experienced statistician looking for an opportunity to use your statistical knowledge and quality mindset to bring clinical projects to registration and market?

Corporate Vice President (CVP) Clinical Reporting within Development

Søborg

Are you a seasoned leader with experience from a large, complex, and international pharmaceutical company?

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