Expert for GLP Quality Assurance at Novo Nordisk
Søborg, Region Hovedstaden, Denmark -
Full Time


Start Date

Immediate

Expiry Date

08 Feb, 24

Salary

0.0

Posted On

09 Nov, 23

Experience

3 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Drug Development, English, Medicine, Biology, Due Diligence

Industry

Pharmaceuticals

Description

Expert for GLP Quality Assurance
Category: Quality
Location:Søborg, Capital Region of Denmark, DK
Would you like to leverage your strong Good Laboratory Practice (GLP) knowledge, process optimization skills, and quality-oriented mindset within a highly professional and dynamic global setting, all while having the opportunity to grow and gain experience in the realm of due diligence and integration? Will you bring a ‘can-do’ attitude to support high quality in the development of innovative treatments for patients? Are you eager to dive into an emerging area, with the opportunity to shape its growth and leave a meaningful mark?
If so, then take the next step in your journey by joining Novo Nordisk as GLP QA Expert. Your exciting job opportunity awaits - apply now!

QUALIFICATIONS

To succeed in this role, you need the following:

  • A Master’s degree in science such as biology, pharmacy, medicine or similar
  • Strong knowledge in non-clinical research and drug development
  • 3-5 years of extensive experience in GLP is essential
  • Prior experience in non-clinical quality assurance or GLP QA tasks
  • Preferred qualifications include experience in due diligence and integration processes, although they are viewed as an advatnageProficiency in both written and spoken English

  • On a personal level, you consistently adopt a constructive and practical approach to problem-solving, demonstrating a keen enthusiasm for optimising and simplifying processes around you. Proactivity and courage characterize your work style, alongside clear communication, and good interpersonal skills. Your organizational ability, paired with a meticulous attention to detail, reflects your ability to maintain a comprehensive perspective on tasks and objectives.

Responsibilities
  • A Master’s degree in science such as biology, pharmacy, medicine or similar
  • Strong knowledge in non-clinical research and drug development
  • 3-5 years of extensive experience in GLP is essential
  • Prior experience in non-clinical quality assurance or GLP QA tasks
  • Preferred qualifications include experience in due diligence and integration processes, although they are viewed as an advatnageProficiency in both written and spoken Englis
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