GMP/GDP Auditor, CMC Development QA

at  Lundbeck

København, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Jan, 2025Not Specified21 Oct, 20245 year(s) or aboveGood communication skillsNoNo
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Description:

GMP/GDP AUDITOR, CMC DEVELOPMENT QA

This is a great opportunity for an international position as GMP/GDP auditor in CMC Development QA, supporting the development of new innovative treatments for brain diseases. You will have an important role as lead auditor conducting external audits of CMC´s vendors as well as internal audits of CMC. We offer an exciting job, auditing a broad range of vendors supplying Lundbeck´s clinical trials from early stage to late phase including both small molecule and biologic projects.

APPLY NOW

Can you see yourself in this role? We want to hear from you. Does this sound like your dream job, but you’re not sure if you meet all the requirements? We still want to hear from you!
Upload your CV and include a few lines about your motivation for applying. No separate cover letter is needed. We ask you not to include a photo or personal information that does not relate to your professional experience.
If you have questions or want to hear more, please feel free to contact Senior Director, CMC Development QA –Charlotte Ullits Houlbjerg phone +45 30 83 21 69. Applications must be received by November 17th, 2024. Relevant candidates will be invited for interviews as applications are received.
We need every brain in the game – and that includes all brains and the different perspectives we bring to the table. At Lundbeck, we embrace the uniqueness of each employee, and we are committed to building a workforce that is as diverse as the people we serve. Read more about our commitment at www.lundbeck.com/global/about-us/our-commitment/diversity-and-inclusion.

EveryBrainInTheGame

This job ad is intended for individuals seeking a career opportunity with Lundbeck. We engage with recruitment and search firms where needed on the basis of a written agreement, and we do not accept unsolicited requests of any kind. If you work as a recruitment consultant, you are kindly instructed to refrain from contacting Lundbeck or the hiring manager directly with suggested candidates. If you violate this policy, you do so at your own risk and for your own account, and Lundbeck will not assume any liability nor pay any associated fees resulting from such violation.

Responsibilities:

You will join a growing department with an exciting future ahead supporting our current pipeline and expected acquisitions of new drug candidates. As our new colleague, you will support the progression of our pipeline of promising drug candidates by conducting initial and routine audits of CMC GMP and GDP vendors.

Tasks:

  • External audits of CMC vendors
  • Internal audit of CMC
  • Contribute to the continuous improvement of the audit process

As auditor you will collaborate with multiple stakeholders in CMC and vendors all over the world. You will contribute to our continued development of the Quality Management System by authoring and approving SOP´s governing the activities.


REQUIREMENT SUMMARY

Min:5.0Max:10.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Biology, Chemistry

Proficient

1

København, Denmark