Drug Product Specialist at Lundbeck
København, , Denmark -
Full Time


Start Date

Immediate

Expiry Date

01 Dec, 25

Salary

0.0

Posted On

02 Sep, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

DRUG PRODUCT SPECIALIST – BIOLOGICS PRODUCTION

As a Drug Product Specialist in Biologics Production, you will play a pivotal role as a Subject Matter Expert (SME), ensuring excellence in biologics manufacturing and contributing to the success of our innovative treatments.

WHAT YOU BRING TO THE TEAM

We are seeking a candidate with a strong scientific background and a passion for biologics manufacturing. You should bring:

  • A Master of Science or PhD in pharmacy, chemistry, biological sciences, or a related field.
  • 3+ years of experience in Drug Product manufacturing, ideally in sterile fill-finish processes.
  • Knowledge of protein formulation, stability, and cGMP requirements.
  • A collaborative mindset, with the ability to work effectively in cross-functional teams.
  • A proactive attitude, ready to take on new challenges and expand your expertise.

Candidates who meet some but not all qualifications are still encouraged to apply, as the role can be adapted to suit your skills and career aspirations.

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. We ask you not to include a photo or personal information that does not relate to your professional experience.
If you have questions, please contact Kenny Jessen, Senior Director, at +45 30833966.
Applications must be received by September 21st, 2025.
Learn more about us www.lundbeck.com, LinkedIn or Instagram (@h_lundbeck).

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 act as the Subject Matter Expert for commercial biologics Drug Product manufacturing, overseeing global Contract Manufacturing Organizations (CMOs). Your responsibilities include:

  • Oversee the execution of commercial manufacturing at CMO´s
  • Provide technical support to commercial manufacture and act as Person in Plant when required
  • Support pre-commercial activities and the transition of project into the commercial portfolio
  • Review of the GMP manufacturing documents
  • Drive change controls and assessment of vendor/internal deviations
  • Support regulatory filings and interactions with Health Authorities.

This role offers a unique opportunity to take ownership of commercial Drug Product manufacturing from development to the end of lifecycle. You will collaborate with internal and external stakeholders to support Lundbeck’s growing biologics portfolio.

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