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Open nowPosted 2 days ago

Supervisor - GMP Environment

EURES job mobility portal411,025 open roles

Where
Gent, Belgium
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Your applicationOpen nowSupervisor - GMP EnvironmentEURES job mobility portal · Gent, Belgium

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on EURES job mobility portal's own form.

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The clock on this job

Early applications get read.

8.2% of postings close within 7 days. Measured by our own scanner across the market. EURES job mobility portal postings stay open a median of 3 days.

Share of postings closed within
  1. 1.8%1 day
  2. 3.6%3 days
  3. 8.2%7 days
  4. 15.2%14 days
  5. 34.0%30 days
This job: posted 2 days ago

EURES job mobility portal median: 3 days open

The posting

Ghent Region | Leadership experience | GMP & cleanroom | Shift system | 1110509

About the organization Our client is an international manufacturing company active in the pharmaceutical and biotechnology sector. From their site in Flanders, they produce innovative therapies that improve patients' lives worldwide. The organization is known for its high-tech environment, strong growth, and a culture where collaboration, quality, and continuous improvement are key.

Your new role As a Production Supervisor, you are the heartbeat of a GMP manufacturing environment. You lead operational teams and ensure that all processes meet the highest standards of quality and safety.

Your responsibilities include:

  • Leadership and coaching: Motivate and guide production teams in a cleanroom environment.
  • Compliance and audits: Ensure adherence to cGMP standards and act as a key contact during inspections.
  • Documentation management: Oversee procedures, batch records, and ensure timely release.
  • Process improvement: Initiate projects to enhance efficiency, quality, and safety.
  • Cross-functional collaboration: Work closely with QA, QC, Engineering, and Supply Chain.
  • Training: Ensure your team is well-trained and foster a culture of ownership and learning.

You will report directly to the Operations Manager.

What we expect from you

  • Bachelor or Master degree in science, bioengineering, pharmacy, or equivalent through experience
  • Minimum 3 years of experience in a GMP environment, preferably in biotech or pharma
  • Knowledge of cGMP regulations and cleanroom operations
  • Strong communication and organizational skills
  • Proficiency in MS Office; experience with MES/EBR systems is a plus
  • Fluent in English (Dutch is an asset)
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