Cell Therapy Operations Specialist

START PEOPLE

Zwijnaarde

On-site

EUR 42,000 - 56,000

Full time

14 days+

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Benefits offered by this job

Permanent contract
Shift premiums
Meal vouchers €7 per worked day
Group and hospitalization insurance
Bonus system
Career growth opportunities
Summer/winter collective leave

Job summary

START PEOPLE in Belgium is seeking an Operations Expert to join a biotech company developing CAR-T cell therapies. A Bachelor's degree in Sciences, Bio-Engineering, Biotechnology, Pharmacy, or related field is required; cell experience and GMP knowledge are highly valued.

You will work in a GMP cleanroom environment producing clinical and commercial ATMPs, participate in process optimization, write SOPs, manage materials, and support a dedicated team delivering life-changing treatments.

Qualifications

  • Bachelor's degree in Sciences, Bio-Engineering, Biotechnology, Pharmacy or related field.
  • Cell experience (internship or work-based) is a strong plus.
  • Knowledge of GMP regulations is a strong plus.
  • Strong teamwork and clear English communication.

Responsibilities

  • Produce clinical and commercial ATMPs in aseptic manual processes in a GMP cleanroom.
  • Perform in-process control tests to ensure cell counts and viability.
  • Maintain equipment by following instructions, troubleshooting, and coordinating repairs.
  • Contribute to process optimization and new product introductions in GMP areas.
  • Support writing/review of SOPs and manage raw materials, consumables, and waste.

Skills

Cell experience
GMP knowledge
Teamwork
English
Problem solving
Independent learning
MS Office

Education

Bachelor's degree in Sciences/Bio-Engineering/Biotechnology/Pharmacy

Tools

Microsoft Office

Job description

START PEOPLE in Belgium is seeking an Operations Expert to join a biotech company developing CAR-T cell therapies. A Bachelor's degree in Sciences, Bio-Engineering, Biotechnology, Pharmacy, or related field is required; cell experience and GMP knowledge are highly valued.

You will work in a GMP cleanroom environment producing clinical and commercial ATMPs, participate in process optimization, write SOPs, manage materials, and support a dedicated team delivering life-changing treatments.

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