Cell Therapy Operations Specialist

START PEOPLE; Zwijnaarde; Sur place; EUR 42 000 - 56 000; Plein temps

Avantages offerts par ce poste

Permanent contract

Shift premiums

Meal vouchers €7 per worked day

Group and hospitalization insurance

Bonus system

Career growth opportunities

Summer/winter collective leave

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Cell experience

GMP knowledge

Teamwork

English

Problem solving

Independent learning

MS Office

Formation

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

Outils

Microsoft Office

Description du poste

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.