Cell Therapy Specialist

Progressive; Limburg; On-site; EUR 52,000 - 78,000; Full time

Benefits offered by this job

Relocation support (may be available)

Job summary

Progressive seeks a Biotech Associate (Cell Therapy Manufacturing) for its South-East Netherlands site. You will contribute to producing life-changing cell therapies in a GMP manufacturing environment, performing cell culture and aseptic processes, and maintaining precise batch records.

The role requires a Bachelor's in Biotechnology or Life Sciences, 2+ years in GMP cleanrooms, and fluent English. Shifts include rotating schedules with a 31.3% shift allowance, with a move to a 5-shift model

Qualifications

• Minimum 2 years of GMP cleanroom experience.
• Experience with cell culture or tissue culture.
• Strong attention to detail and adherence to procedures.

Responsibilities

• Perform cell and tissue culture activities according to GMP procedures.
• Execute manufacturing processes including media prep, cell expansion and harvesting.
• Work in a cleanroom using aseptic techniques.
• Complete batch records and production documentation accurately.
• Identify deviations and support quality standards.
• Collaborate with Manufacturing, QA, QC and MSAT teams.

Skills

GMP experience

Cell culture

Quality mindset

English communication

Education

Bachelor's degree in Biotechnology or Life Sciences

Job description

Biotech Associate (Cell Therapy Manufacturing)

South-East part of Netherlands | Full-time | Permanent

Our client is a leading biotechnology organization specializing in the manufacturing of advanced cell therapy products. To support continued growth, they are looking for a Biotech Associate to join their GMP manufacturing team.

In this role, you will contribute directly to the production of life-changing therapies in a highly regulated cleanroom environment.

Responsibilities

• Perform cell and tissue culture activities according to GMP procedures.
• Execute manufacturing processes including media preparation, cell expansion, and harvesting.
• Work in a cleanroom environment using strict aseptic techniques.
• Complete batch records and production documentation accurately and on time.
• Identify and report deviations while maintaining high quality standards.
• Support continuous improvement initiatives within manufacturing operations.
• Collaborate with Manufacturing, QA, QC, and MSAT teams.

Requirements

• Laboratory education or Bachelor's degree in Biotechnology, Biology, Life Sciences, or a related field.
• Minimum 2 years of experience in a GMP cleanroom environment.
• Experience with cell culture, tissue culture, or aseptic manufacturing.
• Strong attention to detail and quality mindset.
• Ability to follow procedures accurately and work in a structured manner.
• Good communication skills and fluent English.
• Willingness to work shifts, including evenings, nights, weekends, and holidays.

Shift Pattern

The site currently operates in a 6-shift rotation, which includes a 31.3% shift allowance and an average working week of approximately 37.3 hours.

Current shifts:

• 00:00 - 08:00
• 06:00 - 14:00
• 12:00 - 20:00
• 18:00 - 02:00

A transition to a new 5-shift model is planned. Depending on your start date, you may initially work within the current 6-shift system before moving to the new schedule.

• Morning: 07:00 - 15:30
• Evening: 15:00 - 23:30
• Night: 23:00 - 07:30

The new shift model is expected to provide improved work-life balance, including regular extended periods off and opportunities for 4-day weekends.

What's On Offer

• Opportunity to work with cutting-edge cell therapy technologies.
• Extensive GMP and technical training.
• Career growth within an international biotechnology environment.
• Modern manufacturing facilities and collaborative team culture.
• Relocation support may be available for suitable candidates who already hold valid EU work authorization and do not require visa sponsorship.