Biotech Operator

Progressive; Maastricht; Sur place; EUR 42 000 - 64 000; Plein temps

Avantages offerts par ce poste

Relocation support may be available

Résumé du poste

Our client is a leading biotechnology organization manufacturing advanced cell therapies. You will contribute to GMP manufacturing in a cleanroom setting, performing culture, media preparation, expansion, and documentation according to strict procedures.

Join a team that collaborates with Manufacturing, QA, QC and MSAT, receiving extensive GMP training and opportunities for career growth in an international biotech environment. Flexibility for shifts and relocation support may be available.

Qualifications

• 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.

Responsabilités

• 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 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.

Connaissances

GMP cleanroom experience

Attention to detail

Communication skills

Formation

Bachelor's degree in Biotechnology/Life Sciences

Description du poste

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.

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