Biotechnologist - Cell Therapy Manufacturing

Panda International; Geleen; On-site; EUR 42,000 - 62,000; Full time

Job summary

Panda International in Geleen, The Netherlands, is seeking a Biotech Associate to support the manufacturing of advanced cell therapy products in a GMP cleanroom environment. The role involves hands-on manufacturing, documentation, and cross-functional collaboration to ensure compliant operations.

The ideal candidate has a degree in biotechnology/biology with at least 2 years in a GMP cleanroom, experience with cell/tissue culture, and strong attention to detail.

Qualifications

• Completed laboratory training or Bachelor's degree in Biotechnology, Biology, or related field.
• Minimum 2 years in GMP cleanroom environment.
• Experience performing cell and tissue culture activities in GMP procedures.
• Experience executing manufacturing activities such as media preparation, cell expansion, and harvesting.
• Knowledge of aseptic techniques and cleanroom operations.
• Experience completing GMP production documentation accurately and on time.
• Ability to identify and report deviations while maintaining compliance and product quality.

Responsibilities

• Perform cell and tissue culture activities.
• Execute manufacturing processes.
• Complete GMP documentation.
• Collaborate with QA, QC, and MSAT to ensure compliant, efficient manufacturing operations.

Skills

GMP knowledge

Aseptic processing

Cell culture

Documentation

Quality mindset

Communication

English proficiency

Team collaboration

Shift work

Education

Bachelor's degree in Biotechnology/ Biology or related field

Job description

Biotech Associate | Cell Therapy Manufacturing

A global life sciences organisation is seeking a Biotech Associate to support the manufacturing of advanced cell therapy products within a GMP cleanroom environment. This hands‑on manufacturing role requires strong GMP knowledge, aseptic processing experience, and a quality-driven mindset to help deliver life‑changing therapies to patients.

In this role, you will perform cell and tissue culture activities, execute manufacturing processes, complete GMP documentation, and collaborate with cross‑functional teams including QA, QC, and MSAT to ensure compliant, efficient manufacturing operations.

• Completed laboratory training, vocational education, or a Bachelor's degree in Biotechnology, Biology, or a related scientific field
• Minimum 2 years of experience working in a GMP cleanroom environment
• Experience performing cell and tissue culture activities in accordance with GMP procedures
• Experience executing manufacturing activities such as media preparation, cell expansion, and harvesting
• Knowledge of aseptic techniques and cleanroom operations
• Experience completing GMP production documentation accurately and on time
• Ability to identify and report deviations while maintaining compliance and product quality
• Strong attention to detail and a quality-focused mindset
• Ability to follow procedures accurately and work in a structured manner
• Good communication skills with the ability to work collaboratively within a manufacturing team
• Good written and spoken English
• Willingness to work in a shift pattern, including evenings and weekends

Preferred Requirements

• Experience supporting continuous improvement initiatives within a GMP manufacturing environment
• Experience collaborating with QA, QC, and MSAT teams
• Interest in advanced cell therapy manufacturing and innovative biologics production
• Ability to work effectively in a fast‑paced, team‑oriented manufacturing environment

Practicalities

Start Date: ASAP

Location: Geleen, The Netherlands

Environment: GMP cleanroom manufacturing

Industry: Cell Therapy Manufacturing

Shift Pattern: Shift work, including evenings and weekends