GMP Specialist/Technical Writer

Panda International; Geleen; On-site; EUR 45,000 - 65,000; Part time

Benefits offered by this job

On-site role

6-month contract

Job summary

Panda International seeks a Temporary GMP Support Specialist for a 6-month contract in a cell therapy scale-up. On-site, day-shift role from 08:30 to 17:00, English required, Dutch not necessary. Around 3 years of relevant GMP experience preferred.

Moda ES is used for batch records and TrackWise for deviations. Responsibilities include reviewing electronic batch records, supporting deviations and quality events, assisting with GMP documentation, and ensuring release-related docs move smoothly

Qualifications

• English language required.
• GMP production environment experience essential.
• Cleanroom knowledge is a plus.

Responsibilities

• Review electronic batch records.
• Support deviations, investigations, and quality events.
• Assist with technical writing and GMP documentation.
• Help move release-related documents during ramp-up.
• Collaborate with operations and QA to remove blockers.

Skills

English

Attention to detail

GMP experience

Documentation

Tools

Moda ES

TrackWise

Job description

Temporary GMP Support Specialist role for a 6-month contract in a cell therapy scale-up environment. The position supports the team with electronic batch record review, technical writing, quality event support, and GMP documentation. It is an on-site, day-shift role in a GMP production setting.

• 6-month contract.
• On-site preferred, with limited hybrid flexibility.
• Day shift: 08:30–17:00.
• Around 3 years of relevant experience is ideal.
• English required, Dutch not necessary.
• GMP production environment experience is important.
• The team uses Moda ES for batch records and TrackWise for deviations.

Main responsibilities

• Review electronic batch records.
• Support deviations, investigations, and quality events.
• Assist with technical writing and GMP documentation.
• Help keep release-related documentation moving during the ramp-up phase.
• Work closely with operations and QA to remove blockers and keep tasks on track.

Candidate profile

We are looking for someone practical, detail-oriented, and comfortable working in a GMP environment. Cell and gene therapy experience is a plus, but not mandatory. Cleanroom or aseptic knowledge is also a plus.