Senior Purification Operator: Lead GMP Production & Growth

Prothya Biosolutions Belgium BV; Netherlands; Remote; EUR 42,000 - 61,000; Full time

Benefits offered by this job

40-hour work week

End-of-year bonus

Holiday allowance

30 holidays per year

Personal development budget

Travel allowance

Pension PFZW

GMP-regulated environment

Job summary

Prothya Biosolutions Belgium BV is seeking a Senior Operator Purification PRE to lead purification activities in a GMP-regulated manufacturing setting. You will coordinate daily production tasks, operate equipment, document batches, and support QA and Engineering colleagues.

The role requires a relevant bachelor’s degree and at least 5 years of GMP experience, with a focus on purification or downstream processing in the pharmaceutical sector.

Qualifications

• Bachelor's degree or equivalent required.
• At least 5 years in a GMP-regulated production environment.
• Experience in pharmaceutical/biopharmaceutical purification or downstream processing preferred.
• Strong knowledge of GMP, SOPs, deviations and batch documentation.
• Experience coaching and coordinating operators in production.

Responsibilities

• Coordinate purification activities according to SOPs, GMP requirements and production planning.
• Operate production equipment and perform calculations for production activities.
• Monitor processes, identify deviations and troubleshoot issues.
• Ensure accurate batch records, logbooks and GMP documentation.
• Perform quality checks, sampling and inspections for product quality.

Skills

GMP knowledge

Batch documentation

Quality procedures

Cross-department collaboration

Training/coaching

Education

Bachelor's degree or equivalent

Job description

Prothya Biosolutions Belgium BV is seeking a Senior Operator Purification PRE to lead purification activities in a GMP-regulated manufacturing setting. You will coordinate daily production tasks, operate equipment, document batches, and support QA and Engineering colleagues.

The role requires a relevant bachelor’s degree and at least 5 years of GMP experience, with a focus on purification or downstream processing in the pharmaceutical sector.