Process Microbiologist: GMP Hygiene & Biologics Ops

7266-Janssen Biologics B.V. Legal Entity; Amsterdam; On-site; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Flexible working hours

Global market leader

Development opportunities

Excellent Benefits

Job summary

Johnson & Johnson in Leiden, NL, is seeking a Process Microbiologist to strengthen our Large Molecules Operations. You will support GMP production, improve processes, and work with QA microbiologists across sites. A background in biologics or pharmaceutical manufacturing and aseptic processing is valued.

Reporting to the Senior Director of Operations, you will contribute to capacity expansion and risk management while upholding cGMP standards and quality.

Qualifications

• BSc. or MSc degree in science, preferably in microbiology or related.
• Experience in (pharmaceutical) production with interest in processing and operational processes.
• Experience in and/or knowledge of aseptic processing is a plus.
• Awareness and experience with cGMP standards.
• Excellent communication skills in English (required) and Dutch (preferred).

Responsibilities

• Set up microbiological systems required by GMP production process in a redesigned facility and support routine production.
• Identify, document and escalate risks; implement preventive actions from risk assessments and deviations.
• Drive and contribute to improvements reducing contamination risk and improving microbiological hygiene.
• Develop and manage training curricula in microbiological hygiene and contamination prevention for production staff.
• Identify risks and opportunities and follow up in collaboration with employees and managers.
• Transfer knowledge and communicate clearly across organization layers.
• Support the investigation team on deviations and observations.

Skills

GMP knowledge

Communication

Problem solving

Lean manufacturing

Education

BSc/MSc in science

Job description

Johnson & Johnson in Leiden, NL, is seeking a Process Microbiologist to strengthen our Large Molecules Operations. You will support GMP production, improve processes, and work with QA microbiologists across sites. A background in biologics or pharmaceutical manufacturing and aseptic processing is valued.

Reporting to the Senior Director of Operations, you will contribute to capacity expansion and risk management while upholding cGMP standards and quality.