Biotech Deviation Investigator & Technical Writer (cGMP)

Progressive; Sittard; On-site; EUR 60,000 - 80,000; Full time

Job summary

Progressive is seeking a Deviation Investigator / Technical Writer in Sittard, Netherlands. This role involves leading deviation investigations, performing root cause analyses, and working closely with cross-functional teams to enhance compliance and operational excellence.

The ideal candidate will have a Bachelor’s degree in Pharma, Biotechnology, or Supply Chain, along with 5-10 years' experience in a biotech or pharma setting. Key skills include strong knowledge of cGMP environments and excellent technical writing abilities.

Qualifications

• 5-10 years' experience in Validation, Engineering, or Quality Assurance within biotech/pharma.
• Strong knowledge of cGMP environments and procedures.
• Proven expertise in investigations, CAPA, and root cause analysis.

Responsibilities

• Lead and manage deviation investigations and ensure timely closure.
• Perform root cause analysis, impact assessments, and CAPA implementation.
• Collaborate with QA, QC, Manufacturing, and Supply Chain teams.

Skills

cGMP environments

root cause analysis

technical writing

stakeholder management

analytical mindset

Education

Bachelor's degree in Pharma, Biotechnology, or Supply Chain

Job description

Progressive is seeking a Deviation Investigator / Technical Writer in Sittard, Netherlands. This role involves leading deviation investigations, performing root cause analyses, and working closely with cross-functional teams to enhance compliance and operational excellence.

The ideal candidate will have a Bachelor’s degree in Pharma, Biotechnology, or Supply Chain, along with 5-10 years' experience in a biotech or pharma setting. Key skills include strong knowledge of cGMP environments and excellent technical writing abilities.