Deviation Investigator / Technical Writer

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

Deviation Investigator / Technical Writer - Biotech (cGMP Environment)

Are you an experienced investigator with a strong background in biotech quality and a passion for solving complex problems? We are looking for a Deviation Investigator / Technical Writer to play a critical role in maintaining product quality and driving continuous improvement within a dynamic cGMP environment.

Your Impact

In this role, you will act as a technical expert in investigations, leading end-to-end deviation processes-from initiation to root cause analysis and CAPA implementation. You will collaborate with cross-functional teams and contribute directly to compliance, process optimization, and operational excellence.

Key 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
• Develop and revise SOPs and technical documentation
• Track and present process performance metrics
• Support change controls and quality systems improvements
• Facilitate meetings and resolve cross-functional challenges
• Mentor and guide junior team members

What You Bring

• Bachelor's degree in Pharma, Biotechnology, or Supply Chain
• 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
• Excellent technical writing and communication skills
• Ability to manage multiple complex projects simultaneously
• Strong analytical mindset with the ability to interpret and troubleshoot data

What Sets You Apart

• Calm, solution-oriented mindset under pressure
• Strong stakeholder management and influencing skillsAbility to drive change and improve processes
• High level of ownership and accountability