Remote CQV Engineer — Pharma Validation & Compliance Specialist

DPS Group Global; Noord-Brabant; On-site; EUR 70,000 - 100,000; Full time

Job summary

DPS Group Global in North Brabant, The Netherlands, is seeking a CQV Engineer to support commissioning, qualification and validation activities within pharmaceutical manufacturing projects. You will report to the Sr Manager Validation & Compliance and help develop and execute test strategies aligned with CQV procedures and customer requirements.

You will lead documentation, participate in testing, and provide technical guidance to project teams, ensuring compliance with SOPs and industry

Qualifications

• 3+ years of CQV experience in pharmaceutical manufacturing.
• Hands-on commissioning and qualification experience in validation activities.
• Experience with Computerized Systems Validation (CSV).
• Strong written and spoken English.

Responsibilities

• Develop and update validation documents, including system level assessments, validation plans, test protocols, and traceability matrices.
• Lead commissioning, qualification and validation activities.
• Provide guidance to project teams to ensure validation plans are followed and SOPs are met.
• Perform additional tasks assigned by supervisor.

Skills

Strong communication

Technical writing

Stakeholder management

Problem solving

Independent work

Tools

Systech

Cognex

Job description

DPS Group Global in North Brabant, The Netherlands, is seeking a CQV Engineer to support commissioning, qualification and validation activities within pharmaceutical manufacturing projects. You will report to the Sr Manager Validation & Compliance and help develop and execute test strategies aligned with CQV procedures and customer requirements.

You will lead documentation, participate in testing, and provide technical guidance to project teams, ensuring compliance with SOPs and industry