Senior CQV Engineer – Pharma GMP & Validation Lead

Talentmark; Breda; In loco; EUR 70.000 - 100.000; Tempo pieno

Descrizione del lavoro

Talentmark is seeking an experienced Senior Commissioning, Qualification & Validation (CQV) Engineer to support technical projects in an international pharmaceutical manufacturing environment. You will plan, execute and document CQV activities, collaborating with Engineering, Project Management and other stakeholders to ensure GMP compliance and validation deliverables.

Responsibilities include developing CQV plans, risk assessments and test protocols; leading CQV activities; guiding project

Competenze

• Minimum 3 years hands-on CQV experience in pharmaceutical manufacturing.
• Experience with secondary packaging equipment and print/inspection systems (Systech/Cognex).
• Experience with Computerized Systems Validation (CSV); HVAC-CSV preferred.
• Strong GMP knowledge and ability to document validation artifacts.

Mansioni

• Develop and update validation and commissioning documentation (CQV Plans, Protocols, & summaries).
• Lead and execute CQV activities across projects.
• Provide guidance to project teams to meet validation plans and SOPs.
• Support design, testing, commissioning, and validation phases.
• Identify issues, set priorities, and escalate for timely delivery.

Conoscenze

CQV experience

GMP knowledge

Technical writing

Stakeholder management

Independent work

Strumenti

Systech

Cognex

Descrizione del lavoro

Talentmark is seeking an experienced Senior Commissioning, Qualification & Validation (CQV) Engineer to support technical projects in an international pharmaceutical manufacturing environment. You will plan, execute and document CQV activities, collaborating with Engineering, Project Management and other stakeholders to ensure GMP compliance and validation deliverables.

Responsibilities include developing CQV plans, risk assessments and test protocols; leading CQV activities; guiding project