Senior CQV Engineer (m/f/d)

NES Fircroft; Alzey; Vor Ort; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

NES Fircroft is seeking an experienced Senior CQV Engineer in Alzey to lead commissioning and qualification activities for pharmaceutical facilities, equipment and utilities.

The role requires a strong track record in CQV within the pharmaceutical industry, with 8–10 years of relevant experience and the ability to manage workstreams independently while ensuring GMP standards are met.

Qualifikationen

• Degree in engineering or related field.
• 8–10 years of CQV experience preferred.
• Ability to take independent responsibility for CQV workstreams on complex projects.

Aufgaben

• Plan, coordinate and execute commissioning and qualification activities for pharmaceutical facilities, equipment and utilities.
• Prepare, review and approve CQV documentation (FAT, SAT, IQ, OQ) and reports.
• Coordinate suppliers and project stakeholders, manage deviations and closeout outstanding items.
• Ensure CQV activities and documentation meet GMP requirements.

Kenntnisse

CQV experience

GMP knowledge

Independent responsibility

Ausbildung

Engineering degree or related field

Jobbeschreibung

For our client in Alzey, we are looking for an experienced Senior CQV Engineer (m/f/d) to join a pharmaceutical project.

Your responsibilities

• Independently plan, coordinate and execute commissioning and qualification activities for pharmaceutical facilities, equipment and utilities
• Prepare, review and approve CQV documentation, including FAT, SAT, IQ and OQ protocols and reports
• Coordinate suppliers and project stakeholders, and manage deviations and outstanding items through to closure
• Ensure CQV activities and documentation meet GMP requirements

Your profile

• Degree in engineering, chemical engineering or a related field
• Extensive CQV experience in the pharmaceutical industry, ideally at least eight to ten years
• Proven ability to take independent responsibility for CQV workstreams on complex projects
• Strong knowledge of GMP requirements and the qualification of manufacturing equipment, cleanrooms or clean utilities