CQV Engineer (m/f/d)

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

Zusammenfassung

NES Fircroft in Germany seeks an experienced Senior CQV Engineer (m/f/d) to lead commissioning and qualification activities for a pharmaceutical project in Alzey. The role requires a degree in engineering, extensive CQV pharma experience, and strong GMP knowledge.

Fluency in English is required and German is not required. You will plan, coordinate, and execute CQV for facilities, equipment, and utilities, prepare CQV docs (FAT, SAT, IQ, OQ), coordinate suppliers, and drive deviations to closure,

Qualifikationen

• Degree in engineering, chemical engineering or a related field.
• 8–10 years CQV experience in pharmaceutical industry preferred.
• Ability to take independent responsibility for CQV workstreams.
• Strong knowledge of GMP requirements and qualification of equipment/cleanrooms/clean utilities.
• Fluent English; German not required.

Aufgaben

• 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 to closure.
• Ensure CQV activities and documentation meet GMP requirements.

Kenntnisse

CQV experience

Independent responsibility

GMP knowledge

Fluent English

Ausbildung

Engineering degree (incl. chemical)

Jobbeschreibung

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

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
• Fluent English; German is not required