CQV Engineer
Firmenname für PREMIUM-Mitglieder sichtbar
- August 2024
- Januar 2024
- CH-Zürich
- auf Anfrage
- 12.07.2024
- JN -072024-100105_1720776362
Projekt Insights
Projektbeschreibung
We are urgently seeking experienced CQV consultants in Switzerland with the following skill sets:
Responsibilities:
* Milestones: Ensure commissioning and qualification deadlines are met.
* Design Qualification (DQ): Prepare, execute, approve, and release for Installation Qualification (IQ).
* Supervise Commissioning: Oversee vendors and maintain quality standards.
* Qualification (IQ & OQ): Prepare, execute, approve, and release for Operational Performance (OPS).
* Provide Support: Assist with DQ for other key systems.
* Manage Schedules: Control activities and timelines.
* Report Progress: Update on deliverables and project milestones.
* Resolve Issues: Address project issues and keep non-conformance records.
* Manage Risks: Evaluate and mitigate project risks.
Requirements:
* Education: Master's or bachelor's degree in a pharmaceutical capacity.
* Experience: Commissioning/qualification (DQ, IQ, OQ) in a pharmaceutical environment.
* Technical Skills: DeltaV
* Knowledge: Familiar with GMP and regulatory requirements.
* Language: German and English fluent speaking.
We do not ask for a placement fee from Candidates/Employees.
If you wish to contact a specialist regarding this role, or your job search in general, please contact us by the phone.
Responsibilities:
* Milestones: Ensure commissioning and qualification deadlines are met.
* Design Qualification (DQ): Prepare, execute, approve, and release for Installation Qualification (IQ).
* Supervise Commissioning: Oversee vendors and maintain quality standards.
* Qualification (IQ & OQ): Prepare, execute, approve, and release for Operational Performance (OPS).
* Provide Support: Assist with DQ for other key systems.
* Manage Schedules: Control activities and timelines.
* Report Progress: Update on deliverables and project milestones.
* Resolve Issues: Address project issues and keep non-conformance records.
* Manage Risks: Evaluate and mitigate project risks.
Requirements:
* Education: Master's or bachelor's degree in a pharmaceutical capacity.
* Experience: Commissioning/qualification (DQ, IQ, OQ) in a pharmaceutical environment.
* Technical Skills: DeltaV
* Knowledge: Familiar with GMP and regulatory requirements.
* Language: German and English fluent speaking.
We do not ask for a placement fee from Candidates/Employees.
If you wish to contact a specialist regarding this role, or your job search in general, please contact us by the phone.
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