Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Equipment Validation Engineer
Eingestellt von Optimus Search
Gesuchte Skills: Engineer, Support
Projektbeschreibung
EQUIPMENT VALIDATION ENGINEER - 6 MONTHS - ZURICH - 85CHF P/H
Optimus Life Sciences are working with a globally respected Medical Device company based in Zurich. My client requires an Equipment Validation Engineer to validate test instruments and equipment.
RESPONSIBILITIES
- Provide technical support for the validation group by interacting with end user's.
- Establish project timelines and expectations
- Ensure that operational execution is in compliance.
- Validate Test instruments and equipment.
- Provide technical decision-making regarding cGMP compliance, regulatory issues, validation strategy, and quality systems.
- Support Validation management by interacting with regulatory authorities during site inspections relative to facility and equipment cGMP areas; supports successful management of inspections
REQUIREMENTS
- Working knowledge of validation test instruments and equipment.
- At least 4 years' experience of validation of a large number of GxP systems and sterilization processes.
- Proven knowledge on validation of a large number of GxP systems and sterilisation processes.
- Extensive knowledge of 21CFR11 requirements.
- GxP experience
Optimus Life Sciences are working with a globally respected Medical Device company based in Zurich. My client requires an Equipment Validation Engineer to validate test instruments and equipment.
RESPONSIBILITIES
- Provide technical support for the validation group by interacting with end user's.
- Establish project timelines and expectations
- Ensure that operational execution is in compliance.
- Validate Test instruments and equipment.
- Provide technical decision-making regarding cGMP compliance, regulatory issues, validation strategy, and quality systems.
- Support Validation management by interacting with regulatory authorities during site inspections relative to facility and equipment cGMP areas; supports successful management of inspections
REQUIREMENTS
- Working knowledge of validation test instruments and equipment.
- At least 4 years' experience of validation of a large number of GxP systems and sterilization processes.
- Proven knowledge on validation of a large number of GxP systems and sterilisation processes.
- Extensive knowledge of 21CFR11 requirements.
- GxP experience
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Ingenieurwesen/Technik, Sonstiges