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Validation Engineer
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Engineering, Engineer, Client
Projektbeschreibung
POSITION SUMMARY:
Our fast growing Medical Device client is looking for a highly skilled Validation Engineer to prepare validation protocols, master plans and schedules. Also being responsible for executing & reporting validation activities and plans as needed, to maintain validation compliance on site.
PRINCIPLE JOB RESPONSIBILITIES/OUTPUTS:
- Maintain current validation status of Pharma areas.
- Maintain a Validation Master Plan for those areas.
- Preparing a Master Validation Schedule for those areas.
- Prepare SOP's for Validation, Calibration and Maintenance.
- Generate protocols and reports as required.
- Plan and execute validations and co-ordinate and supervise these activities.
- To ensure that the premises, production equipment and process are maintained to the required standards.
- To ensure engineering systems are maintained in a compliant manner.
- To ensure the Pharma areas have a compliant validation system
EXPERIENCE REQUIRED:
- Degree qualified- Engineering/Chemistry
- Strong experience in Validation, preferably in Healthcare industry.
- World Class Manufacturing and GMP Experience.
- Excellent interpersonal and communication skills.
If you are looking to join this fantastic company please apply today with an email highlighting your key skills and relevant experience aligned to this opportunity.
Our fast growing Medical Device client is looking for a highly skilled Validation Engineer to prepare validation protocols, master plans and schedules. Also being responsible for executing & reporting validation activities and plans as needed, to maintain validation compliance on site.
PRINCIPLE JOB RESPONSIBILITIES/OUTPUTS:
- Maintain current validation status of Pharma areas.
- Maintain a Validation Master Plan for those areas.
- Preparing a Master Validation Schedule for those areas.
- Prepare SOP's for Validation, Calibration and Maintenance.
- Generate protocols and reports as required.
- Plan and execute validations and co-ordinate and supervise these activities.
- To ensure that the premises, production equipment and process are maintained to the required standards.
- To ensure engineering systems are maintained in a compliant manner.
- To ensure the Pharma areas have a compliant validation system
EXPERIENCE REQUIRED:
- Degree qualified- Engineering/Chemistry
- Strong experience in Validation, preferably in Healthcare industry.
- World Class Manufacturing and GMP Experience.
- Excellent interpersonal and communication skills.
If you are looking to join this fantastic company please apply today with an email highlighting your key skills and relevant experience aligned to this opportunity.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik