CQV Engineer
- Breda
- 3500.00 - 5000.00
- 32-40 hours
- Bachelor degree
Client
Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world.
Client
Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world. Their reputation is based on forming successful partnerships with clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.
Requirements
- Experienced with Secondary Packaging Systems, including experience with Print and Inspection systems.
- At least 3 years’ experience in executing Commissioning, Qualification and Validation within manufacturing organizations in the pharmaceutical industries.
- Experienced in Computerized Systems Validation.
- Hands on commissioning and qualification experience within Secondary Packaging Operations.
- Ability to work independently and remotely with minimum direct supervision.
- Good English Technical Writing.
- Excellent communication skills.
- Customer relationship management skills.
- Critical thinking skills.
- Able to set clear priorities and escalate to ensure timely delivery of the project phases including design, development, implementation, testing, construction, commissioning, and validation.
- Experience within a GMP compliance environment regarding practices, policies, procedures, legal requirements and goals of project, develop supporting documentation and monitor activity timeliness / scheduling.
- Ability to anticipate, evaluate and resolve multiple, simultaneous project issues, delays and problems by utilizing technical and business expertise.
What do you get?
- Pension entitlement as from day one
- Collective WGA / WIA insurance
- NBBU / ABU collective labor agreement
- 25 holidays days
- 8,33% holiday allowance
- 100% payment in case of illness after one waiting day
- Travel allowance
Duties
- Support technical projects under minimal supervision and will report to Sr Manager Validation& Compliance within the site Engineering organization.
- Demonstrate hands on commissioning/qualification skills.
- Develop, implement and report test strategies for technical solutions in accordance with internal customer requirements and standard CQV procedures.
- Drive the development of system commissioning qualification and validation documentation.
- Develop and Update several Validation documents.
- Lead Commissioning, Qualification and Validation activities
