Your new company:
Our partner, who is a pharmaceutical equipment manufacturing company. We are looking for a validation engineer to their plant.
What you will do as a validation engineer:
Change Management: Change Control process
- management of change requests, approvals, implementation, communication, distribution of information
- manage, coordinate and follow up changes
- perform/ initiate change risk analysis
- trigger customer communication work-flows, collect information
- related document management (SOP, forms, checklists)
Risk Management
- site risk assessment coordinator
- process FMEA responsible
- leading risk assessments, coordinating teams
- related document management (SOP, forms, risk management tools)
Validation & Qualification
- equipment qualification according to "V" model: DQ, IQ and OQ
- equipment validation as per PQ/PV
- participation in projects, being responsible for qualification and validation activities
- create validation/ qualification document, assign targets for qualification/ validation activities
- maintenance of validation master program
What you need to succeed:
- engineer, manager or natural science degree (preferred mechanical engineer, technical manager, field of quality engineering)
- 1-3 years quality/ testing experience in manufacturing industry (preferred in GMP environment)
- fluent English, good coordination skills
- MS Office, technical writing skill
- Advantages: knowledge of ISO 15378/ GMP and validation/ qualification/ change- and risk management experience
What you will get in return:
- competitive salary
- yearly and seasonal bonuses
- travel allowance
- mobile phone and laptop
- relocation bonus if needed
- you will be part of a great community
- you will have a chance to improve vocationally
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