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