A career at Merck is an ongoing journey of discovery: our 52,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
An exciting new opportunity has arisen to join us as Quality Assurance Equipment Qualification Engineer for our Biotech drug substance plant in Corsier s/ Vevey.
As an integral member of the Quality Unit, you provide QA expertise for Equipment Qualification (including Sterilization/Sanitization qualification and software validation). The role consists to elaborate the qualification strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan. You act as Quality Subject Matter Expert on specific topics and participate in risk assessments and handle deviations on these topics. You review and/or approve qualification documents (DQ-IQ-OQ-PQ), risk assessment, SOPs and take quality decisions according to company standards.
The activities of the QA Expert cover all qualification phases from Basic Design until 1st use of equipment/software. You ensure GMP compliance during all phases of qualification/validation.
What we offer: At Merck, there are always opportunities to break new ground. We empower you to fulfill your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at come2merck.com