For more than 19 years, through our consulting and engineering activities, we have supported our clients throughout the entire lifecycle of biotechnology, pharmaceutical and device products.
Part of an organization of more than 750 Life-science experts, Consultys Switzerland supports and develops talented individuals recognized for their technical and scientific expertise. Our activities allow us to be present in both French-speaking and German speaking Switzerland, with agencies in Lausanne and Basel.
At Consultys, we're proving that it's possible to combine people and performance.
Much more than concepts, our 3 values Respect, Recognition and Transparency guide us and are the foundation of our history, the heart of our group's success.
As part of our development, we are recruiting a CQV Coordinator to join our teams in Stein.
Responsibilities:
* The scope of activities includes the coordination on the installation of equipment, HVAC & Utilities (20%)
* Drafting the IQ/OQ/PQ protocols, execution of the IQ/OQ/PQ and documenting the results according to cGMP requirements.
* Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
* Execution of IQ/OQ and PQ for equipment, systems and utilities.
* Write reports of completed validation activities. Work to identify efficiencies in the validation program approach.
* Work to apply lessons learned and stay informed of industry regulatory changes as it applies to equipment/facility validation.
* Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s.
* Writing and/or revising procedures applicable to the Engineering activities.
* Support the Engineering group to prepare the validation, requalification, and maintenance program.
Your Profile:
* Bachelor’s degree in science or technical field
* Advanced Level Pharma Industry 5-10 years
* Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
* Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.
* Excellent organizational and time management skills
Do you want to join the consulting world in a human-sized company that values the individual and performance?
To share your skills within a cohesive team where experiences are freely shared?
CONSULTYS is open to all talents and is committed to diversity and inclusion.
Seniority Level
Associate
Employment Type
Full-time
Job Function
Business Consulting and Services and Biotechnology Research
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