Consultys is looking to for an Senior CQV Engineer to join its consulting team.
As CQV Engineer you will make sure that all systems, facilities and equipment are installed properly and meet the design requirements put in place for the end-users in a pharmaceutical facility. You will document the process of installation, operation and how it performs.
YOUR MAIN DUTIES:
* Monitoring CQV activities in the field (FAT/SAT/commissioning/qualification/validation)
* Defining and updating the qualification and/or validation strategy
* Carry out IQ, OQ, and PQ tests
* Write validation reports
* Analyse the impact on qualification
ABOUT YOU:
* Master’s degree in life sciences or any related field
* Minimum 4 years of experience in the pharmaceutical industry, including at least 3 years in CQV
* Good knowledge of GMP rules
* Good knowledge of the V-cycle
* Autonomous, conscientious and positive problem-solving mindset
* Fluency in French and English is mandatory.
ABOUT US:
For more than 15 years, the largest laboratories in the world have been showing their confidence in our company. Specialized in pharma, biotech and medical devices, we support our customers from research to product launch.
We cultivate a human-scale company spirit that allows us to personally follow our 550 employees – each of them known for their technical and scientific expertise. Through our regional subsidiaries in France, Belgium, Canada and Switzerland, we offer everyone geographical stability, without a mobility clause in the contracts.
Do you want to integrate the consulting world into a human-sized company that values the individual and the performance? Do you want to invest in long-term innovative projects? To share your skills in a close-knit team where experiences are shared freely? So, join us! We offer you an attractive salary and fringe benefits. You will work in a stimulating international environment, with numerous opportunities for personal development.