CQV Lead job in Visp, Switzerland

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First Name*

Last Name*

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Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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Job type: Contract

Discipline: Design

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

Are you a CQV Lead interested in working for one of the most interesting names in High-Tech Biopharmaceuticals?

A Fantastic new role has just opened up at one of our leading Swiss based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.

Key Responsibilities

Experience with CHVI-4999 & CHVI-4888 C&Q process on the Visp site, preferably in MC-1.
5+yrs experience in a lead role, managing a team of C&Q engineers on the day to day document preparation, execution, review and approvals of life cycle documents. Both pre and post execution.
Good communicator, needs to work with other departments to align on ways of working and handling of issues. German language preferred not essential.
Ability to work under pressure to deliver, must be able to work with minimal instruction.
Highly organized, ability to follow the progress of qualification to the correct sequence.
Ability to instruct the team on correct ways of working according to the clients SOPs and Plans.
Ability to priorities and schedule work to meet the project deadlines.
Experience with DMS, Trackwise, COMOS and Microsoft applications (Word, Excel etc.).
Experience with CHVI-4999 & CHVI-4888 C&Q process on the Visp site, preferably in MC-1.
5+yrs experience in a lead role, managing a team of C&Q engineers on the day to day document preparation, execution, review and approvals of life cycle documents. Both pre and post execution.
Good communicator, needs to work with other departments to align on ways of working and handling of issues. German language preferred not essential.
Ability to work under pressure to deliver, must be able to work with minimal instruction.
Highly organized, ability to follow the progress of qualification to the correct sequence.
Ability to instruct the team on correct ways of working according to the clients SOPs and Plans.
Ability to priorities and schedule work to meet the project deadlines.
Experience with DMS, Trackwise, COMOS and Microsoft applications (Word, Excel etc.).

If you are having difficulty in applying or if you have any questions, please contact Sasha Botha at +41 61 568 79 88.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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