This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
NonStop Recruitment is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Pharmacien AQ produit
QA/GPV Drug Safety Specialist - Global Leading Pharma Company
QA/RA Associate Director - International Pharma Company
United Kingdom
Pharmacien de Production : Poste à fort intérêt scientifique
Pharmacien de Production : Faites la différence !

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.

Computer Systems Validation Specialist - Basel - Pharma

Business Type: Pharmaceutical Company, Biotechnology Company, Contract Research Organisation, Drug Development Company, Contract Manufacturing
Job Type: Quality Assurance - Control, Validation
Job Level: Experienced (non manager)
Position: Contract
Location: Switzerland
Reference: 0870120201725
Closing Date: 22/01/20
Job Details:

We are looking forward to speaking with and responsible Computer Systems Validation Specialists to join our client, a world leading pharmaceutical company in Basel, that is going to offer a lot of professional development and learning opportunities, as well as setting up a stepping stone for career advancement.

You would be accountable for the laboratory instruments qualification, including Computer Systems Validation (CSV) in a GMP regulated environment, responsible to integrate ongoing backend validation projects, offering you cross functional resposibilities that are going to expand your network globally whilst learning from the best during this introductory 12 months challenging assignment that is going to add weight to your profile and open future career doors!

The key responsibilities would be:

  • Leading Quality Engineering activities for design, development and GxP manufacturing to ensure a high level of process and product quality
  • Develop, review and improve requirements, specifications, product plans and product drawings
  • Execute QA reviews and approvals of all validation related documentation (IQ, OQ, PQ, URS and Traceability Matrix)
  • Execute and follow up of system testing
  • Contribute to the development and improvement of design and manufacturing for existing and new products
  • Ensure that the projects follow relevant quality regulations
  • Provide Technical Assessments to Change Controls/CAPA''s, Non-Conformities and Technical Suppliers Qualification

Education & Experience

  • Bachelor or engineering degree in a technical field
  • Min 5 years of experience in Instrument Qualification and Computer System Validation (CSV) activities
  • Good knowledge of pharmaceutical regulations: GMP System, GAMP 5, CFR Part 11
  • Fluent in German and English (C1 written and spoken)

We have limited interview slots for the next days, so if this is of interest, apply today to give yourself the best chance.

The job market changes very quickly so do not forget to connect with me on LinkedIn, check other roles that we are hiring for at the moment and follow for any future relevant roles.

Posted: 08/01/2020 | NPJ Ref: 248092
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing

Credit cards image