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Validation Consultant- Basel - Contract

Employer
NonStop Consulting
Location
Zürich
Salary
Negotiable
Closing date
Dec 12, 2019

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Sector
Science, Life Sciences, Cell and Molecular Biology
Contract Type
Contract/Freelance
Hours
Full Time
Organization Type
Corporate
Jobseeker Type
Professional

Job Details

I am looking forward to speaking to talented and responsible Validation Specialist to join my client, a world leading pharma that is going to offer a lot of professional development and learning opportunities, as well as opening future career doors.

You would be accountable for the laboratory instruments qualification, including Computer System Validation (CSV) in the QC laboratories and would also support the deployment of Data Integrity (DI) in the department, offering you cross funtional resposibilities that are going to expand your network globally whilst learning from the best!

Essential duties and responsibilities

  • Ensure computerized system validation strategy within QC department as well as providing laboratory equipment validation expertise
  • Comply with GMP and Data Integrity requirements through applicable guidelines and procedures
  • Define and follow-up the CS Validation Strategy (Validation Plan)
  • Review / Approve User System Requirement (URS), Functional Specification and Design Specifications
  • Lead Risk Assessments
  • Write Design Qualifications
  • Writing qualification protocols (IOPQ) and reports for quality control instruments, including computer systems
  • Ensure the readiness of instruments for validation activities (i.e. with feasibility protocols)
  • Support analytical technical transfer of assays requiring Analytical Instrument Qualification activities (AIQ)
  • Oversee qualification activities executed by QC analysts, provide training and support
  • Coordinate instruments periodic review
  • Support and prepare inspections, audit responses and regulatory submissions

Education & Experience

  • Bachelor or engineering degree in a technical field
  • Min 5 years of experience in Analytical Instrument Qualification (AIQ) and Computer System Validation (CSV) activities
  • Experience in GMP laboratory activities and good knowledge of Data Integrity requirements
  • Fluent in German and English (C1 written and spoken)

Qualifications

  • Excellent computer skills (Word, Excel, Power Point, MS Project)
  • Able to set his/her own priorities and tight timelines
  • Good interpersonal, organizational, and communication skills

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 I am hiring for at the moment and follow for any future relevant roles.

Company

Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries. 

Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery.  Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.

The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors. 

Company info
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