Validation Engineer (Biotech)

Zurich, Switzerland
12 Feb 2019
14 Mar 2019
WAG - 7069
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Validation Engineer - Biological drug development and manufacturing - Schachen, Switzerland

Clintec currently has an exciting opportunity for an experienced Validation Engineer to work in-sourced to our global sponsor at their biological drug development and manufacturing site located in Schachen, Switzerland. This is an excellent opportunity for the right candidate to join our growing, global company on a permanent, full time basis.

Main Responsibilities:
  • Management of Equipment Qualification Projects and Computer System Validation Projects for laboratory equipment as well as manufacturing equipment.
  • Develop, review and approve Validation Plans, Specifications, Test Scripts, Installations Qualification Protocols, Operational Qualification Protocols, Performance Qualifications Protocols, Traceability Matrices and Summary Reports
  • Perform Equipment Qualification/ Computer System Validation tests
  • Generate/review Standard Operating Procedures related to Equipment Qualification
  • Administration of Equipment Change Controls in TrackWise System
  • Bachelors/Master's degree in Engineering, Life Sciences or another closely related discipline
  • 3-5 years of work experience in pharmaceutical environment
  • Significant practical experience with Equipment Qualification and Computer System Validation
  • Strong project management skills with the ability to prioritize assignments
  • High level of accuracy and quality of work
  • Demonstrated problem-solving skills with the ability to prioritize, align and simplify, used to manage multiple projects with changing priorities
  • Strong collaboration skills with the ability to work across boundaries and to develop sustainable professional relationships on all levels of the organization
  • Strong customer focus and solution orientation; proven ability to deliver practical solutions and to drive results
  • Excellent communication and interpersonal skills
  • Fluent in English and German, both verbal and written
Company Information:

Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 40 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.

Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package.

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