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QC validation (CSV)

  • Location:

    Amsterdam, Netherlands

  • Contact:

    Natanael Hazel

  • Job type:

    Permanent

  • Contact phone:

    +31 (0)20 406 97 50

  • Industry:

    Life Sciences, (Petro)Chemistry

  • Contact email:

    natanael_hazel@oxfordcorp.com

As QC validation associate, you are responsible for equipment validation in the QC department. This includes computerized system validation and implementation of new equipment as well. In this role you work together with many of the departments within the organization as part of the QC.

Job description

You work in a large international organization as part of the QC department. You are responsible for maintenance and improvements for equipment validation, including computerized system validation (CSV). You do this by coordinating the implementation of equipment and by communicating with the heads of the various QC departments in terms for equipment validation and planning. Also, you review all the documentation involved in the validation procedures. To make sure the technicians are supported, you write SOPs, reports and are responsible for troubleshooting as well. All in all, you have a crucial role in the QC within the whole organization in a dynamic and responsible position.

Responsibilities

  • Maintenance and improvement of equipment validation, including CSV, from a QC point-of-view
  • Coordinating the implementation of novel equipment, including validation
  • Communicate with QC department heads for planning of equipment validations
  • Writing SOPs, reports and troubleshoot as support for technicians
  • Write and/or review equipment validation documents


Profile

  • Bachelor or university-level degree in Life Science, Biotech or a similar field
  • Minimum of 5 years work experience within equipment validation in a pharmaceutical organization
  • GMP-working experience
  • Professional oral and written communication in both Dutch and English
  • Self starting, organized and communicative personality
  • Knowledge of biopharmaceutical production is a huge plus, but not required


Benefits

  • Long term position, direct contract with our client
  • Salary range: €3700 - €5600 gross per month, depending on previous experience
  • Fulltime position of 40 hours/week, 32 hours is discussable
  • Travel costs are reimbursed
  • Location: Amsterdam

Vacancy number: 22438
IMPORTANT NOTE: Please do not apply if you do not have a working permit to live and work in the Netherlands. Your application will not be processed.