QC Equipment implementation Specialist

Locatie: Leiden

In this role as QC Equipment implementation Specialist you will be responsible for the implementation of standalone analytical equipment as well as new systems which connect to LIMS. Do you have affinity with implementing equipment in a GMP environment? Apply now!

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What will your job be

As QC Equipment implementation Specialist you will be responsible for the technical implementation of new systems within the organization in collaboration with other teams. Lab systems vary from (standalone) analytical equipment to complex global platform projects which connect to LIMS (Laboratory Information Management Systems). Responsibilities include:

  • Documenting administrator procedures, technical installation procedures and maintenance procedures
  • Implementation of equipment within the agreed timelines
  • Infor, lab managers and supervisors of required corrective actions after publication of new regulations to ensure compliance status of systems (USP, GAMP, GMP, ERES).
  • Involved in maintaining the equipment validation master plan for QC equipment
  • Take part in Lab Systems initiatives and projects, in cooperation with the global organization and in alignment with business needs

What are we looking for

For the position QC Equipment implementation Specialist we are looking for a candidate with demonstrable experience and affinity with implementing equipment in a GMP environment. Furthermore you have:

  • Master's or Bachelor's degree in Life Sciences
  • Minimal 4 years of work experience in Pharma with GMP and automation skills
  • Experience with (Computer) System Validation in a GxP environment
  • Experience with the following software is considered as a plus: Empower, Softmax pro, SDMS, Deskman, LIMS, 32Karat, Trackwise, Compliancewire.
  • Analytical thinking and (technical) problem solving. Lean/Six Sigma experience is desirable
  • Planning skills, ability to prioritize multiple commitments
  • Written and oral communication skills in English. Dutch is desirable

What do we offer

  • A contract for 12 months at CheckMark, with the possibility of an extension
  • Salary indication starting at €3087,- gross per month based on fulltime
  • Fulltime position (40 hours/week)
  • Dayshift

Where will you work

A global biotech company that focuses on the development, pro­duction and marketing of vaccines, recombinant proteins and antibodies to prevent and combat infectious and other diseases.

More information

Sebastiaan Loriaux
088 00 211 26
Jurjen Wilschut
088 00 211 22
Ref.nr: 7280
Het is niet meer mogelijk om te solliciteren op deze vacature.