Engineer Process Equipment

  • Randstad
  • 4000.00 - 4750.00
  • 32-40 hours
  • Bachelor degree

Client

Our client is a consultancy in the food and pharmaceutical industry.

Client

Our client is a consultancy in the food and pharmaceutical industry. They participate in very attractive projects for experienced engineers in the pharmaceutical industry. They offer challenging, varied projects with ample opportunities for personal contributions and development.

Requirements

  • Bachelors degree with 4-6 years’ experience in the pharmaceutical industry/biotechnology.
  • Experience with cGMP and EHSS standards is required.
  • Proven experience with handling change controls, deviations, etc.
  • Lean green belt certification is preferred.
  • Project leadership skills.
  • Quality Assurance understanding of regulatory requirements and industry guidelines specific for the pharmaceutical industry (e.g. GMP, NEN 3140, VCA, CE).
  • High degree of accuracy, initiative, and independence.
  • Communicates clearly in English, both verbally and in writing.
  • Affinity with computerized systems and equipment data flows.
  • Proactive, self-starter, curiosity and eye for improvement.

What do you get?

  • Pension entitlement as from day one
  • Collective WGA / WIA insurance
  • NBBU / ABU collective labor agreement
  • 25 holidays days
  • 8,33% holiday allowance
  • 100% payment in case of illness after one waiting day
  • Travel allowance

Duties

  • Act as the first point of contact for Engineering, Validation, and Maintenance (EVM) to introduce new equipment and maintain the existing equipment.
  • Responsible for introducing processes in the pilot facility including documentation and training.
  • Lead to assure the availability of compliant equipment and processes in the department.
  • Be expert about equipment data integrity topics in a cGMP environment.
  • Support troubleshooting and investigation in non-conformances (process and equipment related).
  • Lead and support process excellence activities to continuously improve the work.
  • Initiate and handle equipment related compliance records (change controls, non-conformances and CAPA records).
  • Work precisely and detect opportunities for improvement with proper follow up, both on work processes as well as personal development.

TAGCLOUD

equipment
#process
#engineer
#GMP
#pharma
#CAPA
#changecontrol
#compliance
#bioprocess
Peter Debrichy

Interested

Send your resume to peter@tailorminds.com referring to job id (1120)

More information?

Please contact Peter Debrichy working at our office in Zoetermeer, phone number +31 6-10191580

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