RA Labeling Officer

  • Venray
  • 3000.00 - 3500.00
  • 32-40 hours
  • Bachelor degree

Client

Our client is a leading project management and engineering company for industry around the world.

Client

Our client is a leading project management and engineering company for industry around the world. Their reputation is based on forming successful partnerships with their customers, offering them innovative designs and cost-effective solutions in the context of sound judgment, strong management and technical excellence. They offer Full Service Engineering for their customers, including project and program management, purchasing, design, construction management, health and safety management, commissioning, qualification and start-up for numerous projects in various market sectors.

Requirements

  • Bachelor degree is required.
  • Preferably gained work experience in Regulatory, QA or Supply Chain Department within the pharmaceutical industry.
  • 3-5 years of relevant experience.
  • Preferably experience working with an artwork/document management system.
  • Preferably experience with GMP guidelines within the pharmaceutical industry.
  • Good communication skills.
  • Team Player.
  • Fluent English (speaking, reading and writing).
  • Service minded.
  • Accurate and efficient.

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

  • Coordination and implementation of new and revised product labeling in line with regulatory product files and timelines.
  • Maintain contacts with all major stakeholder e.g. Local Companies, packaging sites, Regulatory Affairs, Supply Chain Dept., Area Management, external artwork center, QA.
  • Responsible for the correct and timely control of the art-work design department (internal and/or external)
  • Collecting all necessary information for the preparation of new product labeling, such as technical specifications, design specifications, registration requirements and texts.
  • Responsible for proper phasing of the modified materials and control of phasing out of the existing packaging materials.
  • Responsible for correct/complete intake of the documents and procedure that trigger initiation of introductions / changes.

TAGCLOUD

regulatoryaffairs
#labeling
#pharma
#GMP
#registration
#artwork
Peter Debrichy

Interested

Send your resume to peter@tailorminds.com referring to job id (1001)

More information?

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

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