Manufacturing GMP Specialist

  • Zoetermeer
  • 3000.00 - 4000.00
  • 32-40 uren
  • HBO

Opdrachtgever

Our client is a leading Project Management and Engineering Company serving industry around the world.

Opdrachtgever

Our client is a leading Project Management and Engineering Company serving industry around the world. Their reputation is based on forming successful partnerships with their clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.

They provide Full Service Engineering for their clients including Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up on numerous projects across a range of market sectors.

functie Vereisten

We are looking for a person who is pro-active, has a strong quality mindset and works accurately. We are a global company and you will be part of a truly global and international organization. You have a MSc/BSc in pharmaceutical sciences or other relevant disciplines (i.e., pharmacy, (bio)chemistry). At least 4 years of experience in QA or aseptic drug product manufacturing is required, experience in (bio-) pharma industry is desirable. Our highly dynamic environment requires you to be flexible, creative and result oriented. Professional English, Dutch is preferred.

Wat krijg je?

  • 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

Werkzaamheden

Inspection readiness, facilitating audits and inspections such as:
  • Being key user in the documentation system, supporting in the creation of documents.
  • Being key user of the quality system (TrackWise).
  • Responsible for creation and on-time closure of change controls, quality investigations and other quality records.

Furthmore:
  • Maintaining the training strategy and program for the department.
  • Requesting purchase orders and facilitate the invoicing process.
  • Aligning with key stakeholders from clinical supply chain, logistics and QA.
  • Driving continuous improvement in our processes

TAGCLOUD

Sander Pupella

Geïnteresseerd?

Send your resume to sander@tailorminds.com referring to job id (700)

Meer informatie?

Please contact Sander Pupella working at our office in Zoetermeer, phone number +31 6-13140754

SOLLICITEER MET ONDERSTAAND FORMULIER

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