Manufacturing Specialist Vaccins

  • Ledien
  • 4500.00 - 5500.00
  • 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 in Biotechnology, Biochemistry, Biomedicine, Process Technology (or equivalent education).
  • 4 years’ experience in the Biotechnology or Biopharmaceutical industry.
  • Expert in cell culture (USP), bioreactors, virus propagation and/or downstream processing (DSP) and single use items.
  • Know-how on continuous improvement projects.
  • Experience with cGMP environment and EHSS standards is required.
  • Knowledge of working with suppliers such as Thermo Fisher, Merck, Cytiva, Sartorius, etc. is an advantage.
  • Certified Lean Yellow Belt, preferably Green Belt.
  • Excellent command of the English language.

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

  • Lead process excellence activities to continuously improve the work
  • Acute troubleshoot and support production of cGMP batches in the facility. This includes processes such as cell and virus culture, purification processes, formulation & fill and in-process testing.
  • Taking the lead in root cause investigations of complex deviations and implementation of CAPA.
  • Initiate and handle compliance records (Change Control, Events, CAPA, Deviations).
  • Initiate and execute test protocols that help to improve the system or process.
  • Give direct support and leading the root cause analysis for operations whenever there is an issue, as well as improving the documentation, training and procedures related to the equipment.
  • Ensure that the production equipment is in validated state, documentation is up to date, well maintained, and capacity meets planning.
  • Have the overview and knowledge of the status of the equipment (e.g. uptime, downtime, breakdowns, lifecycle management, occupancy rate and capacity).
  • Working 50% onsite, 50% remotely.

TAGCLOUD

cGMP
#GMP
#Equipment
#training
#DS
#DSP
#virus
#testing
Quality
#improvement
#biotechnology
#pharma
#CAPA
#EHSS
#Deviation
#Change
Bas Lokhorst

Interested

Send your resume to bas@tailorminds.com referring to job id (1026)

More information?

Please contact Bas Lokhorst working at our office in Zoetermeer, phone number +31 6 82 43 66 08

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