Product Surveillance Associate

  • Brabant
  • 3000.00 - 3750.00
  • hours
  • Bachelor degree

Client

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

Client

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

Requirements

  • HBO level.
  • Several years of experience working with pharmaceutical products/processes and Quality.
  • Project Management: Demonstrates ability to manage assigned tasks within given timelines and available resources.
  • Productive Communication: Demonstrates the ability to distribute accurate information but may need guidance in appropriately crafting messages for target audience,
  • Demonstrates ability to speak and write clearly and concisely and demonstrates skill in selecting appropriate form of communication for the information to be shared.
  • Regulatory Standards and Compliance (Applying): Applies knowledge of internal and external compliance requirements and quality guidelines to all aspects of product specifications, manu-facturing processes, warehousing/ distributions systems and lab functions.
  • Proactive Quality Improvement/ MPS (Learning): Basic understanding of quality improvement tools, MPS and processes and application in isolated SOPs and procedures.
  • Deviation Management (Applying): Applies deviation and investigation process including root cause analyses.
  • Laboratory Data Information Management (Applying): Applies laboratory data information man-agement to support workflow and data tracking.

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

  • Monitoring, trending and assurance of Product quality process performance.
  • Manage product quality systems (e.g. complaints, stability study management).
  • Identify product deviations/ trends, investigate deviations and escalate product issues.
  • Stability Study Management, include set up general stability protocols, set up, ensure and review OGS year plan.
  • Product Quality Report, include perform yearly Product Quality Report assessment, set up Product Quality Report.
  • Product Quality Complaint, include responsible to maintain, perform and support the product quality complaint system.
  • Work Instruction owner, include responsible for metrics/targets for site Quality, global Quality and Business Review meetings, responsible for training on the assigned Quality system.
  • Continuous Improvements, include leads and/or participates in improvement projects.

TAGCLOUD

pharma
#qualityassurance
#productsurveillance
#GMP
Peter Debrichy

Interested

Send your resume to peter@tailorminds.com referring to job id (973)

More information?

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

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