Product Quality Integrator

  • Randstad
  • 4500.00 - 5500.00
  • 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

  • A minimum of a Bachelor’s degree (or University equivalent) in Pharmacy, Biology, Biochemistry, Biotechnology, Engineering, or Life Sciences. A Master’s or advanced degree is preferred.
  • A minimum of 5 years’ experience in the pharmaceutical and/or biotechnology industry is required. A significant part of this experience should be in the area of Quality (Assurance).
  • You have proven knowledge in cGMP standards, policies and procedures.
  • You have demonstrated knowledge of and/or experience in quality systems and processes (change control, deviation handling, CAPA, risk management, complaints handling, (regulatory) inspections, and manufacturing control strategies.
  • Knowledge of and experience in the following areas is preferred: biotechnology, vaccines, API manufacturing, sterile pharmaceutical manufacturing, process development, technology transfer, process validation, developing quality modules of regulatory filings.
  • Working in a matrix structure, you build relations and partnerships that allow you to get things done.

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

  • Ensure that product quality aspects of the vaccines, including the original variant and new variants, are tracked and consistently met.
  • You will ensure that information and data on the vaccine project are structured for easy access and interpretation.
  • In (sub)projects for the vaccine, you will represent PQM on the project team.
  • Working hands-on at operational activities such as complaints, deviations, change controls, and regulatory reviews.
  • Bring creative solutions to define quality solutions with flexibility for business needs, thus providing the best total value to the company.

TAGCLOUD

productquality
#pharma
#qualityassurance
#GMP
#vaccines
#COVID-19
Peter Debrichy

Interested

Send your resume to peter@tailorminds.com referring to job id (940)

More information?

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

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