CheckMark Labrecruitment

Gepubliceerd: ongeveer 2 maanden geleden

Quality Specialist Covid-19

€3,500 - €6,400 (Maand)
Gepubliceerd: ongeveer 2 maanden geleden
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Waar ga je aan de slag - Where will you work

Pharmaceutical company specialised in the development of vaccines. As Quality Specialist Covid-19 you will be part of the Product Quality Management (PQM) team.

Wat ga je doen - What will your job be

As Quality Specialist Covid-19 you support the Product Quality Management (PQM) team in the Covid-19 vaccine project by ensuring that product quality aspects are tracked and consistently met. Are you the quality profesionnal who get things done? Apply now!

As Quality Specialist Covid-19 you will be responsible for ensuring that product quality aspects of the Covid-19 vaccines, including the original variant and new variants, are tracked and consistently met.

  • You will ensure that information and data on the Covid-19 vaccine project are structured for easy access and interpretation.
  • In (sub)projects for the vaccine, you will represent the Product Quality Management (PQM) department on the project team.
  • Also, you will be working hands-on at operational activities such as complaints, deviations, change controls, and regulatory reviews.
  • In all activities, you bring creative solutions to define quality solutions with flexibility for business needs, thus providing the best total value to the company
  • As you will work in a matrix structure, building relations and partnerships that allow you to get things done is an important part of the job.

Wat vragen wij - What are we looking for

For the position as Quality Specialist Covid-19 we are looking for an all-round quality professional who meets the following requirements:

  • BSc or MSc degree in Pharmacy, Biology, Biochemistry, Biotechnology, Engineering, or Life Sciences
  • 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, e.g., 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

Wat hebben we te bieden - What do we offer
  • Long term position, which starts with a 6 months contract at CheckMark
  • Salary indication from €3600,- to €6400,- gross per month based on a full-time position
  • Full-time position (40 hours/week)
  • Flexiblility to accommodate US, EMEA and ASPAC work schedules when necessary; balancing work and personal time is required

Wil je meer weten - More information

Neem voor meer informatie contact op met Jurjen Wilschut: 088 00 211 22 // 06 3024 7453
Vacaturenummer: 7074

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