Supervisor Quality Engineering - Technical Operations

Prothya Biosolutions makes life-saving plasma medicines and is proud of that! Every day, Prothya colleagues take the extra mile to improve the health of millions of patients worldwide. Are you looking for a position at a dynamic and fast-growing company with an exciting history? Then the position of Supervisor Quality Engineering within our Technical Operations department might be something for you! You will be responsible for the leadership of a dedicated team of Quality Engineers who support the needs of the manufacturing departments in the drive to ensure robust and efficient manufacturing processes within Prothya Biosolutions BV.

Your responsibilities:

1) Team Results

  • Timely handling of production issues and deviations to ensure timely batch release and the prevention of compliance gaps. 
  • Establish new and improve current KPIs which help identify gaps and drive improvement. 
  • Provide support in the training of operators and in the handling of quality issues and records for the whole of Production Operations. 
  • Alignment with the Production Support Manager to improve processes based on data. 
  • Working in matrix organization within the value streams to ensure the team supports timely batch releases and on time in full targets.

2) Effective and efficient business processes

  • Data driven improvements to ensure the performance of manufacturing departments is efficient and yields high quality, right first-time product batches. 
  • Key business processes supported will include Deviations, CAPA, Change Control, Training, and all production processes.  

3) Timely availability of the product

  • To ensure we serve our external and internal customers it is vital that all processes are continuously improved and that all potential compliance gaps are addressed on time and in full. Where required the team will also support deviation handling as SMEs to ensure timely batch release.

4) Team management

  • Hire, lead, coach and appraise employees, and develop (the cooperation between) employees of your team using the relevant HR instruments, service and procedures.

 

Your profile:

  • Bachelor qualification in Science, Technology, or Pharmacy.
  • Demonstrable people management experience, strong leadership skills.
  • Technical quality engineering experience within the pharmaceutical sector, demonstrating a successful history of leading complex investigations and enacting meaningful quality enhancements.
  • In depth knowledge of pharmaceutical manufacturing processes, cGMP, and quality system use.
  • Knowledge of risk analysis tools and processes, data analysis, automation, and engineering.
  • Experience with deviation management is a plus.
  • Fluency in English

What We Offer

  • Full-time employment (40h) with flexible working hours in consultation.
  • A salary between € 4.702,26 and € 6.759,41 gross per month (based on full-time employment).
  • A budget of 16,66% (holiday allowance and 13th month) on top of your gross salary, yours to spend or to save monthly
  • 30 holiday days (based on fte).
  • A personal training budget of €2,100 every three years to foster professional growth and development.
  • Contribution to travel expenses from the first kilometer.
  • Excellent accessibility by public transport and private parking available.
  • A pension plan with Zorg & Welzijn, providing security for your future.
  • A dynamic, safe, and challenging working environment with ample opportunities to grow, innovate, and learn, all while making a meaningful impact on the health of millions.

Acquisitie wordt niet op prijs gesteld. Prothya aanvaardt geen ongevraagde hulp van bureaus voor deze vacature. Toegestuurde cv's (in welke vorm dan ook) door bemiddelingsbureaus aan enige medewerker van Prothya zonder geldige schriftelijke zoekopdracht, worden gezien als eigendom van Prothya waarvoor op geen enkele wijze een vergoeding verschuldigd is.

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