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QC Engineering Specialist Amsterdam Prothya Biosolutions

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Gevraagd

  • 37 - 40 uur
  • Medior/Senior

Aanbod

  • Vast contract
  • Eindejaarsuitkering, Pensioenregeling, Opleidingsbudget, Reiskostenvergoeding
 

Vacature in het kort

Amsterdam
Prothya Biosolutions, known for life-saving plasma medicines, is looking for a QC Engineer Specialist to join the QC Support team. This role involves method development, validation, and quality lab support. Benefit from travel expense contributions and a pension plan. Join a team that makes a real difference in global health. Apply now to be part of this innovative journey! Read on to discover why this challenge awaits you.
 

Over het bedrijf

Prothya Biosolutions
Directe werkgever
Bedrijfsprofiel
 

Volledige vacaturetekst

Prothya Biosolutions maakt levensreddende plasmageneesmiddelen en is daar trots op! Elke dag zetten Prothya-collega's met veel voldoening een stapje extra om de gezondheid van miljoenen patiënten wereldwijd te verbeteren.

Are you an experienced QC Engineer Specialist looking for a new challenge? At QC Support, part of Prothya Biosolutions B.V., we are seeking an enthusiastic team player to support our group in the introduction and validation of multiple analytical methods.

About QC Support Global:

  • Our team supports the QC-Operations lab team with method validation, verification, transfer, troubleshooting and specification setting. We coordinate QC topics in global projects across the sites in Amsterdam and Brussels.

Key responsibilities:

  • Method development and validation/verification: Develop and implement methods in the QC lab following Analytical Quality by Design (AQbD ) principles and international guidelines.
  • Validation Documentation: Write and review various essential GMP documents including reports, risk assessments and periodic reviews.
  • Quality Lab Support: Providing support for QC-operations troubleshooting and investigations following quality events, deviations and CAPAs.
  • Continuous improvement: Maintain the quality level of multiple analytical methods and improve processes and collaborations between teams.

Your skills and experience:

  • Masters degree in analytical chemistry or relevant subject, with at least 3 years of experience in a GMP environment.
  • Expertise with chromatography (HPLC, GC, IC) and other analytical techniques. Knowledge of general pharmacopoeia testing and raw material specification setting is a plus.
  • Familiarity with international guidelines, pharmaceutical QC testing per Pharmacopoeia monographs (Ph. Eur and USP) and method verification.
  • Experience in with method development and validation following AQbD, and following ICH Q2 and Q14 guidelines.
  • Quality mindset and project management experience is preferred.
  • Stress-resistant, enthusiastic and proactive mentality to get things done.
  • Strong communication and collaboration skills with different stakeholders, a real team player.
  • Demonstrate excellent written and oral communication skills in English, with proficiency in Dutch being a plus.

Join us and make a difference! Apply now to grow your career and contribute to our innovative team.

What We Offer:

  • A full-time position with a competitive salary.
  • A budget of 16.66% (holiday allowance and year-end bonus) of your gross salary, which can be used monthly.
  • Flexible working hours, subject to agreement.
  • Personal training budget of €2,100 every 3 years.
  • Contribution to travel expenses from the first kilometer.
  • Good accessibility by public transport, with private parking options available.
  • Pension plan with Zorg & Welzijn.

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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