+30 km
Uren
Opleiding
Dienstverband
Ervaring
Salaris
Datum
Bedrijfstype
Zoek vacatures
Soortgelijke vacatures omgeving Boxmeer.
Laad meer vacatures

Qualification Engineer Boxmeer SIRE Life Sciences

Solliciteer nu
Solliciteer als één van de eersten
Opslaan
Solliciteer nu
Opslaan
Delen

Gevraagd

  • 37 - 40 uur
  • HBO of hoger
  • Engels (taal)

Aanbod

  • Vast contract
 

Vacature in het kort

Boxmeer
Join a leading company at the forefront of animal health innovation as a Qualification Engineer. In this role, you'll ensure the reliability and compliance of systems and equipment vital for producing top-notch animal health products. You'll develop protocols, coordinate calibration processes, and support audits, all while driving continuous improvement across departments. Enjoy unique perks like contributing to global animal health advancements and collaborating across multiple locations. Continue reading to see how we can support your professional growth.
 

Over het bedrijf

SIRE Life Sciences
Werving en selectie21 - 50 medewerkers
Bedrijfsprofiel
Medewerkers
Sollicitatieprocedure
 

Volledige vacaturetekst

The Company
Our client is a top company that makes vaccines and medicines for animals. They've been researching and developing these products for 75 years, focusing on preventing infections in pets and farm animals. They also run the Dutch sales office and are committed to improving animal health worldwide.

Role description
As a Qualification Engineer, you will ensure the reliability and compliance of critical systems, equipment, and processes used in the production of animal health products. You will develop validation and qualification protocols, coordinate calibration processes, and provide expertise during audits. You will also contribute to continuous improvement initiatives across multiple departments and locations.

Responsibilities

  • Create and manage validation/qualification protocols, reports, and planning
  • Analyze calibration and qualification data using CMMS systems
  • Provide technical support for complex validation and calibration processes
  • Review and assess qualification and “as-built” documentation
  • Act as subject matter expert in audits and validation discussions
  • Ensure compliance with internal and external safety and GMP regulations
  • Drive improvements by initiating business cases and analyzing operational data
  • Maintain knowledge sharing within Integrated Process Teams and CoEs
  • Coordinate with teams across multiple Dutch locations
Requirements
  • Bachelor’s degree (HBO) in a technical or scientific field
  • 3–5 years of experience in the pharmaceutical industry
  • Solid knowledge of GMP and validation/calibration principles
  • Ability to read and interpret technical documents
  • Strong organizational and analytical skills
  • Skilled in writing reports and validation documentation
  • Fluent in English; Dutch and German reading skills are a plus
  • Service-oriented and communicative with a flexible mindset
  • Candidates with a strong interest in the field are encouraged to apply
Other Information
Are you interested in this or another role? click the apply button below and I will contact you as soon as possible.

 

55122

Vacature opslaan
 Vacature delen
Sluit
Je notitie is succesvol opgeslagen
Voeg een notitie toe aan deze vacature
Opslaan
Sluit
Bedankt, je melding is verstuurd
Rapporteer deze vacature
Leg kort uit waarom je deze vacature rapporteert:
Versturen
Terug naar vacatures
Sluit
Kies 1 of meer
Sluit
Vacature opgeslagen
Klik op het hartje bovenaan de pagina om je opgeslagen vacatures te zien.
Terug naar vacatures
Sluit
Vul een in