QA Specialist (7124)

CTC Resourcing Solutions AG

Wallis

Vor Ort

CHF 85.000 - 110.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden
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Zusammenfassung

CTC Resourcing Solutions AG in the Valais region of Switzerland seeks a QA Specialist for a 6-month contract to support production and process QA of active pharmaceutical ingredients. The role emphasizes material verification, supplier qualification, and ensuring GMP compliance.

Responsibilities include managing material qualifications and deviations in the LIMS, CAPA and change controls, and delivering KPIs for service quality in a high-pressure manufacturing environment.

Qualifikationen

  • Residency permit or Swiss/EU citizenship required.
  • Bachelor’s degree in biology, chemistry or related field.
  • Strong knowledge of GMP regulations and pharmaceutical quality management systems.
  • Familiarity with quality systems, SAP and LIMS.
  • Experience with deviations, CAPA and change controls.
  • Excellent problem-solving and decision-making skills, especially under pressure.

Aufgaben

  • Perform incoming material verification according to applicable procedures.
  • Establish and maintain raw material suppliers, SOPs, and systems.
  • Manage material qualification and release in the LIMS.
  • Handle deviations and changes related to materials.
  • Collect KPIs for material qualification and release services.
  • Escalate critical quality issues tied to materials while ensuring GMP compliance.

Kenntnisse

Problem solving
Decision making
Work under pressure

Ausbildung

Bachelor’s degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related field

Tools

SAP
LIMS

Jobbeschreibung

CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a:

QA Specialist

for a 6-month contract rolebased in the Valais area, Switzerland.

Main responsibilities:

  • Perform incoming material verification according to applicable procedures.
  • Establish and maintain raw material suppliers, SOPs, and systems.
  • Manage the qualification of materials used in the manufacturing process, including physical verification of incoming raw materials and subsequent release in our LIMS (Laboratory Information Management System).
  • Manage deviations and changes associated with materials.
  • Collect KPIs linked to services related to material qualification and release.
  • Ensure the timely escalation of critical quality issues tied to materials while maintaining compliance with GMP (Good Manufacturing Practices).

Qualifications and Experience:

  • Relevant working/residency permit or Swiss/EU-Citizenship required.
  • Bachelor’s degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
  • Strong knowledge of GMP regulations and pharmaceutical quality management systems.
  • Familiarity with quality systems, particularly SAP and LIMS.
  • Experience in managing quality tools, including deviations, CAPA (Corrective and Preventive Actions), and change controls.
  • Excellent problem-solving and decision-making skills, especially in high-pressure environments.
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