Pharma QA Specialist: Materials, GMP & LIMS (Contract)

CTC Resourcing Solutions

Wallis

On-site

CHF 70,000 - 90,000

Full time

2 days ago
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Job summary

CTC is supporting a global market leader in the Life Sciences industry by recruiting a QA Specialist for a 7-month contract in the Valais region of Switzerland. The role focuses on material receipt services, data integrity in systems, and KPI collection to support GMP-compliant operations.

Responsibilities include material verification, supplier and SOP maintenance, material qualification in the LIMS, deviation management, and timely escalation of quality issues.

Qualifications

  • Bachelor’s degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  • Strong knowledge of GMP regulations and pharmaceutical quality management systems.
  • Experience with deviations, CAPA, and change controls; familiarity with SAP and LIMS.

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 release in LIMS.
  • Manage deviations and changes associated with materials.
  • Collect KPIs linked to services related to material qualification and release.
  • Escalate critical quality issues tied to materials in a timely, GMP-compliant manner.

Skills

Problem-solving
Decision-making
High-pressure environments
Quality mindset

Education

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

Tools

SAP
LIMS

Job description

CTC is supporting a global market leader in the Life Sciences industry by recruiting a QA Specialist for a 7-month contract in the Valais region of Switzerland. The role focuses on material receipt services, data integrity in systems, and KPI collection to support GMP-compliant operations.

Responsibilities include material verification, supplier and SOP maintenance, material qualification in the LIMS, deviation management, and timely escalation of quality issues.

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