QA Logistics Specialist

Coopers Group; Oberwallis; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

Coopers Group in Visp, Switzerland, is seeking a QA Logistic Specialist to ensure material incoming verification and alignment with regulatory and corporate standards. The role oversees material receipt services, maintaining data in the QA systems and KPI tracking, with timely escalation of risks.

The successful candidate will manage supplier qualifications, SOPs, and material release in LIMS, while handling deviations, CAPA, and change controls in a high‑pressure GMP environment.

Qualifikationen

• Bachelor's degree required in biology, chemistry, biochemistry, pharmaceutical sciences, or related field.
• Proficient in English; German is advantageous.
• Strong knowledge of GMP regulations and pharmaceutical quality management systems.
• Knowledge of quality systems, SAP and LIMS.
• Experience with deviations, CAPA and change controls.
• Excellent problem-solving and decision-making under pressure.

Aufgaben

• Performs incoming material verification according to applicable procedures.
• Establishes and maintains raw material suppliers, SOPs, and systems.
• Manages qualification of materials used during manufacturing, including physical verification and release in LIMS.
• Manages change notifications and quality alerts and raw material suppliers.
• Manages deviations and changes associated with material.
• Collect KPI linked to material qualification and release services.
• Escalates critical quality issues related to material while ensuring GMP compliance.

Kenntnisse

English proficiency

German advantage

GMP knowledge

Quality systems

SAP

LIMS

CAPA

Change controls

Deviations management

Problem-solving

Decision-making

Ausbildung

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

Tools

SAP

LIMS

Jobbeschreibung

Location: Visp

Start date: Immediately

End date: 15/03/2027

The QA Logistic Specialist, ensures material incoming verification and that company's materials qualification process and services associated, are aligned with regulatory requirements corporate standards and agreements in place with shareholders.

This role is responsible for the oversight and compliance regarding the requirements set out in the respective agreement related to the services provided by the Shareholder regarding material receipt.

Additionally, the role ensures that all raw material data and information are maintained up to date within the appropriate system, KPI associated with the scope of the role are collected and organized, while also timely escalating risks and issues.

Key Responsibilities

• Performs incoming material verification according to applicable procedures
• Establishes and maintains raw material suppliers, SOPs, and systems.
• Manages qualification of materials used during manufacturing process including physical verification of incoming raw material and subsequent release in LIMS.
• Manages change notifications and quality Alerts and raw material suppliers
• Manages deviations and changes associated with material
• Collect KPI linked to services associated with material qualification and release
• Ensure the timely escalation of critical quality issues linked to material, while ensuring compliance with GMPs.

Required Skills

• Bachelor's Degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related fields.
• Proficient English language, German would be an advantage.
• Strong knowledge of GMP regulations and pharmaceutical quality management systems.
• Knowledge of quality systems, especially SAP and LIMS.
• Knowledge in managing quality tools, including deviations, CAPA and change controls.
• Problem-solving and decision-making skills, especially in high-pressure environments.