QA Logistic Specialist

Proclinical; Oberwallis; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Proclinical in Switzerland seeks a Quality Assurance Logistics Specialist to verify incoming materials, oversee material qualification and release in LIMS, and ensure GMP-compliant processes across global supply chains.

You will establish SOPs for raw material suppliers, manage change notifications and quality alerts, and collect KPIs for qualification and release services while escalating critical quality issues promptly.

Qualifikationen

• Degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
• Proficiency in English; knowledge of German is an advantage.
• Strong understanding of GMP regulations and pharmaceutical quality management systems.
• Familiarity with quality systems such as SAP and LIMS.
• Experience managing quality tools, including deviations, CAPA, and change controls.

Aufgaben

• Verify incoming materials according to established procedures.
• Establish and maintain SOPs and systems for raw material suppliers.
• Oversee the qualification of materials used in manufacturing, including physical verification and release in LIMS.
• Manage change notifications and quality alerts from the network and raw material suppliers.
• Handle deviations and changes associated with materials.
• Collect and organize KPIs related to material qualification and release services.
• Escalate critical quality issues promptly while ensuring GMP compliance.

Kenntnisse

GMP Regulations

LIMS

SAP

CAPA

Change Control

Deviation Handling

Quality Systems

English Proficiency

Analytical Skills

Ausbildung

Bachelor's degree in Biology/C Chemistry/Pharmaceutical Sciences

Tools

LIMS

SAP

Jobbeschreibung

Ready to play a critical role in safeguarding pharmaceutical quality while driving compliance across global supply chains?

Proclinical is seeking a Quality Assurance Logistic Specialist to join a dynamic team in Switzerland. In this role, you will ensure the verification of incoming materials and oversee the qualification processes to align with regulatory requirements and corporate standards. You will play a key role in maintaining compliance, managing raw material data, and ensuring timely escalation of risks or issues. This is an onsite position requiring a strong understanding of GMP regulations and quality management systems.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Perform verification of incoming materials according to established procedures.
• Establish and maintain SOPs and systems for raw material suppliers.
• Oversee the qualification of materials used in manufacturing, including physical verification and release in LIMS.
• Manage change notifications and quality alerts from the network and raw material suppliers.
• Handle deviations and changes associated with materials.
• Collect and organize KPIs related to material qualification and release services.
• Escalate critical quality issues promptly while ensuring compliance with GMP standards.

Key Skills and Requirements:

• Degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
• Proficiency in English; knowledge of German is an advantage.
• Strong understanding of GMP regulations and pharmaceutical quality management systems.
• Familiarity with quality systems such as SAP and LIMS.
• Experience managing quality tools, including deviations, CAPA, and change controls.
• Excellent problem-solving and decision-making skills, especially under pressure.