QA Logistic Specialist

Safeguarding Pharmaceutical Quality and Global Compliance

Join a dynamic team in Switzerland to play a critical role in safeguarding pharmaceutical quality while driving compliance across global supply chains. In this position, you will ensure the verification of incoming materials and oversee qualification processes to align with regulatory requirements and corporate standards. You will be instrumental in maintaining compliance, managing raw material data, and ensuring the timely escalation of risks or issues. This onsite role demands a strong understanding of GMP regulations and quality management systems. To be considered, candidates must hold the right to work in this location or possess an EU passport.

Core 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.