GMP Materials QA & Release Specialist

Swisslinx AG; Oberwallis; On-site; CHF 90,000 - 120,000; Full time

Job summary

Swisslinx AG is seeking a QA Logistics Specialist to support GMP-compliant incoming material activities, qualification, and release within our quality systems. You will verify materials, coordinate their qualification and release, and ensure documentation is accurate and up to date.

The role requires a science background and familiarity with SAP or LIMS, plus strong organizational skills and attention to detail to maintain GMP compliance and quality standards.

Qualifications

• Incoming material checks in line with GMP procedures.
• Coordinate qualification and release of raw materials.
• Physical verification of incoming materials and support release in LIMS.
• Maintain raw material supplier information, SOPs and system data.
• Manage supplier change notifications and quality alerts.
• Handle deviations, CAPAs and change controls.
• Track KPIs related to material qualification and release.
• Identify and escalate quality risks or issues in a timely manner.
• Ensure activities remain compliant with applicable GMP and quality requirements.

Responsibilities

• Oversee incoming material verification and release activities within quality systems.
• Coordinate the qualification and release of raw materials used in manufacturing.
• Maintain supplier information, SOPs and data in SAP/LIMS.
• Handle deviations, CAPAs and change controls; manage quality alerts.
• Track KPIs and escalate material-related quality risks promptly.

Skills

GMP knowledge

Quality systems understanding

Attention to detail

Organizational skills

Education

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

Tools

SAP

LIMS

Job description

Swisslinx AG is seeking a QA Logistics Specialist to support GMP-compliant incoming material activities, qualification, and release within our quality systems. You will verify materials, coordinate their qualification and release, and ensure documentation is accurate and up to date.

The role requires a science background and familiarity with SAP or LIMS, plus strong organizational skills and attention to detail to maintain GMP compliance and quality standards.