QA & QMS Specialist: GMP Documentation Expert

Tech'Firm Industrie AG; Basel; Vor Ort; CHF 95.000 - 130.000; Vollzeit

Zusammenfassung

Techfirm Engineering is seeking a QA Specialist / QMS associate (m/w/d) to reinforce our Industrial Services team in Switzerland. Based in Basel, you will focus on GMP documentation review, quality approvals, QMS activities, and audit support.

Ideal candidates have initial GMP-regulated pharmaceutical experience and at least 1 year in Quality Assurance/QMS, with strong attention to detail and excellent collaboration across disciplines.

Qualifikationen

• Attention to detail and strong quality mindset.
• Structured and organized approach.
• Autonomous and proactive working style.
• Good communication and stakeholder management skills.

Aufgaben

• Review and approve quality and GMP documentation.
• Review and manage logbooks, GMP documents, procedures, and deviations.
• Act as a Quality Approver for relevant documentation.
• Support QMS-related activities and quality processes.
• Prepare and maintain quality reports and documentation.
• Support audit activities and provide necessary documentation.
• Assist vendor onboarding ensuring GMP requirements are addressed.
• Participate in governance meetings and collaborate with cross-functional teams.

Jobbeschreibung

Techfirm Engineering is seeking a QA Specialist / QMS associate (m/w/d) to reinforce our Industrial Services team in Switzerland. Based in Basel, you will focus on GMP documentation review, quality approvals, QMS activities, and audit support.

Ideal candidates have initial GMP-regulated pharmaceutical experience and at least 1 year in Quality Assurance/QMS, with strong attention to detail and excellent collaboration across disciplines.