GMP QA Lead: Systems & Process Improvement

Solvias; Schweiz; Vor Ort; CHF 110.000 - 140.000; Vollzeit

Zusammenfassung

Solvias in Switzerland is seeking a QA-oriented professional to oversee the quality management software as a system administrator. You will support users, update SOPs, and harmonize processes across sites while leading various projects and implementing new QMS modules.

The role requires a background in analytical chemistry/biochemistry/life sciences and strong GMP knowledge, with experience in analytical-pharmaceutical environments and QA. Fluency in English is essential; German is a plus.

Qualifikationen

• Background in analytical chemistry, biochemistry or life science.
• Experience in the analytical-pharmaceutical environment, preferably experience in QA.
• Strong ability to resolve problems and build good relationships with various stakeholders.
• Good interpersonal skills and team spirit; capable of collaboration in a dynamic, cross-functional matrix environment.
• Ability to lead projects between sites and work independently.
• Broad knowledge of regulatory GMP frameworks (ICH, FDA, USP, Ph. Eur.).
• Solid background in data integrity and computerized systems risk assessment.

Aufgaben

• Taking care of the quality management software as system administrator.
• Support and train users.
• Improve and update processes including SOPs and documents.
• Harmonization of processes.
• Leading projects.
• Implementing additional modules/functions within the quality management software.

Kenntnisse

Analytical chemistry

Biochemistry

Life sciences

QA experience

Stakeholder management

Team collaboration

IT/data integrity

GMP knowledge

Project leadership

English proficiency

German language

Jobbeschreibung

Solvias in Switzerland is seeking a QA-oriented professional to oversee the quality management software as a system administrator. You will support users, update SOPs, and harmonize processes across sites while leading various projects and implementing new QMS modules.

The role requires a background in analytical chemistry/biochemistry/life sciences and strong GMP knowledge, with experience in analytical-pharmaceutical environments and QA. Fluency in English is essential; German is a plus.