Quality Assurance Associate

Actalent; Bezirk Solothurn; Hybrid; CHF 90.000 - 120.000; Teilzeit

Benefits dieser Stelle

4-day workweek

Hybrid work model

Contract until Feb 2027

Exposure to global quality processes

Fast interview process

Zusammenfassung

Actalent in Solothurn, Switzerland is seeking a Quality Assurance Associate for a GMP-regulated environment. The role targets a junior QA professional with initial Quality Systems experience and a drive to develop further while collaborating with local and global stakeholders.

The position offers 80% workload (4 days/week) with a hybrid model (1 home office day). Contract until February 2027, with potential extension, and exposure to global quality processes.

Qualifikationen

• Initial QA experience in a GMP environment (2–3 years)
• Exposure to QMS processes: Deviations, Change Controls, CAPAs
• Experience with electronic quality systems (Veeva, Oracle) is advantageous
• Strong communication and ability to work with international stakeholders

Aufgaben

• Support a range of Quality Management System (QMS) activities
• Assist with audit and inspection readiness initiatives
• Support supplier and contractor onboarding processes
• Coordinate governance meetings, including scheduling, KPI tracking, and preparation of quality metrics
• Review GMP documentation, procedures, records, and logbooks
• Provide support for deviations, CAPAs, change controls, and vendor management activities
• Collaborate with local and global Quality Assurance teams as a key point of contact
• Support quality reporting and ensure timely follow-up of quality-related actions

Kenntnisse

Quality Assurance

Global collaboration

Strong communication

Independent work

Tools

Veeva

Oracle

Jobbeschreibung

Solothurn, Switzerland | Hybrid | Contract Position

We are currently looking for a Quality Assurance Associate to join a quality-focused team within a GMP-regulated pharmaceutical environment. This position is ideal for a junior QA professional with initial experience in Quality Systems who is looking to further develop their expertise while collaborating with both local and global stakeholders.

Responsibilities

• Support a range of Quality Management System (QMS) activities
• Assist with audit and inspection readiness initiatives
• Support supplier and contractor onboarding processes
• Coordinate governance meetings, including scheduling, KPI tracking, and preparation of quality metrics
• Review GMP documentation, procedures, records, and logbooks
• Provide support for deviations, CAPAs, change controls, and vendor management activities
• Collaborate with local and global Quality Assurance teams as a key point of contact
• Support quality reporting and ensure timely follow-up of quality-related actions

Requirements

• Initial experience in Quality Assurance within a GMP-regulated environment, min. 2-3 years
• Exposure to Quality Systems processes such as:
• Deviations
• Change Controls
• CAPAs
• Experience with electronic quality systems is advantageous (e.g. Veeva, Oracle)
• Strong communication skills and ability to work with international stakeholders
• Fluent English, both written and spoken
• Proactive, organised, and able to work independently
• Comfortable taking initiative and managing multiple priorities

What We Offer

• 80% workload (4 days per week)
• Hybrid working model with 1 home office day per week
• Contract until February 2027 with potential extension
• Exposure to global quality processes and cross-functional collaboration
• Fast interview process with a single interview stage

Start Date: ASAP

If you are looking to build your QA career in a collaborative GMP environment and enjoy working with international teams, we look forward to hearing from you.