Gi Life Sciences
Visp
8 hours ago
QA Project Manager
- Publication date:03 October 2025
- Workload:100%
- Contract type:Temporary
- Place of work:Visp, 3930 Visp
About the job
Gi Life Sciences is looking for a client, a QA Project Manager for the region of Viège.
Temporary Contract (replacement maternity leave)
Start date : immediate
End date: June 2026
Main mission :
Ensure the daily supervision, strategic and tactical leadership of a team of QA project managers, ensuring quality support to internal and external clients as part of technology transfer activities and process validation.
Key responsibilities:
- Supervise, train and develop a team of QA project managers.
- Provide strategic and operational guidance.
- Act as an escalation point for QA issues.
- Ensure compliance with quality requirements at key stages of technology transfer and process validation.
- Oversee sterility assurance assessments, material assessments, deviations, change controls and quality agreements.
- Ensure proactive resolution of issues related to production, regulatory compliance and TT processes.
- Track and analyze key performance indicators (KPIs) for internal and external customers.
- Ensure compliance with SOPs, quality agreements and current regulations.
- Actively participate in risk management and documented decision making.
- Maintain smooth and effective communication with internal and external stakeholders.
- Define team objectives and ensure alignment with site priorities.
- Promote continuous improvement, operational efficiency and innovative thinking.
- Monitor progress, ensure implementation of actions and evaluate results.
- Supervise training, supervise employees and develop quality principles.
- Regularly organize individual and collective meetings to review objectives and provide constructive feedback.
- Take on the role of QA project manager for client projects, if required.
- Participate in the recruitment and integration of new qualified employees.
- Collaborate with internal clients on change controls, deviation, CAPA.
- Intervene as a QA expert on complex or high-risk subjects involving the relevant services (MSAT, engineering, QC, validation, Supply Chain, production)
- Participate in project meetings to identify quality requirements.
- Support the completion of QA deliverables.
- Track Key Performance Indicators (KPIs) and quality measures.
- Represent the QA department during cross-functional meetings.
- Prepare trend reports on deviations for site management.
- Assess trends and propose recommendations for improvement.
- Participate in regulatory and client audits as an QA representative.
Profile :
- BSc/MSc in science, biotechnology or related discipline.
- Minimum 10 years of experience in quality assurance in a regulated environment and team management with direct reports.
- Expertise in deviation, CAPA, change control.
- Ability to work in transversal with technical functions.
- Proven experience in quality assurance in a GMP environment.
- Proven skills in team management, problem solving and project management.
- Excellent ability to work in a transversal way and interact with various interlocutors.
- English (C1), German (B2).
Gi Life Sciences contact :
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Contact
Jessica Liuzzo
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