Visp
6 months
41 hours
Start: February 3, 2025
Deadline: January 22, 2025
SL-000050
SL-000050
Job description:
On behalf of our client, we are seeking a detail-oriented Quality Assurance Specialist to join their team in Visp.
About the customer:
The client is a leader in the Pharmaceutical industry, renowned for its innovative solutions and commitment to quality in healthcare.
Requirements:
- Collaborate with cross-functional teams to manage and execute Quality System-related projects within defined timelines.
- Draft, review, and finalize new procedures to ensure clarity, consistency, and alignment with organizational and regulatory requirements.
Competences:
- Bachelor’s (B.Sc.) or Master’s (M.Sc.) degree in natural sciences or a related field.
- Significant work experience in a GMP-regulated environment, preferably within a Quality System unit.
- Proven ability to manage multiple tasks and interact effectively with diverse stakeholders.
- Strong proficiency in written and spoken English; German is an advantage.
- Expertise with Microsoft tools, particularly Excel and PowerPoint.
Compensation benefits:
- An opportunity to contribute to the development and execution of Quality Systems within a renowned pharmaceutical organization.
- A collaborative and supportive work environment in Visp, a hub for cutting-edge pharmaceutical and biotech projects.
- Potential for professional growth and career development.
