In this role, you will support quality assurance processes by maintaining compliance documentation, assisting with audits, and collaborating across departments to uphold quality standards. You will play a key role in ensuring adherence to GMP regulations and improving quality management systems at our site.

Start Date: 01/10/2025

Duration: 9 Months

Place of Work: Visp

Key Responsibilities

Prepare and update accurate reports on compliance activities and related documents, including monitoring key quality indicators such as non-conformities, CAPAs, change controls, and training status
Assist with the implementation of corporate documents at the local level
Work closely with other departments to ensure consistency and compliance within the Quality Management System across the site
Identify and lead projects aimed at enhancing QMS processes and compliance
Participate actively in audits and inspections, including preparing documentation and following up on findings
Perform additional duties as required

Candidate Profile

Bachelor’s or Master’s degree in natural sciences or a related discipline
Several years of experience working within a GMP-regulated environment, ideally in quality assurance
Strong ability to manage multiple stakeholders and tasks simultaneously
Proficient in Microsoft Office tools, especially Excel and PowerPoint
Languages: Excellent command of written and spoken English, German skills are a plus

Job ID 41181026