QA Engineer
Quality Auditor (m/w/d)
Lucerne
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For one of our clients, we are currently looking for a
Quality Auditor (m/w/d)
to join the Global Development Quality Operations (GDQ OPS) team.
This Specialist-level position plays a key role in supporting quality and compliance activities at the Schachen site. As part of the Global Development Quality Operations team, you will contribute to maintaining and improving GMP compliance by supporting cross-functional projects, quality system enhancements, compliance monitoring, SOP management, and quality initiatives. You will work closely with manufacturing and quality stakeholders to ensure that products, processes, and documentation meet the highest regulatory and quality standards.
Your Responsibilities
- Support the release or rejection of GMP materials and components through batch release activities and participation in critical quality-related investigations and programs.
- Perform reviews of GMP documentation, electronic systems, batch records, and other quality-related records in accordance with Quality Operations requirements.
- Ensure all activities are conducted in compliance with cGMP regulations, internal procedures, and quality standards.
- Support quality system processes, compliance monitoring activities, and continuous improvement initiatives.
- Collaborate with cross-functional teams to maintain inspection readiness and support quality-related projects.
Your Profile:
- Bachelor's or Master's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, Engineering, Quality Management, or a related field.
- Initial experience in Quality Assurance, Quality Operations, or a GMP-regulated environment (pharmaceutical, biotech, or medical device industry).
- Basic understanding of cGMP requirements, quality systems, and manufacturing processes.
- Experience reviewing GMP documentation, batch records, deviations, or change controls is an advantage.
- Strong organizational skills, attention to detail, and the ability to manage multiple priorities.
- Proactive and collaborative approach to problem-solving and continuous improvement.
- Fluent German and English language skills (minimum C1 level, written and spoken).
What We Offer
- An opportunity to work in a highly regulated and innovative biopharmaceutical environment.
- Exposure to global quality processes and cross-functional collaboration.
- A dynamic team culture with opportunities for professional growth and development.
- Hybrid work model. The candidate is expecting to be at minimum 3 days per week on site and might increase depending on business needs.
- Location: Schachen
- Contract duration: This is a 12-month contract position, planned to start in September, with the possibility of extension.
- Type of employment: Temporary staffing
- Latest start entry date that can be considered is 01 October 2026
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