Quality Auditor / Quality Auditress

Job Opportunity: Quality Auditor (m/w/d)

We are currently seeking a Quality Auditor (m/w/d) to join the Global Development Quality Operations (GDQ OPS) team for one of our clients. This specialist-level position is essential for supporting quality and compliance activities at the Schachen site. As a member of the Global Development Quality Operations team, you will play a crucial role in maintaining and enhancing GMP compliance through participation in cross-functional projects, quality system improvements, compliance monitoring, SOP management, and various quality initiatives.

You will closely collaborate with manufacturing and quality stakeholders to ensure that products, processes, and documentation adhere to the highest regulatory and quality standards.

Your Responsibilities

• Support the release or rejection of GMP materials and components through batch release activities and involvement 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 that all activities comply 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 assist in 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 in 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.
• A 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: candidates are expected to be on-site a minimum of three days per week, with the possibility of increasing based 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

Note: Only applications matching the job profile will be considered. Apply online using the form below.