ANALYTICAL VALIDATION SPECIALIST (80 – 100%) (M/F/D) REGION ZURICH / EAST SWITZERLAND / BASEL

About the job

Your expertise for strong automation solutions – become part of our team now!

Since our foundation, we have established ourselves as a reliable partner for building and process automation. Our unique selling point: We offer a comprehensive range of services from the initial concept to final implementation – including execution planning and seamless system integration.

With our broad expertise, many years of experience, and a strong team, we reliably implement innovative solutions as an SME in Zurich and Aesch near Basel. Openness, flexibility, and honest interaction characterise our collaboration. We promote professional development, a strong sense of community, and support our customers throughout the entire life cycle.

We look forward to your application and to successfully implementing new projects together!

• Development and validation of analytical methods to support manufacturing and quality control
• Conducting and evaluating sample analyses as well as data interpretation
• Ensuring compliance with regulatory requirements and quality standards
• Creation and maintenance of the required documentation, including validation plans, reports, and SOPs
• Collaboration with interdisciplinary teams to optimise processes and solve analytical challenges
• Participation in audits and inspections as well as providing expertise in method validation

WHAT WE EXPECT FROM YOU:

• Completed degree in chemistry, biochemistry, or a related field
• At least 3 years of experience in quality control in the pharmaceutical industry
• Sound knowledge of GxP, data integrity, and qualification methods
• Familiarity with regulatory requirements (GMP, ICH)
• Excellent communication skills in German and English

We look forward to your application!