Job Description

This Advanced QA Professional – QMS role is an exciting opportunity because it places you at the heart of shaping and continuously improving a global quality management system that directly impacts patient safety and product excellence. You'll collaborate across functions, lead complex investigations and system implementations, and drive measurable change in a highly regulated, innovation-driven environment.

Your new role

This role offers a rare chance to shape and modernize a global QMS at the Bohumil site, directly influencing patient safety and product quality across the full CMC value chain. It is both exciting and challenging — you will lead complex, high-impact change projects, act as a trusted expert across functions, and navigate regulatory expectations while pioneering innovative quality solutions.

Day-to-day your tasks will include:

• Lead implementation and maintenance of assigned QMS processes (change control, deviations, CAPA, QRM), acting as local process owner and Veeva Vault superuser.
• Ensure ongoing compliance with corporate QMS and Czech regulatory requirements by monitoring obligations and driving corrective actions.
• Design, deliver and manage QMS training programs to ensure personnel competency and timely completion of required training.
• Support audit and inspection readiness, participate in internal audits and regulatory inspections, and coordinate quality management reviews.
• Develop and execute quality assurance strategies and KPIs to monitor, measure and continuously improve QMS performance.
• Perform risk assessments across the value chain (production, QC, storage, distribution), provide mitigation recommendations and ensure implementation.
• Represent QA in cross-organizational process groups, provide expert advice on complex quality issues, and drive change and process optimization with high independence.

Your new department

The QA Systems & Training team at Bohumil drives a mission to ensure robust, user-friendly QMS and a highly competent workforce that together safeguard product quality and patient safety across the CMC value chain. The team combines traditional GMP rigor with innovative, data-driven approaches—leveraging tools like Veeva Vault and advanced quality metrics—to simplify processes and enable faster, risk-based decision making. You will contribute by owning key QMS processes, delivering targeted training, and spearheading improvements that increase compliance, efficiency, and cross-functional alignment.

Your skills & qualifications

This position combines hands-on QMS ownership, cross-functional collaboration, and strategic improvement work in a regulated, innovation-driven environment You’ll bring with you:

• Bachelor’s or master’s degree in pharmacy, Chemistry, Biotechnology or a related field.
• Minimum 3 years in pharmaceutical quality assurance (or related field) with solid knowledge of GMP and regulatory standards.
• Proven ability to manage and improve QMS processes, implement quality assurance strategies, and act as superuser for systems like Veeva Vault.
• Strong analytical thinking and risk assessment skills to identify, evaluate and mitigate risks to patients and products.
• Effective communicator with experience delivering training and presenting quality recommendations to cross-functional stakeholders in Czech and English.
• Able to handle complex tasks, make independent decisions, and drive problem resolution with limited predefined procedures.
• Team player who works across functions, adapts to changing regulatory and operational demands, and contributes to continuous improvement initiatives.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary

results we produce. Being part of a global healthcare company means opportunities to learn and

develop are all around us, while our benefits are designed with your career and life stage in mind.

Deadline

12 January 2026. (Applications are reviewed on an ongoing basis)