Job Description

Advanced Pilot Manufacturing Professional
Bohumil, Czech Republic

Be at the heart of pharmaceutical production where precision meets innovation, and your technical expertise directly contributes to delivering life-saving medicines to patients worldwide.

Your new role

As an Advanced Pilot Manufacturing Professional in our Upstream department, you'll play a critical role in executing and optimizing technological processes that form the foundation of our pharmaceutical production. You'll work in a GMP-regulated environment where attention to detail and technical excellence are essential to our success.

Your responsibilities will include:

• Ensuring execution of manufacturing processes in the Upstream (USP) department in full compliance with GMP requirements and production schedules

• Managing assigned equipment and both GMP and non-GMP supporting processes, including preparation of documentation and validation activities

• Creating, reviewing and maintaining controlled documentation (SOPs, MBRs, forms) that ensures process consistency and quality

• Coordinating and implementing modifications to the DeltaV control system in cooperation with production coordinators and IT/OT teams

• Designing and implementing optimization initiatives to minimize production losses and enhance manufacturing efficiency

• Training and supporting the professional development of team members in operational procedures

• Representing production in cross-functional projects focused on process improvements and change implementation

Your new department

At our Bohumil site, the Upstream Pilot Manufacturing team is responsible for critical early-stage production processes. Working within a state-of-the-art facility, our team combines technical expertise with continuous improvement mindset to ensure robust, compliant manufacturing operations. You'll collaborate closely with Quality Assurance, Quality Control, Process Science & Technology, Maintenance, and other departments to drive operational excellence.

Your skills & qualifications

We're looking for a technically skilled manufacturing professional who thrives in a regulated environment and is passionate about process excellence. You'll bring with you:

• Secondary education with school leaving examination as a minimum (technical or natural sciences background preferred)

• Previous experience in pharmaceutical, biotech, food or technical manufacturing environments with exposure to GMP or regulated operations

• Strong understanding of GMP principles and compliance requirements

• Technical aptitude and proven ability to operate complex manufacturing equipment and control systems

• Problem-solving skills with a structured approach to handling deviations and non-standard situations

• English language proficiency at minimum B1 level for effective communication and documentation

• Strong attention to detail, teamwork orientation, and adaptability in changing operational environments

• Experience with digital process control systems and data analysis is advantageous

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. In manufacturing, your technical expertise and commitment to quality directly impact millions of patients globally. Here, you'll find a culture of mutual respect where collaboration across functions is valued, and where your contribution to continuous improvement genuinely matters. When you join us, you're becoming part of a story that spans generations.

What we offer

Being part of a global healthcare leader means you'll have opportunities to develop your technical skills, work with advanced manufacturing technologies, and contribute to meaningful projects. Our benefits are designed to support you throughout your career journey, and our collaborative culture ensures you're never just a number – you're a valued member of a team united by purpose.

Deadline

Please apply before 13th of May 2026

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.