GMP Quality & Compliance Specialist

Novo Nordisk A/S; Måløv; On-site; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk A/S in Denmark seeks a GMP Supporter to help maintain cGMP standards on the tablet production shop floor, partnering with manufacturing to ensure compliant, efficient operations and ongoing process improvements.

You will manage deviations, change controls, SOPs, and support new product launches, while preparing and reviewing key documents and collaborating across quality, production, and projects. Audit readiness is a key focus.

Qualifications

• Bachelor's or master's degree in Natural Sciences.
• 2–3 years of experience in the pharmaceutical industry in a GMP setting.
• Solid understanding of daily GMP operations with strong ownership of quality and compliance.
• Experience with deviations, change control, SOPs and inspection readiness; English fluency.

Responsibilities

• Being present and handling issues on the shopfloor.
• Ensuring manufacturing processes are executed in a standardised, cGMP-compliant manner.
• Handling deviations and change controls related to processes and equipment, driving them to timely and robust resolution.
• Supporting new product launches through input on process, production, qualification, and facility readiness.
• Preparing, reviewing, and approving SOPs, job instructions, protocols, and reports.
• Participating in cross-functional projects focused on optimisation, digitalisation, and implementation of new systems.

Skills

Quality mindset

Cross-functional collaboration

GMP compliance

Process improvement

Education

Bachelor's or Master's in Natural Sciences

Job description

Novo Nordisk A/S in Denmark seeks a GMP Supporter to help maintain cGMP standards on the tablet production shop floor, partnering with manufacturing to ensure compliant, efficient operations and ongoing process improvements.

You will manage deviations, change controls, SOPs, and support new product launches, while preparing and reviewing key documents and collaborating across quality, production, and projects. Audit readiness is a key focus.