GMP Pilot Technician – Pharmaceutical Process Engineering

Novo Nordisk A/S; Gladsaxe Kommune; On-site; DKK 438,000 - 643,000; Full time

Job summary

Novo Nordisk A/S in Bagsværd, Denmark, seeks a Pilot Technician in Manufacturing Process Engineering to support the manufacture of active pharmaceutical ingredients, intermediates and excipients in a regulated API environment.

You will perform pilot plant operations, ensure quality, safety and data integrity, follow GMP procedures, and contribute to continuous improvements while collaborating with the API team and other stakeholders.

Qualifications

• A technical education at technician level.
• Relevant experience within chemical production or pharmaceutical manufacturing.
• Ability to follow established procedures and perform semi-routine tasks with moderate supervision.

Responsibilities

• Perform general operations in a chemical production facility, supporting the manufacture of active pharmaceutical ingredients, intermediates and excipients.
• Carry out chemical reaction operations, work-up and purification activities, as well as buffer preparation and the general handling of chemicals.
• Complete cleaning, environmental monitoring and good housekeeping activities to help maintain a safe and reliable working environment.
• Plan, perform and document tasks within your area of expertise, following current Good Manufacturing Practice requirements and relevant procedures.
• Operate computer systems, manage data carefully and help ensure data integrity throughout your work.
• Support the maintenance, control and calibration of equipment and systems, including relevant standard operating procedures.
• Contribute to continuous improvement, troubleshooting, colleague training and performance and planning board meetings.

Skills

Technical mindset

Communication skills

Collaboration

Problem solving

Proactive approach

Education

Technical education at technician level

Job description

Novo Nordisk A/S in Bagsværd, Denmark, seeks a Pilot Technician in Manufacturing Process Engineering to support the manufacture of active pharmaceutical ingredients, intermediates and excipients in a regulated API environment.

You will perform pilot plant operations, ensure quality, safety and data integrity, follow GMP procedures, and contribute to continuous improvements while collaborating with the API team and other stakeholders.