Pilot Plant Technician - API Process Engineering

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

Job summary

Novo Nordisk seeks a Pilot Technician at Bagsværd to support manufacturing of APIs, intermediates and excipients in a compliant GMP environment. You will follow established processes, document activities and contribute to improvements with focus on quality, safety and data integrity.

You will collaborate with the API Manufacturing team and liaise with stakeholders across R&D, CMC Development and Product Supply to ensure timely, reliable production.

Qualifications

• Technical education at technician level.
• Experience in chemical production or pharmaceutical manufacturing preferred.
• Ability to follow procedures and complete semi-routine tasks with moderate supervision.
• Good communication and collaboration skills.
• Proactive, flexible and solution-oriented approach.
• Ability to work with documentation, production data and quality requirements.
• Familiarity with regulated manufacturing standards is useful but not essential.

Responsibilities

• Operate general operations in a chemical production facility to manufacture active pharmaceutical ingredients, intermediates and excipients.
• Carry out chemical reaction operations, work-up and purification, plus buffer preparation and general chemical handling.
• Complete cleaning, environmental monitoring and housekeeping to maintain a safe and reliable working environment.
• Plan, perform and document tasks following GMP requirements and relevant procedures.
• Operate computer systems, manage data carefully and ensure data integrity.
• Support maintenance, control and calibration of equipment and systems.
• Contribute to continuous improvement, troubleshooting, training and planning board meetings.

Skills

Communication

Collaboration

Documentation

Data integrity

Problem solving

Education

Technician level technical education

Job description

Novo Nordisk seeks a Pilot Technician at Bagsværd to support manufacturing of APIs, intermediates and excipients in a compliant GMP environment. You will follow established processes, document activities and contribute to improvements with focus on quality, safety and data integrity.

You will collaborate with the API Manufacturing team and liaise with stakeholders across R&D, CMC Development and Product Supply to ensure timely, reliable production.