Pilot Technician, Manufacturing 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

Department: API

Manufacturing Location: Bagsværd

As a Pilot Technician, you will help manufacture active pharmaceutical ingredients, intermediates and excipients for clinical and non-clinical activities. Your practical work in the pilot plant will support reliable production while protecting quality, safety and data integrity. By following established processes and contributing to improvements, you will help the team meet project deadlines and maintain high operational standards.

What You’ll Bring

• A technical education at technician level.
• Relevant experience within chemical production, pharmaceutical manufacturing or a related technical area is preferred.
• The ability to follow established procedures and complete semi-routine tasks with moderate supervision.
• Good communication and collaboration skills.
• A proactive, flexible and solution-oriented approach.
• The ability to work responsibly with documentation, production data and quality requirements.
• Familiarity with regulated manufacturing standards is useful but not essential.

What You’ll Do

• 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.

Who You’ll Work With

You will work within an API Manufacturing department and collaborate closely with colleagues in your immediate team. You will also interact with relevant internal stakeholders across Global Research, CMC Development and Product Supply.

In these relationships, you will explain facts, practices and procedures, share knowledge and contribute to troubleshooting and alignment. The role does not include direct or indirect people-management responsibilities, but you may train colleagues in relevant tasks and support the wider team through practical knowledge sharing.

What You Can Expect Here

You can expect a practical role where your daily work directly supports manufacturing activities in the laboratory and pilot plant. You will have responsibility for the quality and integrity of your work while receiving general guidance on new assignments. The role gives you opportunities to build technical experience, contribute ideas and participate in continuous improvements within the department.

You will work within established Quality Management System, environmental, health and occupational safety standards. You will also contribute to a collaborative environment where colleagues share knowledge, solve operational challenges and work together to meet project timelines.

Salary

For this role, the Annual Base Salary ranges from 437,600 to 643,200 DKK, corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Incentives and Benefits

The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks. Learn more about our Reward Philosophy here.

For further information about the position, please contact hiring manager Martin Hauge Bülow at [e-mail].

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

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