Senior Mechanical Engineer with a Flair for Quality and Documentation

• Fast stilling
• Ansøgningsfrist: 03.08.2026

Arbejdssted: Herlev og Kalundborg

Are you our next Mechanical & Quality Consultant?
At Norconsult Danmark – Life Science, we highly value skilled professionals.

We are currently looking for a Mechanical Engineer with strong competencies in quality and documentation, as well as hands-on experience with testing, commissioning and project handover within the pharmaceutical industry.

This is an exciting opportunity to join a team working on complex life science projects, where quality, compliance and technical excellence are key to successful project delivery.

Your primary responsibilities may include:

• Preparing and reviewing technical and quality related documentation for mechanical systems and process equipment.
• Developing User Requirements Specifications (URS), Design Specifications, Technical Specifications, and Requirements Traceability Matrices (RTMs).
• Reviewing P&IDs, layouts, technical drawings, and mechanical documentation.
• Performing line walks and verifying installations against design requirements and GMP standards.
• Participating in FAT, SAT, commissioning, qualification, and validation activities.
• Reviewing design documentation, including component lists, instrument lists, welding documentation, material certificates, and technical specifications.
• Ensuring compliance with GMP requirements, applicable quality standards, and relevant industry regulations.
• Advising clients on mechanical solutions, machine safety, quality requirements, and regulatory expectations.
• Building and maintaining strong relationships with clients, suppliers, and other stakeholders

Your Qualifications
You may come from a relevant background, such as a Marine Engineer, Mechanical Engineer, or have gained the above experience through roles within the pharmaceutical industry.

More specifically, you have:

• A minimum of 10 years of experience working with mechanical systems, quality and documentation in pharmaceutical industry projects.
• Experience with machine safety, ATEX and various types of process equipment.
• Solid knowledge of GMP and GEP principles and requirements.
• A high level of technical expertise and professional integrity.
• Experience from the engineering consultancy industry is considered an advantage.
• Strong written and verbal communication skills in both Danish and English, enabling you to prepare technical documentation, reports and communicate effectively with stakeholders.

What We Offer
We offer an exciting position with one of the leading engineering consultancies in the Nordic region, where we are committed to supporting both your professional and personal development.

You will have an independent and responsible role, working alongside skilled colleagues in a well-functioning and locally anchored organization.

We foster an open, informal and positive work environment where your opinions are valued and help shape important decisions.

Our department takes great pride in its professional expertise and is dedicated to being a trusted and professional partner to our clients. We also prioritize social activities to strengthen team spirit and collaboration. The atmosphere is informal, welcoming and characterized by a solution-oriented mindset and a good sense of humor.

We offer a competitive benefits package in line with industry standards, including a pension scheme, health insurance, and opportunities for continuous professional development and training.

Location:
Kalundborg or Herlev

Start Date:
As soon as possible

Contact Information:
If you would like to learn more about the position or about Norconsult Life Science, please contact: Asha Mahendran, Department Manager,

Phone: Se telefonnummer på jobbank.dk

We look forward to hearing from you.