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Do you want the unique opportunity to contribute, expand, and influence how our business area of consultancy with Process Engineering – Pharma & Life Science will evolve? Do you want to advise our clients on process design, technology selection, and current production optimization? - If so, this is the right position for you.
You will be working on the client’s side, supporting them in the development and implementation of renovation/new construction of production facilities – mainly on projects in the Pharma and Life Science sectors. The position involves almost all aspects of the project and all its phases. The tasks will be very diverse and varied, ranging from specification and documentation to implementation, supervision, and testing.
The Pharma and Life Science division at Artelia consists of over 100 employees spread across nine departments. We have offices in Holbæk and Buddinge, where you can work from. You will be part of the department: “Process & Mechanical – Pharma”, where you will have 19 competent colleagues who are looking forward to welcoming another colleague to collaborate with. You will have ample opportunity to contribute to shaping the development of the department, where we make a significant effort to foster a strong team spirit in a busy work environment. To ensure the quality of our work, we regularly meet as a team to discuss and share knowledge. Additionally, we prioritize staying updated within our field through courses, visiting relevant trade fairs, and, most importantly, through specific focus days at Artelia.
Artelia is a dynamic company with a flat organizational structure, where there is a short distance from idea to action. Your daily work will be characterized by high professionalism, freedom with responsibility, a high degree of knowledge sharing, and fast execution.
You profile
- You have a background in Process Engineering, Chemical Engineering, Chemistry and Biotechnology Engineering, or similar.
- Minimum 5-10 years of experience in a process engineering role.
- Previous experience as a Project Manager/Package Owner is an advantage.
- You have experience in biopharmaceutical production (e.g., upstream or downstream etc.).
- Experience with equipment in biopharmaceutical production.
- You have a good understanding of GMP requirements.
- You thrive in an interdisciplinary project environment.
- You have good communication skills and can communicate effectively in both Danish and English.
- You can develop and articulate complex topics and results in a report or presentation.
- You must have a valid driver’s license.
Your main tasks
- Establish customer contact and relationships.
- Serve as Subject Matter Expert (SME) lead for process equipment package.
- Continuously monitor the customer’s process and production needs.
- Specify and design process equipment.
- Responsable for dokumentation.
- Provide advice to customers on process and process equipment optimization.
- Manage small, medium, and large projects (review design, planning, and implementation)
- Renovation of process equipment.
- Participation in and execution of FAT and SAT tests.
- Analysis of systems (line walk, process measurement, etc.)
- Customer support/training during process startup.
We offer
- Many exciting and challenging projects
- A strong professional network with committed and competent colleagues
- A culture where well-being, cooperation and working conditions are given high priority
- A dynamic and inspiring environment with ample opportunity for personal development
- A workplace where "freedom under responsibility" is a core value
- Good career opportunities which are supported by internal training courses in Academy, on subjects such as management, project management, BIM and other professional areas
- Attractive employee benefits with health insurance, employee bonuses, lunch arrangements, active staff clubs, sports and cultural events, study and ski trips and an attractive salary package.
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