Join Progress - Experts in Life Sciences as a Senior Design consultant
32 - 38 uur | cGMP engineering | Project Management
Have you performed multiple feasibility studies and/or conceptual or basic designs of GMP cleanrooms for (bio-)pharmaceutical or ATMP manufacturing? Are you ready for a new challenge? Progress might be your perfect match.
Your challenges
As a Senior Design Consultant at Progress you will have the unique opportunity to be deployed in various capacities, consisting of larger and smaller engineering projects within the pharmaceutical and biotechnology
industries or healthcare sector for example by:
- Leading (engineering) projects from design to completion stage and applying fundamental engineering principles, concepts, theories, and techniques to align with customer objectives;
- Developing, conducting or supporting feasibility studies, basic and/or conceptual design studies for production processes, process installations, cleanrooms, clean utilities and facilities.
- Managing or participating in construction projects (greenfield or brownfield) complete with cleanrooms, clean utilities, production processes, labs and all associated equipment and systems.
Our offer to you
Focus on human capital
Informal work environment
Healthy work-life balance
Short communication lines
Company car
Competitive salary and benefits
Our offer
- A varied job in challenging projects at renowned companies in the life sciences & healthcare industry;
- a healthy growing company with an informal work environment and people centric culture;
- a personal development budget and continuous professional development, both in practice and through courses, trainings and networking events;
- short communication lines, personal commitment, team spirit;
- a healthy work-life balance; work part-time (24-32 hours a week) or full-time (38-hours a week);
- a competitive salary with a bonus on top;
- 25 days of paid annual leave, and the opportunity to build up additional leave;
- a flexible mobility scheme: the choice of various options such as a lease car or travel allowance;
- a contribution to your pension scheme;
- an opportunity to take part in our collective employee participation scheme;
- different social and fun activities, like team events, family day and an end-year weekend.
Your profile
As a people-centric company, your personality is what matters most to us. That’s why we expect you to share the same values we hold: integrity, flexibility, customer focus, and expertise.
- Experience: Minimum of 7 years relevant work experience in the (bio-) pharmaceutical industry and/or cGMP engineering environment;
- Expertise: Expert in feasibility studies, basic and/or conceptual design studies for production processes, process installations, cleanrooms, clean utilities and facilities;
- Knowledge of pharmaceutical production equipment and the cGMP/EU/FDA requirements;
- Education: University or Higher Professional Education (HBO) degree in biotechnology, pharmaceutical, chemical of mechanical engineering or similar;
- Project Management: Proven track record on leading projects from design to completion stage with a strong stakeholder management, planning and communication skills in Dutch and English.
Our team
The strength of Progress lies in the interaction between highly qualified and motivated colleagues, supported by a robust management team. Colleagues help each other and share their professional know-how by regularly evaluating projects and sharing experiences. After a training period, you will become part of a close-knit and enthusiastic team.
Meet our experts
For more information please contact
Haris Achterberg
Human Resources Manager
Office: +31 (0)235635016
Mobile: +31 (0)6 48 08 91 78
