Pharmaceutical OSD Engineer (m/f) – Fulltime (100%)

☞ PHARMAPLAN (TTP Group)

View: 226

Update day: 21-03-2024

Location: Montreux Vaud VD

Category: High Technology Mechanical / Technical Electrical / Electronics IT - Software

Industry: Staffing Recruiting Biotechnology Research Pharmaceutical Manufacturing

Position: Associate

Job type: Full-time

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Job content

For our office in Montreux we are looking for a:

Pharmaceutical OSD Engineer (m/f) – Fulltime (100%)

PASSION FOR PHARMA ENGINEERING:This is what Pharmaplan stands for. As one of the leading pharmaceutical consulting and engineering companies in Europe, we are specialized in the integrated and holistic planning and realization of pharmaceutical production facilities and thus shape the future of our industry. With our highly qualified employees working in areas such as project management, process engineering, GMP, laboratory planning, architecture, building services and digital factory, we set the course for the global supply of medicines of tomorrow.

Operating under the umbrella of the TTP Group with over 1´000 employees at 26 international locations, we support the pharmaceutical and biotechnology industry with flexible, GMP-compliant and future-proof solutions. From initiation to construction to handover, we handle projects of all sizes on behalf of our clients.

Ensuring pharmaceutical production in Europe is more important than ever. Join us and become part of our Pharmaplan mission!

The job

As part of our project team you will carry out the pharma process planning within customer projects of pharmaceutical processes and plants at our customers’ premises.

In pharmaceutical projects, you coordinate the stakeholders involved (suppliers, engineers and operators) across all phases.

Your main responsibilities are:

  • Lead the execution of pharma process engineering from design until project handover to the client including C&Q
  • Develop solutions to complex problems
  • Provide technical direction with other engineers
  • Project management support: from proposal (scope definitions, cost calculations, staffing), project execution (reporting) until project handover to the client
  • Contribute to Standards and Guidelines development on your area

Your Qualifications

You have a life science or engineering degree and have a solid knowledge of GMP regulations and industry standards with at least 5 years of relevant job experience.

You have worked on projects within the pharmaceutical area more specifically Oral Solid Dosage process including high potent product and/or material handling/washer. You have work experience within a pharmaceutical company’s technical organisation, a supplier company or an engineering/consulting company.

You speak French and English fluently. German language will be a benefit.

Personally, you are characterised by fast learning, high operational readiness and resilience as well as flexibility.

You enjoy achieving your success within a team and have the necessary assertiveness and communication skills. Even in hectic situations you keep the focus on the essentials.

You have excellent customer understanding, and the ability to inspire and demonstrate leadership in customer relations. Furthermore, you have a personal drive and are passionate about your work.

We offer

  • Exciting and different tasks in a dynamic environment
  • Development opportunities in a fast-growing company
  • A wide range of internal training courses and ongoing education opportunities
  • A working environment that is open to innovative ideas and suggestions
  • Attractive leisure activities and teambuilding events

Contact

For further information contact the HR Recruitment team: 0041 (0) 61 307-9670.

Application

Please submit your application online including your salary requirement and your availability.

We do not accept applications from a recruitment company.
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Deadline: 05-05-2024

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