Project Manager – Equipment Design

Project Manager – Equipment Design

We are looking for a proactive and detail-oriented Project Manager in Equipment Design to lead the development, design, and implementation of process equipment within a regulated environment. You will oversee technical design activities from concept to qualification, ensuring compliance with engineering standards, project timelines, and GMP requirements.

• Lead equipment design projects from feasibility through to commissioning and qualification.
• Coordinate mechanical, automation, and process design activities with internal and external stakeholders.
• Develop and review technical specifications, design documentation, and FAT/SAT protocols.
• Manage supplier relationships, including technical alignment, design reviews, and project follow‑up.
• Ensure budget and schedule control across all project phases.
• Oversee change management and risk assessment related to equipment design and modifications.
• Support CQV teams during qualification phases and participate in design improvement workshops.
• Guarantee compliance with GMP, safety, and quality standards for all equipment.

• Degree in Mechanical Engineering, Process Engineering, or related technical field.
• Minimum 5 years of experience in equipment design or project management in a pharmaceutical, biotech, or industrial environment.
• Strong understanding of GMP requirements and engineering design principles.
• Excellent communication and coordination skills across multidisciplinary teams.
• Fluent in English and French;
  German is a plus.

CDI

We are currently seeking an expert in biotech processes to join our Life Sciences team in Neuchâtel.

• Serve as the primary technical contact for production equipment and systems.
• Support and lead design, installation, commissioning, and qualification activities.
• Troubleshoot issues and drive corrective actions and process improvements.
• Ensure equipment is fit for use, compliant, and safe.
• Coordinate modifications, upgrades, and continuous improvement initiatives.
• Ensure compliance with cGMP, GEP, safety, and engineering standards.
• Participate in audits as a system expert.
• Lead the equipment obsolescence program.
• Work hands‑on with operations in a fast‑paced environment.

• Bioreactors and process vessels
• Chromatography and filtration (incl. UF/DF)

Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.