Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
The Role
The Project Engineer is responsible for the project planning/costing, design, implementation, commissioning and qualification of initiatives identified to improve capacity and reliability in Membrane manufacturing. The project engineer will be responsible for the full project lifecycle, ensuring stakeholders requirements are achieved and will work with other departments and functions to successfully deliver improvements to Membrane manufacturing.
Duties Include:
• Manage all aspects of assigned engineering projects (project feasibility, cost-benefit analysis, budgeting and projections, HAZOP analysis, project proposal and presentation, securing approval, scheduling and project management, contractor selection, site co-ordination and supervision, progress monitoring & reporting, cost management and control, training, procedure development, commissioning and documentation, final handover and any other associated responsibilities).
• Support optimization of production processes through designing improvements in capacity, identifying areas for cost reduction and quality improvements, ensuring waste and downtime reduction, and helping eliminate non-value tasks.
• Provide support to IQ, OQ, and PQ activities as appropriate.
• Help manage the Engineering Documentation archive and ensure that all engineering documentation is appropriately indexed, filed and tagged.
• Communication of project status through regular scheduled communications, both formal and informal with internal and external stakeholders.
• Ensure that all appropriate personnel are fully trained on all new technologies introduced as part of each project.
• There may be a requirement to travel abroad to Vendor premises as part of the project requirements (e.g. for design reviews/ build inspections / FAT execution).
Who You Are
• Level 8 degree in Mechanical or Electrical Engineering or relevant qualification is desired.
• Level 7 degree will be considered.
• Trade qualification an advantage.
• Minimum of 3-5 years working in a Med Device or Pharma regulated cGMP manufacturing environment.
• Proven project management experience, qualification desirable.
• Critical: Proven ability to manage multiple projects on time and within budget. • In depth knowledge of unit operations and process engineering. Experience of DCS and SCADA systems, including associated documentation.
• Detailed knowledge and understanding of both processes and equipment (mechanical, electrical, controls etc.).
• Understanding of adherence to regulatory compliance (change control, audits etc.).
• Ability to work as part of and lead a team when required.
• Ability to manage vendor supply in line with project requirements during a project schedule.
• Previous experience within an ATEX environment an advantage.
• Excellent awareness and experience in relation to Quality and Environmental Health and Safety.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!