Principal Engineer

Life Science Recruitment; Burgenland; Vor Ort; EUR 60 000 - 90 000; Vollzeit

Zusammenfassung

A leading company in the Pharma and Medical Device sector is seeking a Principal Device Equipment Engineer. The successful candidate will manage the specification and delivery of equipment, working across organizational teams on global projects. This role requires a degree in Science/Engineering and at least 7 years of relevant experience, particularly in project management, and will offer competitive benefits including salary and family healthcare.

Leistungen

Competitive salary

Bonus

Pension

Full family healthcare

Qualifikationen

• 7+ years’ experience in pharmaceutical and/or medical device development.
• Strong project management experience preferred.
• Good communication skills and commitment to teamwork essential.

Aufgaben

• Develop engineering systems strategy for program delivery.
• Lead equipment delivery projects with suppliers.
• Accountable for process specification from concept to commercialization.

Kenntnisse

Project Management

Communication

Teamwork

Technical Writing

Ausbildung

Degree in Science/Engineering

Jobbeschreibung

Company:
My client are a Pharma and Medical Device company developing combination products who have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas.


Role:Principal Device Equipment Engineer
Location:Newenham Court, Northern Cross, Malahide rd, Dublin 17
Benefits:Competitive salary, bonus, pension and full family healthcare


Overview:
The Principal Device Equipment Engineer will be an SME in the management and delivery of equipment, inclusive of specification, procurement, delivery, qualification, and project management of the same.

The successful candidate will lead equipment delivery projects with the suppliers, inclusive of budget management, and ownership for specification through to qualification. The candidate will work in collaboration with cross organisational teams.
This is a Global role that is key to the success of GDD’s varied product portfolio delivery and will provide the successful candidate exposure to all aspects of combination device design, development, and production.





Day to day:

• Develop engineering systems strategy for program delivery. Pilot to scale up, subassembly, final assembly, labelling, packaging, transport, and auxiliary systems. Establishing and maintaining timelines against organization requirements and identify external partners/OEMs to meet internal needs.
• Lead for engineering systems in cross departmental teams. Manage engineering system objectives in line with program delivery. Supporting the device program team through communication, plan management, technical review and execution, budgetary management, risk assessment, etc.
• Accountable for the process specification, development and realization from product concept to commercialization, liaising with appropriate internal teams to establish process steps and appropriate controls, using good engineering practices. Identification and management risk through established practices, RAID for engineering systems and program delivery.
• Lead development of bespoke manufacturing processes, manufacturing specifications, equipment, manual or benchtop systems, semi and fully automated equipment that meet product performance and quality requirements. Continuous focus on capacity scale up, whilst managing cost requirements.
• Responsible for site integration; establish training needs, transport, site specification, commissioning and qualification activities, product quality, ensuring process performance metrics, development batch record, process, and product.

Company:
My client are a Pharma and Medical Device company developing combination products who have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas.


Role:Principal Device Equipment Engineer
Location:Newenham Court, Northern Cross, Malahide rd, Dublin 17
Benefits:Competitive salary, bonus, pension and full family healthcare


Overview:
The Principal Device Equipment Engineer will be an SME in the management and delivery of equipment, inclusive of specification, procurement, delivery, qualification, and project management of the same.

The successful candidate will lead equipment delivery projects with the suppliers, inclusive of budget management, and ownership for specification through to qualification. The candidate will work in collaboration with cross organisational teams.
This is a Global role that is key to the success of GDD’s varied product portfolio delivery and will provide the successful candidate exposure to all aspects of combination device design, development, and production.





Day to day:

• Develop engineering systems strategy for program delivery. Pilot to scale up, subassembly, final assembly, labelling, packaging, transport, and auxiliary systems. Establishing and maintaining timelines against organization requirements and identify external partners/OEMs to meet internal needs.
• Lead for engineering systems in cross departmental teams. Manage engineering system objectives in line with program delivery. Supporting the device program team through communication, plan management, technical review and execution, budgetary management, risk assessment, etc.
• Accountable for the process specification, development and realization from product concept to commercialization, liaising with appropriate internal teams to establish process steps and appropriate controls, using good engineering practices. Identification and management risk through established practices, RAID for engineering systems and program delivery.
• Lead development of bespoke manufacturing processes, manufacturing specifications, equipment, manual or benchtop systems, semi and fully automated equipment that meet product performance and quality requirements. Continuous focus on capacity scale up, whilst managing cost requirements.
• Responsible for site integration; establish training needs, transport, site specification, commissioning and qualification activities, product quality, ensuring process performance metrics, development batch record, process, and product.

Experience required:

• Degree in Science/Engineering with 7+ years’ experience in pharmaceutical and/or medical device development or similar role.
• Strong project management experience is highly preferred.
• Enthusiastic, conscientious, highly driven and motivated person.
• Good communication skills and commitment to teamwork are essential.
• Writing technical reports and producing high quality documentation within a regulatory controlled GMP environment

Does this sound like your next career move? For more info forward your application or contact me on 087 0612325 [e-mail]