Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Senior Project Engineer - Cork

Posted Jun 8, 2021
Job ID: JJJP00006732
Location
Cork
Duration
1 year
(Jun 28, 2021 - Jun 26, 2022)
Hours/week
39 hrs/week
Payrate range
30 - 40 €/hr

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.


We are currently recruiting a Senior Project Engineer to join our contingent workforce on a growing team at Depuy Synthes Cork. This will be an initial 12 month contract.


About Depuy Synthes:

DePuy Synthes is a Johnson & Johnson company that is one of the leaders in the medical device industry. Our implants and instruments are used by orthopaedic surgeons to treat patients with conditions resulting from traumatic injuries, degenerative diseases, deformities, and sports related injuries. Our environment is entrepreneurial, learning-driven, and is as challenging as it is rewarding.

 

DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative, and comprehensive orthopaedic and neurological business in the world. DePuy Synthes Companies will offer an unparalleled breadth and depth of products, services, and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, we are creating one organization that will be agile and better equipped in today's evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.   


The Role: 

Development and installation of manufacturing processes and for new product introductions. The successful candidate will provide the technical lead in cross functional teams to set up new processes to meet challenging project commitments in line with agreed stability metrics. The role will involve collaborating with global R&D teams to develop innovative and cost effective devices and delivering highly stable and effective manufacturing processes.


Key Responsibilities:

  • Lead NPI development requirements and work with cross functional teams in the Innovation Centre and with the Value Streams.
  • Lead NPI development requirements and work with cross functional teams in the Innovation Centre and with the Value Streams.
  • Provide design for manufacturing technical input to global design groups to minimise lifecycle cost
  • Project planning to deliver project(s) against agreed milestones and project scope (schedule, resource, cost).
  • Deliver stable manufacturing solutions in line with stability metrics process.
  • Conduct and lead detailed product design reviews
  • Development of advanced manufacturing processes to lean guidelines
  • Manage risk management and validation lifecycle for new process or process changes.
  • Management of the Asset Lifecycle for new equipment and processes (URS/RA/IQ/OQ/PQ).
  • Direct PFMEA studies and lead risk assessment effort for overall process
  • Influence innovative qualification methodologies to apply appropriate statistical and validation techniques based on failure model and overall risk
  • Develop strategic collaborations across functions, business units and geographic boundaries to achieve effective outcomes over the long-term.
  • Provide timely and accurate reporting on project activities.
  • All other duties as directed by direct manager.


Candidate Requirements:

  • Obtained as a minimum a Degree in Mechanical/Production/Manufacturing Engineering and 3 years minimium post graduate (Ideally 5 years plus) experience in a medical device or comparable hi-tech environment. 
  • Proven track record in development, installation and qualification of manufacturing processes for New Products or Product Transfer.
  • Experience using proven problem solving/Root techniques (8D, TRIZ or equivalent)
  • Demonstrated ability to lead sub teams within a project and give direction to fellow team members, contractors, vendors to complete tasks to a defined timeline. 
  • Skilled in preparing documentation such as project plans, schedules / timelines, checklists, protocols, and reports that are often detailed and complex.
  • Self motivated, with focus on Quality, Timelines and Cost.
  • Proficiency of GD&T and ASME Y14.5M 1994 standards
  • Excellent Planning & Organizing Skills
  • Flexible work ethic. 


Desirable Criteria:

  • Certification from an accredited institution in Project/Program Management.
  • Knowledge of medical device quality & regulatory systems and medical device directive (ISO13485, MDD and FDA CFR 820) and other pertinent Design Control requirements.
  • Knowledge of anatomy and physiology.
  • Knowledge of manufacturing processes.


If you meet our requirements and are interested in hearing more about our Senior Project Engineer role, please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!


 


Similar jobs

+ View all jobs