Senior Engineer, Network Manufacturing

at  Johnson Johnson

Senior Engineer, Network Manufacturing
Location: Cork, Ireland, Raynham, MA, USA
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.
That is why we in Johnson & Johnson are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”!
DePuy Synthes, Companies of Johnson & Johnson, is the largest, most comprehensive orthopedic and neurological business in the world, built upon the strong legacies of two phenomenal companies.
DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials.
Our broad array of inspired, innovative, and high-quality offerings helps advance the health and wellbeing of people around the world.
We are now recruiting for a Senior Manufacturing Engineer to join the Network Tech Ops team in DePuy Synthes
Job Purpose:
As part of DePuy Synthes Network Edge strategy we are increasing global Manufacturing capacity within the DPS Orthopaedic franchise. As part of that initiative, we are now recruiting for a Staff Engineer to execute capacity expansion projects.
This role will execute engineering deliverables in support of large-scale manufacturing capacity projects that will yield stable, reliable and cost-effective manufacturing process meeting projects FPO’s of capacity, product cost, budget and timeline. The scope of this position will include both project delivery as well as ensuring knowledge transfer to developing manufacturing site staff and will work in collaboration with the existing DPS functional organisations to ensure standardisation and the implementation of Best-in-Class practices.

1. Key Responsibilities:

• Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
• Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognised Regulatory Standards for relevant markets.
• Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
• Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
• Communicates with internal and external partners to coordinate and execute project plans.
• Provides technical leadership and supports execution of EHS&S policies and procedures
• Supporting technical collaboration across functions
• Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented.

QUALIFICATIONS

• Experienced knowledge of medical device manufacturing and validation
• Minimum two years (preferred 4 years) of relevant professional work experience in medtech or similar regulated industry.
• Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
• Strong interpersonal and communication skills & demonstrated ability to operate as part of a team.
• Track record of innovation and adaptability in project execution, with strong problem-solving skills.
• Proven competence to evaluate communicate and act upon significant risks, demonstrating leadership of the high standards of quality and compliance.
• Strong influencing skills - Excellent interpersonal skills (written and oral).
• Decision Making – Required to make decisions on technical and management issues.

Education/Qualifications:

• Minimum of a Bachelor’s degree or University degree required; focused degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering or in a supply-chain related field preferred.

Other:

• This role may require up to 25 % of domestic & international travel.

Make a unique mark in your career
If you want to be seen for the talent you bring to your work, be the driver of your own career, and work with others who share your real passion for caring and success, then we invite you to join the Johnson & Johnson Talent Community by visiting www.careers.jnj.com
If you decide to apply for the position, any personal data which you provide shall be processed by Johnson & Johnson Medical, a Johnson & Johnson company. Your personal data shall be processed for the purposes of recruitment, recruitment policy and selection.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status

• Supporting delivery of robust and fully developed and qualified orthopaedic implant manufacturing processes to Network Edge projects
• Ensure that all project activities are conducted in line with procedures and controls outlined in the QMS and that the quality and performance of the product conforms to specified standards and in compliance with the recognised Regulatory Standards for relevant markets.
• Collaborate with functional stakeholders to ensure that technical, validation and regulatory strategies are implemented in an efficient and compliant manner and at an appropriate risk level
• Partner with Regulatory to execute the strategy necessary for all filings, inspections, and registrations in multiple sites and countries.
• Communicates with internal and external partners to coordinate and execute project plans.
• Provides technical leadership and supports execution of EHS&S policies and procedures
• Supporting technical collaboration across functions
• Leads effective and timely communication processes and stakeholder management processes within the project scope and ensures project and program activities are consistently documented