Senior Manufacturing Engineer - Network

at  Johnson Johnson

Johnson & Johnson is currently seeking Senior Manufacturing Engineer - Network MedTech to join our TEAM located in Ireland (Cork) / United States (Raynham, MA).
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
About J&J MedTech
At Johnson & Johnson MedTech, we unleash diverse healthcare expertise, purposeful technology, and a passion for people to transform the future of medical intervention and empower everyone to live their best life possible. For more than a century, we have driven breakthrough scientific innovation to address unmet needs and reimagine health. In surgery, orthopedics, vision, and interventional solutions, we continue to help save lives and create a future where healthcare solutions are smarter, less invasive, and more personalized.
Resume
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.

Major Duties & Responsibilities

• Supporting delivery of robust and fully developed and qualified orthopedic 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 recognized 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

• 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.
• 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.
• This role may require up to 25 % of domestic & international travel
  We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
  Don’t miss this exceptional opportunity to join a world-class company and make a lasting impact. Apply now and be part of our ambitious team

• Supporting delivery of robust and fully developed and qualified orthopedic 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 recognized 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