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Senior Manufacturing Engineer - 2406192104W

Description

Johnson and Johnson Med Tech is now recruiting for a Senior Manufacturing Engineer to work fully on-site at our facility in 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/.

Job Purpose:

As part of Johnson and Johnson’s - DePuy Synthes manufacturing strategy we are increasing Global Manufacturing capacity within the DPS Orthopaedic franchise. As part of that initiative, we are now recruiting for a Senior Manufacturing Engineer to deliver on project requirements for the Foundry capacity expansion for specific product platforms in the Raynham, MA.

This role will be responsible for executing engineering deliverables in the areas of process development, tool design and procurement, tool validation, machine programming, machinery & equipment acquisition, continuous improvement and other duties associated with engineering support of production, leading to the successful achievement of program goals and objectives. 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.

Key Responsibilities:

• Responsible for planning, developing, and delivering processes associated with development of new foundry tooling, new equipment and processes

• Participates in highly complex engineering projects with an extensive cross-functional team. This includes developing and executing to the plan and schedule and meeting the goals and objectives of the project.

• 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

• Communicates with internal and external partners to coordinate and execute project plans

• Supporting technical collaboration across functions

• Provides direction and technical support regarding tooling and equipment design and development, testing of materials, preparation of specifications and operator instructions, process studies, investigations, root cause analysis, problem solving and report or presentation preparation.

• Performs assignments designed to continue the development of professional work knowledge and abilities requiring application of standard engineering techniques, procedures, and criteria in carrying out a sequence of related engineering tasks, project management, statistical analysis and presentation of data and technical writing.

• Writes and executes engineering studies and process validation protocols and summary reports (Installation Qualification, Operation Qualification, Performance Qualification, Computer Software Validation and Test Method Validation).

• Leads new tooling and equipment acquisition efforts including user requirement specifications, machine selection, installation, validation, employee training, and other related equipment responsibilities as required.

• Develops and implements manufacturing and inspection procedures.

• Exercises independent judgment on significant details of work and makes selections and adaptations of engineering alternatives.

• Performs assignments that have complex objectives and require the investigation of multiple variables.

• Participates in and leads cross-functional teams which may include, but are not limited to Manufacturing Engineering, Production, Quality Assurance, Finance, personnel from other sites and external resources.

• Acts as a liaison to vendors with regard to contracted products, tools & fixtures, equipment and their manufacture.

• 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.

Qualifications

Experience, skills & proficiencies required:

• Experienced in a Medical Device and/or regulated manufacturing work environment

• Minimum four (4) years of relevant professional work experience

• Strong interpersonal and communication skills & demonstrated ability to operate as part of a team

• Process validation experience.

• Must be able to read and interpret blueprints of parts and machinery (GD&T)

• 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

• Act with speed, flexibility, and accountability to achieve goals. Understands how own work impacts the enterprise and use understanding to make effective decisions and take actions and lead priorities effectively to deliver expected results

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:

• Preferred Candidate will have, hands-on experience with foundry casting processes, machining processes, metal finishing processes, laser processing or production automation.

• This role may require up to 10% of domestic & international travel

• Expected pay range for this role is $76,000 - $121,900.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.

• Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

• This position is eligible to participate in the Company’s long-term incentive program.

• Employees are eligible for the following time off benefits:

• Vacation – up to 120 hours per calendar year

• Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year

• Holiday pay, including Floating Holidays – up to 13 days per calendar year

• Work, Personal and Family Time - up to 40 hours per calendar year

Additional information can be found through the link below.

For additional general information on Company benefits, please go to:

• _https://www.careers.jnj.com/employee-benefits_

This job posting is anticipated to close on June 12, 2024. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location NA-US-Massachusetts-Raynham

Organization DePuy Synthes Products, Inc (6149)

Job Function Manufacturing Engineering

Req ID: 2406192104W