Sr. Manager, Engineering Standards Lead
- Salary
- $127K–$218.5K
- Hiring from
- United States
- Work type
- Hybrid
- Posted
627,515 remote jobs, straight from company career pages
100% free · New jobs every minute
Show job descriptionHide job description
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 jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Project/Program Management GroupJob Sub Function:
Project/Program ManagementJob Category:
People LeaderAll Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of AmericaJob Description:
DePuy Synthes is recruiting for a Sr. Manager, Engineering Standards Lead,locatedinRaynham, MA or in West Chester, PA or Palm Beach Gardens, FL or Warsaw, IN or Raritan, NJ.
Job Overview
The Sr. Manager, Engineering Standards Leadis responsible forleveraginginternal and externalexpertisetodefine,govern, and continuouslyimproveglobal engineering standards thatsupport compliantcapitalprojectdelivery anddriveoperational excellence across DePuy Synthes. This role serves as a strategic leader and subject matter expert, partnering acrossCapital Project Delivery, Facilities,R&D, Quality,andManufacturingfunctions to drive consistent, scalable, and compliant engineering practices that support innovation and patient safety.
Key Responsibilities
Lead the development, implementation, and governance of global engineering standards, specifications, and best practices across thecapital project deliveryorganization.
Ensure engineering standards align with regulatory requirements, quality system expectations, and industry standards (e.g., FDA, ISO, international regulations).
Partner withcross‑functionalstakeholders (Facilities,R&D, Quality, Manufacturing, Supply Chain) to drive consistent application of engineering standards.
Oversee change management, impact assessments, and communication strategies related to engineering standard updates and deployments.
Provide technical leadership and guidance to engineering teams, serving as an escalation point for complexstandards‑relatedissues.
Lead continuous improvement initiatives to simplify, harmonize, and modernize engineering processes and documentation.
Monitor external trends, emerging technologies, and regulatory changes to proactively evolve engineering standards.
Develop metrics and reporting to assess adoption, effectiveness, and complianceofengineering standards.
Qualifications
Education
Required:Bachelor’s degree in Engineering(Mechanical, Biomedical, Electrical, or related discipline).
Preferred:Master’s degree in Engineering, Quality, or related technical field.
Experience and Skills
Required:
Typically8-10 years of progressive experience in engineering, quality, or technical leadership roles within a regulated industry (medical devices strongly preferred).
Demonstrated experience developing, governing, or deploying engineering standards, procedures, or technical frameworks.
Strong working knowledge of quality systems and regulatory requirementsimpactingengineering activities.
Proven ability to leadcross‑functionalinitiatives and influence without direct authority.
Experience managing or mentoringengineersor technical professionals.
Preferred:
Experience in global or matrixed organizations.
Familiarity with ISO standards, design controls, risk management, and product lifecycle management.
Change management or process excellence experience (Lean, Six Sigma, or similar).
Experience supporting audits or regulatory inspections.
Excellent written and verbal communication skills, including technical documentation.
Other:
Language:Englishproficiencyrequired.
Travel:Limited; up to 15%, domestic and occasional international.
Certifications:Professional engineering, quality, or process improvement certifications preferred (e.g., PE, ASQ, Lean Six Sigma).
For more information on how we support the whole health of our employees throughout their wellness,careerand life journey, please visitwww.careers.jnj.com.
Johnson & Johnson announced plans to separate ourOrthopaedicsbusiness toestablisha standaloneorthopaedicscompany, operating as DePuy Synthes. The process of the planned separation isanticipatedto be completed within 18 to24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may berequired, regulatory approvals and other customary conditions and approvals. Should you accept this position, it isanticipatedthat, following conclusion of the transaction, you would be an employee of DePuySynthesand your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes atan appropriate timeand subject to any necessary consultation processes.
Johnson & Johnsonisan 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, disability, protected veteran status or other characteristics protected by federal,stateor local law. We actively seek qualified candidates who areprotectedveterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnsoniscommitted to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to requestan accommodation, external applicants please contact us viahttps://www.jnj.com/contact-us/careers, internal employees contactAskGSto be directed to your accommodation resource.
#DePuySynthesCareers
Required Skills:
Preferred Skills:
Agile Decision Making, Analytics Insights, Developing Others, Inclusive Leadership, Leadership, Organizational Project Management, Performance Measurement, Program Management, Project Management Methodology (PMM), Project Management Office (PMO), Project Management Tools, Project Reporting, Regulatory Compliance, Risk Management, Statement of Work (SOW), Team ManagementThe anticipated base pay range for this position is :
$127,000.00 - $218,500.00Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are 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.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
Additional information can be found through the link below.
Co-Ops and Intern Positions: Please use the following language:
Co-Ops/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan.
Co-Ops and Interns are eligible for the following sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year.
Co-Ops and Interns are eligible to participate in the Company’s consolidated retirement plan (pension).
Positions Represented by CBA: Please use the following language:
This position is eligible for benefits to include medical, dental, vision and time off, as well as any others as provided for in the applicable Collective Bargaining Agreement.
For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits
About Us
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/.
Our Credo calls on us to respect the dignity of every individual and create an environment for all people to thrive. Throughout the recruitment process - from application through hiring - we are committed to providing reasonable accommodations/adjustments for qualified candidates with disabilities. If you need support at any stage of the recruitment process, please complete our candidate accommodation request form so we can assist you.
