Johnson & Johnson

Sr. Manager, Engineering Standards Lead

Johnson & Johnson$122K — $245K *
Manufacturing & Automotive
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering (Mechanical, Biomedical, Electrical, or related discipline) required.
  • Typically 8-10 years of experience in engineering, quality, or technical roles within regulated industries.
  • Demonstrated experience in developing and governing engineering standards and frameworks.
  • Strong knowledge of quality systems and regulatory requirements for engineering activities.
  • Proven capability to lead and influence cross-functional teams without direct authority.

Responsibilities

  • Lead the creation and governance of global engineering standards for capital projects.
  • Ensure standards meet regulatory and quality requirements (e.g., FDA, ISO).
  • Collaborate with various departments (Facilities, R&D, Quality, Manufacturing) for consistent engineering practices.
  • Manage change processes and communications related to engineering standards updates.
  • Provide technical guidance and support to engineering teams on standards issues.
  • Drive continuous improvement in engineering processes and documentation.
  • Monitor trends and regulatory changes to update engineering standards accordingly.

Benefits

  • Participation in a consolidated retirement plan (pension) and 401(k) savings plan.
  • 120 hours of vacation plus additional sick time.
  • 13 paid holidays and floating holidays per year.
  • Parental Leave of 480 hours for birth/adoption/foster care of a child.
  • Caregiver Leave and Volunteer Leave available.
  • Military Spouse Time-Off of 80 hours per year.
  • Opportunities for professional development through certifications.
Full Job Description
Job Function:
Project/Program Management Group

Job Sub Function:
Project/Program Management

Job Category:
People Leader

All 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 America

Job Description:

DePuy Synthes is recruiting for a Sr. Manager, Engineering Standards Lead, located in Raynham, MA or in West Chester, PA or Palm Beach Gardens, FL or Warsaw, IN or Raritan, NJ.

Job Overview

The Sr. Manager, Engineering Standards Lead is responsible for leveraging internal and external expertise to define, govern, and continuously improve global engineering standards that support compliant capital project delivery and drive operational excellence across DePuy Synthes. This role serves as a strategic leader and subject matter expert, partnering across Capital Project Delivery, Facilities, R&D, Quality, and Manufacturing functions 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 the capital project delivery organization.


  • Ensure engineering standards align with regulatory requirements, quality system expectations, and industry standards (e.g., FDA, ISO, international regulations).


  • Partner with cross-functional stakeholders (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 complex standards-related issues.


  • 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 compliance of engineering 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:

  • Typically 8-10 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 requirements impacting engineering activities.


  • Proven ability to lead cross-functional initiatives and influence without direct authority.


  • Experience managing or mentoring engineers or 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: English proficiency required.


  • 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, career and life journey, please visit www.careers.jnj.com.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and 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 at an appropriate time and subject to any necessary consultation processes.

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 Management

The anticipated base pay range for this position is :
122,000.00 - 245,000.00 USD Annual

Additional 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)). 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 For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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