FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Senior Engineer, Network Manufacturing – Orthopaedics
Johnson & Johnson. Execute capacity expansion projects for the DePuy Synthes Orthopaedics manufacturing network .
Posted 9/24/2026full-timeRaynham • Massachusetts • United StatesSenior💰 $79,000 - $127,650 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in executing capacity expansion projects within the medical device manufacturing sector, ensuring compliance with regulatory standards and delivering high-quality, cost-effective manufacturing processes. Strong leadership in project management, technical collaboration, and stakeholder communication is essential.
Highest-signal resume keywords
Medical Device ManufacturingSix Sigma ExpertiseProject ManagementRegulatory ComplianceInterpersonal Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Capacity Expansion ProjectsManufacturing Process DevelopmentStatistical AnalysisProblem-Solving EngineeringQuality Management Systems (QMS)Technical LeadershipRisk EvaluationInnovation in Project ExecutionDocumentation StandardsEHS&S Policies
Soft Skills
Strong Interpersonal SkillsTeam CollaborationInfluencing SkillsDecision-MakingAdaptability
Industry Keywords
Orthopaedic Implant ManufacturingValidationRegulatory FilingsStakeholder ManagementBest-in-Class Practices
About the role
Key responsibilities & impact- Execute capacity expansion projects for the DePuy Synthes Orthopaedics manufacturing network
- Execute engineering deliverables supporting large-scale manufacturing capacity projects
- Deliver stable, reliable and cost-effective manufacturing processes meeting capacity, product cost, budget and timeline objectives
- Support delivery of robust, fully developed and qualified orthopaedic implant manufacturing processes
- Conduct project activities in line with QMS procedures and controls
- Ensure product quality and performance conform to specified standards and recognized regulatory standards
- Collaborate with functional stakeholders on technical, validation and regulatory strategies
- Partner with Regulatory on filings, inspections and registrations across multiple sites and countries
- Communicate with internal and external partners to coordinate and execute project plans
- Provide technical leadership and support execution of EHS&S policies and procedures
- Support technical collaboration across functions
- Lead timely communication and stakeholder management processes within project scope
- Ensure project and program activities are consistently documented
- Transfer knowledge to developing manufacturing site staff
- Collaborate with existing functional organizations to ensure standardization and implementation of best-in-class practices
Requirements
What you’ll need- Minimum five (5) years of relevant professional work experience
- Experienced knowledge of medical device manufacturing and validation
- Statistical and problem-solving engineering expertise (Six Sigma, SE or A3)
- Strong interpersonal and communication skills and ability to operate as part of a team
- Track record of innovation and adaptability in project execution
- Strong problem-solving skills
- Competence to evaluate, communicate and act upon significant risks
- Leadership of high standards of quality and compliance
- Strong influencing skills
- Excellent written and oral interpersonal skills
- Ability to make decisions on technical and management issues
- Minimum of a Bachelor’s degree or University degree required
- Focused degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering or a supply-chain related field preferred
- May require up to 25% domestic and international travel
Benefits
Comp & perks- Consolidated retirement plan (pension)
- Savings plan (401(k))
- Vacation – 120 hours per calendar year
- Sick time – 40 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 period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
- Inclusive interview process and disability accommodations
- Equal opportunity employment