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Sr. Manufacturing Engineer, E2E Delivery

Job in Raynham, Bristol County, Massachusetts, 02767, USA
Listing for: 6149-DePuy Synthes Products Inc. Legal Entity
Full Time position
Listed on 2026-05-30
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 94000 - 151800 USD Yearly USD 94000.00 151800.00 YEAR
Job Description & How to Apply Below

Job Overview

DePuy Synthes is recruiting for a Senior Manufacturing Engineer – E2E Delivery to support our Med Tech Orthopaedics business. This position will be based in our Raynham, MA location.

About Orthopaedics

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. This role requires a diverse manufacturing background, preferably with direct experience in a medium to large scale manufacturing company, with new product introduction (NPI), manufacturing process improvement, capacity expansions and site optimization.

Responsibilities
  • Responsible for leading projects within Raynham site, representing the site on various forums.
  • Develop and maintain detailed Microsoft project plans for impacted product families.
  • Provides direction in supporting the needs of manufacturing areas in terms of meeting the requirements for quality standards, compliant documentation, capacity and product availability.
  • Provides technical support in the development and implementation of manufacturing processes, preparation of specifications and operator instructions, process studies, production readiness, investigations, root cause analysis, problem solving and report or presentation preparation.
  • Support updating procedures, manufacturing specifications, bills, routes and travelers for product & process changes in the PLM system.
  • Lead and implement activities required to transition equipment from installation through IQ, OQ, and PQ phase.
  • Perform hands‑on equipment assessments, testing, and qualification activities.
  • Creation of controlled documentation (SOPs, work instructions, specifications).
  • Play a key role in the preparation of NPI capital justifications and cost‑benefit analysis.
  • Actively support Supply Network programs, including departmental team initiatives on a global scale.
  • Support new asset purchasing and commissioning, work with OEM equipment manufacturers and distributors to develop user requirements.
  • Work with teams across functions (Operations Value Stream, OpEx, Planning, Engineering, and Quality) to align on validation strategy, author validation documents, coordinate execution and document approvals.
  • Ensure compliance with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments when supporting projects.
  • Perform 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.
  • Maintains positive communication and collaboration with all levels of employees, customers, contractors, and vendors.
  • Champions a collaborative, high‑performing environment passionate about achieving outstanding.
Qualifications
  • Education:

    Minimum of a Bachelor’s degree and/or University degree, preferably in Engineering.
  • A minimum of 4 years of relevant work experience is required.
  • Engineering experience required.
  • Process validation experience.
  • Medical Device and/or regulated manufacturing work environment.
  • Dedication to develop and champion innovation, creativity and collaboration.
  • Persuasive communication and social skills.
  • Knowledge of Microsoft Office.
  • Hands‑on experience with machining processes, casting, metal finishing processes, laser processing or production automation.
  • Experience with 3D printing or additive manufacturing technologies.
  • Project management experience, new production line setup or facility ramp‑up activities.
  • Six sigma, green belt or black belt training.
  • Knowledge of Geometric Dimensioning and Tolerancing (GD&T).
  • May require up to 10% domestic and/or international travel to other locations and sites.
Preferred Skills
  • Accelerating
  • Coaching
  • Compliance Risk
  • Critical Thinking
  • Facility Management
  • Good Manufacturing Practices (GMP)
  • Lean Manufacturing Principles
  • Lean Supply Chain Management
  • Manufacturing Engineering
  • Performance Measurement
  • Product Design
  • Program Management
  • Project Engineering
  • Project…
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