Bwxt

60 Bwxt Process Development Engineer Jobs Hiring Near You

We are seeking an experienced Plasma Etch Process Development Engineer to join our advanced packaging team. The successful candidate will be responsible for developing, optimizing, and implementing ...

We are seeking an experienced Plasma Etch Process Development Engineer to join our advanced packaging team. The successful candidate will be responsible for developing, optimizing, and implementing ...

Process Development Engineer

Vernonia, OR · On-site

$148K - $209K/yr

We are seeking an experienced Plasma Etch Process Development Engineer to join our advanced packaging team. The successful candidate will be responsible for developing, optimizing, and implementing ...

We are seeking an experienced Plasma Etch Process Development Engineer to join our advanced packaging team. The successful candidate will be responsible for developing, optimizing, and implementing ...

On-Board Services is hiring a Process Development Engineer For immediate consideration please send your resume to Subject Line: Position Title and State you are Located About Us: On-Board Services ...

New

Showing results 21-40

Bwxt Jobs Information

What other companies are hiring for Process Development Engineer jobs?

Infographic showing various Process Development Engineer job openings at Bwxt in the United States as of August 2026, with employment types broken down into 97% Full Time, 1% Part Time, and 2% Nights. Highlights an 97% Physical, 2% Hybrid, and 1% Remote job distribution.

Process Development Engineer

Search jobs on OhioMeansJobs

Dorado, PR • On-site

Full-time, Contractor

Posted 5 days ago


Job description

Full Time Contract
Role: Process Development Engineer
Location: Dorado, PR
Length of Contract: 12+ Months
Position Description
The Process Development Engineer will lead and support the characterization, validation, optimization, and scale-up of new manufacturing processes and equipment. Operating in an FDA-regulated medical device environment (21 CFR Part 820 / ISO 13485), this role ensures seamless transition from process development to high-volume manufacturing through structured IQ/OQ/PQ protocols, robust statistical methods (DOE/PFMEA), and cross-functional technical leadership.
Responsibilities
  • Process & Equipment Validation: Design, execute, and document Installation, Operational, and Performance Qualifications (IQ/OQ/PQ) and Process Performance Qualifications (PPQ); draft Master Validation Plans (MVP) and Validation Summary Reports (VSR).
  • Test Method & Inspection Development: Develop and validate receiving and in-process inspection systems, fixtures, gauge R&R studies, and test methods for new components and automated processes.
  • Process Optimization & Root-Cause Analysis: Apply Design of Experiments (DOE), PFMEA, CAPA, and structured root-cause investigation tools (5-Why, Fishbone) to characterize manufacturing windows, eliminate process variability, and boost yields.
  • Automation & Equipment Integration: Oversee the integration of automated manufacturing equipment incorporating PLCs, servo motors, pneumatic systems, optical vision systems, and specialized joining tech (e.g., laser welding, heat bonding, micro-assembly, injection molding).
  • Documentation & Technical Standards: Author and update technical documentation including Manufacturing Execution System (MES) routes, standard operating procedures (SOPs), preventative maintenance (PM) routines, calibration procedures, and engineering change orders (ECOs).
  • Project Management & Collaboration: Lead multi-disciplinary project workstreams (Quality, R&D, Operations, Regulatory) from process concept through commercial implementation, tracking deliverables against strict timeline milestones.
Qualifications
  • Experience: 5–7+ years of hands-on process development, manufacturing engineering, or quality engineering experience within an FDA-regulated environment (Medical Devices preferred, Biotech/Pharma).
  • Regulatory Compliance: Expert knowledge of Quality System Regulations (QSR) 21 CFR Part 820, ISO 13485, ISO 14971, and Good Manufacturing Practices (GMP).
  • Technical Mastery: Proven track record in automated/semi-automated equipment qualification, tooling/fixture design, component assembly, and advanced manufacturing processes (laser welding, ultrasonic welding, heat staking, or vision systems).
  • Statistical Tools: Proficiency in Minitab or equivalent software for process capability (
Education
  • Required: Bachelor of Science (B.S.) in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Industrial Engineering, or Chemical Engineering.
  • Preferred: Six Sigma Green Belt or Black Belt certification; Certified Quality Engineer (CQE) or Professional Engineer (PE) license.

Equal Opportunity Employer:
RCM is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Pay Transparency:
RCM believes in transparency and fairness in compensation. We are committed to providing our employees with competitive salaries that reflect their skills, experience, and contributions to our organization. As part of our commitment to pay transparency, we want to provide you with as much information as possible about our compensation practices.
About RCM:
RCM is publicly traded on Nasdaq under the symbol RCMT.  RCM is a business and technology solutions provider with world-class talent in key market segments. We help design, build, and enable the Industries of Tomorrow, Today. Operating at the intersection of resources, critical infrastructure, and modernization of industries, RCM is a provider of services in Life Sciences, Data & Solutions (IT), Healthcare, Engineering, Aerospace & Defense, and Process & Industrial.
Disclaimer:
This job posting is intended to describe the general nature and the level of the work to be performed. It is not intended to include every job duty and responsibility specific to the position. RCM reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.