Top 17 Senior process engineer Jobs in San Juan Pr

Senior Manufacturing Engineer
Weil Group, Inc —Dorado, PR
- Temporary
- Background check
- Bachelor's degree
- Mentoring
Quick Apply
Engineering - Senior Process Engineer
Viant Medical —Vega Baja, PR
- Full-time
- 5 years
- Bachelor of Science
- Bachelor's degree
Quick Apply
Senior Process Engineer Advisor
Business Staffing Solution —San Juan, PR
- From $40 an hour
- Weekends as needed
- Hybrid work
- Spanish
- Computer Science
- 5 years
Quick Apply
12d
Sr. Process Engineer, Energy Remanufacturing
Tesla —Vega Alta, PR
- Full-time
- Engineering
- Analysis skills
- Mentoring
Sr Engineer - Process & Product
Baxter —Aibonito, PR
- Spanish
- English
- 3 years
- Paid parental leave
- Employee stock purchase plan
Sr. Engineer, Process & Product
Baxter —Aibonito, PR
- Spanish
- English
- 3 years
- Paid parental leave
- Employee stock purchase plan
Senior Engineer - Process Optimization & Capital Projects
BioPharma Consulting JAD Group —Juncos, PR
- Contract
- Spanish
- Doctoral degree
- Engineering
Quick Apply
Senior Engineer 35627
ProQualityNetwork —Municipio de Juncos, PR
- Overtime
- Spanish
- Doctoral degree
- Computer literacy
4d
Senior Engineer 35449
ProQualityNetwork —Juncos, PR
- Spanish
- Doctoral degree
- Engineering
JT570 - SR ENGINEER
Quality Consulting Group, LLC —Juncos, PR
- Temporary
- Background check
- Management
- Mid-level
Quick Apply
7d
Sr. Engineering Manager, Film
Novolex —United States
- $155,000 - $170,000 a year
- Full-time
- Engineering
- Travel
- Senior level
- Wellness program
- Paid parental leave

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senior process engineer jobs near san juan pr

Senior Manufacturing Engineer

Weil Group, Inc
Dorado, PR

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Job Details

Temporary | Full-time

Qualifications

Statistics
Industrial automation
Teamwork
New product introduction engineering projects
Project engineering
Content creation for technical audiences
Defect resolution root cause analysis
Engineering development testing
Quality control statistical data analysis
Preventive action implementation
Regulatory compliance
Statistical Process Control
Tooling design
Technical writing experience within manufacturing
Production deviation management
Value stream mapping
Corrective and preventive actions (CAPA)
Project management experience in manufacturing
Minitab
Bachelor's degree in engineering
Production validation processes
Bachelor's degree
Technology transfer (scale-up process)
Leading team collaboration initiatives
Biomedical regulatory compliance
Root cause analysis
Test validation method
Mechanical knowledge
ISO 13485
Cross-functional communication

Full Job Description

Role Summary
The Senior Manufacturing Engineer leads enterprise manufacturing operations support, validation strategy, implementation of manufacturing processes, documentation generation, process optimization, and cross-functional technical execution. The role is expected to operate with a high degree of independence, provide technical leadership to project teams, and mentor junior engineers or technical team members as needed.

Key Responsibilities

Lead IQ/OQ/PQ and process performance qualification activities; develop validation protocols, reports, and master validation plans.
Design and develop in-process and receiving inspection systems, control plans, sampling plans, and inspection methods for components and manufacturing processes.
Generate, review, and approve equipment documentation, PM/calibration procedures, manufacturing instructions, and process control documentation.
Manage enterprise manufacturing projects from concept through implementation; lead cross-functional technical collaboration with Manufacturing, Quality, R&D, Regulatory, Supply Chain, and external suppliers as applicable.
Apply DOE, PFMEA, risk analysis, SPC, MSA, and root-cause methodologies to characterize, optimize, and improve manufacturing processes.
Lead Lean Manufacturing and continuous improvement initiatives to improve yield, cycle time, cost, throughput, process capability, and equipment performance.
Provide technical direction for manufacturing technologies such as laser welding, heat bonding, injection molding, vision systems, fixtures, tooling, test methods, automation, and equipment qualification.
Support change control, CAPA, nonconformance investigations, and product/process scale-up activities while maintaining compliance with site quality procedures.

Experience Requirements

Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field.
5-7+ years in manufacturing engineering, process engineering, validation engineering, or quality engineering within an FDA-regulated environment.
Strong working knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices required in regulated manufacturing environments.
Electrical and mechanical engineering background applied to automated or semi-automated manufacturing systems.
Experience with automation/controls, tooling, fixtures, test method development, equipment qualification, and manufacturing process validation.
Proficiency in DOE, FMEA/PFMEA, CAPA, root-cause investigation, statistical analysis, and process capability tools; experience with Minitab, JMP, or equivalent preferred.
Experience with Lean Manufacturing, Six Sigma, Kaizen, value stream mapping, or other continuous improvement methodologies preferred.
Experience supporting product introductions, process scale-up, design transfer, and improvements to existing manufacturing processes.
Strong project management, communication, technical writing, analytical, and cross-functional leadership skills.

Quality Expectations
Demonstrates commitment to patient safety and product quality by complying with all applicable quality procedures.
Ensures proper documentation discipline and supports Quality System compliance while providing technical guidance to others as needed.

*Weil Group is proud to be an Equal Employment Opportunity Employer.*
#IND2

Education:

Bachelor's (Required)

Experience:

Mechanical, Electrical, Industrial,: 6 years (Preferred)
Manufacturing, Biomedical or related technical field: 6 years (Preferred)
manufacturing & process engineering: 6 years (Preferred)
validation or quality engineering: 6 years (Preferred)
FDA-regulated environment: 6 years (Preferred)
21 CFR Part 820, GMP, ISO 13485: 6 years (Preferred)
documentation practices: 6 years (Preferred)
automated or semi-automated manufacturing systems: 6 years (Preferred)
automation/controls, tooling, fixtures: 6 years (Preferred)
test method development: 6 years (Preferred)
equipment qualification, process validation: 6 years (Preferred)
DOE, FMEA/PFMEA, CAPA, root-cause investigation: 6 years (Preferred)
statistical analysis, and process capability tools: 6 years (Preferred)
Minitab, JMP: 6 years (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

senior process engineer jobs in san juan pr

Senior Manufacturing Engineer

Engineering - Senior Process Engineer

Senior Process Engineer Advisor

Sr. Process Engineer, Energy Remanufacturing

Sr Engineer - Process & Product

Sr. Engineer, Process & Product

Senior Engineer - Process Optimization & Capital Projects

Senior Engineer 35627

Senior Engineer 35449

JT570 - SR ENGINEER

Sr. Engineering Manager, Film

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