More jobs:
Technical Project Manager – Product Development; NPD
Job in
Palo Alto, Santa Clara County, California, 94306, USA
Listing for:
Zenith Services Inc.
Full Time
position
Listed on 2026-11-08
Job specializations:
-
Engineering
Product Engineer, Regulatory Compliance Specialist, Quality Engineering, Manufacturing Engineer
Job Description & How to Apply Below
Technical Project Manager - New Product Development (NPD)
Domain: Pharmaceutical / Manufacturing
Job Description:We are looking for an experienced Technical Project Manager with a strong Mechanical Engineering background to lead New Product Development (NPD) projects in a pharmaceutical manufacturing environment.
The ideal candidate should have experience managing engineering projects, manufacturing processes, regulatory compliance, and product development within FDA-regulated environments.
Key Responsibilities:- Lead end-to-end NPD/NPI projects from concept through design, development, testing, validation, and production launch.
- Manage project timelines, budgets, resources, risks, and deliverables.
- Coordinate mechanical design, manufacturing, quality, regulatory, validation, and supply chain teams.
- Oversee mechanical product development, prototyping, and design reviews.
- Drive Design for Manufacturing (DFM), Design for Assembly (DFA), and manufacturing readiness.
- Ensure compliance with FDA regulations, GMP, and applicable industry standards.
- Coordinate regulatory documentation, design controls, risk assessments, and change control processes.
- Support audits, CAPA, deviations, validation activities, and regulatory submissions, as applicable.
- Manage engineering changes, technical documentation, and stakeholder communication.
Qualifications:
- Bachelor's degree in Mechanical Engineering or related field.
- 8-15 years of engineering experience, including 3-5 years in technical project management.
- Strong experience in Mechanical Engineering and NPD/NPI.
- Knowledge of CAD tools such as Siemens NX, Solid Works, Creo, or CATIA.
- Experience with DFM, GD&T, FMEA, and design validation.
- Knowledge of FDA regulations, GMP, regulatory compliance, and quality management systems.
- Experience with regulatory documentation, change control, CAPA, and validation.
- Pharmaceutical, medical device, or FDA-regulated manufacturing experience preferred.
- Strong project management and cross-functional leadership skills.
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