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Technical Project Manager – Product Development; NPD

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
Salary/Wage Range or Industry Benchmark: 130000 - 190000 USD Yearly USD 130000.00 190000.00 YEAR

Job Description & How to Apply Below

Position: Technical Project Manager – New Product Development (NPD)
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.
Required Skills &

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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