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R&D Project Manager

Job in Mesquite, Dallas County, Texas, 75181, USA
Listing for: BioMed Laboratories LLC
Full Time position
Listed on 2026-02-16
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Product Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Product Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: R&D Project Manager I

Overview

Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions that connect, protect, and purify our world.

Responsibilities
  • Develop, communicate, and execute project plans that describe the Mativ design strategy to take a market or customer idea concept or process/material improvement from the feasibility phase to commercialization, transforming the idea into a commercially viable, financially attractive product for customers.
  • Set project scope and objectives. Define and monitor tasks, milestones, and risks throughout the project. Manage stage-gate processes using appropriate systems and software.
  • Lead cross-functional teams to execute project deliverables, meeting required timelines while communicating changes in scope and/or timing to all appropriate functions.
  • Lead client engagement relationship and communication for projects.
  • Identify, log, analyze, and manage potential and actual issues and risks, taking corrective action by tackling day-to-day problems head-on.
  • Manage relationships between R&D and production; work with teams to scale up final design from the lab to a product that can be reliably manufactured with a validated production process.
  • When applicable, manage internal process improvement projects, including but not limited to raw material qualification and production process improvements.
  • Support continuous improvement initiatives in all aspects of delivering projects.
  • Act as the technical liaison with manufacturing, assisting with production challenges, manufacturing process design, and process upgrades.
  • Ensure compliance with FDA and EU regulatory standards for drug products, OTC products, and medical devices.
  • Work with third-party testing labs on raw material, safety, and finished goods testing.
  • Provide support to the commercial team in communicating with customers.
Qualifications

Required

  • BS degree in an engineering or science discipline.
  • Project management skills: setting and monitoring scope, actions and timelines, risk identification and mitigation.
  • Experience using Microsoft Office products required.
  • Must be able to read/write professionally in the English language.
  • Strong leadership skills to effectively work with all team members.
  • Travel percentage
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