Process Engineer III

Middlesex, MA, US • Posted 9 hours ago • Updated 9 hours ago
Full Time
On-site
USD 80.00 per hour
Fitment

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Job Details

Skills

  • Mergers and Acquisitions
  • Design Of Experiments
  • IT Management
  • Optimization
  • Technical Support
  • Manufacturing Operations
  • IQ
  • OQ
  • PQ
  • Risk Assessment
  • Technical Writing
  • Process Modeling
  • Collaboration
  • Research and Development
  • Mentorship
  • Process Improvement
  • Regulatory Compliance
  • Pharmaceutics
  • Medical Devices
  • Life Sciences
  • GMP
  • ISO 9000
  • Process Engineering
  • Technology Transfer
  • Statistical Process Control
  • Lean Manufacturing
  • Process Optimization
  • Data Analysis
  • SolidWorks
  • Microsoft Office
  • Documentation
  • Management
  • Manufacturing
  • Supervision
  • Communication
  • Project Management
  • Analytical Skill
  • Continuous Improvement
  • Operational Excellence

Summary

Pay Rate Low: 80 | Pay Rate High: 100
Our client is a leading life sciences company that develops and manufactures tools and materials used in the production of biologic drugs. They are looking for a skilled Process Engineer III to join their growing team in Middlesex County, MA! This is a great opportunity to contribute to an innovative life science organization!

Location: Middlesex County, MA
Pay rate: $80 - $100/hr. DOE
Job type: 6-month contract (possibility of extension or hire)

Position Summary
Experienced Process Engineer III responsible for leading technology transfer, manufacturing process support, and strategic engineering projects within a GMP/ISO 9001 regulated environment. Provides technical leadership for process development, equipment qualification, process validation, and manufacturing optimization while supporting new product introductions and continuous improvement initiatives. Collaborates with cross-functional and global engineering teams to ensure efficient, compliant, and reliable manufacturing operations.

Key Responsibilities
  • Lead technology transfer activities and support manufacturing process stabilization across multiple products and manufacturing sites.
  • Manage engineering projects while providing technical support for day-to-day manufacturing operations in a regulated environment.
  • Develop and execute process and equipment qualification/validation (IQ/OQ/PQ) protocols and support process validation activities.
  • Prepare engineering documentation, including change controls, test protocols, validation reports, risk assessments, and technical documentation.
  • Drive continuous improvement initiatives by applying Lean manufacturing principles, statistical process control (SPC), and data analysis to improve process efficiency, quality, and compliance.
  • Support new product introductions by contributing to process design, scale-up, and manufacturing implementation.
  • Collaborate with cross-functional teams, including Manufacturing, Quality, R&D, Validation, and Global Engineering, to execute strategic projects and resolve technical issues.
  • Mentor junior engineers, provide technical guidance, and promote engineering best practices and standardization.
  • Identify and implement process improvements while ensuring compliance with GMP, ISO 9001, and company quality standards.
Qualifications
  • Bachelor's degree in Engineering or a related technical discipline.
  • 5-7 years of engineering experience in biopharmaceutical, pharmaceutical, biologics, medical device, or other life sciences manufacturing environments.
  • Hands-on experience in GMP and/or ISO 9001 regulated manufacturing with knowledge of process engineering, technology transfer, equipment qualification, and process validation.
  • Strong technical expertise in Tangential Flow Filtration (TFF), Statistical Process Control (SPC), automation, Lean manufacturing, process optimization, and data analysis.
  • Proficiency with SolidWorks/CAD, Microsoft Office, and engineering documentation systems.
  • Demonstrated success managing multiple engineering projects, leading cross-functional teams, and solving complex manufacturing challenges with minimal supervision.
  • Excellent communication, project management, and analytical skills with a commitment to continuous improvement, quality, and operational excellence.

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Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10522794
  • Position Id: eecb42676a0cf423f901eaf43197bdd
  • Posted 9 hours ago
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