Process Engineer III

Title : Process Engineer III

Location: Marlborough, MA (Onsite)

Employment Type: Contract

Duration: 8 Months

Job Responsibilities

• Serve as a Subject Matter Expert (SME) for technology transfer of consumable products and manufacturing process stabilization.

• Provide technical leadership in Tangential Flow Filtration (TFF), equipment design and qualification, technology transfer, project management, and facility design.

• Coordinate with global engineering teams to support strategic project initiatives and manufacturing improvements.

• Drive continuous improvement initiatives, regulatory compliance, operational efficiency, and industry best practices.

• Develop engineering documentation, including test protocols, change controls, action plans, and technical reports.

• Support new product implementation and contribute to manufacturing process design during product development.

• Provide technical guidance and mentoring to junior engineers and support process development standards and training.

• Apply statistical methods to engineering tests and process validation activities.

• Lead process improvement initiatives to enhance manufacturing performance.

• Manage multiple projects independently while coordinating cross-functional engineering and manufacturing resources.

• Provide technical direction, communicate project status, and support site manufacturing operations.

• Support process and equipment qualification, technology transfer between manufacturing sites, and ongoing plant operations.

Required Qualifications

• Bachelor's degree in Engineering is required.

• 5 7 years of experience in life sciences, pharmaceutical, medical device, or biologics manufacturing.

• Experience in GMP or ISO 9001-regulated manufacturing environments.

• Hands-on experience with technology transfer and manufacturing process stabilization.

• Strong knowledge of Tangential Flow Filtration (TFF), process engineering, and equipment design.

• Experience with process and equipment validation/qualification.

• Knowledge of statistical process control, data analysis, and lean manufacturing principles.

• Experience managing cross-functional projects and working with global engineering teams.

• Ability to independently manage projects, troubleshoot issues, and provide technical leadership.

• Proficiency in SolidWorks/CAD, Microsoft Office, and electronic document management.

• Strong communication, collaboration, and problem-solving skills.

Preferred Qualifications

• Experience with microfluidics, mass spectrometry, and chemical vapor deposition.

• Knowledge of automation, single-use products, and sterilization processes.

• Biopharmaceutical or medical device product development experience.

• Experience with process improvement and manufacturing scale-up.

• Ability to mentor junior engineers and lead technical project teams.

Pay Scale

Anticipated hourly pay range: $77/hr to $82/hr on W2.

Benefits

Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements:

Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.

Retirement Benefits: A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.

Paid Time Off (PTO): No PTO other than that required by applicable state and local laws.