Top 221 Process engineer Jobs in Needham, Ma

Process Engineer
Grove —Boston, MA
- $75 - $80 an hour
- Full-time
- 5 years
- Bachelor of Science
- Engineering
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Nanofabrication Process Engineer
MIT Lincoln Laboratory —Lexington, MA
- $116,400 - $182,200 a year
- Full-time
- Bachelor of Science
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Process Engineer, Drug Product
Amylyx Pharmaceuticals —Cambridge, MA
- $131,000 - $147,000 a year
- Engineering
- 3 years
- Master's degree
Combat Feeding Process Engineer
Pueo Business Solutions LLC —Natick, MA
- Full-time
- Mid-level
- Assembly
- 2 years
Process Development Engineer II, Upstream
Takeda Pharmaceutical —Lexington, MA
- $71,800 - $112,860 a year
- Full-time
- Mid-level
- Continuous improvement
- Associate's degree
- Paid holidays
- Disability insurance
Process Engineer
Coherent Corp. —Woburn, MA
- $84,295 - $138,000 a year
- Overtime
- Bachelor of Science
- Mid-level
- Office
Electrical Engineer
AMETEK —Chelmsford, MA
- $90,000 - $125,000 a year
- Full-time
- 5 years
- Assembly
- US work authorization
- Health insurance
- Dental insurance
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4d
Process Engineer - FACs/Artiva
The CCS Companies —Norwood, MA
- $50,000 - $70,000 a year
- Full-time
- Background check
- Software troubleshooting
- Basic math
- Paid training
- Health savings account
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4d
Process Technology Engineer
Sartorius —Marlborough, MA
- $95,000 - $120,000 a year
- Full-time
- 7 years
- Engineering
- Master's degree
- Health savings account
- AD&D insurance
Process and Automation Engineer
Mueller Coatings —East Bridgewater, MA
- Full-time
- 5 years
- System design
- Analysis skills
- Health insurance
- Dental insurance
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Manufacturing Engineer-CNC Machining & Process Development
AccuRounds —Avon, MA
- $30 - $40 an hour
- Full-time
- Ability to walk for extended periods
- Mid-level
- Analysis skills
- Health insurance
- Dental insurance
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Senior Manufacturing Engineer
Ardent Staffing Solutions —Chelmsford, MA
- $90,000 - $110,000 a year
- Email
- 6 years
- Engineering
- Senior level
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Manager-Engineering (Wafer Fab)
Microchip Technology —Lowell, MA
- $91,000 - $232,000 a year
- Full-time
- 5 years
- Engineering
- Assembly
- Employee stock purchase plan
- Health insurance
Process Engineer
NN, Inc. —North Attleboro, MA
- From $60,000 a year
- Full-time
- Bachelor of Science
- Engineering
- ERP systems
- Health insurance
- Dental insurance
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Manufacturing Process Engineer
Genuine Search Group —Boston, MA
- $35 - $47 an hour
- Full-time
- 5 years
- Analysis skills
- Experience equivalent to degree accepted
- Health insurance
- Dental insurance
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2d
Pilot Line Supervisor
Lubrizol —Wilmington, MA
- $110,000 - $125,000 a year
- Full-time
- Bachelor of Science
- Master's degree
- Supervising experience
- Health savings account
- Paid holidays
Sr Test & Validation Engineer - 3rd Shift
Raytheon —Andover, MA
- $86,800 - $165,200 a year
- Full-time
- 5 years
- Continuous improvement
- Senior level
- Paid holidays
- Disability insurance
Sr Electrical Engineer - Failure Analysis
Raytheon —Andover, MA
- $86,800 - $165,200 a year
- Full-time
- 3 years
- Analysis skills
- Experience equivalent to degree accepted
- Paid holidays
- Disability insurance
4th Shift Backside Process Support Engineer
Raytheon —Andover, MA
- $86,800 - $165,200 a year
- Full-time
- 6 years
- Mid-level
- SQL
- Paid holidays
- Disability insurance
1st Shift Backside Process Support Engineer
Raytheon —Andover, MA
- $86,800 - $165,200 a year
- Full-time
- 6 years
- Mid-level
- SQL
- Paid holidays
- Disability insurance

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process engineer jobs near needham, ma

Process Engineer

Grove -
Boston, MA

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Job Details

Full-time | Contract
$75 - $80 an hour

Qualifications

Incident investigation techniques for hazard identification
Biotechnology
Teamwork
Project engineering
Content creation for technical audiences
Defect resolution root cause analysis
Requirements specification
Requirements design
Technical documentation
Bachelor of Science
Design of manufacturing processes
Technical writing experience within manufacturing
Production deviation management
Reliability analysis
Corrective and preventive actions (CAPA)
Project management experience in manufacturing
System design for system development
Manufacturing facility experience
Production validation processes
Quality risk management
Requirements analysis
Design engineering
Leading team collaboration initiatives
Quality control problem-solving
Regulatory/legal compliance standards in production
Engineering product development
Biomedical regulatory compliance
Commissioning phase involvement
Escalation handling
Cross-functional team management

Full Job Description

Title: Process Engineer Contractor – Automation of Machinery and Processes
Start Date: ASAP
Duration: 12 Months
Logistics: Fully Onsite – candidate may choose homebase between Boston and Providence but will need to have occasional presence at both sites
Hours/week: 40 hours/week
Manager Notes:

            Experience with FMEA, root cause analysis, CAPA, and change control is required
            Must have GMP-regulated cell & genetic therapy industry experience
            Looking for candidate with strong execution mind-set and strong communication   skills, must be confident in engineering mindset
Process Engineer Contractor – Automation of Machinery and Processes (AMP) TeamAre you ready to revolutionize Cell & Gene Therapy? Join us in shaping the future of therapeutics! We are seeking a Process Engineer Contractor in our journey of developing cutting-edge manufacturing solutions for Casgevy—a first-of-its-kind therapy transforming the treatment of Sickle Cell Disease and Beta Thalassemia.  In this role, you will be at the forefront of automating complex processes in one of the most dynamic and rapidly evolving fields in biotechnology. You will work with a passionate team of scientists, engineers, and innovators, all united by a shared mission: to push the boundaries of what’s possible in Cell & Genetic Therapy.  This position will play a critical role in equipment & systems development, process optimization, and technology transfer to ensure robust and reliable systems that advance our mission. The position is onsite 5 days per week at Providence, RI and/or Boston, MA sites with ad-hoc flexibility.Key Responsibilities:
Process & Systems Engineering Expertise: Provide technical support for the design, specification, selection, and lifecycle management of cell & genetic therapy process equipment and manufacturing systems, ensuring alignment with program objectives, business needs, regulatory requirements, and industry standards.
Process Equipment & Manufacturing System Ownership: Serve as a subject matter expert for cell & genetic therapy process equipment and manufacturing systems during requirements definition, design reviews, commissioning, qualification, validation, and ongoing manufacturing support. Guide teams through complex technical decisions and issue resolution.
Process & Equipment Optimization: Support high-impact initiatives to improve equipment reliability, process robustness, operational efficiency, and scalability. Advance implementation of engineering solutions through structured problem-solving, risk assessment, and change management.
Technical Delivery: Support engineering workstreams and complex equipment development efforts from concept through implementation, including URS/FRS development, technology evaluations, facility & systems simulation, requirements mapping, safety risk assessments, FMEA execution, study design, FAT/SAT execution, technology transfer, and validation support. Collaborate with and manage external vendors to deliver systems on time and within budget.
Troubleshooting and Manufacturing Support: Provide advanced hands-on technical support for equipment and manufacturing operations, including troubleshooting critical issues, supporting rapid development cycles, and enabling long-term manufacturing sustainability.
Documentation and Compliance Excellence: Author, review, and approve technical documentation including protocols, reports, SOPs, work instructions, specifications, and engineering assessments, ensuring compliance with regulatory, quality, and internal standards.
Cross-Functional Influence and Collaboration: Partner closely with Manufacturing, Process Development, Quality, Validation, Facilities, MSAT, Project Management, and external vendors/partners to ensure successful delivery of engineering and equipment initiatives across the product lifecycle.
Deviation, CAPA, and Change Control Leadership: Lead and support complex investigations, root cause analyses, deviation assessments, CAPA development, and change control activities. Ensure timely closure and sustainable corrective actions.
Technical Development: Contribute to the development of engineering best practices, standard work, and technical capabilities across the organization.
Execution and Accountability: Deliver assigned objectives on time and within budget while proactively identifying risks, escalating issues, and communicating impacts and mitigation plans to stakeholders and leadership.
Quality and Regulatory Compliance: Ensure all activities are executed in accordance with applicable regulatory requirements, corporate policies, and Quality System expectations.
Additional Responsibilities: Perform other duties as assigned based on business and program needs.

Required Qualifications:

Education: BS or MS in Engineering or a related technical discipline.
Experience: 7+ years of relevant experience with a BS, or 5+ years of relevant experience with an MS, in process engineering, systems engineering, project engineering, equipment engineering, and/or process optimization within the GMP-regulated cell & genetic therapy industry.
Process & Systems Engineering: Demonstrated experience leading complex equipment and manufacturing systems development initiatives from concept through implementation, including requirements definition, design, specification, documentation, commissioning, qualification, validation, and lifecycle support. Cell & genetic therapy experience desired.
Technical Communication: Excellent technical writing, presentation, and communication skills, with the ability to clearly convey complex engineering concepts to technical and non-technical stakeholders.
Regulatory Knowledge: Strong understanding of cGMP/cGxP principles and practices, including familiarity with 21 CFR Part 210 and 211 and applicable engineering and validation expectations in regulated manufacturing environments.
Problem Solving and Risk Management: Proven success applying structured problem-solving and risk-based decision-making to resolve technical challenges. Experience with FMEA, root cause analysis, CAPA, and change control is required. Lean/Six Sigma Green Belt or DMAIC experience preferred.
Independence and Influence: Ability to operate with a high degree of autonomy, exercise sound engineering judgment, and influence decisions across functions and organizational levels.
Collaboration and Leadership: Strong interpersonal and leadership skills with a demonstrated ability to manage multiple priorities, coordinate cross-functional and external contributors, and drive execution across complex programs.

Execution Mindset: Strong sense of urgency, accountability, and proactive escalation, with the ability to balance strategic thinking and hands-on execution.

Pay: $75.00 - $80.00 per hour

Work Location: In person

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Refine Your Search

process engineer jobs in needham, ma

Process Engineer

Nanofabrication Process Engineer

Process Engineer, Drug Product

Combat Feeding Process Engineer

Process Development Engineer II, Upstream

Process Engineer

Electrical Engineer

Process Engineer - FACs/Artiva

Process Technology Engineer

Process and Automation Engineer

Manufacturing Engineer-CNC Machining & Process Development

Senior Manufacturing Engineer

Manager-Engineering (Wafer Fab)

Process Engineer

Manufacturing Process Engineer

Pilot Line Supervisor

Sr Test & Validation Engineer - 3rd Shift

Sr Electrical Engineer - Failure Analysis

4th Shift Backside Process Support Engineer

1st Shift Backside Process Support Engineer

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