field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Role: Electrical design engineer
Location: Chelmsford, Massachusetts
Required skills:
<ul>
<li>Knowledge of Semiconductor Automation solutions for design of Wafer handling Robotics Automation,</li>
<li>AutoCAD experience</li>
<li>Knowledge of PLC, Automation products is an added advantage</li>
<li>Client will also take Interview.</li>
</ul>
JOB DESCRIPTION
• Knowledge of Semiconductor Automation Solutions
• Relevant experience of designing of Wafer handling Robotics Automation
• Relevant experience with Power and Control schematics
• Relevant experience of resolving manufacturing queries &amp; issues
• Experience of AutoCAD, AutoCAD Electrical
• Excellent in verbal and written communication in English language
• Able to handle Microsoft Office applications
• Able to work independently with minimum supervision

Electrical Design Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
Job Overview
The Production Technician II is responsible for basic production operations within Boston BioProducts. Must have the ability to work independently in a fast-paced lab environment while maintaining high standards for the final product. This position is also responsible for the daily upkeep and cleanliness of the production area, which includes chemicals, materials, and equipment.
 
**Direct Applicants ONLY - No Staffing Agencies or Third-Party Recruiters."
 
Roles &amp; Responsibilities
<ul>
<li> Performs general housekeeping in compliance with the standards required.</li>
<li> Demonstrates a sound knowledge and understanding of GMP requirements.</li>
<li> Demonstrates the care and safety necessary to properly safeguard facilities, equipment, product and co-workers.</li>
<li> Performance and adherence of MFG protocols and batch records pertaining to filtration and assisting peers as needed.</li>
<li> Assembles, cleans and operates production equipment (i.e. filters, pumps, pipettes, BSC, benchtop surfaces, etc.).</li>
<li> Demonstrates GDP by performing real time documentation during production run and maintains accurate records/logs.</li>
<li> Reviews documentation prior to completion of records</li>
<li> Ensures daily/weekly tasks are completed in a timely fashion (i.e. track and stock consumable items, ensure proper storage of raw materials and buffers, delivery of QC samples, execution of proper disposal methods, etc.)</li>
<li> Maintains up to date training records.</li>
<li> Performs finished goods filtration and packing activities independently.</li>
<li> Demonstrates understanding of beliefs, values and behaviors in accordance with company culture.</li>
<li> Shows ability to train new technicians in finished goods filtration and packing activities.</li>
<li> Shows understanding of buffer compositions, (ie. Molecular weights, concentrations and dilutions).</li>
<li> Executes calibration, daily maintenance and operations of production equipment (i.e. pH and conductivity meters, Osmometer, SUMs, fume hood, etc.)</li>
<li> Prepares buffer solutions and properly stores process intermediates. Able to independently manufacture in stock buffers</li>
<li> Performs pH and buffer adjustments accordingly.</li>
<li> Performs calculations for processing.</li>
<li> Weighs all powders, chemicals, and reagents needed and performs all calculations, preparations and reagent additions.</li>
<li> Recognizes and identifies mechanical, chemical, and safety hazards to the proper individuals.</li>
<li> Is capable of working in multiple roles associated with the manufacturing of solutions.</li>
<li> Develop a better understanding of how to be supportive of new processes and initiatives.</li>
<li>Create a company culture which is representative of company values. </li>
</ul>
 
Qualifications and Requirements
<ul>
<li>Requires a High School Diploma or equivalent</li>
<li>Minimum 1-2 years of relevant experience</li>
<li>Fundamental knowledge of solutions and reagents, including properties, functional, application, and precaution</li>
<li>Fundamental knowledge of chemistry concepts such as molarity, concentration, and mass.</li>
<li>Fundamental knowledge with dimensional analysis for basic dilutions and conversions.</li>
<li>Fundamental knowledge of ISO standards and other applicable regulations </li>
<li>Demonstrated ability to meet deadlines, multitask, and change priorities while maintaining productivity. </li>
<li>Ability to work well independently and in a team environment.</li>
<li>Must be able to stand for extended periods and lift at least 25 pounds.</li>
</ul>

Production Technician II

<h3>Job Description</h3>
Job DescriptionDescription:&nbsp;Business Process AnalystWaltham, MA12 Months (possible extension)&nbsp;Role Overview The Business Process Analyst within Workplace Services plays a critical role in designing, standardizing, and implementing business processes across all pillars, including Campus Experience, Event &amp; Conference Management, Office Services &amp; Planning and Warehousing &amp; Logistics. This position partners with stakeholders within Workplace Services to deliver consistent, efficient, and compliant operational practices supporting business goals and world-class workplace experience. Key Responsibilities: Develop, document, and optimize business processes and procedures across all Workplace Services pillars, ensuring alignment with organizational strategy, regulatory requirements, and best practices. Update, maintain and report out on key project plans Map and analyze workflows including roles &amp; responsibilities to identify efficiency opportunities, gaps, and process risks, recommending practical solutions for improvement and standardization. Coordinate cross-functional input to ensure end-to-end process integration, collaborating with other Site Operations teams, third party suppliers and end users. Lead process implementation activities—including training materials, communications and change management in partnership with key stakeholders and process owners Monitor process performance and compliance, establishing and tracking key metrics, running regular audits, and recommending updates for continuous improvement. Maintain detailed process documentation, SOPs, and process maps using approved platforms and tools, ensuring all materials are inspection- and audit-ready. Stay current with industry best practices, trends, and regulatory changes, incorporating innovations and improvements as appropriate. Experience and Requirements: 1-5 years of workplace services experience or equivalent specialties experience required. Additional experience is acceptable. Bachelor’s degree in a related field Business administration, facility management, hospitality management, or similar. Proven experience in business process analysis, design, development, and implementation within facilities management, workplace services, corporate real estate, or a related environment; direct experience in the pharmaceutical industry or similarly regulated sector preferred. Strong knowledge of end-to-end process mapping methodologies (e.g., BPMN, Lean, Six Sigma) and demonstrated proficiency in digital modeling tools such as Visio, Bic or equivalent. Exceptional analytical, organizational, and communication skills, including the proven ability to effectively facilitate workshops and drive successful cross-functional collaboration. Demonstrated ability to work independently and successfully manage multiple concurrent projects in a fast-paced, complex matrixed environment. Proficiency with digital process modeling and documentation tools as well as the full MS Office Suite. Minimum of 3 days a week onsite presence. Preferred Qualifications Experience supporting life sciences or high-compliance environments. Familiarity with sustainability initiatives in workplace operations. Desire to implement AI enabled tools as part of daily activities

Process Analyst

<h3>Job Description</h3>
Job DescriptionTeamware Solutions, a business division of Quantum Leap Consulting Private Limited, offers cutting edge industry solutions for deriving business value for our clients? IT initiatives. Offering deep domain expertise in Banking, Financial Services and Insurance, Oil and Gas, Infrastructure, Manufacturing, Retail, Telecom and Healthcare industries, Teamware leads its service in offering skills augmentation and professional consulting services. With over 1700 professionals deputed across India, USA, Middle East and APAC, our major clients include Captive IT units in North America, India, Product Companies and IT Services firms. Our Vision Our Vision is to be among the top 10 largest global Professional Services firm in the Information Technology Space; we aim to achieve this by 2023, when we complete 20 years. 
Job Role:&nbsp;LIMS Labvantage
Location:&nbsp;Boston, MA&nbsp;(Day 1 Onsite)
Duration:&nbsp;6+ Months
ROLE DESCRIPTION:
·Experience Required:&nbsp;4 – 6 Years
·3-5 years of experience providing IT support for LIMS systems in a pharmaceutical, biotech, or laboratory setting.
·Experience with LabVantage LIMS is a must.
·Strong understanding of laboratory processes, sample management, and analytical workflows.
·Experience with LIMS system configuration, master data updates, and user management.
·Familiarity with ITIL processes (incident, change, and problem management)
·Ability to troubleshoot application issues, system errors, and support ticket resolution.
·Familiarity with GxP, FDA, and other regulatory guidelines related to laboratory systems.
·Knowledge of system integration concepts (LIMS to instruments, ELNs, ERP systems).
·Strong skills in documenting system processes, configurations, and incident resolution procedures.
·Excellent communication and collaboration skills, working with both technical and non-technical teams.
 &nbsp;
Teamware Solutions, a business division of Quantum Leap Consulting Private Limited, offers cutting edge industry solutions for deriving business value for our clients'? IT initiatives. Offering deep domain expertise in Banking, Financial Services and Insurance, Oil and Gas, Infrastructure, Manufacturing, Retail, Telecom and Healthcare industries, Teamware leads its service in offering skills augmentation and professional consulting services. With over 1700 professionals deputed across India, USA, Middle East and APAC, our major clients include Captive IT units in North America, India, Product Companies and IT Services firms. Our Vision Our Vision is to be among the top 10 largest global Professional Services firm in the Information Technology Space; we aim to achieve this by 2023, when we complete 20 years.

LIMS

<h3>Job Description</h3>
Job Description
Job Title: Principal / Senior Electrical Engineer (Medical Devices) Location: Burlington, MA – Hybrid (3 days onsite, no remote) - (Only USC and GC) Domain: Medical Devices – Complex Electro-Mechanical Systems Visa: US Citizens / Green Card holders only &nbsp;
Compensation:
Job Overview
We are seeking a highly skilled Principal or Senior Electrical Engineer with 8–10+ years of experience in medical device design and development. This role is hands-on and will focus on analog/digital circuit design, PCB layout, and embedded programming, working across all phases of product development—from concept through production.
The ideal candidate has a strong background in medical device standards (IEC 60601, ISO 13485, FDA) and thrives in a cross-functional environment delivering innovative, safe, and compliant medical technologies.
Key Responsibilities
<ul>
<li>
Design and develop analog and digital circuits, including low-noise analog, sensor interfaces, and power management systems.
</li>
<li>
Perform PCB layout and ensure compliance with EMC/EMI requirements.
</li>
<li>
Write, debug, and maintain embedded C code for microcontrollers.
</li>
<li>
Collaborate with cross-functional teams (mechanical, systems, software) for system integration.
</li>
<li>
Ensure designs meet medical device regulations and quality standards (IEC 60601, ISO 13485, FDA).
</li>
<li>
Support verification, validation, and transfer to manufacturing activities.
</li>
<li>
Provide documentation, troubleshooting, and technical leadership in design reviews.
</li>
</ul>
Qualifications
<ul>
<li>
B.S. in Electrical Engineering (M.S. preferred).
</li>
<li>
8–10+ years of experience in medical device electrical design.
</li>
<li>
Proven expertise in:
<ul>
<li>
Analog/digital circuit design
</li>
<li>
PCB design tools and layout
</li>
<li>
Embedded C programming
</li>
</ul>
</li>
<li>
Strong knowledge of low-noise analog, sensor interfaces, power management, and EMC/EMI compliance.
</li>
<li>
Hands-on troubleshooting and root-cause analysis skills.
</li>
<li>
Familiarity with medical device regulatory frameworks (IEC 60601, ISO 13485, FDA).
</li>
<li>
Excellent communication, documentation, and cross-team collaboration abilities.
</li>
</ul>

Principal or Senior Electrical Engineer

<h3>Job Description</h3>
Job Description
JOB TITLE: Machinist - Day Shift LOCATION: Chelmsford, MA PAY RATE: $28/hour 
We are a national staffing firm partnering with top-tier aerospace companies, and we are seeking first-class employees to join our clients' teams!
Job Details: 
<ul>
<li>
Contract Length: 12 months (with potential extension)
</li>
<li>
Benefits: Medical, dental, and vision (Cigna)
</li>
<li>
Perks: Bonus potential + Priority as a Tier 1 supplier
</li>
<li>
Opportunities: Thousands of openings nationwide
</li>
</ul>
Qualifying Questions:
<ul>
<li>
Are you a U.S. person as defined under ITAR regulations?
</li>
<li>
Do you meet the educational and experience requirements for this role?
</li>
<li>
Can you commute to the job location or relocate if necessary?
</li>
</ul>
Summary: 
<ul>
<li>
This hands-on contract role offers growth potential in an innovative environment focused on high-quality machining processes and precision products.
</li>
<li>
Ability to obtain Secret Clearance 
</li>
<li>
Operate precision machine tools to produce original parts and components
</li>
<li>
Assemble electronic components and sub-assemblies per work instructions and drawings
</li>
<li>
Read and interpret engineering drawings and work instructions
</li>
<li>
Set up cutting tools, adjust machine settings, and monitor machining processes
</li>
<li>
Perform routine machine maintenance and accurate data entry
</li>
<li>
Collaborate with team members to drive continuous improvement
</li>
<li>
Interim clearance process begins at offer stage
</li>
</ul>
Requirements:
<ul>
<li>
High school diploma or GED required
</li>
<li>
Basic computer and math skills
</li>
<li>
Mechanical aptitude and familiarity with machine operations
</li>
<li>
Attention to detail and ability to work in a fast-paced environment
</li>
<li>
Knowledge of ESD procedures is a plus
</li>
<li>
Strong work ethic, reliability, and eagerness to learn
</li>
<li>
Safety shoes required
</li>
<li>
Must be a U.S. Person (as defined by ITAR).
</li>
</ul>
About Us:
The Structures Company is a leading aerospace staffing agency, providing top-tier talent to major OEMs and Tier 1 suppliers. We specialize in contract, contract-to-hire, and direct hire placements in engineering, production, IT, maintenance, and support roles.
Eligibility Requirements:
U.S. Citizenship required under ITAR regulations: A U.S. person is defined as a lawful permanent resident or a protected individual under 8 U.S.C. 1324b(a)(3).
Keywords: Aerospace, Aviation, Engineering, Maintenance, Aircraft Design
Take your aerospace career to new heights-apply today!
#vij
The Structures Company is a national staffing firm specializing in contract, contract to hire, and direct hire placement opportunities. Our clients rely on us to support their engineering, IT, Production, Maintenance &amp; Repair, and support staff. Our niche recruiting team is one of our biggest strengths and is why we are a top provider of talented professionals to the majority of our clients. They will help you identify the opportunity that best fits your interests while also providing industry-leading customer service. We support the majority of aerospace OEM's and tier 1 suppliers across the United States. The Structures Company LLC is an Affirmative Action/ Equal Opportunity Employer (or AA/ EOE)

Machinist - Day Shift

<h3>Job Description</h3>
Job DescriptionSalary: $24-$27/hour 
Westaff is looking for a Night Quality Assurance Technician in the Claremont NH area for Immediate Start!
 
Pay Rate: $24-$27/hour DOE
 
Location: Claremont NH
 
Shift: M-F 3:30pm -12:00am
 
DUTIES AND RESPONSIBILITIES: 
<ul>
<li>Conduct production room inspections to insure all policies and procedures are being followed</li>
<li>Conduct GMP inspections</li>
<li>Conduct production specific task verifications (can change at discretion of QA Director)</li>
<li>Immediately communicate with QA Director and/or QA Supervisor anything which can result in unsafe or poor-quality product, and will need to be placed on hold</li>
<li>Communicate via teams, email, and radio as needed</li>
<li>Conduct QA and GMP checklists in production room</li>
<li>Monitor Safefoods360 for accuracy and completeness as directed</li>
<li>Communicate with production employees as observations are detected</li>
<li>Properly document all findings and follow up actions to findings </li>
<li>Assisting production as needed </li>
<li>Conduct ATP and Allergen Specific Swabs as needed</li>
<li>Conduct MAP test, product sizes, Aw, and Yields </li>
<li>Conduct Pre-op activities or End of Day activities</li>
<li>Assist in Releasing products as needed </li>
<li>Conduct Internal Audits as needed (Glass and brittle plastic, pest control and food defense)</li>
</ul>
 
Must have prior Quality and Production experience!
 
Benefits for Westaff:
Free Online Skill Building Courses
Medical, Dental, and Vision
 
Apply Now for Immediate Consideration!

Night Quality Assurance Technician-Claremont NH

<h3>Job Description</h3>
Job DescriptionJob Summary (List Format): - Support the Quality Information Systems Management group by collaborating with operational, business, and QA teams. - Facilitate regulatory assessments, change control reviews, requirements gathering, system design, and system testing. - Provide quality oversight and assume quality ownership for all computerized system projects. - Ensure quality compliance and manage quality risks during project implementation and enhancements. - Participate in cross-functional discussions, offering quality guidance and decisions for system projects (including new implementations, enhancements, releases, and reviews). - Review and approve quality events (such as deviations and CAPAs), project deliverables, test scripts, and reports. - Drive system assessments and the resolution of issues related to system quality and compliance. - Communicate quality risks and mitigation plans to project teams while ensuring ongoing quality assurance throughout all stages of systems development and implementation. - Leverage expertise in enterprise computerized systems (e.g., ServiceNow, QMS, ERP, Veeva EDC, Compass, RIM, data analytics, lab and manufacturing systems). - Utilize strong technical writing, communication, and project management skills to deliver innovative and compliant system solutions.

Senior Validation Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
About New England Caseworks
New England Caseworks specializes in commercial casework and millwork solutions, built by experienced craftsmen to meet the needs of the Education, Healthcare, Commercial, Industrial, and Laboratory markets. 
 
Opportunity
New EnglandCaseworks is seeking a Millwork Finisher. A Millwork Finisher needs to be highly detailed, able to handle multiple projects at a time, highly organized, able to solve problems and work with a team to produce results and meet deadlines.
Role 
Responsible for all aspects of the finishing process from setup, color matching, quality control, inventory stock, cleanup and maintenance. 
 Duties &amp; Responsibilities
<ul>
<li>Preparing millwork for spraying (sanding, wiping, inspecting)</li>
<li>Color matching per sample or specification</li>
<li>Oversee and produce all finished material</li>
<li>Manage, use and maintain Superficial reciprocating finish line</li>
<li>Work with Production Manager to identify deadlines for material needed for upcoming projects</li>
<li>Prepare stock requisitions for purchasing</li>
</ul>
Requirements 
<ul>
<li>2-5 years Finish Department experience</li>
<li>1-3 years cabinet making experience</li>
<li>Familiarity with materials and hardware for commercial casework and millwork</li>
<li>Dependable</li>
<li>Driven, strong personal work ethic</li>
<li>Able to effectively manage information, schedules and people</li>
<li>Well organized and able to appropriately prioritize tasks</li>
<li>Enthusiastic and positive approach to position and tasks</li>
<li>Ability to lift 50+lbs</li>
</ul>
 
Disclaimer
The worker will be subject to noise from automated machinery. This position requires someone to cut, lift, and transport wood and other materials from floor to waist height on a regular basis. This is a standing position and frequent movement around shop floor is required. No travel is required for this position. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
 
We are an equal opportunity employer; applicants, employees and former employees are protected from employment discrimination based on race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability and genetic information (including family medical history), or any other characteristic protected by law.
 
Benefits
We offer growth opportunities for motivated professionals and a great compensation package including, dental insurance, medical insurance, vision insurance, pre-tax accounts for health and dependent care, 401K employer match, paid company holidays, and paid vacations.

New England Caseworks - Millwork Finisher

<h3>Job Description</h3>
Job Description
Role Name:&nbsp;&nbsp;Biologics Manufacturing Technician
Location:&nbsp;55 Messina Dr, Braintree, MA, US
Duration:&nbsp;04 Months
Job Description:
Performs process operations including but not limited to: Drug Product:&nbsp;Formulation, Filling, Crimping, Visual Inspection, Labeling/Packaging BSM: Weighing, pH, Centrifugal Filtration, Lyophilization, Milling, Calcination, Cleaning Principal Duties and Responsibilities • Read, understand and follow detailed written procedures • Maintain records in and out of clean room environment to comply with regulatory requirements • Ability to cross train in all manufacturing environments • Exposure to areas that require understanding of SDS and use of PPE to ensure safety • Perform 5S activities in the area. • Maintain training in LMS This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA. Expected Areas of Competence (i.e. KSAs) • Communication skills with ability to interact effectively with lead and/or supervisor. • Ability to follow instructions from Lead and/or Supervisor • Must be able to meet all technical and physical requirements of primary job function • Understands Zimmer’s Quality System including strong familiarity with Measurement Instruction Sheet layout and purpose, and Zimmer’s Compliance Policies • Advocate of Zimmer’s core values and behaviors Education/ Experience Requirements High School Diploma, At least one year of relevant experience preferred.

8,014 Manufacturing Jobs