field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionSalary: $25 
Westaff is hiring Experience Assemblers in Wilmington, MA
 
Benefits to Westaff Associates:
<ul>
<li>Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>Retirement Savings Plan</li>
<li>FREE Online Classes</li>
</ul>
 
This is a temporary assignment lasting 1 week (possibly 2)
 
Schedule:
8am - 5pm
Start date Tuesday 10/7/2025
 
Job Details:
<ul>
<li>The experienced assembler will be putting together carts following blue print schematics</li>
</ul>
 
Experience:
<ul>
<li>MUST be experienced in assembling products following blue prints</li>
<li>Must be committed to length of assignment</li>
<li>Attention to detail</li>
<li>Experience with hand tools, screwdriver, mallet, electric drill</li>
</ul>
 
Apply Now for immediate consideration

Assemblers - Wilmington, MA

<h3>Job Description</h3>
Job Description
Job Title-&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Electrical Engineer
Project Location&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Burlington MA (Hybrid)
Project Duration-&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Full Time Direct Hire
Onsite hybrid – Monday &amp; Friday work from home, Tuesday, Wednesday, Thursday in office.
The client is developing LVAD technology (heart pump) that helps people that are on the heart transplant list.&nbsp; Really cool technology.&nbsp; The preference is someone coming from medical device BUT they are open to other regulated industries like aerospace, DoD, automotive, etc.&nbsp; Preference for experience with battery technology and/or wireless communication.&nbsp; They will be doing new design/development for peripherals for this device – battery, controller, battery charger, etc.
Senior/Staff Electrical Engineer
Requirements
<ul>
<li>Bachelor’s degree in Electrical or Computer Engineering</li>
<li>7+ years of experience in electrical hardware design, ideally for medical or similarly regulated products.</li>
<li>Strong background in battery management (BMS, PMICs) and support for multiple battery chemistries.</li>
<li>Strong understanding of embedded firmware, sensor integration, and analog/digital circuit design.</li>
<li>Proven track record taking a product through its full lifecycle: prototyping, production, field support, and failure analysis.</li>
<li>Proficient with PCB tools (Cadence, Altium), and circuit simulation (LTSpice)</li>
<li>Experience in low-power design and wireless connectivity (Cellular, BLE, NFC).</li>
<li>Experience with using best-practice root cause analysis techniques backed by objective and data-driven engineering analysis</li>
<li>Familiarity with regulatory and compliance standards such as IEC 60601.</li>
<li>Ability to write and develop automated test scripts using Windows or Linux OS, with experience writing or using Python/C for hardware testing and automation</li>
<li>Demonstrated ability to work in a collaborative and fast-paced R&amp;D environment with global team members</li>
<li>Excellent written and verbal communication skills, with experience producing technical documentation.</li>
</ul>

Electrical Engineer

<h3>Job Description</h3>
Job Description
Position: QA Inspector/ Quality Inspector Schedule: Start time can vary 6:30 am 7:30 am
Position summary:
<ul>
<li>With direct guidance in a team environment, responsible for performing basic inspection requirements.</li>
</ul>
Overview:
<ul>
<li>One year inspection or related experience or demonstrated ability to perform</li>
<li>Not required but prefer Level 1 Nondestructive Test Inspector</li>
<li>The certification must be in accordance with MIL-STD-410 and PES1-29</li>
<li>Ability to read and understand blueprints, manufacturer's specifications and electrical instruments/gages.</li>
<li>Possess working knowledge of machine shop mathematics.</li>
<li>Knowledge of applicable military standards may be required.</li>
<li>May be required to lift to 50 lbs.</li>
<li>Must demonstrate effective verbal, written and interpersonal communication</li>
<li>Ability to work effectively with others and be participative team player.</li>
</ul>
Responsibilities:
<ul>
<li>Responsibilities may include some or all the following:</li>
<li>Maintain accurate and up to date records and files.</li>
<li>Inspection Perform basic parts inspection using gages and instruments such as micrometers, calipers, height gages and thread, plug and ring gages, hardness testers, spring tester or related inspection equipment to determine acceptability or rejection of parts.</li>
<li>Operate surface analyzer to determine parts finish.</li>
<li>Observe and perform audits of assembly and test, machining, and other functions for compliance with procedures. Document acceptances and rejections.</li>
<li>Route inspected parts by instructions. Calibration Issue or remove parts from various areas.</li>
<li>Perform basic calibration on various types of measuring and test equipment.</li>
<li>Determine measuring and test equipment acceptability to tolerances.</li>
<li>Use standards to make ups for calibration of measuring and test equipment.</li>
<li>Issue and recall measuring and test equipment.</li>
</ul>

Quality Inspector 1

<h3>Job Description</h3>
Job DescriptionSalary: 
About Aura:
Aura Biosciences is a clinical-stage biotechnology company focused on developing precision therapies for solid tumors that aim to preserve organ function. Our lead candidate, bel-sar (AU-011), is currently in late-stage development for primary choroidal melanoma and in early-stage development in other ocular oncology indications and bladder cancer. Aura Biosciences is headquartered in Boston, MA. Our mission is to grow as an innovative global oncology company that positively transforms the lives of patients. 
For more information, visit aurabiosciences.com. Follow us on X (formerly Twitter) @AuraBiosciences and visit us on LinkedIn.
 
Position Summary:
Aura Biosciences is seeking a highly motivated and detail-oriented QC Scientist to support method validation and routine QC operations for our innovative oncology therapeutics. This role is critical to ensuring the integrity and compliance of analytical methods used in the testing of drug substance and drug product across clinical stages.
 
Key Responsibilities:
<ul>
<li>Lead and execute method qualification and validation activities in alignment with ICH guidelines and GMP standards.</li>
<li>Support and oversight of routine QC testing of plasmid, drug substance (DS) and drug product (DP), including release and stability studies.</li>
<li>Collaborate with CMOs and CROs to ensure timely and compliant execution of analytical activities.</li>
<li>Author and review technical documentation including validation plans, protocols, reports, SOPs, and CoAs.</li>
<li>Manage validation timelines and proactively provide solutions to method challenges.</li>
<li>Participate and lead investigations (OOT/OOS), CAPAs, and continuous improvement initiatives.</li>
<li>Review and trend analytical data routinely for specification evaluation.</li>
<li>Ensure compliance with internal quality systems and regulatory expectations.</li>
<li>Contribute to cross-functional CMC discussions and provide technical input on overall analytical strategy.</li>
</ul>
Key Skills
<ul>
<li>Analytical Method Validation Strong understanding of ICH Q2(R2), GMP principles including compendial methods and data integrity.</li>
<li>Instrumentation Expertise Proficiency in HPLC, UV-Vis, Empower, Bioassays, qPCR other analytical platforms and compendial methods.</li>
<li>Collaboration Effective communication with internal teams and prior experience managing external partners (CMOs/CROs) is preferred.</li>
<li>Technical Writing Skilled in drafting and reviewing protocols, reports, and SOPs.</li>
<li>Problem Solving Experience with OOS/OOT investigations and root cause analysis.</li>
<li>Project Management Ability to manage timelines and deliverables across multiple stakeholders.</li>
<li>Regulatory Knowledge Familiarity with FDA and EMA expectations for QC and validation.</li>
<li>Attention to Detail High level of accuracy in data review and documentation.</li>
<li>Statistical analysis using JMP, Minitab or equivalent.</li>
<li>Minimal travel is required to CMOs.</li>
<li>Role is a hybrid role (minimum 3 days onsite).</li>
<li>Minimum BS in Sciences with at least +5 years experience or MS and 2+ years</li>
</ul>
 
Salary &amp; Benefit Information:
Salary Range: $105,000/yr - $135,000/yr
(Placement within the listed range depends on many factors including, but not limited to: geographic location, degree, years of experience, and internal company equity)
Health insurance with FULL premium coverage
401K with company match
Employee Stock Purchase Program (ESPP)
Competitive paid time off (PTO)
Company-paid short &amp; long-term disability insurance and life insurance

QC Scientist Method Validation & QC Operations

<h3>Job Description</h3>
Job Description
Note :
<ul>
<li>Need Local to MA, with same State I’d Only.</li>
</ul>
Position Overview :
<ul>
<li>Need someone with Lab experience.</li>
<li>We are looking for 4 Senior Commissioning, Qualification, and Validation (CQV) Engineers to perform execution of lab equipment qualification (LEQ) and facility/environmental utility (FEU) commissioning activities to support the reactivation and GMP-readiness of a Boston area client’s QC Laboratory.</li>
<li>This role will focus on drafting and executing URS, IQ, OQ, PQ, and commissioning protocols, ensuring equipment, utilities, and lab spaces are compliant with FDA/EMA requirements and fully audit-ready within a compressed five-week timeline.</li>
<li>Ideally, all candidates will be capable of working cross functionally on both equipment and the facility systems, however in terms of focus we will need two QAV engineers to handle the equipment validation and 2 Commissioning Engineers to handle the FEU validation.</li>
</ul>
Tasks, Responsibilities, and Deliverables:
<ul>
<li>Develop and execute URS for lab equipment and utilities (balances, centrifuges, incubators, freezers, biosafety cabinets, HVAC, gases, freezer room).</li>
<li>Draft and execute commissioning protocols for FEU systems.</li>
<li>Perform and document IQ, OQ, and PQ for lab instruments and support equipment.</li>
<li>Conduct criticality assessments to determine validation scope and depth.</li>
<li>Support traceability matrix development to ensure requirements coverage.</li>
<li>Document test execution results, deviations, and corrective actions.</li>
<li>Prepare and finalize GMP-ready validation reports for submission to QA.</li>
<li>Interface with Client SMEs and QA for review/approval cycles, ensuring alignment with site standards.</li>
<li>Deliver assigned packages within agreed milestones to enable regulatory readiness.</li>
</ul>
Required Skills, Scope, and Experience:
<ul>
<li>Bachelor’s degree in Engineering, Life Sciences, or related field.</li>
<li>8+ years’ experience in commissioning, qualification, and validation within GMP-regulated biopharma/biotech environments.</li>
<li>Strong knowledge of FDA, EMA, and ICH requirements, including 21 CFR Parts 210, 211.</li>
<li>Demonstrated expertise in IQ/OQ/PQ execution for QC lab instruments and utilities.</li>
<li>Experience with commissioning HVAC, environmental monitoring systems (EMS), and building management systems (BMS).</li>
<li>Familiarity with risk-based validation (ISPE Baseline Guides, ASTM E2500).</li>
<li>Strong technical writing and documentation skills (URS, protocols, reports).</li>
<li>Ability to deliver results under compressed timelines with high compliance standards. &nbsp;</li>
</ul>

Urgent On-Site Opening for Senior CQV Engineer - Needham, MA - Need Local to MA Only.

<h3>Job Description</h3>
Job DescriptionOverview:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.&nbsp;&nbsp;&nbsp; &nbsp;Position:&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;Electronics Technician /&nbsp;Validation TechnicianLocation:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Tewksbury, MA - 01876Duration:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp; &nbsp; 12 Months&nbsp;Job Type:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Temporary Assignment&nbsp;Work Type:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;Onsite&nbsp; &nbsp;Shift Timings:&nbsp; &nbsp;Day Shift &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;Summary
<ul>
<li>This is an entry level Validation Technician position.</li>
<li>Perform customer support activities involving the installation, preventative and corrective maintenance, and testing of electronic equipment and sub-systems used for monitoring nuclear power levels in the nuclear industry. </li>
<li>Test and verify the performance and required maintenance of assigned customer equipment. </li>
<li>Interact with customers and co-workers, typically working under general supervision.</li>
</ul>
Responsibilities
<ul>
<li>Perform electrical testing of components, printed circuits, assemblies, and systems.</li>
<li>Document test plans, test procedures, and test results for each assigned job.</li>
<li>Collaborate with Engineering and Assembly to ensure manufacturing, construction, installation, and operations conform to functional specifications and customer requirements.</li>
<li>Identify, diagnose, and repair electronic failures at the component level.</li>
<li>Perform other miscellaneous duties as assigned.</li>
</ul>
Required Skills
<ul>
<li>High School Diploma or equivalent required.</li>
<li>Associate’s degree in a technical discipline is highly preferred</li>
<li>Basic computer proficiency (Microsoft Excel, Word, etc.).</li>
<li>Electro-mechanical assembly experience is an advantage.</li>
<li>Technical Electrical/Electronics/Computer experience (desired but not required).</li>
<li>Knowledge of ESD best practices.</li>
<li>Willingness to learn. </li>
<li>Ability to troubleshoot electronic circuits.</li>
<li>Experience building gaming computers or hobby electronics projects.</li>
</ul>
TekWissen® Group is an equal opportunity employer supporting workforce diversity.&nbsp; 
TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.
TekWissen® is an equal opportunity employer supporting workplace diversity.&nbsp;

Electronics Technician

<h3>Job Description</h3>
Job Description
Skills: Design and create fabrication drawings for custom machine tooling, fixtures, and gages. Provide engineering and technical support for production issues and equipment.

DUTIES &amp; RESPONSIBILITIES*
• Collaboration with internal customers to accept and initiate new tooling requests.
• Collaboration with Manufacturing Engineers &amp; Quality Engineers to evaluate and gain consensus on proper product dimensioning schemes that convey design intent, ensure functionality, aid in ease of manufacturing and ensure ability to use hard gages.
• A highly developed understanding of both design and fabrication skills, to effectively engineer new tools, fixtures, gages, and equipment.
• Effective use of CAD to design tools (like NX), fixtures, and gages.
• Investigation of pertinent design factors such as ease of manufacture, availability of materials and equipment, interchangeability, replaceability, strength-weight efficiency, and cost.
• Creation of layouts of complex assemblies and details of parts of devices, mechanisms, and structures.
• Identification and specification of appropriate materials for use on tools, fixtures, gages, and equipment
• Identification and specification of appropriate purchased components for use on tools, fixtures, gages, and equipment
• Consult with other tool designers to ensure conformance to accepted practices and standards.
• Work directly with engineering &amp; calibration on gage issues.
• Facilitate stakeholder meetings to review designs and intents.
Education
BS in Mechanical Engineering or other Technical Degree, or equivalent professional experience
A minimum of 3+ years’ experience in all phases of CAD design
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS*
• Required Qualifications:
o Working knowledge of GD&amp;T.
o Working knowledge and experience using Siemens NX (Unigraphics) modeling software
o Self-starter with the ability to deliver results under minimal supervision.
• Preferred Qualifications:
o A concentration in the specialized disciplines of Gage Design, GD&amp;T Application, and Design Checking
o Experience working in a regulated medical industry.
o Design for manufacturability
&nbsp;

CAD Engineer at Raynham, MA (Onsite)

<h3>Job Description</h3>
Job DescriptionSalary: $46,742.80 TO $62,826.92 PER YEAR 
POSITION TITLE: LIGHT EQUIPMENT OPERATOR
 DPW WATER DIVISION
 AFSCME LOCAL 1700 GRADE 7
 FULL-TIME (40 HOURS PER WEEK)
 FULL PAY RANGE: $46,742.80 TO $62,826.92 PER YEAR
 HIRING RANGE: $46,742.80 TO $49,116.60 
 
POSITION OVERVIEW:
 General laboring work, requiring some skills such as pipe laying, installing water services, replacing valves and, in emergencies, installing water meters and reading water meters
 Will be able to operate a compressor, jack hammer, water pump, repair leaks, dig trenches by hand, tap water mains, drive truck, repair or replace street valves
 Assist in repairing equipment and cleaning of the garage and stockroom
Be on call for emergencies and will do all work as assigned or required by the Superintendent
Answers directly to the Water Superintendent. In the absence of the Water Superintendent, will answer directly to the Foreman; in the absence of both the Water Superintendent and the Foreman, will answer directly to the Lead Man 
 
QUALIFICATIONS:
Valid Massachusetts Drivers License
 EDUCATION AND EXPERIENCE:
 High school diploma, trade school education, or equivalent training and experience.
 
Diversity &amp; Inclusion is a key component of our success as an organization. The Town of Bridgewater is an Equal Opportunity Employer and encourages all qualified individualsregardless of background, experience, or strengthsto apply.

LIGHT EQUIPMENT OPERATOR

<h3>Job Description</h3>
Job Description
We are a looking for a Sheet Metal Installer to help our company grow while using your skills to advance with us. We have been in business for over 25 years and still going! We have several job opportunities available from residential and commercial work, hanging, installing, wrapping, insulating, and more! Apply here to discuss more about how we can help better your career path.
We offer employees – Competitive Pay – Medical, Dental, and Vision – 401k with Company Match – Tool Reimbursement – Tuition Reimbursement – AND MORE…!!!
Ask us how to earn a $250 referral bonus!

Sheet Metal Installer - Commercial Work

<h3>Job Description</h3>
Job Description
Job Title: Industrial Maintenance Technician Job Location: Devens, MA Job Type: Full-Time
Job Description:
<ul>
<li>Troubleshoot and repair mechanical and electrical issues on plant machinery and systems.</li>
<li>Perform preventive maintenance (PMs) and corrective maintenance to minimize equipment downtime.</li>
<li>Install, modify, and service electrical wiring, conduits, and control systems in an industrial environment.</li>
<li>Interpret mechanical and electrical schematics, blueprints, and technical drawings.</li>
<li>Assist with fabrication, plumbing, welding, and other general maintenance duties as needed.</li>
<li>Adhere to OSHA, fire and electrical safety codes, and company-specific safety procedures.</li>
<li>Collaborate with teammates, management, and vendors to support smooth plant operations.</li>
<li>Maintain accurate records of maintenance work and safety training.</li>
<li>Complete required monthly online safety training.</li>
</ul>

8,014 Manufacturing Jobs