field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
CMM Programmer
BioTalent · Devens, Massachusetts, United States (On-site)
Job Title: CMM Programmer
Introduction
Join a leading manufacturing organization in Devens, MA dedicated to precision engineering and high-quality production standards. We are currently seeking an experienced CMM Programmer with deep expertise in Zeiss CMMs and Calypso software to support our quality inspection and metrology efforts.
This role plays a key part in ensuring dimensional accuracy and quality compliance across the production lifecycle through precise inspection programming and execution.
This Role Will Offer You
<ul>
<li>The opportunity to program and optimize advanced Zeiss CMMs in a high-precision manufacturing environment</li>
<li>A collaborative and technically focused team culture</li>
<li>Competitive compensation and a comprehensive benefits package</li>
<li>Opportunities for ongoing development in inspection automation, metrology systems, and quality engineering</li>
</ul>
You Will Be Responsible For
<ul>
<li>Creating, modifying, and optimizing CMM programs using Calypso software for routine and complex inspections</li>
<li>Performing dimensional inspections of precision parts and assemblies using Zeiss Coordinate Measuring Machines</li>
<li>Analyzing engineering drawings and applying GD&amp;T to ensure inspection accuracy and compliance</li>
<li>Supporting first article inspections (FAI), in-process checks, and final inspections</li>
<li>Troubleshooting and resolving measurement discrepancies or software issues</li>
<li>Documenting results, generating inspection reports, and supporting non-conformance investigations</li>
<li>Collaborating closely with Quality, Production, and Engineering teams to drive continuous improvement in dimensional control</li>
<li>Ensuring proper calibration, maintenance, and functionality of CMM and related metrology equipment</li>
</ul>
You Will Bring the Following
<ul>
<li>Proven experience programming Zeiss CMMs with Calypso software</li>
<li>Strong knowledge of GD&amp;T and the ability to interpret detailed technical drawings and blueprints</li>
<li>Experience in a precision manufacturing environment (e.g. aerospace, medical device, automotive)</li>
<li>Familiarity with quality systems, inspection procedures, and ISO or AS9100 standards</li>
<li>Strong analytical skills, attention to detail, and the ability to work independently and cross-functionally</li>
</ul>
To learn more or apply, please contact me at <a href="mailto:devon.nzepuome@biotalent.com" target="_blank">devon.nzepuome@biotalent.com</a>.
BioTalent Ltd is acting as an employment agency in relation to this opportunity.

Coordinate Measuring Machine Programmer

<h3>Job Description</h3>
Reporting to the Practice Manager, this mission critical position is responsible for administrative tasks that occur on a clinic floor including; scheduling appointments in accordance with the scheduling guidelines; liaising among patients/families/providers/leadership; utilizing institutional and technical knowledge to properly triage patient and provider requests. Enjoys working in a busy clinic setting, offering exemplary customer service, and managing complex high-volume scheduling tasks while balancing multiple real- time priorities.
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. &nbsp;
Primary Duties and Responsibilities:
Reporting to the Practice Manager and working under the guidance of the Lead Clinic Coordinator, this mission critical position is responsible for the following:&nbsp; Appointment Scheduling: • Accurately schedules complex appointment sets across disciplines for oncology patients in accordance with scheduling guidelines • Monitors scheduling reports to ensure accuracy in patient scheduling and to ensure optimization of resource utilization • Maintains confidentiality of Protected Health Information (PHI) • Possesses strategic thinking skills, the ability to learn rapidly, multi-task, and adapt quickly to an ever-changing environment. • Participates in training new team members as requested Patient Experience: • Delivers outstanding customer service to internal and external customers • Timely, accurately and curiously responds to the needs of internal and external customers • Ability to deescalate patient grievances, and maintain customer service standards, and involve floor leadership as necessary Communication and Collaboration: • Demonstrates ability to effectively communicate across leadership levels and with varying audiences • Synthesizes and communicates complex information in patient friendly terms • Obtains detailed scheduling information face-to-face, by telephone, or electronically while performing check-in and check-out functions – i.e. triaging phone calls, double identifying patients, printing appropriate paperwork, coordinating complex schedules; acquiring and entering verbal orders • Works effectively as a member of the team and across functional teams • Fosters a sense of shared responsibility among the team Emergency Response: • Recognizes emergencies and appropriately responds using standard operating procedures Regulatory Compliance and Quality Improvement: • Compliance with DFCI policies and procedures • Understanding their role and responsibility in obtaining successful Joint Commission accreditation&nbsp; • HIPPA regulation compliance • Completion of assigned AEU and Health Stream competencies • Executes registration related processes including: Partners Patient Gateway Enrollment, MASS HiWay, Medicare Secondary Patient Questionnaire (MSPQ), Massachusetts Medical Orders for Life-Sustaining Treatment (MOLST), and Release of Patient Information. • Actively participates and provides constructive feedback on quality improvement projects Information Technology: • Maintains a level of competency in all systems including: Epic, Real Time Locating System (RTLS), Outlook • Actively engaged in system upgrades and effected operational changes&nbsp; • Distribution, maintenance, after-use cleaning, and technical troubleshooting issues of patient-use iPads
Knowledge, Skills and Abilities:
• Excellent verbal and written communication skills • Working knowledge of computers and technology • Excellent customer service • Ability to function as an integral member of the team • Strong organizational skills with the ability to multi-task • Strong problem solving and critical thinking skills • Demonstrated flexibility and ability to take on additional responsibilities as situations require • Ability to adapt to ever-changing environment
Minimum Job Qualifications:
High school diploma, bachelor’s degree preferred. Experience working in a customer service setting preferred. Proficiency in technology and complex computer systems required.
License/Certification/Registration Required:
Supervisory Responsibilities:
None
Patient Contact:
Yes, this position entails patient contact and communication.&nbsp; Methods of contact are in person, via telephone, written letter or email.&nbsp; Age population served will depend upon clinical area assigned, (i.e. Pediatric or Adult clinic).&nbsp; This position may or may not include provision of wheelchair escort services.
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive&nbsp;environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate&nbsp;professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.&nbsp;&nbsp;
EEO Poster.
Pay Transparency Statement
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications.
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).
$45,500.00 - $54,400.00

Clinic Coordinator 1

<h3>Job Description</h3>
The Manufacturing Quality Engineer will be highly involved in the manufacturing aspects of the business, with an emphasis on Quality. The Quality Engineer will handle multiple projects and tasks throughout product development, product launch, and manufacturing. Additionally, this individual will ensure that product meets quality standards consistent with customer and other regulatory requirements. This role also supports plant activities in customer issues, supplier issues, and initiate corrective actions with an emphasis on process improvement. The mission of the Manufacturing Quality Engineer is to enhance the quality of materials and products through detection, analysis, and correction of conditions leading to nonconformance.
 
Job Functions:
 
<ul>
<li>Support, maintain, and sustain QMS.</li>
<li>Audit processes and products.</li>
<li>Complete first piece inspection activities.</li>
<li>Support CMM programming needs. </li>
<li>Support incoming inspection and communicate with suppliers regarding SCARS and other issues.</li>
<li>Confer with engineers about the quality assurance of new products and development of procedures and quality requirements.</li>
<li>Develop and update PFMEAs and Control Plans, as necessary.</li>
<li>Assist in resolving customer quality issues.</li>
<li>Investigate nonconformance reports and coordinate corrective / preventive actions.</li>
<li>Perform internal audits and mentor process owners toward improvement.</li>
<li>Participate on improvement teams for safety, quality, or cost.</li>
<li>Collect and analyze internal/external quality data and report.</li>
<li>Perform other duties as assigned to support the advancement of quality systems and operations.</li>
</ul>
 
Skills:
 
<ul>
<li>Good team player.</li>
<li>Good problem-solving skills.</li>
<li>Effective communication skills.</li>
<li>Strong computer skills and knowledge of MS Office Suite.</li>
<li>Working knowledge of print and specification interpretation.</li>
</ul>
 
Required Experience:
 
<ul>
<li>BS in Mechanical Engineering, or another technical field.</li>
<li>2+ year experience in Quality or Manufacturing background in diecast or injection molded products.</li>
<li>Hands on experience measuring with various gauges and tools.</li>
<li>Experience in 5S, lean or other continuous improvement methods.</li>
<li>PPAP, QMS, NADCAP, and ISO9001 standards experience</li>
<li>CMM Programming experience highly desired.</li>
</ul>

Quality Engineer

<h3>Job Description</h3>
Rangam is seeking candidates for a Direct Hire role as a Senior Process Technician/Tech ops 2 with our client, one of the world’s largest pharmaceutical companies.
 
Seeking candidates in Andover, MA or willing to relocate.
 
Use Your Power for Purpose
Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in client's mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need. 
 
What You Will Achieve
In this role, you will:
<ul>
<li>Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.</li>
<li>Manage personal time and professional development, being accountable for results.</li>
<li>Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.</li>
<li>Identify and solve moderately routine problems.</li>
<li>Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.</li>
<li>Ensure work is reviewed for accuracy, quality, and adherence to standards.</li>
<li>Be responsible for the production of drug substances or active biological ingredients (ABI), assisting in various activities and functions within a manufacturing facility, and ensuring equipment functionality.</li>
<li>Support technical operations, maintain housekeeping standards, keep training status current, and assist in the implementation of new technology for process execution and analysis.</li>
</ul>
 
Here Is What You Need (Minimum Requirements)
<ul>
<li>High School Diploma or GED with 2+ years of relevant experience</li>
<li>Strong verbal and written communication skills</li>
<li>Proficiency in using standard manufacturing equipment and tools</li>
<li>Basic understanding of Good Manufacturing Practices (GMP)</li>
<li>Ability to follow detailed instructions and standard operating procedures</li>
<li>Strong problem-solving skills in a structured environment</li>
<li>Capability to work effectively in a team setting</li>
<li>Basic computer skills, including familiarity with data entry and reporting systems</li>
</ul>
 
Bonus Points If You Have (Preferred Requirements)
<ul>
<li>Experience in a pharmaceutical or biotechnology manufacturing environment</li>
<li>Knowledge of regulatory requirements and quality systems</li>
<li>Strong organizational skills and attention to detail</li>
<li>Ability to adapt to changing priorities and manage multiple tasks</li>
<li>Demonstrated ability to take initiative and drive continuous improvement</li>
<li>Strong analytical skills and the ability to interpret technical data</li>
</ul>
 
PHYSICAL/MENTAL REQUIREMENTS
<ul>
<li>Include Lifting (approx max of 50lbs) , sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis. Does not include requirements that are generally applicable to most or all jobs at client's, such as “ability to communicate,” “ability to work on teams”, “office job involving use of computer”, etc.</li>
</ul>
 
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
 
This is for a rotating second shift position (2pm to 2am).
 
OTHER JOB DETAILS
Last Date to Apply for Job: Dec 9, 2025.
Referral Bonus Eligibility: YES
Eligible for Relocation Package: NO
 
Work Location Assignment: On Premise
 
 
The salary for this position ranges from $26,34 to $43,89 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with client's Matching Contributions and an additional client's Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at client's Candidate Site – U.S. Benefits | (uscandidates.my**benefits.com). Compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Massachusetts - Andover location.
 
 
Relocation assistance may be available based on business needs and/or eligibility.
 
To find out more about Rangam and this role, click the apply button.
 
 
 
Satnam Singh
SA Technical Recruiter | Rangam Consultants, Inc
M: (513) 447-8917
E: <a href="mailto:satnam@rangam.com" target="_blank">satnam@rangam.com</a>| W: <a href="http://www.rangam.com" target="_blank">www.rangam.com</a>

Senior Process Technician/Tech ops 2

<h3>Job Description</h3>
Job Description
Our client in South Burlington, VT is seeking bindery workers to join their team. As a bindery worker, you will assist in making magazines by use of machines and assist with packaging and distribution.[

Job Title: Bindery Worker
Location: South Burlington, VT
Pay Range: 18.00&nbsp;-19.80 an hour
Shift: 7-3pm, 3-11pm or 11-7am &nbsp;
What’s the Job?
<ul>
<li>Using machine operation to package, label and distribute Magazines</li>
<li>Train on Machines and report issues</li>
<li>Assist with maintaining GMP</li>
<li>Warehouse shipping, receiving</li>
</ul>

What’s Needed?
<ul>
<li>Good attendance</li>
<li>Dependable</li>
<li>Willing to Learn</li>
<li>Work Ethic</li>
</ul>

What’s in it for me?
<ul>
<li>Competitive Wages</li>
<li>Weekly Pay</li>
<li>Access to free online courses and certificate programs</li>
<li>Full Time Positions</li>
<li>Career Opportunities</li>
</ul>
If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of:Manpower, Experis, Talent Solutions, and Jefferson Wells
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands –&nbsp;Manpower, Experis, Talent Solutions, and Jefferson Wells&nbsp;– creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

Bindery Worker

<h3>Job Description</h3>
Location: Woburn, MA (on-site 5 days per week)
 
Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess’ patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world.
 
Responsibilities&nbsp;
<ul>
<li>Perform cGMP manufacturing operations according to documented procedures or batch records</li>
<li>Operate automated manufacturing equipment and record relevant in-process data.&nbsp;</li>
<li>Complete production and testing records following Good Documentation Practices (GDP)</li>
<li>Handle, assemble, and visually inspect products, including use of a microscope, automated inspection systems, or&nbsp; other optical systems.&nbsp;&nbsp;</li>
<li>Contribute to root cause analysis (RCA) and help contribute to manufacturing investigations</li>
<li>Support manufacturing related R&amp;D efforts as needed&nbsp;</li>
<li>Perform other assigned duties related to manufacturing, quality control, and/or facility operations.&nbsp;</li>
</ul>
﻿&nbsp;
Qualifications&nbsp;
<ul>
<li>2 + years’ relevant experience working in regulated environments in medical device or biopharmaceutical&nbsp; industries; experience working in a clean room is preferred&nbsp;</li>
<li>High school diploma minimal, associate’s degree or trade certifications preferred&nbsp;</li>
<li>Good written and verbal communication skills, attention to detail, and a demonstrated ability to work effectively&nbsp; within a team</li>
<li>Ability to stand or sit for a full shift on a manufacturing line&nbsp;</li>
<li>Entrepreneurial spirit and drive to positively impact global human health&nbsp;</li>
</ul>
 
At Vaxess, we’re bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to <a href="mailto:careers@vaxess.com" target="_blank">careers@vaxess.com</a>.

Manufacturing Technician

<h3>Job Description</h3>
Job DescriptionDescription:
The TSUBAKI name is synonymous with excellence in quality, dependability, and customer service. U.S. Tsubaki Automotive, LLC is an international tier-one supplier of high-speed chain drive systems to the automotive industry.&nbsp;&nbsp;
Essential Duties and Responsibilities:
<ul>
<li>Operate a variety of machines for metal finishing, i.e., chamfer barrels, polishing machines, spin dryers and shot peen machines.&nbsp;</li>
<li>Follow work instructions to maintain work flow and produce good parts for the line.&nbsp;</li>
<li>Follow safety instructions including P.P.E. Fill out paperwork to accurately track traceability on all parts.&nbsp;</li>
<li>Work to specifications, schedules, orders and general instructions of department group leader and supervisor.</li>
</ul>
Requirements:
<ul>
<li>High school diploma or equivalent preferred; equivalent relevant experience may be considered</li>
<li>Be able to read and write English</li>
<li>2 -5 years’ experience running multiple machines, troubleshooting and performing preventative maintenance.&nbsp;&nbsp;</li>
<li>Moderate physical effort consisting of occasional heavy weights.</li>
</ul>
Tsubaki is an Equal Opportunity Employer - Minorities/Females/Veterans/Disability
PM21
 
Compensation details: 23.11-25.78 Hourly Wage
 
PI0908d8e6a25a-25405-39397624

Metal Finisher - 24/7 Days

<h3>Job Description</h3>
Job Description Description:
We are seeking a Manufacturing Engineer to join our Operations Team. Bigbelly is pursuing an ambitious product roadmap, and this position plays a visible, cross-functional role as the company builds its internal manufacturing and development capabilities. The evolving needs of the growing Operations Team are expected to lead to new opportunities for personal and professional growth. Must be authorized to work in the US and able to commute to work. 
 
In this role, you will develop, implement, and improve manufacturing processes and systems. This role involves working closely with the production teams (domestic and international) to produce our products efficiently, safely, and to the established quality standards. You will be involved in and often leading projects related to troubleshooting production issues, developing process documentation, and reducing costs. You will work with the Development Engineering team to introduce new technologies and products into the manufacturing sites. Ideally, you have had experience working in both the manufacturing and development environments, having brought multiple products into production while managing them through their product life cycle. You will also have a proven track record working with supply chain teams and developing relationships with global suppliers and production partners. 
 
This position reports to the Plant Operations Manager and will provide the necessary methods and processes to drive the production team to achieve excellence in Quality, Execution, Cost, Flexibility, and Methods and Process Innovation. 
 
Responsibilities
 
Safety
<ul>
<li>Champion adherence to safety rules throughout the operation to protect oneself and others from injury.</li>
<li>Ensure all manufacturing equipment (jigs, fixtures, material handling, tools, etc) is designed and deployed to be operated safely. </li>
<li>Assist the Plant Manager by ensuring common practice safety guidelines are followed daily. </li>
</ul>
Cost Management
<ul>
<li>Leveraging Lean tools, initiate and lead projects that improve manufacturing costs by driving improvements in areas such as manufacturability, “touch time”, Value Stream Mapping, part flow, fixturing, packaging, etc. Lead frequent “Gemba” walks.</li>
<li>Support the supply chain team to identify and qualify alternative sources for improved costs.</li>
<li>Sample labor time for tasks, to maintain labor timetables, always seeking time reductions. </li>
<li>Participate in the auditing of the DL “competency” matrix as a member of the evaluation board. </li>
</ul>
Design and Implementation
<ul>
<li>Collaborate with Engineering and suppliers to ensure manufacturability of new products utilizing DFX, PFMEA, DFMEA, GD&amp;T, Tolerance analysis, etc.</li>
<li>Manage the installation and commissioning of new equipment and processes to support NPI (New Product Introduction).</li>
<li>Create and oversee the development of new manufacturing processes, systems, and technologies to expand Bigbelly's capabilities.</li>
<li>When production equipment is required, coordinate collaborative project builds with Engineering.</li>
</ul>
Troubleshooting and Problem Solving
<ul>
<li>Provide engineering support to production teams to resolve technical issues.</li>
<li>Support analysis of field failures and in-process quality escapements</li>
<li>Support the resolution of quality issues through root cause analysis and implementing preventive corrective actions.</li>
</ul>
 
Documentation 
<ul>
<li>Support the creation and maintenance of manufacturing work instructions and process control plans for all products. This includes deploying and maintaining the appropriate tools for conveying the instructions and recording the results.</li>
<li>Coordinate requests for engineering changes, and after evaluating, lead the implementation of ECOs at suppliers and in-house production. </li>
</ul>
 
Project Management and Leadership
<ul>
<li>Lead mid to high-level manufacturing projects, providing direction, guidance, and engineering expertise to team members while delivering formal presentations to leadership regarding project status. This includes resource plans, timelines, and budgets.</li>
<li>Develop and maintain plans for new tooling, equipment, and production capabilities.</li>
</ul>
 
 
Requirements:
<ul>
<li>Bachelor's degree in manufacturing, Industrial, or Mechanical Engineering</li>
<li>10+ years of experience in an electromechanical manufacturing environment </li>
<li>Strong leadership and management skills</li>
<li>Excellent problem-solving and analytical skills (statistical experiment design experience preferred)</li>
<li>Experience with Lean Manufacturing and Six Sigma DMAIC methodologies (Greenbelt certification preferred)</li>
<li>Experienced using SolidWorks 3D CAD design software, desirable</li>
<li>Proficiency using PLM tools (Arena preferred)</li>
<li>Lean-Six Sigma Greenbelt certification utilizing DMAIC principles a plus.</li>
<li>Proficiency in using and understanding GD&amp;T</li>
</ul>
 
PI9f0cfed0d594-25405-35217407

Manufacturing Engineer

<h3>Job Description</h3>
Job Description
Location: New Bedford, MA Pay: $30.00/hour Schedule: [3rd]
About the Role
We are looking for a skilled Industrial Maintenance Technician to join our team in New Bedford. In this role, you will install, maintain, troubleshoot, and repair machinery and equipment involving mechanical, pneumatic, hydraulic, and electrical systems.
Key Responsibilities
<ul>
<li>Troubleshooting &amp; Repair (50%) Diagnose, repair, and rebuild mechanical assemblies—manual or automated—including electric, pneumatic, and hydraulic systems.</li>
<li>Preventive Maintenance (20%) Perform scheduled maintenance to minimize downtime and extend equipment life.</li>
<li>Problem Isolation (20%) Identify sources of equipment issues using prints, schematics, and collaboration with operators, engineers, and vendors.</li>
<li>Fabrication &amp; Support (10%) Conduct basic welding, plumbing, and machining tasks as needed.</li>
</ul>
Additional duties include maintaining accurate work records in a computerized maintenance system and monitoring spare parts inventory.
Qualifications
<ul>
<li>Education: Trade school diploma preferred</li>
<li>Experience: Minimum 3 years in industrial equipment repair</li>
<li>Technical Skills:</li>
<li>Proficiency in mechanical repair techniques</li>
<li>Knowledge of plumbing and piping</li>
<li>Universal Refrigeration License required</li>
<li>Ability to read blueprints and schematics</li>
<li>Basic knowledge of electronic controls</li>
<li>Familiarity with safe work practices</li>
</ul>
Requirements
<ul>
<li>Own trade-related tools</li>
<li>Ability to operate hoisting/lifting devices (cranes, jacks, tractors)</li>
<li>Competence in troubleshooting power transmission, vacuum, and pneumatic systems</li>
<li>Strong communication and interpersonal skills</li>
<li>Ability to obtain forklift, pallet-jack, and/or man-lift license</li>
</ul>
Additional Skills
<ul>
<li>Computer literacy for maintenance systems</li>
<li>Basic math and measurement skills</li>
<li>Ability to use machine tools (drills, lathes, millers)</li>
</ul>

Industrial Technician

<h3>Job Description</h3>
Job Title: Manufacturing Quality Technician
Duration: 6 + Months
Location: Ayer MA
Pay rate: $27 - 30/hr (Without benefits)
3 Days a Week – 6pm-6am
 
Job Summary:
The Associate Manufacturing Technician will operate, troubleshoot, and maintain advanced automated equipment used in producing medical devices. The role involves cross-training across multiple technologies—laser welding, heat staking, PCB handling/testing, robotic automation, metal forming, discrete component assembly, and medical packaging. This position requires strong mechanical aptitude, problem-solving ability, and comfort working in a fast-paced, highly regulated manufacturing environment.
Key Responsibilities
<ul>
<li>Set up, operate, and perform basic maintenance on automated manufacturing equipment with minimal supervision.</li>
<li>Monitor machines, maintain raw material feeds, clear faults/stoppages, and adjust processes using HMIs.</li>
<li>Conduct equipment inspections; create work orders for corrective or preventive maintenance.</li>
<li>Troubleshoot mechanical issues, ensure product quality, and use measurement tools to verify tolerances.</li>
<li>Support new product transfer, process development, and equipment/process v­­­­­­­­­­­­­­­­­­alidations.</li>
<li>Participate in issue investigation and corrective actions within equipment cells.</li>
<li>Manage material handling, documentation, inventory updates, and follow all GMP/SOP requirements.</li>
<li>Maintain a clean manufacturing/cleanroom environment and collaborate across teams to improve processes.</li>
</ul>
Qualifications
<ul>
<li>High school diploma/GED or 3+ years manufacturing experience.</li>
<li>Basic math skills; proficient in English.</li>
<li>Mechanical aptitude with ability to operate, debug, or maintain automated equipment.</li>
<li>Preferred: experience with HMIs, robotics, discrete assembly, medical devices, laser/heat staking/ultrasonic welding, and cleanroom work.</li>
<li>Familiarity with measurement tools (micrometers, calipers, gauges).</li>
</ul>
Physical Requirements
<ul>
<li>Standing/walking most of the shift; ability to lift up to 20 lbs.</li>
<li>Frequent reaching, pushing, and pulling.</li>
</ul>
 
Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit <a href="https://dexian.com/" target="_blank">https://dexian.com/</a> to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status

10,319 Manufacturing Jobs