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<h3>Job Description</h3>
Job Description
Our client is seeking an experienced Industrial Maintenance Technician to support 3rd shift operations. This role focuses on maintaining, troubleshooting, and repairing production equipment to ensure maximum uptime, safety, and efficiency.
Onsite | No Visa Sponsorship | No Relocation Assistance
Work Schedule: Sun-Thurs, 11PM-7AM 3rd Shift (Training on 1st or split 1st/2nd shift)
Location: On-site in Devens, MA (near Ayer/Littleton)
Responsibilities:
<ul>
<li>Follow OSHA, electrical, and company safety standards.</li>
<li>Perform preventive and corrective maintenance to reduce downtime.</li>
<li>Read and interpret mechanical/electrical schematics and technical drawings.</li>
<li>Support fabrication, welding, plumbing, and general facility maintenance.</li>
<li>Collaborate with maintenance and production teams to support plant operations.</li>
<li>Maintain accurate maintenance logs and complete monthly safety training.</li>
<li>Install, modify, and service electrical wiring, conduits, motors, and control systems.</li>
<li>Troubleshoot and repair mechanical and electrical issues on production machinery.</li>
</ul>
Qualifications/Must Haves:
<ul>
<li>Strong mechanical and electrical troubleshooting skills.</li>
<li>Ability to read schematics and diagnose issues independently.</li>
<li>Familiarity with industrial computer systems and networked equipment.</li>
<li>5+ years of industrial maintenance experience OR technical school training + hands-on experience.</li>
<li>Experience with AC/DC motor controls, pneumatics, hydraulics, and PLC interfaces.</li>
</ul>
Preferred Skills:
<ul>
<li>Welding, fabrication, or machining skills.</li>
<li>Corrugated, packaging, or high-volume manufacturing environment.</li>
<li>Experience with corrugators, die cutters, conveyors, or similar machinery.</li>
</ul>
Benefits &amp; Perks:
<ul>
<li>Medical, dental, life, STD/LTD</li>
<li>401(k) with company match</li>
<li>Optional supplemental insurance</li>
<li>Competitive compensation + shift differential</li>
<li>Tuition reimbursement &amp; scholarship opportunities</li>
<li>Monthly Teamshare bonus program (up to 15% additional income)</li>
</ul>

Industrial Maintenance Technician - 3rd Shift (Manufacturing | On-Site)

<h3>Job Description</h3>
Job Description
Date:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; December 26, 2025
Job Title:&nbsp;&nbsp; Plant Engineer - Open
Scope:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Reports to Plant Manager
Plant Engineer
Nyacol® Nano Technologies, Inc., a leader in the development and manufacture of inorganic colloids and nanoparticle technology is seeking a Plant Engineer to join their team.&nbsp; This is a full-time position and reports to the Plant Manager.
Responsibilities and Duties include the following:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for the safety &amp; well being of the Maintenance Department’s employees.&nbsp; This includes an organized &amp; safe operating environment at all times.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hiring all maintenance department employees in conjunction with the Plant Manager &amp; Human Resource Manager.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for abiding by &amp; enforcing the safety programs for the company.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Leads the Maintenance Team to preserve the facility and its’ equipment, improve uptime along with controlling &amp; monitoring costs.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Coordinate training for maintenance and production department employees as needed.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Assist with the development/enhancement of a preventative maintenance program.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Create and maintain a master equipment list.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for maintaining all equipment files – update and make complete.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for keeping accurate equipment records.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for purchasing all parts and materials necessary to keep the facility operating.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for the maintenance and operation of two (2) boilers.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsible for coordinating outside contractors and vendors when they are brought in to provide additional personnel and services to support the Maintenance Department.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Project installations - provide expertise to new equipment design, installation and start-up.
o&nbsp;&nbsp;&nbsp; Assist with the design construction and start-up of new equipment.&nbsp;
o&nbsp;&nbsp;&nbsp; Assist in the implementation of capital projects which includes developing process designs, preparing budgets, obtaining cost estimates, overseeing installation and in some cases designing modifications to existing processes.&nbsp;
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Oversee maintenance schedule, perform internal audits and instrument calibration.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Discipline of maintenance department employees as needed.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Provide support to the Plant Manager in preparation of the plant budget.&nbsp;
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintain software and design-basis documentation for E&amp;I systems (drawings, circuit breaker coordination, arc-flash calculations, etc.)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Communicate and facilitate an understanding of the NNT Quality System and Quality Policy.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Other tasks as directed by the Plant Manager or President.
Required Qualifications:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hands-on experience (minimum 7 years) in both maintenance shop and manufacturing environments.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prior experience (minimum 5 years) in maintenance management and process trouble shooting.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience with Microsoft Outlook, Excel &amp; Word.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Basic PLC skills &amp; experience.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Good supervisory, communication and documentation skills.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Knowledge of pumps, controls (level, pressure, temperature, etc.), motors, valves, electrical systems, etc.
Preferred Requirements:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prior work experience in chemical manufacturing environment.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Massachusetts State licenses -
o&nbsp;&nbsp;&nbsp; Boilers, plumbing, pipe fitting, electrical, hoisting, wastewater, etc.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; BS in Engineering (Chemical or Mechanical).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Process control background (DCS, PLC).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Safety Management involvement (OSHA, PHA, MOC, SOP, etc.).
Related Information:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Works in both manufacturing and maintenance shop environments.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Work week is from Monday through Friday.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Works as part of a maintenance on-call rotation which includes week nights and occasional weekends.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Occasionally fills in for the Plant Manager during their absence.
Company DescriptionLeader in the development and manufacture of nanomaterials with excellent potential for growth. 
<h3>Company Description</h3>
Leader in the development and manufacture of nanomaterials with excellent potential for growth.

Plant Engineer

<h3>Job Description</h3>
Job Description
Job Title: Manufacturing Technician
Job Description
The Manufacturing Technician will be responsible for performing all cell culture manufacturing and aseptic techniques. The role involves documenting all operations in electronic batch records while adhering to all GMP and SOPs. Additionally, the technician will be involved in reviewing and revising production documents.
Responsibilities
<ul>
<li>Perform all cell culture manufacturing and aseptic techniques.</li>
<li>Document all operations in electronic batch records in compliance with GMP and SOPs.</li>
<li>Review and revise production documents as needed.</li>
<li>OOS investigation and batch record review.</li>
<li>Other duties as assigned.</li>
</ul>
Essential Skills Needed 
<ul>
<li>Experience in cleanroom environments.</li>
<li>Knowledge of cell therapy, cell culture, and mammalian cell culture.</li>
<li>Familiarity with GMP regulations and SOPs.</li>
<li>Proficiency in 5S and lean manufacturing principles.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s or higher degree in Life Sciences or related field with 2-4+ years of cGMP experience in the biotech or pharmaceutical industry.</li>
<li>Biotechnology certificate with 4-6+ years of cGMP experience in the biotechnology or pharmaceutical industry.</li>
<li>Experience with cell culture and following SOPs.</li>
</ul>
Work Environment
This is a 100% onsite position with an initial training period of 3-4 months from Monday to Friday. Following training, the schedule will shift to Wednesday through Saturday, 6:30 am to 5:00 pm.
Job Type &amp; Location
This is a Permanent position based out of Cambridge, MA.
Pay and Benefits
The pay range for this position is $60320.00 - $74800.00/yr.
They will get a lot of holidays, vacation, and they will get 401k. they will also get a 10% bonus for this role and restricted stock units.
Workplace Type
This is a fully onsite position in Cambridge,MA.
Application Deadline
This position is anticipated to close on Dec 25, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Manufacturing Technician

<h3>Job Description</h3>
Job DescriptionLeading architectural and engineering firm is adding a Senior Electrical Engineer to their Boston team! 
 
Responsibilities: 
<ul>
<li>Prepare scope, budget and staff after assessing project requirements </li>
<li>Using preliminary review and client meetings, write scope of work for electrical design </li>
<li>Prepare engineering studies/schematic design for new systems </li>
<li>Analyze operation of existing systems </li>
<li>Effectively present complex engineering analysis to owner/design team </li>
<li>Troubleshoot/resolve complex problems (conflicting design requirements, code issues, varying design options, and difficult condition requirements) </li>
<li>Research non-routine code issues and obtain interpretations from code officials </li>
<li>Prepare sketches/system schematics for complicated design tasks </li>
<li>Prepare calculations including whole building electrical loads, lighting calculations, power distribution calculations, equipment sizing, editing specification sections, and creating punch lists </li>
<li>Review contractor cost estimates after preparing engineering opinion of probable cost for electrical systems </li>
<li>Develop/maintain a thorough understanding of construction processes and delivery methods </li>
<li>Review drawings/documents for compliance </li>
<li>Mentor/train junior staff </li>
</ul>
 
Requirements: 
<ul>
<li>BS or MS degree in electrical engineering </li>
<li>12+ years of design experience for a variety of projects (corporate, higher education, or performing arts projects) </li>
<li>Documented experience providing electrical design to an MEP engineering firm or A/E firm </li>
<li>PE License </li>
<li>Extensive knowledge of National Fire Protection Association Codes (NFPA) </li>
<li>Understanding of applicable (city, state, federal) requirements/pertinent standards </li>
<li>Knowledge of IECC, LEED and ASHRAE requirements </li>
<li>Working knowledge of Revit software </li>
<li>Familiar with electrical analysis software (SKM, Easy Power) </li>
<li>Knowledge of the current sustainable technologies applicable to the design of commercial electrical systems </li>
</ul>
 
Salary is commensurate with experience. 
 
Successful applicants must be authorized to work in the USA without sponsorship. 
 
All qualified applicants will receive consideration for employment without regard to protected veteran status, disability, race, color, religion, sex, sexual orientation, gender identity, or national origin. 
 
Please contact Laura Harrison for further information! 
 
<a href="http://www.harrisonconsultingsolutions.com" target="_blank">www.harrisonconsultingsolutions.com</a> 
 
517-906-6926

Electrical Engineer

<h3>Job Description</h3>
A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, the QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing.
Responsibilities:
<ul>
<li>Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing</li>
<li>Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents</li>
<li>Support method transfer, qualification of critical reagents, and other assay-related activities</li>
<li>Participate in the review and basic trending of QC data</li>
<li>Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking</li>
<li>Collaborate with internal teams and external partners as part of cross-functional project support</li>
<li>Contribute to investigations and deviation reports under guidance</li>
<li>Perform other duties, as needed</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's Degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field</li>
<li>Familiarity with basic Lab techniques and Data Analysis methods</li>
<li>Strong organizational, communication, and interpersonal skills</li>
<li>Detail-oriented and eager to develop problem-solving skills in a regulated lab environment</li>
<li>Enthusiasm for learning and the ability to work both independently and within a team</li>
</ul>
Desired Skills:
<ul>
<li>Academic or internship experience with Mammalian Cell Culture and/or ELISAs </li>
</ul>

QC Analyst

<h3>Job Description</h3>
Job DescriptionGrow Your Craft With a Team That Sticks Around
Many of our teammates have built 20+ year careers here. Join Pace as we continue our path to be the premier die casting manufacturer and engineering solutions partner worldwide.
Role Snapshot
We’re hiring a skilled Industrial Painter who can apply a range of coatings to tight tolerances using multiple paint systems. You’ll bring a sharp eye for detail, a steady hand, and a strong commitment to safety and quality.
Schedule &amp; Pay
<ul>
<li>Employment: Full-time, first shift</li>
<li>Hours: 6:00 AM – 2:30 PM, Monday–Friday</li>
<li>Compensation: $20.00–$31.00 per hour</li>
</ul>
A Day in the Life
From the moment your shift begins, you’ll prep, spray, and verify finishes to meet customer specs while keeping the booth pristine and compliant:
<ul>
<li>Pull the correct paint from inventory and prepare it to the proper spraying viscosity with the appropriate thinner.</li>
<li>Accurately mix two-part urethane coatings with reducer.</li>
<li>Apply coatings to parts per specification and tolerance requirements.</li>
<li>Confirm finished parts meet customer standards through careful inspection.</li>
<li>Manage materials responsibly: pour surplus paint into the designated waste bucket by the booth for hazardous waste collection, and clean your spray gun with solvent—collecting used solvent in the second bucket for material handler pickup.</li>
<li>Address spills immediately with absorbent material and follow all hazardous waste procedures.</li>
<li>Replace filters and keep the spray booth clean and orderly.</li>
<li>Move materials as needed and maintain housekeeping in your area.</li>
</ul>
What You’ll Bring
<ul>
<li>Excellent hand–eye coordination, finger dexterity, and strong color recognition.</li>
<li>Clear communication and an ability to follow detailed work instructions.</li>
<li>Safety-first mindset that protects yourself, teammates, and the environment.</li>
<li>Reliable, consistent performance and attendance.</li>
</ul>
Experience Requirements
<ul>
<li>Minimum two years of industrial spray painting (or equivalent experience).</li>
<li>Able to pass a respiratory physical.</li>
</ul>
Physical Requirements
<ul>
<li>Occasionally lift or move equipment up to 30 lbs.</li>
<li>Able to climb and descend stairs.</li>
<li>Capable of sitting, standing, walking, climbing, stooping, and kneeling as needed.</li>
</ul>
Benefits That Back You
<ul>
<li>Medical, dental, vision, and life insurance coverage.</li>
<li>401(k) with a company match to support your retirement goals.</li>
<li>PTO, sick time, and 11 paid company holidays.</li>
<li>Tuition reimbursement and paid company training.</li>
<li>Real opportunities for advancement and long-term growth.</li>
</ul>

Precision Industrial Coatings Painter

<h3>Job Description</h3>
Job Description
Position Summary
The Director of Manufacturing balances the urgency of daily shift operations with the pursuit of long-term goals while ensuring the highest standards of quality and compliance. Work requires excellent teamwork, ability to communicate clearly, and cooperate with other staff members to achieve overall organizational objectives. The individual must have the ability to coordinate work between functions to ensure alignment with overall department vision and promote urgency, ownership, and accountability across the organization.
Duties and Responsibilities







 
<ul>
<li>Manage the execution of shift manufacturing to meet quality, client, and financial objectives as well as supporting technical transfer of clinical production activities across shifts</li>
<li>Oversee the finite scheduling of aseptic formulation and filling operations to ensure timely batch preparation and filling in alignment with production plans, quality standards, and manufacturing priorities</li>
<li>Partner with Quality and Operational Excellence manufacturing management team to ensure consistent product quality; drive efforts to create a right-first time (RFT) culture, reduce and eliminate human errors, manage deviations to ensure true root cause is identified and on time closure is achieved and continuously improve operational performance</li>
<li>Proactively identify, assess, and mitigate operational, quality, and organizational risks, escalating key risks and issues</li>
<li>Assure cGMP compliance with regulatory agencies (FDA, EMA, etc.) while maintaining high standards of quality, compliance, and safety through leadership by example</li>
<li>Implement and drive continuous improvement initiatives across manufacturing operations, leveraging data-driven insights and Operation Excellence methodologies</li>
<li>Develop, implement, and maintain KPIs aligned with site objectives to measure and monitor manufacturing performance across key areas including productivity, yield, utilization, cycle times, compliance, and cost efficiency</li>
<li>Regularly review and refine KPI metrics to reflect changes in business needs and operational priorities</li>
<li>Provide management reporting through use of department metrics aligned with site objectives and balanced scorecard</li>
<li>Balance team and individual responsibilities and exhibit objectivity and openness to others' views</li>
<li>Facilitate effective communication between clients and internal stakeholders to ensure alignment of site objectives</li>
<li>Work to maintain a safe manufacturing environment in accordance with plant/corporate policies and with local, state and federal environmental, health and safety regulations</li>
<li>Other duties as assigned</li>
</ul>
Regulatory Responsibilities 
<ul>
<li>Assure cGMP compliance with regulatory agencies (FDA, EMA, etc.) </li>
<li>Ensure compliance with all local, state, federal, FDA, OSHA, cGMP or other applicable regulations</li>
</ul>
Supervisory Responsibilities
<ul>
<li>Balance team and individual responsibilities</li>
<li>Exhibit objectivity and openness to others' views</li>
<li>Give and welcome feedback</li>
<li>Contribute to building a positive team spirit</li>
<li>Put success of team above own interests</li>
<li>Build morale and group commitments to goals and objectives</li>
<li>Support everyone's efforts to succeed</li>
</ul>
Experience
<ul>
<li>Eight (8) to ten (10) years of supervisory/leadership experience in a GMP manufacturing environment with specific involvement with Operations, Quality and Compliance Management</li>
<li>Direct parenteral manufacturing/quality experience preferred</li>
<li>Experience in a Lean, Six Sigma or similar Operational Excellence system </li>
</ul>
Education
<ul>
<li>Bachelor’s degree from an accredited college or university with a major in Science, Engineering or is preferred </li>
<li>An equivalent combination of education and experience may be considered</li>
</ul>
Knowledge, Skills &amp; Abilities
<ul>
<li>Excellent teamwork</li>
<li>Ability to communicate clearly and cooperate with other staff members to achieve overall organizational objectives</li>
<li>Ability to coordinate work between functions to ensure alignment with overall department vision</li>
<li>Ability to promote urgency, ownership, and accountability across the organization</li>
<li>Skilled in relational databases and ability to use computerized software to support management reporting including word processing, spreadsheets, charts/graphs and presentations</li>
<li>Knowledge of FDA regulations, GMP/GLP/GCP, CFR 210, 211, 610, Part 11, and Parenteral Manufacturing Guidance (FDA/EU Annexes), Lean Manufacturing, Six-Sigma</li>
<li>Ability to set and achieve challenging goals</li>
<li>Ability to demonstrate persistence and overcome obstacles</li>
<li>Ability to measure self against standards of excellence</li>
<li>Ability to take calculated risks to accomplish goals</li>
</ul>
Physical Requirements

<ul>
<li>Ability to meet gowning requirements for cleanroom activities</li>
<li>Able to lift up to approximately 15-50 pounds frequently and up to 50 lbs. occasionally</li>
<li>Frequent standing and walking throughout the facility</li>
<li>Use of both hands and arms in repetitive motion</li>
<li>Fine and gross motor skills</li>
<li>Satisfactory audio-visual acuity</li>
</ul>

Director of Manufacturing

<h3>Job Description</h3>
Job Title: Mechanical Engineer IV
Location: Westboro, MA
Zip Code: 01581
Duration:12 Months
Pay Rate: $ 66.58 /hr
Keyword's: #Westborojobs; #Engineerjobs.
Start Date: Immediate
 
Job Description:
Key job responsibilities:
* Collaborate with cross-functional engineers to design and execute packaging machinery and automation projects
* Lead the mechanical design workstreams encompassing the core system evolution, structural member design including the modular frame, safety/guarding, and incorporation ancillary systems at the project / platform level while ensuring the technical, cost and timeline objectives are achieved
* Deliver engineering workstreams including drive system modeling, load and bearing calculations, static and dynamic torque simulations and analysis, 3D and 2D model design including the mechanical BOM generation
* Execute the detailed design evolution of modules and subsystems for material specifications, geographic requirements and continuous improvement goals aligned with
* MSP"s platform and project level initiatives
* Partner with the Electrical Engineering, ensure project documentation is complete and scalable for electrical schematics, BOM, I/O"s and subsystem programs
 
Qualifications: 
* Experience in developing functional specifications, design verification plans and functional test procedures
* Experience working with interdisciplinary teams to execute product design from concept to production
* BS in Mechanical or Mechatronics Engineering
* 8+ years of design experience for industrial automation
* Design of custom mechanical components
* Integration of sensors, actuators, and controls hardware with automated machinery
Proficiency in 3D design and simulation software including but not limited to Ansys, Creo, Catia, Solidworks
 
Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

Mechanical Design Engineer

<h3>Job Description</h3>
Position: Molding Process Set Up Technician 1st Shift Location: Fiskdale, Massachusetts Duration: Perm Placement Job ID: 173173 Job Overview: We are seeking a dedicated Molding Process Set Up Technician for the 1st shift to join our team. This role involves developing and ensuring manufacturing jobs are running a decoupled molding process, assisting in the design and installation of robotics, performing machine and auxiliary equipment changeovers, assisting in the transition of new jobs from engineering into production, and monitoring press performance on close tolerance jobs. The ideal candidate will have relevant experience and a commitment to quality and innovation. Responsibilities:
<ul>
<li>Develop and ensure manufacturing jobs are running a decoupled molding process.</li>
<li>Assist in the design and installation of robotics.</li>
<li>Perform machine and auxiliary equipment changeovers.</li>
<li>Assist in the transition of new jobs from engineering into production.</li>
<li>Monitor press performance on close tolerance jobs. </li>
</ul>
Qualifications:
<ul>
<li>1-3 years of experience as a Molding Process Technician (Preferred).</li>
<li>Proficiency in English (Required).</li>
<li>Ability to reliably commute or plan to relocate to Fiskdale, MA 01518 before starting work (Required).</li>
<li>Relocation assistance is not available for this position.</li>
<li>Visa sponsorship is not offered for this position.</li>
</ul>
Pay Range: $26.00–$36.00/hour (Full-Time)&nbsp; The specific compensation for this position will be determined by a number of factors, including the scope, complexity and location of the role as well as the cost of labor in the market; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. Our full-time consultants have access to benefits including medical, dental, vision and 401K contributions as well as any other PTO, sick leave, and other benefits mandated by appliable state or localities where you reside or work

Molding Process Set Up Technician 1st Shift

<h3>Job Description</h3>
Title: QC Investigations Specialist
Location: Greater Boston Area, MA (Onsite)
Employment Type: Contract
Status: Accepting Candidates
About the role
This role supports real-time manufacturing operations by leading investigations, resolving on-floor issues, and ensuring high-quality documentation. You’ll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance.
Key Responsibilities
• Triage manufacturing issues and lead analytical investigations and root cause analysis.
• Write clear, compliant quality documentation including deviations and CAPAs.
• Coordinate with SMEs to determine immediate actions, containment, and impact assessments.
• Interpret data to support structured problem-solving and continuous improvement.
• Provide technical operations support across manufacturing and QC functions.
Qualifications
• 6+ years pharmaceutical or biotech manufacturing experience.
• 4+ years analytical investigation and QC-focused experience.
• Strong background in RCA, deviation management, and GxP documentation.
• Ability to interpret analytical data and think scientifically under time-sensitive conditions.
• Experience partnering cross-functionally with manufacturing, QC, materials, and facilities teams.
Compensation (MA Pay Transparency):
• Estimated hourly range: $50–$55/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.
 
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