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New Hampshire Ball Bearing’s Astro Division is located in Laconia, NH—heart of the scenic Lakes Region. Astro is a World-Class 450+ person, climate-controlled manufacturing facility that produces spherical bearings, rod ends, sub-assemblies and other precision metal parts for the aerospace industry.
Manufacturing Supervisor
 This dynamic individual will be responsible for third shift (or 2nd ) department operations, employee supervision and will assist in the facilitation of planning for personnel, machines, equipment, and purchasing of supplies/raw materials. Position requires demonstrated leadership, providing coaching, training, mentoring and direction to employees to achieve department and company goals and metrics.&nbsp;
Must use considerable judgment to work independently toward resolutions and devise new and modify existing methods, techniques and procedures to meet production requirements. Educate and train personnel in relation to their job functions, as well as maintain established housekeeping practices.
 Associate’s Degree is preferred with a minimum of 5 years progressive supervisory experience in a fast paced manufacturing environment. NHBB is a company entrenched in Continuous Improvement. If you are interested in joining our progressive team, please mail, fax or email your resume to Human Resources at:
NHBB, Inc. Astro Division 155 Lexington Drive Laconia, NH 03246 <a href="http://www.nhbb.com" target="_blank">www.nhbb.com</a> Email: <a href="mailto:nparker@nhbb.com" target="_blank">nparker@nhbb.com</a>
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
 Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S.

MANUFACTURING SUPERVISOR

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The MFG Specialist in this role will be part of a cohesive team responsible for Deviation investigations, CAPAs, and Change Controls for all phases of manufacturing. The Manufacturing Specialist uses expert knowledge of cGMP regulations and project management to ensure manufacturing readiness and compliance. The incumbent will also support equipment, documentation and process operations improvement initiatives within Manufacturing. The MFG Specialist works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. 
This position is located in Lexington, MA and reports to the MFG Compliance and Improvement Manager.
ESSENTIAL JOB FUNCTIONS
Primary responsibilities include the following:
<ul>
<li>Practices and promotes safe work habits and adheres to safety procedures and guidelines</li>
<li>Utilizes manufacturing process knowledge and investigation skill to identify and resolve manufacturing issues, improve process operations and affect positive change.</li>
<li>Performs root cause analysis on Manufacturing quality events and leads investigations for minor and major quality events.</li>
<li>Identifies and drives Manufacturing corrective and/or preventative actions.</li>
<li>Provide Manufacturing support for tech transfers</li>
<li>Attend Change Control Review Meetings to present and resolve questions related to changes. Prepare assessments on changes impacting manufacturing.</li>
<li>Participates on cross functional teams to drive complex manufacturing operations changes or improvements</li>
<li>Supports document revisions and/or document management including batch production records and manufacturing procedures</li>
<li>Performs training with staff on the floor</li>
<li>Provides expertise for processing technology (chromatography, filtrations, digital systems, etc…)</li>
<li>Participates in cross-functional equipment and operational process improvement while teaming with Engineering, Validation, Quality Assurance, Quality Control, Facilities, and Manufacturing Science and Technology</li>
<li>Lead by example by demonstrating current good manufacturing practices, complying with standard operating procedures, and maintaining compliant manufacturing documentation.</li>
<li>Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion, with periodic management guidance</li>
<li>Reviews the work of others and provides feedback</li>
<li>Creates and presents trending and metrics reports</li>
<li>Participates in equipment start-up, commissioning, and validation activities</li>
<li>Works in a manner that requires consistent exercise of discretion and judgment</li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Normally requires 2 to 3 years related industry or manufacturing experience with a Bachelor's degree. A Master's degree with 1 to 2 years' experience will be considered as also acceptable.</li>
<li>Some experience with owning, investigating, and writing deviations, creating and executing CAPAs, and writing and managing Change Controls.</li>
<li>Ability to adhere to company internal and regulatory (EMA, FDA) policies, processes and procedures</li>
<li>Some experience in biomanufacturing unit operations (USP and/or DSP)</li>
<li>Good technical writing and oral communication skills</li>
<li>Hands-on experience in writing and reviewing documentation</li>
<li>Prior experience preferred performing root cause analysis using practices, such as Event &amp; Causal Factor Charting, Kepner-Tregoe Problem Analysis, and the basic Quality Improvement Tools (e.g., Pareto Chart, Control Chart, and Process Map, etc. and/or scientific methods</li>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
High School Diploma
Essential
Bachelor's Degree in Life Sciences/Engineering
Essential
Master's Degree in Life Sciences/Engineering
Desired
ON-THE-JOB EXPERIENCE

3-4 years related industry experience
Desired
SKILLS / ABILITIES

Ability to apply systems thinking as part of problem-solving
Essential
Demonstrates industrial empathy when working with stakeholders
Essential
Is detail oriented and able to self-organize
Essential
Is able to communicate in professional way on diverse levels and channels 
Essential
Is able to communicate in professional way on diverse levels and channels
Essential
Takes the initiative to own and resolve issues
Essential
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Regularly sit for long periods of time</li>
</ul>
Movement
<ul>
<li>Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 10 pounds</li>
<li>Rarely lift and/or move up to 25 pounds</li>
</ul>
Vision
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

MFG Specialist II - Compliance (1st Shift)

<h3>Job Description</h3>
Job Description
Empowering a Sustainable Future
Factorial develops breakthrough solid-state battery technology to enable safe, scalable, and high-performance cells for electric vehicles. Our portfolio of solid-state innovations includes the segment-leading FEST® (Factorial Electrolyte System Technology), which has been scaled in 100+Ah cells, works at room temperature, and is compatible with existing lithium-ion battery manufacturing equipment. With strong OEM backing, including joint development agreements with Mercedes-Benz, Stellantis, and Hyundai Motor Company, a world-class team of scientists, engineers, and business professionals, and cutting-edge R&amp;D facilities, Factorial is pushing the boundaries of battery technology. 
The Opportunity:
Factorial Energy is looking for a Cell Design Engineer – All Solid-State Battery, to join its Product Development team in Billerica, Massachusetts. The successful candidate will engage in Lithium rechargeable battery design-oriented tasks and will focus on the optimization of overall battery performance by controlling multiple aspects of the battery. This position requires a thorough understanding of how the battery works, how they are assembled and how the energy density can be affected by various parameters etc. Applicants must demonstrate excellent written and verbal communication skills.
Responsibilities:
- Spend at least 50% of your time inside Factorial's labs, working directly with our development teams - Design the cell by the multiple performance aspects (cycle life, energy density, power density etc.) - Review and feedback on the designed cell parameters to fine-tune them up to the customer's requirements. - Engage in cell failure root cause analysis if required. - Interface and work closely not only with the rest of cell design team but also with internal R&amp;D team, process team and production team to solve/mitigate the problems from the cell level. - Engage in responding to the customer requests by coordinating with the project managers. - Maintain compliance with all company protocols related to confidentiality, assignment of inventions, and other policies or duties as identified and assigned.
Qualifications:
- More than 5 years of industrial experience with all-solid-state cell design, including testing, data, and failure mechanism analysis. - Experience with pouch cell or prismatic cell is required - Strong communication skills (verbal and written) - Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Project). Knowledge of programming (i.e. Python) is a plus - Statistical analysis and Machine learning related skills are preferred. - Strong problem-solving skills and able to come up with creative solutions to challenges. - Willingness to execute multiple tasks in a fast-paced start-up environment.
Location: 805 Middlesex Turnpike, Billerica, MA 01821 
Factorial Energy is an equal opportunity employer that values diversity at all levels. All qualified applicants, regardless of personal characteristics, are encouraged to apply.
To request a reasonable accommodation to complete an application, job interview, and/or to otherwise participate in the hiring process, please contact <a href="mailto:recruitment@factorialenergy.com" target="_blank">recruitment@factorialenergy.com</a>

Cell Design Engineer - All Solid State Battery

<h3>Job Description</h3>
Job Description
Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future!
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness. We offer a competitive benefits package that includes health, dental, vision, wellness programs, employee discounts, retirement plans, tuition reimbursement, ongoing development, advancement opportunities and more. 
Founded in 1846, today HP Hood is one of the largest and most trusted food and beverage manufacturers in the United States. Our portfolio of national and super-regional brands and licensed products includes Hood, Heluva Good, Lactaid, Blue Diamond Almond Breeze, Planet Oat and more.
Job Summary:
The primary responsibility of this position is to safely and efficiently package quality products in a manner that is consistent with HP Hood LLC standards.
Shift: 10pm to 6.30am (Tuesday and Saturday off).
Start pay rate: $25.48 + 7% night shift diff.
Essential Functions:
<ul>
<li>Perform all tasks and functions related to operating and cleaning filling equipment.</li>
<li>Operate and clean multiple high speed filling machines in a sanitary, efficient, and effective manner.</li>
<li>Complete paperwork as per government regulations and HP Hood requirements.</li>
<li>Safely operate all assigned equipment following JHA requirements.</li>
<li>Consistently meet production quotas.</li>
<li>Comply with all policies and guidelines outlined for production and sanitation processes.</li>
<li>Participate in cross-training efforts to maximize departmental efficiency.</li>
<li>Work in a cooperative manner with managers, supervisors and peers.</li>
</ul>
General:
<ul>
<li>Follow all company safety policies and procedures. Able to demonstrate knowledge of safety areas reviewed in the safety orientation program.</li>
<li>Must be able to adapt to changing production schedules as necessary.</li>
<li>Execute assigned duties with minimal supervision.</li>
<li>Available for required overtime to support business needs and/or critical situations.</li>
<li>Perform assigned duties satisfactorily and in a timely manner.</li>
<li>Perform assigned duties following "Good Manufacturing Practices."</li>
<li>Actively participate in special teams representing the production department.</li>
<li>Maintain a clean &amp; safe work environment.</li>
<li>Perform all other related duties as assigned.</li>
</ul>
Qualifications, Education &amp; Experience:
<ul>
<li>High School Diploma or GED equivalent.</li>
<li>Reading &amp; writing proficiency (English language) and ability to identify colors.</li>
<li>Basic math skills.</li>
<li>Ability to work well as part of a team.</li>
<li>Good communication skills.</li>
<li>Multi-tasked individual.</li>
<li>Ability to work independently with little supervision.</li>
<li>Forklift certification required.</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to move at a quick pace. Frequently.</li>
<li>Standing: Long periods (up to 8 hours). </li>
<li>Sitting: Rarely.</li>
<li>Walking: Frequently.</li>
<li>Bending, Twisting &amp; Stretching: Occasional.</li>
<li>Lifting: Heavy (up to 50 lbs): Occasional.</li>
<li>Climbing: Ladders to make connections and add packaging materials. Occasional.</li>
<li>Pushing/Pulling: moving pallets of paper up to 200 lbs. Stock packaging materials: Occasional.</li>
<li>Environment: Wet and dry, temperature variations from 50 to 85 degrees Fahrenheit. Floors are wet and occasionally slippery due to product spills and the cleaning process (slip-resistant footwear is required). Constant.</li>
<li>Use of chemicals: Occasional.</li>
<li>Noise: Moderate to heavy (hearing protection is required). Constant.</li>
</ul>
Exact compensation may vary based on skills, experience and location.
The pay range for this position is$25.48—$27.83 USD
HP Hood is an Equal Opportunity Employer 
Female/Minority/Veteran/Disabled
"VERVRAA Federal Contractor"
Privacy Policy
CCPA
For Applicants in Massachusetts - It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Production Worker

<h3>Job Description</h3>
Job DescriptionCOMPANY OVERVIEW
Cresco Labs is one of the largest public, vertically integrated, multistate operators in the cannabis industry. Our portfolio of in-house cultivated and manufactured brands features some of the highest quality, most awarded and most popular cannabis products in America. With dozens of locations nationwide, our owned and operated Sunnyside® dispensaries provide a welcoming, positive, judgement-free place to shop for anyone at any point on their cannabis journey. Founded in 2013, Cresco Labs' mission is to normalize and professionalize cannabis through our passionate employees. As stewards of the cannabis industry, our teams are constantly focused on supporting the needs of our fellow colleagues, consumers, customers, and communities alike. With a focus on Social Equity and Educational Development, our SEEDTM initiative ensures that our company reflects the communities in which we serve, ensuring equal opportunity for all to have the knowledge and resources to work in and own businesses in cannabis. At Cresco Labs, we aim to revolutionize and lead the nation's cannabis industry with a focus on quality and consistency of product, and to bring legitimacy to the industry with the highest level of integrity and professionalism. If you're interested in joining our mission, click the below links to join our team today!
MISSION STATEMENT
At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
SCHEDULE
Monday to Friday, 7:00am to 3:30pm
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in our facility. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications &amp; checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (vape pens/cartridges), and food products (gummies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry. 
CORE JOB DUTIES
<ul>
<li>Performs incoming inspections  </li>
<li>Performs finished product sampling and inspection  </li>
<li>Maintains retain library  </li>
<li>Performs equipment and product line clearances before processing/production runs including but not limited to cleaning and sanitation verification, metal detector checks, and balance checks.  </li>
<li>Performs regulatory label review and approval prior to start-up  </li>
<li>Performs in-process verifications to ensure product weights, correct labeling &amp; packaging for transfer.  </li>
<li>Performs in-process ANSI inspections. </li>
<li>Performs verifications on finished product including but not limited to metal detection checks, label review, and record review. </li>
<li>Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product. </li>
<li>Inspects packaged orders to ensure correct content and quantities, as deemed necessary. </li>
<li>Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.</li>
<li>Monitors compliance to established Good Manufacturing Practice (GMP) guidance. </li>
<li>Reviews product quality standards and specifications to make sure they are available during production runs.   </li>
<li>Complete all required trainings on time.   </li>
<li>Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines. </li>
<li>Other duties as assigned </li>
<li>May require travel to other states or facilities to assist with inspections or quality issues.  </li>
</ul>
REQUIRED EXPERIENCE, EDUCATION AND SKILLS 
<ul>
<li>Bachelors Degree, OR 1-2 years experience &amp; an Associate Degree, OR 2+ years experience in a production environment   </li>
<li>Prior experience in a highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), FDA, HACCP, or SQ.   </li>
<li>Prior experience in Quality Assurance or Quality Control function desired  </li>
<li>Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired  </li>
<li>Ability to follow written procedures and monitor others for adherence to written procedures  </li>
<li>Ability to create or update written procedures with site operations personnel, as needed  </li>
<li>Strong written and verbal communication skills  </li>
<li>Detail-oriented </li>
<li>Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement solutions. </li>
<li>Requires work around plant material, which could include exposure to plant pollen and/or dust. </li>
<li>Requires ability to sit, stand, kneel, and/or do repetitive actions with your hands for long periods of time.  </li>
<li>Requires ability to lift up to 50 lbs to torso level. </li>
</ul>
BENEFITS
Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&amp;D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position.
In accordance with any local and state compensation laws, the compensation listed is the current estimated range for the position. Final offer details and future compensation may be determined by multiple factors including but not limited to, geographic location, market compensation data, skills, experience, and other relevant factors. For questions about this please discuss with your recruiter during the interview process. 
Pay Range$21—$21 USD
ADDITIONAL REQUIREMENTS
<ul>
<li>Must be 21 years of age or older to apply</li>
<li>Must comply with all legal or company regulations for working in the industry </li>
</ul>
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
California Consumer Privacy Act ("CCPA") Notice to Applicants:Please read the California Employee Privacy Notice ("CA Privacy Notice") regarding Sunnyside* and its affiliate Cresco Labs' policies pertaining to the collection, use, and disclosure of personal information. This CA Privacy Notice supplements the information contained in the Sunnyside* Privacy Policy and applies to California resident employees and job applicants. Applicants with disabilities may access this notice in an alternative format by contacting <a href="mailto:CCPAnotice@crescolabs.comReporting" target="_blank">CCPAnotice@crescolabs.comReporting</a> a Scam: Cresco Labs is aware of fictitious employment offers being circulated from various sources. Many of these schemes consist of an alleged offer of employment with Cresco Labs with the intention of gaining personal information, including payment and/or banking information. Be aware that fraudulent job offers and correspondence may appear legitimate: they may feature a Cresco Labs logo, they may appear to originate from an official-looking email address or web site, or they may be sent by individuals purporting to represent Cresco Labs or an entity which includes the word Cresco Labs in its name. Please note that Cresco Labs does not ask for payment or personal banking information as a condition of employment. Any personal information is requested for payroll or state badging purposes only. Applications can be securely submitted through our career's pages.We are working diligently to block this from happening. Beware if an offer of employment looks too good to be true. Never divulge personal and banking information or send money if you are unsure of the authenticity of an email or other communication in the name of Cresco Labs.If you are in doubt, please contact us at <a href="mailto:Report-a-spam@crescolabs.com" target="_blank">Report-a-spam@crescolabs.com</a> with questions.

Quality Assurance Technician - 1st shift

<h3>Job Description</h3>
Job Description
Position Summary
The Production Assembler III is responsible for assembling individual components into a finished product on a production line while following detailed instructions and quality standards. Assemblers often use hand tools and machinery to accurately position and fasten parts together, ensuring the final product meets required specifications. 
Minimum Qualifications
Education: 
<ul>
<li>High School Diploma or Equivalent</li>
<li>Advanced training in J-STD-001/IPC-620 standards</li>
</ul>
Experience: 
<ul>
<li>5 + years previous assembly experience required.</li>
</ul>
Knowledge: 
<ul>
<li>Working knowledge of basic assembly procedures. Previous knowledge of cable and wire harness assembly required.</li>
</ul>
Skills:
<ul>
<li>Manual dexterity</li>
<li>Attention to detail</li>
<li>Basic mechanical skills</li>
<li>Reading and Interpreting Written Instructions</li>
<li>Oral and Written Communication Skills</li>
</ul>
Job Responsibilities
<ul>
<li>Assemble assigned product parts on assembly line in accordance with production guidelines</li>
<li>Read and understand drawings, travelers, bills of material. </li>
<li>Use measuring tools, crimp tools, wire cutting equipment and stripping machines. </li>
<li>Hand crimping.</li>
<li>Spot tie and continuous lacing.</li>
<li>Heat shrink sleeving and boots. </li>
<li>Solder pins, contacts and solder cups, solder sleeves, bus wire splice</li>
<li>Perform job functions with minimum supervision.</li>
<li>Perform spot checks of products to ensure adherence to approved quality standards. </li>
<li>Notify management of product discrepancies or equipment malfunctions. </li>
<li>Adhere to established company policies and procedures paying special attention to safety regulations. </li>
<li>Wear personal protective equipment in accordance with training guidelines. </li>
<li>Maintain an organized and clean work area. </li>
<li>Perform other related duties as assigned. </li>
<li>Provide on-the-job training and coaching to new assemblers.</li>
<li>Attend required trainings for program specific requirements.</li>
</ul>
Internal and External Relationships
This position interacts with production, quality, and engineering departments on a regular basis
Physical Requirements
The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit or stand as needed. This position requires the ability to lift up to ten (10) lbs. The noise level in the work environment is usually quiet. 
About 603 Manufacturing
Located in Hudson, NH, 603 Manufacturing, a Trexon company, opened for business in 1998. We are an awarded manufacturer of cable assemblies and electro-mechanical assemblies. 603 Manufacturing is truly a diversified contract manufacturer, servicing the Defense, Aerospace, Industrial, Medical &amp; Commercial industries. We offer a comprehensive benefit package including a 9/80 work schedule.
603 Manufacturing is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. 603 Manufacturing is an E-Verify Participant. Pre-employment drug/alcohol/background screening is required.

Production Assembler III

<h3>Job Description</h3>
Job Description
Mechanical / Controls Engineer – Industrial Systems (Full-Time, Direct Hire) Location: Billerica, MA | Type: Direct Hire
We’re looking for a hands-on engineer with experience in instrumentation, controls, or mechanical systems to work on design/build projects in chemical process, life sciences, and environmental industries. If you’ve worked with industrial equipment, automation, or process systems, you’ll fit right in.
What You’ll Do:
<ul>
<li>
Design and specify instrumentation, controls, or mechanical systems for industrial projects
</li>
<li>
Develop I/O lists, loop diagrams, control panel layouts, or mechanical equipment layouts
</li>
<li>
Select and specify sensors, transmitters, PLCs, pumps, valves, and related equipment
</li>
<li>
Coordinate with vendors and assist with procurement
</li>
<li>
Support commissioning, testing, and troubleshooting on site
</li>
<li>
Collaborate across mechanical, electrical, and process engineering teams
</li>
</ul>
What You Bring:
<ul>
<li>
BS in Mechanical, Electrical, Chemical, or related engineering field
</li>
<li>
2+ years in instrumentation, controls, mechanical systems, or process engineering
</li>
<li>
Familiarity with PLC/DCS systems and/or industrial mechanical equipment
</li>
<li>
Knowledge of relevant standards (UL-508A, hazardous areas, ASME, etc.)
</li>
<li>
Strong problem-solving and communication skills
</li>
</ul>
Company DescriptionLooking to join a global leader at the forefront of solving today’s most complex challenges? You’ll work with multidisciplinary teams delivering innovative engineering, technical, and consultancy solutions that build smarter, more sustainable infrastructure—from advanced manufacturing and water systems to life sciences and critical facilities—backed by decades of proven success. 
<h3>Company Description</h3>
Looking to join a global leader at the forefront of solving today’s most complex challenges? You’ll work with multidisciplinary teams delivering innovative engineering, technical, and consultancy solutions that build smarter, more sustainable infrastructure—from advanced manufacturing and water systems to life sciences and critical facilities—backed by decades of proven success.

Mechanical / Controls Engineer

<h3>Job Description</h3>
Job Description
JOB PURPOSE: 
Provide technical support and operating knowledge for our medical extrusion process. This position will lead the effort in developing extrusion processes for new and existing product lines. This engineering position is a hands-on role that will support production extrusion and training extrusion technicians.
A successful candidate will have expertise in the hot melt extrusion of polymers for medical device applications. They shall provide technical support to the operations team as well as new product development. 
This is a unique opportunity to work on a novel material and application that requires adaption of melt extrusion processes. 
DUTIES &amp; RESPONSIBILITIES:
<ul>
<li>Analyze, research, design and develop an extrusion process for new and existing product lines.</li>
<li>Identify and source extrusion process equipment to support and expand production and product development capabilities.</li>
<li>Hands-on support of extrusion for production and development activities.</li>
<li>Gather and analyze product and process data to develop and maintain repeatable extrusion processes.</li>
<li>Develop and execute all validation activities related to the extrusion process.</li>
</ul>
QUALIFICATIONS:
<ul>
<li>A minimum of a Bachelor's degree in Plastics Engineering or Polymer Science, or a related Engineering discipline is required.</li>
<li>Minimum of 8 years of relevant extrusion experience.</li>
<li>Process engineering experience in a manufacturing environment is required.</li>
<li>Medical device experience is strongly preferred</li>
<li>Ability to respond to changing priorities and to multi-task in a dynamic environment</li>
<li>Basic understanding of quality systems and design control.</li>
<li>Working knowledge of a cleanroom environment and associated requirements, and a willingness to work in such environments is required.</li>
<li>Excellent time management, organizational, and prioritization skills to successfully complete a wide variety of complex job duties and responsibilities in a timely manner.</li>
<li>Ability to work in a team environment is required.</li>
<li>Hands-on work/understanding of extrusion theory and practice is required</li>
<li>Mechanical skills, including the ability to manipulate common hand tools, is required.</li>
</ul>
Physical Demands:
The physical activities described within the job posting are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Access Vascular, Inc is a proud Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status or disability status. 
About Access Vascular
Access Vascular was founded in 2015 to address the most common and costly complications of intravenous therapy: infection, thrombosis and phlebitis. The company is developing a suite of venous access devices made from patented biomaterials which are highly biocompatible and have demonstrated 6X fewer complications. .

Sr. Extrusion Engineer

<h3>Job Description</h3>
Job Description
Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity.
Xometry is seeking a highly skilled Staff Computational Engineer with a strong background processing three-dimensional models to help create the next generation of automated design for manufacturing (DFM) tools. In this role, you will analyze three-dimensional models for manufacturing feasibility and risk by combining underlying features with real world manufacturing constraints. This role requires someone with a strong understanding of computational geometry, algorithm analysis and code design.
Responsibilities:
<ul>
<li>Design, develop, and implement computational algorithms to solve complex engineering problems related to manufacturing processes (e.g., quoting, optimization, quality control).</li>
<li>Design, develop and deploy algorithms to extract geometric features from 2D and 3D CAD models.</li>
<li>Design, develop and deploy algorithms to detect Design for Manufacturability (DFM) issues of 2D and 3D CAD models.</li>
<li>Identify practical solutions to problems involving 2D and 3D geometry, topology, numerical analysis, manipulation of curves, surfaces and boundary representation topology.</li>
<li>Leverage machine learning and artificial intelligence techniques to improve efficiency and decision-making within the manufacturing platform.</li>
<li>Collaborate with operations and product teams to understand critical issues and develop novel solutions.</li>
<li>Collaborate with data scientists and software engineers to integrate computational solutions into Xometry's production workflows.</li>
<li>Document code and algorithms for maintainability and knowledge sharing.</li>
<li>Stay up-to-date on the latest advancements in computational engineering and related fields.</li>
</ul>
Qualifications:
<ul>
<li>M.S. or PhD degree in applied math, physics, computer science, or engineering required.</li>
<li>8+ years of progressive experience in applying computational methods to solve engineering problems with a proven track record of success.</li>
<li>Demonstrated experience in using CAD/CAE systems: surface modeling, solid modeling, part/assembly modeling, drafting.</li>
<li>Demonstrated experience in developing geometric modeling kernel, especially working with analytical geometry, parametric modeling, freeform geometry (NURBS, spline surfaces, Bézier curves), topological data structures (B-Rep scheme), geometry healing and repair, high-performance data structures and algorithms.</li>
<li>Participation in the development of 3D modeling applications, like SolidEdge, SmartPlant3D, SurfaceWorks, Autodesk Inventor, Pro-Engineer, SolidWorks, ACIS is a plus.</li>
<li>Demonstrated experience with HOOPS Exchange API, PRC and DXF format and specifications.</li>
<li>Research experience in computational geometry, differential geometry, computational fabrication, computational dynamics, or related fields.</li>
<li>Proficient in linear algebra, multivariable calculus, numerical methods, differential equations and other areas of scientific computation, like floating point arithmetic and numerical error analysis.</li>
<li>Familiarity with industry-specific standards (e.g., ISO, ASME) and guidelines for CAD/CAE software.</li>
<li>Strong knowledge of manufacturing processes and materials science.</li>
<li>Fluent in C++ (C++11/14/17), including tools like CMake, GDB, SWIG, etc.</li>
<li>Experience in Python, Cython, numpy, numba and cloud computing platforms a plus</li>
<li>Proficiency in software engineering best practices, including object-oriented design, code versioning, and testing.</li>
<li>Strong documentation skills for developing user manuals, technical reports, and internal documentation to support maintainability and reproducibility.</li>
<li>Must be a US Citizen or Green Card holder (ITAR).</li>
</ul>
#LI-Hybrid
Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
For US based roles: Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Staff Computational Engineer, 3D CAD

<h3>Job Description</h3>
Job Description
Vicarious Surgical is seeking an Advanced Manufacturing Engineering Co-Op to join our team in Waltham, MA for Fall of 2025. This role will be tasked with daily operational excellence, drive initiatives to develop new and optimize existing manufacturing processes and facilitate smooth transitions through the new product development process. The team is a collaborative group that connects all departments. You will interact with R&amp;D, Manufacturing, and Quality teams. To be considered, you must be available for 6 months and be local to Waltham, MA.
Vicarious Surgical is a next generation robotics company developing a disruptive technology with the goal of increasing the efficiency of surgical procedure, improving patient outcomes, and reducing healthcare costs. 
This is a terrific opportunity for an Engineering student to join our company at a very exciting time and be a member of a team of mission-driven and kind individuals with diverse experiences to lead Vicarious into its next phase of hyper-growth and market disruption. 
Team Focus
As part of the Operations Advanced Manufacturing Engineering team, you will focus on daily operational excellence, drive initiatives to develop new and optimize existing manufacturing processes and facilitate smooth transitions through the new product development process. The team is a collaborative group that connects all departments. You will interact with R&amp;D, Manufacturing, and Quality teams.
Project Work
<ul>
<li>Develop, iterate and optimize manufacturing work instructions and standard operating procedures for Vicarious Surgical's electromechanical capital and single use products</li>
<li>Assist in the design, construction and validation of manufacturing assembly and test equipment</li>
<li> Contribute on product teams supporting Design for Manufacturing (DFM) elements and ensuring process capabilities meet targets for all design specifications</li>
<li> Assemble electro-mechanical components. Conduct basic product testing.</li>
<li>Support our assembly, inspection , supply chain, shop organization and more</li>
<li>Support document control with processing data records</li>
<li>Design, develop, and release templates for product development testing, manufacturing, and inspections</li>
</ul>
About You
<ul>
<li>Currently enrolled in an Undergraduate program in Engineering </li>
<li>Competent with use of Google workspace and Microsoft Office Suite.</li>
<li>Ability to quickly learn business related software including NetSuite, MasterControl, etc.</li>
<li>Well-organized with a right first-time approach</li>
<li>Strong communication skills</li>
<li>Ability to work cross-functionally in a fast-paced environment</li>
<li>Ability to write simple reports and business correspondence.</li>
</ul>

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