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job_organization_name

city

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<h3>Job Description</h3>
Job Description
Position: Multiple Production Operator
???? Location: Franklin, MA | ???? Shift: Multiple Shifts -Full-Time 
2nd Shift 15% -Differential &amp; 3rd Shift 22.5% Differential

???? Join Our Team at Tegra Medical!
We’re a trusted contract manufacturer for some of the biggest names in the medical device industry. Known for taking on complex projects that others can’t, we pride ourselves on precision and innovation. Headquartered in Franklin, MA, Tegra Medical is part of the global SFS Group, based in Heerbrugg, Switzerland. Together, we’re shaping the future of healthcare.

If you’re passionate about making a difference and want to work on challenging, meaningful projects, check out our open positions and apply today!

????Your Role:
As a Production Operator, you’ll play a key part in our daily operations, ensuring products meet quality standards and production goals. You will manufacture medical products/components using manual and/or Laser/CNC/NC machine tools such as mill, lathe, grinder or EDM, applying industry standard machine tool techniques to ensure customer product requirements and Tegra Medical requirements are met.

????️ Responsibilities
<ul>
<li>Operate and monitor production equipment.</li>
<li>Assemble, inspect, and package finished goods.</li>
<li>Follow safety and quality protocols.</li>
<li>Collaborate with team members and supervisors</li>
</ul>

???? Qualifications
<ul>
<li>High school diploma or equivalent required.</li>
<li>Ability to lift up to 50 lbs and stand for extended periods</li>
<li>Strong attention to detail and reliability</li>
<li>Willingness to work flexible shifts and overtime</li>
</ul>

???? Benefits
<ul>
<li>On-the-job training and advancement opportunities</li>
<li>Good hourly wage + shift differentials (2nd &amp; 3rd Shift)</li>
<li>Great benefits like health, dental, vision, life, and disability insurance; 401K and much more.</li>
<li>Paid time off, sick time and holiday pay</li>
<li>Employee Assistance Program/ Tuition Reimbursement</li>
</ul>

Tegra Medical is an Equal Opportunity Employer
M/F/D/V

???? How to Apply: Submit your application via our ADP Career Center.
 
 1st shift 7:00am to 3:15pm 2nd shift 3:00pm to 11:115pm - Offers 15% shift differential 3rd shift 11:00pm to 7:15am - Offers 22.5% shift differential

Manufacturing Production Operator

<h3>Job Description</h3>
Job Description
Responsibilities:
<ul>
<li>Maintain and improve execution of production assignments</li>
<li>Review and distribute&nbsp;supplies and shipments&nbsp;in a timely manner&nbsp;</li>
<li>Confer with other departments to determine progress of work and completion dates</li>
<li>Compile reports on costs and inventory levels</li>
<li>Review and communicate production status reports&nbsp;</li>
<li>Serve as point of contact&nbsp;between production and planning teams</li>
</ul>
Qualifications:
<ul>
<li>Previous experience in production, planning, or other related fields</li>
<li>Strong project management skills</li>
<li>Ability to prioritize and multitask</li>
<li>Excellent written and verbal communication skills</li>
<li>Ability to work well in teams</li>
</ul>
Company DescriptionBlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers. 
<h3>Company Description</h3>
BlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers.

Production Planner

<h3>Job Description</h3>
Job DescriptionCompany Description 
Turner &amp; Townsend is a global professional services company with over 22,000 people in more than 60 countries.&nbsp;
Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people’s lives. Working in partnership makes it possible to deliver the world’s most impactful projects and programmes as we turn challenge into opportunity and complexity into success.&nbsp;
Our capabilities include programme, project, cost, asset and commercial management, controls and performance, procurement and supply chain, net zero and digital solutions.&nbsp;
We are majority-owned by CBRE Group, Inc., the world’s largest commercial real estate services and investment firm, with our partners holding a significant minority interest. Turner &amp; Townsend and CBRE work together to provide clients with the premier programme, project and cost management offering in markets around the world
Job Description 
Turner &amp; Townsend is seeking an experienced Senior Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering construction project control services.&nbsp;&nbsp;&nbsp;
Responsibilities:&nbsp;&nbsp;
<ul>
<li>
Develop, monitor and update owners' Project Integrated Master Schedule (IMS). &nbsp;
</li>
</ul>
<ul>
<li>
Establish the schedule management program and deliverables to be used on large scale capital programs. &nbsp;
</li>
</ul>
<ul>
<li>
Interface with project stakeholders as trusted advisors to provide guidance and recommendations for the project. &nbsp;
</li>
</ul>
<ul>
<li>
Prepare baseline schedules and schedule basis documents for approval by project teams. &nbsp;
</li>
</ul>
<ul>
<li>
Conduct schedule of resource loading and leveling. &nbsp;
</li>
</ul>
<ul>
<li>
Consolidate contractors schedule to incorporate into IMS. &nbsp;
</li>
</ul>
<ul>
<li>
Assess impacts on the critical path and near-critical activities and report to the project team. &nbsp;
</li>
</ul>
<ul>
<li>
Monitor schedule deviations and variances and assist in the development of alternative methods for corrective action. &nbsp;
</li>
</ul>
<ul>
<li>
Apply EVM methodology to measure project progress. &nbsp;
</li>
</ul>
<ul>
<li>
Review schedules with project team members on a regular basis to ensure that accurate and timely data is incorporated into the schedule. &nbsp;
</li>
</ul>
<ul>
<li>
Prepare and provide schedule progress reports, trending charts, and schedule analysis on a periodic basis. &nbsp;
</li>
</ul>
<ul>
<li>
Maintain record of scope changes, trends and variances that potentially affect schedule performance. &nbsp;
</li>
</ul>
<ul>
<li>
Assure the credibility of the information contained in the schedule. &nbsp;
</li>
</ul>
<ul>
<li>
Maintain liaison with clients and other consultants at all projects stages. &nbsp;
</li>
</ul>
<ul>
<li>
SOX control responsibilities may be part of this role, which are to be adhered to where applicable.&nbsp;
</li>
</ul>
Qualifications 
<ul>
<li>
Bachelor’s degree in construction management, cost management, quantity surveying, engineering or field related to construction.&nbsp;
</li>
</ul>
<ul>
<li>
Minimum 5-7 years of applicable experience.&nbsp;
</li>
</ul>
<ul>
<li>
Direct experience working on teams within a complex matrix environment. &nbsp;
</li>
</ul>
<ul>
<li>
Expertise using Primavera P6. &nbsp;
</li>
</ul>
<ul>
<li>
Excellent communication skills.&nbsp;&nbsp;
</li>
</ul>
 Additional Information 
Turner &amp; Townsend is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.&nbsp;Equal Employment Opportunity Posters&nbsp; If you’d like to view a copy of the company’s affirmative action plan, please email&nbsp;<a href="mailto:recruitmentUSA@turntown.com" target="_blank">recruitmentUSA@turntown.com</a>.&nbsp; If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact the Human Resources Department at 713-457-9400 or&nbsp;<a href="mailto:recruitmentUSA@turntown.com" target="_blank">recruitmentUSA@turntown.com</a>.&nbsp; This telephone line and email address is reserved solely for job seekers with disabilities requesting accessibility assistance or an accommodation in the job application process. Please do not call about the status of your job application if you do not require accessibility assistance or an accommodation. Messages left for other purposes, such as following up on an application or non-disability related technical issues, will not receive a response.
*On-site presence and requirements may change depending on our client's needs*&nbsp;
Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change.&nbsp;
We want our people to succeed both in work and life. To support this we promote a healthy, productive and flexible working environment that respects work-life balance.&nbsp;&nbsp;
Turner &amp; Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from all sectors of the community.&nbsp;
Please find out more about us at <a href="http://www.turnerandtownsend.com/" target="_blank">www.turnerandtownsend.com/</a> and <a href="https://www.heery.com/&amp;nbsp" target="_blank">https://www.heery.com/&amp;nbsp</a>;
All your information will be kept confidential according to EEO guidelines.&nbsp;
#LI-ES1
Join our social media conversations for more information about Turner &amp; Townsend and our exciting future projects:&nbsp;
Twitter
Instagram
LinkedIn

Senior Scheduler - Construction

<h3>Job Description</h3>
Job Description
Amphenol is one of the largest manufacturers of interconnect products in the world. The Company designs, manufactures and markets electrical, electronic and fiber optic connectors, coaxial and flat-ribbon cable, and interconnect systems. The primary end markets for the Company's products are communications and information processing. Including cable television, cellular telephone and data communication, storage, and information processing systems; aerospace and military electronics; and automotive, rail and other transportation and industrial applications. 
Position: Production Assembler
Location: Amphenol Ardent Concepts - Hampton, NH
Amphenol Ardent Concepts is a leading designer and manufacturer of high performance multicoax and coaxial assemblies, connectors, and sockets used in the development of next generation semiconductors and electronics systems. Our core technology is the smallest, fastest, and most electrically efficient compression mount connector technology worldwide. As data rate requirements increase and devices and systems shrink, Ardent Concept’s products deliver superior signal integrity in a dense footprint that can be reusable across programs to maximize cost savings.
No experience necessary. Willing to train crew members who demonstrate excellent hand/eye coordination with microscopic parts, who otherwise qualify. Candidates that have experience with arts and crafts, small model building, jewelry making, or small intricate mechanical devices may have the skills applicable to work with these micro assembly products
RESPONSIBILITIES: 
<ul>
<li>Micro assembly product lines while working through microscope</li>
<li>Prepare and assemble materials, build product subassemblies or final assemblies, plate product.</li>
<li>Test and inspect products or subassemblies for functionality and quality.</li>
<li>Set up and operate production fixtures and tools in accordance with good manufacturing practices and standard operating procedures.</li>
<li>Inspect finished products for quality and adherence to engineering prints.</li>
<li>Adhere to all applicable regulations, policies, and procedures for health, safety and environmental compliance.</li>
<li>Clean production equipment, products, and work areas.</li>
<li>Measure and record data associated with products.</li>
<li>Other tasks as assigned by supervisor.</li>
</ul>

QUALIFICATIONS: 
<ul>
<li>High level of hand/eye coordination with ability to work extended periods on a microscope</li>
<li>Ability to perform mathematical calculations</li>
<li>Familiarity with engineering drawings is preferred</li>
<li>High school diploma or equivalent</li>
<li>Physical agility</li>
</ul>
Position Type
This is a full-time, first shift position, M-Th 7:00 to 5:30PM. This job operates in a lab/manufacturing setting. While performing the duties of this job, the employee is frequently exposed to fumes and moving mechanical parts. The noise level in the work environment can be loud. Computers and machines are used, and the employee must be coordinated and have the ability to lift and or move up to 25 lbs. Specific vision abilities required by this job include close, distance, color, and peripheral vision. Must have depth perception and ability to adjust focus.
Amphenol Corporation is proud of our reputation as an excellent employer. Our main focus is to provide the highest level of support and responsiveness to both our employees and our customers, the world's largest technology companies. Amphenol Corporation offers the opportunity for career growth within a global organization. We believe that Amphenol Corporation is unique in that every employee, regardless of his or her position, has the ability to positively impact the business.
Amphenol is an “Equal Opportunity Employer” - Minority/Female/Disabled/Veteran/Sexual Orientation/ Gender Identity or National Origin
For additional company information please visit our website at <a href="http://www.amphenol-icc.com" target="_blank">www.amphenol-icc.com</a>
To apply please visit our website at <a href="https://www.amphenol-icc.com/careers/" target="_blank">https://www.amphenol-icc.com/careers/</a>

Assembler - Ardent Concepts

<h3>Job Description</h3>
Job DescriptionSalary: $32 
Westaff is seeking a Spanish Bilingual Production Supervisor for our client in Amherst NH!
 
3:15 pm - 12:45am Monday - Friday
 
Must be available to train on first shift
 
 
Responsibilities Include:
<ul>
<li>Assign machine operations, setups and material changes ensuring the most effective use of personnel to meetproductionobjectives</li>
<li>Plan and monitor job results. Troubleshoot when needed</li>
<li>Train and mentor employees. Discipline when necessary</li>
<li>Ensure that the prescribed safety measures are followed and that policies and procedures are followed</li>
</ul>
Requirements/Experience:
<ul>
<li>Minimum 5 yearssupervisory experience in a manufacturing environment</li>
<li>Should be familiar with AS9100 standards.</li>
<li>BS degree and experience with rubber or plastics preferred.</li>
<li>Excellent customer service, communication, analytical and problem-solving skills</li>
<li>Must be a team player and work well with all departments and individuals at all levels</li>
<li>Bilingual (Spanish) a plus</li>
</ul>

Benefits of working with Westaff include:
Health, Vision, Dental
Free online courses
Weekly pay
 
Apply now for immediate consideration!

Bilingual Production Supervisor - Amherst NH

<h3>Job Description</h3>
Job DescriptionCompany Overview: Merrimack Manufacturing is a&nbsp;medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that&nbsp;will play a crucial part in bringing innovative and life changing products to life. Position Overview: We’re looking for a detail-driven Production Planner to manage and optimize the manufacturing schedule of high-precision medical devices. This role is critical in ensuring product availability while maintaining regulatory compliance and rigorous quality standards. You’ll work closely with cross-functional teams to align production goals with customer demand, inventory targets, and operational capabilities. Responsibilities:
<ul>
<li>Create and adjust daily, weekly, and long-term production plans for medical device assembly and packaging</li>
<li>Coordinate with supply chain, quality assurance, and engineering to ensure timely material availability and readiness</li>
<li>Manage scheduling in compliance with FDA regulations and ISO 13485 standards</li>
<li>Monitor and analyze capacity, lead times, and productivity to identify constraints and propose improvements</li>
<li>Create and manage work orders to ensure on time delivery of orders.</li>
<li>Collaborate with the Quality and Regulatory teams on deviation reports and corrective actions related to production planning</li>
<li>Provide production forecasting to support new product launches and product lifecycle management</li>
</ul>
 Qualifications and Skills:
<ul>
<li>Experience in production planning within a medical device or highly regulated industry</li>
<li>Familiarity with FDA regulations, ISO 13485, and Good Manufacturing Practices (GMP)</li>
<li>Proficiency in ERP systems (e.g. Oracle, SAP) and advanced Excel skills</li>
<li>Strong analytical skills with keen attention to detail</li>
<li>Excellent communication and teamwork ability</li>
<li>APICS certification (CPIM or CSCP)</li>
<li>Experience working with sterilization, cleanroom environments, or Class I/II/III medical devices</li>
<li>Background in lean manufacturing or Six Sigma initiatives</li>
</ul>
 Education:
<ul>
<li>Bachelor’s degree in Business, Supply Chain, or equivalent experience.</li>
</ul>
Powered by JazzHR
yGfUMLxwuQ

<h3>Job Description</h3>
Basic Qualifications Requires a Bachelor's degree in Manufacturing or Industrial Engineering, or a related Science, Engineering or Mathematics field. Also requires 5+ years of job-related experience, or a Master's degree plus 3 years of job-related experience. CLEARANCE REQUIREMENTS: Department of Defense Secret security clearance is obtainable within a reasonable amount of time after hire. Applicants selected will be subject to a U.S. Government security investigation and must meet eligibility requirements for access to classified information. Due to the nature of work performed within our facilities, U.S. citizenship is required. Responsibilities for this Position As an Advanced Manufacturing Engineer at Pittsfield, Massachusetts, you'll be a member of a highly motivated cross functional team responsible for overcoming daily production challenges and continuously delivering on commitments. You are encouraged to apply if you have the knowledge and skills to develop, implement and maintain methods, operation sequence and processes in the manufacturing or fabrication of parts, components, sub-assemblies and final assemblies. Our Advanced Manufacturing Engineer will work collaboratively with fellow Manufacturing Engineering staff to continuously improve manufacturing process performance, transfer new products into production, product and problem diagnosis and repair. Support the development, qualification, verification, and validation of changes to existing product and manufacturing processes. Maximizes efficiency by analyzing equipment layouts, workflow, assembly methods, and work force and equipment utilization. Develops short-term and long-term operational strategies in partnership with team members and provides input necessary for the successful design, development, and execution of that strategy to achieve measurable outcomes in a timely, cost-effective manner. Primary responsibilities will include, but are not limited to, the following: 
<ul>\n
<li>Identify and improve the results of manufacturing and operational processes to improve efficiencies, reduce cost and increase customer satisfaction.</li>
\n
<li>Ensure the assigned operational processes are always capable to satisfy all GDMS, regulatory and industry requirements, and expectations applicable to our organization.</li>
\n
<li>Provide daily on-the-floor technical support working closely with Cell Leads, Supervisors, and fellow Engineers.</li>
\n
<li>Lead in conjunction with Quality personnel the MRB team meeting for analysis, material disposition, containment, and corrective actions definition.</li>
\n
<li>Lead in the selection, installation, and validation of process/packaging equipment utilizing project management tools, Risk Analysis, and Lean Manufacturing techniques.</li>
\n
<li>Develop and update existing manufacturing processes. Determine in-process testing and product final inspection requirements.</li>
\n
<li>Provide technical guidance to troubleshoot and remediate problems with existing production processes to ensure throughput.</li>
\n
<li>Ensure consistent operation and continuous adequacy of test equipment and test methods.</li>
\n
<li>Write process deviation and rework instructions as required.</li>
\n
<li>Responsible for creating and maintaining key process documentation such as Work Instructions, Workbooks, Routings, among others. Support the development of process documentation for new product(s) and changes to existing product(s).</li>
\n
<li>Responsible for setting up proper calibration plans for equipment and test equipment.</li>
\n
<li>Support process and design validation and equipment qualification tasks in association with project and engineering team(s).</li>
\n
<li>Early engagement in managing Production Readiness activity. Conduct review(s) to ensure that the documentation, production processes, test methods, production specifications, tooling and training are in place to support a controlled production environment.</li>
\n
<li>Responsible for improving manufacturing efficiency by analyzing and planning workflow, space requirements, and equipment layout.</li>
\n
<li>Responsible for Facility/Utility/Environment Design readiness with respect to introduction of new process to the manufacturing platform.</li>
\n
<li>Responsible for coordinating the creation of label templates in Brady Workstation or equivalent software.</li>
\n
<li>Support the engagement of the appropriate production personnel through process development to foster early learning and robust process transfer to production.</li>
\n
<li>Support fellow Manufacturing Engineers and Trainers to support the creation execution of SWIs and training.</li>
\n
<li>Analyze new designs for manufacturability; collaborate to improve product design related to enable process.</li>
\n
<li>Provide technical guidance to compose detailed machine specification documents.</li>
\n
<li>Support the procurement and installation of equipment to support existing equipment replacement.</li>
\n
<li>Collaborate with internal and external fabrication resources to ensure tooling builds are successful.</li>
\n
<li>Collaborate with fellow Manufacturing Engineers related to component builds, process and BOM development and other related activities.</li>
\n
<li>Utilize lean manufacturing tools to improve efficiency and quality of manufacturing operations.</li>
\n
<li>Review of proposed component tolerances and input to manufacturing capability. </li>
\n
<li>Engage in development and approval of packaging concepts for manufactured devices and/or subcomponents.</li>
\n
<li>Promote clear process communication and support training of assembly, test and inspection personnel.</li>
\n
<li>Promote communication, visibility, and accountability of transfer activity within team members and to key stakeholders.</li>
\n
<li>Provide critical input, analysis, support, and approval on engineering documentation; participate in design reviews.</li>
\n
<li>Maintain expertise in all GDMS products, their design details, product structure (BOM), manufacturing processes, and associated risks.</li>
\n
<li>Serve as subject matter expert for applicable areas of audits.</li>
\n
<li>Provide solutions to vendor issues as required.</li>
\n</ul>
\n Additional Responsibilities: 
<ul>\n
<li>Ensure conformance to the Quality Policy and Quality System procedures.</li>
\n
<li>Establish and maintain strong communication across functional areas without direct management responsibilities.</li>
\n
<li>Research, develop, and implement necessary systems, competencies, and tools required to improve capability and capacity of the team.</li>
\n
<li>Responsible for the appropriate record keeping of project outputs in accordance with recognized GDMS procedures.</li>
\n
<li>Provide input on and support for capital equipment purchases including tools and software.</li>
\n
<li>May need to work long hours when necessary to complete time sensitive projects.</li>
\n
<li>All other duties as assigned.</li>
\n</ul>
\n What sets you apart: 
<ul>\n
<li>Outstanding communication skills to interface with various engineering disciplines, manufacturing, senior leadership and our business development teams</li>
\n
<li>Recognized as an expert in your field</li>
\n
<li>Ability to multi-task</li>
\n
<li>Resolves complex problems through the use of ingenuity and creativity</li>
\n</ul>
\n Our Commitment to You: 
<ul>\n
<li>An exciting career path with opportunities for continuous learning and development.</li>
\n
<li>Competitive benefits, including 401k matching, flex time off, paid parental leave, healthcare benefits, health &amp; wellness programs, employee resource and social groups, and more</li>
\n
<li>See more at gdmissionsystems.com/careers/why-work-for-us/benefits</li>
\n</ul>
\n Workplace Options: 
<ul>
<li>This position is fully on-site where you will be part of the Pittsfield, Massachusetts team.</li>
</ul>
 Salary Note This estimate represents the typical salary range for this position based on experience and other factors (geographic location, etc.). Actual pay may vary. This job posting will remain open until the position is filled. Combined Salary Range USD $108,374.00 - USD $120,227.00 /Yr. Company Overview General Dynamics Mission Systems (GDMS) engineers a diverse portfolio of high technology solutions, products and services that enable customers to successfully execute missions across all domains of operation. With a global team of 12,000+ top professionals, we partner with the best in industry to expand the bounds of innovation in the defense and scientific arenas. Given the nature of our work and who we are, we value trust, honesty, alignment and transparency. We offer highly competitive benefits and pride ourselves in being a great place to work with a shared sense of purpose. You will also enjoy a flexible work environment where contributions are recognized and rewarded. If who we are and what we do resonates with you, we invite you to join our high-performance team! Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans

Advanced Manufacturing Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Manufacturing Technician Job Description
We are seeking a dedicated Manufacturing Technician to join our team on the 3rd Shift, which includes a 20% shift differential. The shift runs from Monday to Friday, 11:00 PM to 7:30 AM.
Responsibilities
<ul>
<li>Maintain a clean, organized, and safe work environment in compliance with GMP standards and safety protocols.</li>
<li>Proactively identify and report safety hazards and incidents.</li>
<li>Accurately complete GMP documentation and review basic records such as logbooks.</li>
<li>Assist in revising procedures under direct supervision.</li>
<li>Participate in investigations and support execution of Corrective and Preventive Actions (CAPA).</li>
<li>Contribute to small-scale continuous improvement initiatives.</li>
<li>Perform assigned production activities, ensuring all required training is completed and compliant prior to operations.</li>
<li>Apply basic problem-solving skills to identify abnormal results and escalate issues appropriately.</li>
<li>Demonstrate proficiency in designated process areas.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in pH testing, aseptic technique, buffer preparation, and UV-Vis spectroscopy.</li>
<li>Experience with GMP, UV-Vis, pH meters, purification, chromatography, and biotechnology.</li>
<li>Strong knowledge of basic laboratory instrumentation such as pH meters, UV instrumentation, and solution delivery systems.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High school diploma or equivalent with college-level Chemistry degree or equivalent work experience.</li>
<li>A biotechnology certificate or college degree is preferred.</li>
<li>Two plus years of experience in a cGMP manufacturing environment.</li>
</ul>
Work Environment
The role will be based in a GMP environment with an easygoing atmosphere where employees are encouraged to have fun while getting the work done. The company is committed to teamwork and camaraderie, offering a supportive and intimate setting where each employee can make a significant impact.
Job Type &amp; Location
This is a Contract to Hire position based out of Milford, MA.
Pay and Benefits
The pay range for this position is $29.00 - $34.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Milford,MA.
Application Deadline
This position is anticipated to close on Nov 26, 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 Description
This is a temp. to hire opportunity .
Do you have a mechanical aptitude ?
Are you are looking for a foot in the door opportunity that will include on the job training ?
If yes to the above and you are seeking a career opportunity , not just a job then this position may be for you !
Our client is a global co. with a manufacturing facility in Concord , NH .
This is a manufacturing / industrial environment .
Position requires prolonged standing and lifting up to 50 lbs .
Safety shoes required
Preemployment Drug screening and criminal background check required .
You will be trained in the set up and operation of grinding equipment used in the manufacturing process of compounded rubber components .
Key skills :
Basic computer skills , ability to read and work with precision measuring tools and mechanical prints .
Ability to work safely and follow basic safety precautions .
Experience with Forklift or overhead crane operation is a plus .
Pay rate : 23.00 hr.
&nbsp;
Company DescriptionThis company has little to no turnover and is looking for someone who wants to stay with a great company. Company offers outstanding benefits!! 
<h3>Company Description</h3>
This company has little to no turnover and is looking for someone who wants to stay with a great company. Company offers outstanding benefits!!

2nd Shift Machine Operator ( Grinder )

<h3>Job Description</h3>
Job Description
Start here, end here. There is a reason why we have so many employees with 20+ years with the company-Pace offers careers. Join us in becoming the premier die casting manufacturer and engineering solutions supplier worldwide.
Summary:
We're looking for a skilled Industrial Painter to join our team. In this role, you'll be responsible for spraying a variety of parts to precise tolerances and specifications using different types of paint. You must have a keen eye for detail and a commitment to safety and quality.
Compensation range: $20.00-$31.00
This is a full-time, first-shift position, with hours from 6:00 AM to 2:30 PM, Monday through Friday.
Benefits &amp; Perks
At Pace, we invest in our employees' well-being and future. We offer a comprehensive benefits package designed to support you both professionally and personally.
<ul>
<li>Comprehensive Health Benefits: Medical, Dental, Vision, and Life Insurance.</li>
<li>Secure Your Future: 401K with a generous company match.</li>
<li>Work-Life Balance: Paid time off (PTO), sick time, and 11 paid company holidays.</li>
<li>Invest in Your Growth: Tuition reimbursement and paid company training.</li>
<li>Career Advancement: Opportunities to grow within the company.</li>
</ul>
Job Functions:
<ul>
<li>Obtain paint specified for the job from the paint inventory.</li>
<li>Mix with appropriate thinner as required for spraying viscosity.</li>
<li>Mix two-part urethane paint and reducer</li>
<li>Spray paint parts to specifications</li>
<li>Inspect parts for compliance with customer’s specifications</li>
<li>Pour surplus paint into waste paint bucket beside booth for collection as hazardous waste by the material handler.</li>
<li>Wash gun with solvent and collect used solvent in second bucket beside booth for collection as hazardous waste by the material handler.</li>
<li>Pick up spills of hazardous waste promptly with absorbent material. Exercise care in handling hazardous waste and follow the hazardous waste procedures.</li>
<li>Replace filters and clean spray booth as required.</li>
<li>Move materials and perform housekeeping as required.</li>
</ul>
Skills and Experience:
<ul>
<li>Good eye/hand coordination, finger dexterity, and color sensitivity.</li>
<li>Ability to communicate clearly and effectively with others.</li>
<li>Ability to follow work instructions.</li>
<li>Performs jobs in a manner that minimizes hazards to self, others and the environment. Maintains a physical work environment that contributes to the well-being of others. Being aware of conditions or circumstances that affect one’s own safety or the safety of others.</li>
<li>Demonstrates a high level of dependability in all aspects of the job.</li>
</ul>
Required Experience:
<ul>
<li>Two years industrial spray painting or equivalent.</li>
<li>Must be able to pass respiratory physical</li>
</ul>
Physical Demands
<ul>
<li>
Occasionally moves equipment weighing up to 30 pounds.
</li>
<li>
Must be able to Ascend/Descend stairs.
</li>
<li>
Must be able to Sit, Stand, Walk, Climb, Stoop, Kneel.
</li>
</ul>

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