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Position Type: Full-Time Reports To: Piping Department Manager About Vermont Mechanical, Inc. Vermont Mechanical, Inc. is a leading mechanical contractor headquartered in Williston, Vermont, with a legacy of delivering expert HVAC and plumbing solutions across New England. With a reputation for integrity, craftsmanship, and innovation, the company has successfully executed projects in healthcare, education, manufacturing, hospitality, and government sectors. Notable clients include the University of Vermont Medical Center, Champlain Valley Physicians Hospital, and Dartmouth-Hitchcock. Vermont Mechanical prides itself on a collaborative, safety-first culture supported by over 300 professionals and a state-of-the-art fabrication facility. Role Overview Vermont Mechanical is seeking a skilled and motivated Healthcare-focused Piping Foreman to lead complex piping installations on healthcare projects. This role demands technical proficiency, leadership, and organizational insight to ensure that all work is completed safely, efficiently, and to the highest standard. The Foreman will be responsible for directing onsite activity, maintaining project momentum, and collaborating with internal teams and external partners to drive successful outcomes. Key Responsibilities Interpret blueprints and drawings to ensure precise implementation of plumbing systems; coordinate effectively with other trades to ensure integrated systems. Supervise and mentor onsite personnel, promoting a positive and professional jobsite culture. Monitor job schedule, manpower allocation, and budget adherence while maintaining a high standard of worksite appearance and safety. Generate material take-offs and coordinate procurement and delivery logistics. Oversee the installation of piping systems for water supply, drainage, gas, and mechanical systems. Ensure all work complies with applicable building codes and safety standards. Conduct system tests, troubleshoot issues, and prepare the site for inspections and walkthroughs. Facilitate communication across job sites and with other contractors to support seamless operations. Maintain site cleanliness, uphold safety policies, and properly care for tools and equipment. May assist other departments or operate equipment such as forklifts or construction lifts after training. Qualifications ASME 6010 Medical Gas Certification (or ability to start recertification within 90 days). Holds a current plumbing license in Vermont or New Hampshire, or can obtain one in NH within 90 days. Additional certifications preferred: VT Natural Gas or Propane, NH Gas Fitters. OSHA 10 certification required within 14 days of hire; OSHA 30 strongly preferred for leadership. High school diploma or GED (or equivalent experience). Valid driver's license and willingness to travel across VT, NH, and NY. Strong interpersonal and communication skills with the ability to lead, solve problems, and execute technical tasks independently and collaboratively. Physical capability to lift up to 100 pounds and work in construction environments, including at heights and in variable weather. Benefits Opportunities for ongoing training and certification A collaborative and safety-focused culture A chance to work on meaningful, large-scale healthcare projects Access to state-of-the-art equipment and facilities A Warm Invitation to Apply The Source and Recruit Company has been retained to support Vermont Mechanical in hiring for this important role. All inquiries will be handled with confidentiality. This is a dynamic opportunity for someone who takes pride in delivering high-quality mechanical work in mission-critical environments. Candidates from all backgrounds are encouraged to apply. Join a team where leadership, quality, and teamwork come together to make a difference. Equal Employment Opportunity Statement Vermont Mechanical, Inc. and The Source and Recruit Company are committed to creating a diverse environment and are proud to be equal opportunity employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Healthcare Piping Foreman

<h3>Job Description</h3>
Job Description
We are hiring a Press Operator to safely set up and operate stamping presses in a high-precision manufacturing environment. This role requires experience with single and progressive die sets and a commitment to safety, quality, and teamwork. Ideal candidates will have a strong mechanical aptitude, an eye for detail, and a desire to grow within a supportive and high-performing team.
Responsibilities include but are not limited to:
<ul>
<li>
Set up tools, feeders, payoffs, and coil straighteners
</li>
<li>
Handle, use, and install tooling and materials safely
</li>
<li>Perform visual and dimensional inspections to ensure product quality</li>
<li>Ensure proper materials, tools, and equipment are available and in good condition prior to production</li>
<li>
Follow process instructions to meet customer specifications
</li>
<li>
Operate related handling equipment safely
</li>
<li>
Maintain a clean and safety-oriented work environment
</li>
<li>
Follow all EPA, OSHA, and internal safety guidelines
</li>
<li>
Report incidents, near misses, and support a proactive safety culture
</li>
<li>
Participate in cross-training and perform other duties as assigned
</li>
</ul>
Compensation: Pay will be offered based on several factors including the candidate's education, work experience, work location, specific job duties, and certifications.
Benefits: We offer comprehensive benefits to include health, and an incentive recognition bonus (all benefits are based on eligibility).
Skills &amp; Qualifications:
<ul>
<li>
13 years of press operator experience preferred
</li>
<li>
High school diploma or equivalent preferred
</li>
<li>
Strong attention to detail with solid communication and multitasking skills
</li>
<li>
Ability to read and interpret blueprints and technical documents
</li>
<li>
Proficient with measuring tools including calipers, micrometers, gauge pins, and comparators
</li>
<li>
Must be able to read and write in English and follow both written and oral instructions
</li>
<li>
Must be willing and able to work overtime when needed
</li>
</ul>
Apply Today If youre a dedicated and safety-minded professional looking to grow with a quality-focused team, we want to hear from you!
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, or veteran status.

Press Operator

<h3>Job Description</h3>
Job Description
Position Summary
The Quality Systems Director is responsible for developing, implementing, and maintaining a robust Quality Management System (QMS) to ensure compliance with cGMP regulations (21 CFR Parts 210 &amp; 211), FDA aseptic processing guidelines, and EU GMP Annex 1.
Duties 
and Responsibilities
<ul>
<li>Lead the Quality Systems division within the QA Department, supporting the development, clinical, and commercial activities of pharmaceutical and biotech companies.</li>
<li>Oversee and maintain Quality Systems to ensure compliance with regulatory requirements. Key areas of focus include Document Control, Training Programs, Complaint Handling, Supplier Management, and Quality Management Systems (QMS).</li>
<li>Manage the Complaint Program, ensuring non-conformances are properly documented, investigated, and resolved through effective root cause analysis and corrective/preventive actions.</li>
<li>Oversee the Vendor Approval Program, ensuring outside vendors and suppliers meet compliance requirements through qualification and routine audits.</li>
<li>Develop and maintain Quality Agreements with clients and critical suppliers to ensure alignment on compliance and quality expectations.</li>
<li>Lead the Client Change Notification Program, ensuring timely and accurate communication of company changes to SSM clients.</li>
<li>Oversee the Client Audit Program, collaborating with cross-functional teams (Manufacturing, Quality Control, Warehouse, and Engineering) to maintain a continuous state of audit readiness.</li>
<li>Support regulatory inspections, working closely with the Head of Quality to prepare for inspections and respond to regulatory agency observations and requests.</li>
<li>Prepare and report quality metrics, providing actionable insights to senior leadership for decision-making.</li>
<li>Provide client support for ANDA/NDA submissions and pre-PAI/PLI inspections, ensuring compliance with regulatory expectations.</li>
<li>Conduct Annual Product Reviews (APRs) for client products, analyzing trends and ensuring ongoing compliance.</li>
<li>Stay current with evolving FDA (21 CFR 210/211), EU GMP, and industry regulations, advising executive management on necessary updates to the Quality Management System (QMS) to maintain compliance and drive improvements.</li>
<li>Foster strong cross-functional collaboration and ensure cGMP requirements and quality standards are understood and upheld across the organization.</li>
<li>Represent Quality Assurance at senior management, project, board, and review meetings, providing strategic input and leadership on quality initiatives.</li>
</ul>
Regulatory Responsibilities 
Position requires a broad knowledge of life sciences as they relate to the manufacture and testing of pharmaceutical drug products. Thorough knowledge of FDA / EU regulations, particularly as they relate to 21 CFR 210/211 and GMP manufacturing.
Supervisory Responsibilities
<ul>
<li>Provide leadership in daily quality operations, and have employees incorporate QA compliance practices into their daily routines. </li>
</ul>
Experience
<ul>
<li>Minimum of ten (10) years of pharmaceutical experience in a quality role</li>
<li>Minimum of five (5) years in a supervisor/managerial role </li>
</ul>
Education
<ul>
<li>Minimum of a Bachelor of Science Degree</li>
<li>Master’s Degree preferred </li>
<li>Auditor certification from an accredited institute preferred </li>
</ul>
Knowledge, Skills &amp; Abilities
<ul>
<li>In-depth knowledge in current Good Manufacturing Practices (cGMP), analytical chemistry, FDA requirements, ICH guidelines, USP methodology, and EU requirements as they pertain to the pharmaceutical industry.</li>
<li>Thorough knowledge of aseptic manufacturing processes.</li>
<li>ISO requirements and medical device experience is preferred.</li>
<li>Able to travel to vendors, customers and/or other contractual facilities as needed.</li>
<li>Technical writing and strong complex problem-solving skills.</li>
<li>Ability to effectively and clearly communicate, both written and verbally in English.</li>
<li>Detailed oriented</li>
</ul>
Physical Requirements

<ul>
<li>Ability to sit for prolonged periods of time</li>
<li>Ability to lift up to 10lbs</li>
<li>Ability to stand for prolong periods of time</li>
</ul>

Director of Quality Systems

<h3>Job Description</h3>
Job Description
Your Contribution
<ul>
<li>Provide for corrective, preventative, predictive, safety and emergency repairs to electrical machinery and electronic equipment utilized in manufacturing processes.</li>
<li>Ability to troubleshoot facility wiring, electronic controls, including servo/stepper motor controls, process equipment and general mechanical equipment.</li>
<li>Completes accurate records via an Enterprise Asset Management (EAM)</li>
<li>Troubleshoot machine and system failures on a timely basis in a production environment; provide appropriate corrective actions.</li>
<li>Use schematics, blueprints &amp; diagrams to find the sequence of operations to aid in effective troubleshooting of electronic hardware, vacuum systems, hydraulic systems, basic mechanical systems, and pneumatic systems.</li>
<li>Calibrate electronic controllers and maintain accurate records.</li>
<li>Provides project support on internal projects.</li>
<li>Assist Engineering personnel in conducting process and project evaluation and problem solving, must work in a team environment.</li>
<li>Assist in building and grounds maintenance when needed.</li>
<li>Moves, assembles, installs, adjusts, repairs and services all standard production machinery and equipment.</li>
<li>Maintains good housekeeping.</li>
<li>Works overtime as required and responds to emergency call-ins.</li>
</ul>
Your Profile
<ul>
<li>High School Diploma or equivalent.</li>
<li>Minimum two (2) years’ electromechanical training and PLC knowledge for troubleshooting and repair for production equipment.</li>
<li>Four (4) years’ experience in mechanical, electrical repair, and PLC troubleshooting and repair for production equipment.</li>
<li>Ability to read schematics, blueprints and diagrams.</li>
<li>Must be able to read, write, and speak English.</li>
<li>Effective verbal and written communication skills.</li>
<li>Computer proficiency and experience using Microsoft Office software.</li>
<li>Self-motivated and results oriented.</li>
<li>Ability to work in a team oriented environment.</li>
<li>Good manual dexterity and hand/eye coordination.</li>
<li>Due to the nature of work performed at this facility, US Person status may be required.</li>
</ul>

Electromechanical Technician (2nd shift)

<h3>Job Description</h3>
Job Description
Press Operator 1st shift 7:00am to 3:30pm 
Located in Wolfeboro, NH

About PSI Molded Plastics:
PSI Molded Plastics (PSIMP) is a plastic injection molding manufacturer with over 30 years in the plastics industry. PSIMP specializes in complex, high volume, quality molded products for the automotive, appliance, and furniture industries. PSIMP is focused on customer satisfaction, quality, &amp; continuous improvement with the goal of becoming a world-class plastics manufacturer.
PSIMP recognizes that people are the company’s greatest asset. We are committed to our established Guiding Principles to help build a culture where our team members enjoy coming to work every day. You aren’t just a number here at PSIMP, you’re a valued, appreciated, and respected part of the Team.

Summary/Objective:
The Press Operator is responsible for operating the machines and equipment used in the manufacturing of plastic injection molded product in accordance with standard operating procedures (SOP), including visual inspection, trimming, recordkeeping, packaging, and labeling. While performing the duties of this position, the Press Operator is responsible for maintaining a high degree of quality, safety, and efficiency. 

Duties and Responsibilities:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<ol>
<li>Responsible for operating one or more presses per shift, including operating manual presses within quoted cycle times.</li>
<li>Read and adhere to the information in the Process Operating Manual (POM) including the Point and Touch and any temporary work instructions. </li>
<li>Complete the press sign in sheet at the start of every shift or after starting a new job.</li>
<li>Perform the essential functions of the job within safety, quality, productivity, and performance standards as defined by company policy, procedures, and applicable work instructions.</li>
<li>Perform in-process visual inspection of all parts in accordance with the requirements stated in the POM or as otherwise stated per company quality standards.</li>
<li>Calibrate and use scale to weigh parts as required by POM.</li>
<li>Operate and use all tools safely including cutter, knives, etc.</li>
<li>Document rejected products in IQMS and attribute/SPC charts on an hourly basis. </li>
<li>Identify, properly contain, and label scrap/purging.</li>
<li>Properly and safely use grinder to re-grind parts according to work instructions. </li>
<li>Reporting any out-of-control conditions to the Shift Lead or Quality Auditor.</li>
<li>Perform any secondary processes.</li>
<li>Package and label products accurately as directed in the POM.</li>
<li>Perform rework as necessary.</li>
<li>Operate machines as assigned and assist co-workers at other workstations as needed.</li>
<li>Clean the machine and surrounding work areas to ensure the housekeeping and safety of the plant.</li>
<li>Participate in continuous improvement and safety initiatives.</li>
<li>Complete and pass all required training.</li>
</ol>
Perform other duties as assigned.

Press Operator 1st shift 7:00am to 3:30pm

<h3>Job Description</h3>
Job Description
Rochester Electronics is immediately hiring for a Senior Process Engineer!
At Rochester Electronics, we create an excellent employee experience focused on value, performance, motivation, recognition, and career growth. Many companies say their employees are their most important asset. At Rochester Electronics, we mean it! 
<ul>
<li>Outstanding low-cost medical, dental, vision, and prescription drug coverage, Rochester pays 92% of the premiums on behalf of its full-time employees</li>
<li>Paid time off, including vacation, sick, and holiday</li>
<li>Generous match 401K program</li>
<li>Tuition reimbursement</li>
<li>Flexible spending account</li>
</ul>
And so much more!
For the last 40 years, Rochester Electronics, in partnership with over 70 leading semiconductor manufacturers, has provided our valued customers with a continuous source of critical semiconductors. As an original manufacturer stocking distributor, Rochester has over 15 billion devices in stock encompassing more than 200,000-part numbers, providing the world’s most extensive range of end-of-life (EOL) and broadest range of active semiconductors. As a licensed semiconductor manufacturer, Rochester has manufactured over 20,000 device types. With over 12 billion die in stock, Rochester can manufacture over 70,000 device types.
General Summary
The Senior Process Engineer develops and documents manufacturing techniques, materials, tools and processes related to back-end semiconductor assembly. Performs analyses and selects techniques to solve problems and enhance product yield and process flows. 
Responsibilities
<ul>
<li>Establishes high-yielding, cost-effective processes based on product needs and customer requirements.</li>
<li>Maintains knowledge of new developments in manufacturing and design technologies.</li>
<li>Develops and executes Design of Experiments (DOE) for process optimization utilizing appropriate statistical analysis software, such as JUMP, Minitab, Excel Statistics, or equivalent. </li>
<li>Establishes processes based on product specifications.</li>
<li>Evaluate and validate the cost-effectiveness process and design alternatives based on product manufacturability.</li>
<li>Understands principles of cost of goods sold and develops process improvements to increase cost effectiveness of manufacturing.</li>
<li>Understands intellectual property issues relative to processes being developed.</li>
<li>Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors and vendors.</li>
<li>May serve as a member of cross-functional project teams.</li>
<li>Understands work environment issues (i.e. OSHA regulations, etc.).</li>
<li>Performs other related duties and responsibilities, on occasion, as assigned.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in the engineering discipline</li>
<li>A minimum of 5 years’ experience in manufacturing. Semiconductor experience preferred. </li>
<li>Working knowledge of MIL-PRF-38535, MIL-STD-883, ISO9001 and EIA/JEDEC and standards</li>
<li>Ability to work independently with little or no direct supervision.</li>
<li>Skills:
<ol>
<li>Ability to work within a team and as an individual contributor in a fast-paced, changing environment. </li>
<li>Strong verbal and written communication skills, with the ability to effectively communicate at multiple levels in the organization.</li>
<li>Ability to leverage and/or engage others to accomplish projects.</li>
<li>Proficient with Microsoft Office® software suite</li>
<li>Multitasks, prioritizes, and meets deadlines in a timely manner.</li>
<li>Strong organizational and follow-up skills, as well as attention to detail. </li>
</ol>
</li>
<li>As a Rochester Electronics employee, the individual is expected to positively support the Rochester culture and adhere strictly to work policies and practices set forth within the company. </li>
</ul>
 
Rochester Electronics is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, veteran status, or other characteristics protected by applicable law. Rochester Electronics is committed to a culturally diverse workforce.

Senior Process Engineer

<h3>Job Description</h3>
Job Description
Oar Staffing is conducting a search for PRODUCTION SUPERVISORS WITH FOOD INDUSTRY EXPERIENCE for the Second and Third Shift
6 Days Per Week 
 DIRECT HIRES Second Shift – $67,500 - $70,000 Third Shift - $70,000 - $75,000 MIMIMUM OF 2 YEARS’ SUPERVISORY EXPERIENCE IN FOOD MANUFACTURING 
OVERVIEW Oversee and manage the production to ensure maximize productivity in a safe manner. The Production Supervisor monitors employee’s performance, overseeing and collaborating with upper management to improve the manufacturing process, while assisting in solving technical issues with the maintenance of equipment. RESPONSIBILITIES • Interview, hire and train production staff • Manage the daily workflow • Enforcement of company policies related to food safety and company policies • Provide career guidance including evaluations and development of objectives • Resolve production line issues to ensure production goals are achieved • Other duties as assigned SKILLS/TRAINING • Minimum of 2 years’ experience supervisory role in a food manufacturing • Bachelor’s degree preferred • Excellent time management and Microsoft software skills • Problem Solving

PRODUCTION SUPERVISORS -- FOOD INDUSTRY EXPERIENCE - IMMEDIATE NEED

<h3>Job Description</h3>
Job Description
Press Operator (1st and 2nd Shifts) Position Summary:
We are seeking dedicated and reliable Press Operators to join our team at Cummings Printing in Hooksett, NH, for our 1st and 2nd Shift operations. As a Press Operator, you will play a crucial role in the production of high-quality printed materials using Sheetfed presses and other printing equipment. We offer on-the-job training and opportunities for growth within our dynamic and supportive work environment.
Responsibilities:
<ul>
<li>Operate Sheetfed presses and other printing equipment efficiently and safely.</li>
<li>Perform routine maintenance, cleaning, and troubleshooting on printing equipment as needed.</li>
<li>Monitor and maintain consistent print quality throughout production runs.</li>
<li>Follow job specifications and production schedules to meet deadlines.</li>
<li>Collaborate with team members to identify and address any issues that may arise during production.</li>
<li>Adhere to all safety procedures and regulations in the pressroom.</li>
<li>Ensure a clean and organized work area to maintain an efficient production environment.</li>
</ul>
Qualifications &amp; Requirements:
<ul>
<li>Willingness to learn and grow within the printing industry.</li>
<li>Strong mechanical aptitude and ability to troubleshoot equipment issues.</li>
<li>Attention to detail and ability to maintain consistent print quality.</li>
<li>Excellent communication and interpersonal skills.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Flexibility to work 1st and 2nd shift hours.</li>
</ul>
Work Schedule:
<ul>
<li>8-hour shifts</li>
</ul>
Benefits:
<ul>
<li>401(k) retirement plan.</li>
<li>Dental insurance.</li>
<li>Flexible spending account.</li>
<li>Health insurance.</li>
<li>Life insurance.</li>
<li>Vision Insurance.</li>
<li>Paid time off.</li>
</ul>
Work Location: Hooksett, NH
How to Apply:
If you are a dedicated individual looking to launch or advance your career in the printing industry, we want to hear from you! We look forward to reviewing your application and discussing the opportunity to join our team in Hooksett, NH.
Company DescriptionCummings Printing - A reputable, family run, veteran-owned full-service publication printer, providing quality products and services since 1914, with a strong focus on competitive pricing, flexible scheduling, and exceptional customer service. 
<h3>Company Description</h3>
Cummings Printing - A reputable, family run, veteran-owned full-service publication printer, providing quality products and services since 1914, with a strong focus on competitive pricing, flexible scheduling, and exceptional customer service.

Sheetfed Press Operator (1st and 2nd Shifts)

<h3>Job Description</h3>
Job DescriptionSalary: 
MEP Manager 
Position Overview
The MEP Manager oversees the successful integration, coordination, and execution of mechanical, electrical, plumbing, and related systems on large-scale construction projects. Working closely with the project team, subcontractors, and key stakeholders, the MEP Manager ensures project efficiency, quality, and compliance with design standards, codes, and schedules. This role requires technicalproficiency, exceptional organizational skills, and the ability to lead interdisciplinary teams through planning, execution, and closeout phases.
Key Responsibilities
1. Preconstruction &amp; Design Review 
<ul>
<li>Identifyconstructability issues and potential code violations early in the design phase. </li>
<li>Conduct surveys of existing buildings to ensure MEP system compatibility. </li>
<li>Review design documents to confirm compliance with project requirements and owner standards. </li>
<li>Coordinate MEP design progress to 100% construction readiness, issuing RFIs as needed. </li>
</ul>
2. Planning, Coordination, and Submittals 
<ul>
<li>Collaborate with the VDC department for clash detection and 3D modeling. </li>
<li>Participate in the buyout of MEP trades to ensure proper scoping and procurement. </li>
<li>Oversee submittal reviews to verify alignment with project specifications and schedules. </li>
<li>Manage composite coordination drawings, ensuring they are clash-free andsubmittedtimely. </li>
</ul>
3. Construction Process &amp; Quality Control 
<ul>
<li>Lead weekly coordination meetings andmaintainmeeting minutes. </li>
<li>Oversee field inspections and confirm that installations meet quality, design, and code requirements. </li>
<li>Coordinate shutdowns, impairments, and utility tie-ins as needed. </li>
<li>Work closely with manufacturers to ensure installation quality through workshops and field tutorials.</li>
</ul>
4. Risk Management &amp; Safety 
<ul>
<li>Implement company safety and quality control programs on-site. </li>
<li>EnsureSiteforminspections are performed asrequired. </li>
<li>Identifyrisks related to MEP systems and propose mitigation strategies. </li>
</ul>
5. Commissioning &amp; Closeout 
<ul>
<li>Develop commissioning schedules to meet project milestones.</li>
<li>Collaborate with the commissioning agent to address functional testing and deficiency closeouts. </li>
<li>Ensure proper documentation and inspections are completed for project handoff.</li>
</ul>
Qualifications &amp; Skills 
<ul>
<li>Bachelors degree in Construction Management, Engineering, or a related field (preferred). </li>
<li>Minimum of 3 years of experience in construction MEP management. </li>
<li>Knowledge of Procore, BIM software, and other construction tools. </li>
<li>Strong understanding of construction codes, safety regulations, and MEP systems. </li>
<li>Effective leadership, organizational, and communication skills. </li>
</ul>
Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics.

MEP Manager (MA Location)

<h3>Job Description</h3>
Job Description
Overview
Tradesmen International is looking to expand our team of qualified Trade Professionals for current &amp; future projects in and around Boston, MA. Most positions are first shift with a pay scale based on experience and skill level. If you are a Millwright and want to work alongside other proven Craftsmen who emphasize safety, productivity and superior workmanship, this is your chance to advance your career! 
Job Scope to include any or all of the following:
<ul>
<li>Installation, Maintenance, Repair of Industrial Machinery and Equipment</li>
<li>Conveyor Work</li>
<li>Installing Racking</li>
<li>Helping with Set Up, Remodel &amp; Assembling New Conveyors</li>
<li>Some Welding</li>
<li>General Labor, Job Site Clean Up</li>
<li>Moving/Relocating Machinery</li>
<li>Shut Down Work</li>
<li>Working at Heights at Times</li>
</ul>
Requirements:
<ul>
<li>
<ul>
<li>Mechanically Inclined</li>
<li>Basic Tools for the Trade</li>
<li>Proper PPE must be worn</li>
</ul>
</li>
</ul>
 
Qualifications
Tradesmen International not only offers consistent work, top pay, and employment opportunities, we also provide a benefits package that is among the best in the industry. 

Our comprehensive benefits include:
<ul>
<li>Vacation Pay</li>
<li>Health insurance</li>
<li>401(k) profit-sharing savings plan</li>
<li>Incentive programs</li>
<li>Tool purchase programs &amp; MORE!</li>
</ul>
Tradesmen International is an EO employer - M/F/Veteran/Disability

Click here to visit Tradesmen’s full website.

4,005 Manufacturing Jobs