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<h3>Job Description</h3>
Job DescriptionJOB SUMMARY: The Heat Seal Press Operator level 1 is responsible for transferring heat applied decorations to product while maintaining a high level of quality and production. COMPENSATION: The hourly pay range reflects the actual compensation that Ahead, LLC; the employer reasonably expects to pay for the position at the time of hire. The final offer will be determined by a candidate's experience, skills, and qualifications.
<ul>
<li>$17.00&nbsp;- $18.00&nbsp;per hour</li>
</ul>
SUPERVISORY RESPONSIBILITIES:
<ul>
<li>None</li>
</ul>
DUTIES/RESPONSIBILITIES:
<ul>
<li>Meet and exceed production standards.</li>
<li>Meet and exceed quality standards.</li>
<li>Verifying products and components are correct for order.</li>
<li>Prepare products for production.</li>
<li>Prepare heat press for production.</li>
<li>Ensure excellent quality for decorations/products produced.</li>
</ul>
REQUIRED SKILLS/ABILITIES:
<ul>
<li>Ability to read instructions in English.</li>
<li>Possess a positive attitude.</li>
<li>Excellent attention to detail.</li>
<li>Ability to solve problems.</li>
<li>Ability to multi-task under pressure in a fast-paced environment.</li>
<li>Must possess initiative, energy, and drive.</li>
<li>Excellent organizational skills.</li>
<li>Ability to perform quality control.</li>
<li>Ability to maintain good working relationships with co-workers and management.</li>
<li>Additional duties as assigned.</li>
</ul>
&nbsp;EDUCATION AND EXPERIENCE:
<ul>
<li>High school diploma or GED.</li>
<li>Manufacturing experience preferred.</li>
</ul>
PHYSICAL DEMANDS:
<ul>
<li>Ability to stand for extended periods of time.</li>
<li>Ability to move around the facility.</li>
<li>Ability to move, reach, kneel and crouch.</li>
<li>Ability to use hands, fingers, and arms to touch, handle, pinch, or grasp.</li>
<li>Ability to lift 50 pounds.</li>
<li>Ability to wear Personal Protective Equipment (PPE) as needed.</li>
</ul>
WORK ENVIRONMENT:
<ul>
<li>Exposure to moderate noise level.</li>
</ul>
VISION REQUIREMENT:
<ul>
<li>Close vision</li>
<li>Color vision</li>
<li>Ability to adjust focus.</li>
</ul>
PERSONAL PROTECTIVE EQUIPMENT:
<ul>
<li>Closed toe footwear is required when entering the Production Floor. </li>
</ul>
SCHEDULE:
<ul>
<li>3:30 pm – 12:00 am Monday – Friday with Overtime (during the week) as required.</li>
</ul>
DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended or to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. Ahead, LLC is a socially responsible company and an Equal Opportunity Employer. &nbsp;
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SCxD1jGtK4

Heat Seal Press Operator 1

<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: This positon will support manufacturing quality operations in a dynamic, fast-paced, medical device-manufacturing environment. This environment includes the manufacture, inspection, and test of devices for design verification, design validation, and commercial production. RESPONSIBILITIES:
<ul>
<li>Working under the direction of the Quality Manager, ensure all product, processes, and components are within specifications.</li>
<li>This position may also serve as a member on collaborative cross-functional teams, to support new product development efforts, commercial production, material-related design changes, and manufacturing and process changes, risk management activities, and other compliance projects.</li>
<li>Work in compliance with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016.</li>
<li>Lead the Device History Records (DHR) review and approval process.</li>
<li>Lead nonconformance reports (NCR) and CAPA investigations.</li>
<li>Lead the development and implementation of PFMEAs and control plans. </li>
<li>Lead process and equipment validation activities (IQ, OQ, PQ/PV, TMV).</li>
<li>Lead manufacturing and quality system improvements.</li>
<li>Lead customer feedback process and investigations.</li>
<li>Author Engineering Change Orders (CO); support CO implementation tasks</li>
<li>Use experience with engineering and technology to ensure compliance with applicable standards and regulations. </li>
<li>Position requires daily contact with members of Production, Engineering, Materials, and Quality departments.&nbsp; </li>
<li>Routine contact with design authority and customers; occasional contact with auditors</li>
</ul>
 QUALIFICATIONS AND SKILLS:
<ul>
<li>5+ years of experience related to the manufacturing of medical devices in a QMS environment while being in a Quality Control or Engineering role</li>
<li>Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 is required</li>
<li>Experience with Microsoft Office software (Word, Outlook, Excel) required</li>
<li>Experience participating in internal and external audits</li>
<li>Strong project management, prioritization and leadership skills are required</li>
<li>Must be able to manage multiple priorities</li>
<li>Performing statistical data analysis using Minitab or equivalent</li>
<li>Presenting and leading meetings with an audience of peers and senior management level</li>
<li>Use critical thinking and deductive reasoning to make risk based decisions</li>
<li>Knowledge and comprehensive understanding of CAPAs, root cause analysis, and the 8D method</li>
<li>Excellent oral communication and technical writing skills</li>
<li>High level of attention to detail and accuracy</li>
</ul>
 EDUCATION: Bachelor’s degree or equivalent experience in Manufacturing, Mechanical or related engineering / life sciences related discipline. &nbsp;
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6LGZihpiv4

Sr. Quality Engineer

<h3>Job Description</h3>
Job DescriptionSupplier Quality Engineer (SQE) Job Description: The SQE is a strong leader with demonstrated project management skills coupled with Supply Chain experience. The person will be responsible for developing and executing supply chain strategies and plans in support of proposals and/or awarded programs. The person will serve as the liaison between the Quality Manager, functional support organizations (i.e. engineering, finance, contracts) and the Supply Chain organization, and will enable communications across all these parties and will advise the SC and Quality purchasing on status of material strategies and plans throughout the capture, proposal and program lifecycle. &nbsp;The person will serve as single point of contact to SC and Quality, overseeing all SC activities needed to meet program requirements, and ensuring a strong link within and between the various Supply Chain functions required to execute a successful program. Responsibilities:
<ul>
<li>Must be able to effectively partner with engineering to develop accurate Bill of Materials (BOM’s), control changes in the BOM during the proposal process and promptly flow any changes to material pricing and develop a strategy to get representative costs.</li>
<li>Develop and execute material program plans together with the purchasing team and program managers.</li>
<li>Develop and maintain risk &amp; opportunity plans to meet program objectives.</li>
<li>Work closely with Engineering, Quality and Operations to create common schedule based on Material Requirements Planning (MRP).</li>
<li>Work closely with suppliers to ensure scheduled delivery</li>
<li>Conduct periodic source inspections</li>
<li>Monitor performance metrics and proactively act to address program and functional issues.</li>
<li>Maintain a regular and predictable work schedule.</li>
<li>Audit suppliers as needed.</li>
<li>Perform other duties as necessary.</li>
</ul>
 Requirements:
<ul>
<li>BS/BA in related field plus 5 years or more related experience.</li>
<li>Related technical experience may be considered in lieu of education. </li>
<li>Able to travel up to 60% of your time. (70% local suppliers)</li>
<li>Excellent communication skills</li>
<li>Organizational skills</li>
<li>Familiar with machined parts</li>
<li>Familiar with various types of metals and ceramics</li>
<li>Knowledge of Advanced Product Quality Planning (APQP)</li>
<li>Knowledge of Production Part Approval Process (PPAP)</li>
<li>GD&amp;T (Geometric Dimensioning and Tolerancing) Experience</li>
<li>ISO 9001:2015 or AS9100D awareness</li>
</ul>
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ag7T41X6YZ

Supplier Quality Engineer

<h3>Job Description</h3>
Job DescriptionThe production equipment technician apprentice responsible for routine maintenance of our embroidery machines, heat seal presses, digital printers and laser machines. Work Schedule
<ul>
<li>7:00 am – 3:30 pm Monday – Friday with Overtime (Saturday 7am – noon) as required.&nbsp;</li>
</ul>
Compensation:&nbsp;The hourly pay range&nbsp;reflects the actual compensation that Ahead, LLC; the employer reasonably expects to pay for the position at the time of hire.&nbsp;&nbsp;The final offer will be determined by a candidate's experience, skills, and qualifications.
<ul>
<li>$19.00 - $21.00&nbsp;per hour</li>
</ul>
 Essential Duties and Responsibilities
<ul>
<li>Repair of Cap Frames &amp; other machine attachments.</li>
<li>Cleaning, lubrication and minor repairs of embroidery machines.</li>
<li>PM on all machinery.</li>
<li>Daily record keeping of machine tasks performed.</li>
<li>Additional duties as assigned.</li>
</ul>
Education and Experience
<ul>
<li>High school diploma or equivalent preferred. </li>
</ul>
Skills/Qualifications
<ul>
<li>Ability to follow verbal directions.</li>
<li>Ability to read instructions in English.</li>
<li>Ability to work in a team environment.</li>
<li>Ability to work in a fast paced environment.</li>
<li>Ability to perform troubleshooting/problem solving tasks.</li>
<li>Ability to work with tools and machinery.</li>
<li>Skill set to learn how to troubleshoot and repair all equipment.</li>
</ul>
Supervisory Responsibilities
<ul>
<li>None</li>
</ul>
Physical Demands
<ul>
<li>Ability to stand for extended periods of time.</li>
<li>Repetitive use of hands, fingers and arms.</li>
<li>Ability to demonstrate fine dexterity skills.</li>
<li>Ability to move about the facility.</li>
<li>Ability to climb, bend, reach, kneel and crouch.</li>
<li>Ability to lift up to 25 pounds.</li>
<li>Ability to wear Personal Protective Equipment (PPE) as needed.</li>
</ul>
Vision Requirements
<ul>
<li>Close and distance vision.</li>
<li>Vision to be able to thread a needle.</li>
<li>Color vision.</li>
</ul>
Work Environment
<ul>
<li>Exposure to loud noise level.</li>
</ul>
 The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended or to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. Ahead, LLC is a socially responsible company and an Equal Opportunity Employer. ​​​​​
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1NtsEeaUAC

Embroidery Machine Tech Apprentice

<h3>Job Description</h3>
Job DescriptionWe are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes. Join our growing Clinical QA team ensuring our medical device software meets the highest standards of clinical accuracy and regulatory compliance! Our CQA team&nbsp;collaborates across software development, quality, clinical and regulatory teams, acting as quality advocate on behalf of patient and physician needs throughout the software development lifecycle. As a Senior Clinical Validation Engineer, you’ll be at the forefront of advancing our AI-powered cardiovascular imaging software. In this role, you’ll lead validation for major system enhancements and new product launches, ensuring our software meets the highest standards of clinical performance and regulatory compliance. Leveraging your expertise in SaMD validation, medical device regulation, and cardiovascular imaging, you’ll drive cross-functional initiatives, oversee rigorous testing and documentation, and serve as a trusted subject matter expert. Your work will play a key role in delivering a safe, effective, and potentially life-saving solution empowering physicians and transforming patient care. The ideal candidate will have:
<ul>
<li>Degree in biomedical engineering, radiology technology, computer science or&nbsp;related field with 5+ years of SaMD validation or clinical QA experience. or,&nbsp;Advanced degree in a related field with 3+ years of relevant experience.</li>
<li>Excellent communication, collaboration, and decision-making skills, with the ability to translate complex technical concepts into clear, accessible language and influence stakeholders across diverse teams and organizational levels.</li>
<li>Demonstrated ability to guide cross-functional teams, manage multiple complex projects, and make risk-based decisions to ensure high-quality outcomes in a fast-paced startup environment.</li>
<li>Strong understanding of medical software systems, applicable regulatory standards,&nbsp;and their integration into clinical workflows.</li>
<li>Prior experience working with with medical imaging (CTA), AI-enabled clinical software, or cardiovascular diagnostics.</li>
<li>Strong experience using Jira.</li>
<li>Knowledge of cardiovascular disease and anatomy.</li>
<li>Experience in a startup or small to mid-size organization preferred.</li>
</ul>
Work Location:
<ul>
<li>This role is based out of our office in Boston, MA. For local candidates, we operate in a hybrid model with regular in-office collaboration. Candidates outside of the Boston area are invited to apply as fully-remote employees.</li>
</ul>
Salary Range:
<ul>
<li>The anticipated base salary range for this position at Elucid is $140,000 - $165,000. Compensation will be influenced by a wide array of factors including but not limited to internal pay equity, job-related knowledge, skills, education, relevant experience, certifications, and geography as outlined in the job description.</li>
</ul>
----------------------------------------------------
At Elucid, we believe the best work happens in a flexible hybrid environment. Boston-area employees are encouraged to work from the office on Mondays and Wednesdays, with the option to come in additional days if they prefer. Fully remote employees outside the Boston area come in as needed.
We are an equal opportunity employer and value diversity at Elucid. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability.
We understand that self-doubt can sometimes prevent great candidates from applying. If you believe you can make an impact at Elucid, even if you don’t meet every qualification, we encourage you to apply!
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1vDw9MofRk

Senior Clinical Validation Engineer

<h3>Job Description</h3>
Job Description
In-Process Inspector (Contract)
Location: Natick, MA Company: Busek Co. Inc. Job Type: Full-Time
About Busek:
Busek Co. Inc. is a leading innovator in advanced space propulsion and systems. Our pioneering technologies, including Hall thrusters, electrospray propulsion, and solar electric propulsion, enable next-generation spacecraft to achieve greater performance and efficiency. We seek a meticulous and experienced In-Process Inspector to ensure our high-quality manufacturing standards are upheld.
Position Overview:
The In-Process Inspector will be responsible for performing inspections of precision-manufactured components and assemblies during various stages of production. This role requires a keen eye for detail, strong knowledge of inspection tools and techniques, and the ability to read and interpret engineering drawings and specifications.
Key Responsibilities:
<ul>
<li>
Perform in-process inspections of machined, assembled, and fabricated components to ensure compliance with engineering drawings, specifications, and industry standards.
</li>
<li>
Utilize precision measurement tools such as calipers, micrometers, height gauges, and CMM (Coordinate Measuring Machines) to verify dimensional accuracy.
</li>
<li>
Interpret blueprints, GD&amp;T (Geometric Dimensioning &amp; Tolerancing), and technical documentation.
</li>
<li>
Document inspection results and generate reports, including non-conformance reports (NCRs) when necessary.
</li>
<li>
Collaborate with machinists, engineers, and quality personnel to identify and resolve manufacturing discrepancies.
</li>
<li>
Ensure compliance with AS9100 and ISO 9001 quality management systems.
</li>
<li>
Maintain inspection records and assist with internal and external audits.
</li>
<li>
Recommend process improvements to enhance quality and efficiency.
</li>
</ul>
Qualifications &amp; Experience:
<ul>
<li>
3+ years of experience in in-process inspection within an aerospace, defense, or precision machining environment.
</li>
<li>
Strong proficiency in using precision measurement tools and interpreting engineering drawings.
</li>
<li>
Knowledge of GD&amp;T principles and AS9100/ISO 9001 quality standards.
</li>
<li>
Ability to work independently and in a team-oriented environment.
</li>
<li>
Strong attention to detail and documentation skills.
</li>
<li>
Proficiency with Microsoft Office (Word, Excel) and familiarity with ERP/MRP systems.
</li>
<li>
U.S. Citizenship or Permanent Residency required due to government contract requirements.
</li>
</ul>
Why Join Busek?
<ul>
<li>
Work on cutting-edge space propulsion technology.
</li>
<li>
Competitive compensation and benefits package.
</li>
<li>
Collaborative and innovative work environment.
</li>
<li>
Opportunities for career growth and professional development.
</li>
</ul>
If you are passionate about quality assurance and precision inspection in the aerospace industry, we encourage you to apply for this exciting opportunity at Busek. To comply with U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR), employment at Busek requires that applicants be one of the following:
<ul>
<li>A U.S. citizen</li>
<li>A lawful U.S. permanent resident (i.e., current Green Card holder)</li>
<li>A refugee or an individual granted asylum in the U.S.</li>
<li>Or be eligible to receive the required authorizations from the U.S. Department of State and/or the U.S. Department of Commerce, as applicable</li>
</ul>
For more information about ITAR regulations, visit this resource. &nbsp;Article - DDTC Public Portal
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7NlX0qCmIe

In Process Inspector (Contract)

<h3>Job Description</h3>
Job Description
Kitchen Equipment Technician
Joe Warren &amp; Sons Company Inc., (JWS) a leading provider of commercial refrigeration and food equipment services and sales throughout New England, seeks to add a Commercial Cooking Equipment Field Service Technician to help lead the company through an exciting phase of growth. Established in 1991, JWS is a family owned-operated business and headquartered in Norwood, MA. JWS has a long history of above-market growth driven by strong customer loyalty, a dedicated and thoughtful management team, and an industry leading reputation for quality service.
Kitchen Equipment Technician&nbsp;Responsibilities
<ul>
<li>Properly maintain, service and install commercial cooking/food prep&nbsp;equipment.</li>
<li>Accurately and timely completes assignments for all services&nbsp;performed.</li>
<li>Consults with the Parts Department to accurately identify recommended&nbsp;parts.</li>
<li>Maintains a neat and orderly truck, along with accurate part and tool&nbsp;inventory.</li>
<li>Communicates with manufacturers as needed to help with diagnosing problems with&nbsp;equipment.</li>
<li>Defines equipment problems, collects data, establishes fact and draws valid conclusions about the work needing to be&nbsp;performed.</li>
<li>Provides highest level of service to the customer and professionally communicates the service needed to&nbsp;customers.</li>
<li>Promotes and recommends other services provided by JWS to&nbsp;customers.</li>
</ul>
Kitchen Equipment Technician Qualifications
<ul>
<li>High School diploma or GED and valid driver’s license.</li>
<li>Can work well independently or as part of a cohesive team.</li>
<li>Show passion and empathy towards our customers and team.</li>
<li>Must be able to use hands for fine manipulation of hand tools.</li>
<li>Highly safety conscious and must be able to climb stairs and ladders.</li>
<li>Able to follow through on duties and assignments with minimal supervision.</li>
<li>Background experience in gas, electric, plumbing, and/or steam.</li>
<li>(5) years of experience in commercial equipment repair, or in a related area.</li>
<li>Excellent organizational skills,&nbsp;must be motivated and a self-starter with a team-first attitude.&nbsp;</li>
<li>Physical Requirements:&nbsp;Ability to frequently kneel, bend, squat, push, pull, reach, and occasionally. lift/carry up to 70 lbs.&nbsp;Ability to work on ladders, roofs, and other high places.</li>
<li>Ability to work with moving mechanical parts, pressurized steam equipment, open flames, heated surfaces, liquids, and risk of electrical shock in damp, humid, or freezing conditions.</li>
</ul>
Kitchen Equipment Technician&nbsp;Benefits:
<ul>
<li>Attractive compensation package with periodic reviews, bonuses, and increments</li>
<li>Very competitive 401k with a 4% Safe Harbor Match</li>
<li>Comprehensive Health Benefits: Medical, Dental (FREE), Vision, and HSA</li>
<li>Ready-to-Go Company Vehicles: Equipped with all necessary tools and equipment.</li>
<li>Flexible On-call with Overtime: Infrequent on-call schedules and plentiful OT opportunities with incentive pay.</li>
<li>Career Growth: Paid training, tuition assistance, and numerous advancement opportunities.</li>
<li>Mentoring Incentives: Earn extra by mentoring through our Experienced Training Program.</li>
<li>Life &amp; Disability Insurance for your peace of mind</li>
<li>Benefit from our company-wide Bonus incentive program with quarterly payouts</li>
<li>Enjoy 9 company-funded holidays along with generous PTO</li>
<li>Robust career progression opportunities</li>
<li>Referral bonuses for expanding the JWS family</li>
<li>Vast training and professional development prospects</li>
</ul>
Compensation: $60,000-100,000+
At this time, we are not seeking agency assistance or third-party recruitment services.
We are currently unable to sponsor work visas for this position. Applicants must be authorized to work in U.S. without sponsorship.
Joe Warren &amp; Sons Co. Inc. champions diversity and inclusivity. We provide equal employment opportunities to all, irrespective of age, color, disability, ethnicity, family status, gender, national origin, race, religion, sexual orientation, veteran status, or any other protected classification. Embrace a diverse, inclusive work environment with us.
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LuZOfNANoL

Kitchen Equipment Technician

<h3>Job Description</h3>
Job Description
Capable of working independently to complete the majority of projects from start to finish with limited assistance from a Senior Engineer or Director.&nbsp;&nbsp;

Job Summary
<ul>
<li>Lead the client management and design production activities</li>
<li>Coordinate and ensure the thoroughness and accuracy&nbsp;survey of building systems</li>
<li>Support the development of designs, specifications, systems narratives, and system layouts for a variety of projects and project sizes</li>
<li>Manage all phases of project including basic deliverables including calculations, drawings, and specifications</li>
<li>Design mechanical systems including calculations of heating and cooling loads </li>
<li>Select and layout mechanical equipment such as pumps, chiller, fans and boilers</li>
<li>Perform construction administration and field investigation tasks for assigned projects including conducting field inspections and subsequent detailed inspection reports</li>
<li>Ensure that drawings and designs are in accordance with company production and design standards</li>
<li>Collaborate with Technical Leaders / Sr. Engineers to ensure quality standards and appropriate&nbsp;workload management / changes in project scope or additional services</li>
<li>Attend project meetings and site visits</li>
</ul>

Qualifications
<ul>
<li>Bachelor’s degree in mechanical engineering</li>
<li>Equivalent of 3 - 7+ years of relevant professional experience including engineering design and project management</li>
<li>Revit experience preferred</li>
<li>Knowledge of all aspects of mechanical systems</li>
<li>Understanding of applicable design and building codes</li>
</ul>
Representative tasks include walking the site with clients and partners, doing site surveys and performing other tasks that may have you: carrying, moving, and climbing up a 10-foot ladder, gaining access to infrastructure covered by drop ceilings; and crawling, bending, reaching to gain access to and assess building systems.
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UveFi930dq

Mechanical Project Engineer

<h3>Job Description</h3>
Job DescriptionJOB SUMMARY: The level 1 Machine Operator is responsible for operating one 6-head embroidery machine and ensuring a high level of quality and production. SCHEDULE:
<ul>
<li>3:30 pm – 12:00 am Monday – Friday with Overtime (during the week) as required.</li>
</ul>
COMPENSATION:&nbsp;The hourly pay range&nbsp;reflects the actual compensation that Ahead, LLC; the employer reasonably expects to pay for the position at the time of hire.&nbsp;&nbsp;The final offer will be determined by a candidate's experience, skills, and qualifications.
<ul>
<li>$17.00 - $18.00&nbsp;per hour</li>
</ul>
 DUTIES/RESPONSIBILITIES:
<ul>
<li>Meet and exceed production standards.</li>
<li>Meet and exceed quality standards.</li>
<li>Verify products and components are correct.</li>
<li>Prepare products for production.</li>
<li>Prepare machine for production.</li>
<li>Remove excess threads and debris from product.</li>
<li>Remove Pellon from inside of product.</li>
<li>Minor machine maintenance.</li>
<li>Additional duties as assigned.</li>
</ul>
 REQUIRED SKILLS/ABILITIES:
<ul>
<li>Ability to follow verbal instructions.</li>
<li>Ability to problem solve.</li>
<li>Ability to work in a fast paced team environment.</li>
<li>Ability to perform quality control.</li>
<li>Possess a positive attitude.</li>
</ul>
 &nbsp;EDUCATION AND EXPERIENCE:
<ul>
<li>High school diploma or GED</li>
<li>Manufacturing experience preferred.</li>
</ul>
 PHYSICAL DEMANDS:
<ul>
<li>Ability to stand for extended periods of time.</li>
<li>Ability to use hands, fingers, and arms to touch, handle, pinch, or grasp.</li>
<li>Ability to demonstrate fine dexterity skills.</li>
<li>Ability to walk, bend, reach, kneel and crouch.</li>
<li>Ability to lift 50 pounds.</li>
<li>Ability to wear Personal Protective Equipment (PPE) as needed.</li>
</ul>
 WORK ENVIRONMENT:
<ul>
<li>Exposure to moderate noise level.</li>
</ul>
VISION REQUIREMENT:
<ul>
<li>Close Vision</li>
</ul>
PERSONAL PROTECTIVE EQUIPMENT:
<ul>
<li>Closed toe footwear required when entering the Production Floor (as needed).</li>
</ul>
&nbsp;Ahead, LLC is a socially responsible company and an Equal Opportunity Employer.
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0116edlcd1

Machine Operator I (2nd shift hours)

<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: Merrimack Manufacturing is looking for a Manufacturing Team Lead to perform various functions in ensuring production processes run efficiently and effectively. They must have excellent attention to detail, be self-sufficient in assembly, testing and documentation of mechanical and electrical assemblies. The Team Lead will know all processes and procedures on the line and be able to monitor workers and the efficiency of the line.&nbsp; &nbsp;&nbsp;3rd Shift Hours - 11pm - 7am RESPONSIBILITIES:
<ul>
<li>Monitor workers on site during production activities to ensure adherence to ethics and safety procedures</li>
<li>Evaluate manufacturing equipment for safety and functionality</li>
<li>Ensure that products and goods manufactured meet quality standards obtainable in the industry</li>
<li>Lead workers to enhance production quantity and at the same time maintain high production standards. </li>
<li>Check finished products to ensure quality, and that industry standards are met before they are declared ready for use</li>
<li>Keep records of line performance </li>
<li>Work as middleman between workers and management to create healthy communication</li>
<li>Follow and contribute to production schedule for the execution of projects in a timely manner</li>
<li>Ensure that work materials are present when needed.</li>
<li>Maintain neat, orderly and clean work area to ensure efficiency and no safety hazards. Participate in safety programs, meetings, and trainings as required. Bring safety concerns to the attention of management.</li>
<li>Participate in continuous improvement activities as part of a cross-functional team.</li>
<li>Maintain Clean Room integrity by using proper attire and adherence to Clean Room environment practices and procedures as applicable.</li>
<li>Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations.</li>
</ul>
 QUALIFICATIONS AND SKILLS:
<ul>
<li>Minimum of 3 years hands-on experience in a manufacturing environment with at least 1-year lead experience (preferred).</li>
<li>Knowledge of production practices and procedures in a cGMP &amp; GDP environment.</li>
<li>Experience with assembly, testing and the documentation of mechanical and electrical devices</li>
<li>Possess excellent interpersonal skills and ability to relate effectively with all members of the team from various backgrounds </li>
<li>Strong verbal and written communication skills to effectively relate with team members and the management</li>
<li>Strong ability to motivate, lead, and give directions to team members</li>
<li>Willingness to undertake various tasks and adapt to unexpected situations within dynamic company environment</li>
<li>Medical device manufacturing experience preferred</li>
<li>Working knowledge of Microsoft Office and basic computer skills. </li>
<li>Good hand eye coordination and manual dexterity required</li>
<li>Willingness to attend leadership trainings and any other trainings that management determines valuable to a lead’s role</li>
<li>Other assignments as assigned by management</li>
</ul>
 EDUCATION: H.S. Diploma or GED. &nbsp;
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