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<h3>Job Description</h3>
Job DescriptionThe NPI Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role focuses on coordinating the development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other QMS documentation to support initial qualification and commercial launch of medical products. The role will have direct interaction with suppliers, engineers, and manufacturing personal. How you will make an impact as a NPI Quality Specialist:&nbsp;
<ul>
<li>Collaborate with suppliers to ensure that tooling and manufacturing processes meet quality standards and specifications for medical products.</li>
<li>Develop and maintain relationships with suppliers to ensure timely delivery of validated tooling, equipment, and components.</li>
<li>Work with suppliers to address non-conformances related to tooling or materials, and develop corrective actions in collaboration with engineering and validation teams.</li>
<li>Coordinate tooling qualifications, ensuring tools meet all performance, safety, and regulatory standards before product manufacturing.</li>
<li>Ensure process changes (e.g., tool changes, equipment upgrades) are assessed and validated appropriately to maintain product quality.</li>
<li>Communicate effectively with validation personnel to align on protocols, testing, and timelines for process and tooling validation activities.</li>
<li>Act as a liaison between suppliers, engineering, and quality teams to ensure alignment and resolution of issues related to tooling and process validation.</li>
<li>Ensure proper documentation of tooling qualifications, process validations, and supplier-related activities according to standards</li>
<li>Coordinate the Review and approval of documentation related to tooling and process changes, ensuring traceability and compliance with design history files (DHF) and production records.</li>
<li>Provide regular updates on the status of NPI tooling and process validation activities, including any challenges or risks.</li>
<li>Track and report the status of validation milestones, tooling approvals, and supplier progress, ensuring adherence to project timelines.</li>
</ul>
Skills you need to be successful:&nbsp;
<ul>
<li>Bachelor’s degree with 1 year of supplier management experience or 5 years of supplier management experience</li>
<li>Project coordination and/or project management experience</li>
<li>Experience working in an engineering or technical environment</li>
<li>Experience with JIRA</li>
<li>Advanced proficiency in Microsoft Word &amp; Excel</li>
<li>Strong computer skills with databases and software applications</li>
<li>Strong written and verbal communication skills</li>
<li>Demonstrated aptitude for learning technical information quickly and accurately</li>
<li>Ability to shift priorities efficiently in as fast paced environment&nbsp;</li>
</ul>
About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research &amp; Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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NPI Quality Specialist

<h3>Job Description</h3>
Job DescriptionV-Tron Electronics Corporation is looking for a Cost Estimator to join our team in our Attleboro location. The Cost Estimator is a key member of the Quoting department who will establish standard routings and costed parts list associated with customer provided documentation. The ideal candidate will be curious, have a strong attention to detail and passion for customer success. Responsibilities: Establish material costs to prescribe customer parameters by soliciting bids from suppliers. Build standard parts list in V-Tron Electronics parts list database. Documents costs in parts master database. Develop standard routings by identifying required operations on customer blueprints in the most efficient way possible. Experience Requirements:&nbsp;
<ul>
<li>High School graduate or GED equivalent.</li>
<li>Minimum 2-years assembly, supervisory or management experience in manufacture of wire harnesses/cable assembly operations.</li>
</ul>
Candidates who do not meet these requirements but show a strong aptitude for success may be considered by V-Tron Electronics management. Skills Required:
<ul>
<li>Must possess a working knowledge of windows-based software including but not limited to MS word, MS excel and MS outlook.</li>
<li>Have in-depth understanding related to output of process equipment and techniques related to wire harness and cable assembly manufacturing.</li>
<li>Communicate well with specific engineering departments assigned to develop and prove time standards for operations relating to cable and wire harness assembly.</li>
<li>Exhibit strong negotiating and communications skills with external suppliers.</li>
<li>Must be well organized and precise in documenting and storing data related to material cost, and time estimates &nbsp;</li>
</ul>
Required Training:
<ul>
<li>Meet the experience criteria documented above. </li>
<li>Must display in depth understanding of assembly techniques associated with cable and wire harness assembly.</li>
</ul>
 About V-Tron Electronics Corporation: V-Tron Electronics Corporation is a privately held, veteran owned small business incorporated in 1970.&nbsp; We began as an electronics service provider to the emerging Massachusetts computer industry in the 1970’s and quickly grew to offer these services to a wide variety of industries including Semi-Conductors, Medical, Military and Industrial Electronics, all while shipping worldwide. Join our team and become an invaluable part of our future. Your time at V-Tron Electronics will be marked by the trust and empowerment needed to achieve your best work. V-Tron Electronics' benefits include a skill-based pay structure, healthcare benefits, paid time off, paid holidays and a 401(k)-Retirement plan with company match. &nbsp;
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Cost Estimator in Manufacturing

<h3>Job Description</h3>
Job DescriptionDEKA R&amp;D has an immediate opening for a Quality Specialist to work in the Quality Department in a dynamic Medical Device Research and Development environment.&nbsp; The position reports to the Director of Quality.&nbsp; The Quality Specialist is actively involved with everyday quality assurance operational tasks for ongoing product development projects and commercially released products. How you will make an impact:
<ul>
<li>Review and Approve Quality System Records</li>
<li>Support updating procedures and processes to support the QMS</li>
<li>Support the site Corrective and Preventive Action program</li>
<li>Provide QA support relative to DHR Review/inspections and final acceptance of materials/products</li>
<li>Review labels for accuracy and precision</li>
<li>Initiate non-conforming materials reports and segregate / control non-conforming materials as required</li>
<li>Review and close complaint files per complaint requirements</li>
<li>File and maintain records manually and electronically</li>
<li>Support QMS collection and trending of quality data</li>
<li>Manage QMS databases for action items and implementation</li>
<li>Support vendor qualification and management</li>
<li>Support external and internal audits</li>
<li>Support as backup to Training Coordinator, CAPA Coordinator, and Calibration Coordinator</li>
<li>Provide training as required to DEKA personnel&nbsp;</li>
<li>Promote QMS awareness to non-QA departments throughout DEKA</li>
</ul>
Skills needed to be successful:&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;
<ul>
<li>Preferred 2+ years’ experience in Quality Assurance in an FDA regulated environment – with QSR (21 CFR Part 820) and ISO 13485 experience if possible.</li>
<li>Experience with documentation in a regulated field such as medical device</li>
<li>Prior auditing experience is a plus</li>
<li>Strong written/verbal communication skills</li>
<li>Ability to:
<ul>
<li>Learn custom software programs</li>
<li>Multitask and carry tasks through to completion</li>
<li>Manage multiple sources of data and develop reports</li>
</ul>
</li>
</ul>
About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
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Quality Specialist

<h3>Job Description</h3>
Job DescriptionThe Production Quality Inspector is responsible to ensure that products meet established standards and specifications by identifying defects and ensuring compliance with regulations. This role is vital for maintaining product integrity and customer satisfaction. KNOWLEDGE, SKILLS AND ABILITIES:
<ul>
<li>Strong attention to detail skills related to product inspection and documentation. </li>
<li>Effective communication and ability to communicate cross functionally with all levels.</li>
<li>Knowledge of GDP (Good Documentation Practices)</li>
<li>Knowledge of visual and mechanical inspection.</li>
<li>Knowledge of sampling techniques or equivalent.</li>
<li>Ability to interpret inspection procedures, drawings, and instructions </li>
<li>Ability to raise issues to supervision/management for resolution.</li>
<li>Ability to work under pressure balancing multiple demands </li>
<li>Ability to use mechanical equipment that may include but not limited to Optical comparator, CMM, micrometers, pin gages, etc.</li>
<li>Self-starter and independent individual with strong organizational, time management and computer skills.</li>
</ul>
 ESSENTIAL FUNCTIONS:
<ul>
<li>Work with the Production department to effectively and efficiently inspect manufactured products.</li>
<li>Work with Quality Engineers to collect data and drive nonconformance resolution.</li>
<li>Drive containment actions as needed when a non-conforming action has been determined, following all Quality Management System (QMS) requirements.</li>
</ul>
EDUCATION: H.S. Diploma or equivalent EXPERIENCE: 
<ul>
<li>Minimum of 3 years’ experience as a quality inspector. 5+ years desired.</li>
<li>Prior experience in medical device and or electro mechanical assembly required.</li>
<li>Prior experience working with an ERP/MRP system (SAP, InforXA, ExactMax, etc.).</li>
<li>Prior experience working in an ISO9001, AS9100, or ISO13485 environment </li>
<li>Prior experience handling/disposition of non-conforming material a plus.</li>
</ul>
 &nbsp;
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Production Inspector

<h3>Job Description</h3>
Job Description
Job Title: QA Inspector – Receiving (Contract)
Location: Natick, MA
Job Type: Full-time
About Busek: Busek Co. Inc. (<a href="http://www.busek.com" target="_blank">www.busek.com</a>) researches, develops, and produces spacecraft subsystem technologies for space missions. Our talented staff possess expertise in in-space propulsion, space-borne sensors, materials science, manufacturing, and high-fidelity electronic design for challenging space missions. Busek is recognized in the spacecraft on-orbit propulsion community for numerous achievements, including developing the first U.S. Hall Effect Thruster in space. Our efforts span research, development, and manufacturing of aerospace systems, with low-volume production of high-reliability in-space components and subsystems. Our facilities include over 30,000 sq. ft. of R&amp;D labs and more than 40 vacuum chambers. Founded in 1985, Busek is located in Natick, MA, approximately 20 miles west of Boston. For more information, visit <a href="http://www.busek.com" target="_blank">www.busek.com</a>.
Job Summary: As a Quality Assurance (QA) Inspector – Receiving, you will play a critical role in ensuring the quality of incoming and in-process parts and components. You will work closely with design and test engineers, manufacturing staff, and fabrication technicians (both internal and external) to verify compliance with Busek’s documentation and customer requirements. This role provides a direct contribution to spaceflight programs, including groundbreaking NASA, commercial space, and defense missions.
Key Responsibilities:
<ul>
<li>
Conduct inspections of incoming and in-process components per documentation requirements.
</li>
<li>
Interpret engineering blueprints, specifications, and drawings.
</li>
<li>
Operate and utilize various inspection tools and gauges to verify part quality.
</li>
<li>
Maintain accurate inspection records and documentation.
</li>
<li>
Adhere to GD&amp;T (Geometric Dimensioning and Tolerancing) principles and processes.
</li>
<li>
Coordinate inspection efforts with coworkers to ensure workflow efficiency and quality compliance.
</li>
</ul>
Desired Qualifications:
<ul>
<li>
Prior experience in a technical QA parts inspection role.
</li>
<li>
Previous work experience in quality control or related field.
</li>
<li>
Proficiency in Microsoft Office Suite (Word, Excel).
</li>
<li>
Knowledge of AS9100 or ISO 9001 standards is a plus.
</li>
<li>
Experience working with small precision components.
</li>
</ul>
Additional Information: To conform to U.S. Government regulations, applicants must be a U.S. citizen, lawful permanent resident of the U.S., or a protected individual as defined by 8 U.S.C. 1324b(a)(3).
Benefits:
<ul>
<li>
Competitive Salary
</li>
<li>
SEP Retirement Savings
</li>
<li>
Performance Bonuses
</li>
<li>
Medical, Dental, and Vision Insurance
</li>
<li>
Life Insurance
</li>
<li>
Long-Term / Short-Term Disability Coverage
</li>
<li>
Paid Vacation, Sick Leave, and Holidays
</li>
<li>
Education Assistance 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:
</li>
<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>
<li>For more information about ITAR regulations, visit this resource. &nbsp;Article - DDTC Public Portal</li>
</ul>
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Quality Inspector - receiving (Contract)

<h3>Job Description</h3>
Job DescriptionDEKA Research and Development, located in Manchester, NH, has an immediate opening for a Verification and Validation Test Engineer&nbsp;to work in a dynamic medical device R&amp;D environment. Test Engineering is a high-visibility role with a significant, direct impact on the success of the project. How you will make an impact as a&nbsp;Verification and Validation Test Engineer:
<ul>
<li>Developing and writing test procedures&nbsp;assessing end-to-end performance and reliability of user interfaces and hardware</li>
<li>Understanding device design and core technologies in order to inform test method development</li>
<li>Determining test coverage for revisions to design</li>
<li>Creating and evaluating test fixtures if needed for product design verification</li>
<li>Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs</li>
<li>Contributing toward&nbsp;regulatory and agency submissions</li>
<li>Authoring Test Summaries and other documents</li>
</ul>
To be successful in this role as a Verification and Validation Test Engineer, you will need the following skills and experience:
<ul>
<li>Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering.</li>
<li>Experience with research, development, and product testing</li>
<li>Experience writing procedures for others to follow</li>
<li>Experience with data and failure analysis</li>
<li>Broad measurement instrument knowledge</li>
<li>Knowledge and deep understanding of engineering fundamentals</li>
<li>Demonstrated problem solving ability and techniques</li>
<li>Ability to work as part of an interdisciplinary team</li>
<li>Self-motivated and able to self-prioritize</li>
<li>Ability to clearly explain objectives</li>
<li>Must be detail oriented and have excellent verbal and written communication skills</li>
<li>Experience in medical devices, knowledge of FDA&nbsp;Quality System Regulations (QSRs) and/or ISO&nbsp;13485, and other medical device industry experience preferred</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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Verification and Validation Test Engineer

<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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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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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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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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