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<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 position reports to the Lead Quality Systems Engineer and plays a crucial role in managing and facilitating feedback processes within an organization. The role contributes to the continuous improvement of processes, products, and services within an organization. Responsibilities:
<ul>
<li>Manage the complaint handling process, from intake to resolution.</li>
<li>Analyzing and categorizing feedback to identify patterns, trends, and common themes.</li>
<li>Setting up and managing channels through which feedback can be submitted</li>
<li>Review documentation for compliance and Good Documentation Practices</li>
<li>Participate in product evaluations associated with field complaints.</li>
<li>Ensure timely closure of complaints and maintain complete complaint documentation files.</li>
<li>Facilitating prompt responses to feedback, especially when immediate action or acknowledgment is required</li>
<li>Work with product-specific Quality Engineer to collect data and document investigation, and initiate Corrective Actions when required</li>
<li>Sharing feedback with relevant departments, teams, or individuals who can address specific issues or identify improvements</li>
<li>Creating regular reports summarizing feedback data, insights, and any actions taken or planned in response to the feedback</li>
<li>Track the progress of changes or improvements made in response to feedback and ensure that they are effectively implemented.</li>
<li>Assist with post-market surveillance activities, including planning, data collection, trend analysis, and risk assessments.</li>
<li>Work closely with cross-functional teams to evaluate field performance and identify areas for product improvements.</li>
</ul>
 Qualifications and Skills:
<ul>
<li>Bachelor's degree in Engineering or related field.</li>
<li>Knowledge of global regulatory requirements for medical devices or pharmaceuticals, and combination products. FDA requirements for Quality Systems and Medical Device Reporting regulations (21 CFR 803, 820, and 211) is preferred</li>
<li>Strong organization skills, ability to track and evaluate outstanding tasks at a large scale, prioritize multiple projects and ensure compliance with standard operating procedures</li>
<li>Solid written/verbal communication and organizational skills</li>
<li>Strong deduction, decision-making and critical thinking abilities</li>
<li>Ability to work with cross-functional teams and to interact positively, effectively with peers, management, and customers</li>
<li>Previous experience in complaint handling and processes a strong plus</li>
<li>Experience developing and implementing complaint handling and PMS processes within quality management systems.</li>
</ul>
 Education: H.S. Diploma or GED &nbsp;
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Customer Feedback Engineer

<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 position will support manufacturing quality operations in a dynamic, fast-paced, medical device manufacturing environment. This environment includes the manufacture, inspection, and testing of devices for process validation and commercial production. RESPONSIBILITIES:
<ul>
<li>Working under the direction of Quality Engineers support, drive, and coordinate final inspection and acceptance of medical devices.</li>
<li>Support quality engineers in processing nonconformances, deviations, and rework authorizations by gathering data, updating logs, or drafting documentation.</li>
<li>Perform Device History Record (DHR) reviews for completeness, accuracy, and compliance to internal and regulatory requirements.</li>
<li>Identify and document errors or missing information in DHRs and coordinate with production or quality teams for timely correction. </li>
<li>Work cooperatively with team members on commercial production lines to support quality requirements and projects.</li>
<li>Provide administrative and technical support for change orders, training records, and CAPA follow-up as assigned.</li>
<li>May perform inspections for components, materials, devices and documents. </li>
<li>Position requires daily contact with members of Production, Engineering, Materials, and Quality departments and occasional contact with auditors and customers</li>
</ul>
 QUALIFICATIONS AND SKILLS:
<ul>
<li>2 + years of experience in occupation related to Manufacturing or Quality Control of medical devices.</li>
<li>Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 is preferred. </li>
<li>Experience with Microsoft Office software (Word, Outlook, Excel) required.</li>
<li>Self-starter and independent individual with strong organizational, time management and communication skills.</li>
<li>Ability to drive assigned tasks to closure</li>
<li>Must be able to manage multiple priorities. </li>
<li>Use critical thinking and deductive reasoning to make risk based decisions.</li>
</ul>
 EDUCATION: Associate degree or equivalent experience in Manufacturing, Quality, Mechanical or related engineering / life sciences related discipline. &nbsp;
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Quality Operations Specialist

<h3>Job Description</h3>
Job DescriptionMentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.&nbsp; Job Responsibilities:
<ul>
<li>Experience performing calibrations in Pharmaceutical Industry Environment. Biotechnology preferred.&nbsp;&nbsp;</li>
<li>Strong Knowledge in tolerance calculation</li>
<li>Experience in Calibration system assessment</li>
<li>Strong knowledge in process tolerance evaluation.</li>
<li>Process&nbsp;Instrumentation/ Calibration to manage calibration program.</li>
<li>Experience performing calibrations to Bioreactors, Utilities, Formulation, Aseptic Areas.</li>
<li>Experience in Blue Mountain (RAM), Calman, or Procal Software is highly preferred.</li>
</ul>
Must possess experience in:
<ul>
<li>Temperature</li>
<li>Technologies</li>
<li>Pressure</li>
<li>Humidity</li>
<li>Flow</li>
<li>Mass</li>
<li>PH</li>
<li>Conductivity</li>
<li>Dimension and Electrical</li>
<li>Knowledge in cGMP</li>
<li>Associate degree in Instrumentation Engineering</li>
</ul>
 Qualifications Requirements/Knowledge/Education/Skills:
<ul>
<li>AD, Instrumentation Technology, and or Electronics.</li>
<li>AD, Tecnología de Instrumentación y / o Electrónica.</li>
</ul>
 Physical Requirements and Working Environment:&nbsp;
<ul>
<li>While performing the duties of this job, the employee is regularly required to use hands to finger, handle, feel, or operate equipments, tools, or controls. The employee frequently is required to stand, walk, talk, or hear; sit; climb or balance, stoop, kneel, crouch or crawl; and smell. The employee may lift and/or move up to 25-35 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus.</li>
<li>He / she may frequently work inside weather conditions, near moving mechanical parts, exposed to wet and or humid conditions, and an odorous atmosphere, may be exposed to fumes and the risk of electrical shock, and occasionally work on ladders in high places, in small spaces, such as lift/metering stations, manholes, tanks and wet wells. The noise level in the work environment is usually moderately loud.</li>
</ul>
 Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.
Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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Instrumentation/Calibration Technician

<h3>Job Description</h3>
Job DescriptionQualification Engineer Location: Busek Co. Inc. – Natick, MA About Busek Busek Co. Inc. is a leading developer of advanced space propulsion and power systems. Our technologies support NASA, the Department of Defense, and commercial aerospace partners. We design, build, and test mission-critical hardware that enables groundbreaking space exploration and defense applications.Position Summary The Qualification Engineer will play a key role in validating the performance and reliability of Busek’s cutting-edge space propulsion and power systems. This role is highly hands-on, combining test planning, hardware setup, execution of environmental and functional tests, and data analysis. The Qualification Engineer will collaborate closely with design engineers, subject matter experts, and cross-functional teams to ensure all systems meet rigorous customer and industry requirements.Key Responsibilities
<ul>
<li>Develop and maintain test plans and procedures in alignment with product requirements, customer specifications, and industry standards.</li>
<li>Design and validate test fixtures and support equipment, including 3D CAD modeling and creation of technical drawings.</li>
<li>Oversee procurement and validation of test hardware, equipment, and materials.</li>
<li>Lead and execute qualification and acceptance tests, including vibration, shock, thermal vacuum, EMI/EMC, leak, and proof tests.</li>
<li>Perform hands-on test setup, inspections, troubleshooting, and data collection.</li>
<li>Analyze test results, drive root cause investigations, and recommend corrective actions.</li>
<li>Maintain thorough documentation of test activities, results, and observations.</li>
<li>Collaborate across engineering and program teams to ensure efficient communication and alignment.</li>
<li>Ensure compliance with safety requirements and cleanroom/test facility protocols.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Mechanical, Aerospace, Electrical Engineering, or related field; equivalent hands-on experience will be considered.</li>
<li>Strong troubleshooting and problem-solving skills, with hands-on experience working with complex hardware.</li>
<li>Proficiency with SolidWorks CAD (or equivalent 3D CAD software).</li>
<li>Excellent attention to detail, with strong technical documentation and organizational skills.</li>
<li>Ability to thrive in a fast-paced, cross-functional environment and manage multiple priorities.</li>
<li>Self-directed, proactive, adaptable, and able to work effectively under tight deadlines.</li>
</ul>
Additional Information
<ul>
<li>Must be a U.S. citizen or permanent resident (Green Card holder).</li>
<li>Competitive benefits package including:
<ul>
<li>Performance bonuses</li>
<li>Medical, dental, and vision insurance</li>
<li>Life insurance and disability coverage</li>
<li>Paid time off and holidays</li>
</ul>
</li>
</ul>
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 &nbsp;
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Qualification Engineer

<h3>Job Description</h3>
Job DescriptionQuality Inspector Level 2 / Mechanical Inspector&nbsp; 2nd Shift Differential &amp; OT Eligible!!! About Prototek Prototek is a leading national provider of digital based manufacturing services including CNC machining, precision sheet metal fabrication, EDM, and additive manufacturing services. Prototek serves a variety of customer end markets, including aerospace, defense, medical, robotics, electronics, consumer, and general industrial. Prototek has manufacturing locations across the United States including&nbsp;facilities in New Hampshire, Wisconsin, California, Colorado, and Pennsylvania. Prototek is ISO 9001:2015 and AS9100D:2016 certified as well as ITAR Registered.&nbsp;For more information, visit&nbsp;<a href="http://www.prototek.com.&amp;nbsp" target="_blank">www.prototek.com.&amp;nbsp</a>; &nbsp;Position Summary&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The Quality Inspector Level II is responsible for performing quality inspections on in-process and final products. Utilizing a range of inspection techniques and equipment, the Inspector will ensure that all products meet company and customer standards. &nbsp;Essential Functions&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<ul>
<li>Conduct quality inspections, including First Article, in-process, and final inspections on products.</li>
<li>Inspect parts using hand tools, measurement equipment, and advanced systems such as CMM and Optical Comparators.</li>
<li>Prepare inspection reports, Certificates of Conformance, and assist with FAI (First Article Inspection) reports and customer certification requirements.</li>
<li>Route parts to appropriate secondary processes and ensure timely delivery to the Shipping department.</li>
<li>Communicate project status and quality challenges with department leads and Project Managers.</li>
<li>Train and mentor employees on department operations, procedures, and quality standards.</li>
<li>Guide less experienced inspectors, providing solutions and maintaining rigorous quality control procedures.</li>
<li>Support production teams in adhering to ISO9001 processes.</li>
<li>Inspect incoming products from outside processes for compliance with specifications.</li>
<li>Participate in audits and compliance projects as assigned.</li>
<li>Follow applicable procedures and work instructions while offering ideas for improvement.</li>
<li>Perform other duties as assigned by management.</li>
</ul>
Technical Competencies
<ul>
<li>Competences indicated for Inspector I.</li>
<li>Advanced knowledge of GD&amp;T per ASME Y14.5.</li>
<li>Proficient in reading and interpreting detailed manufacturing drawings.</li>
<li>Strong understanding of hand measurement tools and measurement equipment. </li>
<li>Proficient in Microsoft Office Suite, using Mie Trak, SolidWorks, and CMM tools. </li>
</ul>
Behavioral Competencies
<ul>
<li>Demonstrate motivation, accountability, and effective written and verbal communication skills.</li>
<li>Ability to manage multiple projects, solve complex problems, and adapt to changing circumstances. </li>
<li>Strong attention to detail and commitment to high-quality work and team collaboration. </li>
<li>Ability to handle conflict resolution, mentor others, and respond effectively under pressure. </li>
<li>Demonstrate effective written and verbal communication skills to manage their teams. </li>
</ul>
Education &amp; Professional Experience
<ul>
<li>Experience indicated for Inspector I</li>
<li>Minimum of 5 years of inspection experience preferred.</li>
<li>Extensive knowledge of applicable manufacturing processes.</li>
<li>Comprehensive understanding of ISO 9001, AS 9100, and/or Medical ISO13485 standards.</li>
<li>GD&amp;T training certificate from recognized instructor. </li>
</ul>
Physical Requirements/Work Environment
<ul>
<li>Ability to sit, stand, bend, kneel, and crouch for extended periods. </li>
<li>Capability to use hands and fingers for operating equipment and handling parts of various sizes.</li>
<li>Ability to lift, push or pull up to 50lbs, moderately throughout the workday. </li>
<li>Visual acuity for close vision, color vision, depth perception, and sharp focus.</li>
<li>Work in a fast-paced environment with noise conditions ranging from moderate to extreme; hearing protection is provided if needed. &nbsp;</li>
<li>Exposure to fumes, airborne particles, moving mechanical parts, and vibration.</li>
</ul>
** This role is crucial for maintaining high-quality standards and ensuring that all products meet rigorous specifications while supporting and mentoring team members.** &nbsp;Work Hours/Travel
<ul>
<li>2nd shift work schedule:&nbsp; Monday - Thursday / 10 hour shift</li>
<li>Overtime as necessary (including occasional weekends if needed)</li>
<li>Travel: N/A</li>
</ul>
 What Prototek Offers:
<ul>
<li>Career advancement opportunities</li>
<li>Competitive pay scale</li>
<li>Paid time off (PTO) starting at 80 hours with annual increase for each year of service</li>
<li>9 paid Holidays annually</li>
<li>Education reimbursement program</li>
<li>Health, dental, vision, life and short-term disability insurance </li>
<li>Company paid life and long-term disability insurance </li>
<li>Employee Assistance Program (EAP) </li>
<li>401(k) match: 100% of 3% and 50% for 4% and 5%</li>
</ul>
 Additional Information:&nbsp; Prototek maintains International Traffic in Arms Regulations (ITAR) compliant operations in United States based facilities.&nbsp; This position is subject to ITAR which requires U.S. Person status. ITAR defines U.S. Person as U.S. Citizens, lawful permanent residents, or foreign nationals granted refugee or asylee status. &nbsp;
We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, national origin, sexual orientation, gender, gender identity, veteran status, disability, or any other protected class.
EEO is The Law - click here for more information: <a href="https://www.eeoc.gov/sites/default/files/migrated_files/employers/poster_screen_reader_optimized.pdf" target="_blank">https://www.eeoc.gov/sites/default/files/migrated_files/employers/poste…</a>
We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact 603-746-2001 or email us: <a href="mailto:HR@PROTOTEK.COM" target="_blank">HR@PROTOTEK.COM</a>. You may also write to us and we will be happy to assist you with the application: Prototek, 205 Pine St., Hopkinton, NH 03229
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Quality Inspector Level II - 2nd Shift

<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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