Quality control inspector jobs in Lowell, MA

Primary Skills: Electrical testing (Expert), Oscilloscopes (Expert), Python (Intermediate), Soldering (Advanced), Test-Execution (Proficient) Contract Type: W2 Duration: 6 Months with possible extension Pay Range: $37.00 - $41.00 Per Hour #LP Job Summary: Join our dynamic Hardware Test Engineering team as a Quality Assurance Engineer, focused on groundbreaking robotic system design. This position involves collaborating with hardware developers and program management to enhance testing capabilities utilizing your critical thinking and problem-solving skills. Ideal candidates will bring in-depth electrical experience to the forefront of new technological advancements in robotics. Key Responsibilities: Collaborate with Test Engineers and developers on tooling and techniques for testing. Maintain and maximize fixture uptime for existing systems. Troubleshoot electrical and control issues efficiently. Develop comprehensive test subsystems and documentation. Execute detailed tests and accurately acquire test data. Must-Have Skills: Proficient in reading and understanding electrical schematics. Experienced with board-level soldering and capable of performing board reworks. Skilled in using standard electrical test equipment (oscilloscopes, multi-meters). Industry Experience: Robotics, Electrical Engineering or related fields with a strong emphasis on testing and troubleshooting hardware. ABOUT AKRAYA Akraya is an award-winning IT staffing firm consistently recognized for our commitment to excellence and a thriving work environment. Most recently, we were recognized Inc's Best Workplaces 2024 and Silicon Valley's Best Places to Work by the San Francisco Business Journal (2024) and Glassdoor's Best Places to Work (2023 & 2022)! Industry Leaders in IT Staffing As staffing solutions providers for Fortune 100 companies, Akraya's industry recognitions solidify our leadership position in the IT staffing space. We don't just connect you with great jobs, we connect you with a workplace that inspires! Join Akraya Today! Let us lead you to your dream career and experience the Akraya difference. Browse our open positions and join our team!

Our client is a global leader in e-commerce and cloud technology, recognized for innovation, customer obsession, and large-scale operational excellence. Based out of Westborough Massachusetts they are looking to hire a Quality Assurance Tech 1 on a Contract basis. Contract Duration: 6 Month Contract (Potential for extension) Required Skills & Experience Read and understand electrical schematics Ability to fabricate fixturing and perform board re-works, based on schematics Board-level soldering experience Experience with cable assembly and bring up AS or BS in Electrical Engineering or equivalent industry experience experience testing hardware Experience using standard electrical test/laboratory equipment Oscilloscopes Data acquisition devices Digital multi-meters Signal generators Understand and execute documented test procedures collect test data, document test artifacts and conditions Troubleshoot electronic devices under test Clear written and verbal communication for Test Engineers and external stakeholders Proficiency working in a Linux/Unix environment, and executing simple scripts is a plus Daily Responsibilities Working with other Test Engineers, Hardware and Software developers regarding tools and techniques required for testing. Maintain fixture uptime of existing fixtures Troubleshoot electrical and control issues Develop test subsystems and documentation Execute tests and acquire test data You will receive the following benefits: Medical Insurance - Four medical plans to choose from for you and your family Dental & Orthodontia Benefits Vision Benefits Health Savings Account (HSA) Health and Dependent Care Flexible Spending Accounts Voluntary Life Insurance, Long-Term & Short-Term Disability Insurance Hospital Indemnity Insurance 401(k) including match with pre and post-tax options Paid Sick Time Leave Legal and Identity Protection Plans Pre-tax Commuter Benefit 529 College Saver Plan Motion Recruitment Partners (MRP) is an Equal Opportunity Employer. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under MRP's Employment Accommodation policy. Applicants need to make their needs known in advance.

Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess' patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. The Role The Research Associate/Quality Engineer will be responsible for performing mechanical testing of materials and components using instruments such as Mecmesin, Instron, or equivalent force-measurement systems. This role will support tensile, compression, shear, puncture, and force displacement characterization to ensure product performance, robustness, and compliance with internal quality standards. In addition, the individual will contribute to method development, qualification activities, and routine QC release testing to support clinical and commercial manufacturing programs. This is a unique opportunity to be part of an emerging early-phase clinical company bringing innovative technology to the global market. Key Responsibilities Essential duties and responsibilities include the following. Other duties may be assigned. Perform mechanical testing of materials, components, and finished MAP products using Mecmesin, Instron, or comparable systems, including tensile, compression, shear, puncture, and force displacement profiling. Develop, optimize, and maintain mechanical test methods to support product characterization, comparability studies, and design verification/validation activities. Execute routine QC mechanical release testing aligned with cGMP expectations and data integrity standards. Troubleshoot mechanical testing issues, support instrumentation maintenance, and ensure proper calibration and documentation Analyze mechanical test data, prepare technical reports, and document all activities in audit-ready laboratory records. Collaborate cross-functionally with QC, Analytical Development, Process Development, Manufacturing, and Regulatory teams to enable program success. Assist in broader QC testing efforts as needed, including support for analytical, functional, and stability assays. Independently author method SOPs, analytical protocols, technical reports, and contribute to regulatory submissions. Maintain rigorous laboratory documentation and complete, audit-ready analytical records. Collaborate effectively with QC, Manufacturing, Process Development, and Regulatory teams to enable program success across phases. Thrive in a fast-paced, cross-functional environment with excellent communication and organizational skills. Qualifications Bachelor's degree in Mechanical Engineering, Materials Science, Biomedical Engineering, or a related discipline; 1-3 years of relevant mechanical testing or QC experience, or a master's degree with applicable laboratory experience. Hands-on experience with mechanical testing instruments such as Mecmesin, Instron, Texture Analyzer, or equivalent force-measurement systems. Demonstrated proficiency in tensile, compression, shear, puncture, and force-displacement mechanical characterization. Experience developing, optimizing, and/or qualifying mechanical test methods for materials, components, or finished products. Familiarity with GMP, GLP, or ISO 17025 laboratory environments and strong understanding of data integrity (ALCOA+). Ability to analyze mechanical test data, generate clear technical reports, and maintain accurate documentation. Experience supporting QC release testing, method qualification, method transfer, or equipment qualification is a plus. Strong organizational skills with the ability to manage multiple workflows and prioritize effectively in a fast-paced environment. Excellent verbal and written communication skills and comfort working within interdisciplinary teams. Commitment to collaborative work within interdisciplinary project teams. At Vaxess, we're bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to ****************** .

We are seeking a highly motivated Entry-Level Quality Control (QC) Analyst to join our Gene Therapy QC Bioassay group. This is an excellent opportunity for recent graduates or individuals early in their careers to gain hands-on experience in a dynamic and cutting-edge environment supporting AAV-based gene therapy programs. The QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing. Responsibilities: Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing. Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents. Support method transfer, qualification of critical reagents, and other assay-related activities. Participate in the review and basic trending of QC data. Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking. Collaborate with internal teams and external partners as part of cross-functional project support. Contribute to investigations and deviation reports under guidance. Qualifications: Bachelor's degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field. Academic or internship experience with mammalian cell culture and/or ELISAs strongly preferred. Familiarity with basic lab techniques and data analysis methods. Enthusiasm for learning and the ability to work both independently and within a team. Strong organizational, communication, and interpersonal skills. Detail-oriented and eager to develop problem-solving skills in a regulated lab environment.

The Alexander Technology Group is looking for a Quality Technician for a client in the Portsmouth, NH area. This is a full-time role No 3rd party applicants/agencies will be considered, do not reach out. Salary: 60-75k Must be on-site Requirements: Quality Technician Perform in-process and final product inspections/testing for device products: Conduct visual/functional checks on assembled devices Support environmental monitoring and cleanliness in manufacturing/assembly areas: Execute routine sampling and testing (e.g., viable/non-viable particulates, settle plates) in ISO-classified cleanrooms used for assembly, escalate excursions, and assist in gowning qualification and line clearance activities. Execute sampling and basic analytical testing of incoming materials and in-process samples: Test device components Document deviations, non-conformances, and support CAPA investigations Assist in equipment qualification, process validation, and cleaning validation activities If interested, please send resume to ************************

Job Description About Us Stellar Industries is a rapidly growing industry leader in manufacturing metalized ceramics. We are a major supplier of innovative, high-quality parts to the Aerospace, Photonics, Telecommunications, and Commercial industries. The company was acquired by TRUMPF Photonics in 2019 and has significant growth goals. About the Role The Quality Control Inspector Level II maintains quality standards by inspecting incoming materials from outside suppliers, in-process production, and finished products in accordance with the quality standards and operating procedures set forth by the Head of Quality Control/Quality Assurance. What You Get to Do Works independently with minimal supervision. Maintain an organized and clean work area. Uses Hand tools, including but not limited to tweezers, calipers, and micrometers. Confirms specifications by conducting visual and measurement tests. Works with a variety of blueprints and technical drawings; must be able to interpret changing requirements as products and builds vary. Completes a General Inspection Report by documenting inspection findings regarding product dimensions, quantity of parts accepted/rejected, and basis of rejection. Uses Vision Systems and documents results into the computer. Follow all safety protocols. Cross-train as requested in other areas of the company. About You Minimum of 3 years of quality control experience. Must be able to work in a sitting position for up to 10 hours. Must be able to wear a lab coat, spittle mask, and gloves while working. The position requires working with measuring devices and microscopes. Individuals must have previous experience working in a similar environment. Must be able to work independently and demonstrate extremely high levels of precision and accuracy. line, High-Temperature BTU Furnaces, as well as various facility-related items, including air handlers, air compressors, air filtration units, etc. What We Offer Competitive pay A generous benefits package that includes medical, dental, 401K plan, and PTO Employer-paid vision plan, Employer paid Basic Life and AD&D Insurance, and Employer Paid Disability Insurance Tuition Reimbursement 4-Day workweek, Monday-Thursday 12 pm-10:30 pm Monday-Thursday 12:00 pm - 10:30 pm

So why join Hologic? You will have the opportunity to get in on the ground floor at a high growth facility to create a manufacturing process working on life-saving medical devices with potential for future growth. This is a great opportunity to enhance you manufacturing operation skills and knowledge to further your career. The Quality Control Inspector is a critical member of the Quality Assurance team, responsible for ensuring that finished products and in-process components meet all regulatory, quality, and customer requirements before release to inventory. This role involves the meticulous review of Device History Records (DHRs), performing inspections, and providing support to manufacturing and quality processes, such as Incoming Inspection, Material Review Board (MRB), Calibration and Returned Material Authorization (RMA) activities. The Final Inspector 2 is instrumental in upholding Hologic's commitment to excellence by ensuring compliance with Good Manufacturing Practices (GMP), ISO standards, and quality systems, while fostering a culture of continuous improvement and collaboration. What to expect: Lead with Ownership - Demonstrate integrity and always aim to do the right thing. Be highly accountable for your work, follow through on commitments, and take responsibility when things don't go as planned. Embrace opportunities to try new things and learn from mistakes. Act with Speed - Approach tasks with a strong sense of urgency and a bias toward action. Keep stakeholders informed by providing regular updates early and often, ensuring transparency and avoiding unexpected surprises, even when working at a fast pace. Foster Partnerships - Collaborate effectively with teammates and stakeholders to achieve shared goals. Invest in building strong working relationships and contribute to efforts that fulfill the organization's Purpose, Promise, and Passion. Delight Customers - Strive to exceed expectations by delivering high-quality work, exceptional experiences, and innovative solutions. Engage in proactive communication, provide excellent service, and develop a deep understanding of customer needs to create positive, lasting impressions and build trust-based relationships. Celebrate WINS! - Take pride in delivering impactful results. Contribute to a positive team environment by celebrating both individual and team accomplishments. Support colleagues, recognize collective successes, and embody the mindset of an 'A-player' who inspires others. What we expect: Perform detailed reviews of Device History Records (DHRs) as part of final inspection and release activities for finished products, ensuring accuracy and compliance with documentation standards. Conduct reviews of manufacturing records for replacement components, subassemblies, and in-process inspections to ensure alignment with quality requirements. Support manufacturing personnel by ensuring proper documentation of Failure Investigation Reports and processing of Non-Conforming Materials in the Product Lifecycle Management (PLM) system, including identification, quarantine, and documentation. Perform routine inspections, including field service and special inspections, to support validations, studies, and incoming inspection activities. Communicate and reinforce Good Manufacturing Practices (GMP) to manufacturing personnel to uphold quality standards. Review and provide input on new releases of Inspection and Test documents to ensure adherence to Good Documentation Practices (GDP). Maintain QA Activity Collection Plans, First Pass Yield reports, and other applicable tracking mechanisms to monitor quality metrics. Collaborate with Engineering to provide feedback on documentation improvements and process changes. Support Incoming, product returns and calibration teams as needed as needed. Perform other duties as assigned by leadership to meet organizational and operational needs. Education and Experience: High school degree and/or an equivalent technical school education preferred. Minimum of 3 to 5 years related Quality Inspection experience in Medical Manufacturing environment. Experience with Oracle, and Agile preferred. The annualized base salary range for this hourly role is $46,100-$69,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand. Agency and Third Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Acute Care TechnologySee attached Job Description At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary Verification of procured materials, sub-assemblies, finished products and processes to the companies Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Essential Functions Inspect measure and/or test material to established methods and standards. Utilize various inspection tools, such as Vision System, Verniers, Micrometers, Rulers, Oscilloscopes, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. Document inspection and test results according to established procedures. Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. Process returned material to established procedures. Read and interpret documentation such as Standard Operating Procedures (SOP), schematics, technical drawings, PDAs and ECOs. Interface with other functions and departments as required. Required/Preferred Education and Experience High School Diploma Or equivalent. required 1-3 years experience in a related position. required Knowledge, Skills and Abilities Good written and oral communication skills. Ability to read specifications, procedures and engineering drawings. Familiar with use of mechanical and electronic test equipment. IPC-A-61OD for Incoming Inspection, preferred. Basic computer skills: Microsoft Office, Oracle and MES. Physical Demands Ability to lift up to 50 lbs. ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. #LI-LV1 The hourly pay rate for this position is: $24.00 to $25.00 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

Summary: The Lead Housing Quality Standard (HQS) Inspector is responsible for conducting any mandatory inspection for all leased units under the Rental Assistance Program in accordance to the Department of Housing and Urban Development (HUD) and Department of Housing and Community Development (DHCD) program guidance. As the Lead HQS Inspector the incumbent is expected to assist the Inspections' Supervisor in providing training to newly hired inspectors and with administrative duties as assigned. Why Work for SMOC? Paid Time Off: All full-time employees can accrue up to 3 weeks of vacation, and 2 weeks of sick time and are eligible for 12 paid holidays during their first year of employment. Employer-paid Life Insurance & AD&D and Long-Term Disability for full-time employees. Comprehensive Benefits Package including Medical Plans through Mass General Brigham with an HRA Employer cost-sharing program, Dental Plans with Orthodontic Coverage, and EyeMed Vision Insurance available to full-time employees. 403(B) Retirement Plan with a company match starting on day one for all full-time and part-time employees. Additional voluntary benefits including; Term and Whole Life Insurance, Accident Insurance, Critical Illness, Hospital indemnity, and Short-Term Disability. Flexible Spending Accounts, Dependent Care Accounts, Employee Assistance Program, Tuition Reimbursement and more. Primary Responsibilities: Conduct thorough HUD/DHCD HQS inspections of all SMOC RAPS existing units, potential new units, and the reinspection of those units as required including physical and remote virtual inspections. Verify unit compliance based on health and safety requirements. Verify unit conditions for rent reasonableness comparisons. Enter all inspection data into the MRI Tenmast Software Systems' Inspection module and monitoring information as needed; printing all required inspection-related letters for participating tenants and owners. Assist the Inspection Supervisor in providing "on the job" training for newly hired HQS inspectors in the field Assist the Inspection Supervisor in monitoring the various types of inspections conducted by the HQS Inspection team including remote virtual inspections, re-inspections, inspections conducted using an owner self certification and physical inspections Make recommendations to the Inspection Supervisor on behalf of the HQS inspectors on process and procedure Monitor HQS supplies and make requests to the Program Director on orders for necessary equipment such as gloves, shoe coverings and personal protective equipment as needed Utilize and maintain inspection-related equipment on a regular basis, including camera, hand-held inspection devices or tablets, flashlight, cell phone, tick tester, and inspection-supply cache. Engage all clients by understanding and addressing their needs whether within or outside the scope of work. Attend & participate in engagement team meetings as requested and communicate effectively with clients and staff in other areas. Maintain confidentiality of client, employee and agency information in accordance with federal and state laws and funder requirements. Ensure compliance with program/department, agency and/or funder requirements, as well as SMOC policies & procedures. Other duties as assigned. Knowledge and Skill Requirements: Education: High school diploma or equivalent Minimum years of related experience: 1-2 years preferred Knowledge of Excel, Windows, Word and PCs, ability to work well in a very high volume and productivity environment, ability to handle potentially stressful situations and sensitivity to the needs of economically- disadvantaged clientele. Valid Mass. driver's license and insurance Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Must meet all required DHCD program certifications within 1 year. Organizational Relationship: Directly reports to HQS Inspection Supervisor. Indirectly reports to Program Director, Assistant Director and Division Director. Direct reports of this position are none. Indirect reports of this position are HQS Inspectors. Physical Requirement: Physical effort required to do the job: Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Working Conditions: This job requires working in many different conditions and places. About 80% of the time is outside the office either on the road or at a tenant's unit. Therefore, conditions range from an office environment to an outdoor environment that can be dirty, wet, cold, hot, difficult and risky. As part of the responsibilities of this position, the Lead Inspector will have direct or incidental contact with clients served by SMOC in various programs funded or administered through the Executive Office of Health and Human Services. A successful background check is required. Remote Work Option: Remote work is permissible in some positions at SMOC depending on the key functions and responsibilities. The Lead Inspector position is eligible to work from home 0% of the week in scheduling coordination with the department manager. Monday-Friday; 9am-5pm 35

Rennscot MFG, founded in 2017, started as a motorsports-focused shop in the aftermarket automotive industry. Now, they are a leading provider of advanced manufacturing services located in Woburn, MA. Rennscot MFG strives to be more than just a machine shop; they solve problems in innovative ways, using a suite of integrated services to fuel a passion for ideation. With a focus on diversifying into commercial and critical technology sectors, Rennscot MFG delivers cutting-edge technologies and unwavering commitment to quality. They offer a comprehensive range of services, including reverse engineering, metal & polymer additive manufacturing, and precision machining to support various industries' needs. For more information, visit rennscotmfg.com. Description The Quality Control Inspector is responsible for ensuring that manufactured components meet engineering and customer specifications through precise inspection processes. This role places a strong emphasis on visual inspections, along with manual inspection methods, and requires a keen understanding of technical drawings and GD&T. Candidates will be considered for either an L1 (entry-level) or L2 (experienced) inspector position based on experience and qualifications. Responsibilities Operate pre-programmed CMM inspections (Zeiss/Calypso preferred) Load/unload parts and verify setups Interpret CMM results and compare them against engineering requirements Document findings in the MES (ProShop) and communicate deviations Perform manual inspections using a variety of precision metrology tools Calipers, micrometers, height gauges, thread gauges, bore gauges, etc. Visual inspections for defects such as nicks, scratches, and finish inconsistencies Review technical drawings and apply GD&T principles to inspections Conduct receiving, in-process, and final inspections Assist in non-conformance investigations, root cause analysis, and corrective actions Maintain accurate inspection records and ensure compliance with AS9100/ISO9001 standards Collaborate with machinists, engineers, and quality team members to resolve inspection-related concerns Adhere to company safety protocols, including proper PPE usage (eye protection, hearing protection, etc.) Step into other support roles as needed based on company demands; assist with CNC machine operation, post-processing additively manufactured parts, mechanical assembly, or logistics tasks (e.g., driving components to/from outside processing vendors) Required Skills & Qualifications Experience in quality inspection within a manufacturing environment Strong ability to interpret technical drawings, GD&T, and work instructions Proficiency in basic metrology tools (calipers, micrometers, etc.) Familiarity with non-conformance documentation and quality reporting Attention to detail and ability to work independently in a fast-paced environment Preferred Skills & Qualifications Experience running CMM programs (Zeiss/Calypso preferred) Ability to make minor adjustments to Calypso programs Understanding of statistical process control (SPC) and quality tools (FMEA, control plans, etc.) Experience working in regulated industries (aerospace, medical, automotive, etc.) Physical Demands Standing for extended periods Lifting/moving objects up to 50 lbs Fine motor skills for handling small precision components Working in an industrial environment requiring PPE (eye protection, hearing protection, etc.) ITAR Requirement To conform to US Government export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a US citizen, lawful permanent resident of the US, protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the US Department of State. Learn more about the ITAR here: **************************************************************************************** Rennscot MFG is an Equal Opportunity Employer; employment with Rennscot MFG is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

Job Description The Quality Control Technician - Troubleshooting is responsible for inspecting and testing cable and wire products and processes to ensure they meet all quality standards, specifications, and regulations. This includes performing visual inspections, dimensional measurements, electrical, and functional tests. The primary function of this role is to evaluate nonconforming products and to determine the necessary actions to rework the product. The QC Technician must also be able to read and interpret blueprints, engineering drawings, and specifications. This position requires the use of High Voltage, all safety guidelines, procedures, and regulations to prevent accidents and ensure a safe working environment must be followed. The Quality Control Technician - Troubleshooting is a respectful team-player that works well with diverse internal team members. This position is ambitious, self-motivated, results-driven, and demonstrates problem solving skills with sound judgment. This role is also responsive, flexible, accessible, detail oriented, willing to embrace change and proactively adjust plans. Partnering with and elevating others by communicating with peers to increase awareness and ensure team success. Essential Duties and Responsibilities: Troubleshoot nonconforming cables, fill out nonconformance reports and communicates findings to Production Quality Supervisor and Quality Manager Detect and report unusual or non-conforming documentation, materials, conditions, or product to Production Quality Supervisor and Quality Manager. Assist and sometimes lead Root Cause and Corrective Action efforts. Inspect materials, components, and final product to ensure they meet quality standards. Measure dimensions of cable and wire products to ensure they meet specifications. Conduct visual and electrical tests on cable and wire products to ensure they meet performance requirements and identify any defects. When required, perform functional tests on cable and wire products to ensure they operate as designed. Document the results of all tests and inspections. Create, update, compile, save and maintain documentation into internal database. Work with various internal personnel and departments to communicate and resolve quality issues. Comply and support company policies and quality management system. Maintain and create a clean, uncluttered environment that reduces waste and optimizes productivity by following the 5S steps: sort, set in order, shine, standardize, and sustain. When required, help with continuous improvement efforts. More additional responsibilities may be applicable per the Quality Manager. Qualifications: High school diploma or equivalent. 1+ year of experience in quality control, preferably in the cable and wire manufacturing industry. Experience with visual inspection and dimensional measurement. Basic understanding of Microsoft Office and Adobe. Ability to read and interpret blueprints, engineering drawings, and specifications. Strong attention to detail. Ability to work independently and as part of a team. Strong communication skills. Proficient with computers and comfortable using Microsoft Office Suite (Word, Excel, etc.). Physical Qualifications: The physical demands described are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to sit; stand; crouch; stoop; walk; talk; hear; use hands to handle or feel assemblies; reach with hands and arms for materials and tools. The employee must occasionally lift and/or move up to twenty-five (25) pounds. They must also have the ability to see details at close range (within a few feet of the observer), color vision, depth perception and ability to focus. This position requires use of information or access to hardware and documents which are subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. Benefit Conditions: Waiting period may apply Only full-time employees are eligible This Job Is: A job for which military experienced candidates are encouraged to apply Job Type: Full-time Salary: $20.00 - $25.00 per hour Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Experience level: 1 year Schedule: 8 hour shift Day shift Monday to Friday Overtime Work setting: In-person Experience: Blueprint reading: 1 year (Required) Quality control: 2 years (Preferred) Work Location: In person

Job Description 1. Qualifications: a. High school diploma or GED required b. Minimum 3 years of relevant quality experience, within ISO13485/GMP manufacturing environment preferred, within extrusion is a plus c. Demonstrated efficiency and competency in core and advanced methods and gages for the inspection of tightly toleranced products d. Ability to read and interpret Engineering drawings e. Demonstrate initiative and self-motivation to create efficiencies and improve productivity within the inspection process f. Able to adapt and apply inspection knowledge to an array of product geometries and materials g. Work independently and prioritize assignments h. Will receive ongoing training to support competency and growth within the role i. Will receive opportunity and training to support growth within QC 2. Basic Position Skills: a. Organization - Able to react and maintain order and focus across shifting priorities and tasks b. Time Management - Able to balances multiple responsibilities and create efficiencies within the inspection process and achieve due dates c. Critical Thinking - Able to apply and adapt training and experience effectively to assigned tasks; ability to interact with data and identify risk d. Communication - Able to contribute across the team and coordinate with and support others to achieve departmental goals e. Mature work ethic - professional and positive attitude; provide constructive feedback and ownership to drive improvement within areas of responsibility 3. Reports to: Quality Supervisor 4. Primary job responsibility: The QC Inspector Level 2 is a mid-level position within the QC department for individuals who have demonstrated proficiency in all Level 1 competencies and responsibilities. The Level 2 Inspector utilizes core and advanced inspection methods and gages efficiently to perform inspections of extruded product across a broad range of product geometries and material to determine conformance to defined specifications. This position may include responsibility for an assigned Quality workflow and/or area of focus within an area of demonstrated expertise, efficiency and experience. 5. Essential functions of position: Perform Final Inspection for product Lot Release a. Prepare, follow, perform and document final inspections as defined on inspection paperwork for lot release b. Adapt inspection method techniques to accommodate the inspection of an array of products, including prototypes, profiles, multi-lumen and thin wall extruded tubes c. Demonstrate acceptable measurement error within inspection methods and techniques d. Assess conformance to defined specifications and requirements and identify and document non-conformance reports (NCR) e. Perform boundary inspections and actions as required to contain non-conforming product f. Complete thorough and detailed end-of-shift reporting Perform Start up and In-process inspection of manufacturing extrusion lines a. Prepare, follow and perform start-up and in-process inspections for multiple extrusion lines within a shift for an array of parts with varying degrees of difficulty relating to raw material properties, geometries, tolerances and methods b. React, adjust and communicate appropriately to challenges encountered during the extrusion process c. Identify and document non-conformances to defined specifications and requirements during the extrusion process d. Communicate inspection results and work with extrusion technician or operator to address non-conformances and at-risk product e. Identify, document, and perform boundary inspection to contain at-risk product encountered during the extrusion process Assigned Quality Workflow or Area of Focus a. Support assigned workflow or area of focus with accountability and action b. Create documented procedures and provide training as warranted c. Maintain appropriate documentation and tracking of workflow outcomes and performance as warranted d. Identify under performance and risk within the workflow and action needed to sustain and/or improve workflow outcomes and performance as warranted e. Coordinate and work with others as needed in support of assigned workflow f. Provide and maintain active communication and updates of assigned workflow to Quality Manager and/or Supervisor. Inspection Methods, Gages and Equipment a. Utilize pin gages, ring gages, calipers, rulers, vision systems, and other applicable gages as specified and within scope of training b. Utilize advanced inspection methods including automated OGP routines and advanced vision system techniques such as modeling and construction c. Recognize and respond to basic visual and dimensional quality indicators and erroneous data d. Create efficiencies within the inspection process e. Identify and report equipment and gages outside of calibration dates and exhibiting damage, wear, or malfunctions Documentation and Compliance f. Adhere to Good Documentation Practices (GDP) requirements g. Maintain accurate and complete records in all required documentation h. Follow defined processes and procedures appropriately and effectively identify gaps and/or misalignment with requirements i. Maintain product and lot traceability throughout the workflow and in all inspection documentation Safety and Housekeeping a. Follow all requirements and equipment safety procedures b. Identify and report safety hazards c. Keep work area clean and organized Communication a. Professional and courteous interactions b. Effective use of email and daily reporting to facilitate follow-up and action c. Proactive and constructive communication and support across the team to drive improvement and collaboration 6. Is the work described above checked by another individual? ? YES ? NO 7. Work Environment: a. Dynamic and fast-paced manufacturing floor, prone to interruptions b. Exposure to noise, high temperatures, moving machinery, and high-voltage equipment c. Clean room and gowning requirements Is the work described above checked by another individual? YES Consistent motor skills and other requirements of the position: Persistent: Standing: 10% Sitting: 75% Walking: 15% Consistent lifting of up to 35 lbs. - Rarely lifting of 1 lb. - Frequently Maximum carrying distance of up to 30 ft. - Occasionally Reaching - must be able to reach machines and/or materials up to 6 ft. from - Frequently Kneeling - N/A Climbing stairs - N/A Repetitive motion - right/left hand/wrist - Frequently Repetitive motion - right/left foot/ankle - N/A Continuous arm motions - Yes Must be able to avoid potentially moving which could cause injury - Yes Must be able to grasp and move object consistently and regularly - Yes Vision: intricate nature of work requires of 20/20 with or without corrective lenses - Yes Must be able to use gaging equipment and tools - Yes Must demonstrate to work productively and efficiently with others - Yes Microspec offers competitive wages and benefits, including: Sign-On Bonus Comprehensive Health Insurance Matching 401K plan annually after 1 year Entry-level 2 weeks paid vacation 64 Hours personal/sick time (unused time paid out at the end of the year) Annual discretionary bonus Salary range-$26.50-$28.00 per hour based on experience 20% Second Shift Differential

Salary: $17-$19 Innofiber, LLC specializes in the development and manufacturing of fiber optic illumination for medical and industrial applications that meet the highest industry standards. We are committed to lean manufacturing and continuous improvement programs. Job Description: Performs mechanical inspections/optical finishes on materials to Standard Operating Procedures (SOP) and mechanical drawing specifications. Ability to perform first article inspections and generate a report for both incoming and final inspections. Perform a variety of duties to inspect incoming material per Innofibers drawings specifications. Check work with appropriate test equipment and measuring instruments. Keep and maintain records as required. Helps with internal calibrations of tools according to ISO Procedures. Maintain the equipment and work area in a clean and orderly condition. Perform all assignments in conformance with all safety and health requirements. Perform all other related duties required or directed by your supervisor or QA Manger. Key Responsibilities Maintaining workflow to meet customer shipment requirements. The ability to work independently or as a team with little or no assistance. The ability to complete the required documentation that is required to maintain ISO requirements and customer requirements. Data entry for material transfer into inventory control system using Access database and FishBowl. Works with QA Manager should requirements be needed to update material specifications and SOPs. Keep and maintain appropriate QC records as required, including MRB weekly reviews with appropriate department personnel. Qualifications/Experience/Education Mechanical knowledge with the use of micrometers, calipers, go/no go gages, optical comparators, measuring tools, vision system, and various other test equipment. Ability to perform precise measurements check work with appropriate test equipment and measuring instruments. Report unusual conditions or circumstances to management. Possesses solid organizational & analytical skills. Good oral, written and communication skills with the ability to interact with various departments within the organization as well as communicate quality issues to management. Works under general supervision and follows established procedures and instructions. Solid computer skills using Microsoft Word and excel. Understanding of ACESS database is a plus. Ability to read and interpret mechanical blueprints. Have worked in an environment that is ISO certified. Physical Demands and Work Environment While performing the duties of this position, the employee is frequently required to use hands or fingers, handle or feel objects, tools, or controls. The employee is required to stand, walk, sit, and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate.

Job DescriptionJob Title: Quality Control Inspector Pay: $17. 50-$18. 50/hr Shift: 3rd Shift | 11:00 PM -7:00 AMLocation: Gardner, MA

So why join Hologic? You will have the opportunity to get in on the ground floor at a high growth facility to create a manufacturing process working on life-saving medical devices with potential for future growth. This is a great opportunity to enhance you manufacturing operation skills and knowledge to further your career. The Quality Control Inspector is a critical member of the Quality Assurance team, responsible for ensuring that finished products and in-process components meet all regulatory, quality, and customer requirements before release to inventory. This role involves the meticulous review of Device History Records (DHRs), performing inspections, and providing support to manufacturing and quality processes, such as Incoming Inspection, Material Review Board (MRB), Calibration and Returned Material Authorization (RMA) activities. The Final Inspector 2 is instrumental in upholding Hologic's commitment to excellence by ensuring compliance with Good Manufacturing Practices (GMP), ISO standards, and quality systems, while fostering a culture of continuous improvement and collaboration. What to expect: * Lead with Ownership - Demonstrate integrity and always aim to do the right thing. Be highly accountable for your work, follow through on commitments, and take responsibility when things don't go as planned. Embrace opportunities to try new things and learn from mistakes. * Act with Speed - Approach tasks with a strong sense of urgency and a bias toward action. Keep stakeholders informed by providing regular updates early and often, ensuring transparency and avoiding unexpected surprises, even when working at a fast pace. * Foster Partnerships - Collaborate effectively with teammates and stakeholders to achieve shared goals. Invest in building strong working relationships and contribute to efforts that fulfill the organization's Purpose, Promise, and Passion. * Delight Customers - Strive to exceed expectations by delivering high-quality work, exceptional experiences, and innovative solutions. Engage in proactive communication, provide excellent service, and develop a deep understanding of customer needs to create positive, lasting impressions and build trust-based relationships. * Celebrate WINS! - Take pride in delivering impactful results. Contribute to a positive team environment by celebrating both individual and team accomplishments. Support colleagues, recognize collective successes, and embody the mindset of an 'A-player' who inspires others. What we expect: * Perform detailed reviews of Device History Records (DHRs) as part of final inspection and release activities for finished products, ensuring accuracy and compliance with documentation standards. * Conduct reviews of manufacturing records for replacement components, subassemblies, and in-process inspections to ensure alignment with quality requirements. * Support manufacturing personnel by ensuring proper documentation of Failure Investigation Reports and processing of Non-Conforming Materials in the Product * Lifecycle Management (PLM) system, including identification, quarantine, and documentation. * Perform routine inspections, including field service and special inspections, to support validations, studies, and incoming inspection activities. * Communicate and reinforce Good Manufacturing Practices (GMP) to manufacturing personnel to uphold quality standards. * Review and provide input on new releases of Inspection and Test documents to ensure adherence to Good Documentation Practices (GDP). * Maintain QA Activity Collection Plans, First Pass Yield reports, and other applicable tracking mechanisms to monitor quality metrics. * Collaborate with Engineering to provide feedback on documentation improvements and process changes. * Support Incoming, product returns and calibration teams as needed as needed. * Perform other duties as assigned by leadership to meet organizational and operational needs. Education and Experience: High school degree and/or an equivalent technical school education preferred. Minimum of 3 to 5 years related Quality Inspection experience in Medical Manufacturing environment. Experience with Oracle, and Agile preferred. The annualized base salary range for this hourly role is $46,100-$69,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand. Agency and Third Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture on the second shift. The position also performs inspection activities during in-process manufacturing for second shift. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Job Description Summary: The Lead Housing Quality Standard (HQS) Inspector is responsible for conducting any mandatory inspection for all leased units under the Rental Assistance Program in accordance to the Department of Housing and Urban Development (HUD) and Department of Housing and Community Development (DHCD) program guidance. As the Lead HQS Inspector the incumbent is expected to assist the Inspections' Supervisor in providing training to newly hired inspectors and with administrative duties as assigned. Why Work for SMOC? Paid Time Off: All full-time employees can accrue up to 3 weeks of vacation, and 2 weeks of sick time and are eligible for 12 paid holidays during their first year of employment. Employer-paid Life Insurance & AD&D and Long-Term Disability for full-time employees. Comprehensive Benefits Package including Medical Plans through Mass General Brigham with an HRA Employer cost-sharing program, Dental Plans with Orthodontic Coverage, and EyeMed Vision Insurance available to full-time employees. 403(B) Retirement Plan with a company match starting on day one for all full-time and part-time employees. Additional voluntary benefits including; Term and Whole Life Insurance, Accident Insurance, Critical Illness, Hospital indemnity, and Short-Term Disability. Flexible Spending Accounts, Dependent Care Accounts, Employee Assistance Program, Tuition Reimbursement and more. Primary Responsibilities: Conduct thorough HUD/DHCD HQS inspections of all SMOC RAPS existing units, potential new units, and the reinspection of those units as required including physical and remote virtual inspections. Verify unit compliance based on health and safety requirements. Verify unit conditions for rent reasonableness comparisons. Enter all inspection data into the MRI Tenmast Software Systems' Inspection module and monitoring information as needed; printing all required inspection-related letters for participating tenants and owners. Assist the Inspection Supervisor in providing "on the job" training for newly hired HQS inspectors in the field Assist the Inspection Supervisor in monitoring the various types of inspections conducted by the HQS Inspection team including remote virtual inspections, re-inspections, inspections conducted using an owner self certification and physical inspections Make recommendations to the Inspection Supervisor on behalf of the HQS inspectors on process and procedure Monitor HQS supplies and make requests to the Program Director on orders for necessary equipment such as gloves, shoe coverings and personal protective equipment as needed Utilize and maintain inspection-related equipment on a regular basis, including camera, hand-held inspection devices or tablets, flashlight, cell phone, tick tester, and inspection-supply cache. Engage all clients by understanding and addressing their needs whether within or outside the scope of work. Attend & participate in engagement team meetings as requested and communicate effectively with clients and staff in other areas. Maintain confidentiality of client, employee and agency information in accordance with federal and state laws and funder requirements. Ensure compliance with program/department, agency and/or funder requirements, as well as SMOC policies & procedures. Other duties as assigned. Knowledge and Skill Requirements: Education: High school diploma or equivalent Minimum years of related experience: 1-2 years preferred Knowledge of Excel, Windows, Word and PCs, ability to work well in a very high volume and productivity environment, ability to handle potentially stressful situations and sensitivity to the needs of economically- disadvantaged clientele. Valid Mass. driver's license and insurance Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Must meet all required DHCD program certifications within 1 year. Organizational Relationship: Directly reports to HQS Inspection Supervisor. Indirectly reports to Program Director, Assistant Director and Division Director. Direct reports of this position are none. Indirect reports of this position are HQS Inspectors. Physical Requirement: Physical effort required to do the job: Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Working Conditions: This job requires working in many different conditions and places. About 80% of the time is outside the office either on the road or at a tenant's unit. Therefore, conditions range from an office environment to an outdoor environment that can be dirty, wet, cold, hot, difficult and risky. As part of the responsibilities of this position, the Lead Inspector will have direct or incidental contact with clients served by SMOC in various programs funded or administered through the Executive Office of Health and Human Services. A successful background check is required. Remote Work Option: Remote work is permissible in some positions at SMOC depending on the key functions and responsibilities. The Lead Inspector position is eligible to work from home 0% of the week in scheduling coordination with the department manager. Monday-Friday; 9am-5pm 35

Job Description Qualifications: a. High school diploma or GED required b. 0-3 years of relevant experience preferred; prior quality experience preferred, within GMP manufacturing environment is a plus Skills d. Familiarity with the fundamental concepts of Engineering drawings, inspection and documentation e. Demonstrate initiative and self-motivation to grow and succeed within the position f. Able to work semi-independently after initial training g. Display aptitude and willingness to learn and accept coaching h. Will receive hands-on training to support competency within the role i. Will receive opportunity and training to support growth within QC 2. Basic Position Skills: a. Flexibility - Able to adapt to shifting priorities and tasks b. Time Management - Able to balance multiple responsibilities and complete them efficiently c. Aptitude - Able to apply training effectively to assigned tasks d. Attention to Detail - Able to complete all documentation thoroughly and correctly e. Communication - Able to receive and give feedback and work well with others to achieve shared goals f. Mature work ethic - punctual with demonstrated good attendance record 3. Reports to: Quality Supervisor 4. Primary job responsibility: The QC Inspector Level 1 is an entry-level position within the Quality Control department. This position is focused on developing and applying foundational knowledge and the hands-on skills and competencies necessary for the inspection of extruded components utilized in Medical Devices. The Level 1 Inspector utilizes basic and foundational methods and gages to perform inspections of extruded product to determine conformance to defined specifications, adheres to GDP documentation requirements, and contributes to the daily productivity of the QC Team. This position is performed with guidance and supervision with increasing independence with experience 5. Essential functions of position: Perform Final Inspection for product Lot Release a. Prepare, follow and perform final inspections as defined on inspection paperwork for lot release b. Perform inspections using defined methods, gages and equipment c. Apply and follow ANSI and C = 0 Sampling Plans d. Document inspection results and complete all inspection paperwork as required e. Assess conformance to defined specifications and requirements f. Identify and document non-conformances to defined specifications and requirements g. Recognize, document and escalate quality concerns and issues h. Complete end-of-shift reporting Perform Start up and In-process inspection of manufacturing extrusion lines a. Prepare, follow and perform start-up and in-process inspections as defined on inspection paperwork of high-volume extrusion lines for production parts exhibiting recurring similar and consistent product geometries and materials and inspection methods b. Perform inspections using defined methods, gages and equipment c. Document inspection results and complete all inspection paperwork as required d. Assess conformance to defined specifications and requirements e. Identify and document non-conformances to defined specifications and requirements f. Communicate inspection results to the extrusion technician or operator g. Recognize, document and escalate quality concerns and issues h. Identify, document, and communicate at-risk product to appropriate personnel Inspection Methods, Gages and Equipment a. Utilize pin gages, ring gages, calipers, rulers, vision systems, and other applicable gages as specified and within scope of training b. Recognize and respond to basic visual and dimensional quality indicators and erroneous data c. Create efficiencies within the inspection process d. Identify and report equipment and gages outside of calibration dates and exhibiting damage, wear, or malfunctions Documentation and Compliance e. Adhere to Good Documentation Practices (GDP) requirements f. Maintain accurate and complete records in all required documentation g. Follow defined processes and procedures appropriately and effectively h. Maintain product and lot traceability throughout the workflow and in all inspection documentation Safety and Housekeeping a. Follow all requirements and equipment safety procedures b. Identify and report safety hazards c. Keep work area clean and organized Communication a. Professional and courteous interactions b. Effective use of email and daily reporting Work Environment: a. Dynamic and fast-paced manufacturing floor b. Exposure to noise, high temperatures, moving machinery, and high-voltage equipment c. Clean room and gowning requirements Is the work described above checked by another individual? YES Consistent motor skills and other requirements of the position: Persistent: Standing: 10% Sitting: 75% Walking: 15% Consistent lifting of up to 35 lbs. - Rarely Minimum lifting of 1 lb. - Frequently Maximum carrying distance of up to 30 ft. - Occasionally Reaching - must be able to reach machines and/or materials up to 6 ft. from floor - Frequently Kneeling - N/A Climbing stairs - N/A Repetitive motion - right/left hand/wrist - Frequently Repetitive motion - right/left foot/ankle - N/A Continuous arm motions - Yes Must be able to avoid potentially moving object which could cause injury - Yes Must be able to grasp and move object consistently and regularly - Yes Vision: intricate nature of work requires vision of 20/20 with or without corrective lenses - Yes Must be able to use gaging equipment and tools - Yes Must demonstrate ability to work productively and efficiently with others - Yes Microspec offers competitive wages and benefits including: Sign-On Bonus Comprehensive Health Insurance Matching 401K plan annually after 1 year Entry level 2 weeks paid vacation 64 Hours personal/sick time (unused time paid out at end of year) Annual discretionary bonus Salary range-$23-$26 per hour based on experience 20% Second Shift Differential