Quality control inspector jobs in Nashua, NH

Title: QC Investigations Specialist Employment Type: Contract Status: Accepting Candidates About the role This role supports real-time manufacturing operations by leading investigations, resolving on-floor issues, and ensuring high-quality documentation. You'll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance. Key Responsibilities • Triage manufacturing issues and lead analytical investigations and root cause analysis. • Write clear, compliant quality documentation including deviations and CAPAs. • Coordinate with SMEs to determine immediate actions, containment, and impact assessments. • Interpret data to support structured problem-solving and continuous improvement. • Provide technical operations support across manufacturing and QC functions. Qualifications • 6+ years pharmaceutical or biotech manufacturing experience. • 4+ years analytical investigation and QC-focused experience. • Strong background in RCA, deviation management, and GxP documentation. • Ability to interpret analytical data and think scientifically under time-sensitive conditions. • Experience partnering cross-functionally with manufacturing, QC, materials, and facilities teams. Compensation (MA Pay Transparency): • Estimated hourly range: $50-$55/hr (W-2). • Final rate within this range will be based on skills, experience, and interview results.

Quality Control Inspector (CWI) Base Salary: $40-55/hr About the Role Seeking a qualified Quality Control Inspector (CWI) to ensure all structural steel fabrication meets applicable codes, standards, and client specifications. This position is responsible for visual and dimensional inspection of welded products, documenting results, and coordinating with production and QA management to maintain top-tier quality standards. Key Responsibilities Conduct visual and dimensional inspections of structural steel components. Verify welding procedures, materials, and tolerances meet AWS/CWB and project standards. Complete inspection and test plans, weld maps, and related documentation. Perform NDT (VT/MT/PT/UT) if qualified and record results. Communicate with production, supervisors, and QA Manager to resolve issues. Support training and mentorship of team members in QC practices. Qualifications CWI certification required (active and in date). Minimum 5 years of welding or QC experience in a structural steel environment. Strong understanding of AWS, AISC, and fabrication tolerances. Ability to read shop drawings, measure accurately, and complete QA forms. Experience with coatings, traceability, and documentation processes preferred. Able to lift up to 60 lbs and work both independently and as part of a team.

Contract Length: 6 month with potential extension About the Role We are seeking a highly motivated and independent QC Equipment Technician to be the operational and compliance expert for all laboratory equipment within our state-of-the-art biopharmaceutical Quality Control (QC) facilities. This specialized role is critical for ensuring the continuous qualification, calibration, and maintenance of high-precision analytical instrumentation, directly supporting the compliance and integrity of our clinical and commercial testing programs. Key Responsibilities The QC Equipment Technician manages the full lifecycle of laboratory assets and supports the robust quality system that governs their use: Equipment Lifecycle & Maintenance Coordinate and schedule calibration, maintenance, and Installation, Operational, Performance Qualification (IOPQ) activities with Facilities, Metrology, and QC end-users to minimize equipment downtime and address Out of Tolerance (OOT) events immediately. Monitor, coordinate, and communicate equipment lifecycle timelines-from acquisition and induction to qualification, implementation, and decommissioning-utilizing project management tools. Submit asset induction, work, and administrative requests to ensure equipment failures are addressed immediately and data in the Computerized Maintenance Management System (CMMS) is accurate and in the proper state. Serve as the primary QC point person for all equipment inquiries, acting as the liaison between the laboratory team and appropriate external vendors. Ensure all vendor representatives strictly follow site safety and cGMP procedures when working on equipment. Perform minor, non-invasive repairs on high-precision systems like UHPLC (e.g., changing capillaries, flow cells, needles/seats) and execute basic troubleshooting to diagnose complex failures. Quality & Compliance Documentation Support the authoring, review, and maintenance of high-stakes quality system records, including Deviations, Change Controls, and CAPAs (Corrective and Preventive Actions) as required. Author, revise, and maintain Equipment/Instrument Standard Operating Procedures (SOPs). Review preventative maintenance reports, calibration certifications, CMMS records, and perform system inventory audits to ensure compliance. Ensure all equipment documentation meets stringent cGMP, GDP (Good Documentation Practices), and data integrity requirements (ALCOA+) throughout its operational life. Ensure all tasks are performed in compliance with safety and cGMP requirements. Inventory & Logistics Order supplies and maintain inventory for equipment consumables and accessories. Assist with locating and collecting assets due for service and returning them to the laboratory promptly once service is complete. Basic Qualifications Education: Bachelor's degree (BS) in a relevant scientific discipline (e.g., Chemistry, Biology, Engineering, or related field). Experience: Minimum of 5 years of experience in a regulated laboratory setting with a BS degree. OR Minimum of 3+ years of experience in a GMP Quality Control (QC) laboratory setting. Knowledge: Demonstrated aptitude and ability to learn quickly to develop a strong understanding of GxP principles (cGMP, GLP). Skills: Proven expertise in laboratory equipment IOPQ, calibration, maintenance, and troubleshooting. Familiarity with electronic Quality Management Systems (eQMS) and CMMS software.

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.

We are seeking a Senior Quality Control Inspector to join our growing team in Littleton, MA. In this hands-on role, you will perform precise mechanical inspections to ensure our products meet the highest standards of quality and compliance. You will work closely with cross-functional teams, supporting manufacturing and R&D processes while maintaining adherence to FDA and ISO 13485 requirements. If you have a passion for precision, attention to detail, and experience in medical device inspection, this is an excellent opportunity to advance your career in a dynamic and collaborative environment. Key Responsibilities: Perform dimensional, visual, and functional inspections of components, subassemblies, and finished products. Conduct First Article Inspections (FAI), in-process, final, and RMA inspections. Maintain and calibrate inspection equipment within the Quality Control Lab; assist with internal calibrations. Create and maintain part-specific inspection forms and quality documentation. Support R&D projects and new product development with inspection expertise. Interpret engineering drawings, specifications, and GD&T to ensure product compliance. Document and process non-conformances, and assist with root cause investigations. Prepare inspection records for internal and external audits. Collaborate with suppliers for product verification and technical clarification. Participate in continuous improvement initiatives to enhance inspection accuracy and efficiency. Qualifications: Required: High school diploma or equivalent (Technical degree a plus) 7+ years of Quality Control inspection experience in a manufacturing environment (medical device preferred) Strong knowledge of mechanical inspection, metrology, and calibration processes Proficient in reading engineering drawings and interpreting GD&T symbols Skilled in using inspection tools such as calipers, micrometers, microhite, pin gages, and thread gages Experience with ERP/MRP systems and electronic Quality Management Systems (eQMS) Familiarity with IPC standards for inspection Benefits: Competitive salary based on experience Comprehensive health, dental, and vision insurance Paid time off (PTO) and paid holidays 401(k) plan with company match Professional development and career advancement opportunities

DEKA R&D has an immediate opening for and Quality Control Inspector to work in a dynamic Medical Device Research, Development, and Manufacturing company. This position is a highly visible role with significant and direct impact on the development and success of multiple engineering projects. Responsibilities as a Quality Control Inspector: Interpret Mechanical and Electrical print reading and apply to incoming inspection practices Operate CMM equipment and utilize various measuring tools for inspection of medical device components Communicate effectively across multiple projects to provide feedback on inspection of parts Inspect various mechanical and electrical components and assemblies through incoming inspection Interpret ASME Y14.5 and GD&T standards throughout the inspection process for compliance and best practices Provide feedback on inspection activities to improve efficient whether individually or in a cross-functional setting To be successful as a Quality Control Inspector, you will need the following qualifications: 3+ years of experience in a regulated industry Mechanical Engineering degree or Equivalent education/experience CMM programming, Metrology and/or CQI certified is a plus Ability to read and understand complex GD&T on prints using ASME Y14.5 standards Basic GD&T knowledge required, Advanced GD&T knowledge preferred Proficient with mechanical measuring equipment such as micrometers, calipers, optical comparator Ability to understand and operate CMMs preferred Inspection of soldered components and Printed Circuit Board (PCB) assemblies; IPC-A-610 certification preferred Computer skills and knowledge; comfortable learning new software (Experience with Jira is a plus) 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 & 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.

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.

About Us: As a global manufacturer of complex aircraft engine components, Pursuit Aerospace is founded on a commitment to relentless, continuous, operational improvement and extraordinary customer service. We pride ourselves on competitive cost structure, exceptional on-time delivery, and industry-leading quality. About the Opportunity: The Quality Team Lead will play a critical role in maintaining and improving the quality systems, processes, and culture at Pursuit Aerospace. This position provides leadership to the quality team and serves as a key liaison between quality, operations, engineering, and customers to ensure products meet or exceed internal and external requirements. Location: Malden, MA Responsibilities: Supervise and lead a team of Quality Inspectors and Technicians in day-to-day activities. Ensure that incoming, in-process, and final inspections are performed to quality standards and customer specifications. Assist in the implementation and maintenance of AS9100/ISO9001 standards and quality procedures. Participate in root cause analysis and corrective/preventive action processes (RCCA/CAPA). Monitor and report quality performance metrics, driving continuous improvement initiatives. Provide training, guidance, and development to quality team members. Collaborate with Production, Engineering, and Supply Chain teams to resolve quality issues and support production goals. Lead the team with a strong sense of urgency to meet customer delivery needs while ensuring there is never a compromise on safety or quality standards. Escalate significant quality issues and customer complaints as necessary. Promote a culture of quality, accountability, and continuous improvement. Required Qualifications: High School diploma or equivalent required. 5+ years of experience in aerospace manufacturing or a similar regulated industry. 5+ Experience with inspection tools, GD&T, and reading technical drawings. 1+ years in a supervisory or team lead role. Must be authorized to work in the U.S. on a full-time basis without sponsorship now or in the future. The Company cannot offer employment to visa holders who require employer sponsorship in the future or cannot work now on a full-time basis. Must be able to perform work subject to ITAR/EAR regulations. Preferred Qualifications: Associate's or bachelor's degree in engineering, Quality, or a related field preferred. Experience working with CNC machinery, PLCs, and automated systems. Familiarity with lean manufacturing practices and continuous improvement initiatives. Comfortable using manufacturing software systems and basic Microsoft Office applications. Strong knowledge of production processes, safety standards, and quality systems (e.g., AS9100, ISO 9001). Demonstrated ability to lead by example, motivate teams, and hold others accountable. Excellent communication, organizational, and problem-solving skills. Proficiency in root cause analysis tools (e.g., 5 Whys, Fishbone, 8D). Ability to work in a fast-paced and collaborative environment. Pre-Employment Screening: As a federal contractor in the defense industry, Pursuit Aerospace is subject to federal regulations. All offers of employment are contingent upon successful completion of background checks, drug and alcohol screening, and employment eligibility verification. Physical Requirements: Requires mobility in a manufacturing plant environment while using Personal Protective Equipment. Must be able to frequently sit, stand, and walk. Must be able to lift and carry up to 15 pounds. Compensation & Benefits: Pursuit Aerospace also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, schedule type, and the applicability of collective bargaining agreements, among other things. Pursuit is an Equal Opportunity Employer

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 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

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

Full-time Description The Quality Control Inspector, reporting to the Quality Control Supervisor is responsible for all aspects of incoming, in-process, and final inspections, including measurements, recordkeeping, calibration, documentation, production support on an as needed basis and other urgent matters for the Quality Control Department. Principal Responsibilities Perform dimensional and visual first article and in-process/final inspection on raw material, parts, gages, and other equipment, accepting material/product or referring for quality review based on findings. Prepare inspection reports; ensure material traceability. Initiate Nonconformances (NCR) and Supplier Corrective Action Reports (SCARs); facilitate Material Review Board (MRB) meetings. Use a variety of fixed and variable measuring instruments. Monitor and coordinate Engineering Change Order (ECO) activity across the organization ensuring compliance with the Quality Management System (QMS); support QMS maintenance for compliance with FDA QSR, ISO 13485, and other regulatory requirements. Ensure compliance with electronic document control workflows in QCBD or similar document control tool. Ensure documents are being filed and organized. Support audits in the role as a “Runner”, extracting documents, review them to ensure regulatory compliance and correctness, and present to the Lead Auditor for presentation. Coordinate QA/QC tasks with cross functional teams across the organization: support production and product development teams; review Device History Records (DHRs) for completeness and accuracy; execute receiving procedures & support shipping activities. Support and promote continuous improvement initiatives to meet business objectives. Maintains a safe and healthy work environment by following standards and procedures and complying with legal regulations. Perform miscellaneous duties and projects as assigned and required. Requirements Training, Skills, Knowledge and/or Experience Minimum 1 year of experience performing mechanical inspections in a manufacturing environment; optical inspection experience preferred. Experience working in medical devices and FDA QSR and ISO 13485 preferred. Understanding quality control processes, methods, and standards. Proficiency with Microsoft 365 apps suite. Competencies Strong data collection & analysis, problem solving, presentation and communication skills. Strong attention to detail. Ability to collaborate effectively with cross-functional teams. Education Requirements High School Diploma or GED required. Supervisory Responsibility None Working Conditions This job operates in manufacturing and engineering laboratory environments including ISO class 7 cleanrooms. PPE required when in controlled environment rooms or cleanrooms. Physical surroundings This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. Physical Effort While performing duties of this job, the employee is occasionally required to stand, walk, sit, use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; talk and hear. Work Schedule / Travel In-person, Mon to Fri in Gardner, MA; occasional travel, with periodic presence in the Windham, ME site. Other Requirements This position involves access to technology that is subject to U.S. export controls. Any job offer made will be contingent upon the applicant's capacity to serve in compliance with U.S. export controls.

Full-time Description Summary/Objective Quality Control Inspector is responsible for performing and documenting FAIs, receiving, in-process and final inspection to ensure product conforms to all applicable requirements. Essential Functions Performs receiving, in process and final inspection of products. Records inspection results by completing reports, summarizing re-works and wastes and inputting data into quality database Resolves issues and answer questions from Operators as well as from Inspectors and Engineers. Participates in special projects related to tooling fixtures and gages. Identifies and participate in cost reduction projects utilizing Lean Manufacturing principle. Reviews and approve material and special process certifications Follows detailed work instructions on shop routers for compliance with customer requirements Works closely with the team to determine efficiency gaps, and to implement improvements. Provides inspection support to all departments in the organization, perform part inspection and FAIs. Performs other responsibilities as required. Requirements Competencies Ability to read and interpret specifications and inspection instructions to determine product conformance. Self-starter; able to work independently with minimal supervision in a fast-paced environment. Highly organized with meticulous attention to detail and follow-through while maintaining a safe, clean and organized workspace. Must be able to interact and communicate with coworkers at all levels of the organization. Knowledge of mechanical inspection and proficiency in the use of manual & visual inspection equipment: e.g., Calipers, gauges, micrometers, digital indicators, etc. Basic computer skills (including Microsoft Office). Understands production travelers and work instructions. Strong desire to learn and to apply new skills. Supervisory Responsibility None Work Environment This job operates in a manufacturing environment. This role routinely uses shop floor tools and machinery. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Manual dexterity sufficient to operate machinery for precision work Visual acuity (corrected) to read directions and prints and to inspect machined parts closely to ensure that they meet specifications Frequently required to sit, stand, move about the shop floor, talk, hear, bend and reach with hands and arms Occasionally lift and/or move up to 50 pounds Ability to squat or kneel occasionally Position Type/Expected Hours of Work This is a full-time hourly position which operates Monday through Friday, 7:00am to 3:30pm. Travel Occasional (Less than 5%) Required Education and Experience High School diploma or equivalent required Knowledge of blueprint reading 4 years of experience in a manufacturing environment and mechanical inspection of precision parts. 4 years of experience with inspection equipment and tools. Please note this job posting is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Harmonic Drive LLC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. U.S. Export Controls Requirements: This job may require access to technology, materials, software or hardware that is controlled by the export laws of the United States. Candidates are required to provide proof of either US citizenship, Permanent US residency or classification as a protected individual as defined in 8 USC 1324b (a) (3). This position is not eligible for immigration sponsorship.

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

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.

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