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Systems Quality Assurance I (Co-Op) - United States
Cisco Systems, Inc. 4.8
Quality control inspector job in Maynard, MA
Please note this posting is to advertise potential job opportunities. This exact role may not be open today but could open in the near future. When you apply, a Cisco representative may contact you directly if a relevant position opens.
Applications are accepted until further notice.
Please note this posting is to advertise potential job opportunities. This exact role may not be open today but could open in the near future. When you apply, a Cisco representative may contact you directly if a relevant position opens.
Meet the Team
Acacia, now part of Cisco, provides innovative silicon-based high speed optical interconnect products to accelerate network scalability through advancements in performance, capacity, and cost. Our DSP ASICs, silicon photonic PICs and coherent modules empower cloud and service providers to meet the fast-growing demand for data. Cisco is well known for developing ground-breaking products in short time intervals. To support new product development at an exciting pace the Systems Quality Assurance team is challenged to architect, develop and maintain test automation software using scalable and maintainable methods. If you have a passion for test automation, working on complex systems and for delivering high quality best-in-class technology, then this position is calling your name.
Your Impact
The SQA Engineering Co-op will perform one or more of the following tasks while working on Cisco's elite optical communication products. The Co-op will be assigned relevant work assignments to challenge them according to their current level of experience and capability.The Co-op may find themselves working in the following areas:
* Contribute to design and development of test plans, test facilities and test automation software (C++, C#, Python or LabVIEW)
* Implement manual and automated tests on new Cisco product software releases under supervision of senior SQA team members
* Work closely with senior SQA team members to resolve issues by analyzing Cisco product under test while using various measurement instruments and automated debug software
* Document detailed test results; analyze test results data for trends and anomalies
* Learn to produce high quality code that is robust and maintainable
Minimum Qualifications
* Currently enrolled in an undergraduate degree program. Relevant fields include: Computer Science, Software Engineering, Computer Engineering or Electrical Engineering
* Knowledge of Python
* Knowledge of C# or C++
* Knowledge of LabVIEW
* Must be able to be onsite in Maynard, MA five days a week
Preferred Qualifications
* Good interpersonal and organizational skills
* Passion about engineering
* Enjoys working with hardware AND software
* Enjoys working in lab environments
* Likes to be challenged to understand systems and figure out ways to break it
* Previous internship experience
Why Cisco?
At Cisco, we're revolutionizing how data and infrastructure connect and protect organizations in the AI era - and beyond. We've been innovating fearlessly for 40 years to create solutions that power how humans and technology work together across the physical and digital worlds. These solutions provide customers with unparalleled security, visibility, and insights across the entire digital footprint.
Fueled by the depth and breadth of our technology, we experiment and create meaningful solutions. Add to that our worldwide network of doers and experts, and you'll see that the opportunities to grow and build are limitless. We work as a team, collaborating with empathy to make really big things happen on a global scale. Because our solutions are everywhere, our impact is everywhere.
We are Cisco, and our power starts with you.
Message to applicants applying to work in the U.S. and/or Canada:
Individual pay is determined by the candidate's hiring location, market conditions, job-related skillset, experience, qualifications, education, certifications, and/or training. The full salary range for certain locations is listed below. For locations not listed below, the recruiter can share more details about compensation for the role in your location during the hiring process.
U.S. employees are offered benefits, subject to Cisco's plan eligibility rules, which include medical, dental and vision insurance, a 401(k) plan with a Cisco matching contribution, paid parental leave, short and long-term disability coverage, and basic life insurance. Please see the Cisco careers site to discover more benefits and perks. Employees may be eligible to receive grants of Cisco restricted stock units, which vest following continued employment with Cisco for defined periods of time.
U.S. employees are eligible for paid time away as described below, subject to Cisco's policies:
10 paid holidays per full calendar year, plus 1 floating holiday for non-exempt employees
1 paid day off for employee's birthday, paid year-end holiday shutdown, and 4 paid days off for personal wellness determined by Cisco
Non-exempt employees** receive 16 days of paid vacation time per full calendar year, accrued at rate of 4.92 hours per pay period for full-time employees
Exempt employees participate in Cisco's flexible vacation time off program, which has no defined limit on how much vacation time eligible employees may use (subject to availability and some business limitations)
80 hours of sick time off provided on hire date and each January 1st thereafter, and up to 80 hours ofunused sick timecarried forwardfrom one calendar yearto the next
Additional paid time away may be requested to deal with critical or emergency issues for family members
Optional 10 paid days per full calendar year to volunteer
For non-sales roles, employees are also eligible to earn annual bonuses subject to Cisco's policies.
Employees on sales plans earn performance-based incentive pay on top of their base salary, which is split between quota and non-quota components, subject to the applicable Cisco plan. For quota-based incentive pay, Cisco typically pays as follows:
.75% of incentive target for each 1% of revenue attainment up to 50% of quota;
1.5% of incentive target for each 1% of attainment between 50% and 75%;
1% of incentive target for each 1% of attainment between 75% and 100%; and
Once performance exceeds 100% attainment, incentive rates are at or above 1% for each 1% of attainment with no cap on incentive compensation.
For non-quota-based sales performance elements such as strategic sales objectives, Cisco may pay 0% up to 125% of target. Cisco sales plans do not have a minimum threshold of performance for sales incentive compensation to be paid.
The applicable full salary ranges for this position, by specific state, are listed below:
New York City Metro Area:
$44,000.00 - $185,000.00
Non-Metro New York state & Washington state:
$44,000.00 - $185,000.00
* For quota-based sales roles on Cisco's sales plan, the ranges provided in this posting include base pay and sales target incentive compensation combined.
** Employees in Illinois, whether exempt or non-exempt, will participate in a unique time off program to meet local requirements.
$44k-185k yearly 1d ago
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Quality Control Technician
JVT Advisors 3.7
Quality control inspector job in Rochester, MA
Location: Rochester MA (100% On-site), 1st shift only 6:30A-3:30P M-F, salary range $72K-$82K, full-time role:
health insurance with an HRA, dental, vision, LTD, and a 401(k) retirement plan with an employer match. 3 weeks PTO, 1 week sick. Generous relocation package offered. Qualified candidates are encouraged to apply.
Large precast concrete supplier in Massachusetts and New Hampshire, providing high-quality products for over 70 years. Their extensive product range includes septic tanks, manholes, drainage structures, bulkheads, curbing, residential steps, and retaining wall systems, all crafted to precise specifications. They cater to engineers, contractors, and homeowners, emphasizing superior performance and exceptional customer service.
The Quality Control Technician (“QC Technician”) will work within the production plant and is ultimately responsible for product testing. The QC Tech will assist in the execution of quality control processes, procedures and protocol associated with the production of pre and post concrete pours.
Responsibility
Responsible for ACI concrete field tests
Responsible for quality control inspections in manufacturing plant
Inspect forms before pouring (Pre-Pour).
Inspect product after removed from forms (Post-Pour)
Notifies Production Supervisor if deficiencies are found.
Perform and/or schedule repairs on products as needed.
Housekeeping - maintain a clean work area. Including cleanliness within breakroom, restroom, and general facility areas.
Expected to maintain knowledge of precast plant techniques and procedures.
May assist with precast production operation as needed.
Characteristics
Always committed to safety. Maintain a safe work area. Follow safe work practices as outlined in the Safety Program.
Always committed to quality. Follow and implement quality control measures.
Excellent attendance.
Reliable means of transportation to and from work.
Ability to learn, organize and prioritize work and handle multiple tasks.
Outstanding attitude, honesty, and ethic at all times.
Expected to use sound judgment, diplomacy, and discretion.
Work independently or cooperatively with others.
Self-drive in carrying out the functions of the job.
Requirements:
ACI Concrete Field-Testing Grade 1 Certified (preferred)
NPCA PQS Training
Must be at least 18 years of age per federal guidelines.
Good communication skills, both verbal and written to all levels of staff
Ability to remain focused in busy environment.
Computers and tablets skills in order to perform tasks.
Ability to read blueprints and sketches.
$72k-82k yearly 1d ago
Quality Control Inspector
Biotalent
Quality control inspector job in Devens, MA
Quality Inspector III - Weekdays
About Us
Founded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, our client is reshaping how the world manufactures critical products. They build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through vertically integrated capabilities, including scalable additive manufacturing and precision machining, they deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship.
Their team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. They foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because diverse perspectives lead to better outcomes.
Job Purpose
As a Quality Inspector III at our client, you will work in a diversified role within the Quality Inspection team dedicated to ensuring every product delivered meets the highest standards of precision, safety, and reliability. By applying expertise in inspection methods, quality systems, and problem-solving, this role safeguards customer trust, drives continuous improvement, and supports innovation in metal additive manufacturing.
This position operates on the weekday shift: Monday-Friday, 6:00 AM to 2:30 PM.
Key Responsibilities
Perform First Article Inspections (FAI) and routine part inspections using calipers, micrometers, and other gauges.
Verify that materials, equipment, processes, and products comply with quality specifications.
Develop and validate inspection and test methods; assist in creating SOPs and inspection protocols.
Monitor, analyze, and report on product quality metrics.
Support compliance with customer, internal, and industry requirements (AS9100, ISO 9001, ISO 13485) through audits and gap analysis.
Assist in developing and implementing process controls, corrective actions, and continuous improvement initiatives.
Ensure workflows, processes, and products comply with safety regulations.
Investigate and troubleshoot product or production issues.
Inspect manufactured parts, issue non-conformance reports, and facilitate MRB hardware disposition and corrective action tasks.
Work independently and manage daily priorities with minimal supervision.
Communicate and collaborate with operations personnel to ensure production needs are met.
Initiate and communicate identified nonconformances.
Qualifications
5+ years of experience performing part inspections with strong drawing interpretation skills.
Extensive knowledge of GD&T principles.
Experience with First Article Inspections (FAI), Test Method Validation (TMV), and developing inspection methods.
Proficiency in AQL sampling techniques.
Skilled in performing dimensional and visual inspections.
Experience with root cause analysis, data analysis, and troubleshooting.
Experience in medical device, aerospace, or defense manufacturing required.
Hands-on experience with advanced inspection equipment and software, including CMMs, PCMMs, vision systems, profilometers, and blue-light scanners (e.g., Zeiss, Faro, Keyence).
Ability to troubleshoot issues encountered with inspection equipment.
Self-motivated, hands-on team player with excellent communication skills; adaptable to fast-paced environments and excited by new challenges in metal additive manufacturing.
$30k-52k yearly est. 5d ago
Quality Control Analyst II
Talentburst, An Inc. 5000 Company 4.0
Quality control inspector job in Norton, MA
Industry: Pharmaceuticals
Title: Quality Control Analyst II
Duration: 11 months contract (+Possibility of extension)
This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
Description:
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.
Key Responsibilities'
Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep.
Review data timely and qualify as a data reviewer.
Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
Contribute to updating controlled documents (SOPs, work instructions, test methods).
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).
Participate in continuous improvement initiatives and cross-functional collaboration.
Support regulatory submissions, inspection readiness, and audits
Qualifications:
B.S. in chemistry, biology, biochemistry, or related field.
4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
Experience in method transfer/implementation; understanding of method lifecycle management preferred.
Strong technical writing, data analysis, problem-solving, and organizational skills.
Excellent communication and teamwork.
Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
$60k-83k yearly est. 4d ago
Quality Control Analyst II - Mansfield, MA area - Contract (Weekend Shift)
Yoh, A Day & Zimmermann Company 4.7
Quality control inspector job in Norton, MA
Please send your updated resume to ****************** Quality Control Analyst II - Mansfield, MA area- Contract (Weekend Shift) Mansfield, MA area Contract - (Weekend Shift)
Experienced in performing routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the . All qualified applicants are welcome to apply
Estimated Min Rate: $30.80
Estimated Max Rate: $44.00
What's In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
Health Savings Account (HSA) (for employees working 20+ hours per week)
Life & Disability Insurance (for employees working 20+ hours per week)
MetLife Voluntary Benefits
Employee Assistance Program (EAP)
401K Retirement Savings Plan
Direct Deposit & weekly epayroll
Referral Bonus Programs
Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************
$30.8 hourly 4d ago
QC, Chemistry, Sample Management
JMD Technologies Inc.
Quality control inspector job in Norwood, MA
Title: QC Specialist - Chemistry
Employment Type: Contract
Status: Accepting Candidates
About the role
This role supports Quality Control Chemistry operations by leading QC Sample Management activities across multiple lab functions. You will ensure compliant, on-time sample processing while partnering with digital and quality teams in a fast-paced cGMP environment. Shift: Wednesday-Saturday, 6:00 AM-4:00 PM.
Key Responsibilities
• Lead QC Sample Management operations supporting Chemistry, Microbiology, Bioassay, and Raw Materials
• Oversee daily schedules to ensure compliant sample processing and documentation
• Author and maintain SOPs, deviations, CAPAs, and change controls
• Act as primary support for audit readiness and regulatory inspections
• Partner with Digital teams to optimize LIMS (LabVantage) and data workflows
• Manage CTU systems, investigations, and compliance issue resolution
Qualifications
• BA/BS with 3-5 years or MS with 1-3 years of cGMP Quality Control experience
• Strong hands-on experience with QC Sample Management
• Proficiency with LIMS and Veeva Quality Systems
• Working knowledge of FDA, EU, and ICH regulations
• Experience with gowning, aseptic technique, and lab safety practices
• Proven people management and cross-functional leadership skills
Compensation (MA Pay Transparency):
• Estimated hourly range: $40-$45/hr (W-2)
• Final rate within this range will be based on skills, experience, and interview results.
$24k-37k yearly est. 2d ago
Quality Control Analyst II
Advantage Technical
Quality control inspector job in Norton, MA
Quality Control Analyst II Norton 45 per hour
This is an onsite role in Norton, MA.
First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
Perform routine and non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies in accordance with SOPs
Support weekend laboratory operations and maintain required training records
Assist with laboratory equipment and inventory maintenance, including reagent and sample preparation
Review data in a timely manner and serve as a qualified data reviewer
Perform operational assignments such as raw material processing, environmental monitoring, and in-process testing
Contribute to the creation and updating of controlled documents, including SOPs, work instructions, and test methods
Follow internal policies, SOPs, and applicable regulatory standards (GMP, GLP, ICH)
Participate in continuous improvement initiatives and cross-functional collaboration
Support regulatory submissions, inspection readiness, and audits
Qualifications
Bachelor's degree in Chemistry, Biology, Biochemistry, or a related field
4-8 years of pharmaceutical or biotech experience in GMP QC or equivalent environments
Experience with method transfer and implementation; understanding of method lifecycle management preferred
Strong technical writing, data analysis, problem-solving, and organizational skills
Excellent communication and teamwork abilities
Proficiency in LabWare LIMS, Microsoft Excel, Word, and PowerPoint preferred
$49k-79k yearly est. 4d ago
QA Technician
Granite Telecommunications 4.7
Quality control inspector job in Lincoln, RI
Granite delivers advanced communications and technology solutions to businesses and government agencies throughout the United States and Canada. We provide exceptional customized service with an emphasis on reliability and outstanding customer support and our customers include over 85 of the Fortune 100. Granite has over $1.85 Billion in revenue with more than 2,100 employees and is headquartered in Quincy, MA. Our mission is to be the leading telecommunications company wherever we offer services as well as provide an environment where the value of each individual is recognized and where each person has the opportunity to further their growth and achieve success.
Granite has been recognized by the Boston Business Journal as one of the "Healthiest Companies" in Massachusetts for the past 15 consecutive years.
Our offices have onsite fully equipped state of the art gyms for employees at zero cost.
Granite's philanthropy is unparalleled with over $300 million in donations to organizations such as Dana Farber Cancer Institute, The ALS Foundation and the Alzheimer's Association to name a few.
We have been consistently rated a "Fastest Growing Company" by Inc. Magazine.
Granite was named to Forbes List of America's Best Employers 2022, 2023 and 2024.
Granite was recently named One of Forbes Best Employers for Diversity.
Our company's insurance package includes health, dental, vision, life, disability coverage, 401K retirement with company match, childcare benefits, tuition assistance, and more.
If you are a highly motivated individual who wants to grow your career with a fast paced and progressive company, Granite has countless opportunities for you.
EOE/M/F/Vets/Disabled
Summary of Position:
The Quality Assurance Representative is responsible for performing detailed quality checks on all equipment being shipped from the Rhode Island Warehouse. This role ensures accuracy in documentation, labeling, and compliance with operational standards, reducing errors and improving customer satisfaction.
Duties and Responsibilities:
Perform QC checks on all orders to be shipped verify accuracy and functionality.
Ensure compliance with standardized procedures.
Collaborate with configuration technicians and fulfillment teams to resolve discrepancies.
Maintain QC records and contribute to process improvement initiatives.
Analyze trending quality issues conduct root cause analysis to be able to reduce the frequency of errors
Required Qualifications:
High school diploma or equivalent
Strong attention to detail and ability to follow standardized procedures.
Entry-level experience with basic computer systems, ticketing tools, and documentation platforms
Ability to prioritize and manage multiple tasks in a fast-paced environment
Strong communication and teamwork skills
Ability to lift and move equipment as needed
Preferred Qualifications:
Associate's degree, technical certification, or equivalent experience.
Familiarity with Network equipment and other communications hardware.
Proven experience in analytical process improvement, including identifying inefficiencies, implementing corrective actions, and documenting results.
Working knowledge of internal ticketing and order management systems.
Strong problem-solving skills and ability to adapt to shifting priorities.
Prior experience in a fast-paced lab, logistics, or telecom environment.
$31k-45k yearly est. 1d ago
QC Analyst
Tandym Group
Quality control inspector job in Woburn, MA
A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, 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
Perform other duties, as needed
Qualifications:
Bachelor's Degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field
Familiarity with basic Lab techniques and Data Analysis methods
Strong organizational, communication, and interpersonal skills
Detail-oriented and eager to develop problem-solving skills in a regulated lab environment
Enthusiasm for learning and the ability to work both independently and within a team
Desired Skills:
Academic or internship experience with Mammalian Cell Culture and/or ELISAs
$48k-78k yearly est. 4d ago
Environmental monitoring QC Associate
Planet Pharma 4.1
Quality control inspector job in Bedford, MA
Responsibilities:
• Perform environmental monitoring (EM) tasks for the aseptic environment, other controlled areas, and plant utility systems following specified instructions and techniques from Standard Operating Procedures (SOP), Training Material, and other GMP documents.
• Incubate and enumerate microbial growth on EM plates.
• Ensure all tasks are completed in a GMP compliant and safe manner.
• Document all tasks within LIMS or standard laboratory paper documentation utilizing GDP principles.
• Entry of information into logbooks as applicable for tasks per SOP.
• Partner and communicate with operations, manufacturing, facilities, and other site departments as required for support of operations and GMP processes.
• Actively participate in daily and weekly laboratory meetings.
• Accurately complete task management tools and handover communications.
• Perform general lab tasks including cleaning and equipment preparation.
• Maintain training for all required tasks.
• May assist in laboratory investigations with limited scope.
Requirements:
• Bachelor's degree with no experience, associate degree with 2+ years' experience, or High School Diploma [or Equivalent (GED)] with 4+ years' experience.
• Good oral, written, and interpersonal communication skills.
• Basic math skills and computer skills such as data entry, along with a high level of attention to detail.
• A demonstrated ability to organize time independently, be able to perform several tasks concurrently (ability to multi-task) and be able to meet objectives in a team-oriented environment.
• Must maintain aseptic qualifications
Shift is Sunday - Wednesday, 10 hour days, after a 3 month training period of Monday - Friday, 8 hour days
$41k-66k yearly est. 3d ago
Quality Engineer, Analytical Development and Quality Control
Vaxess Technologies
Quality control inspector job in Woburn, MA
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
******************
.
$69k-95k yearly est. 4d ago
Fall 2026 Co-Op - MES and Quality
Keurig Dr Pepper 4.5
Quality control inspector job in Burlington, MA
Job Overview:Fall 2026 Co-Op - MES and Quality - Burlington, MA As a Fall 2026 Co-Op - MES and Quality Co-Op in Burlington, MA at Keurig Dr Pepper (KDP), you will be a part of the beverage revolution. You will be working in a fast-paced, highly technical manufacturing environment that produces some of KDP's most popular beverages.
Each co-op will lead high-impact projects and will be provided with opportunities to grow professionally.
Come learn what it takes to succeed at an industry-leading company and help contribute to our ongoing success.
You will be able to directly participate in the implementation of new technology that improves our manufacturing process.
Shift/Schedule: The KDP 2026 Fall Co-op Program will run from July 13 - Decemeber 11, 2026Full-time; 40 hours per week Monday-Friday 8:00am until 5:00pm In-Person As a Co-op you will: Gain knowledge in executing operational plans and projects, including data analytics and developing visualizations for DMS (Daily Management Systems) and QMS(Quality Management Systems).
Participate in AGILE project management and lead the development, verification, and testing of Data Analytics dashboards and visualization tools.
Influence software capabilities to achieve six sigma quality performance and enhance Quality Management System.
Assist with TPM (Total Productive Maintenance) implementation and Lean activities, including participation in Continuous Improvement or Kaizen events.
Test and verify new technology systems implemented for the Quality management and Manufacturing process.
Elements of the KDP Co-op Program include: Engaging and partnering on innovative projects to gain experience in a challenging, cross functional team environment Participate in meet & greets and lunch & learns with KDP executives and other organization leaders Receive professional development training such as networking, professional skills development and presenting Be paired with a mentor to enhance your knowledge of other parts of the business and build your network Complete a project from start to finish and present it and your takeaways to your team, department vice president and other KDP stakeholders Total Rewards:$31/hour Paid bi-weekly $5,000 Sign-on Bonus, paid within first 30 days of employment Requirements:Must be an undergraduate currently enrolled in a full-time academic program from an accredited college or university, majoring in Information Technology, Computer Science, Analytics, Engineering or another related field Available to work 40 hours per week (M-F, 8am-5pm) Excellent organizational skills and attention to detail with a demonstrated ability to manage multiple projects, prioritize requests, and meet deadlines Strong communication skills including excellent listening, written, and verbal abilities Ability to work cross-functionally, be independently driven, and a self-starter Strong skills in Microsoft Excel and PowerPoint Please note: This position is limited to persons with permanent right to work in the United States.
We incorporate HireVue, an automated interview tool, into our campus recruitment process.
Please visit this link to learn more about HireVue and how to prepare.
*We recommend checking with your campus career center for additional preparation resources such as InterviewStream, Big Interview and more Company Overview:Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partners brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere.
We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values.
We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale.
Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth.
Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop.
We offer robust benefits to support your health and wellness as well as your personal and financial well-being.
We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work.
Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law.
A.
I.
Disclosure: KDP uses artificial intelligence to assist with initial resume screening and candidate matching.
This technology helps us efficiently identify candidates whose qualifications align with our open roles.
If you prefer not to have your application processed using artificial intelligence, you may opt out by emailing your resume and qualifications directly to kdpjobs@kdrp.
com.
$31 hourly Auto-Apply 60d+ ago
2nd shift Quality Control Operator Level II
Stellar Industries Corp 3.5
Quality control inspector job in Millbury, MA
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 ControlInspector 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
$34k-41k yearly est. 15d ago
Quality Control Inspector
Plansee USA
Quality control inspector job in Franklin Town, MA
Job Description
**What makes us strong? **Our employees in 50 countries worldwide - all working with passion to enable high-tech applications with our strong metals: tungsten and molybdenum.
At our Plansee site in Franklin, USA, we specialize in transforming semi-finished molybdenum and tungsten products into complex components-leveraging decades of precision manufacturing and engineering excellence.
Join a highly motivated team in Franklin, USA, where local expertise meets the global knowledge and values of the Plansee Group.
RESPONSIBILITIES
Perform first piece, in-process and finished machined part inspections including first article inspection for conformance to quality assurance standards.
Accurately completes all quality control documentation such as non-conforming material, travelers and control charts.
Create and store electronic inspection reports using customer drawings and specifications.
Follows verbal and/or written instructions such as blueprints, traveler, work instruction, process specifications, and sketches, in completing a variety of inspection tasks.
Verify that inspection equipment, machinery and tools used are calibrated per Company standards.
QUALIFICATIONS
High School diploma or GED. Technical school education in manufacturing technology and/or ASQ certified inspector a plus.
Strong knowledge of GD&T and ability to read and interpret machining and fabrication drawings.
Proficiency in the use of the MS Windows (Word, Excel, Outlook) and MRP systems.
Strong attention to detail and advanced shop math skills.
Ability to calculate trigonometry formulas a plus.
Knowledge of running and programming Zeiss Calypso CMM software a plus.
Understanding of aerospace requirements (AS9100, AS9102, ASTM's) preferable.
Meet the requirements under ITAR - U.S. Citizen or Permanent Resident (Green Card holder).
**BENEFITS
**
Medical - 90% paid for with 100% reimbursement on deductible
Dental
Vision
Flexible spending accounts
Company paid life and disability insurance
401 K w/ company match
Time off Benefits
Pay range: $25-$32 per hour + bonus plan
And much more!
Equal Employment Opportunity
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class.
You should be proficient in:
GD&T
Quality Inspection Experience
Standard Operating Procedures (SOPs)
AS9100
AS9102
Quality Control Experience
Quality Control Data Analysis
AS9100 Experience
Machines & technologies you'll use:
Coordinate Measuring Machine (CMM) (Zeiss)
$25-32 hourly 10d ago
QC Inspector
Tech Talent Express 3.5
Quality control inspector job in Fall River, MA
We are seeking a Quality ControlInspector with experience in conducting first article inspection processes to ensure the quality of finished products. The ideal candidate will have some prior experience with FAI, knowledge of quality assurance techniques, and the ability to interpret engineering drawings and technical documents.
Responsibilities:
Assist in Conducting First Article inspection (AS9102) processes and document activities
Interpret test results for acceptance or rejection
Record test results and compile nonconforming output report
Mechanical Inspection
Electrical Point to Point wiring continuity testing
Maintain calibration logs
Qualifications:
Minimum experience with first article inspection processes (Will Train)
Knowledge of quality assurance techniques and functions
Previous experience with calipers and micrometers
Ability to read and interpret engineering drawings, specs, and other technical documents
Mechanical aptitude
Excellent communication skills both verbally and in writing
$38k-46k yearly est. 60d+ ago
QC Incoming Inspector I
Anika Therapeutics 4.3
Quality control inspector job in Bedford, 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.
$41k-60k yearly est. Auto-Apply 60d+ ago
Lead Inspector, HQS
South Middlesex Opportu
Quality control inspector job in Framingham, MA
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.
$51k-86k yearly est. Auto-Apply 10d ago
Quality Control Inspector
Bendon Gear & MacHine 3.7
Quality control inspector job in Rockland, MA
We are a growing manufacturing company looking for an individual to assist or lead our quality control department
Requirements
A qualified individual would:
Be able to read and interpret drawings. Understand GD&T. Understand a variety of sampling plans.
Utilize best practice inspection methods to ensure product conforms to customer and drawing specifications.
Be familiar with and able to use a variety of inspection tooling (micrometers, calipers, CMM, indicators, optical comparator, etc).
Have good computer skills (Microsoft Office, Outlook, be able to learn a robust ERP system).
Be familiar with completing first article inspections per AS9102 and complete utilizing specialized software.
Have a good organizational skill set as each customer has a different set of requirements that are critical to product acceptance.
Be familiar with the requirements of ISO9001.
Attention to detail is critical.
FULL TIME EMPLOYEE BENEFITS:
Competitive compensation based on experience
BCBS Medical, Altus Dental and Vision, Disability and Life Insurance - 100% Company Paid.
Paid personal and vacation time (PTO)
10+ Paid holidays
401K plan
Potential for Growth
OT based on business conditions
COMPANY:
Bendon Gear is a precision machine and gear company doing business for over 40 years, with a stable set of excellent customers.
We are a good, solid company, and we wish to build a team of good people who are motivated, flexible, and capable.
Job Types: Full-time, Part-time
Salary: $18.00 - $27.00 per hour
Benefits:
401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Professional development assistance
Vision insurance
Schedule:
10 hour shift
8 hour shift
Monday to Friday
Salary Description $18 - 27.00 / Hr
$18-27 hourly 10d ago
QC Inspector
Trexon
Quality control inspector job in Braintree Town, MA
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
$20-25 hourly 2d ago
Quality Control Inspector
Rennscot MFG
Quality control inspector job in Woburn, MA
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 ControlInspector 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.
How much does a quality control inspector earn in Smithfield, RI?
The average quality control inspector in Smithfield, RI earns between $22,000 and $63,000 annually. This compares to the national average quality control inspector range of $25,000 to $47,000.
Average quality control inspector salary in Smithfield, RI
$37,000
What are the biggest employers of Quality Control Inspectors in Smithfield, RI?
The biggest employers of Quality Control Inspectors in Smithfield, RI are: