Medical Device Quality Inspector - FDA/ISO 13485 Compliant
SANMINA-SCI TECHNOLOGY INDIA PRIVATE LIMITED
Sanmina Corporation is seeking a Quality Control Inspector at our Carrollton, TX facility to ensure devices meet FDA/ISO 13845 standards. The role focuses on inspecting parts and assemblies, recording results, and performing audits to validate conformance to process requirements. Ideal candidates have a high school diploma, 1-2 years in QC in manufacturing, proficiency with inspection equipment, and comfort with standard office tools. Prior Sanmina experience is a plus; EOE. #J-18808-Ljbffr SANMINA-SCI TECHNOLOGY INDIA PRIVATE LIMITED
- Sanmina-SCI Systems de México in Carrollton seeks an experienced Quality Control Inspector to ensure that products meet FDA and ISO 13845 standards in our Medical Device manufacturing operation. The Quality Control Inspector will inspect parts and materials for compliance...Suggested
- ..., delivering superior quality and support to Original... ...systems, medical, multimedia, computing... ...in the maintenance of ISO 13485. Conduct internal and... ...maintenance of an ISO 13485 compliant system.Provide day-to-... ...preferably in the medical device industry. Experience with...Suggested
- ...Description Job Title: Quality Control Inspector - PCB & Medical Electronics... ..., PCB assemblies , and FDA-regulated medical electronics... ...components for the medical device industry. Key Responsibilities... ...(21 CFR Part 820), ISO 13485, and other applicable standards...SuggestedWork at office
- ...DescriptionProduction Planner/Scheduler (Medical Device)Sanmina Corporation (Nasdaq: SANM)... ...solutions, delivering superior quality and support to Original Equipment... ...forecasting processesWorking knowledge of FDA QSR (21 CFR Part 820), ISO 13485 and ability to understand other...Suggested
- ..., TX is seeking a Production Planner/Scheduler for our Medical Device operations. You will develop daily/weekly production schedules... ...of planning experience, strong MRP knowledge, and familiarity with FDA QSR (21 CFR 820) and ISO 13485. #J-18808-Ljbffr Sanmina CorporationSuggested
- Quality Control Inspector Our Carrollton facility is looking for an experienced Quality Control Inspector to work in our Medical Device manufacturing operation to ensure that products meet FDA and ISO 13845 standards. Job Purpose: Inspects parts, assemblies, accessories...Full timeTemporary workWork at officeAfternoon shift
- ...facility is seeking a Production Planner/Scheduler for Medical Device manufacturing. You will develop daily/weekly... ...equivalent, 5+ years in manufacturing with strong MRP expertise, and knowledge of FDA QSR (21 CFR Part 820) and ISO 13485. #J-18808-Ljbffr Sanmina
$20 - $24 per hour
...Quality Control InspectorThe Quality Control Inspector performs receiving, in-process, and final inspections... ...for submission to the FDA while ensuring that all... ....Adhere to FDA and ISO requirements, safety guidelines... ...the following: • Medical, dental & vision • Critical...Full timeContract workTemporary workMonday to FridayFlexible hours- Swiss American Products seeks a Quality Control Inspector to ensure products meet regulatory and quality specifications. Reporting to the Quality... ...checks, sampling for testing, and adherence to SAP SOPs and FDA/GMP guidelines. Strong communication and analytical skills are...
- VIRA in Texas seeks a Quality Inspector to ensure incoming materials, in-process parts, and finished goods meet defined standards. You will perform visual and dimensional inspections, document results, and support root-cause analysis with cross-functional teams. Responsibilities...
- ...listings, and registration of medical devices. Trains and mentors lower-... ...by third parties e.g., BSI, FDA and others, as required.Initiates... ...feedback / approval of compliant labeling e.g., IFUs, marketing... ...knowledge of applicable FDA, ISO, MDR requirements, consensus...
- ...have an exciting opportunity at our Carrollton, TX facility for a Quality Control Lab Manager! The Role The Quality Control Lab... ...inorganic chemistry, semiconductor process chemicals Knowledge of ISO 9000 certification and Quality Management Systems Experience...Full timeLocal areaShift workAfternoon shift
- ...Insight Global is looking for a Quality Assurance Inspector that will be responsible for performing... ...standards. • Ensure compliance with FDA, ISO, safety, and company policies and... ...Quality Inspection experience with Medical Devices or Aerospace Background • Experience...
- ...the design, manufacturing, and sales of medical devices (including Class I and II devices,... ...maintaining regulatory approvals, supporting quality management system (QMS) objectives,... ...requirements. In-depth knowledge of ISO 13485, FDA regulations (including 21 CFR Part 820...
- ...seeks a Clinical Study Manager to lead planning, execution, and oversight of clinical studies across the medical device lifecycle, ensuring alignment with ISO 14155, FDA, EU MDR, and GCP. You will coordinate timelines, budgets, site performance, and vendor relationships...
- ...regulatory interpretations in the medical device industry. Creates and trains... ...compliance with applicable ISO and CFR regulations/guidance.... ...the duties described in the Quality Manual.... ...Proficiency with ISO-10993, ISO-14971, FDA and EU-MDR regulations and application...Full time
$112.9k - $188.1k
...OnsiteStryker is hiring a Staff Software Quality Engineer, Post Market Integration... ...PreferredExperience working within the medical device industry, including knowledge of U.S. and... ...standards, and quality systems such as ISO 13485, Good Documentation Practices (GDP), and...Full timeFor contractors- ...Description Job Description Quality Inspector (Dimensional)... ...operations within a regulated medical device manufacturing environment... ...engineering specifications, FDA regulations, and ISO quality standards.... .... Follow all FDA, ISO 13485, GMP, safety, and company...Contract workLocal areaMonday to Friday
- ...expertise to deliver innovative, compliant, and sustainable design... ...pharmaceutical, biotechnology, and medical device sectors. This will be a... ...standards, best practices, and quality benchmarks for life science projects... ...compliance with GMP, FDA, EMA, and global standards.Integrate...
- ...Envision Paid Life Insurance. Medical, Dental, Vision, FSA Plans. 10... ...Responsible for maintaining Envision quality standards on all product lines... ...complexity. Participate in ISO internal audits as scheduled.... ...for defects; using measuring devices; and/or assembling parts with...Contract work
- ...Quality Inspector It's fun to work in a company where people truly BELIEVE in what they're doing... ...of inspection tools and measurement devices. Assist in the implementation and continuous... ..., ERP, or QMS systems). Knowledge of ISO or quality system principles preferred....
- ...direct-hire position at our innovative medical device client. If you’re passionate about... ...studies are conducted in alignment with ISO 14155, FDA regulations, EU MDR, and Good Clinical... ...functionally with Regulatory Affairs, Quality, Medical Affairs, and Product Development...
$86.7k - $173.3k
...and products in diagnostics, medical devices, nutritionals and branded... ...Job Title Senior Development Quality Engineer Working at AbbottAt... ...activities in accordance with ISO 14971, FDA QMSR, EU MDR, and industry... ...of FDA 21 CFR Part 820, ISO 13485, ISO 14971, EN 45502-1, ISO...Contract workWork experience placementWorldwideShift work$40 - $44 per hour
...improve operational performance, quality, and cost. The engineer... ...-functional teams to ensure compliant, efficient, and scalable... .... Ensure compliance with FDA, ISO, GMP, and internal quality system... ...Preferred Experience Medical device, pharmaceutical,...$99.3k - $198.7k
...and products in diagnostics, medical devices, nutritionals and branded generic... ...the organization to maintain quality system and product compliance... ...ongoing compliance with FDA regulations (21 CFR Parts 803... ...standards (e.g., FDA, EU MDR/IVDR, ISO 13485, ISO 14971). Establish...Worldwide- Join to apply for the Quality Control Inspector - Dzung Troung - JKF role at Delta Electronics Americas . Be among the first 25 applicants. Delta... ...Conduct visual and dimensional weld inspections per AWS D1.1, ISO, or equivalent welding standards. Verify weld quality,...Full timeLocal areaWorldwide
- Sanmina-SCI Systems de México is looking for a Receiving Quality Inspector to ensure that materials received meet quality standards. The role includes comparing items against procurement data, inspecting materials for defects, and recording data accurately. Candidates should...
- Position Summary Under supervision of the Quality Control Supervisor, the Quality Control Inspector (QCI) is responsible for assuring that all products produced at... ...are performed in accordance with SAP SOP's and FDA/GMP guidelines. Assist in execution of product/process...Work at office
- Sanmina-SCI Systems de México, located in Carrollton, Texas, is looking for a Quality Control Inspector. This role involves inspecting parts and assemblies for conformance to specifications and ensuring quality through accurate documentation and audits. Candidates should...
- Sanmina-SCI Systems de México is looking for a Quality Control Inspector to perform inspections and audits for quality compliance. Responsibilities include inspecting parts against specifications, documenting results, and participating in the construction of inspection...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Medical Device Quality Inspector - FDA/ISO 13485 Compliant. Be the first to apply!
- quality inspector Carrollton, TX
- quality assurance assistant Carrollton, TX
- quality operator Carrollton, TX
- quality control inspector Carrollton, TX
- quality assurance inspector Carrollton, TX
- quality control assistant Carrollton, TX
- medical device Carrollton, TX
- rn quality Carrollton, TX
- quality Carrollton, TX
- quality intern Carrollton, TX


