Quality Control Inspector jobs at Orchid Orthopedic Solutions

- 117 jobs

QC Inspector, Visual Inspector
Orchid Orthopedic Solutions 4.2
Quality control inspector job at Orchid Orthopedic Solutions
ABOUT US The Oregon City, OR site was established in 1973 and joined the Orchid team in 2012. Our 80,000 square foot facility employs approximately 300 team members. We specialize in hip and knee joint implants that enable our customers to live a longer active life. We are a full-service plant, meaning our team can manufacture medical implants from start to finish in-house. A career with Orchid provides growth opportunities, a great benefits package including performance bonuses, insurance, 401(k) with company match, and paid time off. For more information, please visit ********************* SHIFT ORE - Shift 1 ($0) (United States of America - Oregon) A BRIEF OVERVIEW The QC Inspector, Visual, Orchid Oregon, performs tasks to visually inspect machined and machined & polished parts to ensure compliance to customer acceptance criteria in accordance with established policies and procedures. The QC Inspector, Visual, Orchid Oregon reports to the Quality Control Supervisor. WHAT YOU WILL DO Ensure compliance to Orchid requirements in inspection and record keeping. Collect inspection data and report results. Maintain accurate documentation at all times during the manufacturing and inspection process per Good Manufacturing Practices. Perform complete Device History Record review including inspection documentation Ensure all raw materials received meet specifications. Perform testing and inspection at various stages of production, including visual and dimensional inspection Ensure customer specifications and other applicable internal external requirements are followed. Use handheld inspection tools for measurement purposes, such as micrometers, calipers, height gages, optical comparator, gage blocks, and dial indicators. Conduct physical inspection of product with gauging such as: Thread gages, plug gages, pin gages, functional gages. Perform visual and/or cosmetic inspection of product following applicable procedure(s) using appropriate light sources. Monitor equipment to ensure proper operation and escalate any equipment-related issues. Communicate potential nonconforming situations to Quality Engineering and Quality Management. Demonstrate an understanding of basic manufacturing concepts and processes. Quarantine non-conforming or potential non-conforming parts or materials. Work modified schedules to support production requirements as necessary. Complete First Article Inspections as well as receiving, in-process, and final and packaging inspections against customer requirements with minimal supervision Train inspection personnel. Inspect customer-returned parts Under guidance, perform first piece inspections to support production and perform internal manufactured first articles. Advocate for the health and safety of self, co-workers, customers, and the community. Support quality and compliance by adhering to all procedures, work instructions, and forms per the Quality Management Systems (QMS). Complete all required training. Visually inspect machined and polished parts Confirm discrepancies using appropriate tools including, but not limited to calipers, pin gages, measuring instruments and surface profilometers as required Route non-conforming product for rework operations to ensure compliance of customer acceptance criteria Accurately document inspection results Communicate nonconformance's and work with Quality to drive corrective actions Complete proper documentation as required including, but not limited to, process routing card, salvage router, scrap tags, dimensional reports, etc. EDUCATION QUALIFICATIONS High School Or Equivalent (Required) EXPERIENCE QUALIFICATIONS No previous work experience required Experience in a Scientific Field (Preferred) Experience in Quality Inspection and Lean Manufacturing (Preferred) LICENSES AND CERTIFICATIONS Any Technical Trade School (Preferred) Any American Society for Quality (Preferred) KNOWLEDGE & SKILLS THAT ENABLE SUCCESS Mathematical Ability - Working Experience Data Entry - Working Experience Computer Knowledge - Working Experience Communication - Working Experience Collaboration - Working Experience Handwriting - Working Experience Accuracy and Attention to Detail - Working Experience Quality Inspection Metrology Tools - Working Experience Information Processing - Working Experience Blueprint Reading - Working Experience GD&T - Working Experience Visual Quality Assurance - Working Experience Layout Inspection - Working Experience Time management - Working Experience Problem Solving - Working Experience PHYSICAL DEMANDS Must be able to remain in a stationary position - Frequently Must be able to move about the inside of the building - Occasionally Must be able to move equipment around the building - Occasionally Must be able to position oneself and move under/around/over equipment - Occasionally Must be able to handle/adjust/inspect/position various items and equipment - Constantly Must be able to communicate and exchange information with others - Frequently Must be able to perform tasks that require repetitive handling/adjusting/inspecting/positioning of items and equipment - Constantly Must be able to distinguish and detect information such as writing and defects - Constantly Must be able to move equipment - Occasionally WORKING CONDITIONS Noise - Occasionally WHAT WE OFFER Opportunity to work in a growing company Ability to help people live a longer, more active life Comprehensive benefit package Ability to work in an organization that values: Integrity First: We do the right thing Teamwork: We are one Orchid Results: Our results matter ADDITIONAL REQUIREMENTS Candidates offered employment may be required to submit to a pre-employment background check and pre-employment drug-screening based on position requirements Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time Candidates must be able to provide proof of eligibility to work in the United States through eVerify At Orchid, we fully support a diverse and inclusive workplace and we are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, hair type, age, status as a protected veteran, or disability. Orchid Orthopedic Solutions only pays fees for solicited presentations of job seekers submitted through our preferred vendor job board by recruiters, employment agencies, or other parties.
$39k-50k yearly est. Auto-Apply 9d ago
Quality Control Specialist
Cutting Edge Supply 4.5
Colton, CA jobs
QUALITY CONTROL Cutting Edge Supply Company is North America's Largest Independently Owned Distributor of Ground Engaging Tools.” In operation since 1950; we have been a leader in the Heavy Equipment parts business for over 75 years. Our focus is to provide the highest quality and largest selection of wear parts for the Mining, Construction, and Material Processing. Description The quality control inspector performs assessment, documentation and organization tasks to support the efficiency and effectiveness of their organizations supply chain. Their duties and responsibilities include, but not limited to the following: Position Qualification and Physical Requirements Inspect output samples using industry-appropriate methods, such as comparing to standards, measuring dimensions and examining functionality Experience inspection both large & small, fabricated assemblies Experience with calipers, micrometers and other inspection tools Position requires accurate use of a tape measure Drive and operate a forklift Must have experience handling big loads such as rebar, I Beams, or heavy material Ensure that production line adheres to standards and procedures Review blueprints and specifications to compare to produced goods Record inspection results by completing reports, summarizing re-works and wastes and inputting data into quality database Train production team on quality control measures to improve product excellence Propose improvements in the production process Monitor the use of equipment to ensure it is safe and discard or red tag any equipment that do not meet requirements Keep measurement equipment operating accurately by following calibration requirements and scheduling repairs as needed Must be able to lift up to 70/lbs. and use lifting devices Must be able to communicate questions, issues, and discrepancies to supervision. Sufficient math skills to be able to add and subtract dimensions and perform basic shop math. Experience in heavy equipment industry a PLUS Must be a team player Pay Scale: Based on Ability and Experience. We offer 100% paid HMO employee insurance with PPO options available for a shared cost, dental, vision, life insurance, paid time off, 401(k) retirement savings plan that matches .50 cents on the dollar, and 5% profit sharing! Come work with us! Please, No Agencies Please, No phone calls
$38k-54k yearly est. 1d ago
Quality Control Analyst
Aequor 3.2
Vacaville, CA jobs
QC Analyst I Duration: 6+ Months With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals. Job Responsibilities ● Perform a broad variety of basic and moderately complex tests with documentation according to GMP ● Review data and assess against established acceptance criteria ● Perform technical review of peer-generated data ● Evaluate data to identify trends and/or establish limits ● Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed ● Identify and troubleshoot technical problems ● Identify gaps in systems and procedures ● Receive and provide training ● Participate in assay transfer and assay validation ● Perform equipment qualification / maintenance ● Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures ● Support the maintenance and compliance of operational areas ● Assure and apply GMP throughout operations ● Coordinate with customers to support multi-site operational activities ● Support internal and external audits and regulatory inspections ● Works to meet schedules, timelines, deadlines ● Participate in and/or lead group and project teamwork; project and process improvements ● Write protocols and reports under limited supervision ● Meets scheduled performance of 95% on time ● Perform other duties as requested by managers to support Quality activities Job Requirements ● B.S./B.A. degree and 1-3 years experience or Master's Degree plus one year experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry. ● Strong verbal and written communication skills, ability to organize and present information both formally and informally. ● Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures. ● Routinely exercises sound judgment, reasoning and problem solving. ● Capable of working under limited supervision and determining own short term priorities.
$41k-68k yearly est. 1d ago
Quality Control Inspector II - Redmond, OR
Medline 4.3
Redmond, OR jobs
Under minimal supervision, the QC Inspector II oversees quality projects, ensures compliance with Medline SOPs, and maintains product integrity at the distribution center. Responsibilities include investigating and documenting held finished goods, managing holds and releases, completing rework assignments, inspecting raw materials and finished goods using various methods, recording inspection results, providing product disposition, ensuring inventory control, performing final inspections, and ensuring compliance with quality procedures and company policies. Job Description MAJOR RESPONSIBILITIES Apply and remove holds in the system and Q-Tag. Assess and repackage inbound damaged goods. Communicate with divisional partners to determine product disposition. Maintain communication with branch personnel and divisional partners. Operate material handling equipment (e.g., reach truck, order picker) to manage inventory. Assist with item adjustments and other inventory-related tasks. Prioritize and perform recall activities, including stock checks, deviations, relabels, product rework, and pedigree verification. Coordinate project/rework areas and resources. Maintain daily reports of held stock using SAP, Excel, and other systems. Ensure compliance with SOPs and regulations; communicate with management to address non-conformances. Maintain hazardous waste logs and perform weekly audits. Use computer systems for communication, reporting, and tracking project time. Recommend methods to increase efficiency. Ensure shipments are from licensed vendors and maintain electronic logs. Perform in-process and final inspections; complete inspection documentation. Operate test equipment and perform measurements. Identify defects and initiate non-conforming material reports. Communicate effectively with quality assurance and production groups. Verify and approve line start-up and equipment requirements. Participate in continual improvement and customer satisfaction efforts. Read and interpret engineering instructions and other documents. Comply with quality systems, GMP, GDP, OSHA, and company regulations. Review manufacturing/production documents to ensure accuracy. Perform line clearance procedures for product release. Review and approve Engineering Change Notices (ECNs) and substitutions. Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. The anticipated salary range for this position: $19.75 - $27.75 Hourly The actual salary will vary based on applicant's location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold. Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here. Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
$19.8-27.8 hourly Auto-Apply 43d ago
Quality Technician
Steris 4.5
Birmingham, AL jobs
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. You will support manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. This is a day shift position, Mon-Fri, 8am-5pm. Can include overtime and occasional Saturdays. Facility is climate cooled. What You'll Do as a Quality Technician • Assist in production line Quality investigations and associated problem-solving activities. • Will coordinate and conduct in-process and final QC product acceptance testing, depending on facility. • Investigates production line stoppages to identify corrective actions. • Participates on a Material Review Board to review and process non-conformance reports. • Enters and retrieves Quality data from local and global systems. • Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release. • Complete other duties as assigned. The Experience, Skills and Abilities Needed Required: • Minimum of three (3) years of experience in a manufacturing or repair environment or other technical production tasks with a high school diploma or equivalent. • Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks with an associate degree. • Familiarity working with and using a microscope. • Experience working with a Quality Management System (ISO 13485). • Experience using basic hand tools i.e., utility knife, screwdrivers, hammers. • Proficiency using MS Office including Work, Excel and Outlook. • High level of professionalism, good communication skills, able to work individually and as part of a team. Preferred: Knowledge of metrology (mics, calipers, gauges). Ability to sit and stand for long periods of time. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future. Here is a brief overview of what we offer: • Market Competitive Pay with shift differential ⦁ Climate controlled facility • Extensive Paid Time Off and (9) added Holidays • Excellent Healthcare, Dental and Vision Benefits • Long/Short Term Disability Coverage • 401(k) with a company match • Maternity and Paternity Leave • Additional add-on benefits/discounts for programs such as Pet Insurance • Tuition Reimbursement and continued education programs • Excellent opportunities for advancement in a stable long-term career #LI-KL1 Pay rate for this opportunity is $21.50 $25.00 per hour. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
$21.5-25 hourly 8d ago
Quality Technician (Birmingham, AL, US, 35222)
Steris Corporation 4.5
Birmingham, AL jobs
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. You will support manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. This is a day shift position, Mon-Fri, 8am-5pm. Can include overtime and occasional Saturdays. Facility is climate cooled. What You'll Do as a Quality Technician * Assist in production line Quality investigations and associated problem-solving activities. * Will coordinate and conduct in-process and final QC product acceptance testing, depending on facility. * Investigates production line stoppages to identify corrective actions. * Participates on a Material Review Board to review and process non-conformance reports. * Enters and retrieves Quality data from local and global systems. * Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release. * Complete other duties as assigned. The Experience, Skills and Abilities Needed Required: * Minimum of three (3) years of experience in a manufacturing or repair environment or other technical production tasks with a high school diploma or equivalent. * Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks with an associate degree. * Familiarity working with and using a microscope. * Experience working with a Quality Management System (ISO 13485). * Experience using basic hand tools i.e., utility knife, screwdrivers, hammers. * Proficiency using MS Office including Work, Excel and Outlook. * High level of professionalism, good communication skills, able to work individually and as part of a team. Preferred: * Knowledge of metrology (mics, calipers, gauges). * Ability to sit and stand for long periods of time. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future. Here is a brief overview of what we offer: * Market Competitive Pay with shift differential ⦁ Climate controlled facility * Extensive Paid Time Off and (9) added Holidays * Excellent Healthcare, Dental and Vision Benefits * Long/Short Term Disability Coverage * 401(k) with a company match * Maternity and Paternity Leave * Additional add-on benefits/discounts for programs such as Pet Insurance * Tuition Reimbursement and continued education programs * Excellent opportunities for advancement in a stable long-term career #LI-KL1 Pay rate for this opportunity is $21.50 $25.00 per hour. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
$21.5-25 hourly 16d ago
Quality Control Inspector II - Lynwood, CA
Medline 4.3
Lynwood, CA jobs
Under minimal supervision, the QC Inspector II oversees quality projects, ensures compliance with Medline SOPs, and maintains product integrity at the distribution center. Responsibilities include investigating and documenting held finished goods, managing holds and releases, completing rework assignments, inspecting raw materials and finished goods using various methods, recording inspection results, providing product disposition, ensuring inventory control, performing final inspections, and ensuring compliance with quality procedures and company policies. Job Description MAJOR RESPONSIBILITIES Apply and remove holds in the system and Q-Tag. Assess and repackage inbound damaged goods. Communicate with divisional partners to determine product disposition. Maintain communication with branch personnel and divisional partners. Operate material handling equipment (e.g., reach truck, order picker) to manage inventory. Assist with item adjustments and other inventory-related tasks. Prioritize and perform recall activities, including stock checks, deviations, relabels, product rework, and pedigree verification. Coordinate project/rework areas and resources. Maintain daily reports of held stock using SAP, Excel, and other systems. Ensure compliance with SOPs and regulations; communicate with management to address non-conformances. Maintain hazardous waste logs and perform weekly audits. Use computer systems for communication, reporting, and tracking project time. Recommend methods to increase efficiency. Ensure shipments are from licensed vendors and maintain electronic logs. Perform in-process and final inspections; complete inspection documentation. Operate test equipment and perform measurements. Identify defects and initiate non-conforming material reports. Communicate effectively with quality assurance and production groups. Verify and approve line start-up and equipment requirements. Participate in continual improvement and customer satisfaction efforts. Read and interpret engineering instructions and other documents. Comply with quality systems, GMP, GDP, OSHA, and company regulations. Review manufacturing/production documents to ensure accuracy. Perform line clearance procedures for product release. Review and approve Engineering Change Notices (ECNs) and substitutions. MINIMUM JOB REQUIREMENTS Education Typically requires High School Diploma or equivalent. Certification / Licensure At least 1 years of quality control experience in a regulated industry setting. Work Experience Knowledge / Skills / Abilities Proficiency in using powered warehouse equipment. Ability to read, write, speak, and understand English. Strong attention to detail, including the ability to read and understand labeling information, discern differences in similar products or packaging, and identify differences in character sequences (e.g., Lot, Expiration, Date of Manufacture). Basic math skills, including addition, subtraction, and fractional to decimal conversions. Basic computer skills, including the ability to generate Non-Conforming Material Reports (NCMRs) or certificates as necessary, and proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.). Ability to work in hot and cold environments. Capability to sit, walk, or stand for prolonged periods, with frequent twisting and bending. Ability to lift up to 50 lbs. Ability to prioritize quickly in a fast-paced manufacturing environment. Ability to process all relevant details, understand and prioritize their importance, and draw concise conclusions. Basic knowledge of quality regulations such as GMP, GDP, ISO, or 21CFR 820, 210-211. PREFERRED JOB REQUIREMENTS Education Certification / Licensure Work Experience At least 2 years of quality control experience in a regulated industry setting. Knowledge / Skills / Abilities Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. The anticipated salary range for this position: $23.75 - $33.25 Hourly The actual salary will vary based on applicant's location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold. Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here. Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws. Medline Industries, LP complies with the Los Angeles County Fair Chance Ordinance for Employees (FCO) and the State of California Fair Chance Act (FCA). In accordance with the FCO and FCA, an applicant's criminal history will not result in automatic disqualification from employment. Qualified applicants with arrest or conviction records will be considered for employment
$23.8-33.3 hourly Auto-Apply 60d+ ago
Quality Control Inspector ( Temp - Hire ) - Long Beach, CA
Hydrafacial Company 3.8
Long Beach, CA jobs
About Us Hydrafacial is a global category-creating company focused on bringing innovative products to market and delivering beauty health experiences by reinventing our consumer's relationship with their skin, their bodies and their self-confidence. Every person here is a key player in our success. We are firm believers in making the little things count each day so the big things will follow. If this sounds like you, come check us out! This is the perfect opportunity to work with some of the best leaders in the industry while you gain the global and strategic experience to add to your professional toolbox. Job Description: The Quality Control Inspector - Inspection is responsible for performing inspections and testing activities throughout the manufacturing process to ensure compliance with quality standards. This role includes conducting First Article Inspections (FAI), Incoming Quality Control (IQC) In-Process Quality Control (IPQC), and Final Quality Control (FQC) inspections, and maintaining detailed inspection records. The Quality Control Inspector will collaborate with cross-functional teams to address quality and safety issues and contribute to continuous improvement initiatives. This is an on-site position based in Long Beach, CA and requires on-site presence five days a week. This is a full-time role with a schedule of Monday-Friday, 6:00 AM to 02:30 PM or 7:00 AM to -3:30 PM or 08:00 AM to 04:30 PM. What you'll do: Primary Responsibilities: Perform inspection and testing activities during First Article Inspections (FAI), manufacturing processes, and Incoming Quality Control (IQC), In-Process Quality Control (IPQC), and Final Quality Control (FQC) inspections. Generate detailed and accurate inspection data sheets in compliance with current Good Manufacturing Practices (cGMP) and Hydrafacial Quality Management System (QMS) requirements. Properly document inspections, prepare first article documentation, and compile certification packages. Conduct product build documentation reviews and end-item data package reviews. Generate nonconformance reports for discrepancies found during inspection processes. Utilize conventional inspection tools such as calipers, gauges, etc., to ensure precise measurements. Ensure all inspection equipment is qualified and calibrated before use. Interpret engineering drawings and specifications accurately. Conduct visual inspections to identify defects or non-conformities in products. Collect and analyze quality data to identify trends and areas for improvement. Collaborate with cross-functional teams to address quality issues and drive continuous improvement initiatives. Maintain accurate documentation of inspection results and quality records. Participate in continuous improvement initiatives to enhance product quality. Report quality related issues to leads and managers in a timely manner. Adhere to all company safety procedures and perform job functions in a safe and effective manner. Performs other duties as assigned What you need to know: Experience/Skills/Education: Required: High school diploma or equivalent; technical training or certification in quality inspection is a plus. Minimum of 2-3 years of experience in a quality inspection role within a manufacturing environment. Proficiency in using conventional inspection tools such as calipers, micrometers, and gauges. Strong understanding of GDP, cGMP, and QMS requirements. Ability to read and interpret engineering drawings and specifications. Experience with generating nonconformance reports and inspection documentation. Strong analytical and problem-solving skills. Excellent attention to detail and organizational skills. Basic understanding of ERP systems, Micro Office, etc. Ability to work independently, cross train, and collaborate professionally in a team environment. Experience with handling pallet jacks and other various moving equipment. Manufacturing environment with exposure to machinery, equipment, and various temperatures. Requires bending, twisting, heavy lifting, pulling/pushing, standing, sitting, reaching, and walking handling inspection tools for extended periods. Must adhere to all safety guidelines and wear the required personal protective equipment (PPE). Must be able to lift and move 50lbs. Desired: Associate degree or higher in a related field preferred. We mean it when we say you'll LOVE this role. Base Pay : $20.00- $23.00/hour Hydrafacial is proud to be an equal opportunity employer. We prohibit discrimination and harassment of any kind based on race, sex, religion, sexual orientation, national origin, gender identity, gender expression, age, disability, genetic information, pregnancy or any other protected characteristic as outlined by color, federal, state or local laws. We are committed to working with and providing accommodation to applicants with physical and mental disabilities. Hydrafacial does not accept unsolicited assistance or resumes/CVs from third party search firms. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral or CV/resume submitted by a search firm to any employee at our company without a valid written search agreement. If we need additional support, we will be sure to reach out directly to one of our preferred providers. Please no phone calls or emails.
$20-23 hourly Auto-Apply 18d ago
QC Inspector II
Alphatec Spine 4.4
Carlsbad, CA jobs
Job Description Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities Perform Quality Control inspections, as required per ATEC procedures Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) Perform transactions in ERP system, as necessary to release product from Inspection Read and conform to all company policies and procedures Perform documentation evaluations Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives Assist auditors during internal audits Other duties as assigned Requirements The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Good communication skills, both verbal and written Strong organization skills and attention to detail Basic math and computer skills required Firm understanding of 21 CFR (Code of Federal Regulations), Part 820, ISO 13485, Good Documentation Practices (GDP) Firm understanding of ASTM (Association of Systems & Test Methods) standards and Heat Treat conditions per ASTM standards Experience in a controlled or regulated environment required Inspection experience with Optical Comparators, Vision Systems, hand tools Education and Experience High School Diploma or equivalent and 2-5 years of experience; experience working in a medical device industry preferred. Familiarity with quality concepts such as visual inspection and defect identification. For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate's qualifications, education, skill set, years of experience, and internal equity. $22.00 to $31.00 Full-Time Hourly Salary.
$22-31 hourly 6d ago
Quality Control Inspector - Irvine
Applied Medical Distribution Corporation 4.4
Irvine, CA jobs
Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions. Position Description Are you detail-oriented with a passion for maintaining the highest standards of quality in manufacturing? Join Applied Medical as a Quality Control Inspector and play a vital role in ensuring the excellence of our raw materials, components, and finished products. As part of our Quality Assurance team, you'll utilize precision measurement tools, review engineering documentation, and uphold strict compliance with industry standards. Key Responsibilities: * Conduct thorough inspection activities, including receiving, in-process, and final product verification. * Assess raw materials, components, subassemblies, and finished products for adherence to standards, guidelines, and specifications outlined in company procedures. * Interpret engineering drawings, shop order operations, and process controls to ensure accuracy in production. * Inspect products and materials following standard operating procedures and work instructions. * Utilize technical measuring devices to confirm product conformance to defined specifications. * Document and report nonconforming materials, ensuring accurate record-keeping. * Maintain detailed inspection results using data management software. Position Requirements * Forklift certified and/or willingness to learn. * 2+ years of experience working within quality management systems (ISO 9001, ISO 13485, or 21 CFR Part 820). * Ability to read, write, and communicate in English effectively. * Understanding and adherence to Applied Medical's Quality Systems and training guidelines. * Compliance with safety rules and company policies. * Ability to work Monday through Friday 8:00am - 4:30pm. Preferred * Hands-on manufacturing experience, particularly within the medical device industry. Benefits * Competitive compensation range: $18 - 23 / hour (California). * Comprehensive benefits package. * Training and mentorship opportunities. * On-campus wellness activities. * Education reimbursement program. * 401(k) program with discretionary employer match. * Generous vacation accrual and paid holiday schedule. Please note that the compensation range may be adjusted in the future, and bonus and incentive compensation plans may apply. Our total reward package reflects our commitment to employee growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life. All compensation and benefits are subject to plan documents and written agreements. Equal Opportunity Employer Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.
$18-23 hourly Auto-Apply 58d ago
Quality Control Laboratory CLS I
San Diego Blood Bank 4.4
San Diego, CA jobs
The anticipated salary range for candidates who will work in San Diego, CA is $72,000 to $90,000 annually. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and years of experience within the job, type and years of experience within the blood banking industry, education, etc. Job Summary Under minimal supervision of management, Medical Laboratory Scientists perform manufacturing processes in a highly regulated environment-from receipt of unprocessed apheresis platelets, through maintaining accurate records of finished components in preparation to distribute to available inventory. The QC lab CLSs test products across the three stages of production (before, in-process, and final) and review the data to ensure the high quality and maximum efficacy of blood components. Responsibilities Perform essential laboratory responsibilities according to established procedures. Support the SDBB safety, GMP and Quality Plan. Adheres to GMP guidelines. Safely operate laboratory equipment in accordance with established SOPs. Obtain samples for product QC testing and further manufacturing. Perform donor and product quality control evaluations. Perform sterility testing on apheresis platelets and operate Bact/ALERT instrument. Perform pathogen reduction process using illuminator instrument. Operate Hematology analyzer to manufacture platelets using large volume delayed sampling and pathogen reduction methods. Perform pH analysis using pH Meters Perform residual WBC testing using Fluorescence Microscopy method. Perform routine equipment QC and maintenance. Evaluate, gather data, trend, and assess results. Assist in training new personnel and other staff members. Assist in laboratory paperwork documenting information accurately and completely in a timely manner. Complete all tests required for each product. Initiate and participate in the investigations and assess any potential impact on product quality. Conduct retesting of product as needed to support quality investigations. Participate in research projects. Participate in department meetings and educational programs. Review and approve quality control on products, reagents, and various test kits. Receive / Review, Upload and Commit IDM test results. Provide support for the donor notification/look-back process. Perform Iso titration on platelet components. Communicate with production personnel and Quality Assurance department. Assist with validations, special projects, and new process developments. Monitor supply inventory levels and assist with material ordering. Understand and adhere to the policies and standards as developed as part of the San Diego Blood Bank Compliance Program. Perform other related duties as assigned or requested. Working Environment Normal laboratory environment with biohazard precautions. May be exposed to blood or bodily fluids that may be capable of transmitting diseases. May be exposed to chemicals that may be hazardous. May be called on to work or attend meetings at other than routinely scheduled hours. Physical Requirements Must be able to stand or sit long hours. Must be able to work on a computer 4 - 8 hours a day. Must be able to communicate clearly. May be required to lift to 40 pounds. Equipment Used General office equipment (computer, printer, fax, copy machine). Various software systems (Blood Establishment Computer System, Quality Management System). Laboratory equipment, including, but not limited to: Centrifuges. Heat sealers. Scales. Refrigerators/incubators. Sterile Connection Devices. BacT/ALERT 3D analyzer. Hematology cell counter. Illuminators. ADAM rWBC analyzer. pH Meter. Qualifications Education: MLS/MT (ASCP)cm or equivalent experience. CA Clinical Laboratory Scientist (CLS)- Generalist. Experience: Laboratory experience preferred but not required. Understanding of technical aspects of lab department, blood banking concepts, hematology, microbiology, serology, and flow cytometry. Skills: Organized and able to efficiently prioritize and handle multiple tasks at one time to provide a productive workflow. Professional communication both written and oral, which is clear and precise. Provide direct and constant supervision over unlicensed laboratory personnel. Must be detail oriented, well organized and display good time management skills. Ability to perform under pressure and work under stressful situations. Interpersonal skills to establish and maintain professional relationships. The San Diego Blood Bank is an Equal Opportunity Employer. EOE/Minority/Female/Disability/Vets The above statements are intended to describe the general nature and level of work being performed. This job description is not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.
$72k-90k yearly Auto-Apply 60d+ ago
QC Inspector II
Atec Spine 4.4
Carlsbad, CA jobs
Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities * Perform Quality Control inspections, as required per ATEC procedures * Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) * Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred * Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed * Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms * Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) * Perform transactions in ERP system, as necessary to release product from Inspection * Read and conform to all company policies and procedures * Perform documentation evaluations * Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives * Assist auditors during internal audits * Other duties as assigned
$44k-53k yearly est. 7d ago
Quality Control Inspector I (1st shift)
Glaukos Corporation 4.9
San Clemente, CA jobs
GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection Receiving inspection of components following procedures, specifications and drawings. Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. Read engineering drawings and interpret geometric dimensioning and tolerancing. Review associated paperwork, complete inspection records using good documentation practices, and release components. Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) Carefully handle and process extremely small components without damaging them. In-Process Inspection Perform Line Clearance for Operations activities Inspect and release labeling Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform inspections on components and assemblies in manufacturing Final Inspection Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform final inspection on finished goods Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing Perform in-house peel testing on sealed packages Maintain sample retain area Other Duties Work with engineering in the design of high quality inspection / metrology fixtures. Support equipment and process validation activities by inspecting process outputs Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. Coordinate the monthly environmental monitoring of the cleanrooms. Coordinate quarterly dose audits. How will you get here? High School Diploma required. 0-2 years industry experience. Knowledge, Skills, and Abilities Medical device experience and working knowledge of QSR a must Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable Attention to detail and accuracy a must Must have excellent documentation skills Team player, good written/oral communicator Must be organized and able to coordinate activities with outside vendors #GKOSUS
$39k-50k yearly est. Auto-Apply 36d ago
Quality Control Inspector I (1st shift)
Glaukos 4.9
San Clemente, CA jobs
GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection * Receiving inspection of components following procedures, specifications and drawings. * Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. * Read engineering drawings and interpret geometric dimensioning and tolerancing. * Review associated paperwork, complete inspection records using good documentation practices, and release components. * Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) * Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) * Carefully handle and process extremely small components without damaging them. In-Process Inspection * Perform Line Clearance for Operations activities * Inspect and release labeling * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform inspections on components and assemblies in manufacturing Final Inspection * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform final inspection on finished goods * Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. * Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing * Perform in-house peel testing on sealed packages * Maintain sample retain area Other Duties * Work with engineering in the design of high quality inspection / metrology fixtures. * Support equipment and process validation activities by inspecting process outputs * Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. * Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. * Coordinate the monthly environmental monitoring of the cleanrooms. * Coordinate quarterly dose audits. How will you get here? * High School Diploma required. * 0-2 years industry experience. Knowledge, Skills, and Abilities * Medical device experience and working knowledge of QSR a must * Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable * Attention to detail and accuracy a must * Must have excellent documentation skills * Team player, good written/oral communicator * Must be organized and able to coordinate activities with outside vendors #GKOSUS
$39k-50k yearly est. 36d ago
Post-Market Quality Inspector
Applied Medical Distribution Corporation 4.4
Rancho Santa Margarita, CA jobs
Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions. Position Description The Quality Inspector plays a critical role in maintaining the safety, reliability, and compliance of Applied Medical's medical devices following clinical use. This post-market quality inspector position ensures that returned products meet Applied Medical's stringent quality standards while supporting patient safety and continuous product improvement. Working within an ISO 13485 and FDA-regulated environment, the Quality Inspector performs detailed inspections, documentation, and collaboration with cross-functional teams to support ongoing product integrity and regulatory compliance. Key Responsibilities * Inspect and assess returned medical devices to verify condition, cleanliness, and compliance with safety and decontamination standards. * Use calibrated measuring tools to confirm product integrity against specifications. Document findings in Applied Medical's enterprise resource planning (ERP) and electronic quality management system (eQMS) platforms with accuracy and traceability. * Collaborate cross-functionally with the Servicing, Regulatory Affairs, and Customer Relations teams to resolve documentation discrepancies and product concerns. * Maintain compliance with applicable regulatory standards, including 21 CFR Part 820, ISO 9001, and ISO 13485. * Support continuous improvement initiatives by contributing feedback. * Adhere to safety protocols when handling decontaminated or potentially biohazardous materials in accordance with bloodborne pathogen procedures. Success in This Role Looks Like * Conducts accurate and efficient inspections that uphold Applied Medical's quality and safety standards. * Contributes to clear, compliant, and timely documentation that supports post-market surveillance and regulatory reporting. * Demonstrates precision, consistency, and accountability in all inspection and verification activities. * Builds strong working relationships with cross-functional partners to resolve quality issues and improve processes. * Supports Applied Medical's mission of delivering reliable, high-quality devices that advance patient care and clinical outcomes. Position Requirements This position requires the following skills and attributes: * High school diploma or equivalent education. * Minimum of two years of experience in quality assurance or inspection within a regulated manufacturing environment (e.g., medical device, pharmaceutical, or aerospace). * Working knowledge of ISO and FDA regulatory frameworks, including 21 CFR Part 820. * Strong analytical skills with meticulous attention to detail. * Proficiency in ERP and eQMS systems for data entry and documentation (e.g., SAP). * Clear written and verbal communication skills in English. * Ability to lift between fifteen and twenty-five pounds on an occasional to regular basis. * Organizational discipline and the ability to manage time effectively in a fast-paced environment. Preferred The following skills and attributes are preferred: * Experience working in a medical device manufacturing or clinical servicing environment. * Familiarity with bloodborne pathogen protocols, product decontamination, and sterilization processes. * Exposure to continuous improvement methodologies such as Lean or Six Sigma. * Understanding of ISO 13485 quality systems and regulatory documentation practices. Benefits * Competitive compensation range: $18 - 23 / hour (California). * Comprehensive benefits package. * Training and mentorship opportunities. * On-campus wellness activities. * Education reimbursement program. * 401(k) program with discretionary employer match. * Generous vacation accrual and paid holiday schedule. Please note that the compensation range may be based on factors such as relevant education, qualifications, experience. The compensation range may be adjusted in the future, and special discretionary bonus or incentive compensation plans may apply. Our total reward package reflects our commitment to team member growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life. Equal Opportunity Employer Applied Medical is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other basis protected by federal, state or local laws in the locations where Applied Medical operates.
$18-23 hourly Auto-Apply 34d ago
Quality Inspector
Rani Therapeutics 4.5
Fremont, CA jobs
GENERAL INFORMATION Quality Inspector (II, III, or Senior) Department: Quality Assurance Reports to: Quality Engineering Purpose of the Job This Quality Inspector position will report to Quality Engineering. Main responsibilities include performing incoming inspections of materials/parts/products and reviewing and approval of manufacturing batch records and inspection records. This position will require to perform disposition of materials/parts/products. As a Quality Inspector, you will also support Quality Engineering with other Quality Management System (QMS) activities, such as assisting with environmental monitoring and quality metrics. Major Duties and Responsibilities Interpret drawings and specification documents. Perform incoming inspection of materials/components/subassemblies/finished products following standard operating procedures and using standard inspection tools, including the MicroVu and Keyence. Determine inspection sample size based on procedures, specifications, and standards. Help develop inspection methods, including automated inspection programs using the MicroVu and Keyence. Review/approve executed batch records for manufacturing and inspection records in accordance to QMS procedures and Good Documentation Practices. Approve/perform final disposition of materials/components/subassemblies/finished products. Assign and apply expiration dating labels to materials/parts/products, as per specifications/quality procedures. Initiate Non-Conformance Material Reports (NCMRs) and deviations when discrepancies are observed during inspections and record review process. Report discrepancies and issues to QA Engineering and affected function(s). Maintain materials in Quarantine (pending disposition) and MRB (under NCMR and deviations) in order. Maintain accurate records as per Document Control procedures. Support training of IQC personnel. Assist with performing environmental monitoring of Controlled Environment Rooms (CERs), as needed. Support Quality in the collection of quality metrics data. Interact closely with different functions of the organization. Education and/or Job Experience 2-5 years of experience performing inspections and reviews/approvals of manufacturing batch records/inspection records Government Regulated Environment experience such as FDA and ISO 13485 Must have adequate computer experience (knowledge of Microsoft Word, Excel) Experience working in a cGMP environment Skills and Specifications Attention to detail and organizational skills Good interpersonal and communication skills Ability to work as a part of a team and promote a team environment
$38k-49k yearly est. 25d ago
Quality Control Lab CLS II
San Diego Blood Bank 4.4
San Diego, CA jobs
Under minimal supervision of management, Medical Laboratory Scientists perform manufacturing processes in a highly regulated environment-from receipt of unprocessed apheresis platelets, through maintaining accurate records of finished components in preparation to distribute to available inventory. The QC lab CLSs test products across the three stages of production (before, in-process, and final) and review the data to ensure the high quality and maximum efficacy of blood components.
$32k-44k yearly est. Auto-Apply 60d+ ago
Laboratory Support, Quality Control
Avid Bioservices 4.2
Tustin, CA jobs
Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: Join our team as Laboratory Support, Quality Control where your expertise and organizational skills will play a crucial role in maintaining a well-ordered and safe laboratory working environment. This role is perfect for individuals who are detail-oriented and passionate about supporting scientific research through meticulous laboratory upkeep and efficient handling of supplies and waste management. You'll find fulfillment in ensuring that our state-of-the-art lab operates smoothly and is always ready for groundbreaking research. Laboratory maintenance such as cleaning glassware, dusting/wiping bench, restocking of laboratory consumables on shelves, benches, cabinets, and other efforts to support the laboratories. Maintain/organize/distribute stockroom inventories of general supplies needed for use in the laboratory and reorder items as necessary. Record equipment daily readings and function checks of storage units. Clean/monitor/maintain laboratory equipment such as autoclaves, centrifuges, incubators, refrigeration units, cryotanks, fume hoods and water baths. Proper collection and disposal of biohazardous waste, hazardous waste, and recyclable waste in accordance with EHS guidelines. Verify that supplies have been received on time. Perform inventory counts. Prepare and package outgoing shipments via FedEx or World Courier as needed. Prepare buffers/reagents/various solutions for lab personnel and general lab use. Perform duties such as (but not limited to) data entry or manual inventory of lab items, cell lines, etc. Maintain equipment records and daily work logs. Read and comply with necessary SOPs pertaining to the Laboratory Technician position. Perform other duties as assigned. Minimum Qualifications: A Certificate in Biotechnology Lab Assistant or relevant laboratory experience is required for the position. 2+ years of related experience and/or training; or equivalent combination of education and experience. Preferred Qualifications: An understanding of aseptic handling, sterile technique, laboratory etiquette, GDP and GMP is preferred. Position Type/Expected Hours of Work:This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $20.52 to $24.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
$20.5-24 hourly Auto-Apply 57d ago
Laboratory Support, Quality Control
Avid Bioservices 4.2
Tustin, CA jobs
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: Join our team as Laboratory Support, Quality Control where your expertise and organizational skills will play a crucial role in maintaining a well-ordered and safe laboratory working environment. This role is perfect for individuals who are detail-oriented and passionate about supporting scientific research through meticulous laboratory upkeep and efficient handling of supplies and waste management. You'll find fulfillment in ensuring that our state-of-the-art lab operates smoothly and is always ready for groundbreaking research. * Laboratory maintenance such as cleaning glassware, dusting/wiping bench, restocking of laboratory consumables on shelves, benches, cabinets, and other efforts to support the laboratories. * Maintain/organize/distribute stockroom inventories of general supplies needed for use in the laboratory and reorder items as necessary. * Record equipment daily readings and function checks of storage units. * Clean/monitor/maintain laboratory equipment such as autoclaves, centrifuges, incubators, refrigeration units, cryotanks, fume hoods and water baths. * Proper collection and disposal of biohazardous waste, hazardous waste, and recyclable waste in accordance with EHS guidelines. * Verify that supplies have been received on time. * Perform inventory counts. * Prepare and package outgoing shipments via FedEx or World Courier as needed. * Prepare buffers/reagents/various solutions for lab personnel and general lab use. * Perform duties such as (but not limited to) data entry or manual inventory of lab items, cell lines, etc. * Maintain equipment records and daily work logs. * Read and comply with necessary SOPs pertaining to the Laboratory Technician position. * Perform other duties as assigned. Minimum Qualifications: * A Certificate in Biotechnology Lab Assistant or relevant laboratory experience is required for the position. * 2+ years of related experience and/or training; or equivalent combination of education and experience. Preferred Qualifications: * An understanding of aseptic handling, sterile technique, laboratory etiquette, GDP and GMP is preferred. Position Type/Expected Hours of Work: This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $20.52 to $24.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: * You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. * Your written and verbal skills are out of this world, and you communicate with clarity and confidence. * You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. * You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
$20.5-24 hourly Auto-Apply 58d ago
Fluorescent Penetrant Inspector
Tecomet 4.7
Lansing, MI jobs
Performs non-destructive testing on products using fluorescent penetrant inspection as required to conform to customer and/or national standards, by performing the following duties. The role requires the above to be accomplished within Tecomet's principles of continuous improvement, customer driven innovation and a win first culture, while meeting company financial and other performance metrics. **Principle Responsibilities** + Performs inspection procedures following customers' specifications. + Determines acceptability of product based on results of testing. + Interprets results, and determines probable cause of defects. + Performs daily system checks. + Documents and publishes results of FPI testing. + Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. + Write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization. + Add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. And compute rate, ratio, and percent and to draw and interpret bar graphs. + Apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. And deal with problems involving several concrete variables in standardized situations. + Maintain confidentiality. + Work well under pressure and to remain flexible to changing schedules and demands. + Additional duties as requested by management. **Qualification Requirements** **Credentials/Experience:** + 2 years related experience and/or training preferred **Experience/Educational/Training Preferred:** + High school diploma or general education degree (GED) + SNTC Level I or II preferred + NAS 410 Level I or II preferred **Knowledge, Skills, and Abilities:** + Excellent communication and interpersonal skills + Ability to work independently and exercise judgment + Working knowledge of fluorescent penetrant inspection equipment **Other Requirements** **Work Environment** The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. **Physical Requirements** While performing the duties of this job, the employee could be required to stand. The employee could frequently be required to walk; use hand to finger, handle, or feel; reach with hands and arms and talk or hear. The employee could be required to sit; climb or balance and stoop, kneel, crouch, or crawl. The employee could occasionally lift and or move up to 50 pounds. Specific vision abilities required by the job could include close vision, distance vision, peripheral vision, and ability to adjust focus. **Travel Requirements** N/A **Americans with Disabilities Act (ADA):** Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. _The statements herein are intended to describe the general nature and level of work being performed by employees and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company._ **Pay Range** $20.00 - $26.10 / hour **Pay Transparency** In order to support the Fair Compensation Strategy by the US Govt., HR Dept., clients are required to adhere to "Pay Transparency Law"; in the impacted states; that have mandated the employers to list the salary ranges in Job advertisements or postings for job opportunities and Job promotions.
$20-26.1 hourly 26d ago