Inspector jobs at Globus Medical - 222 jobs

rms Company provides contract manufacturing of high-quality, tight-tolerance medical implants, components and sub-assemblies using cutting-edge technology. rms is part of the Cretex Medical family of companies. Learn more at ******************** and ********************** Quality Inspector Position Summary The Quality Inspector supports the production floor & reports to the Production Supervisor, ensuring product compliance to quality and industry specifications. 1st Shift: Monday - Friday 6:00am - 2:30pm Responsibilities Quality Inspector Responsibilities: * Conduct mechanical and visual inspections, reporting and isolating non-conforming product * Perform in-process inspections and document findings as required * Inspect finished products to determine conformance through inspections to specifications; conducting visual and dimensional testing; creating rejections for nonconforming products and confirming re-work. * Perform and document inspection results through paperwork review, completion of IP forms (inspection plan documents), enter data into data base when required, create shipping packets * Communicate quality issues to Supervisor Qualifications Desirable Requirements/Qualifications: * High school diploma or equivalent * 1 year of experience in a manufacturing environment * Understanding of ISO 13485 * Experience with measurement and testing equipment * Vision System experience a plus * Proficient in blue print reading rms Company Benefits As a Cretex Medical company, rms offers a full benefit package to its employees. Benefits include medical, dental, vision and life insurance options. rms also offers a 401(k) retirement plan with employer match, profit sharing, short- term and long-term disability insurance, paid time off, holiday pay, and an onsite medical clinic. rms Company also offers company specific benefits, such as: * Onsite Clinic * Paid Parental Leave * Monthly Social Events * Annual Employee Appreciation Week * Volunteer Opportunities * Training and Development Opportunities * Tuition Reimbursement * Wellness Program Cretex Companies use cutting oils, solvents, and other chemicals in the manufacturing process. Testing is conducted on a periodic basis to ensure that all chemicals are kept well below the OSHA permissible exposure levels. Pay Range USD $18.22 - USD $25.53 /Hr. Pay Range Details This pay range reflects the base hourly rate or annual salary for positions within this job grade, based on our market-based pay structures. Actual compensation will depend on factors such as skills, relevant experience, education, internal equity, business needs, and local market conditions. While the full hiring range is shared for transparency, offers are rarely made at the minimum or maximum of the range. Company Benefits All Employees: Our 401k retirement savings plan with a company match contribution; onsite health clinics, discretionary holiday bonus program (based on years of service), Cretex University, 24/7 employee assistance program with access to five confidential visits with a licensed counselor at no cost, wellness program with incentives, an employee death benefit, and employee sick and safe leave are available to all Cretex employees. 20+hours: Cretex's medical benefit package includes: comprehensive medical insurance with access to virtual providers; dental insurance (Little Partners Dental benefit covers services 100 percent for children 12 and younger when seen by a Health Partners in network provider); vision insurance; a pre-tax health savings account, healthcare and dependent care pre-tax reimbursement accounts; paid holidays, paid time off; and our discretionary profit sharing program are available to employees working 20+ hours/week. 30+ hours: Parental Leave, accident and critical illness benefits, optional employee, spouse, and child life; short and long term disability; company provided life insurance; and tuition assistance programs are available to employees working 30+ hours per week. (Some benefits are subject to eligibility criteria.) Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, gender identity, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law. Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit *********************

Working at Freudenberg: We will wow your world! Responsibilities: Measure and record product quality using, visual, mechanical and optical gauging instruments. Inspect incoming raw material to insure that all quality requirements have been met per acceptance activities and material specifications. Ensure conformance to certifications for all materials and components received. Identify and segregate non-conforming material for material review board (MRB) disposition Generate NCMR's and assign owners. Participate in Gauge R&R's Perform applicable materials testing per acceptance activities and/or specification. Strong knowledge of interpreting drawings, customer specification, test methods, and inspection criteria. Maintain complete, legible, and accurate records. Independently handle problems that arise within area of responsibility. Knowledge of cGMP's. Knowledge of scheduling methods and ability to change priorities when directed by Supervisor/Manager. Interact effectively with other employees within the department and the company. Release product to next location upon completion within SAP system. Qualifications: High School/Trade School Diploma or GED 1-2 years of experience in Quality Control Experience in the medical device industry preferred The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Medical LLC

Job Description Inspection & Packaging Lead (3rd shift) This position reports directly to the Inspection and Packaging Supervisors as well as the VILP Manager. The role is responsible for general support of the Visual Inspection, Labeling, and Packaging of finished sterile compounds. The Lead is responsible for ensuring the accuracy for label reconciliation, document completeness and correctness of all product identification. Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further - Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company - we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positivelyimpactpatients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-EdgeTechnology: Work withstate-of-the-artfacilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today! Essential Functions: Lead and perform the line/area clearance of the visual inspection or label, and packaging activities. Review of batch record during and end of visual inspection, label, and packaging activities. Assist Inspection & Packaging Supervisors in overseeing employees who are responsible for visual inspection/labeling/packaging of finished goods. Collaborate with Inspection & Packaging Supervisors to ensure timely visual inspection and labeling of products to meet scheduled batch release dates. Ensure that training on SOPs and processes remains current. Analyze Production efficiencies downtime and waste. Lead teams to improve the results. Write investigations and CAPA actions for non-conformances in the department. Work with QA to quickly resolve any variance or document errors so that product may be released on time. Lead Problem Solving activities. Assist with maintaining batch and label inventory and managing daily staffing for visual inspection and labeling. Other duties as assigned. Supervisory Responsibilities: Lead a team of Associates, providing direction, support, and training. Provide a positive and collaborative work environment through effective communication and accountability, escalating conflict promptly and fairly. Experience and Necessary Skills: 1-year previous leadership experience or comparable experience preferred. Minimum 1 years' experience in aseptic processing preferred. Knowledge of cGMP guidelines/standards. Bachelor's degree or relevant experience preferred. Demonstrated written and oral communications skills including strong presentation skills. Excellent organizational skills and results oriented. Strong results orientation. Strong Microsoft Office skills are essential, proficient in the use of spreadsheets and word processing programs Ability to effectively bring others together and reconcile differences. Able to lift up to 50 lbs. and stand for extended periods when required Must pass an eye exam confirming 20/20 near vision corrected (with contacts or glasses) or uncorrected Must pass an eye exam confirming the ability to accurately perceive color Benefits: Smart healthcare coverage options that rewards wellness (and puts money back in your pocket!) Flexible Spending & Health Savings Accounts (FSA & HSA) available Dental & Vision insurance Employer Paid Life Insurance & Employee Assistance Program Short Term & Long-Term Disability Insurance Up to 4% 401K Matching (100% vested on day one!) Generous Paid Time Off Options - vacation,sick, paid leave and holidays! $5,250 Annual Tuition Reimbursement after 6 months $1,000 Referral Bonus Program with no limit Eligible for annual bonus program Timeline: We will be accepting applications on an ongoing basis until position is filled. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. *Please note that we do not work with third-party recruiters or agencies for this position. If you are a qualified candidate and wish to apply for this job, please do so directly through our official application process. We appreciate your understanding and cooperation in this matter. Monday - Friday 1130pm to 8am

Inspection & Packaging Lead (3rd shift) This position reports directly to the Inspection and Packaging Supervisors as well as the VILP Manager. The role is responsible for general support of the Visual Inspection, Labeling, and Packaging of finished sterile compounds. The Lead is responsible for ensuring the accuracy for label reconciliation, document completeness and correctness of all product identification. Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further - Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company - we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positivelyimpactpatients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-EdgeTechnology: Work withstate-of-the-artfacilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today! Essential Functions: Lead and perform the line/area clearance of the visual inspection or label, and packaging activities. Review of batch record during and end of visual inspection, label, and packaging activities. Assist Inspection & Packaging Supervisors in overseeing employees who are responsible for visual inspection/labeling/packaging of finished goods. Collaborate with Inspection & Packaging Supervisors to ensure timely visual inspection and labeling of products to meet scheduled batch release dates. Ensure that training on SOPs and processes remains current. Analyze Production efficiencies downtime and waste. Lead teams to improve the results. Write investigations and CAPA actions for non-conformances in the department. Work with QA to quickly resolve any variance or document errors so that product may be released on time. Lead Problem Solving activities. Assist with maintaining batch and label inventory and managing daily staffing for visual inspection and labeling. Other duties as assigned. Supervisory Responsibilities: Lead a team of Associates, providing direction, support, and training. Provide a positive and collaborative work environment through effective communication and accountability, escalating conflict promptly and fairly. Experience and Necessary Skills: 1-year previous leadership experience or comparable experience preferred. Minimum 1 years' experience in aseptic processing preferred. Knowledge of cGMP guidelines/standards. Bachelor's degree or relevant experience preferred. Demonstrated written and oral communications skills including strong presentation skills. Excellent organizational skills and results oriented. Strong results orientation. Strong Microsoft Office skills are essential, proficient in the use of spreadsheets and word processing programs Ability to effectively bring others together and reconcile differences. Able to lift up to 50 lbs. and stand for extended periods when required Must pass an eye exam confirming 20/20 near vision corrected (with contacts or glasses) or uncorrected Must pass an eye exam confirming the ability to accurately perceive color Benefits: Smart healthcare coverage options that rewards wellness (and puts money back in your pocket!) Flexible Spending & Health Savings Accounts (FSA & HSA) available Dental & Vision insurance Employer Paid Life Insurance & Employee Assistance Program Short Term & Long-Term Disability Insurance Up to 4% 401K Matching (100% vested on day one!) Generous Paid Time Off Options - vacation,sick, paid leave and holidays! $5,250 Annual Tuition Reimbursement after 6 months $1,000 Referral Bonus Program with no limit Eligible for annual bonus program Timeline: We will be accepting applications on an ongoing basis until position is filled. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. *Please note that we do not work with third-party recruiters or agencies for this position. If you are a qualified candidate and wish to apply for this job, please do so directly through our official application process. We appreciate your understanding and cooperation in this matter. Monday - Friday 1130pm to 8am

Element Materials Technology is seeking a motivated and detail-oriented NDT FPI Inspector (3rd Shift) to join our growing team. The successful candidate will perform nondestructive testing using Fluorescent Penetrant Inspection (FPI) techniques in accordance with applicable procedures, specifications, and standards. This position plays a key role in ensuring product integrity and quality in support of our aerospace and industrial customers. Salary: $20.50 - $26.50/hr DOE + shift differential Hours: 11pm - 7:30am Responsibilities * Perform Fluorescent Penetrant Inspections (FPI) in accordance with customer specifications, procedures, and applicable standards. * Interpret and evaluate test results to determine conformance to acceptance criteria. * Accurately document inspection results, nonconformances, and associated data. * Conduct pre- and post-cleaning operations to prepare parts for inspection. * Set up, calibrate, and verify equipment performance as required. * Maintain a clean, organized, and safe work environment in compliance with Element's safety standards. * Collaborate with team members and supervisors to ensure efficient workflow and timely completion of testing. * Support continuous improvement efforts and uphold Element's commitment to quality and integrity. Skills / Qualifications * Certification to NAS 410 in Fluorescent Penetrant Inspection (FPI) required (Level I considered with training and experience). * Previous experience performing FPI in a materials testing, aerospace, or manufacturing environment preferred. * Ability to read and interpret engineering drawings, specifications, and work instructions. * Strong attention to detail and ability to work independently with minimal supervision. * Basic computer literacy and proficiency with data entry systems. Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) "If you need an accommodation filling out an application, or applying to a job, please email ***********************"

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.

Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures Dept. and on the off-line inspection area and therefore must be knowledgeable of procedures and (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping equipment in each area Pay Range: $19.91 - $21.66 Responsibilities The Specialist performs some or all of the following accountabilities as assigned: * Visually inspects products for various defects. * Documents work accurately and timely. * Complies with current SOP's and cGMP's. * Sets-up, adjusts, and operates equipment such as inspection machines, cappers, etc. * Performs and documents critical start-up procedures for filling operation such as filter integrity test, line clearance, component verification, etc * Performs and documents quality checks on product. * Calculates percent defective on inspection results and reconciles components on batch record. * Loads and unloads vials from turntables. Stacks, wraps and moves pallets of product. Performs other duties as assigned. Additional Information We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program. Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

Element has an opportunity for a Nondestructive Etch Trainee (2nd Shift) to join our growing team. To conduct daily Etch tests in accordance with company approved procedures while paying close attention to safety and project timelines. Salary: $20.50 - $23.50/hr DOE Hours: 4:30pm - 3am Responsibilities * Conduct daily Etch logs in accordance with written company procedures• Process parts per Element procedures and/or specifications• General knowledge of chemical processes performed at EMT• Conduct Chemical additions• Maintain related test equipment and tools in good working condition• Complete assigned tasks in a safe and efficient manner• Perform other duties as assigned Skills / Qualifications * High school graduate or equivalent• Etching metal plating experience a plus• Familiar with testing codes and standards• Experience in interpreting testing procedures and requirements.• Proficiency in Microsoft Applications (Word, Excel, Outlook)• Availability, flexibility, and maturity to represent the company at a broad range of events/projects in the community• Ability to remain calm when faced with mounting pressure related to deadlines and multiple priorities.• Well developed oral and written communication skills to meet a variety of communication needs Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) "If you need an accommodation filling out an application, or applying to a job, please email ***********************"

- AUTHORIZED INSPECTOR Bureau Veritas is looking for a hardworking, observant, and mechanically inclined inspector for the metal fabrication and pressure vessel industry. This role is ideal for individuals who are self-motivated and prefer to work independently. Excellent pay and benefits, plus opportunity for a long-term career. WE PROVIDE TRAINING. Key Responsibilities Performs ASME and National Board shop and field inspection services at assigned clients, including review and verification of code required activities, implementation and applicability of the manufacturers written quality control system, and witnessing of all required tests. Monitors client quality control system for compliance with relevant codes and requirements. Documents all inspection activities per established policies. Ensures compliance with applicable sections of the ASME Code, the National Board Inspection Code, and Jurisdictional requirements for the construction and repair of boilers and pressure vessels. Acquires and maintains knowledge of the applicable sections of the ASME code, the National Board code, and the Jurisdiction. Continually enhances knowledge through self-study, internal training, and approved courses. Required Education and/or Experience Must have 4 years of demonstrated experience in nuclear reactors or the boiler and pressure vessel industry, such as design, welding, fabrication, operation, repair, inspection, nondestructive examination, or quality control system oversight. A STEM BS or AS degree, CWI, or technical certificate may be substituted for 2 years of experience. Must have a high school diploma Must complete a 2-week preparatory training course provided by Bureau Veritas on ASME Sections I, IV, V, VIII, IX, and B31.1. Must be able to obtain a National Board Authorized Inspector Commission with "R" Endorsement. Obtaining this commission requires attendance at a 72-hour course and a 32-hour course provided by the National Board, passing (2) exams administered by the National Board, and 80- hours of on-the-job training with another Commissioned Inspector. OR Must have a National Board Authorized Inspector Commission with "R" Endorsement. Competencies Ability to read, write, speak clearly and informatively, use a computer, and perform basic arithmetic. Ability to understand and interpret the boiler and pressure vessel codes. Ability to interact with clients. Ability to apply industry knowledge, technical skill, and sound business practice to decision making. Ability to adhere to established company policies, directives, and procedures, and to ensure accurate and timely reporting and submission of results for assigned activities.

Description: The Inspector I- LFP is an entry level, non-exempt position that reports to the LFP Production Supervisors. The Inspector I is responsible for complying with Charm Sciences, Inc. standard operating procedures, inspecting product, and operating packaging machines. The pay range for this position is $15.50 to $20.00 per hour. Compensation will be determined based on education, experience, and other factors in accordance with applicable laws. Essential Functions: Comply with all Charm Sciences, Inc. Standard Operating Procedures (SOP's). Inspect ROSA diagnostic tests as outlined in SOP: FLA-152: Lateral Flow Inspection. Always maintain a clean safe work environment. Load ROSA tests on both manual machine and automatic loaders. Works efficiently on a production line where priorities can shift throughout the day. Report any line issues, product issues or other work-related concerns to the inspector-II, inspector-III or the LFP Production Supervisor. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Requirements: Required: Excellent verbal and written communication skills. Work hours for the LFP Department are 7:30 am to 4:00 pm with occasional overtime. Preferred: Basic English vocabulary. 1-2 years' experience in a GMP manufacturing environment. Familiarity with Microsoft Windows and Excel. Bilingual: English/Spanish. Physical Requirements The person in this position must be able to frequently lift up to 10 pounds. Must be able to work continuously in a low humidity environment. The person in this position must be able to remain stationary for an extended length of time while working at a machine. Able to visually inspect lateral flow strips. The person in this position occasionally must operate a computer, a packaging machine and other production equipment. Will be exposed to fluctuating environmental conditions, i.e., temperatures ranging from 4°ree;C in a walk-in cold-room where finished product is stored to 28°ree;C in LFP Dry Rooms.

The Inspector I- LFP is an entry level, non-exempt position that reports to the LFP Production Supervisors. The Inspector I is responsible for complying with Charm Sciences, Inc. standard operating procedures, inspecting product, and operating packaging machines. The pay range for this position is $15.50 to $20.00 per hour. Compensation will be determined based on education, experience, and other factors in accordance with applicable laws. Essential Functions: * Comply with all Charm Sciences, Inc. Standard Operating Procedures (SOP's). * Inspect ROSA diagnostic tests as outlined in SOP: FLA-152: Lateral Flow Inspection. * Always maintain a clean safe work environment. * Load ROSA tests on both manual machine and automatic loaders. * Works efficiently on a production line where priorities can shift throughout the day. * Report any line issues, product issues or other work-related concerns to the inspector-II, inspector-III or the LFP Production Supervisor. * Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Requirements Required: * Excellent verbal and written communication skills. * Work hours for the LFP Department are 7:30 am to 4:00 pm with occasional overtime. Preferred: * Basic English vocabulary. * 1-2 years' experience in a GMP manufacturing environment. * Familiarity with Microsoft Windows and Excel. * Bilingual: English/Spanish. Physical Requirements * The person in this position must be able to frequently lift up to 10 pounds. * Must be able to work continuously in a low humidity environment. * The person in this position must be able to remain stationary for an extended length of time while working at a machine. * Able to visually inspect lateral flow strips. * The person in this position occasionally must operate a computer, a packaging machine and other production equipment. * Will be exposed to fluctuating environmental conditions, i.e., temperatures ranging from 4°C in a walk-in cold-room where finished product is stored to 28°C in LFP Dry Rooms. Salary Description $15.50 to $20.00 per hour.

Element has an opportunity for a NDT FPI/MPI Inspector Trainee our rapidly expanding team. As a member of the operations team, the Test Technician position performs a variety of routine and non-routine testing assignments within the department assigned and insures timely and accurate test results under direct supervision. The technician positions must be proficient in a number of core business skills including but not limited to compliance to established safety rules, code of conduct, and company policies and procedures. Salary: $20.50- $22/hr DOE Responsibilities * Counts, inspects articles to verify contents of shipments against the travelers by performing the following duties. * Verifies that traveler matches identification on customer's' containers/product. * Unpack customers 'parts from the containers they were received in and store empty containers in a neat manner to ensure they do not become damaged or contaminated * If product has none of the above continue prepping parts for processing (vapor degrease, hand clean etc.) * Visually inspect parts for any incoming damage, also verify the quantities and show acceptance by initialing the traveler. Skills / Qualifications Language Skills: * Must be able to speak, read and write and comprehend English fluently. Must be able to converse with the operators in a calm fashion when issues are brought to you. Mathematical Skills: * Must be able to perform the four basic mathe functions, addition, subtracting , multiplication and division. Must be able to count parts and reconcile against travelers. Reasoning Ability: * Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Computer Skills: * To perform this job successfully, and individual should have knowledge of database software, spreadsheet software and word processing software including e-mailing. Physical Demands: * Lifting up to 50 lbs. is expected. Mechanical aids are available for weights over 50 lbs. * Must be able to stand for an extended period of time. Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

FORTNA partners with the world's leading brands to transform omnichannel and parcel distribution operations. Known world-wide for enabling companies to keep pace with digital disruption and growth objectives, we design and deliver solutions, powered by intelligent software, to optimize fast, accurate and cost-effective order fulfillment and last mile delivery. Our people, innovative approach and proprietary algorithms and tools ensure optimal operations design and material and information flow. We deliver exceptional value every day to our customers with comprehensive services and products including network strategy, distribution center operational design and implementation, material handling automated equipment, robotics and a comprehensive suite of lifecycle services. At FORTNA, we believe in fostering a workplace that isn't just a job but a movement - a collective effort to redefine success and transform challenges into opportunities. "Join the Movement" encapsulates our commitment to a workplace culture that thrives on collaboration, celebrates diversity, and empowers every individual to contribute to something greater than themselves. Our Team. Our Passion. Our Approach. JOB SUMMARY: The Quality Inspector will be responsible for inspection of cut, formed, weld fabricated, machined or assemblies for adherence to engineering drawings. ESSENTIAL FUNCTIONS: 1. Interpretation and understanding of shop drawings to determine if a part is made to print. Examples are: o Weld symbols o Geometric dimensioning and tolerancing symbols o Print legend and notation 2. The ability to use measuring instruments to verify whether a product is conforming to shop drawings. Examples include Micrometer, Caliper, Jo blocks, Pin gage, Tape measure, Dial indicator 3. Manual Dexterity and ability to lift to 30 lbs. 4. Must be able to distinguish color in this position and the ability to read small print and distinguish fine details. 5. Reading skills to understand instructions, plans, or purchase orders. 6. Good communication skills enabling verbal and written communication using active listening and learning. 7. Tasks include but are not limited to: o Process Production reject tags, issuing a Quality Hold. o File Maker system for accurate product disposition with basic computer skills. o Issue Quality Hold for all nonconforming material. o Help investigate out of process activities and assist with containment of nonconforming material. o Review process check sheets for completeness. o Data collection with part verification inspection o Audit defined processes for adherence to the process. QUALIFICATIONS: 1. High school diploma (or GED). 2. Prior manufacturing experience, with some aspect of Quality inspection (preferred). 3. Prior experience in metal fabrication a plus or welding/layout experience (preferred). 4. Basic blueprint reading skills and welding symbols. 5. The ability to use basic computer programs such as Word, Excel, PowerPoint, and Outlook. (preferred) 6. Must have ability to use appropriate tools related to the task. This describes the general nature and level of work expected of a person assigned to this position. All job requirements listed indicate the minimum level of knowledge, skills and/or ability deemed necessary to perform the job proficiently. Starting pay will be $21.00 This job description describes the general nature and level of work expected of a person assigned to this position. All job requirements listed indicate the minimum level of knowledge, skills and/or ability deemed necessary to perform the job proficiently. Employees may be required to perform any other job-related duties as requested by their supervisor. It is the policy of FORTNA and its affiliated companies to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, pregnancy or pregnancy-related condition, status with regard to public assistance, veteran status, citizenship status (if authorized to work in the U.S.), or any other characteristic protected by federal, state or local law. In addition, FORTNA will provide reasonable accommodations for qualified individuals with disabilities.

- AUTHORIZED INSPECTOR Bureau Veritas is looking for a hardworking, observant, and mechanically inclined inspector for the metal fabrication and pressure vessel industry. This role is ideal for individuals who are self-motivated and prefer to work independently. Excellent pay and benefits, plus opportunity for a long-term career. WE PROVIDE TRAINING. Key Responsibilities: Performs ASME and National Board shop and field inspection services at assigned clients, including review and verification of code required activities, implementation and applicability of the manufacturers written quality control system, and witnessing of all required tests. Monitors client quality control system for compliance with relevant codes and requirements. Documents all inspection activities per established policies. Ensures compliance with applicable sections of the ASME Code, the National Board Inspection Code, and Jurisdictional requirements for the construction and repair of boilers and pressure vessels. Acquires and maintains knowledge of the applicable sections of the ASME code, the National Board code, and the Jurisdiction. Continually enhances knowledge through self-study, internal training, and approved courses. Required Education and/or Experience Must have 4 years of demonstrated experience in nuclear reactors or the boiler and pressure vessel industry, such as design, welding, fabrication, operation, repair, inspection, nondestructive examination, or quality control system oversight. A STEM BS or AS degree, CWI, or technical certificate may be substituted for 2 years of experience. Must have a high school diploma Must complete a 2-week preparatory training course provided by Bureau Veritas on ASME Sections I, IV, V, VIII, IX, and B31.1. Must be able to obtain a National Board Authorized Inspector Commission with "R" Endorsement. Obtaining this commission requires attendance at a 72-hour course and a 32-hour course provided by the National Board, passing (2) exams administered by the National Board, and 80- hours of on-the-job training with another Commissioned Inspector. OR Must have a National Board Authorized Inspector Commission with "R" Endorsement. Competencies Ability to read, write, speak clearly and informatively, use a computer, and perform basic arithmetic. Ability to understand and interpret the boiler and pressure vessel codes. Ability to interact with clients. Ability to apply industry knowledge, technical skill, and sound business practice to decision making. Ability to adhere to established company policies, directives, and procedures, and to ensure accurate and timely reporting and submission of results for assigned activities.

- AUTHORIZED INSPECTOR Bureau Veritas is looking for a hardworking, observant, and mechanically inclined inspector for the metal fabrication and pressure vessel industry. This role is ideal for individuals who are self-motivated and prefer to work independently. Excellent pay and benefits, plus opportunity for a long-term career. WE PROVIDE TRAINING. Key Responsibilities Performs ASME and National Board shop and field inspection services at assigned clients, including review and verification of code required activities, implementation and applicability of the manufacturers written quality control system, and witnessing of all required tests. Monitors client quality control system for compliance with relevant codes and requirements. Documents all inspection activities per established policies. Ensures compliance with applicable sections of the ASME Code, the National Board Inspection Code, and Jurisdictional requirements for the construction and repair of boilers and pressure vessels. Acquires and maintains knowledge of the applicable sections of the ASME code, the National Board code, and the Jurisdiction. Continually enhances knowledge through self-study, internal training, and approved courses. Required Education and/or Experience Must have 4 years of demonstrated experience in nuclear reactors or the boiler and pressure vessel industry, such as design, welding, fabrication, operation, repair, inspection, nondestructive examination, or quality control system oversight. A STEM BS or AS degree, CWI, or technical certificate may be substituted for 2 years of experience. Must have a high school diploma Must complete a 2-week preparatory training course provided by Bureau Veritas on ASME Sections I, IV, V, VIII, IX, and B31.1. Must be able to obtain a National Board Authorized Inspector Commission with "R" Endorsement. Obtaining this commission requires attendance at a 72-hour course and a 32-hour course provided by the National Board, passing (2) exams administered by the National Board, and 80- hours of on-the-job training with another Commissioned Inspector. OR Must have a National Board Authorized Inspector Commission with "R" Endorsement. Competencies Ability to read, write, speak clearly and informatively, use a computer, and perform basic arithmetic. Ability to understand and interpret the boiler and pressure vessel codes. Ability to interact with clients. Ability to apply industry knowledge, technical skill, and sound business practice to decision making. Ability to adhere to established company policies, directives, and procedures, and to ensure accurate and timely reporting and submission of results for assigned activities.

Oversees logs and procedures and ensures Q.C. and Production are abiding by GMP and GLP company rules set forth by company SOPs. Ensuring things are made right in the first place is the best way of preventing out of specification products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Includes the following, but other duties may be assigned as the company's needs dictate. Reviews and approves the Production filling batch records. Checks and audits the documents for accuracy and GMP compliance during and at the completion of filling. Checks and confirms that the correct components and compounding batch have been set-up and are being used on the appropriate packaging line. Reviews the data reported by the mechanics, machine operators, and line leads to ensure that the information is correct and entered appropriately. Responsible for placing compounded batches and finished goods that do not conform to company specifications into Quarantine status with applicable labeling. Reports any quality issues to Quality management and participates in investigations, as necessary. Performs daily housekeeping audits of the Production area logbooks and reports results to Quality management. Supports GMP training of employees. Participates in Quality System audits as directed by Quality management. Complies with Health, Safety, and Environmental responsibilities for the position. Inspects the production lines to ensure that both Production and Quality control personnel are following the required SOP to perform their jobs. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. 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. EDUCATION and/or EXPERIENCE: High school diploma or GED (general education degree) and some college (science-based courses preferred). Minimum 6-months of hands-on experience as Quality audit/inspector in cGMP environment; preferably in pharmaceutical, biomedical, or medical device field (regulated industry). Experience with batch record keeping, CAPA initiation, and deviation investigation. Should have experience working on the floor of a manufacturing facility. LANGUAGE SKILLS: Fluent in reading, writing, and speaking the English language, as well as having experience with technical writing (knowing Spanish is a plus). Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from departmental manager/supervisor or other employees. MATHEMATICAL SKILLS: Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. COMPUTER SKILLS: To perform this job successfully, an individual should have knowledge of Database software, Spreadsheet software and Word Processing software. REASONING ABILITY: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. 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 frequently required to sit, use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to stand, walk, talk or hear, and taste and smell. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. 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. While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles (herbal powders). The noise level in the work environment is usually quiet. Sunrider Manufacturing provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Oversees logs and procedures and ensures Q.C. and Production are abiding by GMP and GLP company rules set forth by company SOPs. Ensuring things are made right in the first place is the best way of preventing out of specification products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Includes the following, but other duties may be assigned as the company's needs dictate. Reviews and approves the Production filling batch records. Checks and audits the documents for accuracy and GMP compliance during and at the completion of filling. Checks and confirms that the correct components and compounding batch have been set-up and are being used on the appropriate packaging line. Reviews the data reported by the mechanics, machine operators, and line leads to ensure that the information is correct and entered appropriately. Responsible for placing compounded batches and finished goods that do not conform to company specifications into Quarantine status with applicable labeling. Reports any quality issues to Quality management and participates in investigations, as necessary. Performs daily housekeeping audits of the Production area logbooks and reports results to Quality management. Supports GMP training of employees. Participates in Quality System audits as directed by Quality management. Complies with Health, Safety, and Environmental responsibilities for the position. Inspects the production lines to ensure that both Production and Quality control personnel are following the required SOP to perform their jobs. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. 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. EDUCATION and/or EXPERIENCE: High school diploma or GED (general education degree) and some college (science-based courses preferred). Minimum 6-months of hands-on experience as Quality audit/inspector in cGMP environment; preferably in pharmaceutical, biomedical, or medical device field (regulated industry). Experience with batch record keeping, CAPA initiation, and deviation investigation. Should have experience working on the floor of a manufacturing facility. LANGUAGE SKILLS: Fluent in reading, writing, and speaking the English language, as well as having experience with technical writing (knowing Spanish is a plus). Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from departmental manager/supervisor or other employees. MATHEMATICAL SKILLS: Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. COMPUTER SKILLS: To perform this job successfully, an individual should have knowledge of Database software, Spreadsheet software and Word Processing software. REASONING ABILITY: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. 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 frequently required to sit, use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to stand, walk, talk or hear, and taste and smell. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. 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. While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles (herbal powders). The noise level in the work environment is usually quiet. Sunrider Manufacturing provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Description: Job Purpose The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards. Duties and Responsibilities Preparation of the QC Labeling areas as specifically described in SOPs. Performs final inspection of products for proper specifications, label accuracy, and compliance with applicable regulations, standards and Vivex Biologics, Inc. quality requirements. Combines components for final products. Applies labels to final product and adds package inserts, boxes, etc. Maintains accurate inventory of post-processing, quarantine products (frozen and room temperature). Performs disposition of nonconforming products as directed. Coordinates and stages products for sterilization. Monitors freezers and responds to alarms. Supports nonconformance investigations, when applicable. Maintains knowledge of applicable regulations and standards related to storage, handling, labeling and inspections of tissue. Maintains effective communication with management when issues arise to obtain appropriate instructions to address the issues. Performs other duties as assigned by management. Requirements: Qualifications High School/Minimum of 4 Years of Relevant Experience. Associate/Minimum of 1 Years of Relevant experience. Bachelors/Minimum of 0-1 Years of Relevant experience Working Conditions Work is indoors in environmentally controlled conditions. Overtime may be required to meet production deadlines. Some on-call and weekends may be required. Physical Requirements Able to stand for extended period. Able to lift 25 lbs. without assistance. Must be able to infrequently lift, push, pull and carry boxes weighing up to 25 pounds. Walk, squat and bend over for intervals of 15-30 minutes, with or without reasonable accommodation. Direct Reports No direct reports. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job any time. Vivex Biologics, Inc. is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, transfers, leaves of absence, compensation and training. Vivex Biologics, Inc. with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.

Job Purpose The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards. Duties and Responsibilities Preparation of the QC Labeling areas as specifically described in SOPs. Performs final inspection of products for proper specifications, label accuracy, and compliance with applicable regulations, standards and Vivex Biologics, Inc. quality requirements. Combines components for final products. Applies labels to final product and adds package inserts, boxes, etc. Maintains accurate inventory of post-processing, quarantine products (frozen and room temperature). Performs disposition of nonconforming products as directed. Coordinates and stages products for sterilization. Monitors freezers and responds to alarms. Supports nonconformance investigations, when applicable. Maintains knowledge of applicable regulations and standards related to storage, handling, labeling and inspections of tissue. Maintains effective communication with management when issues arise to obtain appropriate instructions to address the issues. Performs other duties as assigned by management. Requirements Qualifications High School/Minimum of 4 Years of Relevant Experience. Associate/Minimum of 1 Years of Relevant experience. Bachelors/Minimum of 0-1 Years of Relevant experience Working Conditions Work is indoors in environmentally controlled conditions. Overtime may be required to meet production deadlines. Some on-call and weekends may be required. Physical Requirements Able to stand for extended period. Able to lift 25 lbs. without assistance. Must be able to infrequently lift, push, pull and carry boxes weighing up to 25 pounds. Walk, squat and bend over for intervals of 15-30 minutes, with or without reasonable accommodation. Direct Reports No direct reports. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job any time. Vivex Biologics, Inc. is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, transfers, leaves of absence, compensation and training. Vivex Biologics, Inc. with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.