Laboratory technician jobs in Kingsport, TN

Title: RCAM Lab Assistant (Part-time/Temporary) (Pool) Employee Classification: Skilled Crafts Institution: Northeast State Community College Department: Regional Center for Advanced Manufacturing (RCAM) Salary: $30.00/hourly Job Summary Reporting to the Regional Center for Advanced Manufacturing (RCAM) Director of Operations, the RCAM Lab Assistant delivers standardized lab content to support training programs in a hands-on lab environment. They must complete the necessary training to qualify as an NCCER craft instructor. Job Duties * Deliver field-specific lab training content to a diverse audience. * Occasionally serve as an SME for advanced development work of programs. * Drive improvement in process effectiveness and efficiency. * Adhere to RCAM schedule and inclement weather policies, which may differ from other NESCC schedules and/or closures. * Complete other assignments as directed by supervision. Minimum Qualifications Industrial Operations Lab Assistant: * Craft qualified at the journey level of any instructional material being delivered * Experience in an industrial setting or other qualifying experience as approved by supervision Electrical, Mechanical, Machining, or Welding Lab Assistant: * Experience at a minimum journey or technician level in their area of expertise * Experience in an industrial setting or other qualifying experience as approved by supervision Construction Lab Assistant: * Experience at a minimum journey or technician level in their area of expertise * OR a minimum of three years' experience as a certified teacher in a vocational/technical construction or maintenance-related training program Preferred Qualifications * Expertise in the field * Previous teaching experience in skilled trades * Apprenticeship Graduate * Associate Degree * Conversational ability or fluency in a second language Knowledge, Skills, and Abilities * Technology Skills: MS Office skills, Word, Excel, Outlook; digital records management systems; general operating systems and data information systems * Capable of learning new technology and applying the new technology in the lab environment * Ability to self-direct and make sound decisions independently. For assistance regarding the job ad, application process, or application status, please contact the Office of Human Resources at ************ or *****************************. Special Instructions to Applicants: To be considered for a position at Northeast State, you must create an online application. A resume and unofficial transcripts are required; a cover letter is optional. You will also be required to provide the contact information for a minimum of three (3) professional references. References WILL be contacted if you are selected for an interview. Your skills, abilities, qualifications, and years of experience will be evaluated using only what is recorded on your application. Please note that attaching a resume does not substitute for completion of the application form. Part-time work experience is calculated at 50% of full-time experience.

QA Technician (Nights) Work Schedule: Monday - Friday 8-hours shifts (Nights) Benefits: Medical, Dental, Vision, Life, Short-Term/Long-Term Disability Insurance effective 30 days after first full month 401(k) Match 7 Paid Holidays, 3 Floating Holidays for use at employee's discretion Immediate eligibility for holiday and vacation pay Work-Life Balance Climate-Controlled and cleanest work environment in Morristown Education Reimbursement Fitness Reimbursement Employee Product Giveaways Referral Program Associate discount programs Overtime available POSITION SUMMARY: The Quality Assurance Technician provides support for production, purchasing, product development, project managers, and customer to ensure that all applicable regulations and customer expectations are met in the production process. ESSENTIAL ACCOUNTABILITIES: * Provide daily support to all manufacturing cells and other internal customers for Quality related issues and concerns. * Performing the first piece inspection process for all finished goods. * Investigate non-conforming material; write investigation reports. Update NCM raw materials and finished product disposition. * Work on special projects as assigned by the QA Manager or QA Supervisor. * Train and develop future QA technicians. * Maintain the training and ability to review each document within the DHR. * Train and develop production floor associates in quality, procedures, and production records. * Sample/Inspect all applicable incoming raw materials. Perform testing as needed. * Monitor and maintain solution and finished product retain samples. Perform annual inspection of drug product retains. * Manage QA Hold/Quarantine area. * Obtain environmental samples per schedule. * Demonstrate commitment to Rockline/Iatric's RRITE Values of Renew, Respect, Integrity, Teamwork, and Excellence. * Associates have a direct and important role in ensuring that all work is performed in a safe manner. Effectiveness in carrying out this responsibility is part of each associate's essential accountabilities. * Contribute to a cooperative working effort by demonstrating a willingness to perform other job-related work, as needed or requested This position is designated as Safety-Sensitive (A safety-sensitive position is one in which the associate's inability or impaired ability to perform their job-related tasks could result in a direct threat to the associate's safety or the safety of others). QUALIFICATION REQUIREMENTS: (To perform this job successfully, an individual must be able to perform each of the essential accountabilities satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.) * High School Diploma/GED, required plus a minimum of 3 years' experience in Quality, a Laboratory setting or Wet Wipes manufacturing; Associate's or Bachelor's degree in technical, quality or life science preferred, or any combination of equivalent education and experience. * Working knowledge of Microsoft tools (Word, Excel, PowerPoint) required. * Strong problem-solving skills. * Ability to communicate across all levels of the organization. * Working knowledge of the FDA's regulations (21 CFR) is highly recommended. * Ability to work in a fast-paced, high-pressure environment with limited supervision is a plus. * Work prioritizing is essential for success. * Ability to make sound decisions and influence others. PHYSICAL AND MENTAL REQUIREMENTS: (The physical demands described here are representatives of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions) * Must be able to communicate face-to-face and over the phone * Occasional lifting up to 50 lbs. * Frequent standing/walking. Occasional sitting, bending, twisting, kneeling, climbing, pushing/pulling, and reaching. * Repetitive hand and foot movement. * Work environment includes occasional noise >85db, hot and cold temperatures. * Requires ability to read, write, calculate, and analyze. * Requires good visual acuity with depth perception and color vision. 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.) * Production and office environment FLSA Status: Non-Exempt Grade: 06

USAntibiotics, the only U.S. manufacturer of Amoxicillin products, is part of the Jackson Healthcare family of companies. We're always looking to add new talent to our teams, and we value diverse professionals who have strong leadership skills, align with our culture, and are committed to excellence. The Chemist will provide analytical support for QC testing of antibiotic products which include raw materials, in-process samples, stability samples, validation samples, product surveillance, and finished products according to Quality Assurance standard procedures, as assigned. Assist with development and validation of chemical assays. Assist with installing, validating, and trouble-shooting new and existing equipment, including automated systems, as assigned. Accurately generate and document all analytical test results per written procedures and corporate policies and support management in the evaluation and review of all test results and investigations as needed. RESPONSIBILITIES: Maintains the QC laboratories to comply with cGMP and US Antibiotics standards of safety, quality, and cleanliness. Follows all safety precautions and guidance from training sessions, chemical hygiene plan, MSDSs (Material Safety Data Sheets), and other technical literature and resources. Performs efficient and reliable analytical tests following validated procedures for raw material, in process, validation, product surveillance, finished product, stability, water, and environmental samples, as assigned. Documents all results in accordance with cGMPs and written procedures. Troubleshoots and solves problems with assays and laboratory equipment and reports all observations. Strictly follows written procedures to minimize analytical variability. Recommends any potential improvements or changes to methods and lab operations (changes implemented via the change control process). Interprets analytical results correctly, notifying supervision promptly of any situation that indicates analytical issues or product issues. Participates in analytical method validations or transfers as required. Performs satisfactorily on all analyst qualification studies, indicating technical proficiency. Plans, performs, and documents non-routine tests (or special studies) and investigations under the direction of supervisor and/or manager. Evaluates and utilizes state-of-the-art equipment, including automated systems and computerized systems to perform and document testing and meet the goals of improved performance, including reliability and efficiency. Maintains and improves proficiency of technical skills through training. Conducts special studies in accordance with protocols and direction of management. Prepares well-documented reports of results. Carries out other departmental duties as deemed appropriate by supervisor/manager. Reviews (i.e., validates) analytical test results for other laboratory personnel, as required. Assists supervision in conducting analytical failure investigations, as required, following all procedures. Calibrates and maintains assigned laboratory equipment as needed according to schedules and procedures, documenting all results. Assists with equipment qualification testing as required by management. Assists with sampling tasks as required. Ensures that testing of products manufactured at the facility is performed per approved procedures and appropriate regulations and those lab operations conform to company standards for safety and performance. Reports all test results and any concerns with accuracy of analytical data and/or any issues that may impact product quality, efficacy, safety, or purity. Supports production needs by efficient laboratory turnaround of samples with right-first-time testing. Evaluates test results versus established test criteria and/or product specifications. Must be able to follow procedures for investigative analytical results as required. Advises, in a technical role, less-experienced staff, notifying supervisor or manager of problems/issues or additional training needs. Initiates ideas for operational changes and continuous improvement in laboratory, within constraints of policies and procedures to improve cGMP compliance, efficiency, cost, and performance. Must be able to assure the accuracy and integrity of analytical results/documentation generated. Exercises careful attention to testing procedures, and sampling handling and preparation as to avoid known degradation failure modes for materials under test, and to documentation. EDUCATION, WORK EXPERIENCE, CERTIFICATIONS: BS/BA degree in Chemistry (or related science) or equivalent related analytical experience. Minimum of 0-5 years of analytical experience in pharmaceutical industry and/or other scientific experience. Strong knowledge/experience of cGMPs in areas beyond QC laboratory. KNOWLEDGE, SKILLS, AND ABILITIES: Skills/Abilities: Demonstrate ability to perform a wide variety of chemical, instrumental, and chromatographic analyses in an efficient, reliable, and safety conscious manner. Advanced computer skills. Appropriate interpersonal and leadership skills Strong verbal communication skills and technical writing skills. Ability to prioritize and decide appropriate course of actions for routine issues. Ability to recognize possible compliance, technical, or safety-related issues and notify supervisor or manager promptly. Ability to suggest appropriate corrective and/or preventive action(s) and assist with implementation. Ability to work in a multi-disciplinary team environment Demonstrate visual acuity per SOP requirements Required Knowledge: Understanding of analytical techniques, test methodology, method development, method validation and reporting for data integrity. Comprehensive skills related to chemical, instrumental, chromatographic analysis, Operational Excellence, statistical applications and tools Understanding of equipment installation, validation, calibration, and troubleshooting, etc. Strong knowledge of cGMPs, USP and FDA's laboratory related requirements. REQUIREMENTS & WORKING CONDITIONS: 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 stand; walk; sit; use hands to finger, handle, or feel; write; type; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; and smell EEO Statement: We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected status under the law.

Company / Location Information A.O. Smith is a global leader applying innovative technologies and energy-efficient solutions to products manufactured and marketed worldwide. The company is one of the world's leading manufacturers of residential and commercial water heating equipment and boilers, as well as a manufacturer of water treatment products for residential and light commercial applications. A. O. Smith is headquartered in Milwaukee, Wisconsin, with approximately 12,000 employees at operations in the United States, Canada, China, India, Mexico, the Netherlands, and the United Kingdom. Primary Function Responsibilities Hands-on laboratory work in a variety of different science / engineering labs Model making, including use of a lathe and mill Building units for testing at multiple facilities Uses verbal and written instructions, drawings, diagrams, and schematics to accomplish tasks. Follows specified methods to inspect and test equipment Demonstrates complete technical understanding of all lab test set ups and procedures. Works with engineers to develop protocols and schedules for testings Reviews and interprets test data for engineer review Collecting and analyzing data Generating reports Provides safety leadership in the lab Works independendently to run efficiency testing, agency safety, or performance testing processes Creates standard operating procedures for completing standard lab tests Independently runs analytical instrumentation Limited project management that is engineer led Other duties may be assigned as needed Keeps abreast of competitor and new product activity Qualifications Associate's degree in Engineering Technology, HVAC, Mechanical Engineering. Electrical Engineering, Electronics, Chemistry, Biology, or related field preferred. 5+ years of related work experience with degree or 7+ years without Associate Degree. Additional Qualifications: Communicates technical material effectively both written and orally. Good general problem solving skills Provien history of effective mentoring and developing other technicians or interns/co-ops. Knowledge of CAE software such as Solidworks, MATLAB, LabView Effective use of Microsoft Products (Excel, Word, etc.) Model Shop experience Education Associate Degree in Related FieldHigh School Diploma or GEDWe Offer Competitive compensation package and comprehensive benefits plans which include medical and dental insurance, company-sponsored life insurance, retirement security savings plan, short- and long-term disability programs and tuition assistance. #LI-Onsite #LI-AO ADA Statement & EEO Statement In developing this job description care was taken to include all competencies needed to successfully perform in this position. However, for Americans with Disabilities Act (ADA) purposes, the essential functions of the job may or may not have been described for purposes of ADA reasonable accommodation. All reasonable accommodation requests will be reviewed and evaluated on a case-by-case basis. We consider all applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, gender identity and expression, marital or military status. We also provide reasonable accommodations to qualified individuals with disabilities in accordance with the Americans with Disabilities Act and applicable state and local law.

Leclerc is a family business with 120 years of experience, tradition and know-how passed down from people with heart. Thanks to our 1,900 employees in eight plants in Canada and the United States, we are constantly innovating to exceed the expectations of both small and large appetites. Position Summary The Quality Control Technician reports to the Quality Manager. S/he is responsible for ensuring controls relative to the food transformation process with heavy concentration on hygiene and sanitation. In addition, s/he will be responsible for ensuring efficient and effective operational functionality of product by performing a number of quality control analytical processes. Responsibilities Requirements Associates degree in Food Science and Technology, Biology, or equivalent combination of education/experience; Minimum of 2 years' experience in technical field (engineering, food science, chemistry) with industry experience; Knowledge of GFSI / BRC, SQF, GMP and other food safety standard including HACCP or similar food industry regulations is preferred; Experience using Microsoft Office and other computer based applications (I pad, One Note, etc.); Excellent people skills, maintain a positive attitude and ability to motivate people, specifically mentoring and coaching individuals; Ability to communicate effectively, both orally and written; Must be able read, interpret and comprehend weights, measurements, and mathematical equations; Be able to effectively understand and adhere to a variety of guidelines and work procedures (including health, safety, hygiene and sanitation), along with prioritizing and organizing workload; Ability to learn quickly and work both independently and as a team; Ability to work in a fast-paced, challenging, and consistently changing environment; Excellent manual dexterity; Ability to stand; walk; for long periods of time; Able and willing to work 10-12hrs daily; Must be flexible with work hours and be able to work overtime and weekends when needed; This position has been identified as a safety sensitive position within Leclerc Foods USA, Inc Essential Functions: Must be able to lift from floor to waist 20 lbs. 33% of the time. Regular and reliable attendance. #200 Working at Leclerc is : Earn a competitive salary Enjoy cookies at will Benefit from a comprehensive benefits program Save on our products Embrace high velocity technology

You put the pro in medical laboratory professional. You've got problem-solving instincts, a passion for patient care, and the technical training to deliver quality results. You're also looking for great benefits, the support of an all-star team, and an opportunity to grow your career. Join our front line of #HealthcareHeroes! Our mission is to advance the health and wellbeing of our communities as a leader in clinical laboratory solutions. Quality is in our DNA -- is it in yours? This opportunity is full-time during third shift. Location: Knoxville, TN Nights: Monday - Friday Hours: Third Shift, 10:30PM to 7:00AM Full-time benefits available In this role, you will: * Perform a vital part of the patient care process through moderate and high complexity testing * Analyze, review, and report testing results * Recognize when corrective action is needed and implement effective solutions * Work in a fast-paced laboratory environment with biological and chemical hazards * Champion safety, compliance, and quality control All you need is: * High school diploma or equivalent and the completion of an AMA-approved Medical Laboratory training program to qualify as a Medical Laboratory Technician (MLT) * Or * Bachelor of Science degree or equivalent preferred and completion of an AMA-approved program of Medical Technology to qualify as a Medical Technologist (MT) * Current TN licensure as a Medical Laboratory Technician (MLT) or Medical Technologist (MT). * Certification or eligible by ASCP or equivalent * 6 months of laboratory training or experience * Strong reading, writing, and analytical skills * Ability to operate general laboratory equipment, including but not limited to: telephones, computers, automated analyzers, centrifuges, microscopes, manual and automated pipettes, and audible alarms. Bonus points if you've got: * 2+ years of laboratory training or experience performing high complexity testing within area of specialty We'll give you: * Competitive Wages plus shift differential * Appreciation for your work * A feeling of satisfaction that you've helped people * Opportunity to grow in your profession * Free lab services for you and your dependents * Work-life balance, including Paid Time Off and Paid Holidays * Competitive benefits including medical, dental, and vision insurance * Help saving for retirement, with a 401(k) plus a company match * A sense of belonging - we're a community! We also want you to know: This role will have routine access to Protected Health Information (PHI). Employees will be trained on reasonable safeguards and are expected to maintain strict confidentiality, as well as abide by all applicable privacy and security standards. Employees are expected only to access PHI when it is required to fulfill job duties. Scheduled Weekly Hours: 40 Work Shift: Job Category: Laboratory Operations Company: American Esoteric Labs Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

The Quality Assurance (QA) Technician is responsible for monitoring, inspecting, and ensuring product quality and compliance within an HDPE (High-Density Polyethylene) pipe manufacturing environment. This role requires close attention to detail, technical knowledge of testing standards, and the ability to support production teams in maintaining compliance with industry regulations. Key Responsibilities Product Inspection & Testing Examine product (internal and external) for surface defects such as discoloration, cracks, splits, waves, or dimples. Inspect coils for proper taping and inside diameter. Review all product printing to verify accuracy of markings; escalate deviations immediately. Measure and record product dimensions: wall thickness, OD, ID, ovality, and OOR. Conduct visual inspections of pipe, retains, and samples to identify defects. Test and evaluate all retains submitted by Production QC. Inspect returned goods, complete required documentation, and determine disposition. Documentation & Reporting Ensure specification sheets are correctly completed, current, and aligned with retains submitted. File all specification sheets and associated test results. Accurately record and communicate scrapped inventory quantities for proper adjustments. Confirm that production-line specification sheets are up-to-date and accessible for supervisors. Report all suspected quality or process issues to the QA Supervisor and Production Management; follow through on required resolution steps. Quality Systems, Audits & Compliance Verify proper handling, labeling, packaging, and bundling of finished product through routine line checks and dock audits. Monitor manufacturing processes by performing audits, collecting samples, verifying lengths, and checking adherence to specifications. Conduct ISO 9001 internal audits and process audits alongside the QA Supervisor; track and close findings. Review and comply with all required QTs, SQPs, and L4 documents relevant to testing and material compliance. Manage calibration and measurement system requirements for gauges, testing, and measuring equipment; maintain accuracy of database (IQMS) and escalate needs for repair or replacement. Support to Production & Cross-Functional Collaboration Communicate quality issues to Production and Supervisors promptly. Work with cross-functional teams to resolve in-process concerns in a timely manner. Support QA and Production supervisors in investigating and resolving internal and external non-conformance issues. Provide training and coaching to Production personnel on quality standards, best practices, and correct use of gauges and measurement tools. Customer Samples & Regulatory Testing Manage the collection, inspection, documentation, retention, and shipment of customer samples. Ensure timely execution and proper documentation of periodic testing requirements (e.g., stiffness tests, semi-annual hydro tests, NSF annual samples, FM Approval tests). Prepare customer documentation packages as required by individual inspection and test plans or Sales Orders. Maintain all quality records according to company policies and retention requirements. Health & Safety Actively participate in Health & Safety training. Promote and maintain safe work practices at all times. Qualifications High school diploma or equivalent required, technical diploma in manufacturing or quality an asset. Prior experience in a manufacturing or quality control role preferred. Strong attention to detail and ability to interpret specifications and technical documents. Competency in using measuring tools (calipers, micrometers, gauges). Basic computer skills; familiarity with ERP/QMS systems such as IQMS is an asset. Strong communication skills and ability to collaborate with production teams. Ability to stand, walk, bend, and lift up to 50 lbs as required. Work Environment This position operates in both laboratory and production floor settings. Regular exposure to manufacturing noise, machinery, and physical activity is expected. Shift work or overtime may be required to ensure continuous quality coverage.

Our Company Amerita Amerita, Inc. is a leading provider in home Infusion therapy. We are looking for a Pharmacy Technician - Compounding to join our Pharmacy team as we grow to be one of the top home infusion providers in the country. The Pharmacy Technician will report to the Pharmacy Manager and work in our City, State branch. Amerita is an entrepreneurial-founded company and a wholly owned subsidiary of PharMerica. The home infusion market is positioned for rapid growth driven by the aging population, increase in chronic diseases, robust pipeline of infusible drugs coming to market, and an industry shift from hospital delivery settings to lower-cost, high-quality alternative providers such as Amerita. As a core member of the Pharmacy team, you will be expected to prepare technical and clerical tasks associated with the preparation, labeling and dispensing of pharmaceuticals. We will help you achieve your goals through continuous professional development and regular career progression discussions. Schedule: Monday - Friday 8:00am - 5:00pm • Competitive Pay • Health, Dental, Vision & Life Insurance • Company-Paid Short & Long-Term Disability • Flexible Schedules & Paid Time Off • Tuition Reimbursement • Employee Discount Program & DailyPay • 401k • Pet Insurance Responsibilities Coordinates and schedules the preparation of sterile mixtures and home medical equipment orders with the assistance of the Pharmacist Completes all calculations on product preparation as necessary Compounds sterile mixtures and non-mixtures, including, but not limited to parenteral nutrition, antibiotics, chemotherapy, hydration and narcotic analgesics, using aseptic technique where state laws permit Ensures compounding/clean room areas and related equipment are cleaned, sanitized and maintained in compliance with company policies and procedures, and USP 797 and USP 800 standards Documents all activities on appropriate logs Participates in branch management, department and intra-departmental meetings and quality improvement activities Adheres to all accreditation, OSHA, FDA, state, local and federal regulations, and USP 797 and USP 800 standards relevant to infusion pharmacy and home medical equipment Documents all temperature logs, pressure and humidity monitors, records all sterility testing done in the clean room in compliance with company policies and procedures, and USP 797 and USP 800 standards Documents all activities on the appropriate logs Other duties as assigned Supervisory Responsibility: No Qualifications Successful completion of an approved/accredited Pharmacy Technician training program; IV certification preferred Registered Pharmacy Technician license in state of practice per state regulations National Pharmacy Technician Certification as required by the state board of pharmacy in state of practice 1-3 years of related pharmacy experience in a home care setting, retail or pharmacy setting, preferred At least 1 year of aseptic preparation of infusion-related pharmaceuticals in a hospital or home infusion setting preferred General knowledge of drug terminology, pharmaceutical calculations, drug use and aseptic techniques Flexible schedule with the ability to work on-call evenings and weekends on an as-scheduled basis Effective mathematical and communication skills required Basic pharmacy knowledge of reading and interpreting prescriptions Ability to work independently, accurately and efficiently Valid driver's license Driving Position: Yes-Minimal driving for patient deliveries may be required **To perform this role will require constant sitting and typing on a keyboard with fingers, and ocassionally standing and walking. The physical requirements will be the ability to push/pull and lift/carry 21-30 lbs** About our Line of Business Amerita, an affiliate of BrightSpring Health Services, is a specialty infusion company focused on providing complex pharmaceutical products and clinical services to patients outside of the hospital. Committed to excellent service, our vision is to combine the administrative efficiencies of a large organization with the flexibility, responsiveness, and entrepreneurial spirit of a local provider. For more information, please visit ****************** Follow us on Facebook, LinkedIn, and X. Salary Range USD $22.50 / Hour

IMMEDIATE NEED FOR QUALITY LAB TECHNICIAN! Duties/Responsibilities: Examine product for internal and external surface defects, such as discoloration, cracks, splits, waves, or dimples. Inspect product for proper taping and inside diameter. Test and evaluate all Measure wall thickness, outside diameter, inside diameter & ovality, Evaluate Specification sheets to confirm they are being filled out correctly and that the information on them applies to the products submitted. File all specification sheets with the test results. Accurately record and communicate the quantity of inventory scrapped so proper adjustments can be made. Inspect returned goods. Confirm specification sheets on the production line are up to date and readily available for the production supervisors. Communicate all problems to the Quality Assurance Supervisor. Qualifications/Requirements: 2 years Quality Assurance experience Inspection & Inventory auditing experience Apply here ASAP!

Temp To Full-Time IMMEDIATE NEED FOR QUALITY LAB TECHNICIAN! Duties/Responsibilities: Examine product for internal and external surface defects, such as discoloration, cracks, splits, waves, or dimples. Inspect product for proper taping and inside diameter. Test and evaluate all Measure wall thickness, outside diameter, inside diameter & ovality, Evaluate Specification sheets to confirm they are being filled out correctly and that the information on them applies to the products submitted. File all specification sheets with the test results. Accurately record and communicate the quantity of inventory scrapped so proper adjustments can be made. Inspect returned goods. Confirm specification sheets on the production line are up to date and readily available for the production supervisors. Communicate all problems to the Quality Assurance Supervisor. Qualifications/Requirements: 2 years Quality Assurance experience Inspection & Inventory auditing experience Apply here ASAP! 19.00

Information Job Title Orthotics and Prosthetics Laboratory Technician Department Rehabilitative Sciences - 21755 Pay Grade 7 Job Category Support Staff Job Summary The Department of Rehabilitation seeks an experienced laboratory coordinator with a broad spectrum of skills and experience to manage laboratory operations, new technology development, device fabrication, and fabrication instruction in the inaugural Master of Science in Orthotics and Prosthetics (MSOP) program. The position is a full-time staff position and reports to the director of the Orthotics and Prosthetics program. The MSOP program anticipates admission of its first cohort in the Spring of 2025. The successful candidate is expected to participate as a full member of the department with all relevant duties, responsibilities, and benefits. The staff member is expected to be responsible for the organization, coordination, supervision, and some instruction of laboratory operations in the MSOP program. The value of employment at ETSU goes far beyond salary. Regularly benefited ETSU employees enjoy a full range of benefits, services, and programs, including paid time off & leave, paid holidays, health and life insurance, retirement planning, access to university facilities and services, and much more! Check out the ETSU Human Resources Benefits page for additional information. *********************************************** ETSU is an Equal Opportunity Employer Disclaimer: The Job Summary is intended to describe the general nature and level of work being performed by individuals in this classification. It is not intended to be a complete list of all responsibilities, duties, and skills required. Management reserves the right to revise the job or require different tasks to be performed as assigned to reflect changes in the position. Employee must be able to perform the essential functions of the position satisfactorily with or without reasonable accommodations. Knowledge, Skills and Abilities * Must be skilled at operating machinery including power tools, mills, lathes, and welders while maintaining a high level of hand-eye coordination. * Attention to detail. * Excellent communication skills. * Ability to work under pressure and meet demanding deadlines. * Ability to multitask. * Basic mathematical skills. * Ability to relay concepts. * Basic budgeting/inventory skills. * Willing to pursue certification as an Orthotic and Prosthetic Technician by the American Board for Certification in Orthotics, Prosthetics and Pedorthics, Inc. * Possess awareness of digital shape capture and additive manufacturing (3-0 printing) methods. * Ability to fabricate, fit, maintain, and repair artificial limbs, carbon, silicone, plastic appliances, and other prosthetic devices, according to Prosthetist specifications. * Ability to maintain and repair prosthetic devices under the guidance of the prosthetic staff and/or the lab manager. * Ability to follow instructions from the Prosthetist to determine type of prosthesis to be fabricated and the materials and tools required. * Ability to lay out and mark dimensions of parts using appropriate measuring instruments and templates. * Ability to saw, carve, cut, and grind wood, plastic, metal, or fabric to fabricate parts, using appropriate tools. * Ability to drill and tap holes for rivets and screws using drill press. * Ability to glue, weld, bolt, sew, and rivet parts together to form prostheses. * Ability to test prostheses for freedom of movement, alignment of parts, and mechanical stability, using all appropriate tools. * Ability to fabricate cosmetic covers. * Ability to apply silicone skin covers to the prosthesis. Required Qualifications * High school diploma or equivalent. * One year of technical experience working in an Orthotics and/or Prosthetics laboratory. Preferred Qualifications * Certified Orthotic and Prosthetic Technician by the American Board for Certification in Orthotics, Prosthetics and Pedorthics, Inc. OR commensurate experience. * Working knowledge and skills in digital shape capture and additive manufacturing methods * Extensive technical design and fabrication experience in Orthotics and Prosthetics. * An associate degree (or higher degree) or strong desire to pursue an associate degree (or higher degree). * Management/supervision experience in an active Orthotic and Prosthetic fabrication laboratory. * Mentoring/teaching experience in fabrication methods of orthoses, prostheses and footwear. Salary Posting Detail Information Posting Number SS01908P Is this position subject to a criminal background check? No Is any part of the funding for this posting coming from a grant or outside funding source? No Open Date 11/25/2025 Close Date Open Until Filled No Special Instructions to Applicants Please apply at the link below: ********************************************************** UI/CandidateExperience/en/job/515/share/300000069885896?utm_medium=jobshare&utm_source=Internal%20Job%20Share

The Quality Control Analyst II is a key technical role, responsible for ensuring the accuracy, reliability, and regulatory compliance of all analytical results that support the release of raw materials, in-process samples, bulk products, stability studies, and finished goods manufactured at Crown Laboratories. This position performs a broad range of qualitative and quantitative analyses using validated methods and cGMP/GLP-compliant laboratory practices. The QC Analyst II level includes additional responsibilities such as troubleshooting, supporting method validation and verification activities, leading portions of investigations, and contributing to continuous improvement initiatives across the QC organization. The Analyst will work collaboratively with Quality Assurance, Manufacturing, and Research & Development to ensure product quality, regulatory compliance, and operational efficiency. Reporting to: Quality Control Supervisor/Manager Location: Johnson City, TN - onsite Responsibilities/Essential Duties: * Performs routine and non-routine analytical testing of raw materials, in-process samples, finished products, bulk intermediates, and stability samples in accordance with approved SOPs, compendial requirements (USP, EP), and regulatory expectations. * Prepare reagents, standards, and sample solutions with precision, ensuring proper documentation and traceability of materials used in analytical activities. * Operate, maintain, and troubleshoot laboratory instrumentation including but not limited to HPLC, GC, UV-Vis, FTIR, Karl Fischer, viscometers, and other analytical systems. * Execute environmental monitoring activities (where applicable), interpret data trends, and escalate deviations per SOP. * Accurately document all analytical data in laboratory notebooks and electronic systems (e.g. LIMS) in accordance with ALCOA+ data integrity principles and cGMP/GLP guidelines. * Assist in laboratory investigations including OOS, OOT, and atypical results, supporting root cause analysis and corrective action implementation. * Participate in the qualification, verification, and validation of analytical methods, equipment, and laboratory systems under the guidance of senior QC or Validation personnel. * Support continuous improvement initiatives, including 5S, workflow optimization, and implementation of corrective/preventative actions (CAPA). * Comply with all site-wide safety, EHS, and hazardous material handling requirements; promptly report safety concerns and near misses. * Maintain laboratory cleanliness, readiness for internal/external audits, and adherence to cGMP expectations. * Collaborate cross-functionally with QA, manufacturing, Supply Chain, R&D, and Validation to resolve analytical issues and support timely batch disposition. * Perform additional duties, projects, or training assignments as delegated by QC leadership. Basic Qualifications: * Bachelor's degree & 2+ years' directly related experience; OR Preferred Qualifications: * Bachelor's degree in Chemistry, or related scientific discipline. * 2+ years' experience in a GMP/GLP laboratory environment (industry, academic, or internship). * Demonstrated ability to follow written procedures accurately and maintain high-quality documentation. * Strong attention to detail, analytical thinking, and problem-solving skills. * Effective written and verbal communication skills. * Proficiency with Microsoft Office applications (Word, Excel, PowerPoint). * Experience working in a regulated pharmaceutical, OTC drug, cosmetic, or medical device manufacturing environment. * Familiarity with LIMS or other laboratory information management systems. * Working knowledge of compendial methods (USP, EP, JP) and pharmacopeial requirements. * Exposure to method validation/verification, analytical troubleshooting, and instrument qualification. * Experience with data integrity, FDA 21 CFR Part 211, and ICH Q2(R2) expectations. * Laboratory-based role requiring daily use of PPE, including lab coats, safety glasses, and gloves. * Routine standing, walking, bending, lifting up to 25 lbs., and handling chemical reagents and laboratory materials. * Work involves exposure to chemical substances, solvents, and analytical instrumentation in a controlled laboratory setting. Company Summary: Crown is a proud member of the Revance Portfolio of skincare offerings. Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings throughout every stage of life. With a differentiated portfolio of products spanning 60 countries, Revance meets the evolving needs of patients and consumers worldwide through continued innovation and commercialization of new products and treatments. What Revance invests in you: * Competitive Compensation including base salary and annual performance bonus. * Flexible PTO, holidays, and parental leave. * Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more! This section of the is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job." Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

At BWX Technologies, Inc. (NYSE: BWXT), we are People Strong, Innovation Driven. A U.S.-based company, BWXT is a Fortune 1000 and Defense News Top 100 manufacturing and engineering innovator that provides safe and effective nuclear solutions for global security, clean energy, environmental restoration, nuclear medicine and space exploration. With more than 7,800 employees, BWXT has 14 major operating sites in the U.S., Canada and the U.K. We are the sole manufacturer of naval nuclear reactors for U.S. submarines and aircraft carriers. Our company supplies precision manufactured components, services and fuel for the commercial nuclear power industry across four continents. Our joint ventures provide environmental restoration and operations management at a dozen U.S. Department of Energy and NASA facilities. BWXT's technology is driving advances in medical radioisotope production in North America and microreactors for various defense and space applications. For more information, visit ************ . Follow us on LinkedIn , X , Facebook and Instagram . BWXT Ordnance Tennessee (NOGJ) has an immediate need for a Quality Technician 2 in Jonesborough Tennessee. The Quality Technician 2 position performs inspection of in-process and finished products, performs a variety of testing techniques, completes and reviews inspection documents, and accepts or rejects material based on customer specifications and guidelines while maintaining traceability and acceptable quality standards. The Quality Technician 2 will work within the Quality Assurance Department and will report directly to the Sr. Manager of Quality Assurance. This position requires the ability to work any shift as dictated by production requirements (1st, 2nd or 3rd), the ability to work overtime, weekends and shifts of 10 to 12 hours per day. Location: Jonesborough, Tennessee Your Day to Day as a Quality Technician 2 for NOGJ: Create and maintain accurate records including records of inspection. Prepare simple to complex reports. Read and interpret complex drawings. Effectively present information to customers, client departments and other employees within the organization. Read, interpret and understand written or verbal requirements, procedures and specifications to perform assigned tasks. Prepare inspection reports. Record and maintain accurate records and files. Prioritize work to meet critical deadlines. Follow Safety Practices. Work effectively in a team environment and interface effectively with all levels of employees within the organization. Perform mathematical calculations accurately and efficiently. Perform visual inspection or product. Set-up inspection processes. Inspection of in-process or finished product. Initiation, preparation and follow through of inspection reports to include screening, rework and re-inspection. Compile and prepare reports; Perform statistical analysis. Performance of all types of inspection processes including use of micrometers, indicators, CMM, comparators, vision equipment, etc. Accept or reject material based on approved inspection equipment and methods. Assume lead/supervisory role, as required. Review and make suggestions for changes to inspector plans, inspector procedures for processes defined by Engineering. Work with customer representatives for lot acceptance. Assist Manufacturing with troubleshooting quality deficient products. Provide support and give recommendations during audits. Maintain quality documents/reports per procedures. Maintain a clean and safe work environment and work area. Perform work in other areas of the facility as required Required Qualifications: Requires a High School Diploma or equivalent and a minimum of 6 years of prior relevant experience or an Associate's degree with 2 years of related experience. Selected candidate may be required to complete training and certifications in two or more non-destructive testing (NDT) methods. Demonstrated knowledge of all standard measuring and gaging equipment, quality standards and techniques; applicable laws, codes, ordinances, and regulations, non-destructive and destruction testing techniques and principles; gaging methods and sampling plans Ability to read and interpret simple to complex blueprints and engineering Drawings Ability to perform visual setup and dimensional inspection of complex parts and assemblies Intermediate math skills. Numbers, their operation and inter-relationships, including arithmetic, algebra, geometry, statistics, trigonometry, and their applications Calibration and Metrology principles Techniques, tools and instruments involved in the use of precision technical plans, inspection plans, blueprints, drawings and/or models Microsoft Office, Word, Excel, and Outlook Familiarity with Statistical Process Control methods Requires the ability to interface with all levels of personnel and work in a team environment Must be able to wear and use personal protective equipment including but not limited to safety shoes, eyeglasses, coveralls, ear plugs and various monitoring equipment Requires the ability to pass a visual acuity exam upon hire and annually thereafter (Near Vision must meet the Jaeger #1 test at less than 12 inches with one eye, natural or corrected) (NAS410) Effective verbal and written communication skills are essential Ability to work effectively in a fast-paced and dynamic environment Must be a U.S. citizen with no dual citizenship Must be able to obtain and maintain a U.S. Department of Defense (DoD) clearance Preferred Qualifications: Prior experience with BWXT Ordnance Tennessee (NOGJ) product lines is strongly desired Coordinate Measuring Machine (CMM) operation and programming experience is desired A certification in two or more non-destructive testing (NDT) methods is desired. What We Offer: Competitive salary and benefits package, including health, dental, and retirement plans. Flexible work schedules and paid time off to promote a healthy work-life balance. Professional development opportunities, including mentorship programs and sponsorship for continuing education. An inclusive atmosphere that celebrates new perspectives and supports collaboration between different generations. The chance to be part of a mission-driven organization making a positive impact on the future of energy. Opportunities for continuous learning and training to grow throughout your career! Pay: $$23.58 to $34.61 - $$23.58 The base salary range for this position in Tennessee (US-TN) at the start of employment is expected to be between $$23.58 to $34.61 and $$23.58 per year. However, the base salary offered is based on local job market factors, and may vary further depending on factors specific to the selected job candidate, such as job-related knowledge, skills, experience, and other objective business considerations. Subject to these considerations, the total compensation package for this position may also include other elements, such as an annual cash incentive in addition to a full range of medical, retirement, and/or other benefits. Details of participation in these benefit plans will be provided at such time the selected job candidate receives an offer of employment. If hired, the selected job candidate will be employed 'at-will,' unless employed at a location and in a position subject to a collective bargaining agreement. The company further reserves the right to modify base salary (as well as any other discretionary payment, compensation or benefit program) at any time, including for reasons related to individual performance, company or individual department/team performance, and other market factors. As a federal government contractor, BWX Technologies, Inc. and any subsidiaries, affiliates and related entities ("BWXT" or the "Company") complies with all federal, state, and local laws and customer requirements regarding health and safety protocols. As such, all BWXT new hires will be required to adhere to applicable Company health and safety requirements within the workplace as a condition of employment. Applicants selected will be subject to a Federal background investigation and must meet eligibility requirements for access to classified information or matter. Position requires U.S. citizenship with (no dual citizenship) ability to obtain and maintain a Department of Energy (DOE) security clearance which involves an extensive criminal and financial background investigation, drug test and previous employment reference verifications. BWXT is committed to the concept of Equal Employment Opportunity. We have established procedures to ensure that all personnel actions such as recruitment, compensation, career development, benefits, company-sponsored training and social recreational programs are administered without regard to race, color, religion, sex, national origin, citizenship, age, disability, protected veteran or other protected status. BWX Technologies, Inc. and its affiliates and subsidiaries (BWXT) is not responsible for and does not accept any liability for fees or other costs associated with resumes or candidates presented by recruiters or employment agencies, unless a binding, written recruitment agreement between BWXT and the recruiter or agency exists prior to the presentation of candidates or resumes to BWXT and includes the specific services, job openings, and fees to be paid ("Agreement"). BWXT may consider any candidate for whom a recruiter or agency has submitted an unsolicited resume and explicitly reserves the right to hire such candidate(s) without any financial obligation to the recruiter or agency unless an Agreement is in place prior to presentation and such Agreement explicitly encompasses the job opening for which such fees or costs are sought. An email, verbal or other informal contact with any person within BWXT will not create a binding agreement. Agencies or recruiters without an Agreement are directed not to contact any hiring managers of BWXT with recruiting inquiries or resumes. Recruiters and agencies interested in partnering with BWXT may contact BWXT's Talent Acquisition team at [email protected]. Nearest Major Market: Asheville Nearest Secondary Market: Knoxville Job Segment: Inspector, QC, Nuclear Engineering, DoD, Defense, Quality, Engineering, Government

Job Details Duffield - Duffield, VA Full TimeDescription We are seeking a detail-oriented and proactive Manufacturing Quality Control Technician to ensure that our products meet established quality standards and customer specifications. This role involves inspecting materials and products, conducting tests, maintaining records, and working closely with production teams to resolve quality issues and improve processes. Key Responsibilities: Perform in-process and final inspections of manufactured products to ensure compliance with specifications and standards. Conduct dimensional and visual inspections using tools such as calipers, micrometers, gauges, and other measurement instruments. Review production documentation, including work orders, specifications, and inspection criteria. Identify and report non-conformances, initiate corrective actions, and assist in root cause analysis. Maintain accurate inspection and testing records, logs, and reports. Ensure compliance with company procedures, ISO standards, and regulatory requirements. Collaborate with production, engineering, and quality teams to resolve issues and suggest improvements. Support internal and external audits and inspections. Monitor and calibrate inspection tools and testing equipment. Follow safety and environmental protocols in the workplace. Qualifications Qualifications: High school diploma or GED required; associate degree or technical certification in a related field preferred. 1-3 years of experience in a quality control or inspection role within a manufacturing environment. Familiarity with quality standards (e.g., ISO 9001, GMP) and statistical process control (SPC). Ability to read and interpret technical drawings, blueprints, and specifications. Proficient in using measuring and testing equipment. Strong attention to detail, analytical skills, and problem-solving ability. Basic computer skills, including proficiency with Microsoft Office and quality management systems (QMS). Physical Requirements: Ability to stand, walk, and move for extended periods. Capability to lift up to [25/50] pounds. Manual dexterity for handling small components and precision instruments. Preferred Qualifications: Experience with Six Sigma, Lean Manufacturing, or other quality improvement methodologies. Previous experience in [industry type: automotive, electronics, medical devices, etc.].

Laboratory Assistant, General Laboratory Full Time, 72 Hours Per Pay Period, Night Shift Morristown-Hamblen Healthcare System has 167 licensed beds and 23 emergency suites. The hospital offers outstanding ancillary services including Laboratory, Radiology and Therapy services. At our Breast Imaging Center of Excellence, women can have their annual mammograms, biopsies, and can meet with a nurse navigator if needed. The Women's Center offers six newly remodeled labor and delivery suites and has a secure nursery for the care of our newborns. It serves an eight-county region in the Lakeway Area and is equipped with modern technologies and expert staff to provide the best possible patient care. Learn more about our amazing facility at *********************************** Position Summary: An employee in this position must be able to perform in the following areas: collection and proper handling of venous and capillary blood specimens for both in and out patients, responsibility for the safety and comfort of customers, clerical/computer duties, and courier responsibilities as required for the position. Recruiter: Alexa Robbins || ***************** Responsibilities Customer service and specimen collection is recognized as the first priority. Transcribes medical orders in a timely manner, orders the appropriate laboratory tests as indicated for patients, lab contracts, and specimens. Follows-up on all verbal orders with requests for written orders. Responsible for answering the departmental telephones and transferring calls to proper laboratory/pathology section; follows through with problem resolution; assists physicians/staff in obtaining, faxing or telephone receipt of laboratory test results; and responsible for strict adherence to proper handling of confidential test results. Responsible for use of HIS, LIS and reference lab computer systems (i.e. Mayo, etc.) as appropriate for specific hospital facility. Knowledgeable of manual systems for ordering, collection, verification, and charting in instances of computer failure. Properly processes, all specimens including accessioning; recognition of test priorities; centrifugation; separation/processing, logging and special collection requirements. Properly collects blood samples from venous and/or capillary (heel or finger) sites as required by facility. Proper use of aseptic technique in the collection of blood culture specimens. Accurately labels all specimens. Proper use of blood bank armband and labeling system. Strict adherence to proper identification of patient's name and DOB by hospital armband and asking the patient his/her name, or by asking the RN to visually identify the patient. Strict adherence to proper disposal of needles/sharps, and used gloves during phlebotomy. Maintain clerical and phlebotomy work areas in a neat and sanitary manner. Responsible for participation in Laboratory performance improvement activities. Complies with Laboratory policies and procedures, including Exposure Control, Chemical Hygiene Plan, Disaster Plan, the Joint Commission standards, CLIA and State regulations. May be a resource for difficult sticks. Follows policies, procedures, and safety standards. Completes required education assignments annually. Works toward achieving goals and objectives, and participates in quality improvement initiatives as requested. Performs other duties as assigned. Qualifications Minimum Education: None specified; will accept any combination of formal education and/or prior work experience sufficient to demonstrate possession of the knowledge, skill and ability needed to perform the essential tasks of the job, typically such as would be equivalent to a high school diploma or GED. Preference may be given to individuals possessing a HS diploma or GED. Minimum Experience: None Licensure Requirement: Certification by NCA, ASCP, ASPT, or comparable institution is desirable.

Launch Your Medical Career with Purpose - No Experience Required! *Sign on Bonus $4000* Are you detail-oriented, calm under pressure, and eager to make a real impact in the world? Have you dreamed of working in the medical field but weren't sure where to begin? At Tennessee Donor Services, we're offering a unique opportunity to start your healthcare career as a Tissue Recovery Technician - with paid, hands-on training and no prior medical experience required. When you join us, you're not just learning surgical skills - you're opening the door to a long-term career in healthcare. Tissue Recovery Technicians will participate in the recovery, packaging, and labeling of human tissue. The recovery process consists of cleaning and setting up the recovery room, surgical prep of the donor, aseptic recovery of human tissue, restoration of the donor, and decontamination of the recovery room and instruments. COMPANY OVERVIEW AND MISSION Tennessee Donor Services is a designated organ procurement organization (OPO) within the state of Tennessee - and is a member of the DCI Donor Services family. For over four decades, DCI Donor Services has been a leader in working to end the transplant waiting list. Our unique approach to service allows for nationwide donation, transplantation, and distribution of organs and tissues while maintaining close ties to our local communities. DCI Donor Services operates three organ procurement/tissue recovery organizations: New Mexico Donor Services, Sierra Donor Services, and Tennessee Donor Services. We also maximize the gift of life through the DCI Donor Services Tissue Bank and Sierra Donor Services Eye Bank. Our performance is measured by the way we serve donor families and recipients. To be successful in this endeavor is our ultimate mission. By mobilizing the power of people and the potential of technology, we are honored to extend the reach of each donor's gift and share the importance of the gift of life. With the help of our employee-led strategy team, we will ensure that all communities feel welcome and safe with us because we are a model for fairness, belonging, and forward thinking. 🧠 What Skills Will Set You Up for Success? Strong attention to detail - Accuracy is essential when working in surgical settings and handling donor tissue. Comfortable in clinical or operating room environments - You'll learn sterile technique and surgical protocol. Team player with strong communication skills - You'll work closely with a skilled, mission-driven team. Adaptability and emotional resilience - This is meaningful, life-changing work that requires compassion and professionalism. Motivated to learn and grow - We'll equip you with all the tools and support to succeed. 🛠 What You'll Learn: Real surgical procedures and sterile techniques used in tissue recovery How to operate in an OR-like environment with professional tools and standards Human anatomy and surgical protocols, providing a foundation for future roles in healthcare Skills that translate directly into clinical, surgical, or emergency medical careers You'll gain experience that many people don't get until much later in their medical careers - making this role a powerful steppingstone or an opportunity to build a lasting career in the medical and donation field. 🌟 What You'll Get: On-the-job training - We teach you everything you need to know. Valuable medical experience - Get hands-on with human anatomy and surgical recovery procedures. Career advancement opportunities - Build a future in the healthcare field. Make a difference - Play a vital role in saving and healing lives through tissue donation. Up to $4,000 in sign-on bonuses 💼 Employee Benefits: Generous Paid Time Off (PTO) to recharge and refresh Extended Sick Bank (ESB) for added peace of mind Comprehensive Health Insurance - medical, dental, and vision Holiday Pay - Earn extra pay when you work on recognized holidays A workplace that values purpose, growth, and teamwork 🤝 Our Culture: We believe in working hard, supporting each other, and getting the job done right - together. Our team is tight-knit, mission-driven, and always ready to lend a hand. If you're looking for a place where people have your back and your work truly matters, you'll fit right in. This is more than a job - it's a chance to start a career that truly matters. Ready to make a difference and build your future in healthcare? Apply now and join the mission at Tennessee Donor Services. As a condition of employment, you must be able to obtain Hospital Badge and EMR Access from all of the DCI Donor Services Hospital partners. You will receive a confirmation e-mail upon successful submission of your application. The next step of the selection process will be to complete a video screening. Instructions to complete the video screening will be contained in the confirmation e-mail. Please note - you must complete the video screening within 48 hours from submission of your application to be considered for the position. DCIDS is an EOE/AA employer - M/F/Vet/Disability.

QA Technician (Nights) Work Schedule: Monday - Friday 8-hours shifts (Nights) Benefits: Medical, Dental, Vision, Life, Short-Term/Long-Term Disability Insurance effective 30 days after first full month 401(k) Match 7 Paid Holidays, 3 Floating Holidays for use at employee's discretion Immediate eligibility for holiday and vacation pay Work-Life Balance Climate-Controlled and cleanest work environment in Morristown Education Reimbursement Fitness Reimbursement Employee Product Giveaways Referral Program Associate discount programs Overtime available POSITION SUMMARY: The Quality Assurance Technician provides support for production, purchasing, product development, project managers, and customer to ensure that all applicable regulations and customer expectations are met in the production process. ESSENTIAL ACCOUNTABILITIES: Provide daily support to all manufacturing cells and other internal customers for Quality related issues and concerns. Performing the first piece inspection process for all finished goods. Investigate non-conforming material; write investigation reports. Update NCM raw materials and finished product disposition. Work on special projects as assigned by the QA Manager or QA Supervisor. Train and develop future QA technicians. Maintain the training and ability to review each document within the DHR. Train and develop production floor associates in quality, procedures, and production records. Sample/Inspect all applicable incoming raw materials. Perform testing as needed. Monitor and maintain solution and finished product retain samples. Perform annual inspection of drug product retains. Manage QA Hold/Quarantine area. Obtain environmental samples per schedule. Demonstrate commitment to Rockline/Iatric's RRITE Values of Renew, Respect, Integrity, Teamwork, and Excellence. Associates have a direct and important role in ensuring that all work is performed in a safe manner. Effectiveness in carrying out this responsibility is part of each associate's essential accountabilities. Contribute to a cooperative working effort by demonstrating a willingness to perform other job-related work, as needed or requested This position is designated as Safety-Sensitive (A safety-sensitive position is one in which the associate's inability or impaired ability to perform their job-related tasks could result in a direct threat to the associate's safety or the safety of others). QUALIFICATION REQUIREMENTS: (To perform this job successfully, an individual must be able to perform each of the essential accountabilities satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.) High School Diploma/GED, required plus a minimum of 3 years' experience in Quality, a Laboratory setting or Wet Wipes manufacturing; Associate's or Bachelor's degree in technical, quality or life science preferred, or any combination of equivalent education and experience. Working knowledge of Microsoft tools (Word, Excel, PowerPoint) required. Strong problem-solving skills. Ability to communicate across all levels of the organization. Working knowledge of the FDA's regulations (21 CFR) is highly recommended. Ability to work in a fast-paced, high-pressure environment with limited supervision is a plus. Work prioritizing is essential for success. Ability to make sound decisions and influence others. PHYSICAL AND MENTAL REQUIREMENTS: (The physical demands described here are representatives of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions) Must be able to communicate face-to-face and over the phone Occasional lifting up to 50 lbs. Frequent standing/walking. Occasional sitting, bending, twisting, kneeling, climbing, pushing/pulling, and reaching. Repetitive hand and foot movement. Work environment includes occasional noise >85db, hot and cold temperatures. Requires ability to read, write, calculate, and analyze. Requires good visual acuity with depth perception and color vision. 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.) Production and office environment FLSA Status: Non-Exempt Grade: 06

Immediate positions available for QUALITY LAB ASSOCIATE at ArtaZn (formerly Jarden Zinc) $17.00/hr to start, increase to $18.00/hr in 60 days 6pm-6am or 6am-6pm schedules available Long term positions If interested please apply HERE, come by our office @2290 East Andrew Johnson Hwy or call us today at 423-639-7123!

Temp Immediate positions available for QUALITY LAB ASSOCIATE at ArtaZn (formerly Jarden Zinc) $17.00/hr to start, increase to $18.00/hr in 60 days 6pm-6am or 6am-6pm schedules available Long term positions If interested please apply HERE, come by our office @2290 East Andrew Johnson Hwy or call us today at 423-639-7123!!