Medical laboratory technician jobs in Bloomington, IN

Contemporary Staffing Solutions is seeking a Laboratory Technician to join our client to support laboratory testing efforts for commercial pharmaceutical products. This role involves analyzing in-process and final product samples to ensure accuracy, compliance, and product integrity. Based onsite in Medora, IN , this temporary-to-hire position plays a key role in maintaining quality standards and meeting regulatory requirements. The ideal candidate will be detail-oriented and comfortable working in a fast-paced laboratory environment. Compensation: Up to $26/hour, based on experience Work Schedule: Monday through Friday, 8:30 AM to 5:30 PM with a break Key Responsibilities of the Laboratory Technician: Perform analytical testing on in-process, release, and stability samples to verify product quality and compliance with established procedures and safety standards. Operate and maintain laboratory instruments such as HPLC, GC, pH meters, and dissolution equipment while following cGMP practices. Document laboratory activities, results, and observations in accordance with regulatory and internal documentation standards. Review data, reports, and laboratory records to support accuracy, traceability, and peer validation. Qualifications and Skills for the Laboratory Technician: Bachelor's degree in Chemistry or a related scientific field; equivalent experience in pharmaceutical testing may be considered. Previous experience working in a cGMP-regulated laboratory, with knowledge of USP/NF and FDA guidelines. Familiarity with analytical techniques and instrumentation including HPLC, GC, dissolution testing, and wet chemistry methods. Strong attention to detail, organizational skills, and ability to collaborate within a cross-functional team. Proficiency with Microsoft Word, Excel, and laboratory data management systems such as LIMS or CDS. Why Join Us? You'll gain valuable experience in a regulated pharmaceutical environment while contributing to the production of high-quality drug products. This role offers hands-on exposure to industry-leading laboratory practices, collaboration with experienced professionals, and the potential for long-term career growth through a temporary-to-hire opportunity. About Us: Contemporary Staffing Solutions (CSS) is a trusted leader in providing contract, temporary, temp-to-hire, and direct hire staffing solutions. With decades of experience, we've grown from a staffing agency to a nationwide provider of workforce management solutions. Our niche recruitment expertise spans Accounting & Finance, Call Center & Office Support, Human Resources, Sales & Marketing, and Information Technology. Explore more about CSS and how we connect great talent with exceptional opportunities by visiting *****************************

Job Description Job Duties/Responsibilities: Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Associate degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 2-4 years of clinical laboratory testing experience is required. State Medical Technician license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

Indiana University Health is Indiana's most comprehensive health system, with 16 hospitals and more than 34,000 team members serving Hoosiers across the state! We're looking for team members who are inspired by challenging and meaningful work for the good of every patient. People who are compassionate and serve with a purpose. People who aspire to excellence every day. The laboratories of IU Health offer some of the most comprehensive laboratory services in Indiana! Open 24 hours a day, seven days a week, the laboratories perform more than 19 million tests a year. In addition to IU Health, laboratory testing services are provided to hospitals and physicians across the country. SHIFT: Full-Time, Days The Medical Laboratory Technician at the LAB assists with laboratory testing on patient specimens. Under direction, may provide information for the diagnosis and treatment. Helps to maintain records of performance and utilizes independent judgment to generate acceptable test results. Performs all tasks according to standard operating procedures. Assists with development and modification of procedures and assumes additional responsibilities as outlined by management or the laboratory director. Requires Bachelor's degree in a related science (Certification is not required); Associate Degree in an approved Medical Laboratory Technician Program or a Medical Laboratory Specialist (Laboratory Technician) certification from an official military medical laboratory procedures course of at least 50 weeks duration, dependent on when coursework was completed. Associate degree requires certification (NCA, AMT, ASCP, HEW, and CLA) within 12 months of employment. Failure to achieve would result in downgrade to Lab Assistant II position until certification is achieved or loss of employment, dependent on business need. Requires knowledge of various laboratory techniques and procedures. Requires working knowledge of laboratory testing equipment and routine maintenance procedures. Requires ability to maintain quality control and other records. Requires working knowledge of computers. Requires knowledge of all laboratory safety regulations and protocols. As Indiana's largest and most comprehensive healthcare system, and the number 1 ranked healthcare system in Indiana, we offer: Increased pay scale for bedside nurses. 401(K) retirement savings with employer match Tuition reimbursement Student loan forgiveness - Government program that may allow qualifying participants to have the remainder of their student loan balance forgiven (after a set amount of time and specific qualifications have been met). Employee Assistance Program - Counseling at no cost to you Healthy Results - Participation in our team member wellness programs award points that contribute toward a biweekly financial incentive in your paycheck! The more you participate, the more you earn!

Franciscan Health Indianapolis Shift: Start time between 1:00 PM and 2:30 PM; Weekends and holidays as assigned; Hours may vary as needs dictate FTE: 0.4 WHY ALVERNO We are a highly reliable scientific organization building a culture of service. Our commitment advances the health, wellness and continuity of care in the communities we serve. We are one of the largest integrated laboratory networks serving hospitals in the Midwest region. Our network includes 32 hospitals and multiple physician offices. WHAT WILL YOU DO This individual is responsible for specimen processing, test performance and reporting test results. Testing performed will include waived, moderate and high complexity tests as authorized by the Director. He/she will report results of all tests performed according to established procedures. In addition this individual will participate fully in all quality control procedures and comply with quality assurance and quality management standards within the department as outlined by the department, JCAHO, CAP, CLIA and other applicable agencies. He/she will perform specimen collection as necessary. WHAT WE ARE LOOKING FOR MLT Associates degree in a laboratory science or medical laboratory technology from an accredited institution. MT Bachelor degree in medical laboratory science/medical technology from an accredited college or university. Or Bachelor degree in chemical, physical or biological sciences. At least 1 year of pertinent full-time clinical laboratory experience or training preferred.

Pay Range: $19.66 - $34.59 Responsible for laboratory testing, quality control, phlebotomy, instrument maintenance and troubleshooting. Perform manual and automated routine blood tests. Prepare specimens for microscope examination. Operate laboratory equipment including centrifuges, dry bath incubators, and blood bank refrigerators. Key Performance Areas * Responsible for performing proper quality control procedures before proceeding with patient testing. * Ensure that proper documentation including test report logs, quality control logs, equipment records, and all lab procedure and training checklists are completed on the correct time schedule. Will be responsible to ensure this is performed in central lab. * Maintain adequate inventory of laboratory supplies. Place order with purchasing as needed. * Perform technical laboratory procedures with accuracy and precision, meeting the standard of all accreditation/regulatory agencies. * Perform instrument maintenance at the required times and as needed. * Initiate troubleshooting procedures when instrument malfunction occurs and contact instrument service company, if necessary. * Comply with established safety guidelines and maintains cleanliness of the laboratory and equipment. * Complete any and all duties required to keep laboratory in compliance with state and federal regulatory agencies. Must be able to perform compliance testing. * Maintain and ensure the confidentiality of all patient and employee information at all times. * Comply with all Federal and State laws and regulations pertaining to patient care, patient's rights, safety, billing, and collections. Adhere to all AON and departmental policies and procedures, including IT policies and procedures and the Disaster Recovery Plan. * Must maintain MLT license and required CEUs. * Assist in training new employees to related job duties. * Will be expected to work overtime when given sufficient notice of required overtime. Qualifications Education * A.A. or A.S. degree License and Certification * Appropriate state license required. * National lab certification preferred. * BLS preferred. Experience * Minimum of four years experience in the healthcare field, preferably in a clinical setting is required. #AONC #LI-ONSITE

Apply for this great opportunity as a Medical Technologist/MLT position in the Indianapolis, Indiana area for permanent hire! Position is interviewing now! *Multiple shifts open (evening and night comes with shift differentials) *Full-time, permanent hire *Full benefits package (401k, medical/dental/vision insurance, PTO, etc) *Room for career growth *Competitive pay *SIGN ON/RELOCATION BONUS Position Requirements: *MT, MLS, or MLT ASCP certificate (or eligibility) *Experience preferred but will consider new graduates! *Associate Degree in Science (minimum) Interested in more information? Apply now or send a resume to marissak@ka-recruiting.com. (Reference Code: MK1196)

Pay Range: Responsible for laboratory testing, quality control, phlebotomy, instrument maintenance and troubleshooting. Perform manual and automated routine blood tests. Prepare specimens for microscope examination. Operate laboratory equipment including centrifuges, dry bath incubators, and blood bank refrigerators. Key Performance Areas Responsible for performing proper quality control procedures before proceeding with patient testing. Ensure that proper documentation including test report logs, quality control logs, equipment records, and all lab procedure and training checklists are completed on the correct time schedule. Will be responsible to ensure this is performed in central lab. Maintain adequate inventory of laboratory supplies. Place order with purchasing as needed. Perform technical laboratory procedures with accuracy and precision, meeting the standard of all accreditation/regulatory agencies. Perform instrument maintenance at the required times and as needed. Initiate troubleshooting procedures when instrument malfunction occurs and contact instrument service company, if necessary. Comply with established safety guidelines and maintains cleanliness of the laboratory and equipment. Complete any and all duties required to keep laboratory in compliance with state and federal regulatory agencies. Must be able to perform compliance testing. Maintain and ensure the confidentiality of all patient and employee information at all times. Comply with all Federal and State laws and regulations pertaining to patient care, patient's rights, safety, billing, and collections. Adhere to all AON and departmental policies and procedures, including IT policies and procedures and the Disaster Recovery Plan. Must maintain MLT license and required CEUs. Assist in training new employees to related job duties. Will be expected to work overtime when given sufficient notice of required overtime. Qualifications Education A.A. or A.S. degree License and Certification Appropriate state license required. National lab certification preferred. BLS preferred. Experience Minimum of four years experience in the healthcare field, preferably in a clinical setting is required. #AONC #LI-ONSITE

At Monroe Hospital, our dedicated team of professionals is committed to our core values of quality, compassion, and community. As a member of Prime Healthcare, a Top-15 hospital system in the United States, Monroe Hospital is actively seeking new members to join its award-winning team! Monroe Hospital is a 32-bed community hospital located in beautiful Bloomington, Indiana. Monroe Hospital is committed to providing superior healthcare, ever mindful of each patient's individuality and unique needs. Monroe Hospital has been recognized by Healthgrades as a Patient Safety Excellence Award recipient, a distinction that places Monroe Hospital among the top 10% of all short-term acute care hospitals. For more information, please visit *********************** Responsibilities Medical Laboratory Technician (MLT) can perform waived, highly and moderately complex testing, as stated in CLIA (42 CFR 493.1489). Must possess a degree of skill commensurate with individual's education, training or experience and technical abilities Each individual performing the above procedures must: 1) adhere to the laboratory's procedures for the collection, processing, analysis, and reporting of patient test results, 2) follow the laboratory's established quality control policies and procedures in documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications, 3) be capable of identifying problems that may adversely affect test performance and either correct the problem or immediately notify your immediate supervisor, Director, or Medical Director, 4) perform waived or highly and moderately complex laboratory procedures using both manual and automated methods in, Hematology, Chemistry, Urinalysis, Coagulation, Microbiology and Immunology, 5) perform and document maintenance - daily, weekly, monthly, or as needed on instruments and equipment as appropriate, 6) review the accuracy of patient results prior to releasing or reporting, 7) recognize age specific differences in expected results for newborns to geriatrics, 8) ensure that the testing of proficiency testing samples are tested in the same manner as patient samples and that collaboration with other laboratories is prohibited prior to the reporting of proficiency testing results to the appropriate agencies, 9) may be required to perform venipuncture or capillary puncture on various age groups from newborn to geriatrics, 10) assist in the development and maintenance of laboratory policies and procedures, 11) adheres to all department and hospital policies and procedures related to safety, infection control, emergency preparedness, and human resources, 12) in the absence of a supervisor, may be assigned/identified as Lead Tech, having responsibility for the section or department during their shift, 13) other tasks or responsibilities may be assigned by the department manager/director. Qualifications 1. ASCP certification, or equivalent, preferred.2. Associates Degree in chemical, physical, biological science, or completion of coursework in a program for MLT.3. 1 year of hospital laboratory work experience preferred #LI-AS2 Employment Status Full Time Shift Nights Equal Employment Opportunity Company is an equal employment opportunity employer. Company prohibits discrimination against any applicant or employee based on race, color, sex, sexual orientation, gender identity, religion, national origin, age (subject to applicable law), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. The Company also prohibits harassment of applicants or employees based on any of these protected categories. Know Your Rights: ********************************************************************************************

WinField United SureTech Lab Intern, Summer 2026 When you intern at Land O'Lakes, you're joining a Fortune 250 agribusiness and food production leader with more than 100 years of operations as a farmer- and member-owned cooperative. With business units spanning crop insight and inputs, animal nutrition, dairy foods, and sustainability solutions, you will experience a hands-on, purpose-driven internship. You'll have opportunities to network with industry leaders, tour our state-of-the-art facilities, and be challenged with a business-critical project, all while gaining skills that will impact your career trajectory. We are hiring a SureTech Lab Intern based in Indianapolis, IN for Summer 2026! SureTech is a full-service agricultural lab that provides retailers access to the timely, cost-effective, reliable data their farmers need to make better decisions. With over 50 years of experience, a dedicated team of chemists and lab technicians using the most innovative technology, and a new location with ample space and resources, SureTech has earned its reputation as a trusted partner to retailers across the U.S. As a SureTech Lab Intern you will execute laboratory experiments designed by the Technical Lead Chemist and Intern Manager. This includes test sample organization, sample handling, the running of laboratory instrumentation, and documentation and organization of experimental data. With guidance from the Technical Lead Chemist, you will participate in the analysis of the experimental data. You will be called upon to use the experimental data to draw conclusions and have an understanding of how the data can be used to drive agronomic decisions. Internship Duration: May - August 2026 Interns are paid $25.00/hour. Relocation assistance may be provided to eligible candidates for the duration of the summer internship. Experience-Education (Required) Sophomore (preferred) or Junior undergraduate pursuing a bachelor's degree in agronomy, crop & soil science, horticulture, plant biology, plant pathology, agriculture, or other related field of study. Required GPA of 3.0 or higher Competencies-Skills (Required) Ability to work without direct supervision. Excellent communication, writing, and critical thinking skills. Manage time and effectively prioritize and implement projects and general work tasks. Resourceful and innovative in finding solutions to problems. Flexible and can adapt to changing business surroundings. Ability to adhere to strict safety standards when handling crop protection products in lab and field settings. Properly wear chemical application equipment and personal protective equipment while working as required by job duties. Competencies-Skills (Preferred) Proficient in Microsoft Office Suite tools (Excel, PowerPoint) About Land O'Lakes, Inc. Join us and be part of a Fortune 250, farmer- and member-owned cooperative that is reimagining the business of food. We have been named a Top Workplace by Indeed and LinkedIn, and to the TIME 100 Most Influential Companies list. Benefits for most full-time roles include medical, dental, vision, PTO, life & disability insurance, education assistance, a 401k and a variety of well-being resources. Most part-time employees are eligible for prorated PTO, holiday pay, employee development programs, prorated education assistance, and a 401(k). Land O'Lakes, Inc. is an Equal Opportunity Employer (EOE) M/F/Vets/Disabled. The company maintains a drug-free workforce, including post-employment substance abuse testing pursuant to a Drug and Alcohol Policy. Neither Land O'Lakes, nor its search firms, will ever contact you and ask for confidential information over the phone or in email. If you receive a call or email like this, please do not provide the information being requested.

**$7,500 Sign-on Bonus** Labcorp Employees not eligible for sign-on bonus At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 60,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on peoples lives. We have an exciting opportunity for a Medical Technologist I to join our Safety Testing Team in Indianapolis, IN! Scheduled Shift: Monday-Friday 2pm-10:30pm, rotating Tuesday-Saturday 2pm-10:30pm Pay Range: All job offers will bebased on a candidates skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.For more detailed information, pleaseclick here. Essential Functions Perform assigned clinical laboratory testing accurately and in a timely manner. o Resolve pendings. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved. o Prepare workstation and instrumentation for the assigned testing. o Properly handle specimens and independently resolve technical specimen issues in preparation for analysis and specimen storage. Contact internal customers for clarification as needed. o Operate instruments to perform testing in accordance with established written procedures. o Performs routine testing and calculations as required. o Resolve routine and non-routine assay problems. Ensure the validity of tests results through the performance of established quality assurance and quality control procedures. o Perform experiments, as scheduled, for evaluation of new Calibrator and/or QC lots. Summarize results of investigations and compile data for review by management. o Document quality control results. Interpret quality control results according to Westgard rules or other established departmental procedures and accurately document biases, warnings and violations of control values. o Document corrective action for unusual occurrences (e.g. QC violations, instrument related problems). o Analyze proficiency testing survey samples as patient specimens. Reagents/Materials/Supplies: o Receive, open and place in service all reagents/materials according to SOPs. o Prepare and properly label reagent, quality control, calibrator material. o Document implementation of new reagents/materials according to SOPs. o Perform parallel testing, linearitys, stability, other quality control practices needed to ensure validity of material prior to being placed into service. o Perform inventory control of supplies and reagents as approved by management. Result Entry (Auto-verification and manual entry). o When data is manually entered (e.g. QC, patient data) ensure peer review is performed and documented prior to release of results. o Prepare proper documentation of test results and enter into the information system. o Generate an appropriate audit trail for all activities Document and communicate any result reporting problems or inconsistencies to laboratory management. o Complete testing within the expected turnaround time to meet customers expectations. Ensures maintenance of instruments and equipment is performed according to manufacturer and SOP requirements and documented according to SOP. o Calibrate instruments, equipment and/or assays as required and document. o Perform basic instrument and equipment troubleshooting. o Perform pipette calibrations and document according to SOP. o Notify laboratory management when an instrument or equipment does not meet specifications. Complies with regulatory guidelines and Labcorp Standard Operating Procedures (SOPs) at all times. Training o Individual is responsible for maintaining his/her complete up-to-date training file and is accountable for correcting and deficiencies found in his/her training file. o Individual is responsible for ensuring he/she is trained, and training is documented prior to performing a task. o Individual successfully completes, as scheduled, competency assessment and ensures competency testing documentation is provided to management for review/retention. o Competently performs department duties as set forth in the department training checklist(s). o May assist in training new employees and follows-up to ensure training is understood. o Attends, as scheduled, department, mandatory and other meetings and training, as required according to training matrices. Work to achieve partnership with both internal customers and external clients by: o Pull data in a timely manner for review by QA and external clients. o Contribute to the provision of accurate verbal or written response to internal QA and client audit findings. Coordinate, where needed, with other resources to resolve issue. o Researches and prepares a response following investigation for quality purposes. Coordinate, where needed, with other resources to resolve issue. o Research and responds in a timely manner to internal customer inquiries regarding status of test results, retrieval of samples for testing/storage and other needs. o Understand department metrics and goals. Demonstrate proficiency in applicable computer systems and software. Adheres to established safety policies and universal precaution guidelines at all times. Maintains a clean, organized and safe work environment. Minimizes biohazard waste. Cleans workstation and materials daily. Takes action for the department when additional responsibilities and opportunities are presented. Provide laboratory management with a report of activities upon request. Other duties as assigned. Education/Qualifications/Certifications and Licenses U. S. Requirements Individual must qualify as testing personnel under the following CLIA 1988 and New York State Department of Health requirements: Bachelors degree in Medical Technology or Clinical Laboratory Science or other life science with completion of at least a 12-month training program in Medical Technology. OR Bachelors degree in a chemical, physical or biological science from an accredited college or university and one year training and/or experience in the specialty in which testing is to be performed. Such training must be equivalent to that received in a school of Medical Technology. OR 90 semester hours from an accredited institution that include the following: 1) 16 semester hours of biology courses, which are pertinent to the medical sciences 2) 16 semester hours of chemistry (at least 6 semester hours of Inorganic Chemistry) 3) 3 semester hours of math Completed an accredited clinical laboratory training program, or six months to one year documented laboratory training or experience in the specialty that testing is to be performed. Preferred Experience Automated chemistry and hematology #LI-AB1 Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us at Labcorp Accessibility. Formore information about how we collect and store your personal data, please see our Privacy Statement. RequiredPreferredJob Industries Other

QUALIFICATIONS Education SCCH Laboratory requires the following qualifications for Medical Laboratory Technician: · Has earned an associate degree in a chemical, physical or biological science or medical laboratory technology from an accredited institution, or 1. Has previously qualified or could have qualified as a technologist under CFR 493.1489, on or before 02/28/1992, and 2. Currently possesses certification or passes a certified registry examination within 6 months from hire date Experience/Skills · One to two years' experience · Typing skills · Possesses basic knowledge of laboratory policies and procedures · Works collaboratively and professionally with co-workers, patients, outside agencies, and physicians · Performs waived, moderate, and high complexity testing and participates in proficiency testing programs · Performs other duties as defined under CLIA 493.1495 of CFR Title 42 of Federal Register Required Licenses/Certifications · CPR Working Conditions · Works in a clean, well-lit environment with good ventilation ROUTINE RESPONSIBILITIES Behavioral Expectations · Consistently complies with established Behavioral Expectations Responsibilities/Technical Skills · Practices courtesy, tact, and diplomacy-essential elements of the job-when in contact with lab customers · Maintains a professional and friendly atmosphere for patients and co-workers · Answers telephone · Faxes · Files and organizes · Sends mail to mailroom daily · Checks equipment temperatures daily, making sure they are in range, and that corrective action is taken if a temperature is out of range · Receives and logs specimens coming into clinical laboratory · Reads and understands requisitions and physicians' orders for laboratory requests · Has knowledge of the correct order of draw · Has knowledge of test requirements such as specimen collection container, specimen collection processing, and specimen storage and transportation · Assembles equipment, such as needles, appropriate containers, etc. according to specified procedures · Adequately performs venipuncture and heel sticks according to procedures · Consistently draws blood competently and expediently with as little patient discomfort as possible · Properly labels all specimens collected · Is responsible for specimen processing, test performance, and reporting results · Performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities · Follows the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results · Documents and reports patient results accurately and in a timely manner · Consults with appropriate lab personnel when test findings are abnormal · Completes duties in a timely and productive manner, responding to workload as necessary · Knows how to prioritize STATs, ASAP, time scheduled test, etc. · Conducts drug screen-Non DOT and DOT-collection and processing · Reports and documents critical value within established time frames · Stocks work area and supplies prior to leaving and throughout the day as needed · Disinfects work area and equipment according to laboratory procedure · Reports to the director when results are unacceptable · Participates in at least 80% of monthly departmental meetings · Other duties as assigned · Demonstrates competency in performing testing in the following areas: o Blood collection (venous and heel stick) o Drug Screen Collection o Hematology o Urinalysis o Coagulation o Blood Banking o Immunology/Serology o Chemistry o Microbiology Quality Control/Quality Assurance · Consistently performs, analyzes, and records quality control data · Identifies problems that may adversely affect test performance or reporting of test results, and o Corrects the problems; or o Immediately notifies the general supervisor, technical supervisor, clinical consultant, or director · Documents all corrective actions taken when test systems deviate from the laboratory's established performance specification · Takes necessary and appropriate corrective action, and documents consistently · Reports NO patient results when quality control values are unacceptable · Participates in quality assurance monitoring programs · Performs necessary quality assurance documentation consistently · When performing high complexity testing adheres to the laboratory's quality control policies, documents all quality control activities, instrument and procedural calibrations, and maintenance performed · Adheres to the laboratory's quality control policies, document all quality controls activities, instrument and procedural calibrations and maintenance performed · Maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens · Follows the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance. · Documents all corrective actions taken when test systems deviate from the laboratory's established performance specification · Other duties as assigned by Director Budget/Cost Containment/Miscellaneous · Conscious of cost containment and complies as feasible · Monitors inventory and orders supplies on a weekly basis · Conducts monthly review of supplies to check for expiration dates · Notifies the Manager when supplies are low and have not been received · Follows the SCCH attendance policy · Utilizes time clock in a professional manner · Clocks out for breaks if leaving the hospital grounds · Works overtime hours only when approved by manager Competency/Education · Documents competency of job performance at 6 months and on an annual basis according to CLIA guidelines · Performs required education in HealthStream · Performs required mandatory education in MediaLab Rotating Shifts 80 hrs/Bi-Weekly

Division:Eskenazi Health Sub-Division: Hospital Schedule: Part Time Shift: Days Eskenazi Health serves as the public hospital division of the Health & Hospital Corporation of Marion County. Physicians provide a comprehensive range of primary and specialty care services at the 333-bed hospital and outpatient facilities both on and off of the Eskenazi Health downtown campus including at a network of Eskenazi Health Center sites located throughout Indianapolis. FLSA Status Non-Exempt Job Role Summary The Medical Technologist Point of Care Testing utilizes laboratory science knowledge, experience and skills to ensure that the point of care tests and the non-laboratory staff performing these tests meet all regulatory requirements. Through quality control/assurance monitoring and instrumentation/methodology troubleshooting, assistance is delivered to other healthcare providers in the diagnosis and treatment of patients as well as in disease monitoring and prevention Essential Functions and Responsibilities * Assists the Point of Care Testing (POCT) Coordinator with quality audits to ensure that Point of Care Tests meet or exceed standards established by all applicable regulatory agencies. * Is a technical resource for nursing and medical staff with identification, evaluation, review and troubleshooting of all Point of Care Testing issues and concerns. * Performs or oversees repairs/maintenance on POCT equipment. * Performs and documents supply inventory, instrumentation calibration, methodology comparisons, reagent validation and maintenance following established procedures and policies. * Serves as a mentor/teacher for others using respectful and effective communication and identifies and solves problems independently. * Functions as a self-starter, arrives to work on time and on scheduled days, begins work promptly and balances multiple priorities simultaneously. * Manages time effectively and efficiently completes work assignments through prioritization and organization. * Is able to represent the Point of Care Testing section in the absence of the POCT Coordinator. * Performs other job duties as assigned (examples include but are not limited to: training students, assisting in method validation and implementation of new test systems Job Requirements * Bachelor's Degree in Medical Technology or related science from an accredited U.S. college or university. Foreign degrees must be officially assessed to determine U.S. equivalency. * Current coursework toward a BS may be considered (must have at least 3 years complete and BS must be obtained within 18 months). ASCP or other certification preferred * 2 years' experience in a clinical laboratory Accredited by The Joint Commission and named as one of Indiana's best employers by Forbes magazine for two consecutive years and the top hospital in the state for community benefit by the Lown Institute, Eskenazi Health's programs have received national recognition while also offering new health care opportunities to the local community. As the sponsoring hospital for Indianapolis Emergency Medical Services, the city's primary EMS provider, Eskenazi Health is also home to the first adult Level I trauma center in Indiana, the only verified adult burn center in Indiana and Sandra Eskenazi Mental Health Center, the first community mental health center in Indiana, just to name a few. Nearest Major Market: Indianapolis

Full-time Description Medical (12 HR Shift) Provides 26 full weekends off (not including vacation). Weekend includes Friday - Sunday off! Provides 182 days off per year (not including vacation) 6:00AM - 6:30PM (Days) 6:00PM - 6:30AM (Evening) Week starts Sunday and ends Saturday 2 Days Work-2 Days Off, 3 Days Work - 2 Days Off, 2 Days Work - 3 Days Off Work every other weekend PURPOSE A Medical Device Packaging Lead is a motivated self-starter who effectively follows PMC's operator instructions to assemble and package products on time while ensuring specifications are met and maintaining the production environment. The associate will complete visual inspections, and other testing as required, to identify non-conformities in parallel with production. A successful Medical Device Packaging Lead must be capable of working with minimal supervision, have a “can do” attitude, possess creative problem-solving skills and be willing to do “whatever it takes” to complete assigned tasks efficiently and effectively. This team member should have excellent interpersonal skills, great attention to detail and be highly organized with the ability to multi task with minimum interruption to work progress. RESPONSIBILITY Responsible for packing of medical devices according to PMC's Standard Operating Procedures (SOP) Responsible for following all established policies, practices and procedures related to all job duties Responsible for following all Good Documentation Practices (GDP), Good Manufacturing Practices (GMP) and PMC policies Prepare work area and keep it safe, clean and organized per PMC standards Verify accuracy of product produced against specification and resolve discrepancies as directed by PMC standards Use manufacturing and quality assurance specifications to determine acceptance on all packaging Train, coach, and mentor team members to ensure proficiency in packing. Packaging and Labeling - Set up and operate the packaging operation with minimum down time and interventions. Perform all cleaning, line clearance, staging, set-up and batch reconciliation activities to support the packaging operations. Participate in the review of Operator Instructions Inspecting labels for quality to the customer's expectations. Perform additional duties as necessary that contribute to the overall efficiency of the company. CORE COMPETENCIES Exhibits objectivity and openness to others' views. Takes personal accountability for contributions to the team and organizational results. Demonstrated accuracy and thoroughness; looks for ways to improve and promote quality. Consistently checks all documents for errors and constantly strives for right the first time mentality. Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. Demonstrate the ability to portray the appropriate level of integrity and professionalism. Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure environment. Results-oriented and efficient. Professional attitude and detail orientation. Ability to troubleshoot minor to immediate issues. Takes initiative to identify issues, troubleshoot, propose solutions, and keep management informed. Requirements EDUCATION, EXPERIENCE AND SPECIAL SKILLS: High school diploma or equivalent; additional education or training in manufacturing or logistics is a plus. Strong leadership skills with the ability to motivate and inspire team members to achieve production goals. Excellent organizational and time management abilities, with a focus on prioritizing tasks and meeting deadlines. Attention to detail and commitment to maintaining high standards of quality and accuracy. Effective communication skills, both verbal and written, for interacting with team members and other departments. Must be able to work in a manufacturing work cell and cleanroom environment Must be able to perform repetitive work for extended periods of time Extended hours, including weekends may be required to support the organizations objectives Must have excellent documentation and organizational skills. Experience with sterile barrier packaging is a plus. Experience working in a clean room is a plus. Experience with single use disposable medical devices is a plus. Experience with seal integrity and seal strength testing is a plus. Must maintain an acceptable level of performance and attendance. Team Member will be placed on a Performance Improvement Plan if they reach 4 points under the Attendance Policy and/or reach a Written level under the Corrective Action steps. QUALIFICATIONS: Maintain OEE above 95% Maintains Scrap rates below standard Quality standards maintained Maintains organized workspace

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. Why join Team Simtra? Because we: Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways. Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health. This role: The Microbiology Quality Lab Associate I performs complex routine and non-routine sampling and processes samples in support of the Microbiology department. This position reports to a Microbiology Supervisor. The responsibilities: Performs testing (bioburden, sterility, growth promotion, etc.) on finished products and in process samples. Performs investigational work in support of out of specification samples, using training and scientific method to identify root cause and corrective actions. Documents and processes samples in a Laboratory environment. Investigates and authors Microbiology investigations. Enter test data into Laboratory Information Management System (LIMS) Participate in continuous improvement activities. Required qualifications: Bachelor's degree required in a science related field, preferably Microbiology. Previous experience working in a GMP regulated environment preferred. Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples JDE, BPLM, Pilgrim, Trackwise, etc.) Physical / safety requirements: Must be able to wear applicable Personal Protective Equipment. Position requires handling of laboratory chemicals. Duties may require overtime work, including nights and weekends Use of hands and fingers to manipulate office equipment is required Position requires sitting or standing for long hours. In return, you'll be eligible for[1]: Day One Benefits Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance Spouse Life Insurance Child Life Insurance Short and Long-Term Disability Insurance 401(k) Retirement Savings Plan with Company Match Time Off Program Paid Holidays Paid Time Off Paid Parental Leave and more Adoption Reimbursement Program Education Assistance Program Employee Assistance Program Community and Volunteer Service Program Additional Benefits Voluntary Insurance Benefits Vision Coverage Accident Critical Illness Hospital Indemnity Insurance Identity Theft Protection Legal and more Onsite Campus Amenities Workout Facility Cafeteria Credit Union [1] Current benefit offerings are in effect through 12/31/24 Disclaimer This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. Equal Employment Opportunity Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: ********************************************************************************

Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? * Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. * Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. * Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always. * Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Laboratory Supervisor As the Laboratory Supervisor you will be responsible for overseeing the facility's laboratory function to ensure that tests are performed accurately, according to regulations and in a timely manner. Essential Functions & Requirements: * Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times * Supervises the laboratory and laboratory personnel to ensure the accurate, compliant, and productive operations of the department * Reviews analytical data to confirm data accuracy and acceptability of material for disposal * Provides oversight of the redirection and testing of off-spec materials * Coordinates additional testing with third-party laboratories or other service providers as needed * Manages the purchases and distribution of departmental operating supplies; ensures adherence to laboratory budget to promote profitability and performs functions to control costs * Provides technical expertise as needed to the Operations and Sales teams; supports Sales by ensuring pre-acceptance testing is completed appropriately * Supports, maintains and troubleshoots various laboratory instruments and equipment * Prepares various reporting as requested by location or organizational leadership * Participates in hiring, performance evaluation, promotion and discipline decisions for team members as needed * Takes on additional duties as assigned to support the team and organization Education: * Bachelor's degree (required); degree in chemistry or science-related field (preferred) Experience: * 3+ years of progressive experience in a laboratory environment (required) Competencies: * Hands-on approach to effectively complete testing, equipment maintenance and training * Strong communication skills to effectively and timely communicate details of questionable or hazardous materials to appropriate authorities, respond to incidents, and train other laboratory personnel * Chemical knowledge including characteristics, reactions and hazards of substances encountered in the hazardous waste industry * Strong computer skills including Microsoft Office Suite applications * Working knowledge of Laboratory Information Management (LIM) systems * Strong time management and multi-tasking skills * Detailed understanding of regulatory requirements and familiarity with industry trends * Ability to effectively troubleshoot and conduct maintenance on laboratory equipment * Regular and predictable attendance to perform the functions and requirements of this role Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. Equal Opportunity Employer - Veterans & Disabilities A post-offer drug screen and background check will be required.

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description Job Summary: Manage equipment maintenance and qualification activities while supporting team development and cross-functional collaboration. Key Responsibilities: Equipment Maintenance & Scheduling: Coordinate preventive and corrective maintenance with schedulers, shops, and lab personnel. Act as technical expert and troubleshoot equipment issues. Qualification & Documentation: Execute and review qualification protocols for new and existing equipment. Document activities in logbooks and electronic systems; ensure timely requalification. Process Improvement: Recommend process enhancements to improve efficiency and streamline operations. Cross-Functional Collaboration: Communicate with internal teams, external vendors, and global quality functions to align on equipment policies and operational goals. Team Leadership: Coach and develop staff, monitor workflow to meet turnaround times (TAT), conduct performance reviews, and manage training and succession planning. Best Practices & Networking: Share and implement best practices across teams related to equipment lifecycle activities. Qualifications Education & Experience: Bachelor's degree in physical sciences (e.g., chemistry, physics) 4+ years of relevant lab experience, including leadership responsibilities. Technical & Analytical Skills: Strong computer, scientific, and organizational skills. Ability to troubleshoot equipment and understand CMMS systems. Leadership & Collaboration: Proven leadership with a focus on team engagement, morale, and retention. Ability to work independently and collaboratively across teams and with external vendors. Communication & Work Style: Excellent written and verbal communication skills. Detail-oriented, self-motivated, adaptable, and able to manage multiple priorities in a fast-paced environment. Proactive and solution-oriented with strong focus on quality and productivity. Compliance & Documentation: Ability to maintain accurate records, follow instructions, and comply with company policies. Additional Information Position is full-time, 8:00 am- 5:00 pm Overtime as needed. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always. Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Laboratory Supervisor As the Laboratory Supervisor you will be responsible for overseeing the facility's laboratory function to ensure that tests are performed accurately, according to regulations and in a timely manner. Essential Functions & Requirements: Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times Supervises the laboratory and laboratory personnel to ensure the accurate, compliant, and productive operations of the department Reviews analytical data to confirm data accuracy and acceptability of material for disposal Provides oversight of the redirection and testing of off-spec materials Coordinates additional testing with third-party laboratories or other service providers as needed Manages the purchases and distribution of departmental operating supplies; ensures adherence to laboratory budget to promote profitability and performs functions to control costs Provides technical expertise as needed to the Operations and Sales teams; supports Sales by ensuring pre-acceptance testing is completed appropriately Supports, maintains and troubleshoots various laboratory instruments and equipment Prepares various reporting as requested by location or organizational leadership Participates in hiring, performance evaluation, promotion and discipline decisions for team members as needed Takes on additional duties as assigned to support the team and organization Education: Bachelor's degree (required); degree in chemistry or science-related field (preferred) Experience: 3+ years of progressive experience in a laboratory environment (required) Competencies: Hands-on approach to effectively complete testing, equipment maintenance and training Strong communication skills to effectively and timely communicate details of questionable or hazardous materials to appropriate authorities, respond to incidents, and train other laboratory personnel Chemical knowledge including characteristics, reactions and hazards of substances encountered in the hazardous waste industry Strong computer skills including Microsoft Office Suite applications Working knowledge of Laboratory Information Management (LIM) systems Strong time management and multi-tasking skills Detailed understanding of regulatory requirements and familiarity with industry trends Ability to effectively troubleshoot and conduct maintenance on laboratory equipment Regular and predictable attendance to perform the functions and requirements of this role Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. Equal Opportunity Employer - Veterans & Disabilities A post-offer drug screen and background check will be required.

Lead Quality at the Heart of Ceramic Innovation Reports to: Director of Operations Founded in 1919, American Art Clay Company (AMACO) is a fourth-generation, family-owned leader in ceramic materials, glazes, kilns, and wheels. Our purpose is simple and powerful: make it easier and safer for people of all ages to create. We believe creativity fuels well-being and strengthens communities, and we operate with a culture of continuous improvement from the factory floor to the executive suite. A day in this role You start your morning in the quality lab, confirming instrument calibration and reviewing overnight SPC charts from production. By mid-morning you're mentoring a technician on a newly validated test method, then walking the line to verify CTQ checks are executed consistently across shifts. After lunch, you lead root-cause analysis on an in-process nonconformance flagged by Supplier Quality, translate attribute criteria into measurable limits, and partner with Production to implement a sustainable fix. You close the day by updating the training matrix, prepping for a Gemba review, and aligning schedules and KPIs with your team. What you will lead Quality lab excellence: Build and sustain a fully capable lab; validate methods, calibrate equipment, standardize data capture, and train staff. Process stabilization: Define baseline parameters, lock in fundamentals, and drive consistency across shifts and departments (formulated lab, mechanical, shipping, and manufacturing). In-process controls: Ensure CTQ specifications are verified using the right methods and tools during inspections. Issue ownership: Lead investigations and corrective actions for in-process issues raised by Supplier Quality; deliver durable countermeasures with Production. Quality system rollout: Implement the Amaco and Brent Quality System; create standardized test protocols (TWI), maintain training matrices, and use data to recommend improvements. Continuous improvement: Conduct audits, facilitate Kaizen and A3 problem solving, and report outcomes during Gemba walks and virtual reviews. Team leadership: Set objectives, handle scheduling and reviews, coach on quality and ceramics fundamentals, resolve employee issues, and coordinate scrap controls, inventory accuracy, and safety audits. How success will be measured Noticeable reductions in in-process defects, scrap, and customer complaints. Consistent application of CTQ specs and prompt resolution of discrepancies. Improved stability and repeatability of key processes across all shifts. What you bring Bachelor's degree in Ceramics, Engineering, Materials Science, Industrial Technology, or equivalent (Associate's plus substantial experience considered). 5-7+ years leading quality teams, preferably with significant lab supervision. Hands-on experience building a Quality System and authoring/standardizing quality standards, including converting attribute criteria into numeric limits. Working knowledge of ceramic chemistry, materials testing, and mechanical processes; proven ability to stand up and stabilize a quality lab. ISO 9001, SPC, and problem-solving (DMAIC, A3, 5-Why); familiarity with Lean and Six Sigma (Green Belt preferred) and Minitab. ERP/QMS exposure (NAV, Business Central or SAP) and strong documentation and communication skills. Proficiency with SOPs, Manufacturing Instructions (MI), Kaizen, and people leadership. Work environment, schedule, and travel Full-time, Monday-Friday, 40+ hours; occasional evenings/weekends as needed. Up to 20% travel. Work may require extended standing, heavy lifting, and time in hot or cold areas. Physical demands Regularly talk and hear; frequently stand, walk, use hands, and reach. Occasionally sit, climb/balance, and stoop, kneel, crouch, or crawl. Frequently lift and/or move up to 50+ pounds. Vision needs include close, distance, color, peripheral, depth perception, and focus adjustment. Legal and equal opportunity Reasonable accommodations may be made to enable individuals with disabilities. EEO Statement: AMACO is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: AMACO is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at AMACO are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the location where we operate. AMACO will not tolerate discrimination or harassment based on any of these characteristics. Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Description Full job description We are searching for a detail-oriented, dependable, full-time Electrical Lab Technician to join our growing team. Our Lab Technician will support our research and development alongside our engineering team. As the lab tech will report to the engineering or program manager. Responsibilities include: Preparing and maintaining lab equipment and workspaces Collecting, recording and analyzing data Comply with safety protocols and standards Managing inventory of lab supplies Maintain a clean and safe work environment Other duties as assigned by Rel-Micro leadership Expected hours: 40 per week - Monday to Friday Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Requirements Qualifications: Must be US Citizen Electrical Engineering Tech Degree or High School Diploma with relevant experience Previous experience desired in Soldering, Bench Testing, SMT, Printed Circuit Board Design Experience in electronics repair Laser Safety Ability to explain problems simply and clearly. Ability to understand verbal and written instructions Experience: Soldering: 1 year (Preferred) PCB Assembly: 1 year (Preferred) lab equipment (power supplies, Oscilloscopes, etc.): 1 year (Preferred) Working with Optics / Photonics Equipment: 1 year (Preferred) Ability to Commute: Crane, IN 47522 (Required) Work Location: In person