Chemist jobs in Greensboro, NC - 56 jobs

Job Description Job Title: Research Scientist Reporting: Director of Innovation Ascent Industries Co. is seeking a Research Scientist to join our Research and Development team. This role will serve as the technical focal point for new custom and contract manufacturing projects and drive successful execution from proof of concept through commercial-scale production. This role will collaborate with cross-functional stakeholders in R&D, Sales, Marketing, Engineering, and Manufacturing to drive commercial success with a focus on speed to solution, commercial-scale viability, deep technical rigor, and a proactive safety mindset. The ideal candidate combines strong technical skills in experiment design, synthesis, process chemistry, commercial-scale unit operations, and scale up within the chemicals or materials industry. This role is expected to serve as the subject matter expert for all analytical testing related to the contract manufacturing projects, implementing customer specified tests and introducing new test methods that are critical for ensuring product quality. Duties and Responsibilities: Serve as the technical focal point for new contract manufacturing opportunities. Identify fastest and most efficient route to commercial scale solutions for new contract manufacturing opportunities based on a deep understanding of process chemistry and plant unit operations. Design experiments based on sound scientific principles and statistical methods to validate technical packages for proof of concept, optimize processes, and develop technical package for manufacturing to support First Time in Spec production. Rapidly produce samples for customer evaluation based on a thorough understanding of plant equipment capabilities and technical requirements Establish R&D lab capabilities for synthesis, process development, sample preparation, and testing by evaluating current capabilities and additional needs to support project pipeline. Demonstrate expertise in a broad array of analytical instruments and drive new method development to align internal test methods and capabilities with customer methods and protocols. Leverage external labs for specialized test capabilities. Collaborate with key stakeholders in Sales, Engineering, Manufacturing, Procurement, and Product stewardship to drive successful commercialization. Engage with customers to gather process details, develop experimental plans, communicate project progress, present key findings, results, and support successful qualifications. Create Standard Operating Procedures and Work Instructions for core lab activities. Assure safe lab operations and compliance with site regulations while ensuring zero recordables. Skills, Qualifications, Experience, Special Physical Requirements: Ph.D. or master's degree in chemistry, Chemical Engineering, or Materials Science and Engineering Proven hands-on product development and industrial scale-up (3+ years) in specialty chemicals or materials industry with subject matter expertise in on or product categories: Surfactants, Emulsions, Dispersions, Specialty Additives, Acrylic Adhesives, and Reactive Blends. Know-how of product requirements for one or more market segments: Oil and Gas Chemicals, Water Treatment Chemicals, Personal Care, Lubricants, and CASE. Strong lab scale synthesis skills, working knowledge of commercial-scale process equipment, and prior experience scaling a product from the laboratory scale through robust commercial scale production. Solid understanding of interplay between raw materials, formulations, manufacturing process variables, product specifications, and product performance. Prior experience with development of detailed technical packages for scale up. In depth analytical and method development experience with techniques such as GPC, GC, HPLC, FTIR, NMR, Rheology, Particle Size, and wet chemistry. Design of Experiments and Six Sigma Green Belt Experience Preferred. Ability to prioritize tasks, manage multiple projects simultaneously, and meet tight deadlines. Strong communication skills both written and verbal. Success Metrics On time execution of R&D work for new contract manufacturing projects per milestones established in NPD process Improve technology transfer from lab to plant with a focus on developing detailed technical packages for achieving target specifications in the first production run. Develop detailed understanding of customer technical protocols for testing and drive quick internal implementation Serve as a technical interface to provide outstanding customer engagement in all technical aspects and help position R&D as our unique value proposition to contract manufacturing customers

Are you an experienced Medical Lab Professional? Are you looking to looking to embark on a new challenge in your career? If so, LabCorp wants to speak with you about exciting opportunities to join our Mass Spectrometry team as an Associate Chemist in Burlington, NC! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at Labcorp: "Improving Health, Improving Lives". **Work schedule: Saturday-Tuesday, 6:00am-4:30pm.** **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. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here (************************************************************** . **Job Duties/ Responsibilities:** + Review and certify LC/MS data from instruments utilizing Analyst and Ascent software + Determine if data is acceptable or not and then upload results + Responsible for the verification of the calibration, quality controls, and patient data up to and including result entry + Maintain, calibrate, and clean instrumentation; perform scheduled/routine maintenance and critical function checks on analytical equipment such as GC, GC-MS, HPLC, and UPLC-MS/MS as well as other chromatographic and laboratory equipment + Diagnose and repair issues occurring in the above listed equipment; recognize significant changes in instrument function; troubleshoot as indicated. + Gains knowledge of department operations and procedures under direct supervision and in an entry level capacity + Conducts qualitative and quantitative analyses on organic and inorganic samples to determine their chemical properties. Participates in development of new analytical procedures + Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures + Demonstrate the ability to make technical decisions regarding testing and problem solving + Evaluate raw and final data for accuracy; recognize and correct errors or unusual results + Provide guidance to technical staff with the analysis and interpretation of final results + Assist with training and orientation of new employees as needed + Perform and document preventive maintenance and quality control procedures + Identify and replenish testing bench supplies as necessary **Requirements:** + Bachelor's degree in chemical or Biological science, Clinical Laboratory science, Medical Technology or meet regulatory (CLIA & State) requirements + Minimum 2 years of clinical laboratory testing experience is required + Experience with Chromatographic Data Review preferred but not required + Demonstrated success in clinical testing technical proficiency and scientific knowledge + Advanced knowledge and understanding of specific laboratory and/or department functions + Ability to exercise judgment to determine methods and procedures on new assignments + Proficient with computers and familiarity with laboratory information systems + High level of attention detail along with strong communication and organizational skills + Ability to work independently and within a team environment + Must be able to pass a standardized color vision screen + Flexibility to work overtime or other shifts depending on business needs **_If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!_** **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 our accessibility site (**************************************************** or contact us at Labcorp Accessibility. (Disability_*****************) For more information about how we collect and store your personal data, please see our Privacy Statement (************************************************* .

About Covanta Environmental Solutions: Covanta Environmental Solutions offers comprehensive industrial material management services to companies seeking solutions to some of todays most complex environmental challenges. With a nationwide network of treatment, recycling and energy-from-waste facilities, Covanta Environmental Solutions enables customers to mitigate risk and reach their sustainability goals. For more information, visit *************** . About Covanta: Covanta is a world leader in providing sustainable waste and energy solutions. Annually, Covanta's modern Energy-from-Waste facilities safely convert approximately 20 million tons of waste from municipalities and businesses into clean, renewable electricity to power one million homes and recycle approximately 500,000 tons of metal. Through a vast network of treatment and recycling facilities, Covanta also provides comprehensive industrial material management services to companies seeking solutions to some of today's most complex environmental challenges. For more information, visit *************** . Information on our facilities is available at ***************/Our-Facilities. For career opportunities, visit ***************/Careers . Covanta is an Equal Opportunity Employer. Job Description At Covanta Environmenatl Solutions(CES), the Field Chemist is responsible for the direction of a specific phase of chemical and / or physical testing activities and to perform related work as required. Working at customers locations (inside / outside) segregating, packing and loading hazardous and non-hazardous waste for transportation and ensure safety processes at all time for each job and lab pack service. Responsible for compliance with all RCRA, state, and federal guidelines. Essential Functions and Responsibilities Certifying that Health and Safety is the number one precedence by complying with all safe work practices, guidelines, procedures and acting in a safe manner at all times. Assists in characterizing materials at field project sites and is capable of doing standard field analytical tests. Responsible for collecting, identifying, segregating and packaging hazardous/non-hazardous waste produced within customer facilities by hazard class, and completing all necessary paperwork per job. Preparing waste drums for pick-up and delivery. Develop good client relations by effectively communicating and educating waste generators and fellow employees. Directs and assists field technicians with waste collection and waste practices. Follows proper placarding and load segregation requirements when transporting hazardous materials. Track waste in 10-day hazardous waste transfer facility. Housekeeping in waste storage area, which includes inspections and quality control. Assisting in preparing shipments to hazardous waste disposal facilities. Capable of sending off samples and understanding analytical reports Maintain at least a Class B CDL with HazMat endorsement Any other duties as assigned by supervisor Qualifications Education: Four year college degree ( Science or Environmental majors preferred ) Experience: 2 + Prior lab packing and environmental waste experience. Competent computer skills, including MS Office. All current certifications / licenses required. Ability to lift 50lbs or more. Highly motivated with strong problem solving and interpersonal skills. Must have knowledge of all RCRA and DOT regulations. Knowledge, Skills and Abilities: Knowledge and understanding of all federal, state, local laws and regulation pertaining to the Environmental Services Industry. Excellent interpersonal skills necessary to effectively communicate with internal and external contacts. Certifications (if applicable): Hazardous Materials Handling Certification for DOT 49 CRF Transportation Regulations Other Requirements: Travel +50% of the time. Additional Information Job ID # 7551 All your information will be kept confidential according to EEO guidelines.

Are you ready to gain new skills to help run and maintain the latest production technology and equipment for the world's biggest brands? We're looking for team-players who know how to take charge of business-related challenges and keep us running smoothly. As a Microbiologist at the P&G Greensboro PHC site, you are responsible to ensure that all assigned testing is completed in a cGMP compliant manner per the required timing. You are also responsible for ensuring the Micro Lab is maintained per the cGMP's and meets all applicable global and national laws and regulations. Responsibilities Include: Completing essential non-testing tasks, including but not limited to the following: Media Preparation Glassware Washing General Housekeeping and Disinfection of Lab Area Finishing all maintenance and calibration on assigned equipment Handling Biohazard Light travel may be required (less than 5%) In order to perform the work described above in our manufacturing atmosphere, plant technicians must: Use basic hand and power tools Lift 50 pounds by bending and stooping Climb, stand, and move around on stairs, ladders and platforms Twist, turn and bend Enter confined spaces Stand on concrete floors for an extended period Micro Analysts must demonstrate skills in manufacturing processes, including operating, maintaining and cleaning automated equipment; maintaining accurate records and data; strong technical, interpersonal and problem-solving skills; and knowledge of computers. Additionally, the safety of Technicians is of great importance to Procter & Gamble. Technicians will be required to wear appropriate safety equipment, such as safety shoes, ear protection, and eye protection. The Greensboro Personal Health Care Procter & Gamble Plant operates 7-days per week. Technicians work any day of the week, including weekends. Work on weekends may be as overtime or as part of the Technician's normal schedule. Changes in business volume and production requirements can cause the plant to occasionally change the length of work shifts or the rotation schedule. The hours of work vary from 8 to 12 hours per day. Shift rotations vary from working two or three rotating shifts. Technicians must be willing to rotate and to work any shift. Overtime may be required. Job Qualifications 1. Minimum Associate's Degree in the Life Science field with 1 year of work experience and/or 2 years of work experience in Microbiology preferred. 2. Knowledge of cGMP's as it relates to Microbiology. 3. USP testing experience preferred. 4. Be willing to work weekends, holidays and overtime, as business needs require. 5. Be willing to rotate shifts in the future as the business grows. What we offer: Responsibilities as of Day 1 _ you will feel the ownership of your project from the beginning, and you will be given specific projects and responsibilities. Continuous mentorship - you will engage with passionate people and receive both formal training as well as day-to-day mentoring from your manager. Work in a dynamic and encouraging environment - working over a diverse array of exciting problems. Promote agility and work/life effectiveness and your long-term well-being. Get a competitive salary and benefits package. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, disability status, age, sexual orientation, gender identity and expression, marital status, citizenship, HIV/AIDS status or any other legally protected factor. Immigration sponsorship is not available for this role. As a general matter, Procter & Gamble does not sponsor candidates for nonimmigrant visas or permanent residency. However, Procter & Gamble may make exceptions on a discretionary basis. Any exceptions would be based on the Company's specific business needs at the time and place of recruitment as well as the particular qualifications of the individual. Procter & Gamble participates in e-verify as required by law. Qualified individuals will not be disadvantaged based on being unemployed Job Schedule Full time Job Number R000142211 Job Segmentation Plant Technicians Starting Pay / Salary Range $29.14 / hour

**Work Schedule** **Rotating schedule from 7pm - 7am** **Job Description** Join the Thermo Fisher Scientific team to contribute to global impact through meaningful work. Support our Mission daily to empower customers in creating a healthier, cleaner, and safer world. **Location/Division Specific Information:** Within the Pharma Services Group (PSG), the High Point, NC location specializes in gelatin-based drug delivery dosage forms (softgels). Our expertise lies in the development and production of various softgel technologies. How Will You Make an Impact? The Formulation Technician II will be responsible for operating an encapsulating machine to produce products from pre-mixed ingredients, ensuring accurate temperatures, machine settings, equipment set-ups, in-process measurements, and quality product. **A Day in the Life:** + Manufacture simple, bulk products + Observe machine operation, adjust as needed, take samples of product, and perform in-process testing + Assist Set-Up person to set up machine, empty basket, clean and prepare machine for changeover, and assist with the actual changeover + Assist with cleanup and other encapsulation duties as needed + Operate inline printing equipment **Education:** High school diploma or equivalent experience required. **Experience:** + At least 1 year of professional experience in a manufacturing, operations, production, or lab environment or a relevant field + Desired: Background in a cGMP setting **Knowledge, Skills, Abilities:** + Excellent verbal and written skills + Ability to interpret data, perform basic calculations, and troubleshoot + Ability to work a 12-hour shift in a 24-hour, 7 day per week operation + Meet DEA security clearance requirements if requested + Must have the flexibility to work additional hours when needed **Physical Requirements / Work Environment:** + Must have the ability to regularly lift, push, pull, or transport items weighing up to 50 pounds + Adherence to all GMP Safety Standards + Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed + Loud noises (equipment/machinery) + Some degree of PPE required (safety glasses, gowning, gloves, lab coat, ear plugs, etc.) + Standing for full shift + Working at heights **What We Offer** Compensation: + Competitive hourly pay rate + Additional shift differential for night shift positions + Annual performance-based bonus + Annual merit performance-based increase Excellent Benefits! + Medical, Dental, & Vision benefits effective Day 1 + Paid Time Off & Designated Paid Holidays + Retirement Savings Plan + Tuition Reimbursement + Employee Referral Bonus + Career Advancement Opportunities Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Job Description Role: Sr. Analytical Chemist Pay Rate Range: $140,000 - $190,000 / yr. DOE Schedule: Monday-Friday, 8:00 AM - 5:00 PM Relocation Assistance: Available Employment Type: Full-Time, Permanent Benefits: Comprehensive benefits package available Are you looking for a growth opportunity for a reputable company with a positive work environment? Our client is looking for a Sr. Analytical Chemist to join their team. Please contact us today to discuss this opportunity! About the Role We are seeking a Senior Analytical Chemist to join our specialty chemicals organization focused on personal care applications (e.g., shampoos, body washes, and surfactant-based formulations). This is a highly technical, hands-on role supporting product development, troubleshooting, and analytical excellence within a collaborative laboratory environment. The position is fully onsite in Salisbury, North Carolina, which is commutable from the Greater Charlotte area and located between Charlotte and Greensboro. Occasional travel to nearby facilities and international collaboration opportunities may be available. Key Responsibilities · Design and execute advanced analytical and wet chemistry methods to support personal care and surfactant-based products · Perform and interpret analyses using chromatography (GC, HPLC) and complementary analytical techniques · Apply expertise across spectroscopy, thermal analysis, mass spectrometry, microscopy, and physical testing · Conduct wet analytical techniques including titrations, solids analysis, salts, and activity testing · Partner with R&D, manufacturing, and quality teams to solve complex formulation and performance challenges · Document methods, results, and technical findings clearly and thoroughly · Contribute to continuous improvement, method development, and best laboratory practices · Serve as a technical resource and mentor within the analytical chemistry team Required Qualifications · PhD in Analytical Chemistry, Organic Chemistry, or a closely related discipline · Strong hands-on experience with chromatography (GC, HPLC) and wet chemistry · Demonstrated expertise in surfactant chemistry and personal care or specialty chemicals · Background in analytical techniques including spectroscopy, thermal, physical, mass spectrometry, and microscopy · Passion for laboratory-based problem solving and applied chemistry Preferred Qualifications · 5-10 years of industry experience in specialty chemicals or personal care o Exceptional recent PhD graduates with strong hands-on experience will be considered · Experience working with consumer or personal care formulations (shampoos, body washes, cleansers) · Stable career progression with demonstrated long-term commitment in prior roles · Educational background from a well-recognized technical institution is a plus Note: This role is not aligned with polymer chemistry-focused backgrounds. Compensation & Benefits · Best in industry compensation and comprehensive benefits package · Relocation assistance provided · Long-term growth and career stability within a technically driven organization Work Environment · Fully onsite laboratory role (no remote or hybrid option) · Collaborative, high-accountability culture focused on technical excellence · Opportunity for domestic and potential international collaboration Why choose Addison? • Pay: We negotiate high salaries using U.S. Bureau of Labor Statistics • Benefits & Bonuses: You are eligible for medical, dental, vision insurance benefits, 401K, and monetary bonuses • Permanent Employment: Many of Addison's job openings lead to potential permanent employment • Connections: You connect directly with hiring managers from renowned organizations • Options: You are presented multiple employment options near your home • Professional Development: You are provided hiring process advice, resume revision, and employment term negotiation Addison Group is an Equal Opportunity Employer. Addison Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Addison Group complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Reasonable accommodation is available for qualified individuals with disabilities, upon request. IND 005-009

Winston-Salem, NC, USA Full-time ** 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. **Job Description** + Applies GMP/GLP in all areas of responsibility, as appropriate + Applies the highest quality standard in all areas of responsibility + Demonstrates and promotes the company vision + Demonstrates strong client service skills, teamwork, and collaboration + Proactively plans and multitasks to maximize productivity + Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration + Regular attendance and punctuality + Applies 17025 compliance standards in all areas of responsibility, as appropriate + Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, GC-MS, ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) + Operates and maintains job-related equipment as required + Performs advanced troubleshooting of laboratory equipment + Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipette verifications) + Performs laboratory tasks as assigned following supervisor direction, SOPs, WI, and other documentation + Assists other staff in the edits and updates of SOPs, WI, and other documentation + Follows all Good Documentation Practices appropriately, including digital platforms + Maintains working areas appropriately (cleaning, disinfecting, etc.) + Possesses strong organizational skills + Provides clear feedback + Keeps accurate records, follows instructions, and complies with company policies + Proactively checks and stays current with all training across multiple learning platforms + Provides instruction/training to new staff + Recognizes errors, identifies root causes, and applies process improvements + Provides analysis support for method validation as needed + Evaluates, reviews, and approves data by other analysts + Independently drafts, edits, and updates SOPs, WI, and other documentation + Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision + Makes recommendations for technical improvements, as needed + Assists in Method Development and executes method validation protocols + Assist in method transfer from the MDV group + Write validation protocols and reports + Communicates effectively with client staff members + Conducts all activities in a safe and efficient manner + Performs other duties as assigned **Qualifications** + Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) + 7+ years of related experience **Additional Information** + Position is full-time, Monday - Friday 8am to 5 pm + Ability to work overtime as required. + Tasks require repetitive motion and standing for long periods of time. + May be required to respond to off-shift operational issues. + Candidates currently living within a commutable distance of **Winston-Salem, NC** are encouraged to apply. + 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** + Authorization to work in the United States indefinitely without restriction or sponsorship **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

TAT Technologies (Greensboro Facility) is part of a multi-site, global aerospace company dedicated to our customer experience of exceeding expectations. We are the leading APU leasing and repair station for key commercial and military aircraft solutions with over 50 years of experience in the industry. We have an ambitious and fast-growing environment that believes in the power of team collaboration with the deep-rooted belief that there is no substitution to personal relationships and interactions. We offer a flexible work environment enabling talented individuals to fulfill their development goals through drive, energy, and passion for the customer. TAT Technologies is looking for qualified LG Analytical Technicians. This is a Monday - Friday, 1st Shift (7:00am - 3:30pm) position. These techs will perform the following duties: Must understand the purpose and scope of each process area, including disassembly, machining, inspection, measurement, paint inspection, and reassembly. Must be familiar with and follow FAA requirements related to inspection and repair. Must be able to read and interpret OEM repair manual instructions. Have an aptitude for detailed mechanical work and methodical trouble-shooting is essential. Is expected to practice exemplary conduct and work ethics at all times. Function as a compatible team is imperative to our overall success, and the Associate must participate with initiative, positive approaches to problem solving/prevention, and commitment to quality. Becomes proficient in precise measurement and use of instruments such as micrometers, dial indicators, etc. Practices safe and appropriate use of repair tools. Learns to write concessions. Learns reassembly techniques. Becomes familiar with manuals. Keeps abreast of relative Service Bulletins. Completes all WO paperwork relative to task. Achieves efficiency and broader understanding of reference materials. Accesses and follows instructions in a timelier manner. Knows and follows FAA/ISO guidelines. Knows and follows safety requirements. Requirements One to two years of mechanical repair experience. Familiarity with aviation industry is advantageous. Ability to interpret and follow repair instructions from OEM manuals. Understanding of FAA regulations helpful. An aptitude for detailed mechanical work and methodical trouble-shooting is essential. Writing skills and accuracy are required for documentation. Ability to safely and properly operate Shop equipment and precise measuring equipment. Benefits Piedmont Aviation Component Services, a subsidiary of TAT Technologies, is dedicated to providing an inclusive, fun, and unique workplace. We believe in acknowledging and appreciating the value of our team members. One way we value our team is by providing a comprehensive and expansive benefits offering to include Major Medical, Dental, Vision, Life, 401K with company matching, STD, LTD, accidental coverages, EAP, and more. Insurance carriers vary based on location. TAT Technologies is dedicated to providing an inclusive, fun, and unique workplace. We believe in acknowledging and appreciating the value of our team members. One way we value our team is by providing a comprehensive and expansive benefits offering to include Major Medical, Dental, Vision, Life, 401K with company matching, STD, LTD, accidental coverages, EAP, and more. Insurance carriers vary based on location. Equal Employment Opportunities - TAT TECHNOLOGIES is committed to maintaining a supportive, healthy, and productive work environment free from discrimination, harassment, or bullying, and complying with all legislative requirements. This includes equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran.

Primary Purpose: Maintain a quality environment through proper cleaning processes that meet the requirements of the contract.. Offices: Dust, Vacuum, Sweep and Mop Floors, Clean Tables and Empty Trash Outside of Building: Remove Trash and Debris Restrooms: Clean, Sanitize, Remove Trash and Restock Breakrooms: Sweep, Mop, Clean Tables and Remove Trash Entrance and Exit Doors: Clean Windows, Sanitize Door Handles, Vacuum Mats, Sweep Around Doors and Clean Thresholds Conference Rooms: Dust, Vacuum, Sweep and Mop Floors, Clean Tables and Empty Trash Lab: Sweep and Mop Floors, Clean Tables and Empty Trash Requirements: Background Check Drug Testing Must be 18 years of age or older Must be able to lift 40 pounds for the entire shift Must be able to stand for the entire shift Must be able to climb stairs during the entire shift Must be capable of bending, pushing, pulling and squatting during the entire shift Must be capable of pushing a manual broom and mop Must be detailed oriented Must have reliable transportation arrangements Must be comfortable working in a commercial setting Must be willing to wear all required PPE during the entire shift Must be willing to follow all safety protocols Benefits: Weekly Pay Insurance Packages Opportunity to Advance Continuous Training One Week of Vacation After One Year Physical Demands and Work Environment Must be able to lift 40 pounds during the entire shift Must be able to stand for the entire shift Must be able to climb stairs during the entire shift Must be capable of bending, pushing, pulling and squatting during the entire shift Must be capable of pushing a manual broom and mop

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Demonstrates and promotes the company vision Demonstrates strong client service skills, teamwork, and collaboration Proactively plans and multitasks to maximize productivity Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Regular attendance and punctuality Applies 17025 compliance standards in all areas of responsibility, as appropriate Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, GC-MS, ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) Operates and maintains job-related equipment as required Performs advanced troubleshooting of laboratory equipment Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipette verifications) Performs laboratory tasks as assigned following supervisor direction, SOPs, WI, and other documentation Assists other staff in the edits and updates of SOPs, WI, and other documentation Follows all Good Documentation Practices appropriately, including digital platforms Maintains working areas appropriately (cleaning, disinfecting, etc.) Possesses strong organizational skills Provides clear feedback Keeps accurate records, follows instructions, and complies with company policies Proactively checks and stays current with all training across multiple learning platforms Provides instruction/training to new staff Recognizes errors, identifies root causes, and applies process improvements Provides analysis support for method validation as needed Evaluates, reviews, and approves data by other analysts Independently drafts, edits, and updates SOPs, WI, and other documentation Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision Makes recommendations for technical improvements, as needed Assists in Method Development and executes method validation protocols Assist in method transfer from the MDV group Write validation protocols and reports Communicates effectively with client staff members Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) 7+ years of related experience Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply. 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 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Demonstrates and promotes the company vision Demonstrates strong client service skills, teamwork, and collaboration Proactively plans and multitasks to maximize productivity Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Regular attendance and punctuality Applies 17025 compliance standards in all areas of responsibility, as appropriate Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, GC-MS, ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) Operates and maintains job-related equipment as required Performs advanced troubleshooting of laboratory equipment Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipette verifications) Performs laboratory tasks as assigned following supervisor direction, SOPs, WI, and other documentation Assists other staff in the edits and updates of SOPs, WI, and other documentation Follows all Good Documentation Practices appropriately, including digital platforms Maintains working areas appropriately (cleaning, disinfecting, etc.) Possesses strong organizational skills Provides clear feedback Keeps accurate records, follows instructions, and complies with company policies Proactively checks and stays current with all training across multiple learning platforms Provides instruction/training to new staff Recognizes errors, identifies root causes, and applies process improvements Provides analysis support for method validation as needed Evaluates, reviews, and approves data by other analysts Independently drafts, edits, and updates SOPs, WI, and other documentation Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision Makes recommendations for technical improvements, as needed Assists in Method Development and executes method validation protocols Assist in method transfer from the MDV group Write validation protocols and reports Communicates effectively with client staff members Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) 7+ years of related experience Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply. 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 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Title: Quality Control ChemistJob Description As a Quality Control Chemist, you will be responsible for performing routine analysis of raw materials, in-process, and finished products. This includes conducting tests such as titrations, FTIR, GC, HPLC, Color, and using a viscometer. Your role involves performing calculations for batch tests in a lab environment using instrumentation and physical test methods. You will follow setup procedures and work instructions for laboratory equipment while adhering to customer and company quality standards. Safety is paramount, so you must follow all safety rules and regulations, including the use of appropriate PPE at all times. Responsibilities + Conduct routine analysis of raw materials, in-process, and finished products. + Perform tests including titrations, FTIR, GC, HPLC, Color, and viscometer. + Carry out calculations for batch tests using lab instrumentation and physical test methods. + Set up and operate laboratory equipment according to established procedures. + Ensure compliance with customer and company quality standards. + Follow all safety rules and regulations, using appropriate PPE at all times. Essential Skills + Minimum 1 year of industry experience in analytical testing, troubleshooting, and quality assurance. + Proficiency in gas chromatography (GC), high-performance liquid chromatography (HPLC), and FTIR. + Strong understanding of quality control processes in chemical manufacturing. Additional Skills & Qualifications + BS in Chemistry or other Sciences preferred; AS in Chemistry is acceptable. + Experience in chemical manufacturing is preferred. + Familiarity with basic laboratory equipment (GC/LC/FTIR) and techniques (titration, liquid-liquid partition). Work Environment You will work independently on the night shifts in the lab, handling chemical products. The lab is equipped with newer equipment to assist with testing. The work schedule is a 12-hour night shift, following a 2/2/3 non-rotating pattern in a 7-day x 24-hour chemical operation, from 7PM to 7AM. The role offers opportunities for cross-training and education in certifications, contributing to employee development and career growth. Job Type & Location This is a Contract to Hire position based out of Greensboro, NC. Pay and Benefits The pay range for this position is $26.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Greensboro,NC. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

AAR Corp. (NYSE: AIR) is a global aerospace and defense aftermarket solutions company that employs more than 6,000 people across over 60 sites in over 20 countries. Headquartered in the Chicago, Illinois area, AAR supports commercial and government customers in more than 100 countries through four operating segments: Parts Supply, Integrated Solutions, Repair and Engineering and Expeditionary Services. AAR's purpose is to empower people to build innovative aerospace solutions today so you can safely reach your destination tomorrow. The company's mission is to go above and beyond to provide value-driven aerospace aftermarket solutions to meet the evolving needs of our customers worldwide. AAR constantly searches for the right thing to do for its customers, employees, partners and for society. **Description:** The Chemical Management Technician I manages and controls chemical product usage and waste through the proper handling, storing, transporting, and disposing of hazardous materials in accordance with local, state, and federal regulations. **What you will** **be responsible for** **:** + Service and collect hazardous waste for compacting from all satellite drums, compact, and transport to chemical storage building. + Service and transport liquid hazardous and non-hazardous waste collection drums and totes and store for disposal. + Service and collect aerosol can collection drums, transport and puncture to remove contents, and recycle cans. + Service and collect universal waste from satellite locations and transport for storage and/or processing. + Service and transport the collection barrels for used oil, speedy dry, and oily rags and store for disposal/recycle. + Assure all hazardous/universal waste is labeled, weighed, and stored according to 40 CFR 262 Subpart C requirements and assure all non-hazardous waste is labeled properly. + Dispose/recycle inspected empty containers per chemical container training and procedural requirements. + Complete remove of international garbage from assigned aircraft per training and procedural requirements. + Complete collection and discharge of O2 generators per training and procedural requirements. + Assist with the loading of hazardous and non-hazardous waste for shipping and escorting onsite collection of waste by vendors and assure manifests are delivered to the Environmental Compliance Technician. + Conduct the cleaning of equipment used to support operational activities. **What you will need to be successful in this role** **:** **Minimum** + Must have successfully completed high school or a GED program. + Must be able to secure and maintain certification as a hazardous material technician in accordance with 40 CFR 265.16 within the **first ninety (90) days of employment** . + Must have a valid driver's license and meet company requirements for insurance coverage for driving a company vehicle. + Must be able to read, write and understand English. + Successfully complete background check for PTIA AOA badging and KC10 badging. + Must have basic typing skills. + Ability to work with confidential data and assure it is safeguarded to protect the integrity of the company. + Must be able to read and understand Material Safety Data Sheets (MSDSs). **Preferred** + Previous chemical handling experience. + Current certification of Hazardous Material Incident Response and RCRA training. **The rewards of your career at AAR go far beyond just your salary** **:** + Competitive salary + Comprehensive benefits package including medical, dental, and vision coverage. + 401(k) retirement plan with company match + Generous paid time off program + Professional development and career advancement opportunities **P** **hysical** **D** **emands** **/W** **ork Environment** **:** The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. + Normal or corrected hearing is required. + Normal or corrected vision is required along with the ability to distinguish color. + Frequent trips to the hangar and full access to the facility arerequired. + Duties requirebending stooping, reaching, stretching, climbing stairs, etc. handling supplies and equipment weighing up to 50 lbs. + A normal range pulmonary functions test is required and physiological determination of the ability to wear a respirator and other safety equipmentas necessary. + Possible exposure to inclement weather. + Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. + While performing the duties of this job, the employee may be regularly required to sit, stand, bend, reach and move about the facility. + The environmental characteristic for this position is an office setting. + Candidates should be able to adapt to a traditional business environment. AAR provides accommodation in accordance with applicable laws through all stages of the hiring process. If you require accommodation for any part of the application and/or hiring process, please advise Human Resources. **Compensation:** The anticipated salary range for this position is $17.66 to $23.84 hourly. This range reflects the base pay for candidates who meet the requirements of the role, including experience, education, and location. AAR offers a competitive benefits package, including medical/dental/vision/life/and AD&D insurance, 401(k) savings plan with employer match, paid time off and holiday pay, as well as opportunities for professional development and growth. **_This company considers candidates without regard to their race, color, religion, sex, sexual orientation, gender identity, and national origin._** **Job Details** **Job Family** **EHS** **Job Function** **Environmental** **Pay Type** **Hourly** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status.

Work Schedule 12 hr shift/nights Environmental Conditions Able to lift 40 lbs. without assistance, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift Work Schedule Rotating schedule from 7pm - 7am Job Description Join the Thermo Fisher Scientific team to contribute to global impact through meaningful work. Support our Mission daily to empower customers in creating a healthier, cleaner, and safer world. Location/Division Specific Information: Within the Pharma Services Group (PSG), the High Point, NC location specializes in gelatin-based drug delivery dosage forms (softgels). Our expertise lies in the development and production of various softgel technologies. How Will You Make an Impact? The Formulation Technician II will be responsible for operating an encapsulating machine to produce products from pre-mixed ingredients, ensuring accurate temperatures, machine settings, equipment set-ups, in-process measurements, and quality product. A Day in the Life: Manufacture simple, bulk products Observe machine operation, adjust as needed, take samples of product, and perform in-process testing Assist Set-Up person to set up machine, empty basket, clean and prepare machine for changeover, and assist with the actual changeover Assist with cleanup and other encapsulation duties as needed Operate inline printing equipment Education: High school diploma or equivalent experience required. Experience: Necessary: At least 1 year of professional experience in a manufacturing, operations, production, or lab environment or a relevant field Desired: Background in a cGMP setting Knowledge, Skills, Abilities: Excellent verbal and written skills Ability to interpret data, perform basic calculations, and troubleshoot Ability to work a 12-hour shift in a 24-hour, 7 day per week operation Meet DEA security clearance requirements if requested Must have the flexibility to work additional hours when needed Physical Requirements / Work Environment: Must have the ability to regularly lift, push, pull, or transport items weighing up to 50 pounds Adherence to all GMP Safety Standards Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed Loud noises (equipment/machinery) Some degree of PPE required (safety glasses, gowning, gloves, lab coat, ear plugs, etc.) Standing for full shift Working at heights What We Offer Compensation: Competitive hourly pay rate Additional shift differential for night shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits! Medical, Dental, & Vision benefits effective Day 1 Paid Time Off & Designated Paid Holidays Retirement Savings Plan Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities

AAR Corp. (NYSE: AIR) is a global aerospace and defense aftermarket solutions company that employs more than 6,000 people across over 60 sites in over 20 countries. Headquartered in the Chicago, Illinois area, AAR supports commercial and government customers in more than 100 countries through four operating segments: Parts Supply, Integrated Solutions, Repair and Engineering and Expeditionary Services. AAR's purpose is to empower people to build innovative aerospace solutions today so you can safely reach your destination tomorrow. The company's mission is to go above and beyond to provide value-driven aerospace aftermarket solutions to meet the evolving needs of our customers worldwide. AAR constantly searches for the right thing to do for its customers, employees, partners and for society. Description: The Chemical Management Technician I manages and controls chemical product usage and waste through the proper handling, storing, transporting, and disposing of hazardous materials in accordance with local, state, and federal regulations. What you will be responsible for: Service and collect hazardous waste for compacting from all satellite drums, compact, and transport to chemical storage building. Service and transport liquid hazardous and non-hazardous waste collection drums and totes and store for disposal. Service and collect aerosol can collection drums, transport and puncture to remove contents, and recycle cans. Service and collect universal waste from satellite locations and transport for storage and/or processing. Service and transport the collection barrels for used oil, speedy dry, and oily rags and store for disposal/recycle. Assure all hazardous/universal waste is labeled, weighed, and stored according to 40 CFR 262 Subpart C requirements and assure all non-hazardous waste is labeled properly. Dispose/recycle inspected empty containers per chemical container training and procedural requirements. Complete remove of international garbage from assigned aircraft per training and procedural requirements. Complete collection and discharge of O2 generators per training and procedural requirements. Assist with the loading of hazardous and non-hazardous waste for shipping and escorting onsite collection of waste by vendors and assure manifests are delivered to the Environmental Compliance Technician. Conduct the cleaning of equipment used to support operational activities. What you will need to be successful in this role: Minimum Must have successfully completed high school or a GED program. Must be able to secure and maintain certification as a hazardous material technician in accordance with 40 CFR 265.16 within the first ninety (90) days of employment. Must have a valid driver's license and meet company requirements for insurance coverage for driving a company vehicle. Must be able to read, write and understand English. Successfully complete background check for PTIA AOA badging and KC10 badging. Must have basic typing skills. Ability to work with confidential data and assure it is safeguarded to protect the integrity of the company. Must be able to read and understand Material Safety Data Sheets (MSDSs). Preferred Previous chemical handling experience. Current certification of Hazardous Material Incident Response and RCRA training. The rewards of your career at AAR go far beyond just your salary: Competitive salary Comprehensive benefits package including medical, dental, and vision coverage. 401(k) retirement plan with company match Generous paid time off program Professional development and career advancement opportunities Physical Demands/Work Environment: The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Normal or corrected hearing is required. Normal or corrected vision is required along with the ability to distinguish color. Frequent trips to the hangar and full access to the facility are required. Duties require bending stooping, reaching, stretching, climbing stairs, etc. handling supplies and equipment weighing up to 50 lbs. A normal range pulmonary functions test is required and physiological determination of the ability to wear a respirator and other safety equipment as necessary. Possible exposure to inclement weather. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee may be regularly required to sit, stand, bend, reach and move about the facility. The environmental characteristic for this position is an office setting. Candidates should be able to adapt to a traditional business environment. AAR provides accommodation in accordance with applicable laws through all stages of the hiring process. If you require accommodation for any part of the application and/or hiring process, please advise Human Resources. Compensation: The anticipated salary range for this position is $17.66 to $23.84 hourly. This range reflects the base pay for candidates who meet the requirements of the role, including experience, education, and location. AAR offers a competitive benefits package, including medical/dental/vision/life/and AD&D insurance, 401(k) savings plan with employer match, paid time off and holiday pay, as well as opportunities for professional development and growth. This company considers candidates without regard to their race, color, religion, sex, sexual orientation, gender identity, and national origin.

**Quality Control Analyst III (Full-Time, Contract)** **Department: Quality Control** **Reports To: QC Manager, Analytical** **2 positions** **Hourly Pay Rate: $35-$45** **Schedule: Sun-Thu 8:30a-5p shift and Tue-Sat 8:30a-5p** **Position Summary** The Quality Control Analyst is responsible for performing a variety of analytical and bioanalytical tests to support Quality Control operations. This role includes testing of raw materials, in-process samples, stability samples, and final product. The analyst will maintain accurate data, support investigations, ensure compliance with cGMP/GxP requirements, and contribute to continuous improvement within the QC laboratory. _This is a contract position and does not include company-sponsored benefits._ **Key Responsibilities** + Perform routine bioanalytical testing and support release of in-process, stability, and final product samples. + Conduct routine and non-routine analyses on raw materials, in-process items, and finished products using established procedures, including: + Flow cytometry + ELISA + Kinetic assays + Cell counting/viability + Visual inspections + Initiate and support deviation and OOS investigations within electronic quality systems. + Support completion of action items and AQEM activities in the quality system. + Follow test methods, SOPs, work instructions, and protocols accurately. + Author or revise test methods, SOPs, work instructions, forms, and protocols as needed. + Assist with sample receipt and coordination with manufacturing. + Train and mentor incoming QC Analysts across all levels. + Track and trend QC testing performance, including patient lot data and critical reagent monitoring. + Maintain lab inventory and coordinate material requests with warehouse/supply chain teams. + Participate in change control activities and document assay failures or invalidations. + Ensure all documentation is completed accurately and on time. + Support special projects related to analytical method development or instrumentation troubleshooting. + Perform additional duties as assigned. **Minimum Qualifications** + Bachelor's degree in chemistry, biochemistry, microbiology, or related scientific field. + 3-5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacturing, or medical device industry. + Strong understanding of cGMP, GxP, and FDA regulations. + Familiarity with bioassays and raw material testing methods. + Experience with LIMS or other electronic quality/data systems. + Experience with deviation handling, change control, and OOS investigations. + Subject matter expertise in relevant analytical assays. + Strong communication skills and ability to work cross-functionally. + Excellent attention to detail, problem-solving skills, and decision-making ability. As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

The Quality Control Analyst position involves performing various testing activities to support the Quality Control department, including bio-analytical testing, raw material testing, and protocol testing. The role requires maintaining quality systems and data generated by team members, contributing to investigations, and ensuring compliance with industry standards Responsibilities: Performs routine Bioanalytical testing and release of in-process, stability and REACT Final Product samples as scheduled Executes routine and non-routine analysis, including but not limited to raw materials, in-process items and finished product according to established operating procedures; may include: Flow Cytometry ELISA Kinetic Assays Cell Counting/Viability Visual Appearance Initiates and Supports Deviation/OOS investigations in MasterControl Initiates and Supports Action Item completion as assigned in MasterControl Initiates and Supports AQEM activities as assigned in Master Control Follows Test Methods (TSMs) Standard Operating Procedures (SOPs), Work Instructions (WRKs), and Protocols Authors originals, revisions, and training on TSMs, SOPs, WRKs, Test Forms, and Protocols Support QC Analytics with sample receipt from Manufacturing Trains and mentors incoming QC Analysts (all levels) Track and trend all QC Analytical testing performance of patient lot data along with critical reagent trending Maintain inventory levels in QC labs and coordinate material requests with Warehouse/Supply Chain Initiates, and participates in Change Control (MOC) management Authors/Initiates Aborted/Invalidated Assays in the QC Analytical Lab. Complete documentation accurately and in a timely manner Partakes in special projects on analytical methods and instrumentation problems related to execution of assays. Other duties as assigned Minimum Qualifications: Minimum of Bachelor's Degree (or better) in chemistry, biochemistry, microbiology or related science 3-5 years' experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry Knowledge of cGMP and understanding of GxP, good clinical practices, and FDA guidelines Familiarity with bioassays, and raw material test methods Knowledge of LIMS systems Deviation Handling Change Control Management OOS Investigation experience Subject Matter Expertise in assays relevant to the QC Labs Strong communication skills with the ability to interact with various individuals Detail-oriented with problem-solving and decision-making abilities ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

Job Description Essent Group Ltd. (NYSE: ESNT) is a Bermuda-based holding company (collectively with its subsidiaries, "Essent") which serves the housing finance industry by offering private mortgage insurance, reinsurance, risk management products and title insurance and settlement services to mortgage lenders, borrowers, and investors to support homeownership. We are focused on managing risk and dedicated to serving as a strong and fair counterparty. As a company, we bring strong private capital and a commitment to risk management to the mortgage insurance industry. Title: Quality Assurance Analyst Location: Radnor, PA or Winston Salem, NC (fully on-site) This is an individual contributor position which works under regular supervision and is responsible for completing Quality Assurance Reviews. As a dynamic and resourceful professional, we will rely on you to perform the following duties: Complete quality assurance files reviews for certified loans underwritten under Delegated or Non-Delegated authority. This entails completing a re-underwrite of the loan file for acceptable risk based on published guidelines/credit policy, and a review of completed re-verifications. Complete re-verifications of occupancy, employment/income, and funds for loan closing as required and make referrals to the Special Investigations Unit (SIU) as appropriate. Maintain a strong knowledge of Agency, USPAP and Essent guidelines/eligibility requirements. Complete second level reviews on loans cited with any level of defect by the third-party vendor. Participate in system testing and enhancement requirements as part of a coordinated corporate effort. Perform other duties as assigned by management. Minimum Education & Experience Requirements: High School Diploma/GED; bachelor's in business administration or related field is preferred. Mortgage insurance experience is preferred. Seven (7) years or more of experience in the mortgage banking industry with specific mortgage insurance industry experience desired Practical experience in Conventional mortgage underwriting and/or quality assurance required. Ability to travel as needed. Knowledge of all Agency underwriting guidelines. Proficient in Microsoft applications such as Word and Excel. Strong appraisal review skills and knowledge of USPAP requirements. Outstanding oral and written communication skills. Self-motivated and detail oriented. Excellent organizational, technical and customer service skills. Ability to present difficult responses/findings in a consultative manner while preserving client relationships. Our commitment to your success is enhanced by our competitive salary and comprehensive benefits package including paid time off, medical, dental, vision, 401(k) and disability benefits. We work to maintain a positive environment for our employees, where people can learn and grow with the company. Essent is an Equal Opportunity Employer.

New job opportunity we have available in High Point. Below are the details: Product Quality Technician Shift: 7:00 PM - 7:00 AM (12-hour night shift) Pay Rate: $15.00/hour Collecting samples Performing various product checks to ensure accuracy and quality No lifting involved #LIND26