Quality control analyst jobs in Lynchburg, VA - 687 jobs

The R&D Lab Technician is a key contributor to daily laboratory operations and sensory testing activities. This role supports panel training, test execution, and the maintenance of lab spaces and materials. The position ensures accurate, high-quality sensory evaluations that guide product development and quality assurance. Key Responsibilities: Analytical Testing: Conduct analytical tests and prepare detailed reports for all sensory evaluations and projects. Lab Maintenance: Maintain a safe, clean, and organized environment in the R&D kitchen, laboratory, and sensory rooms. Testing Management: Coordinate and oversee sensory testing for all projects, including scheduling and reporting results. Training Leadership: Deliver sensory and shelf-life training sessions for R&D, Quality, and Operations teams throughout the year. Technology Oversight: Manage and maintain sensory software and hardware to ensure smooth testing processes. Supply Management: Monitor and maintain inventory of kitchen and sensory supplies, finished products, and benchtop ingredients. Recipe for Success: Experience: R/D, in process, finished products, analytical testing, HPLC/GC preferred Technical Skills: Proficiency in Microsoft Office applications (Excel, Word, Outlook). Math Skills: Comfortable with basic math, including percentages and conversions. Organizational Skills: Strong planning and organizational abilities; detail-oriented with a service-focused mindset. Initiative: Ability to work independently and proactively. Education: Bachelor's degree in a related field.

Job Title: QC Environmental Monitoring Technician Department: Quality Control The QC Environmental Monitoring Technician is responsible for supporting parenteral manufacturing operations through routine environmental monitoring of classified manufacturing areas, as well as conducting clean utility sampling and analysis within both manufacturing and QC laboratory facilities. This role plays a critical part in ensuring compliance with cGMP requirements and maintaining a controlled manufacturing environment to support the production of safe and effective pharmaceutical products. Key Responsibilities: Adhere to and promote compliance with all cGMP procedures, Quality Systems, and Good Documentation Practices (GDP). Perform routine environmental monitoring of classified manufacturing areas to support both standard operations and Environmental Monitoring Performance Qualification (EMPQ) activities. Conduct clean utility sampling and analysis, including but not limited to: Compressed air Potable water Purified water Water for Injection (WFI) Clean steam Support manufacturing and laboratory activities by providing timely and accurate environmental monitoring data. Enumerate, review, and document sampling results in LIMS or other laboratory data systems. Perform Second Person Verification (SPV) of environmental monitoring results on a routine basis. Participate in continuous improvement projects and quality initiatives. Assist with authoring and updating Standard Operating Procedures (SOPs) and Work Instructions as required. Adhere to and promote compliance with all site safety standards. Minimum Requirements: High School Diploma or equivalent required; Associate degree preferred. 2+ years of experience performing Environmental Monitoring in a GMP pharmaceutical manufacturing environment, preferably supporting aseptic or parenteral production. Demonstrated experience with environmental monitoring techniques, including: Viable surface monitoring Viable air monitoring Non-viable air monitoring Compressed air sampling Water and clean utility sampling and analysis Experience with laboratory systems such as LIMS, LES, and/or MODA. Preferred Qualifications: Strong understanding of cGMP requirements and regulatory compliance. Experience performing environmental monitoring within filling isolators or restricted access barrier systems (RABS). Ability to train and mentor junior Environmental Monitoring Technicians. Strong verbal and written communication skills. Ability to work effectively with cross-functional teams. Physical & Work Environment Requirements: Ability to work in laboratory and cleanroom environments while wearing appropriate PPE. Ability to gown into facility-dedicated cleanroom attire as required. Ability to stand or walk for extended periods and perform repetitive tasks. Ability to lift, push, pull, and carry up to 30 pounds. Work Schedule & Travel: Ability to work 12-hour shifts. Flexibility to work day or night shifts as required, especially during training and startup phases. Role may initially support project/startup activities and transition into a routine operational support role.

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

This role contains the following responsibilities covering 2nd shift hours (2:00 pm through 10:30 pm), Monday through Friday: The Senior QC Analyst (2nd Shift) will be trained to execute analytical test methods and their corresponding analytical techniques. The core function is composed of completing QC testing for in-process, characterization, release, or stability samples. Additionally, when need arises, Senior QC Analyst will assist with troubleshooting and support In-process Support Associates with STAT samples during 2nd shift. Responsibilities include: In-process, characterization, stability, and/or release testing as assigned. Capabilities include (but not limited to) HPLC, ELISA, qPCR, SoloVPE, other spectrophotometric techniques, capillary electrophoretic techniques, and compendial testing per USP with near-zero error and minimal guidance or direction Execution of method transfer, method qualification, and/or method validation testing performed under protocol Solution preparation Organizes and processes samples according to GxP standards Independent analysis and collation of data to draw conclusions Enter data into control charts and LIMS, if applicable Supports lab investigation and deviation reports Supports implementation of Corrective and Preventive Actions Revises SOPs and technical documents Supports team to troubleshoot testing or project challenges with comfort in presenting and communicating data Tracks department metrics upon request; actively engages in improvement of department metrics Partakes in continuous improvement projects or leading simple improvement projects Ensures state of safety and regulatory audit readiness at all times Maintains work to current Good Manufacturing Practices (cGMP) Ensures Trainer qualification status to expand team matrix Laboratory support - ensures areas are neat, clean, organized, and equipment is functioning Participates in data review activities Duties may include support in STAT testing coordination It is the expectation that this position is required to be onsite full time with a minimum of 75% of time in the laboratory/facility Minimum Requirements: Relevant degree and 4-8 years' biopharmaceutical industry experience, preferably in protein analytics Salary: $63,000-$86,900 KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Requirements Complete ride out edits Understanding of FTTH plant design Quality control Inspection and contractor compliance Reconciliation of close out packages Cost control for the client and Conexon Understanding of NESC standards Production verification and invoice reconciliation with production Assist in promotion and sales of Conexon services Participation in weekly client conference calls Evaluate and advise on FTTH construction techniques Weekly status reporting General computer skills Standard Company Benefits Include: Three (3) weeks of paid time off Comprehensive benefits package, including health, dental, and vision coverage Life insurance Short-term and long-term disability insurance Retirement benefits

Work Schedule 12 hr shift/nights Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Will work with hazardous/toxic materials Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: Greenville, NC/DPD How Will You Make an Impact?: As a Formulation Technician II, you will play a vital role in producing sterile injectables and working on moderate-scale problems that require analysis and critical thinking. You will follow written and verbal instructions to ensure that pharmaceutical products are manufactured in accordance with industry guidelines and regulations. Night and day full time shifts available. Shift hours are 6pm-6am or 6am-6pm on a 2-2-3 rotating schedule. A Day in the Life: Ensure pharmaceutical products are manufactured in strict accordance with area SOPs and current cGMP. Verify and document production activities in batch records, logbooks, and controlled forms. Complete tasks vital to manufacturing drug products in an aseptic filling area, including cleaning cGMP areas, performing line changeovers, parts preparation, filter integrity testing, operating parts washers and autoclaves, performing tray loading and unloading, operating the filling isolator, and general material handling. Troubleshoot equipment alarms. Education: High school diploma or equivalent required. Experience: Required: Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field Preferred: Experience in a cGMP environment Knowledge, Skills, Abilities: Ability to excel in a team environment, follow standard operating procedures, and perform repetitive work duties Basic math skills. Good verbal/written communication. Attention to detail while maintaining a quality product. Physical Requirements / Work Environment Work in a clean-room environment with controlled temperature, humidity, and low ambient noise. Wear appropriate gowning and personal protective equipment. Infrequently lift and manipulate up to 50 pounds unassisted. Stand and move about, including reaching, bending, stooping, grasping. Use hand tools and equipment. What We Offer: Compensation Competitive Pay Performance Related Bonus where eligible Annual merit performance-based increase Excellent Benefits Medical benefits Paid Time Off/Annual Leave Employee Referral Bonus Career Advancement Opportunities

Come join our family! Microbac Laboratories is an essential business offering competitive pay and benefits including medical, dental, vision, life insurance, disability, generous paid time off including vacation, holidays and flex-time, a wellness program, referral bonus, tuition reimbursement and more! Whether you are just starting your career in science or looking to further it, Microbac will put you on the path of an exciting career with room to grow. Quality, safety, giving back to our communities, diversity and inclusion, customer success and employee wellbeing are part of our core culture. We are looking for motivated individuals to join our family as a Microbiology Analyst II. ABOUT MICROBAC Microbac serves our clients with the utmost expertise and respect for their market requirements, constraints and challenges. We embody a company-wide commitment to exceptional customer experience, which has been refined over nearly 50 years of trusted, analytical and measurement experience. Through our network of laboratories, offices, and field services, we have the flexibility to meet the unique requirements for each client, project and scope. As a privately held third-party testing company, Microbac operates with a commitment to safety, quality and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and life science markets. JOB SUMMARY We are currently seeking a full-time Microbiology Analyst II, working in an accredited commercial laboratory, responsible for performing microbiological testing, data analysis, and documentation to ensure product quality and regulatory compliance. This role involves operating specialized lab equipment, supporting method development, and supervising junior staff. The analyst also collaborates with Quality Assurance, contributes to investigations and audits, and helps maintain a high standard of laboratory accuracy, safety, and efficiency. ESSENTIAL FUNCTIONS: Operate, calibrate, and maintain specialized laboratory instrumentation for microbiological testing, such as incubators, autoclaves, microscopes, and particle counters. Prepare media, reagents, and samples for analysis following SOPs (Standard Operating Procedures). Ensure proper aseptic techniques to prevent contamination. Identify microorganisms using traditional and/or rapid methods (e.g., Gram staining, biochemical tests, MALDI-ToF). Maintain microbial culture collections and growth promotion. Monitor sample workflows and proactively address backlogs to ensure timely completion of testing. Manage laboratory supplies and support procurement activities for relevant departments. Perform advanced microbiological testing on raw materials, finished products, and environmental samples. Accurately record detailed observations, analyze data, interpret test results, and maintain documentation in lab notebooks and LIMS. Assist in the development, validation, and implementation of new test methods and procedures. Investigate anomalies or inconsistencies in analytical data and implement corrective actions. Explore and evaluate new technologies or methodologies to enhance laboratory capabilities. Prepare and review Certificates of Analysis (CoAs) and other technical documentation. Ensure all documentation complies with internal SOPs and external regulatory standards. Adhere to and enforce Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant quality standards as well as relevant guidelines, such as FDA, USP. Participate in quality investigations (e.g., OOS, deviations) and support root cause analysis and CCP development. Collaborate with the Quality Assurance team to review, revise, and maintain SOPs. Support internal and external audits by ensuring laboratory readiness and documentation accuracy. Provide day-to-day supervision, mentorship, and training to laboratory technicians and junior analysts on equipment usage, testing protocols, and laboratory practices. Assign and oversee daily testing activities to ensure efficient and compliant lab operations. Review and approve analytical results and reports, including peer review of data generated by junior staff to ensure accuracy and compliance. Support ongoing staff training and contribute to performance evaluations and development planning. Other duties as assigned MINIMUM REQUIREMENTS: Bachelor's degree from a four-year accredited institution in a related field of applied science; plus, five or more years of related experience; or six plus years of related laboratory experience with no degree Strong understanding of principles, terminology, practices, techniques and instrumentation commonly used in a laboratory setting Ability to interpret data, record observations, prepare reports, and perform peer review Ability to effectively prioritize work and manage time to meet deadlines and rush orders Computer literacy Ability to work with delicate laboratory equipment Ability to communicate effectively in both written and verbal formats Ability to understand and adhere to established SOPs PREFERRED QUALIFICATIONS: A general understanding of terms and concepts typically used throughout the industry is preferred WORKING CONDITIONS AND PHYSICAL REQUIREMENTS: The physical demands and working conditions described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Requirements: While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel objects, tools; talk or hear. The employee is occasionally required to stand, walk, and sit. The employee must regularly lift and/or move up to 25 pounds. Specific vision abilities required by this job include color vision and depth perception. Working Conditions: While performing the duties of this job, the employee will be in a general office environment. The noise level in the work environment is usually moderate. This job may require travel less than 20% As a privately held third-party testing company, Microbac operates with a commitment to safety, quality and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and life science markets. OTHER: This is not an exhaustive list of all duties an employee may be required to perform. Microbac reserves the right to revise the job description at any time. Employment is at-will. Microbac, promotes a drug-free, alcohol-free workplace. Applicants considered for hire must pass a drug test before beginning work. Refusal to submit to testing will result in disqualification of further employment consideration. Microbac is an Equal Opportunity Employer - We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. All qualified applicants will receive consideration for employment.

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our lab location in Chester, VA is hiring a full-time Food Laboratory Technician. (40 hours/week plus benefits included). We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option along with profit sharing. Check out our website to learn more about what we do at ******************* Compensation : Starting hourly rates $21 - $22.50 D.O.E. plus a competitive benefits package. Shift Available: Wednesday - Saturday 11:30am - 9pm Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of microbiology and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly.All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences.SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our lab location in Chester, VA is hiring a full-time Food Laboratory Technician. (40 hours/week plus benefits included). We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option along with profit sharing. Check out our website to learn more about what we do at ******************* Compensation : Starting hourly rates $21 - $22.50 D.O.E. plus a competitive benefits package. Shift Available: Wednesday - Saturday 11:30am - 9pm Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of microbiology and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly.All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences.SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

Cornerstone Building Brands is a leading manufacturer of exterior building products for residential and low-rise non-residential buildings in North America. Headquartered in Cary, N.C., we serve residential and commercial customers across the new construction and Repair & Remodel (R&R) markets. Our market-leading portfolio of products spans vinyl windows, vinyl siding, stone veneer, metal roofing, metal wall systems and metal accessories. Cornerstone Building Brands' broad, multi-channel distribution platform and expansive national footprint includes more than 18,800 team members at manufacturing, distribution and office locations throughout North America. Corporate stewardship and Environmental, Social and Governance (ESG) responsibility are embedded in our culture. We are committed to contributing positively to the communities where we live, work and play. For more information, visit us at cornerstonebuildingbrands.com . Job Description JOB DETAILS Base Pay Rate: Starting at $17 per hour DUTIES AND RESPONSIBILITIES Work safely and efficiently in a quality assurance production environment. A trainee will be required to learn and perform various quality tasks related to the inspection of profiles with direct guidance and assistance from the senior quality team to ensure product compliance with established manufacturing standards. Inspect and document in-process vinyl products Communicate and provide samples to initiate corrective action for non-conforming material Quarantine and re-inspect material when an issue is identified Introduce and record inventory of finished products Document scrap/downtime, revise scheduling board as run cycles are completed Maintain Quality area of responsibility for efficient workflow Support/assist quality staff as needed Pull, file and make copies of quality audit sheets Support production floor with various tasks: material handling, general housekeeping, etc Basic knowledge and use measurement devices: calipers, tape measure, impact testers, spectrometer, PLV and the tools required for sample collection Basic knowledge of Data Color Tools, Excel, Word, and Image Tools Manufacturing plant environment. Exposed to routine industrial hazards/safety hazards that require PPE Walks/stands for 12 hours, frequently carries 0 - 10 lbs. occasionally carries 10-20 lbs. Must use hands frequently for grasping and fine manipulation Position requires agility and mobility performing such activities as stooping, kneeling, crouching, standing, walking, pushing, pulling, and lifting Must be able to work in a hot environment The principal responsibilities and duties are intended to describe the functions that are essential to the performance of the job In addition, employees holding this position will be required to perform other job-related duties as requested by supervisor/management/senior quality staff Qualifications Ability to lift to 50 pounds on a continual basis above shoulder height and below the waist Perform function checks throughout the day to insure we are meeting standards Additional Information Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play. Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. All your information will be kept confidential according to EEO guidelines Why work for Cornerstone Building Brands? Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play . Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. *Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement. Cornerstone Building Brands is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster here . You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here . If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or [email protected] . If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or [email protected] . This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. All your information will be kept confidential according to EEO guidelines. California Consumer Privacy Act (CCPA) of 2018 Must be at least 18 years of age to apply. Notice of Recruitment Fraud We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description The CQ Lab Analyst I, will perform basic analysis for raw materials, incoming materials, in process and/or finished products in a safe, compliant, and efficient manner. The Job responsibilities include performing visual, dimensional, and physical testing in support of commodity, wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. • Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified. • Follows procedures at all times, adopting cGMP, cGDP practices. • Follows supervisor directions at all times. • Able to function independently, but asks questions as necessary • Accepts dynamic work sequences • Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed • Consistently communicates work sequence status to supervisor in a timely manner. • Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement. • Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals. • When faced with roadblocks and issues, routinely offers suggestions for improvements • Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift wherever possible. • Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter • For Incoming Material CQ lab analyst, has understanding of Assurance Quality Limit (AQL) and sampling procedures and tables for inspection by attributes (ANSI/ASQ Z1.4). Qualifications Bachelors or Masters Additional Information Sneha Shrivastava Sr Technical Recruiter 862 - 579 - 4236

Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. Your Work Matters. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today! Job Overview The Scientist 2 - Quality Control role performs routine analytical testing on raw materials, intermediate, and final products as well as in-process testing; performs data entry; draft deviations, and participates in OOS investigations for their testing. Ensures compliance with applicable Company SOPs and regulatory guidance's. This role will support our pilot plant and other work needed on the weekends. 3 days (12 hour shifts) - 36 hour weekly role with full benefits and shift differential pay on top of full time salary. Responsibilities Perform routine testing of raw materials, intermediate, and final products (may include stability) Provide support to the plant by performing in-process testing and analyzing cleaning samples. Maintain laboratory notebook. Ensure equipment is left in good working order after use. Perform laboratory upkeep (wash glassware, reorder supplies, check for expired chemicals). Draft their deviations. Be an active participant in their laboratory investigations. Qualifications/Skills Analytical Chemistry Knowledge: Some understanding of the principles of Analytical Chemistry or Quality Control Cross Discipline Knowledge: Early practical industry exposure to cross functional technical departments, including organic chemistry GMP/Regulatory Knowledge: With less manager supervision, able to better understand need for SOPs and basic regulatory guidance Instrumentation: Basic understanding of key analytical R&D equipment, can operate independently once instructed Communication: Good oral and written communication skills Problem Solving: May be asked to support peer-led laboratory investigation process with manager support Time Management: Ability to handle key assignments, with supervision Leadership: Shares ideas with peers Technical Documentation and Review: Ability to keep a good laboratory notebook and perform data entry, compliance with GDP External Influence: Ability to work within a matrix team Industry Credibility and Rapport: Willing to learn and grow within the local Cambrex Team Operational Excellence: Strives to engage in group/team improvement projects Change Orientation: Able to understand the importance of Cambrex initiatives Education, Experience & Licensing Requirements M. S. in Chemistry or related field or B. S. degree in Chemistry or related field with 2 years minimum experience, or Technical Degree with 4 years minimum experience, or High School Degree with 6 years minimum experience. Experience with and fundamental understanding of several of the following analytical technologies (* - most important): HPLC* FTIR* Titration Basic wet chemistry* NMR XRPD cKF Working knowledge of other analytical equipment common to the pharmaceutical industry This position works with and handles hazardous materials and wastes at Cambrex. This person has the appropriate qualifications to read, understand, apply and communicate written and verbal information regarding handling and managing hazardous wastes. He/She is also responsible for recognizing emergency situations concerning hazardous materials and wastes. All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law. #LI-RD1M. S. in Chemistry or related field or B. S. degree in Chemistry or related field with 2 years minimum experience, or Technical Degree with 4 years minimum experience, or High School Degree with 6 years minimum experience. Experience with and fundamental understanding of several of the following analytical technologies (* - most important): HPLC* FTIR* Titration Basic wet chemistry* NMR XRPD cKF Working knowledge of other analytical equipment common to the pharmaceutical industry Perform routine testing of raw materials, intermediate, and final products (may include stability) Provide support to the plant by performing in-process testing and analyzing cleaning samples. Maintain laboratory notebook. Ensure equipment is left in good working order after use. Perform laboratory upkeep (wash glassware, reorder supplies, check for expired chemicals). Draft their deviations. Be an active participant in their laboratory investigations.

No Visa Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. The Senior Microbiologist is a critical technical resource in the QC Microbiology laboratory supporting the manufacturing of sterile injectable products. This position is responsible for independently performing and overseeing complex microbiological testing and environmental monitoring (EM) in compliance with cGMP, USP, FDA, and internal quality standards. This position is in a fast-paced, FDA regulated environment in the Pharmaceutical Industry. This role is mainly responsible for completing deviation investigations, OOS/OOT and CAPA development related to EM and microbiological testing. Maintains spreadsheets and databases to track and monitor department/company data, KPIs and metrics. Accountable for QC Microbiology inventory control including ordering materials, maintaining stock and resolving material complaints as needed. This role will serve as a Subject Matter Expert (SME) to provide guidance and support junior microbiologists. Train team members in aseptic technique, microbiological methods, EM sampling, and good documentation practices. Participate in the qualification of microbiology lab equipment. Identify and implement continuous improvement opportunities to optimize workflows in the quality control microbiology laboratory. OVERALL JOB RESPONSIBILITIES: Operational Excellence: * Models the principles and behaviors of Glenmark and ensures personnel follow the company code of conduct. * Communicate progress, status, and roadblocks as required. * Drive projects, assignments, and complete presentations within timelines and budgets. Create and maintain relevant metrics for department/site. * Spreadsheets and databases will be leveraged for departmental and company metrics, presentations, and data/testing tracking/verification. The Senior Microbiologist is responsible for keeping these sheets and databases up to date. * Ability to perform routine testing of samples submitted to the laboratory as appropriate. Schedules and participates in cleaning, inventory, and maintenance tasks in the lab. * Supports inventory management and ordering/stocking of all QC department laboratory supplies. * Ensures laboratory equipment is in compliance with procedures and GLP requirements. * Troubleshoots laboratory issues related to all instrumentation. Recommends potential corrective and/or preventive actions and implements these actions within the laboratory. * Performs GMP review of test data to ensure that test results meet all specifications. Trends data and analyzes trends to proactively mitigate equipment and reagent performance issues. Verifies laboratory equipment and associated equipment logs to ensure proper operation Stakeholder: * Preparation, review and approval of sampling matrix and hold time schedule Conducts and communicates results of lab investigations when test results fall outside pre-established specifications (OOS). * Performs routine equipment maintenance. * Performs maintenance of spare parts inventory, calibrations and supervises third party maintenance and repair when necessary. * Establishes good working relation with contract laboratories. * Supports in the development of methods transfer and validation, troubleshooting, cross validation, IQ/OQ/PQ protocols. * Supports activities regarding audits of suppliers and contract labs in support of vendor certification program. * Conducts statistical evaluation of the manufacturing and inspection process and training QC staff. * Ensure that all equipment is calibrated. * Responsible to develop and validate new test procedures * Perform data analysis, compile data and generate reports for management review. * Review lab test data and their integrity and adherence to SOPs and cGMP. Compliance: * Maintain current knowledge of regulatory and industry standards, trends and advancements. * Responsible for ensuring compliance to systems and procedures in the EM/Microbiology laboratory and cleanroom areas. And prepare the lab for internal and external audits. * Support Continuous Improvement initiatives by providing support on updating SOPs, WIs, and OJT * Complete and maintain certified investigator training requirements. Perform investigation of the quality events assigned using root cause analysis tools, maintain timelines for closure of investigations and identify/initiate CAPAs * Complete and maintain status as a certified trainer * Ensure Quality Systems are compliant with cGMPs and internal/external regulations and procedures * Evaluates and assists in the implementation of new changes at the site, including providing training on an as needed basis * Provide support to collect and prepare EMPQ reports, EM Trend reports, QMR board presentations with associated documentation. * Performs regular self-audits of the Microbiology and EM laboratory areas (including storage areas) and assists/leads activities to address audit findings. Stakeholder: * Works collaboratively with other department stakeholders to ensure the services provided to the site are developed, tested, and delivered according to established procedures and regulations. Innovation: * Supports purchasing QC EM laboratory supplies. Makes sound, well considered decisions to make the most of available funds and resources. Monitors lab supply costs and looks for ways to work with suppliers to reduce consumables cost when appropriate. * Consults with management, when appropriate, about laboratory supply variances. Demonstrates the ability to assess upcoming laboratory supply needs and prepare accordingly. Makes realistic and actionable plans to address supply chain issues. * Maintains the QC department ordering system to reduce costs and waste due to expiry. Keeps current on physical and computerized tracking systems for materials and supplies. Safety: * Appropriately utilizes PPE (Personal Protective Equipment) as required to perform routine and non-routine laboratory duties KNOWLEDGE, SKILLS AND ABILITIES: Education: * Minimum BS/BA in Pharmaceutical Sciences, Chemistry, Biology Experience: * Minimum of 3+ years in a pharmaceutical environment * Strong organizational skills. Displays the ability to prioritize work and manage multiple tasks independently. * Excellent written communication and technical writing skills. Clearly demonstrates competence in the selection and use of root cause analysis tools and techniques (e.g., 5 Whys, Pareto Analysis, 5M +E). * Displays strong interpersonal skills and ability to work with all levels of an organization. Clearly expresses ideas (verbal and written) and demonstrates the ability to apply a quality mindset when completing Microbiology/EM laboratory tasks. * Demonstrates the ability to read, understand, author, redline and execute standard operating procedures (SOPs). * Displays ability to achieve Glenmark Monroe QE investigator certifications for product/process/testing/facility issues with product and non-product impact. * Exhibits both analytical and problem-solving skills. Proven ability to problem solve/troubleshoot and provide solutions for laboratory issues. * Able to assess safety and environmental risks to ensure laboratory tasks adhere to EHS management system. * The ability to work independently and within team structure and on multiple projects, with flexibility to adapt to changing priorities is required. This candidate must be a technical expert and have excellent written and oral communication as well as interpersonal relationship skills. Ability to lift 30 lbs. and work within different extreme temperature / humidity environments as encountered in the various Incubator conditions.

Job Description ABOUT THE ROLE The quality control group monitors, supports, and influences the design, configurations, and actual construction necessary to guide our design and production teams to manufacture high quality industry leading homes and components for our customers in accordance with regulatory requirements. The quality control inspector undertakes the inspection of materials, components, and final products to confirm adherence to quality, regulatory, and engineering specifications. He/she works collaboratively with production departments to identify ways to continuously improve production quality. The quality control inspector may work independently or under direct supervision executing specific process steps under continuous quality review and coaching as needed. ESSENTIAL DUTIES & RESPONSIBILITIES Works in a safe manner following all safety policies while performing job duties. Undertakes to maintain a safe and healthy work environment for all employees by identifying any safety standards, procedures, or regulations that are not optimally addressed. Maintains open communication with supervisor regarding safety concerns. Follows work orders and instructions in order to accurately and efficiently review the preparation and assembly of building components based on production area specifications and regulatory requirements including HUD specifications. Inspects incoming materials, in-process production, and finished products to ensure materials and products meet specifications, regulatory requirements, and applicable drawings; conducts visual and measurement tests; documents and communicates rejections of unacceptable items and required corrections; ensures defective products are not delivered to the customer. Works collaboratively with production supervisors, team leads, and line assemblers to discuss inspection results and provides guidance as needed. Documents inspection results by completing inspection reports and checklists; communicates any violations of the quality process or adherence to job performance requirements to Production Supervisors and QC Manager. Maintains a good attendance record and proactively communicates and coordinates with supervisors regarding attendance. Keeps inspection and measurement equipment operating by following operating instructions and notifying management when repairs are necessary. Assists in maintaining and keeping tools, machinery, and work area clean and organized. Performs various other job duties as assigned and needed. MINIMUM QUALIFICATIONS Must be 18 years of age. This can be a physically demanding job requiring the ability to lift 40+ pounds, to grip, work over head, pull at chest height, bend, stand, walk, kneel, crawl, push, pull, reach, climb and carry various materials and equipment. High school diploma and substantial experience in and clear understanding of the requirements and expectations across multiple production areas in a fabrication / manufacturing environment expected. Must have experience reading and interpreting schematics and excellent problem-solving skills. Experience in quality control Inspection preferred including building code knowledge, ability to gain an understanding of construction manuals, standards, regulations, and specifications regarding the products. Bilingual Spanish preferred. Ability to build effective relationships with fellow employees and supervisors including when providing constructive feedback and inspection results. Excellent written and oral communication skills required. Ability to handle multiple projects while maintaining attention to detail. Ability to work in a team, to be trained, and take direction. Flexible to work in a fast paced, changing environment. Not afraid to get dirty and handle tools/equipment daily. Must be able to pass a pre-employment drug screen.

Full-time Description Generous PTO starting your first day, plus 11 paid holidays Medical and Dental: IV pays 100% of employee-only premiums plus a contribution toward dependents; includes HSA with employer contribution Life and Short-Term Disability: 100% employer-paid 401(k) with up to 4% match (eligible first of the month after 90 days) Voluntary add-on policies available: vision, additional life, accident, pet insurance, LegalShield Employee Assistance Program for you and your household. Work Location: This position currently supports a hybrid work arrangement once the training period is completed. You must live within commuting distance from our Christiansburg, VA facility. FLSA Status: Non- Exempt Summary Responsible for managing the Stability Assessment Program (SA) through product testing, data collection and review, proofing and reporting. Responsible for the accuracy, integrity, archival, and retrieval of processed data. Works with various departments as required to help resolve customer inquiries, internal defects, and nonconformances. Performs Trace Metallic Impurity (TMI) testing and provides recommendations on protocol starting materials and other production critical materials such as gloves, bottles, etc. Authority The Non-Production Testing Specialist has the authority to perform all tasks and duties as assigned herein. Authority is also granted for the following: Approve customer complaint resolutions; Manage and determine the disposition of products in the Quarantine area; Create, edit and/or review policy, procedures, and work instructions Authority to stop work. This authority permits any employee at any level to halt a job or task when a hazardous situation appears imminent or they feel unsafe. Essential Duties and Responsibilities · Prepare and analyze solutions using instrumental and wet chemical methods in accordance with current work instructions. · Use computer techniques for analysis, data entry, statistical analysis, and properly record all data in electronic lab notebooks and SA records. · Maintain the Stability Assessment Program to ensure that all products are prepped and tested as scheduled. · Properly record and assess the results of stability testing. Communicate potential stability failures to appropriate parties. · Maintain the stability sample inventory ensuring that all samples are accounted for and properly TCT'd for long term storage. · Assist the Quality Assurance Specialist with investigations related to customer complaints, internal defects, and nonconformances. · Perform and assess Trace Metallic Impurity (TMI) testing of protocol starting materials. · Perform leaching studies of critical materials and consumables such as gloves, bottles, tubing, etc. using the TMI method, and provide recommendations. · Adhere to all laboratory safety policies/practices and procedures as related to areas of responsibility. · Other duties as assigned Requirements Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Required · Bachelor's Degree in Chemistry or related field · 1+ years of assay method testing (instrumental, wet assay, etc.) · Keen attention to detail · Excellent interpersonal skills with the ability to build effective working relationships · Excellent organizational, time management and planning skills · PC Proficiency with willingness to learn new skills as needed · Excellent skills with word processing, data entry, spreadsheet, and database maintenance · Ability to work independently or as part of a team with minimal supervision · Knowledge of the Periodic Table, basic algebra, laboratory safety practices and procedures Preferred - · 1+ Years of stability and/or TMI testing experience · Schedule flexibility to accommodate evolving testing needs Salary Description $27.88- $29.81

Apply for this opportunity as a Microbiology MT/MLT in Southeastern Virginia for permanent hire. Opportunities on the day and night shift! Job Title: Microbiology Medical Technologist / Technician Job Description: We are looking for a dedicated Microbiology Medical Technologist to join our laboratory team. You will be responsible for performing microbiological tests, analyzing samples, and ensuring accurate and timely results. Key Responsibilities: Conduct microbiological testing on various specimens. Identify and characterize microorganisms. Maintain laboratory equipment and ensure compliance with safety standards. Collaborate with healthcare professionals to interpret results. Qualifications: Minimum Associate's degree in Medical Technology or related field. ASCP or equivalent certification preferred. Strong analytical and problem-solving skills. Benefits: Competitive salary Health insurance Professional development opportunities Click to apply or send a resume to marissak@ka-recruiting.com for immediate consideration. (Reference Code: MK1024)

The Lab Technologist III will process and analyze patient samples, monitor quality control, ensure all instruments are properly maintained, and enter patient results in their department. This position may require conducting training for new employees and ensuring regulatory compliance standards are met. Responsibilities * Read and follow Departmental Standard Operating Procedures (SOPs). * Judge the acceptability of quality control results with proficiency. * Communicate sample issues within and outside the department to ensure proper client communication. * Participate in internal and external proficiency testing. * Perform maintenance on departmental equipment with proficiency. * Perform, interpret, and troubleshoot assays with proficiency. * Assist in the evaluation and development of new procedures. * Achieve training goals as established by Human Resources. * Understand and follow all safety rules and regulations. * Apply value statements and quality principles to work. * Assist supervisors in daily department operations. * Perform daily, weekly, and monthly maintenance on all department instruments. * Participate in training new employees. * Work closely with other lab personnel. * Assist in research projects as needed. * Assist in maintaining adequate supplies in the department. Essential Skills * Proficiency in clinical microbiology testing/assays at a major hospital or research institution. * Experience with blood, wound, and urine cultures, and microbial identification using various techniques such as bench biochemicals, Vitek, and MALDI-ToF. * Parasitology microscopic analysis and identification, including trichrome and concentrate preparations. * Bachelor's Degree in a Biological or Chemical Science, Medical Technology, or MLT Certification. * Competency in multiple assays and routine issue troubleshooting. * Ability to train others on sample analysis. * Problem-solving skills, detail-oriented, self-motivated, and teamwork. Additional Skills & Qualifications * Must pass a colorblind test for the Microbiology position. * Minimum of 6 years of clinical laboratory training or experience post-MLT degree. * Minimum of 4 years of clinical laboratory training or experience post-MT or BS degree. * Leadership potential within 18-24 months, with potential for advancement to Assistant Technical Supervisor. Work Environment Work in a CLIA-certified clinical diagnostics laboratory. You will be part of a pioneering team dedicated to advancing personalized healthcare. The collaborative culture values innovation, diversity, and inclusion, and supports professional growth through ongoing training and mentorship programs. Job Type & Location This position is based out of North Carolina. Job Type & Location This is a Permanent position based out of Asheville, NC. Pay and Benefits The pay range for this position is $43680.00 - $62400.00/yr. Benefits would be available to them after they complete their time through protouch and would have a waiting/probationary period of 60 days once they are a Genova employee. Once they meet their 60-day waiting period with Genova they are eligible for health, dental, and vision benefits. We offer PPO and HDP plans through Aetna. After 90 days of employment through Genova you are eligible for 401k. There is an employer contribution. For each dollar you contribute, Genova will match dollar for dollar up to a maximum of 3% and $0.50 on the dollar for the next 2% of compensation. That is 100% vested. Vacation- When employees are hired, they begin accruing vacation at a rate of 3.08 hours per pay period and up to 80 hours per year. Personal Leave- Employees will receive personal leave after 6 months of employment. Full time employees will receive 40 hours. Holidays-After 60 days employees are eligible for paid holidays. The company's seven paid holidays are: New Year's Day, Easter, Memorial Day, July 4th, Labor Day, Thanksgiving, Christmas. Workplace Type This is a fully onsite position in Asheville,NC. Application Deadline This position is anticipated to close on Jan 31, 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 for other accommodation options.

JLA International, a Leader in Food Safety, is now accepting applications for a Microbiology Analyst - 2nd shift position at its facility in Edenton, NC. Ideal candidates will possess the following: - An associate degree (required); a BS or BA in the Microbiology or related field (preferred) - Strong attention to detail - Proficiency with data entry and computer applications - Ability to multitask and work in a fast paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Microbiology Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, compositing and plating samples using aseptic technique, data entry, laboratory reporting, quality control, media preparation, dish washing, and other duties as assigned. This is a full-time position in which the employee will be eligible for standard benefits after a brief waiting period. The schedule for this position is Monday through Friday, from 12:00pm - 8:30pm. The laboratory operates weekends, so candidates must be willing to work some weekends. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

Work Hours: 8:30am-5:00pm or 3:00pm-11:30pm Monday-Friday Training Hours: 8:30am -:00pm or 3:00pm-11:30pm Monday - Friday The Lab Technologist will process and analyze patient samples, monitor QC, ensure all instruments are maintained properly, and report patient results in their department. This position requires a Bachelor's Degree in Biological or Chemical Science or MLT Certification. Upon hire candidates must provide official transcripts and a copy of their diploma. No previous professional experience is required however prior clinical experience is desirable. Candidates must be an excellent problem solver, detail oriented, self-motivated, and a good team player. You must successfully past a colorblind test. The employee must be able to work in an environment containing biohazards, toxic chemicals, pungent odors, corrosive acids, noise, sharp objects, and other normal hazards found in the clinical laboratory. Laboratory safety measures are in place and protective equipment provided to help minimize possible exposure to these environmental risks.