Quality control analyst jobs in Johnson City, TN - 898 jobs

About This Role We are seeking a motivated R&D Food Technologist to join our innovative R&D team in Murfreesboro, TN. In this role, you will be responsible for developing and testing new food products, ensuring high-quality standards, and improving existing products. Responsibilities include conducting research, performing laboratory experiments related to food technology and food science, analyzing ingredients, and maintaining compliance with food safety and industry regulations. The role requires collaboration with cross-functional teams to innovate and support the company's product development goals. Key Responsibilities New product development from research and raw ingredient sourcing to lab prototype development, sampling preparation, costing, trial run, product's SOP & product's specification, develop and refine recipe formulation for mass production purposes. Evaluate current and alternative food ingredients, create product recipes, and conduct sensory evaluation of new food products to ensure to meet customer needs and requirements. Participates on cross-functional teams to ensure effective resolution of technical issues and support product innovation. Assist the QA Department in evaluating the HACCP program for new products to ensure the proper function of the Quality Assurance Department including but not limited to Quality, Regulatory, Food Safety, HACCP, SSOP, Labeling, and USDA. Assuring that operations have a consistent understanding of quality programs and actively participate in process improvement designed to achieve quality and company goals. Other duties as assigned by Management. Qualifications Master's or Bachelor's degree in Food Science/Food Technology, or related field Bilingual is preferred (in English and Chinese) Food Technology and Food Science knowledge Experience in Research and Development (R&D) Laboratory skills Knowledge of the food industry and market trends Ability to create and develop new food products Excellent problem-solving and analytical skills Good communication and teamwork skills Attention to detail and ability to follow protocols Experience with food safety and quality standards Benefits Health insurance Paid time off 401(k) retirement plan Company offers H1B sponsorship

Job Title: QC Environmental Monitoring Technician Department: Quality Control Pay: $25-$30/hr The QC Environmental Monitoring Technician supports parenteral manufacturing operations by performing routine environmental monitoring of classified manufacturing areas and conducting clean utility sampling and analysis across manufacturing and QC laboratory facilities. This role is essential in ensuring compliance with cGMP requirements and maintaining a controlled manufacturing environment to support the production of safe, high-quality pharmaceutical products. Key Responsibilities Adhere to and promote compliance with cGMP regulations, Quality Systems, and Good Documentation Practices (GDP). Perform routine environmental monitoring of classified manufacturing areas in support of both routine operations and Environmental Monitoring Performance Qualification (EMPQ) activities. Conduct clean utility sampling and analysis, including: Compressed air Potable water Purified water Water for Injection (WFI) Clean steam Support manufacturing and QC laboratory operations by providing accurate and timely environmental monitoring data. Enumerate, review, and document environmental monitoring results using LIMS or other laboratory data systems. Perform Second Person Verification (SPV) of environmental monitoring data on a routine basis. Participate in continuous improvement initiatives and quality-focused projects. Assist in the development, revision, and maintenance of SOPs and Work Instructions as needed. Adhere to and promote compliance with all site safety policies and procedures. Minimum Qualifications High School Diploma or equivalent required; Associate degree preferred. Minimum of 2 years of experience performing Environmental Monitoring in a GMP-regulated pharmaceutical manufacturing environment. Prior experience supporting aseptic or parenteral manufacturing operations strongly preferred. Hands-on 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 working with laboratory systems such as LIMS, LES, and/or MODA. Preferred Qualifications Strong understanding of cGMP regulations and regulatory compliance expectations. Experience performing environmental monitoring within filling isolators or Restricted Access Barrier Systems (RABS). Ability to train and mentor junior Environmental Monitoring Technicians. Strong written and verbal communication skills. Proven ability to collaborate effectively in a cross-functional team environment. Physical & Work Environment Requirements Ability to work in laboratory and cleanroom environments while wearing appropriate PPE. Ability to gown into facility-specific cleanroom attire. 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, particularly during training and startup phases. This role may initially support project/startup activities and transition into a routine operational support position.

Role: Entry-Level QC Chemist Duration: 06 months What You'll Do Perform hands-on quality control testing on raw materials, in-process samples, and finished products Conduct analytical testing using techniques such as HPLC, GC, FTIR, Dissolution, Titration, and related methods Accurately document, analyze, and report test results in compliance with SOPs and regulatory standards Calibrate, operate, and maintain laboratory instruments and equipment Follow all safety, GMP, and laboratory hygiene practices Work collaboratively in a fast-paced, “flow-to-the-work” team environment Support peer reviews, SOP updates, and continuous improvement efforts What We're Looking For Bachelor's degree in Chemistry, Biology, Chemical Engineering, Life Sciences, or related field Entry-level candidates welcome; QC laboratory experience is a plus Strong attention to detail and ability to perform accurate testing under pressure Comfortable working overnight shifts and standing for extended periods Ability to multitask, meet deadlines, and adapt to changing priorities Basic knowledge of lab equipment, safety practices, and analytical techniques Proficient in Microsoft Word and Excel Strong written and verbal communication skills in English

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.

Welcome to Your Next Career Chapter At Afton Scientific, every role contributes to advancing the quality and reliability of sterile pharmaceutical manufacturing. Our team is driven by innovation, collaboration, and a commitment to excellence. We support employees at every stage of their career by fostering an environment where development, learning, and meaningful impact are possible. We invite you to explore opportunities to join our organization and contribute to our mission. We are currently seeking a Quality Control Technician (I-III) to support our growing biopharmaceutical operations at our on-site facility in Charlottesville, Virginia. Overview of this Position: The Quality Control Technician (I-III) supports daily production activities by performing environmental monitoring, water sampling and testing, and cleanroom support. Depending on experience level, the QC Technician may also contribute to deviation/excursion investigations, documentation revisions, and biologics testing as we expand our capabilities. Non-Negotiable Requirements: •Must be legally authorized to work in the United States; no type of sponsorship is available • At least three (3) years of experience in a Quality Control environment (Senior Techs) • At least one (1) year of experience in a GMP manufacturing facility • At least one (1) year of experience working with Laboratory Information Management Systems (LIMS) Preferred Requirements: • Experience working with Master Control, and/or SAP. • Experience writing or contributing to deviations, excursions, CAPA documentation, or investigations. •Demonstrated ability to anticipate operational needs, plan ahead, and contribute to lab efficiency. •Exceptional communication skills •Experience with OFCCP Compliance Regulation •Bachelor's degree in biology and /or Life Sciences Responsibilities Include: •Perform environmental monitoring in cleanrooms and supporting areas (Grade C/Grade D spaces) •Conduct testing to support material and product release •Conduct routine water sampling, testing, and daily production‑support activities •Support onboarding tasks such as facility orientation and early‑stage lab workflows •Document results accurately and maintain logbooks, records, and reports in alignment with GMP and audit‑ready expectations •Collaborate with Production, Materials, Inspection, and other groups to ensure smooth daily operations (Senior Techs Only) Participate in deviation and excursion writeups Revise controlled documents Provide technical insight and help develop higher‑level QC capabilities Potentially support emerging biologics testing and expanded lab instrumentation Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of this job. This role may require sitting, standing, or walking for extended periods; using a computer; and working in a standard office environment. Specific physical or environmental requirements will be addressed through the reasonable accommodation process. We do not discriminate based on disability and will provide reasonable accommodation as required by law.

Founded in 1992, InServ is a full-service industrial contractor working in the life science, advanced manufacturing, and food and beverage industries. We specialize in four trades (mechanical, hygienic piping, HVAC, and electrical, instrumentation and controls), working from multiple locations across North Carolina and for clients across the Southeast. InServ is both a knowledgeable and reliable partner for our clients. We assist with design, adhere to schedules, and execute with the highest quality to provide a total solution. ESSENTIAL DUTIES AND RESPONSIBILITIES: Conduct daily walk-through surveillances on assigned project(s) and/or fabrication facilities. Evaluate to ensure conformance and compliance with contractual specifications, government regulations, and InServ's QA/QC policies and procedures. Inspect materials and fabricated products, on-site materials/equipment, and verify installation processes to ensure compliance with contract specifications and regulatory standards. Document and communicate inspection results. Identify and recommend solutions for non-conforming items and nonconformance of QA/QC policies and procedures. Follow-through to ensure nonconformances are resolved. Disseminate written policies and procedures related to compliance activities. Interpret specifications and clarify procedural issues for workers. Verify that all contractual and regulatory policies and procedures have been documented, implemented, and communicated for the project, and as directed by QA/QC Manager or Supervisor. Assess product for compliance to specifications and procedures. Assist with the development of risk management strategies. Contribute to suggestions for improvements in communication and monitoring. Maintain daily logs of project quality and surveillances. Support logged information with photographs/videos - photographing must be in accordance with client's privacy policies. File appropriate and timely inspection and compliance reports. Updated: 1/31/25 JD-QA/QC Inspector: Page 2 of 2 Discuss violations of QA/QC policies and/or specifications for potential stop-work orders with the QA/QC Manager and project management. Explain specifications, regulations, and/or QA/QC procedures and recommend rectifications. Train subcontractors on quality requirements and compliance, as necessary. Perform additional assignments per supervisor's direction. Travel Requirements: Skills, Knowledge, Qualifications & Experience: High school diploma or equivalent; some advanced education and/or technical training is desired. Self-motivated with a desire to be among a strong supportive team. AWS Certified Welding Inspector is desired. Prior NDT Level II (VT) certification is required, in accordance with SNT-TC-1A and endorsed by an ASNT NDT Level III. 3 years minimum experience in Visual Testing (VT). Welding experience is preferred but not required. Biopharmaceutical, high-purity inspection experience is required. Thorough knowledge of all aspects of construction (technology, equipment, processes, and methods). Thorough knowledge of company QA/QC policies, procedures and standards. Strong oral and written communication skills. Ability to identify, troubleshoot and resolve problems before major difficulties develop. Auditing skills. MS Office skills and ability/desire to learn new software. Excellent communication, organizational, and planning skills. Employment is contingent upon satisfying all jobsite-specific access requirements, with no outstanding restrictions from any jobsite or from working with any of InServ's partnering General Contractors, Owners, Customers, etc.

Job Title: Chemist Duration: 06 Months Pay Rate: $25/hr on W2 Shift: 7:00AM-5:30PM (Mon -Thurs) but there is some flexibility in start time Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory. Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs. Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting. Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency. Aid other group members as required. Ensure that equipment and working areas are maintained with good safety and housekeeping practices. Re-stock chemicals and consumables used in analysis. Performs other related assignments and duties as required and assigned. Skills: Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy - UV/Vis, NIR, IR, or AA/AE). Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting. Lift and maneuver equipment and materials weighing up to 20 pounds. Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums. Use small hand and power tools to perform incidental maintenance. Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces. Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required. Education: The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred.

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

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

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

Microbiology Analyst - Owensboro KY Be a part of a revolutionary change! At Philip Morris International (PMI), we've chosen to do something incredible. We're totally transforming our business and building our future on one clear purpose - to deliver a smoke-free future. With huge change, comes huge opportunity. So, if you join us, you'll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Our success depends on people who are committed to our purpose and have an appetite for progress. This position sits with our Swedish Match affiliate. Your 'day to day' * Perform standard microbiology work such as isolating microorganisms, culturing samples, staining, and using aseptic techniques. Use both traditional methods and automated microbiology equipment. * Keep the Microbiology Lab clean, organized, and well‑maintained. * Maintain accurate and complete records for all assigned projects. * Conduct both routine and non‑routine microbiological tests. * Provide microbiology support to teams across the organization, including Production, Product Development, Quality Assurance, Regulatory & Scientific Affairs, and Leaf Operations. * Complete special projects as assigned by the Owensboro Analytical Science (OAS) Assistant Manager. * Perform OAS analytical methods and assist the OAS Analytical team when needed. * Handle equipment sterilization, culture media preparation, and autoclave operation/maintenance. * Write and maintain Standard Operating Procedures (SOPs) for validated methods and help develop new microbiology techniques and procedures. * Support Senior Analytical Chemists, Analytical Chemists, Senior Chemical Analysts, Chemical Analysts, and Laboratory Technicians as needed. Who we're looking for: Education * Bachelor's degree in a scientific field such as Microbiology or a related discipline, or equivalent hands‑on experience. Experience * Strong working knowledge of standard microbiology techniques. * Experienced in validating microbiological methods. Skills * Skilled in microbiology and familiar with ISO 17025 procedures and compliance. * Able to troubleshoot microbiology instruments and work with laboratory automation. * Customer‑focused, goal‑oriented, and motivated to support OAS goals and objectives. * Strong understanding of microbiology, including lab procedures, automation, computer tools, project management, and manufacturing processes. * Knowledgeable in microbiology lab safety practices and methodologies. Annual Base Salary Range: $ 60,000 - $80,000 What's 'nice to have' Legally authorized to work in the U.S. (required) What we offer * We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, and much more! * Seize the freedom to define your future and ours. We'll empower you to take risks, experiment and explore. * Be part of an inclusive, diverse culture where everyone's contribution is respected; Collaborate with some of the world's best people and feel like you belong. * Pursue your ambitions and develop your skills with a global business - our staggering size and scale provides endless opportunities to progress. * Take pride in delivering our promise to society: To improve the lives of millions of smokers. PMI is an Equal Opportunity Employer. PMI is headquartered in Stamford, Conn., and its U.S. affiliates have more than 2,300 employees. PMI has been an entirely separate company from Altria and Philip Morris USA since 2008. PMI's affiliates first entered the U.S. market following the company's acquisition of Swedish Match in late 2022.Philip Morris International and its U.S. affiliates are working to deliver a smoke-free future. Since 2008, PMI has invested $12.5 billion globally to develop, scientifically substantiate and commercialize innovative smoke-free products for adults who would otherwise continue to smoke with the goal of transitioning legal-age consumers who smoke to better alternatives. In 2022, PMI acquired Swedish Match - a leader in oral nicotine delivery - creating a global smoke-free champion led by the IQOS and ZYN brands. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA. For more information, please visit ************** and ******************* #PMIUS #LI-DH1

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. Glenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark Generics Limited has a fast growing and robust US generics business. The subsidiary also markets APIs to regulated and semi-regulated countries. POSITION SUMMARY : The Microbiology Analyst is responsible for performing microbiological tests that support the release of intermediates and finished products. These include routine and non-routine microbiological tests on in-process and final container products, as well as environmental monitoring samples. This position also contributes to the completion of regular routine technical tasks. JOB RESPONSIBILITIES : Help maintain inventory by reporting needed supplies. Take appropriate steps to reduce wastages and losses in the Microbiology department. * Monitoring samples, in-process product samples, raw materials, and environmental monitoring (EM) samples. * Successfully complete a gown qualification program to enter and work inside the aseptic manufacturing area. * Perform critical manufacturing process interventions for viable and non-viable EM. * Maintain sample logs on a daily basis to ensure timely testing and tracking of all samples. * Perform routine sampling of critical process utilities (e.g., Water-for-Injection, Purified Water, Clean Compressed Air, Nitrogen Distribution System, etc.) * Count colony forming units (CFU) on Petri plates. * Perform sterility testing on final products and raw materials. * Perform Growth Promotion and Biological Indicator testing. * Perform preparation of reagents, materials, and equipment used in microbiological testing in sterile environments, such as HEPA hoods. * Maintain accurate and complete test records. * Enter test results in the Laboratory Information Management Systems (LIMS). * Maintain Instrument Usage and Calibration Logs based on instrument usage during the preparation and testing of samples. * Maintain current knowledge of regulatory and industry standards, trends and advancements. * Other duties as identified by direct supervisor * 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 and/or limits (OOS/OOL). * 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 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. * Assures laboratory databases are maintained and accurate. * Ensures control of laboratory documentation (Raw Material COA, testing instructions, testing. * Ensure that all equipment is calibrated. Education : * Minimum BS/BA in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or equivalent. * Microbiology degree preferred Experience : * 1-3 years of experience in a cGMP/GLP laboratory. * Pharmaceutical & FDA/GMP industry experience is preferred. * Microbiology laboratory experience, such as aseptic techniques required Knowledge and Skills : * Knowledge of current cGMP regulations for laboratory setting * Proficient in Windows, Microsoft Word, Excel. * Good written, verbal, and communication skills. * Good documentation skills. * Strong organizational skills.

Microbiology Lab Tech needs 1 year microbiology testing experience, Microbiology Lab Tech requires: Bachelors degree in science field or relevant work experience Skilled in use of PC software and Microsoft Office (Excel, Word, PowerPoint) Experience with SAP, relevant ISO standards, and/or auditing preferred Ability to work on multiple projects and priorities Minimum 1 year experience with microbiological testing required Experience with hygienic sampling & hygienic plating required Microbiology Lab Tech duties: Finished product and raw material testing Gram-staining Stocking of inventory, media, and reagents, managing laboratory waste Environmental monitoring including testing process water, air sampling, and swabbing of equipment (limited) Plate reading and communication of results

Description: At Monarca Food Solutions (Palmex / Evans) we are committed to our valued employees, leading innovation, quality, and community. We bring better-for you snacking to consumers with brands dating back nearly a century. We are proud to bring high quality snacking happiness to the hearts and bellies of our consumers daily. If you are an individual who likes to be challenged and make a difference in a fast-paced team-oriented environment, look no further. Come join a company committed to its employees and inspiring wellness in consumers everywhere. Competitive Benefits offered to employees: Low-cost Health, Vision and Dental insurance coverage Company paid Short-Term and Long-Term Disability Company paid Life Insurance Voluntary Life and AD&D insurance 401(k) retirement savings plan with company match We are hiring for a Quality Control Tech in our Kingsport, TN location. Individual will be an independent worker with close supervision of QA supervisor, performs routine test set-up tasks and operational support tasks, including sampling, inspections of facilities and products, keeps accurate records and logs and maintains a clean working environment. WHAT YOU'LL DO: Use of specific testing equipment that may involve oil frying and handling of extremely hot materials and equipment Use of Lab equipment such as grinding, measuring, and screening Deal with people in a manner which shows sensitivity, tact, and professionalism. Good communication capabilities Make decisions based on data and observations about food safety and product quality Follow written and/or oral instructions Maintain confidentiality Enter, transcribe, record, store, or maintain information in either written or electronic form. Operate a tablet or computer keyboard Find, gather and collect information or data Use cleaning agents, and other chemical products Requirements: WHAT WE'RE LOOKING FOR: Associates degree and 1 year of experience in Quality, or equivalent combination of education and experience. Training requirements: GMP's, Allergen control, Employee safety, Food quality, Food safety, HACCP, Fire and evacuation, Food defense, Quality safety culture. Experience in Quality checks and controls, Preoperational inspections, Operational SSOPs, Weight control checks, Traceability and recall, Environmental swabbing Basic computer skills in Word and Excel WORK ENVIRONMENT: This position requires the use of special safety precautions and/or equipment, e.g., working around operating machines, working with hazardous chemicals and materials, etc. While performing the essential functions of this position, the employee is regularly required to talk and hear. The work requires some physical exertion such as long periods of standing; walking over slippery surfaces; recurring bending, crouching, stooping, stretching, reaching, or similar activities; recurring lifting of moderately heavy items such as samples and record boxes. This position requires frequent pulling, carrying, and lifting up to 50lbs. OTHER DUTIES: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. We consider applicants for all positions without regard to race, color, religion, creed, gender, national origin, age, disability, martial or veteran status, sexual orientation, or any other legally protected status. We are an Equal Opportunity Employer.

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)

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

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.