Quality Control Analyst jobs at Lockheed Martin - 387 jobs

Apply for JobJob ID696518 Full/Part TimeFull-Time Regular/TemporaryRegular Add to Favorite JobsEmail this Job About Sandia Sandia National Laboratories is the nation's premier science and engineering lab for national security and technology innovation, with teams of specialists focused on cutting-edge work in a broad array of areas. Some of the main reasons we love our jobs: Challenging work with amazing impact that contributes to security, peace, and freedom worldwide Extraordinary co-workers Some of the best tools, equipment, and research facilities in the world Career advancement and enrichment opportunities Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home) Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance* World-changing technologies. Life-changing careers. Learn more about Sandia at: *These benefits vary by job classification. What Your Job Will Be Like We are seeking an outstanding synthetic materials chemist to establish both an independent research program and a develop a user program with capabilities on offer to the external user community at the Center for Integrated Nanotechnologies (CINT), a DOE-funded user facility. Our ideal candidate is a recognized synthetic materials chemistry expert with a substantive body of doctoral-level research performed in an academic or other professional research and development settings who has the proven capability to operate at a high level within a DOE user facility or other such formal research center. The successful candidate will be a synthetic chemist working in an area of interest to the Soft, Biological, and Composite Nanomaterials Thrust at CINT. Of particular interest are synthesis, characterization, and applications of polymers and/or nanoparticles, but outstanding candidates working to synthesize other materials that have synergistic opportunities will be considered. The successful candidate will support AI-guided design, combinatorial synthesis, and circular materials workflows On any given day, you may be called on to: Lead the development of new synthetic techniques in materials chemistry. Collaborate with other researchers at the laboratory, around the country, or around the world. Lead or collaborate in the development of new projects from a variety of funding agencies. Communicate results through high impact journals and conference presentations. Due to the nature of the work the selected applicant must be able to work onsite in Albuquerque, New Mexico Relocation will be provided for those that qualify. Salary Range $114,000 - $227,500 *Salary range is estimated, and actual salary will be determined after consideration of the selected candidate's experience and qualifications, and application of any approved geographic salary differential. Qualifications We Require A bachelor's degree in a relevant discipline and five (5) years of directly relevant experience, or an equivalent combination of directly relevant education and engineering or scientific experience that demonstrates the knowledge, skills, and ability to perform independent research and development. Qualifications We Desire Graduate degree in a Materials Science or a highly related field where an independent research project was a graduation requirement (e.g., independent project, thesis, or dissertation). Familiarity with operation of standard laboratory equipment, and standard laboratory processes. Ability to prioritize and teach others basic chemistry tasks, including the operation of standard laboratory equipment, and standard laboratory processes. Excellent communication skills, written and oral, and preferably prior experience in writing both published peer-reviewed articles and grant proposals. Effective interpersonal skills and the ability to contribute and work in a multidisciplinary team environment. Experience in a research and development environment. Experience with materials characterization techniques. Experience working on teams consisting of multidisciplinary and multi-disciplinary experimentalist, modelers, and theorists with a common goal Also, for this posting we are seeking individuals with the following experience: PhD in chemistry, chemical engineering, materials science, or a related discipline. Significant experience in the synthesis of nanomaterials. Record of technical achievement as evidenced by peer-reviewed publications in high profile journals. Experience with modern tools of AI-based synthesis and characterization. 2 or more years of relevant experience after PhD. Experience in the synthesis, characterization, and applications of nanoparticles or polymeric nanosystems. Experience with advanced characterization of nanomaterials or nanocomposites using appropriate nanoscale techniques, such as x-ray characterization or electron microscopy. Experience with any of the unique capabilities of CINT's SBCN thrust, including microfluidic systems, advanced optical microscopy, experiment automation using artificial intelligence or machine learning, and cryogenic or environmental TEM. Experience in CINT's strategic areas of growth, including artificial intelligence-based synthesis and manufacturing, metastable materials discovery, and sustainable critical materials recovery or replacement. Experience with proposal writing, managing multi-institution collaborations, and managing lab personnel. About Our Team The Nanosystems Synthesis and Analysis Department consists of CINT scientific research staff assigned to the Physical, Chemical, & Nanosciences Center at Sandia National Laboratories. CINT is a DOE/Office of Science National User Facility operated jointly by Sandia and Los Alamos National Laboratories with facilities at both Laboratories. The CINT Science Department is dedicated to establishing the scientific principles that govern the design, performance, and integration of nanoscale materials into microscale and macroscale systems and devices. Posting Duration This posting will be open for application submissions for a minimum of seven (7) calendar days, including the 'posting date'. Sandia reserves the right to extend the posting date at any time. Security Clearance This position does not currently require a Department of Energy (DOE) security clearance. Sandia will conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Furthermore, employees in New Mexico need to pass a U.S. Air Force background screen for access to Kirtland Air Force Base. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of untrustworthiness can cause access to be denied or terminated, resulting in the inability to perform the duties assigned and subsequent termination of employment. Under federal law, citizens and agents of the People's Republic of China, the Islamic Republic of Iran, the Democratic People's Republic of North Korea, and the Russian Federation are generally prohibited from accessing Sandia National Laboratories. Accordingly, such individuals will not be considered for employment unless they are also a citizen of the United States. If hired without a clearance and it subsequently becomes necessary to obtain and maintain one for the position, or you bid on positions that require a clearance, a pre-processing background review may be conducted prior to a required federal background investigation. Applicants for a DOE security clearance need to be U.S. citizens. If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted. Members of the workforce (MOWs) hired at Sandia who require uncleared access for greater than 179 days during their employment, are required to go through the Uncleared Personal Identity Verification (UPIV) process. Access includes physical and/or cyber (logical) access, as well as remote access to any NNSA information technology (IT) systems. UPIV requirements are not applicable to individuals who require a DOE personnel security clearance for the performance of their SNL employment or to foreign nationals. The UPIV process will include the completion of a USAccess Enrollment, SF-85 (Questionnaire for Non-Sensitive Positions) and OF-306 (Declaration of for Federal Employment). An unfavorable UPIV determination will result in immediate retrieval of the SNL issued badge, removal of cyber (logical) access and/or removal from SNL subcontract. All MOWs may appeal the unfavorable UPIV determination to DOE/NNSA immediately. If the appeal is unsuccessful, the MOW may try to go through the UPIV process one year after the decision date. EEO All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status and any other protected class under state or federal law. NNSA Requirements for MedPEDs If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs. If you have a MedPED and you are selected for an on-site interview at Sandia National Laboratories, there may be additional steps necessary to ensure compliance with NNSA security requirements prior to the interview date.

Formulation QC Specialist Associates Shift Timing: Mon - Friday 40.00 Hours Per Week Duration: 12 Months contract and the possibility to be extended the contract. Working hours are typically 6:00AM to 2:30 PM, M-F* 1st shift position Job description: **Experience in formulations, quality control and/or wet lab experience is preferred **Seeking a highly organized and detail-oriented individual with proven ability to accurately manage multiple priorities, and who can contribute effectively both independently and within a team environment The Opportunity Conduct quality control testing on formulations Ensure compliance with GMP and regulatory requirements Monitor formulation processes for consistency and accuracy Document and report quality assurance findings Assist in troubleshooting and resolving quality issues Who You Are • 0-5 years of experience • Strong problem-solving skills • Excellent communication abilities • Knowledge of industry best practices Preferred (Optional): Experience in pharmaceutical or biotech QC preferred

ID 2025-17927 Element has an opportunity for a Chemistry Technician for testing, sample preparation and delivery/collection of samples and preparation of test reports. Salary: $45,000- $75,000/yr DOE Responsibilities * Determination of chemical and physical properties of metallic and non-metallic materials * Familiarity/Operation of instruments such as ICP/OES, Leco, pH, XRF, MFR, FTIR, DSC, TGA, TMA, DMA, GC/MS, hardness meters, analytical balances, etc. * Prepare the reagents, standard solution and ensure standardization of the solution used in the laboratory. * Handling and storage all chemicals as per the Material Safety Data Sheet (MSDS). * Responsible for conducting, developing, witnessing, and executing tests and experiments using both established methods and newly developed / novel techniques with minimal to no supervision. Some tests can be done at our laboratory or on-site at the customer's location. * General maintenance, cleaning and checking of instruments. * Manage verification and calibration of instruments. * Responsible for adhering to safety procedures and appropriate regulatory and company standards. * Interaction with clients during witnessed testing. * Prepare written quotations, proposals, schedule tests, analyze test results, prepare reports, and submit invoices for approval with limited supervision and oversight. * Ensuring compliance to all Element quality standards as well as ISO 17025 requirements. Skills / Qualifications * Associates degree or higher in Chemistry or equivalent, and/or at least 2 years' experience in a similar role. * Ability to work in teams under pressure and flexible to work different working overtime hours, if required or necessary. * Excellent oral and written communication skills along with strong interpersonal skills and listening ability to communicate effectively with peers, superiors, customers and vendors. * Basic math skills. * Knowledge and experience of safe operation of testing equipment and operating in an independent / chemistry / consultant laboratory. * Frequency of required physical force: Occasional - Moderate. * Work is primarily preformed indoors but may require occasional work outdoors when at customer sites. Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

TITLE: CHEMICAL TECHNICIAN FLSA STATUS: NON-EXEMPT D SHIFT: FRIDAY THRU SUNDAY AND EVERY OTHER THURSDAY 6:00 PM TO 6:00 AM REPORTS TO: PRODUCTION SUPERVISOR Under the direction of the Production Supervisor, the Chemical Technician is responsible for the routine changing of solvents, etch tank fluids, and resist bottles; making, pouring, and maintaining develop solution and lapping slurries; performing tests using various laboratory tools and analyzing the results to ensure consistency; and disposing of chemical waste as needed. This position is located in Milpitas, California. *Must be willing to train on F Shift (Friday thru Sunday and every other Thursday 12:00 PM-12:00 AM) for a minimum of two months before moving to assigned shift. ESSENTIAL FUNCTIONS: Performs routine changing of solvents, etch tanks fluids, and resist bottles to ensure a ready supply of fresh chemicals Prepares, pours, and maintains various chemicals, developing solutions, and etch slurries Manages, monitors, and stocks chemical supplies; informs Materials department when inventory is low or needs to be replenished Performs routine chemical testing to ensure consistency of products using various laboratory tools; analyzes results and reports deviations Properly disposes of chemicals to ensure compliance with Environmental Health and Safety requirements Responds to chemical spills quickly and according to established procedures; participates in the Headway Spill Response team Responds to inquiries from other team members, managers, or departments Overtime may be required contingent on business need Adheres to all safety policies and procedures as required Performs other duties of a similar nature or level* MINIMUM QUALIFICATIONS: High School or General Education Diploma (GED) Experience working in a semiconductor or high volume manufacturing environment or similar industry Experience working with and disposing of chemicals, solvents, or similar compounds Proficient in the use of Microsoft Office Applications Knowledge, Skills, and Abilities: Knowledge and ability to handle, maintain, and properly dispose of hazardous chemicals, solvents, or similar compounds Knowledge and ability to use basic analytical tools to test chemicals for consistency and quality Knowledge and ability to use Microsoft Office applications to create spreadsheets, Word documents, and presentations Ability to follow written or verbal instructions regarding appropriate chemical handling procedures Able to communicate effectively, both verbally and in writing, with all levels of consultants, employees, management, and vendors Able to work productively and collaboratively with all levels of employees and management Able to comply with all safety policies and procedures Able to comply with all clean room protocols and procedures for handling hazardous chemicals Demonstrated ability to resolve equipment maintenance issues quickly and efficiently Demonstrated organizational and time management skills Demonstrated problem-solving and trouble shooting skills Flexible and able to prioritize The hourly rate for this full-time position is between $22.00-$35.00+ bonus target + benefits. Within the range the individual pay may differ depending on additional factors including job responsibilities, job related knowledge, skills, abilities, education, and experience. The hourly pay range shown is subject to change and may be modified periodically. WORKING CONDITIONS: The Chemical Technician works in an indoor environment on a rotating schedule on D shift which is Friday thru Sunday and every other Thursday from 6:00 PM to 6:00 AM. The work hours may be altered from time-to-time contingent on business needs. Technician works in a class 100 ESD sensitive wafer fab manufacturing facility; adheres to OHSA required safety and dress standards. May travel from building-to-building as needed. Technician may be subject to high noise levels, hazardous chemicals, and particulate matter from time-to-time; must be clean-shaved in order to wear a respirator when required. Stands and walks; performs various fine grasping movements, bends, kneels, crawls, and twists; operates a computer and enters information using a keyboard, operates a telephone, and other office equipment; must be able to push, pull, lift, or carry above the waist up to 75 pounds. *Other duties of a similar nature or level are duties that may be required, but may not be specifically listed in the job description or posting. TDK/Headway Technologies, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, national origin, age, disability, or genetics. Applicants requiring accommodation in order to complete the application process should contact the Headway Human Resources Department.

Are you an experienced R&D Technician with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced R&D Technician to work in Arden Hills, MN. The Systems Test Tools and Lab Support Technician will play a critical role in ensuring the availability and reliability of testing tools and infrastructure used in the development and validation of advanced medical systems. This position supports the engineering team by maintaining test tools and software, ensuring 100% uptime, and assisting with testing activities as needed. Primary Responsibilities/Accountabilities: Tool Availability & Maintenance Ensure Systems Eval lab testing tools and equipment are always operational and available. Perform routine checks, preventive maintenance, and troubleshooting of hardware and software tools. Maintain inventory and calibration records for lab equipment. Software Tools Management Install, configure, and update software tools used for system testing. Monitor tool performance and apply patches or upgrades as required. Collaborate with development teams to integrate new testing utilities and frameworks. Testing Support Assist engineers in executing test plans and validating system functionality. Prepare test environments and ensure proper setup for verification and validation activities. Document test results and report issues promptly. Process & Compliance Follow established protocols for tool maintenance and testing activities. Ensure compliance with regulatory standards and internal quality procedures. Contribute to continuous improvement initiatives for lab operations and tool management. Qualifications: Associate or Bachelor's degree in Electronics, Computer Science, Engineering Technology, or a related discipline (or equivalent practical experience). 2+ years of hands-on experience supporting engineering labs, maintaining test tools/equipment, or assisting with system-level testing. Working knowledge of hardware and software troubleshooting, including Windows-based systems and mobile platforms (Android and iOS). Proficiency with Python scripting for basic automation, data handling, or tool support tasks. Strong organizational skills with excellent attention to detail, including accurate documentation and tracking of lab assets and activities. Ability to prioritize tasks and work effectively in a fast-paced, collaborative team environment. Preferred: Experience in medical device testing or regulated environments. Knowledge of automated test tools and scripting languages. Understanding of design controls and traceability requirements. Hands-on experience with lab instrumentation and calibration.

We have an exciting opportunity for a Bioanalytical Chemist to join the Metabolomics team in Crop Health Research and Development located in Indianapolis, IN. This role is focused on providing essential bioanalytical support to advance fermentation research goals. The candidate will conducts experiments and complex technical operations, recognize erroneous or unexpected results, interpret and analyze results, and makes suggestions based on their analyses and conclusions. Responsibilities: Execute established quantitative bioanalytical UPLC methods to support fermentation based programs by analyzing various small molecules. Handle and extract from varied biological matrices including microbial broths and extracts. Conduct basic data interpretation and processing of analytical results to ensure data quality and consistency. Maintain accurate records of instrument performance, results, and experimental procedures. Communicate technical results and instrument status clearly to team members and stakeholders in a dynamic environment. Requirements: B.S. in Chemistry, Biochemistry, Chemical or Biochemical Engineering, Biotechnology, or a related scientific field. Proven hands-on experience with HPLC or UPLC systems for analytical or bioanalytical chemistry applications. Strong work ethic and a proactive, collaborative approach to teamwork. Effective verbal and written communication skills. Preferred Qualifications: Previous research experience in an industrial or academic laboratory setting. Experience with Beckman-based automation or similar robotic liquid handling systems. Experience with Mass Spectrometry (MS) systems and software. Experience with Gas Chromatography (GC) based systems.

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day. Mailroom Quality Control Operator Location: Onsite in Lexington, KY Training Pay: $15 an hour, which may be below your state's minimum wage. Please take this into consideration when applying. Production Pay: Piece rate - production-based pay with no limits to your earning potential. Schedule: Monday-Friday 10:30am-clean desk About the Mailroom Quality Control Operator role: We are seeking a dedicated and detail-oriented Mailroom Quality Control Operator to support our quality processes and help ensure client satisfaction and operational excellence. The ideal candidate is highly organized, has a strong understanding of standard operating procedures, and thrives in a fast-paced production environment. What You'll Do: * Quality control of digital files created by the scanning process * Use a PC to look for errors such as double feeds, checks, notary documents, missed or errored barcodes, etc. * Once completed, place the stacks into a box and when box is full, place on a shelf to be taken to warehouse and stored * Enter information into a computer, print files, and process documents * Simple problem solving and troubleshooting for computers and printers What We're Looking For: * Able to sit and use a computer for long periods of time * Must be able to multi-task while maintaining accuracy * Attention to detail * Able to lift to 35lbs * Must be at least 18 years old and able to pass a criminal background check * High school diploma or GED required * Able and willing to work clean desk schedule * Dependable and able to work full-time onsite Why You'll Love It Here: * Full-time, stable employment (up to 40 hours/week) * Benefits start day one - health, dental, vision, and more * Growth and career advancement opportunities * Friendly, professional work environment Pay Transparency Laws in some locations require disclosure of compensation and/or benefits-related information. For this position, actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, and performance. In addition to base pay, this position, based on business need, may be eligible for a bonus or incentive. In addition, Conduent provides a variety of benefits to employees including health insurance coverage, voluntary dental and vision programs, life and disability insurance, a retirement savings plan, paid holidays, and paid time off (PTO) or vacation and/or sick time. The estimated salary range for this role is $15 an hour. Conduent is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, creed, religion, ancestry, national origin, age, gender identity, gender expression, sex/gender, marital status, sexual orientation, physical or mental disability, medical condition, use of a guide dog or service animal, military/veteran status, citizenship status, basis of genetic information, or any other group protected by law. For US applicants: People with disabilities who need a reasonable accommodation to apply for or compete for employment with Conduent may request such accommodation(s) by submitting their request through this form that must be downloaded: click here to access or download the form. Complete the form and then email it as an attachment to ********************. You may also click here to access Conduent's ADAAA Accommodation Policy.

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day. **Mailroom Quality Control Operator** **Location:** Onsite in Lexington, KY **Training Pay:** $15 an hour, which may be below your state's minimum wage. Please take this into consideration when applying. **Production Pay:** Piece rate - production-based pay with no limits to your earning potential. **Schedule:** Monday-Friday 10:30am-clean desk **About the Mailroom Quality Control Operator role:** We are seeking a dedicated and detail-oriented Mailroom Quality Control Operator to support our quality processes and help ensure client satisfaction and operational excellence. The ideal candidate is highly organized, has a strong understanding of standard operating procedures, and thrives in a fast-paced production environment. **What You'll Do:** - Quality control of digital files created by the scanning process - Use a PC to look for errors such as double feeds, checks, notary documents, missed or errored barcodes, etc. - Once completed, place the stacks into a box and when box is full, place on a shelf to be taken to warehouse and stored - Enter information into a computer, print files, and process documents - Simple problem solving and troubleshooting for computers and printers **What We're Looking For:** + Able to sit and use a computer for long periods of time + Must be able to multi-task while maintaining accuracy + Attention to detail + Able to lift to 35lbs + Must be at least 18 years old and able to pass a criminal background check + High school diploma or GED required + Able and willing to work clean desk schedule + Dependable and able to work full-time onsite **Why You'll Love It Here:** + Full-time, stable employment (up to 40 hours/week) + Benefits start day one - health, dental, vision, and more + Growth and career advancement opportunities + Friendly, professional work environment Pay Transparency Laws in some locations require disclosure of compensation and/or benefits-related information. For this position, actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, and performance. In addition to base pay, this position, based on business need, may be eligible for a bonus or incentive. In addition, Conduent provides a variety of benefits to employees including health insurance coverage, voluntary dental and vision programs, life and disability insurance, a retirement savings plan, paid holidays, and paid time off (PTO) or vacation and/or sick time. The estimated salary range for this role is $15 an hour **.** Conduent is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, creed, religion, ancestry, national origin, age, gender identity, gender expression, sex/gender, marital status, sexual orientation, physical or mental disability, medical condition, use of a guide dog or service animal, military/veteran status, citizenship status, basis of genetic information, or any other group protected by law. For US applicants: People with disabilities who need a reasonable accommodation to apply for or compete for employment with Conduent may request such accommodation(s) by submitting their request through this form that must be downloaded: click here to access or download the form (********************************************************************************************** . Complete the form and then email it as an attachment to ******************** . You may also click here to access Conduent's ADAAA Accommodation Policy (***************************************************************************************** .

Piper Companies is seeking a Quality Control Analytical Scientist (Flow Cytometry) to support GMP analytical testing for a late-stage biopharmaceutical organization advancing gene therapies for rare genetic disorders. This onsite role in Exton, PA offers hands-on experience with flow cytometry and related cell-based assays supporting clinical manufacturing. Responsibilities of the Quality Control Analytical Scientist (Flow Cytometry): * Perform GMP-compliant flow cytometry assays to support in-process, drug substance, and drug product testing. * Execute methods such as percent transduction efficiency and CD90 analysis. * Support additional testing platforms including cell culture, ELISA, and qPCR. * Review results for accuracy, data integrity, and compliance with GMP documentation standards. * Conduct investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, equipment calibration, and readiness for audits. Qualifications of the Quality Control Analytical Scientist (Flow Cytometry): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong experience with flow cytometry, gating strategies, and data analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiar with analytical assays such as ELISA and qPCR. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (Flow Cytometry): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included) * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 1/5/2026 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, Flow Cytometry, FACS, GMP, Analytical Testing, Biologics, Gene Therapy, Cell Culture, ELISA, qPCR, Transduction Efficiency, CD90, Gating Strategy, Data Integrity, CAPA, SOP, Aseptic Technique, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

Piper Companies is seeking a Quality Control Analytical Scientist (qPCR) to join a growing biopharmaceutical organization pioneering gene therapies for rare genetic disorders. This onsite position in Exton, PA provides the opportunity to perform advanced molecular testing and DNA-based assays that directly support GMP manufacturing and product quality operations. Responsibilities of the Quality Control Analytical Scientist (qPCR): * Perform GMP-compliant qPCR testing to support bulk, drug substance, and final product analysis. * Conduct DNA extraction and assays including Vector Copy Number (VCN) and VSVG testing. * Support complementary methods such as cell culture, ELISA, and flow cytometry. * Review data for accuracy, integrity, and compliance with GMP and documentation standards. * Execute OOS investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, calibration schedules, and audit readiness. Qualifications of the Quality Control Analytical Scientist (qPCR): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong proficiency in qPCR methodology, DNA extraction, and molecular analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiarity with analytical platforms such as ELISA and flow cytometry. * Excellent attention to detail, communication, and documentation skills. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (qPCR): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 1/5/2026 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, qPCR, Vector Copy Number, VCN, DNA Extraction, VSVG, GMP, Biologics, Gene Therapy, Molecular Testing, Analytical Methods, Cell Culture, ELISA, Flow Cytometry, CAPA, SOP, Data Integrity, Aseptic Technique, ALCOA, Good Documentation Practices, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement. Our services are vast and we produce software and web products. We specialize in Mobile development, i.e. iPhone and Android apps. We use Objective C and Swift programming languages to create native applications for iPhone, whereas we use Android Code to develop native applications for Android devices. To create applications that work on cross-platforms, we use a number of frameworks such as Titanium, PhoneGap and JQuery mobile. Furthermore, we build web products and offer services such as web designing, layouts, responsive designing, graphic designing, web application development using frameworks based on model view controller architecture and content management system. Our services also extend to the domain of Cloud Computing, where we provide Salesforce CRM to effectively manage one's business and ease out all the operations by giving an easy platform. Apart from this, we also provide IT Staffing services that can help your organization to a great extent as you can hire highly skilled personnel's through us. We make sure that we deliver performance driven products that are optimally developed as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change. Job Description Title/ Designation: Software Quality Control Analyst Duration: 2+ Months Interview Type : In Person Only Location : Raleigh, NC 27607 Qualifications Selenium - Web Driver SOAP UI SQL, rational database, and understanding Data Model Experience on large-scale Web-based project Proficient in various Software Development Life Cycle (SDLC) methodologies Creation and maintenance of automated scripts All types of testing (performance, functional, usability, regression, load, web services, data creation, persistent layer verification, stress, etc.) Additional Information Thanks and Regards, Amrita Sharma 408 766 0000 EXT. 426 amrita.s@)360itpro.com

Vicor is seeking a Wet Chemistry Lab Technician to join 3rd shift operations Sunday - Thursday. This individual will work in the wet chemistry process lab to support all plating fabrication operations. The candidate will work with the wet chemistry lab team for day to day production analysis as well as special projects. Job Description * Perform basic chemical analysis techniques. * Utilize chemical analysis equipment to include Auto-Titration, CVS, ICP, and UV-VIS. * Ability to input analysis results into TrueChem. * Maintain lab safety policies and procedures. Education / Qualifications * 1+ years of prior laboratory experience required. * Experience with Titration analysis, ICP or AA, UV-VIS. * Knowledge of operation and maintenance of lab equipment highly desired. * Knowledge of Microsoft Word, Excel, and PowerPoint required. * Must pay high attention to detail, possess self-motivating skills, and have the ability to self-inspect for quality and accuracy. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status. Vicor is an EO employer - M/F/Veteran/Disability Compensation Data Salary Range: $22 - $25/hour Please note: This range is based on our current market driven pay structures. Individual salaries are determined based upon a variety of factors including but not limited to, a candidates overall qualifications, such as skills, education, and experience as well as company internal equity.

shijo KRG Technologies, Inc., ******************** 25000 Avenue Stanford, Suite #243, Valencia, CA 91355 Direct : ************ Ext : 203 Job Description Role: Sr. Paper Claims QC Analysts Location: Scottsdale, AZ • Review the scanned paper claims document and extracted information in an OCR application to ensure that there is no missing or incomplete information • Review couple of claims systems to identify the missing information and accurately capture the data/information necessary for processing • Correct the data elements extracted in OCR Application for self-learning where needed • Validate the claims that fall out while pre-load batch job into adjudication system, correct and re-load. Qualifications Review the scanned paper claims document and extracted information in an OCR application to ensure that there is no missing or incomplete information • Review couple of claims systems to identify the missing information and accurately capture the data/information necessary for processing • Correct the data elements extracted in OCR Application for self-learning where needed • Validate the claims that fall out while pre-load batch job into adjudication system, correct and re-load.

Piper Health & Sciences is seeking a full-time iPSC Production Scientist to join a growing organization's Bio/Engineering Production team onsite at their Massachusetts location. The ideal candidate will have a strong biology background and hands-on experience in iPSC stem cell culture, differentiation, and QC within a pharmaceutical or biotech environment. Responsibilities of the iPSC Production Scientist Include: * Full-time onsite schedule: Monday-Friday, 9:00 AM - 5:00 PM * Lead and support iPSC production and related lab activities * Perform hands-on stem cell culture and differentiation * Execute QC-related tasks in accordance with SOPs * Maintain accurate lab documentation and records * Support Bio/Engineering Production workflows * Follow all safety, GMP, and GLP standards Qualifications of the iPSC Production Scientist Include: * Biology degree is strongly preferred (Biomedical Engineering degrees are NOT a fit) * Proven hands-on experience with: * iPSC cell culture * Stem cell differentiation * Quality Control (QC) processes * Pharmaceutical or biotech industry experience preferred Compensation of the iPSC Production Scientist Includes: * Salary Range: $83,200.00 - $114,000.00 per year (equivalent to $40.00 - $55.00 per hour), based on experience and certifications. * Comprehensive Benefits: CIGNA Medical, Dental, Vision; 401k through ADP and sick leave as required by law. * Ability to work with a well renowned and growing organization that has a robust pipeline and quality culture. This job opens for applications on 1/12/2026. Applications for this job will be accepted for at least 30 days from the posting date. #LI-AW1 #LI-ONSITE keywords: Scientist, iPSC Production, stem cell culture, induced pluripotent stem cells, cell differentiation, quality control, QC, laboratory scientist, cell biology, biotechnology, pharmaceutical production, bioengineering, GMP, GLP, SOP compliance, tissue engineering, regenerative medicine, bioprocessing, cell therapy, stem cell research, lab operations, onsite scientist, Medford MA jobs, contract scientist, PhD biology, master's biology, postdoctoral research, biotech scientist, pharma scientist, cell culture specialist, stem cell specialist, iPSC scientist, QC scientist, bio production scientist, laboratory techniques, cell-based assays, biotech careers, pharma careers, stem cell manufacturing, cell culture workflows, life sciences jobs, biopharma jobs, laboratory compliance, scientific documentation, biotech industry experience, pharmaceutical industry experience, cell line development, research scientist, production scientist, laboratory QC, stem cell differentiation protocols, cell culture maintenance, full-time onsite scientist, bioengineering production team, regenerative biology, tissue culture, cell therapy manufacturing, biotechnology research, pharmaceutical QC, biomanufacturing, cell biology techniques, stem cell QC testing, scientific method, laboratory safety standards, GMP compliance, GLP compliance, biotech contract role, scientist contract position, iPSC culturing, stem cell production, biotech Medford MA, pharma Medford MA, scientific careers, laboratory scientist jobs, cell therapy scientist, bioprocess scientist, QC laboratory scientist, stem cell lab work, biotech production workflows, pharmaceutical production workflows, life sciences contract jobs, biotech contract scientist, pharma contract scientist.

360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement. Our services are vast and we produce software and web products. We specialize in Mobile development, i.e. iPhone and Android apps. We use Objective C and Swift programming languages to create native applications for iPhone, whereas we use Android Code to develop native applications for Android devices. To create applications that work on cross-platforms, we use a number of frameworks such as Titanium, PhoneGap and JQuery mobile. Furthermore, we build web products and offer services such as web designing, layouts, responsive designing, graphic designing, web application development using frameworks based on model view controller architecture and content management system. Our services also extend to the domain of Cloud Computing, where we provide Salesforce CRM to effectively manage one's business and ease out all the operations by giving an easy platform. Apart from this, we also provide IT Staffing services that can help your organization to a great extent as you can hire highly skilled personnel's through us. We make sure that we deliver performance driven products that are optimally developed as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change. Job Description • This role will report to the Manager of QC Microbiology for support of product testing area. The candidate will support release testing for commercial, clinical and PV products. The candidate will support a variety of GMP activities in the QCM laboratory area. Analyst will be assigned testing roles via QCM standard work process • Performs traditional microbiology testing (Bio burden, endotoxin) in support of commercial product release testing • Performs laboratory support functions such as review of data, maintenance of equipment and support of investigations • May act as delegate /representative for QCM area on cross functional teams for investigations and continuous improvement projects • Receives some supervision on routine work and instructions on new assignments. • Organizes daily activities to ensure timely completion of assignments. Receives direction from scheduling. Reports on missed tasks • Communicates straightforward • This position will interact with peers of same or higher level QCM management and may interact with QA Qualifications • BS in Microbiology preferred • 5-8 years in biopharmaceutical setting preferred. • Proficiency in aseptic technique • Endotoxin testing using Kinetic Methods • Bio burden testing using membrane filtration methods • Familiarity with general lab equipment • Knowledge of cGMP requirements • Must be able to perform lab bench testing Additional Information Thanks and Regards, Karan Sharma 510-254-3300 ext. 150

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.

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.

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.

Shift: 1st shift, Monday-Friday, Standard working hours Duration: 12 Months Pay range: $25.00 Hourly - $25.00 Hourly Onsite Job The Formulations Lab Wash Technician supports the manufacturing process by cleaning, sanitizing, and preparing lab equipment and materials used in buffer and reagent production. This role ensures all cleaning procedures meet cGMP and safety standards, playing a critical role in maintaining a clean and compliant lab environment. Key Responsibilities: •Clean and sanitize stainless steel tanks, glassware, utensils, and other lab equipment according to SOPs and cGMP requirements •Operate and maintain washers, autoclaves, and other sterilization equipment •Prepare tanks and materials for sterilization, including wrapping and loading/unloading from the autoclave •Assist in routine preventive maintenance and minor troubleshooting of washroom equipment •Transport clean equipment and materials to appropriate staging areas for use in production •Maintain accurate cleaning logs and documentation •Follow safety procedures when working with cleaning agents and potentially biohazardous materials •Notify supervisor of any damaged equipment, procedural deviations, or safety concerns •Maintain stock of cleaning supplies and request resupply as needed •Perform other duties as assigned Minimum Requirements / Qualifications: •High school diploma or equivalent required •Previous experience in a laboratory, pharmaceutical, or manufacturing environment preferred •Ability to follow written and verbal instructions precisely •Strong attention to detail and good documentation practices •Ability to lift up to 50 lbs and work on feet for extended periods •Comfortable working in a cleanroom or controlled lab environment Non-Negotiable Hiring Criteria: •Must comply with GMP, QSRs, ISO, and IVD regulations at all times •Ability to read, write, and understand English instructions •Basic math skills for measurements and inventory counts •Willingness to work in an environment with chemical and biological materials •Basic computer skills;familiarity with Microsoft Outlook and Excel preferred Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.