Chemist jobs in North Carolina

We are hiring Chemist - I. Please let me know if you are interested or anyone who might be interested. Client: Major Pharmaceutical Manufacturing Client Chemist - I Duration: 6+ months on W2 ONLY Pay Rate: $24.00-$25.00/ Hr ***LOOKING FOR ENTRY LEVEL GRADUATES WITH CHEMISTRY BACKGROUND*** __________________________________________________________________ DESCRIPTION: Work Location: Wilson - NC Onsite Job Summary Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Primary Responsibilities 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. Education and Experience Requirements The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred. Necessary Knowledge, Skills, and Abilities 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. Regards Vishnu Das Natesan ********************

Title: Sterility Assurance Scientist Duration: 6 Month Contract (potential of extension) Responsibilities: The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to sterility assurance contamination control strategies are established. Key Objectives/Deliverables • (Associate/Senior) Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level. • Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to: • Airflow Pattern Testing • Environmental Monitoring Performance Qualifications • Aseptic Process Simulations • Cleaning, Sanitization, and Disinfection • Gowning within GMP Classified Areas • Aseptic Processing Techniques • Contamination Control • Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies. • (Senior) Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program. • (Principal) Knowledge in pharmaceutical Microbiology, related to microbiological media, microbiological enumeration techniques, and microorganism isolation and identification. • (Principal) Lead/provide technical oversight for one or both the Environmental Monitoring (EM) or Aseptic Process Simulation (APS) program: • (EM) Authoring EM Performance Qualifications (EM PQ) and overseeing the execution. • (EM) Evaluating EM data and authoring EM Trend Reports. • (EM) Assist with identifying facility environmental isolates and how to create and maintain environmental isolated cultures. • (APS) Authoring APS protocols and overseeing the execution. • (APS) Evaluating the APS data, including personnel qualifications, and authoring APS reports. • (APS) Assist with tracking and tending APS to ensure all regulatory requirements and Global Quality Standards are met for each manufacturing line/process. • Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination. • Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements.• Lead or provide technical support for root cause investigations associated with sterility assurance programs. • Participate and/or provide technical sterility assurance support during internal and external audits. • Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs. • Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives. Basic Qualifications: • Bachelor's or master's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline. • Demonstrated understanding and relevant experience of scientific principles required for manufacturing parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. • (Senior) 2+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). • (Principal) 5+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). Additional Skills/Preferences: • Possess strong interpersonal skills to work cross-functionally within a team. • Possess strong self-management and organizational skills. • Possess strong oral and written communication skills for communicating to colleagues, management, and other departments. • Experience with data analysis and trending. • Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing warehouse, or laboratory areas. • Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Additional Information: • Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hours and / or off-hour work may be required. • Tasks may require repetitive motion and standing or walking for long periods of time. • Travel may be required during the project phase for training and implementation of sterility assurance programs. This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the . For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Job Title: Associate Specialist, QC Duration: 23 Months Pay Rate: $31/hr on W2 Shift: Monday - Friday 10:00 AM to 6:00 PM EST Education/Experience Requirements • Associate's degree in Biology, Microbiology, Biochemistry, or related field plus 1-2 years of relevant laboratory/pharmaceutical experience • Bachelor's degree in Biology, Microbiology, Biochemistry, or related field Required Experience and Skills • Understanding and application of Good Laboratory Practices and cGMPs • Aseptic technique • Performance of environmental and water systems monitoring • Working in a team environment Preferred Experience and Skills • Strong verbal and written communication skills • Experience with LIMS, SAP or other laboratory/production software systems Working Relationships • Reports to Quality Control manager • Interacts with employees within own department and other departments Additional Information Our Quality group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe. The main function of the Associate Specialist, Quality Control is to assist in the assurance of the quality of product through the performance of microbiological, chemical and analytical sampling and assays as well as interacting with Production, Quality Assurance, Validation and Facilities, and external resources, as necessary to support Manufacturing. Responsibilities General • Conducts release testing in support of finished product • Conducts microbiological testing; evaluation of environmental microbiological samples • Conducts environmental monitoring sampling to include active air and surface sampling and water sampling • Evaluates data, conducts trouble shooting, process improvements, report writing, involvement in interdepartmental committees and projects • Maintains lab materials and reagents Business & Functional Expertise • Completes assignments in alignment with department objectives • Conducting In-Process and Release testing • Conducting Environmental Monitoring of processes and on a routine basis Problem Solving o Identifies and resolves technical and operational problems in collaboration with colleagues and under guidance from department head Impact Influence o Communicates information, asks questions and checks for understanding Accountability o Accountable for own performance Decision Making o Makes decisions - guided by policies and procedures - on the shop floor o Consults on an as-needed basis with next-level manager on more complex decisions and/or issues that impact other units with inter-related processes

R&D Partners is seeking to hire a Quality Control Analyst in Holly Springs, NC. Your main responsibilities as a Quality Control Analyst: Performs testing and associated tasks without errors per applicable SOPs and protocols within Immunology/Biochemistry function. Properly documents test results in appropriates records and computer systems Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written. Participates in lean lab operation, 6S laboratory layout, preventive action & continuous improvement programs to reduce operating costs. Participates and performs in cross-training to support staff availability within QC department. What we are looking for in a Quality Control Analyst: Bachelor's degree (Biochemistry preferred, recent graduates ok) 1+ years of laboratory experience (ok if degree related) Knowledge of analytical methods and related instrumentation (ok if academic) Must already have or be willing to get a flu shot 1+ years of GMPs safety regulations and data integrity is preferred Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance - PPO, HMO & Dental & Vision insurance 401k plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval Pay Scale: $52,000 - $62,400 Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - ******************************************* Desired Skills and Experience BS Biochemistry, or related. Knowledge of analytical methods and instrumentation, ELISA, BCA, SRID, SDS-PAGE

Essential Responsibilities · Perform dose formulation analysis in support of GLP Toxicology assays · Perform method validations for HPLC and correlating stability studies for analysis of test articles or other chemicals. · Setup, maintenance and daily operation of HPLC system and related equipment. · Aid in the writing and editing of analytical and formulation sections within protocols and reports. · Prepare reagents, vehicles, solutions and suspensions following applicable SOPs, Protocols, and GLPs. · Receipt of controlled and non-controlled chemicals · Assures proper labeling, handling, and storage of all chemicals. · Maintain up-to-date chemical inventory · Perform solubility testing · Perform dose formulation calculations and preparations · Ensure chemical disposal is handled per local, state, and federal regulations · Communicate with Study Directors, Program Managers, and analytical labs to ensure adherence to study protocols Additional Responsibilities · Prepare dose formulations for in vitro and in vivo experiments as needed · Training of junior staff as needed. · Work in a team environment with a professional and positive attitude · Other duties as needed Minimum Acceptable Qualifications · Education: o B.S. in chemistry or related field · Experience: o Two years' experience in a GLP scientific environment · Skills: o Ability to perform basic unit conversion calculations o Experience working under GLP or regulatory requirements o Ability to use, troubleshoot, and maintain standard chromatography laboratory equipment. o Excellent written and oral communication skills o Excellent computer skills working with MS Word/Excel/Powerpoint o Attention to detail o Excellent organizational skills o Ability to exercise independent judgment *This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Are you an experienced Medical Lab Professional? Are you looking to looking to embark on a new challenge in your career? If so, LabCorp wants to speak with you about exciting opportunities to join our Mass Spectrometry team as an Associate Chemist in Burlington, NC! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at Labcorp: “Improving Health, Improving Lives”. Work schedule: 2nd shift, Thursday-Sunday, 1:00pm-11:30pm. Position is eligible for 10% shift differential due to 2nd shift hours. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Job Duties/ Responsibilities: Review and certify LC/MS data from instruments utilizing Analyst and Ascent software Determine if data is acceptable or not and then upload results Responsible for the verification of the calibration, quality controls, and patient data up to and including result entry Maintain, calibrate, and clean instrumentation; perform scheduled/routine maintenance and critical function checks on analytical equipment such as GC, GC-MS, HPLC, and UPLC-MS/MS as well as other chromatographic and laboratory equipment Diagnose and repair issues occurring in the above listed equipment; recognize significant changes in instrument function; troubleshoot as indicated. Gains knowledge of department operations and procedures under direct supervision and in an entry level capacity Conducts qualitative and quantitative analyses on organic and inorganic samples to determine their chemical properties. Participates in development of new analytical procedures Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures Demonstrate the ability to make technical decisions regarding testing and problem solving Evaluate raw and final data for accuracy; recognize and correct errors or unusual results Provide guidance to technical staff with the analysis and interpretation of final results Assist with training and orientation of new employees as needed Perform and document preventive maintenance and quality control procedures Identify and replenish testing bench supplies as necessary Requirements: Bachelor's degree in chemical or Biological science, Clinical Laboratory science, Medical Technology or meet regulatory (CLIA & State) requirements Minimum 2+ years of clinical laboratory testing experience is required for Associate Chemist level Experience with Chromatographic Data Review preferred but not required Demonstrated success in clinical testing technical proficiency and scientific knowledge Advanced knowledge and understanding of specific laboratory and/or department functions Ability to exercise judgment to determine methods and procedures on new assignments Proficient with computers and familiarity with laboratory information systems High level of attention detail along with strong communication and organizational skills Ability to work independently and within a team environment Must be able to pass a standardized color vision screen Flexibility to work overtime or other shifts depending on business needs If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today! Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

As we create a colorful, capable and cleaner world through chemistry, we invite you to join our team to harness the power of chemistry to shape markets, redefine industries and improve lives for billions of people around the world. CREATING ESSENTIAL CHEMISTRY THAT THE WORLD NEEDS At Chemours, our people are redefining how the world thinks of chemistry by approaching everything we do with a commitment to delivering Trusted Chemistry that creates better lives and helps communities thrive. That begins with how we use our science, data, and unmatched technical expertise to develop market-leading products with the highest levels of performance, sustainability, and safety in the industry. Powered by chemistry, our products are used in applications that make the products we rely on, processes, and new technologies possible. In key sectors such as clean energy, advanced electronics, high-performance computing and AI, climate friendly cooling, and high-quality paints and coatings for homes and industrial infrastructure---sustainable solutions and more modern living depend on Chemours chemistry. The Chemours Company headquartered in Wilmington, DE has a Chemist position available in Fayetteville, NC. This is a highly visible, key role within Chemours and the Advanced Performance Materials Business. This position is in the Monomers Manufacturing Technology team and will report to the Manufacturing Technology Manager. The work will primarily involve providing day-to-day support to the lab facilities by providing guidance to the lab technicians in maintaining accurate analytical methods and results as well as troubleshooting operating problems with the lab equipment. The individual will be involved in the implementation of new analytical equipment and the development of new analytical methods, as the need arises. The responsibilities of the position include, but are not limited to, the following: Providing technical support of the analytical instruments used for routine analysis in the Monomers manufacturing quality control and customer service labs, including creation of standards, validation of results, and troubleshooting lab equipment failures Support PSM, EHS, as well as continuous improvement efforts. Participate in and lead Internal Quality audits to maintain the plant's ISO 9000 certification. Routine monitoring of quality data from the lab to look for abnormal results and determine the reason (process upset, equipment failure, sample cross contamination, etc.). Routine monitoring of analytical methods to ensure consistency and statistical accuracy via techniques such as Gage R&R analysis. Initiate and/or review changes to improve the safety, accuracy, consistency, or cycle time of the various lab methods in operation. Selection of new analytical equipment and development of new methods in support of the manufacturing processes as needed. Development of new analytical methods in support of new specifications or targets in the manufacturing processes Improve reliability of lab instrumentation by implementing new methods using alternative equipment Analysis of non-routine samples to assist with troubleshooting of manufacturing problems or in conjunction with manufacturing plant tests / product trials. In order to be qualified for this role, you must possess the following: At least a Bachelor's degree in Chemistry or related fields At least 3 years of experience providing technical support for lab technicians in an analytical setting; equivalent related experience will be considered Knowledge of an array of analytical instruments including, but not limited to: Gas Chromatography Liquid Chromatography Mass Spectroscopy Raman Spectroscopy FTIR (across variety of samples - solids and liquids) Wet chemistry (pH, ion selective electrode, titration, etc.) ICP Analysis Knowledge of NMR spectroscopy a plus The following skill sets are preferred by the business unit: Experience with handling and preparation of standards containing highly toxic liquids and liquefied gases Experience using statistical tools such as Minitab. Experience using lab software (LIMS) and other chromatography data software (Atlas and Chromeleon) Familiarity with fluorine chemistry Six Sigma certified as Green Belt Process Safety Management (PSM) experience Benefits: Competitive Compensation Comprehensive Benefits Packages 401(k) Match Employee Stock Purchase Program Tuition Reimbursement Commuter Benefits Learning and Development Opportunities Strong Inclusion and Diversity Initiatives Company-paid Volunteer Day We're a different kind of chemistry company because we see our people as our biggest assets. Instead of focusing just on what our employees do each day, we look at how they do it-by taking a different approach to talent development, employee engagement, and culture. Our goal is to empower employees to be their best selves, at Chemours and in life. Learn more about Chemours and our culture by visiting Chemours.com/careers. Chemours is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, race, religion, color, gender, disability, national or ethnic origin, ancestry, marital status, family status, sexual orientation, gender identity or expression, or veteran status. Jurisdictions may have additional grounds for non-discrimination, and we comply with all applicable laws. Chemours is an E-Verify employer Candidates must be able to perform all duties listed with or without accommodation Immigration sponsorship (i.e., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant status) is not currently available for this position In our pursuit to be the greatest place to work, we know that a critical element to enhancing our employee experience is to assure we're operating with a solid foundation of trust. At Chemours, this means being transparent about how we pay our employees for the work that they do. Pay Range (in local currency): $93,184.00 - $145,600.00 Chemours Level: 25 Annual Bonus Target: 8% The pay range and incentives listed above is a general guideline based on the primary location of this job only and not a guarantee of total compensation. Factors considered in extending a compensation offer include (but are not limited to) responsibilities of the job, experience, knowledge, skills, and abilities, as well as internal equity, and alignment with market data. The incentive pay is dependent on business results and individual performance and subject to the terms and conditions of the specific plans. At Chemours, you will find sustainability in our vision, our business and your future. If you want to work on the leading edge of your field and have a desire to make a difference, join Chemours and discover what it means when we say "We Are Living Chemistry."

Analytical Chemist - Urgent Need Duration : 12 Months Total Hours/week : 40.00 1 st Shift Client: Medical Device Company Job Category: Research & Development Level of Experience: Entry Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Job Description: This position will function within the Chemical Sciences Unit of Corporate Preclinical Development & Toxicology (CPDT) and will participate in/support the conduct of nonclinical laboratory investigations of medical devices and materials in accordance with GLP regulations and the client CPDT Quality System. The incumbent will be responsible for analytical chemistry testing on medical devices and materials in an ISO 17025 certified lab that performs biocompatibility and chemical testing as required by FDA for medical devices and/or therapeutics and in compliance with ISO 10993. Responsibilities: Conducts non-routine analytical chemistry studies utilizing GC/MS, LC/MS, ICP and other instrumental methods to characterize and identify unknown extractable and leachable compounds in sample extracts. Performs sample preparation, sample extraction and analyses. Performs qualitative and quantitative analyses. Operates chemical instrumentation including GC, LC, ICP, IC, GC/MS, LC/MS, pH, UV/VIS. Records raw data according to GLP documentation requirements. Interprets results and prepares technical reports on completed studies. Prepares chemical reagents and solutions needed for testing. Develops and validates new analytical methods. Maintains a safe chemical laboratory environment. Performs other technical writing functions as requested. Performs duties required for the metrology program in BM RAM as well as manage the schedule, vendors, and unexpected events Qualifications: Typically requires a minimum of a BS Degree in Chemistry or related field. 0-2 years minimum relevant experience or a combination of equivalent education and relevant experience. B.S. degree in Chemistry or related field preferred. Higher level degrees and/or experience may also be considered. Must be well organized and detail oriented. Must be able to multitask and operate effectively within a diverse work environment. Must be team oriented and have strong interpersonal skills. Must have excellent written and verbal communication skills. A working knowledge of computers (including software such as Word, Excel, Access, PowerPoint, SharePoint) is required.

LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada. Title: QC Chemist Location: Rocky Mount, NC Duration: 18 Months Job Description: The CQ Lab Analyst I, will perform basic analysis for raw materials, in process and/or finished products in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. • Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified. • Follows procedures at all times, adopting cGMP, cGDP practices. • Follows supervisor directions at all times. • Able to function independently, but asks questions as necessary • Accepts dynamic work sequences • Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed • Consistently communicates work sequence status to supervisor in a timely manner. • Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement. • Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals. • When faced with roadblocks and issues, routinely offers suggestions for improvements • Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift wherever possible. • Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter Additional Information Regards, Anuj Mehta ************

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description: The CQ Lab Analyst I, will perform basic analysis for raw materials, in process and/or finished products in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. • Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified. • Follows procedures at all times, adopting cGMP, cGDP practices. • Follows supervisor directions at all times. • Able to function independently, but asks questions as necessary • Accepts dynamic work sequences • Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed • Consistently communicates work sequence status to supervisor in a timely manner. • Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement. • Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals. • When faced with roadblocks and issues, routinely offers suggestions for improvements • Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift wherever possible. • Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter Education experience required: BS/MS in Chemistry or BS Science Degree, 0-2 years of experience Qualifications Education experience required: BS/MS in Chemistry or BS Science Degree, 0-2 years of experience Additional Information All your information will be kept confidential according to EEO guidelines.

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

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

Job Description - The Quality Control Raw Materials Chemist III ensures that testing, data review, and documentation is compliant with GMP regulations, internal procedures, and applicable compendial requirements. The position will be operating within a GMP environment for a Quality Control CDMO. The ideal candidate will additionally possess superior communication skills, presenting to internal and potentially external clients Essential Functions Perform testing of raw materials, packaging components, and other samples. Author or act as author for lab investigations, analytical testing methods, deviations, protocols and SOPs for raw materials and raw material instrumentation. Provide technical support to the laboratory for method and instrument troubleshooting as needed. Lead the Raw Materials laboratory implementation project by overseeing installation, qualification, and training on new instruments and techniques. Provide training for other analysts for raw materials testing Schedule the QC laboratory Raw Materials workload appropriately to meet manufacturing release testing schedules and timelines. Monitor weekly laboratory and data review activities for accuracy and track hours needed for completion of tasks. Oversight for review of QC Raw Material data for compliance with specifications and regulatory requirements Interact with third party laboratories for any microbial and analytical testing of raw materials Generate and/or review shipping paperwork for third party testing and prepare samples for shipment. Create purchase requisitions for lab supplies and third-party testing Perform weekly laboratory audit inspections Perform sampling of raw materials as needed Review third party laboratory investigations and protocols. Other duties as assigned Powered by JazzHR IhEoyEcRDL

Job Description: Provides analytical support to client groups. Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes early stage prototypes, lab samples, pilot plant samples, production samples, stability samples and competitor samples. Possesses extensive knowledge of various laboratory instruments like HPLC, GC, AA, Dissolution, IC, etc. Years of Experience 0-3. Qualifications What will the resource be working with, or, have exposure to?: Biohazardous Agent work (such as menigiditis, staph aureus, Lenti Virus, streph pneumoniae) Neisseria meningitidis serogroup A,C, Y,W Staph aureus Strep Pneumoniae Additional Comments Regarding Surveillance / Clearance: Potential exposure to Tetnus Toxin. Minimal risk of exposure, but some fermentation samples potentially have active cells and/or toxin present. Will the Resource be working with or in support of government reimbursed products?: No - government reimbursements Please list out the (up to) top 3 critical skills: analytical chemistry Precision pipetting technique Data integrity management using laboratory notebook Will overtime be needed?: No If Yes, how many hours of overtime (on average) per week?: Will you consider Veteran candidates?: Yes How many years experience are required?: 0-2 years What is the minimum education experience required?: BS Chemistry, Biochemistry, Microbiology, Biology, or similar Additional Information All your information will be kept confidential according to EEO guidelines.

Codetta Bio is a venture-backed life sciences company with innovative solutions to some of the most significant challenges in the life sciences and healthcare industries. We are developing advanced multi-omic biomarker measurement tools supporting data-driven approaches to understanding the unique genetic, environmental, lifestyle, and clinical factors that contribute to individual health and wellness. Guided by an experienced leadership team, Codetta offers a high-energy, collaborative work environment with opportunities for professional advancement. The ideal candidate will be self-motivated, organized with excellent communication skills, as well as excellent writing skills. As this position relies heavily on working with a cross-functional team, time flexibility is important. The candidate must be comfortable in a fast-paced environment where everyone holds each other accountable and have the flexibility to meet during normal work hours and alternative hours as needed. Major Responsibilities: Responsible for manufacturing key bead-based reagents for Codetta Bio product lines Works with cross-function team to develop, qualify and validate methods to support reagent characterization and product release Optimizes reagent manufacture methods and contributes to improvement of process efficiency Responsible for maintaining appropriate documentation, including Batch Records, compliant with ISO9001 and GMP regulations electronically, and via paper record, as indicated Supports final product quality control Present data at regular meetings and contribute to scientific publications Occasional evening or weekend work when Required Qualifications: BS, or MS in chemistry, biochemistry, chemical engineering or related field 2 years experience working in biological reagent manufacturing, preferably in industry Direct experience with buffer formulation, general lab techniques (pipetting, use of pH meter, analytical balances, volumetric glassware), preferably in industry Direct experience with conjugation of protein and nucleic acids as well as surface (bead or other assay solid support) functionalization methods Exceptional organization skills and attention to detail Ability to work independently and manage time effectively Excellent written and verbal communication skills Collaborative and team-oriented Preferred Qualifications: Demonstrated knowledge and understanding of GMP, QA and QC functions associated with the manufacturing of assay-related products and compliance with ISO 9001 or similar. BSL-2 laboratory experience Direct experience with conjugation of protein and nucleic acids as well as surface (bead or other assay solid support) functionalization methods Direct experience with PCR and immunoassay methods and instruments Direct experience with ELNs, Benchling or similar Additional Information At this time, we are unable to sponsor visas for this position. All applicants must be authorized to work in the United States without company sponsorship. Work Location: On-site in Morrisville, NC

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Analytical Chemist needs 2 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry Analytical Chemist requires: BS/BA Degree in Science/related field with experience in biotech or pharmaceutical industry Experience in the biotech or pharmaceutical industry Analytical Chemistry and/or Microbiology techniques and instrumentation, Laboratory Information Management System (LIMS), Microsoft Office™ applications specifically Word and Excel Analytical Chemist responsibilities include: Performs tasks associated with maintaining GMP compliant Quality Control and Stability laboratories with a specific focus on Performs testing including, but not limited to clinical and/or commercial standards/controls/critical reagents, product, raw materials and validation samples. Additional Information $26HR 6 Months

Essential Responsibilities * Perform dose formulation analysis in support of GLP Toxicology assays * Perform method validations for HPLC and correlating stability studies for analysis of test articles or other chemicals. * Setup, maintenance and daily operation of HPLC system and related equipment. * Aid in the writing and editing of analytical and formulation sections within protocols and reports. * Prepare reagents, vehicles, solutions and suspensions following applicable SOPs, Protocols, and GLPs. * Receipt of controlled and non-controlled chemicals * Assures proper labeling, handling, and storage of all chemicals. * Maintain up-to-date chemical inventory * Perform solubility testing * Perform dose formulation calculations and preparations * Ensure chemical disposal is handled per local, state, and federal regulations * Communicate with Study Directors, Program Managers, and analytical labs to ensure adherence to study protocols Additional Responsibilities * Prepare dose formulations for in vitro and in vivo experiments as needed * Training of junior staff as needed. * Work in a team environment with a professional and positive attitude * Other duties as needed Minimum Acceptable Qualifications * Education: o B.S. in chemistry or related field * Experience: o Two years' experience in a GLP scientific environment * Skills: o Ability to perform basic unit conversion calculations o Experience working under GLP or regulatory requirements o Ability to use, troubleshoot, and maintain standard chromatography laboratory equipment. o Excellent written and oral communication skills o Excellent computer skills working with MS Word/Excel/Powerpoint o Attention to detail o Excellent organizational skills o Ability to exercise independent judgment * This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada. Title: QC Chemist Location: Rocky Mount, NC Duration: 18 Months Job Description: The CQ Lab Analyst I, will perform basic analysis for raw materials, in process and/or finished products in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. • Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified. • Follows procedures at all times, adopting cGMP, cGDP practices. • Follows supervisor directions at all times. • Able to function independently, but asks questions as necessary • Accepts dynamic work sequences • Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed • Consistently communicates work sequence status to supervisor in a timely manner. • Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement. • Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals. • When faced with roadblocks and issues, routinely offers suggestions for improvements • Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift wherever possible. • Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter Additional Information Regards, Anuj Mehta ************

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