Chemist jobs in Rocky Mount, NC

We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.** **Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement **Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline + **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience + **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience **Responsibilities** + Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation + Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships + Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities + Participate in computer system validation activities associated with new or upgraded equipment or software packages + Support the purchase, installation, and equipment qualification of new laboratory equipment + Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support + Originate and progress Notice of Event (NOE) and Change Management (CM) records + Perform and document investigations and assist in developing/implementing CAPA plans + Represent the laboratory on all aspects of laboratory equipment during audits + Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures **Required Skills and Experience** + Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system validation requirements + Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks + Capable of working independently under moderate supervision + Strong verbal and written communication skills + Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators **Desired Skills and Experience** + Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them. + Experience with computerized standalone systems GMP validation requirements + Familiarity with authoring relevant instrument standard operating procedures (SOPs) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Job Description Chemist - North Carolina as a Chemist with a well-known chemical manufacturer? Essential Duties and Responsibilities: Prepare and apply formulations to customer substrates using various methods (e.g., spray, gravure, dip/nip). Test finished parts for physical properties, color, aesthetics, and flammability. Modify existing formulations, simulate customer parts, and scale up production as needed. Collaborate with cross-functional teams globally to support chemistry development. Present findings to Technical Sales, Customers, internal R&D, and Applications. Education and Experience: Bachelor's Degree in Chemistry, Chemical Engineering, Plastic Engineering, Mechanical Engineering, or a related field. Less than 3 years of industrial experience, with a focus on coatings formulation, color matching, processing, quality control, and technical service. Additional Requirements: Must be eligible to work in the US.

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 ************

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.

Perform a variety of analytical laboratory testing of raw material, processed material and finished products and assure compliance with applicable laws, rules and regulations. Major Job Duties: Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality. Qualifications: Essential Skills- 0-3 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques. Perform a variety of laboratory testing. Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others. Must be able to read, write, speak and understand fluent English. Strong understanding of GMP concepts and requirements. Able to demonstrate accuracy and thoroughness while completing work in a timely manner. Follows instructions, policies, and procedures. Non-Essential Skills - Operate, maintain and repair equipment required to perform related duties. Observe health and safety regulations. Education Requirements: Bachelors of Science degree in chemistry or closely related field. Physical Demands: While performing the duties of this job, the employee is frequently required to stand and use hands to finger, handle, or feel. The employee is occasionally required to walk; sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. The employee is occasionally exposed to moving mechanical parts or airborne particles. The noise level in the work environment is usually moderate. These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of this job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of this job What is the minimum education experience required? Bachelors in Chemistry (preferred) or Science, 0-2 years of Pharmaceutical 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 Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Role Overview Complete Technology Transfer activities by performing manufacturing process development for Injectables products to commercial lines. Using experimental design, establish formulation processes, product pathway and select components for successful scaleup. Support client calls, prepare necessary documentation (including but not limited to work orders, protocols, summaries, with minimum supervision), and provides scientific justification as needed and update status of project work. Discover Impactful Work! Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. Leads technical/scientific process/product/project activities to implement strategies and technical solutions. Drives creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. Makes decisions that involve direct application of technical knowledge. A Day in the Life. Design, implement, and evaluate studies, lead tech transfer, commercial scale-up and support process validation. Represent the organization on formal technical and scientific forums. Lead and/or participate in problem solving and project work for formulations, equipment and processes. Write/revise work orders for new processes, FORMs, reports, memos, and protocols as required. Independently manage projects, proficient in evaluating and organizing all technical aspects of the project to achieve necessary landmarks and turning points. Support manufacturing operations, change controls, investigations as subject matter expert (SME), resolve accurate CAPAs. Assess material changes and determine change impact. Support development of proposals and timelines for projects, leading relevant client meetings. Review new bid quotes, protocols, technical documents, results, and reports. Keys to Success Education: Bachelor's of Science in Chemistry, Biochemistry, Biology, Pharmaceutical or related physical science. Experience: Bachelors and 3+ years confirmed experience CMO or Pharmaceutical product development experience PREFERRED Equivalency: Equivalent combinations of education, training, and meaningful work experience may be considered. Knowledge, Skills, Abilities: Advanced knowledge of variety of aspects of a subject area and working knowledge of principles and concepts in other relevant technical subject areas. Excellent knowledge of scientific methodology and development as related to the pharmaceutical industry. Detailed knowledge of Good Manufacturing Practices. Strong proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint). Excellent critical and logical thinking skills. Effective written, interpersonal, and presentation skills, including leading technical discussions with internal and external clients. Ability to work on multiple projects simultaneously. Proficiency at developing knowledge and skills in pharmaceutical processes, equipment, instrumentation, and procedures. Capability to keep current with scientific literature and industry trends relating to process technologies. Ability to develop technical solutions. Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand and walk; ability to lift and/or carry light objects of up to 25 lbs. for brief periods.

We are seeking a dynamic and forward-thinking food scientist who can bring their technical expertise to the table and play a vital role in developing and refining formulations for our current and future products. As a valued member of our project teams, you will have the opportunity to channel your creativity and innovation to bring new products to life, from initial concept to market launch. With your invaluable contributions, we will unlock the full potential of our brand and enhance the nutritional quality, taste, and texture of our food products. Stay ahead of the curve by exploring new advancements and driving product innovation in partnership with our company. To thrive in this role, you must possess the ability to interpret and apply scientific findings to the world of food, converting them into groundbreaking product concepts. Additionally, a firm grasp of business objectives is crucial for translating them into clear project goals. Excitingly, we are looking for individuals who are team players and share our unwavering passion for product development. Our Food Scientist is responsible for developing, testing, and maintaining high-quality food products that meet company standards, regulatory requirements, and customer expectations. This role involves hands-on product tasting, analytical testing, and collaboration across departments to ensure consistency, safety, and innovation in all products produced by the facility. Key Responsibilities Product Development & Research Conduct research and development (R&D) for new product formulations, line extensions, and process improvements. Experiment with ingredient functionality, flavor profiles, textures, and stability to achieve desired product characteristics. Maintain accurate records of formulations, processing parameters, and sensory evaluations. Evaluate and approve raw materials and new ingredient suppliers based on quality, performance, and compliance standards. Liaising with relevant stakeholders to address concerns about food quality and safety. Utilizing advanced formulation software to create and maintain formulations. Playing a pivotal role in bringing new products to life, from conceptualization to successful launch. Coordinating the arrangement and shipment of sales samples. Updating product information sheets and labels for effective sales presentation. Accurately recording, analyzing, and summarizing research data for informed decision-making. Collaborating with independent laboratories for comprehensive testing. Maintaining the MRP system by keeping it up to date and accurate. Ensuring strict compliance with GMP and other safety regulations. Performing any additional duties assigned by the supervisor. Product Tasting & Evaluation Taste and evaluate all products during development and production for flavor accuracy, consistency, texture, and appearance. Lead sensory panels and coordinate tasting sessions with internal staff and customers as needed. Document results and recommend adjustments to formulations or processes based on sensory and analytical data. Analytical Testing & Data Review Prepare, perform, and review all analytical testing and quality data, including but not limited too, pH, Brix, viscosity, color, moisture, and microbiological analysis. Ensure testing equipment is properly calibrated and maintained for accuracy and reliability. Analyze test results to identify trends or deviations and recommend corrective actions when necessary. Prepare technical reports summarizing findings for management and customer review. Customer Collaboration Work one-on-one with customers to establish and refine recipe standards that align with their brand and quality expectations. Translate customer requirements into production-ready formulas while ensuring cost efficiency and manufacturability. Participate in customer tastings, product trials, and formulation meetings to ensure satisfaction and consistency. Cross-Department Coordination Collaborate closely with the Customer Success Department to address customer feedback, troubleshoot issues, and develop improvement plans. Partner with Cook Room and Bottle Room Associates to ensure recipes are prepared, cooked, and packaged according to approved standards. Provide technical guidance to production staff during scale-up, batching, and process trials. Assist the Quality Assurance team in developing and implementing product specifications, SOPs, and regulatory documentation. Regulatory & Documentation Ensure all product formulations and processes comply with FDA, SQF, GMP and other company compliance regulations, as well as applicable food safety regulations. Maintain up-to-date records of all formulations, test results, and production data in accordance with company documentation standards. Support the preparation of product labels, ingredient statements, and nutritional facts panels. Qualifications Bachelor's degree in Food Science, Food Technology, Chemistry, or related field required; Master's degree preferred. Minimum 3-5 years of experience in food product development, manufacturing, or quality assurance. Strong knowledge of food chemistry, microbiology, sensory science, and process engineering. Hands-on experience with analytical testing equipment and sensory evaluation. Excellent communication skills and ability to collaborate with cross-functional teams. Strong organizational and data analysis skills with attention to detail. Knowledge of FDA, SQF regulations, HACCP, Acid/Acidified, PCQI and GMP standards. Working Conditions On-site position within a food manufacturing environment. Requires daily tasting and sensory evaluation of products. Involves working in production areas (Cook Room, Bottle Room, all GMP zones) and laboratory settings. Occasional customer visits or off-site product demonstrations may be required. Physical Requirements Ability to stand for extended periods in production areas. Must be able to safely handle ingredients, lab equipment, and small production tools. Capable of lifting up to 25 lbs. BENEFITS: Experience a diverse range of comprehensive benefits, including medical, vision, and dental coverage. Take time away from work and recharge with generous paid time off and "dream" days off. Participate in exciting company events that foster camaraderie and team spirit.

Job Title: Quality/Validation Engineer III / Laboratory Instrument Validation Duration: 09 months contract, extendable up to 18 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. : The Quality Engineer III - Instrument Validation will be responsible for: Serving as validation representative for instruments Partnering with the laboratories, quality system administrators, BT, instrumentation and quality on implementing new instruments at the site Performing analytical instrument validation including computerized system validation if applicable Performing any validation change control during the life-cycle of the system Performing system periodic review Performing system decommissioning This position will be responsible for providing end-user support for all Quality Laboratory groups as well as compliance to global and site internal policies and procedures. ROLE RESPONSIBILITIES Initiates and leads change control for implementation of new instruments or changes to existing analytical instrumentation and associated instrument control software where applicable in Quality Control laboratories. Authors cGMP risk assessments, user requirements & functional specifications, validation plans, protocols (i.e. IQ, OQ, PQ), reports, addendums and other validation deliverables as required by the site validation SOPs. Assist the system owner with evaluating recommending the appropriate user roles and privileges for data integrity (where applicable), writing instrument operation instructions and preventive maintenance plans. Ensures lab instrument's adherence to national and international regulatory guidelines on Electronic Records and Electronic Signatures and Data Integrity, cGMP, FDA 21 CFR Part 11/210/211, EU Annex 11, MHRA guidelines. Authors protocol to challenge the main aspects of these requirements during validation to demonstrate adherence. For systems found unable to fully comply, formulate workarounds/strategies with core stake holders to mitigate the gaps. Initiates and leads risk assessment, gap analysis, and deviation management associated with validation of lab instruments. Completes periodic reviews of instruments and instrument control software with focus on change control, deviation investigations, and CAPA to ensure compliance and validated state of the instrument. Previous experience with PR/CAPA systems preferred. Reviews validation deliverables created by others for adherence to site validation SOPs and acts as validation approver as needed. All other duties as assigned. QUALIFICATIONS Bachelor's degree in a science or engineering related discipline with knowledge in quality operations laboratory processes. 5-7 years of experience in the validation of laboratory instruments including those with computerized systems attached in a cGMP environment (required). 5-7 years of experience in the Pharmaceutical industry or relevant business experience within Quality Assurance or Validation cGMP Compliance. Hands on experience operating instrument systems. Demonstrated attention to detail. Good oral and legible written communication skills. Must be able to work independently. Mastery of core computer software/systems (Word, Excel, Sharepoint, etc.). Demonstrated ability to work in a team environment and manage workload to meet deadlines. Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form. PHYSICAL/MENTAL REQUIREMENTS (not all roles will have physical or mental requirements) Use a computer terminal for up to 8 hours per shift, occasionally lift a maximum of 5 pounds per activity 4 times per shift, work around moving equipment, work with biological materials. Occasionally lift a computer system and/or instrument up to 50 pounds. Stand for up to 8 hours, sit for up to 8 hours, walking, climbing stairs, responding to visual warning indicators, respond to audible warning indicators, respond to color or special visual indicators, wear specialized protective. Mathematical and scientific reasoning ability. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS May be required to work non-standard hours including weekends and holidays to support laboratory processes at the Rocky Mount site. Some gowning may be required to enter laboratory areas. Work safely in laboratory areas where biological and chemical hazards are present. ORGANIZATIONAL RELATIONSHIPS Position interacts with laboratories within the Quality unit and impacts their compliance and continuous improvement. Other functions key to the instrument validation process include Laboratory System Administrators, Calibration and Documentation. Position Comments visible to MSP and Supplier: Other Considerations: 1. The official job description of the candidate is Quality Engineer III - Laboratory Instrument Validation. 2. If the candidate has less than the required 5-7 years of experience in the validation of laboratory instruments, will consider the candidate for Quality Engineer II 3. Please post this position in an area geared for the laboratory. 4. In Appendix B, CANDIDATE SCREENING - RESUME COVERSHEET, it would be helpful if the vendors would include the information for at least the 4 skills identified below in addition to anything else they want to add/highlight. Additional Information Anuj Mehta ************

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

At DraftKings, AI is becoming an integral part of both our present and future, powering how work gets done today, guiding smarter decisions, and sparking bold ideas. It's transforming how we enhance customer experiences, streamline operations, and unlock new possibilities. Our teams are energized by innovation and readily embrace emerging technology. We're not waiting for the future to arrive. We're shaping it, one bold step at a time. To those who see AI as a driver of progress, come build the future together. The Crown Is Yours As an Associate Quality Control Analyst, you'll be part of a team of passionate individuals dedicated to the sports industry and data collection, focused on maintaining accuracy and integrity in fast-paced, high-intensity environments. In this role, you'll monitor and verify the accuracy of data feeds related to college and professional sports, providing support to our data collection scouts. Your work will play a critical role in ensuring the reliability of our sports data, supporting our organization's operations and decision-making processes, all while fostering continuous improvement and personal growth. What you'll do as an Associate Quality Control Analyst * Monitor and ensure the accuracy and consistency of real-time data feeds for college and professional sports. * Identify, report, and resolve discrepancies or errors in sports data promptly by verifying data consistency across multiple sources and platforms. * Collaborate with technical teams to troubleshoot and communicate in real-time with internal teams to address and resolve data feed issues. * Stay up-to-date with sports schedules, team rosters, and key statistics. * Provide feedback on scout performance and identify areas for improvement. What you'll bring * Strong passion and in-depth knowledge of college and professional sports (e.g., schedules, teams, players, and statistics). * Exceptional attention to detail with the ability to work quickly and accurately under tight deadlines while using strong analytical, troubleshooting, and problem solving skills. * Basic proficiency with data tools and platforms (e.g., Excel, Google Sheets, or database systems). * Ability to work independently while maintaining effective team communication. * Experience in data monitoring, sports analytics, or a related field. * Familiarity with sports data platforms, APIs, and real-time data feed systems. The US hourly rate for this part-time position is 17.00 USD - 22.00 USD, plus bonus, equity, and benefits as applicable. Our ranges are determined by role, level, and location. The compensation information displayed on each job posting reflects the range for new hire pay rates for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific pay range and how that was determined during the hiring process. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. #LI-SA2 Join Our Team We're a publicly traded (NASDAQ: DKNG) technology company headquartered in Boston. As a regulated gaming company, you may be required to obtain a gaming license issued by the appropriate state agency as a condition of employment. Don't worry, we'll guide you through the process if this is relevant to your role.

Job DescriptionBenefits: 401(k) 401(k) matching Company car Competitive salary Health insurance Opportunity for advancement Paid time off Vision insurance Benefits/Perks Flexible Schedule Competitive Pay Career Advancement Opportunities Job Summary We are seeking a HVAC Quality Control to join our team. In this role, you will monitor the quality of incoming and outgoing materials and ensure they meet our high-quality standards. You will inspect randomly selected samples, use our proven methods to inspect them, and approve or reject them based on their quality. The ideal candidate has an eye for detail and is committed to our high standards of quality. Responsibilities Review blueprints and written instructions to understand quality requirements for each product Select random samples and test using our standard methods Approve or reject samples based on quality standards and inspections Use necessary tools in the course of testing products Maintain accurate and detailed records of testing outcomes Ensure compliance with health and safety standards at all times Qualifications Previous experience as a Quality Inspector or in a similar role is preferred Attention to detail Familiarity with Microsoft Office and other software applications Excellent verbal and written communication skills

DSA Doors is looking for a talented Quality Control Technician. The primary purpose of a Quality Control Technician is to ensure the finished products have zero defects before it is sent to the customers. The position requires keen eye for details and detecting defects that can cost the company time, resources and reputation. Essential Functions: · Visually and tactile inspection of all finished products for defects and blemishes. · Notify supervisors when defects or blemishes are detected. · Take photographic images in assigned angles for each finished unit and upload to database for future warranty maintenance inquiries. · Manage daily work priority by reviewing and assessing Work Tickets and ready for the Wrapping Team to shipment. · Track and document all order that are damaged, missing, wrong, poor quality, extra items. · Provide supervisors with reports. · Able to maintain clean and organized working area. · Additional duties as assigned. Requirements Skills and Requirements: A keen eye for detail and a results-driven approach. Must have a can-do attitude Ability to work independently to carry out assignment. Must be able to report to superior with accurate information. Ability to meet physical demands as listed below. Ability to work standing up for an 8 hour shift. Ability to work overtime as needed

We are looking to fill a **Scientist 3 - Analytical Chemist** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.** **Responsibilities** + General understanding of analytical method development and method validation + Hands-on experience with chromatographic analysis using various ultra-high-performance liquid chromatography (UPLC), high-performance liquid chromatography (HPLC), and gas chromatography (GC) techniques + General knowledge of separations science + Experience with Empower chromatographic software and with analysis of drug formulations + Hand-on experience with Fourier transform infrared (FTIR) spectroscopic analysis and ultraviolet-visible (UV-VIS) spectroscopic analysis + Skilled on method and instrument troubleshooting, specifically for HPLC and GC methods and systems **Required Skills** + Strong computer, scientific, and organizational skills + Excellent organization to multi-task and manage multiple ongoing projects in parallel including routine testing (for example, assay and impurity testing) and data processing and interpretation + Excellent communication (oral and written) and attention to detail + Proficient in written and spoken English, is required **Desired Skills and Experience** + Empower software + Analysis of drug products + Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude **Qualifications** + BS degree and 3-5 years of relevant experience, or + MS degree with at least 1-2 years relevant experience **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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 ************

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Title: Sr. Quality Specialist/ Quality Control Chemist Location: Rocky Mount - NC Duration: 18 Months Job Description: · The Sr. Quality Specialist shall independently conduct and write complex formal investigation reports with input from area SMEs. · The candidate will function as an independent reviewer of drafted investigations providing constructive feedback and in some instances act as a coach to the investigator. · This position will also perform impact risk assessment as well as assist in root cause determination and plans appropriate corrective action and preventative action. · The incumbent will assist in the tracking and trending of corrective and preventative action to assure timely closure. · This person will also perform reviews and evaluate sensitive, confidential information and develops recommendations for use by the plant quality assurance department. POSITION RESPONSIBILITIES: · In order of importance, list the primary responsibilities critical to the performance of the position. · 2-5 years' experience in pharmaceutical quality environment required. · Experience in sterile manufacturing and an understanding of the sterilization process and its impact to products. · Working knowledge of environmental monitoring and aseptic manufacturing. Understanding of process validation requirements. · American Society for Quality (ASQ) certification is an asset. · Pharmaceutical operations experience and/or knowledge. Experience in a solutions facility preferred. · Working knowledge of FDA regulations. · Knowledge of various quality tools such as root cause analysis, DMAIC process, fishbone analysis, etc. · Prior investigation writing experience (with determination of product impact). · Strong oral and written communication presentation, interpersonal skills and adept at communication with employees at all levels within the organization. · Excellent facilitation skills and ability to facilitate strategy meetings. · Superior technical writing and problem solving skills. · Organize data, extract key information and write technical summary reports. · Expertise with word-processing, spreadsheet, and presentation software. TrackWise experience a plus. ORGANIZATIONAL RELATIONSHIPS: · Ability to interface with multiple levels of people in the organization, including plant personnel and senior management. Qualifications EDUCATION AND EXPERIENCE: · Bachelor's degree with 3-5 years experience in the FDA regulated industry. Additional Information All your information will be kept confidential according to EEO guidelines. With Regards, Abhishek Singh 650-399-0881 Clinical Recruiter Integrated Resources, Inc.

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

Job Description Food Scientist We are seeking a dynamic and forward-thinking food scientist who can bring their technical expertise to the table and play a vital role in developing and refining formulations for our current and future products. As a valued member of our project teams, you will have the opportunity to channel your creativity and innovation to bring new products to life, from initial concept to market launch. With your invaluable contributions, we will unlock the full potential of our brand and enhance the nutritional quality, taste, and texture of our food products. Stay ahead of the curve by exploring new advancements and driving product innovation in partnership with our company. To thrive in this role, you must possess the ability to interpret and apply scientific findings to the world of food, converting them into groundbreaking product concepts. Additionally, a firm grasp of business objectives is crucial for translating them into clear project goals. Excitingly, we are looking for individuals who are team players and share our unwavering passion for product development. Our Food Scientist is responsible for developing, testing, and maintaining high-quality food products that meet company standards, regulatory requirements, and customer expectations. This role involves hands-on product tasting, analytical testing, and collaboration across departments to ensure consistency, safety, and innovation in all products produced by the facility. Key Responsibilities Product Development & Research Conduct research and development (R&D) for new product formulations, line extensions, and process improvements. Experiment with ingredient functionality, flavor profiles, textures, and stability to achieve desired product characteristics. Maintain accurate records of formulations, processing parameters, and sensory evaluations. Evaluate and approve raw materials and new ingredient suppliers based on quality, performance, and compliance standards. Liaising with relevant stakeholders to address concerns about food quality and safety. Utilizing advanced formulation software to create and maintain formulations. Playing a pivotal role in bringing new products to life, from conceptualization to successful launch. Coordinating the arrangement and shipment of sales samples. Updating product information sheets and labels for effective sales presentation. Accurately recording, analyzing, and summarizing research data for informed decision-making. Collaborating with independent laboratories for comprehensive testing. Maintaining the MRP system by keeping it up to date and accurate. Ensuring strict compliance with GMP and other safety regulations. Performing any additional duties assigned by the supervisor. Product Tasting & Evaluation Taste and evaluate all products during development and production for flavor accuracy, consistency, texture, and appearance. Lead sensory panels and coordinate tasting sessions with internal staff and customers as needed. Document results and recommend adjustments to formulations or processes based on sensory and analytical data. Analytical Testing & Data Review Prepare, perform, and review all analytical testing and quality data, including but not limited too, pH, Brix, viscosity, color, moisture, and microbiological analysis. Ensure testing equipment is properly calibrated and maintained for accuracy and reliability. Analyze test results to identify trends or deviations and recommend corrective actions when necessary. Prepare technical reports summarizing findings for management and customer review. Customer Collaboration Work one-on-one with customers to establish and refine recipe standards that align with their brand and quality expectations. Translate customer requirements into production-ready formulas while ensuring cost efficiency and manufacturability. Participate in customer tastings, product trials, and formulation meetings to ensure satisfaction and consistency. Cross-Department Coordination Collaborate closely with the Customer Success Department to address customer feedback, troubleshoot issues, and develop improvement plans. Partner with Cook Room and Bottle Room Associates to ensure recipes are prepared, cooked, and packaged according to approved standards. Provide technical guidance to production staff during scale-up, batching, and process trials. Assist the Quality Assurance team in developing and implementing product specifications, SOPs, and regulatory documentation. Regulatory & Documentation Ensure all product formulations and processes comply with FDA, SQF, GMP and other company compliance regulations, as well as applicable food safety regulations. Maintain up-to-date records of all formulations, test results, and production data in accordance with company documentation standards. Support the preparation of product labels, ingredient statements, and nutritional facts panels. Qualifications Bachelor's degree in Food Science, Food Technology, Chemistry, or related field required; Master's degree preferred. Minimum 3-5 years of experience in food product development, manufacturing, or quality assurance. Strong knowledge of food chemistry, microbiology, sensory science, and process engineering. Hands-on experience with analytical testing equipment and sensory evaluation. Excellent communication skills and ability to collaborate with cross-functional teams. Strong organizational and data analysis skills with attention to detail. Knowledge of FDA, SQF regulations, HACCP, Acid/Acidified, PCQI and GMP standards. Working Conditions On-site position within a food manufacturing environment. Requires daily tasting and sensory evaluation of products. Involves working in production areas (Cook Room, Bottle Room, all GMP zones) and laboratory settings. Occasional customer visits or off-site product demonstrations may be required. Physical Requirements Ability to stand for extended periods in production areas. Must be able to safely handle ingredients, lab equipment, and small production tools. Capable of lifting up to 25 lbs. BENEFITS: Experience a diverse range of comprehensive benefits, including medical, vision, and dental coverage. Take time away from work and recharge with generous paid time off and "dream" days off. Participate in exciting company events that foster camaraderie and team spirit.