Chemist jobs in Tennessee - 51 jobs

We are looking to fill a **Scientist 3 -** **Third Shift** **Analytical Chemist Pilot Plant** 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. **Description** The Scientist III **Third Shift** - Analytical Chemist Pilot Plant operates and maintains a myriad of analytical instrumentation and other duties as assigned by the client. **Responsibilities** + Experience in routine and real-time testing for high-performance liquid chromatography (HPLC), gas chromatography (GC), ultraviolet (UV) spectroscopy, infrared (IR) spectroscopy, titrations, Karl Fischer (KF) testing, and other wet chemistry methods + Experience in HPLC and GC is required with an interest in expanding the knowledge and background in method development and optimization, validation, data analysis, and sample preparation techniques + Routine use of modern analytical techniques such as HPLC, GC, KF, ultraviolet-visible spectroscopy (UV-VIS), and IR spectroscopy + Comfortable working in a cGMP environment; knowledgeable in various GMP analytical activities, such as documentation procedures, abiding by relevant department SOPs and generation and second scientist review of GMP data + Experience with automated liquid handling systems (Tecan) for high throughput testing + Experience with a myriad of software platforms used in the compilation, processing, and reporting of data, such as Waters Empower, Relational Laboratory Information Management System (RLIMS), Lab X, etc. **Qualifications** + BA/BS (3-5 yrs.) of relevant experience in n chemistry or a related discipline testing lab + MS (1-2 yrs.) of relevant experience in chemistry or a related discipline testing lab **Desired Skills and Experience** + Effective organizational, multi-tasking, and oral/written communications skills + Ability to work under pressure and provide reliable results with quick turnarounds + Consistently deliver high quality and fully compliant results and interact with a diverse customer base daily + Proficient in written and spoken English, is required **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.

* Maintain the highest standards of scientific professionalism. When in doubt, get feedback from other R&D/Technical professionals. * Maintain detailed and comprehensive documentation of all work performed. * Stay current with the scientific literature, particularly in areas that may affect company's product line, existing processes or potential commercial opportunities. * Evaluate technology packages from external sources for chemical and cost-effective viability, as directed. * Perform literature searches for development work, potential projects, and to support QA/QC and Environmental/Health & Safety. * Provide ideas for investigation with an emphasis on commercialization, patent opportunity, or publication on a regular basis. * Provide support to QA/QC by writing analytical SOPs. * Communicate results by providing timely reports and project updates, to include technical reports and summaries for company business units and customers. * Provide monthly report on progress of work to the department head. * Provide help on preparation of quarterly/yearly R&D summaries of ongoing work to peers and senior management. * Plan and develop robust analytical methods including troubleshooting and validation, as appropriate. * Work closely with Synthesis group and support on routine analysis. * Work closely with Quality Assurance (QA) and Quality Control (QC) to identify project needs and to insure strict compliance with internal quality and/or cGMP/ICH guidelines. * Work closely with QA on validation efforts for new API processes to insure strict cGMP compliance, where appropriate. * Work closely with R&D team to answer DMF deficiencies and customer queries. * Maintain rigorous accountability and documentation of work related to controlled substances in accordance with established SOPs and requirements of federal regulations (21 CFR Part 1300-1399). * Adhere to all relevant company SOPs and guidelines, and provide input for correcting and changing existing procedures and processes. * Provide technical support as needed for company products, analytical methods and customer-driven issues, as needed. * Provide necessary information on cost-saving and time-saving alternatives to current analytical and laboratory practices whenever and wherever possible. * Assist in supervision of R&D laboratory operations in general, including troubleshooting of lab systems and instrumentation. * Work with Health, Safety and Environmental representative to identify waste stream data and possible hazards for potential products and processes. * Assist in the maintenance and cleaning of the R&D laboratory in general and in individual workspace in particular. * Seek out opportunities for professional development. * Select and purchase R&D chemicals, glassware and supplies, and track these orders using the established R&D purchase requisition system. * Execute R&D stability program, to include writing and following stability protocols, and packaging and testing APIs, as well as compiling and reporting stability results to R&D manager. * Facilitate the training system within the R&D department in coordination with the requirements set forth by QA. * Other duties as assigned. Position Requirements: * B.S. degree in Chemistry (preferable), Chemical Engineering, or related discipline. * Ability and attitude to assume a leadership role and work in a productive technical team within an industrial research environment. * Ability to communicate effectively through verbal, written, presentation and computer modes of expression. * Ability to confidently represent company on technical matters to customers, senior management, and at scientific venues (conferences and publications). The presently-anticipated base compensation pay range for this position is $102,500 to $125,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Long Term Incentive Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time. The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s). We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law. Nearest Major Market: Chattanooga

Job Title: Quality Control Chemist About the Company: IPS Corporation is a global, market-leading provider of solvent cements, adhesives, and specialized plumbing products. Founded in 1954 in Los Angeles, CA, IPS began by producing clear cements for laminating acrylic sheets for aircraft canopies. Today, IPS, with its three operating companies, has eight manufacturing plants and nine distribution centers supporting sales to a diverse set of end markets in 85 countries. About Weld-On: Weld-On Adhesives, the largest subsidiary of IPS Corporation, is the pioneer and leading manufacturer of Weld-On solvent cements, primers, and cleaners for PVC, CPVC, ABS and other plastic piping systems. Weld-On products are globally recognized as the premium products for joining plastic pipes and fittings and are used by professional installers around the world in a variety of applications such as, but not limited to, construction (residential & commercial), industrial (chemical process, water treatment, mining, etc.), irrigation (landscaping & agricultural) and others. About the Job: We are seeking a Quality Control (QC) Chemist to join our team at the Weld-On Adhesives manufacturing facility in Hartsville, TN. Reporting directly to the Quality Manager, this role plays a critical part in ensuring that all products meet the highest quality standards through rigorous analytical testing and inspection. The QC Chemist will also collaborate with cross-functional teams to support new product introductions, validation processes, and compliance with certification requirements Responsibilities: Perform quality assurance testing using Gas chromatography, Infrared spectroscopy, viscometers, moisture analyzers, and other analytical techniques to verify product conformance with specifications. Maintain and calibrate laboratory equipment to ensure accuracy, reliability, and compliance with standards. Develop, write, and implement Standard Operating Procedures (SOPs) for laboratory processes and equipment usage. Accurately record and document QC test results, deviations, and corrective actions in compliance with internal protocols and customer requirements. Conduct lab experiments to support new formula introduction, validation, and troubleshooting of quality issues. Assist with product certification and compliance activities, including audits, testing, and sample submissions. Education/ Experience Qualifications: Bachelor's degree in Chemistry, Polymer Science, Materials Science, or a related field. Minimum of 3 years of relevant experience in the chemical industry, preferably in adhesives, sealants, or coatings. Strong technical expertise in chemical formulation, quality control, and analytical testing. Familiarity with regulatory requirements and standards related to hazardous chemicals. Proficiency in data analysis, with the ability to identify trends and draw valid conclusions; experience with statistical tools is a plus. Excellent written and verbal communication skills, with the ability to collaborate effectively across all organizational levels and with external partners. Comfortable working in a global, multi-disciplinary team environment. Willingness to travel up to 25%. This description reflects management's assignment of essential functions; it does not proscribe or restrict the tasks that may be assigned. Weld On is an equal opportunity employer and makes employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other status protected by law.

Requisition Id 14972 The Centrifuge Science (CS) Section within the Enrichment Science and Engineering Division (ESED) at Oak Ridge National Laboratory (ORNL) is seeking a Senior Electric Motor Researcher for the Mechanical Systems Modeling (MSM) Group. The Senior Electric Motor Researcher will perform analysis on electric motors and motor drive systems for gas centrifuges. In addition, the Senior Electric Motor Researcher will guide experimental testing and validation of electric motors and electromagnetics. Purpose: ESED serves the nation in two critical areas: advancing enrichment technologies and exploring enriched stable isotope production and applications. The division leverages an elite staff of scientists and engineers with the world-leading capabilities of ORNL to deliver groundbreaking advancements with a variety of applications, from national security to life-saving medical treatments. ESED is the national steward for research, development, and demonstration of centrifuge technology. The successful candidate will provide research and development (R&D) leadership to the group that strategically advances science and technology focused on gas testing of prototype enrichment devices for processing uranium-bearing and stable isotope compounds. The Mechanical Systems Modeling Group applies first principles and empirical approaches to advance the physics and engineering understanding of enrichment devices using analytical methods and computational tools such as finite element analysis (FEA). The Senior Electric Motor Researcher will provide research and development (R&D) leadership to the group/section/division in the area of FEA on electric motors and development, testing, and demonstration of motors and motor drives. Major Duties and Responsibilities Major duties will be to perform complex analysis in the field of electromagnetics as it relates to motors and electromagnetic assemblies compatible with enrichment devices and technologies. The successful candidate will also be involved with developing and coordinating tests to determine mechanical and thermal properties for use in and to validate simulations. Finally, the candidate will be responsible for providing direction in detailed formal designs, test plans, test data analytics, and fabrication plans in coordination with stakeholder personnel. Additional duties include the following: Establish and conduct research within the field of electric motors and motor drives as it relates to centrifuge and enrichment technologies. Interact and collaborate with management and group/section/division members to define, execute, and report on relevant project elements. Actively collaborate with the domain experts from U.S. government laboratories and academia involved in similar efforts. Significantly contribute to R&D, design, and experimental troubleshooting activities. Publish high-quality research results in peer-reviewed classified reports. Publish and present nonsensitive research in journals and conferences, if authorized by the sponsoring agency. Basic Qualifications: PhD degree and 8 years relevant postgraduate experience or a MS degree with 12 years postgraduate experience in electrical engineering or closely related engineering or science discipline. Excellent communication (verbal and written), strategic planning, organization, and decision-making skills. Experience testing motors, motor drives, and magnetic material. Experience designing fixtures and apparatuses for testing magnetics and motors. Preferred Qualifications: Active DOE Q clearance Demonstrated prior leadership experience. Experience with ANSYS Maxwell and related software. Experience with MATLAB, C++, or Python. At least 7 years' relevant experience with modeling of electric motors and electromagnetics. Experience in designing and fabricating electric motors. Knowledge of motor control techniques used in motor drive systems. Knowledge of motor drive modulation techniques and their impact on motor design. Knowledge of position feedback systems and their integration in electric machines. Special Requirements: This position requires the ability to obtain and maintain a DOE Q clearance from the US Department of Energy. As such, this position is a Workplace Substance Abuse (WSAP) testing designated position. WSAP positions require passing a preplacement drug test and participation in an ongoing random drug testing program. ================================================================================ About the Isotope Science and Enrichment Directorate (ISED): Established in 2020, ISED is strengthening ORNL's leadership in isotope production and enrichment technology innovation. ISED is guiding the laboratory's pursuit of the fundamental science and technology that broadens the application of isotopes for energy, environmental, medical, and national security purposes. These efforts are made possible through the High Flux Isotope Reactor, the Radiochemical Engineering Development Center, ORNL's other nuclear facilities, and an assemblage of world-leading scientists and engineers. Please visit ***************************************** for more information about ISED. Benefits at ORNL: UT-Battelle offers a quality benefits package, including a matching 401(k), contributory pension plan, paid vacation, and medical/dental plan options. Onsite amenities include a credit union, medical clinic, cafeteria, and fitness facilities. Relocation: Moving can be overwhelming and expensive. UT-Battelle offers a generous relocation package to ease the transition process. Domestic and international relocation assistance is available for certain positions. If invited to interview, be sure to ask your Recruiter (Talent Acquisition Partner) for details. For more information about our benefits, working here, and living here, visit the “About” tab at ********************** #LI-DC1 This position will remain open for a minimum of 5 days after which it will close when a qualified candidate is identified and/or hired. We accept Word (.doc, .docx), Adobe (unsecured .pdf), Rich Text Format (.rtf), and HTML (.htm, .html) up to 5MB in size. Resumes from third party vendors will not be accepted; these resumes will be deleted and the candidates submitted will not be considered for employment. If you have trouble applying for a position, please email ***********************. ORNL is an equal opportunity employer. All qualified applicants, including individuals with disabilities and protected veterans, are encouraged to apply. UT-Battelle is an E-Verify employer.

USAntibiotics, the only U.S. manufacturer of Amoxicillin products, is part of the Jackson Healthcare family of companies. We're always looking to add new talent to our teams, and we value diverse professionals who have strong leadership skills, align with our culture, and are committed to excellence. POSITION SUMMARY: Provide specialized technical support within the Quality Assurance Laboratory as assigned. Provide leadership/training to less experienced staff, as assigned to assure efficient and valid analytical laboratory support the Bristol site. Assist with supervisory duties in the absence of Management (including review and approval of analytical data per cGMPs and regulatory requirements). Perform analytical testing of all sample types as assigned. Assist with development and validation of chemical assays. Lead installation, validation and troubleshooting new and existing equipment, including automated systems, as assigned. Assist Management in improving efficiency and compliance status of laboratories. Roles & Responsibilities: Perform technical duties in specialized area or function as leader in absence of management, as assigned. Assist laboratory supervisors with tasks, as needed Perform efficient and reliable analytical tests following validated procedures for a wide variety of methods and sample types as assigned Document all results in accordance with cGMPs and written procedures Trouble-shoot and solve problems with assays and equipment with little or no supervision. Report all observations Recommend changes to methods and operations as appropriate Interpret analytical results correctly, notifying Management promptly of both situations that indicate analytical issues and manufacturing or product issues Develop/implement appropriate corrective and preventative actions (CAPA) Maintain the QC laboratories to comply with cGMP and USAntibiotics' standards of safety, quality, and cleanliness Participate in analytical method validations or transfers as required Perform satisfactorily on all analyst qualification studies, indicating technical proficiency Plan, perform, and document non-routine tests (or special studies) and investigations under the direction of Manager Evaluate and utilize state-of-the-art equipment including automated systems and computerized systems to perform testing and meet the goal of improved assay performance, including reliability , cost and assay characteristics Maintain and improve proficiency of operations through training Write validation reports, analytical procedure SOPs and equipment SOPs as required Notify Management of any SOPs that may require revision and initiate change requests per written policy, providing sufficient evidence/documentation to support change request Conduct special studies in accordance with protocols and direction of management. Prepare well documented reports of results Carry out other departmental duties as deemed appropriate by supervisor/manager Broaden understanding of subtleties of the techniques utilized by keeping current with technical and professional literature, attending technical discussions both inside and outside the USAntibiotics' community Provide technical and professional expertise to less experienced staff in the laboratory Serve as technical resource during Regulatory inspections and internal audits as required. Also, conduct internal audits and self-inspections as required. Provide information to outside vendors and technical representatives in a professional manner Review (i.e., validate) and approve analytical results for other laboratory personnel as assigned Assist management in conducting analytical failure investigations, as required, following all procedures Responsible for calibrating and maintaining assigned laboratory equipment according to schedules and procedures, documenting all results Lead equipment qualifications, drafting protocols and summary reports, as directed by management Specialized area of responsibility as assigned: Analytical Methodology/Instrumentation Mastery LIMS SAP Compendial/Regulatory Expertise QUALIFICATIONS - EDUCATION, WORK EXPERIENCE, CERTIFICATIONS: BS/BA degree in Chemistry (or related science) or equivalent related analytical experience PREFERRED QUALIFICATIONS: Master's Degree in Chemistry (or related science) and/or approximately 7 years scientific work experience, which includes a specialized skill Previous pharmaceutical industry experience EXPERIENCE REQUIRED: Minimum of 5-10 years of analytical experience in pharmaceutical industry and/or other scientific experience Strong knowledge/experience of cGMPs in areas beyond QC laboratory KNOWLEDGE, SKILLS, AND ABILITIES: Demonstrated ability to perform a wide variety of chemical, instrumental, and chromatographic analyses Demonstrated mastery of skills at Chemist level and/or expertise in specific topic Advanced computer skills Advanced method development and trouble-shooting skills Thorough understanding of chemical theory on which test methodology is based with strong laboratory testing skills Appropriate interpersonal and leadership skills Advanced verbal and written communication skills Ability to prioritize and decide appropriate course of actions. Consistently notifies Management of possible compliance and technical issues and suggests/implements corrective actions Ability to handle multiple priorities efficiently and make/implement decisions Fully versed in cGMPs, FDA, and other regulatory agency requirements Ability to function independently on special projects and follow through to successful completion Ability to maintain confidentiality Ability to work in a team multi-disciplinary environment interacting on a professional level with peers, subordinate and senior personnel ACCOUNTABILITY: Assures that testing of products manufactured at the facility is performed per approved procedures and appropriate regulations and that lab operations conform to company standards for safety and performance Performs technical functions based on mastery of specialized topic, and advises/assists less experienced personnel in the laboratories Assures the quality of laboratory documentation, i.e., documentation is comprehensive and accurate Provides leadership in the laboratory in the absence of Management and make appropriate decisions regarding product release and quality Assists laboratory supervisors with duties, as needed COMPLEXITY: Serves as backup to management for routine lab operations and in planning laboratory investigations, determining validity of results and appropriate actions Advises in a technical role less experienced staff, notifying Management of problems/issues or additional training needs Performs statistical analysis as required for annual product reviews, special studies, investigations, etc. Also must use judgement to raise possible issues to upper management Initiates operational changes in laboratory, within constraints of policies and procedures to improve cGMP compliance, efficiency, cost, and performance Assures the integrity of analytical results/documentation generated Assists the Quality Assurance Department in meeting goals established TRAVEL REQUIREMENTS & WORKING CONDITIONS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job While performing the duties of this job, the employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel; write; type; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; and smell The employee must frequently lift and/or move up to 50 pounds Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. EEO Statement: We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected status under the law.

Come make a difference in our community by Making Healthy Happen! TITLE: Chemist I SHIFT: Rotating 1st Shift; 7:00PM-7:00AM 2-2-3 Rotating Work Schedule (every other weekend) Great for work-life balance! Only work 3 to 4 days per week!!! BENEFITS: 401k w/company match. Medical, Dental, Vision, Life, Short-term/Long-term Disability Insurances effective 30 days after first full Month! 7 Paid Holidays & 3 Floating Holidays for use at employee's discretion Immediately eligible for holiday and vacation pay! Annual allowance for prescription safety glasses Climate-controlled and cleanest work environment in Morristown! Education & Fitness reimbursement Employee Product Giveaways! Employee Referral Program $$$! Associate Discount Programs Overtime available POSITION SUMMARY: The Chemist I will be responsible for daily QC testing to be in compliance with ISO, USP CFR or other Regulatory entities. Testing of incoming WIP, Finished Goods and raw materials which include using GC, HPLC, FTIR, TOC, UVvis Spectroscopy, Autotitration, organoleptic, pH etc. Additionally, this role will learn industrial microbiology techniques and be fully cross trained to perform aseptic sampling and traditional plating methods. Other routine responsibilities include solution preparation, standardization and maintaining general laboratory conditions to comply with cGDP's, cGMPs and cGLPs to ensure RFT results. ESSENTIAL ACCOUNTABILITIES: Microbiological Testing Sample preparation and testing following USP and Aseptic technique Gram staining and phenotypic ID using API Environmental Monitoring in Plant Maintain Micro Test Logs CPM of Plant water loop Chemical Testing GC HPLC Titration Solution prep TOC FTIR pH/Density/Conductivity Physical Testing: Weights, diameters, thickness, flow rates, OB Checks Demonstrate commitment to the company's RRITE Values of Renew, Respect, Integrity, Teamwork, and Excellence. Associates have a direct and important role in ensuring that all work is performed in a safe manner. Effectiveness in carrying out this responsibility is part of each associate's essential accountabilities. Contribute to a cooperative working effort by demonstrating a willingness to perform other job-related work, as needed or requested. This position is designated as Safety-Sensitive (A safety-sensitive position is one in which the associate's inability or impaired ability to perform their job-related tasks could result in a direct threat to the associate's safety or the safety of others). QUALIFICATION REQUIREMENTS: (To perform this job successfully, an individual must be able to perform each of the essential accountabilities satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Must be qualified through Phase I or higher. To be considered for this position, an associate must be below 5 attendance points and have no active performance-related corrective actions. Selected candidates must complete the HR Predictive Index Assessment to understand strengths and areas for improvement. PHYSICAL AND MENTAL REQUIREMENTS: (The physical demands described here are representatives of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions) Associates degree in Chemistry or Biology or Physics (BA preferred). 0-3 years of experience in a QC Lab. Qualitative and quantitative analysis skills. Strong math skills. Ability to handle a fast pace, high stress environment while still maintaining RFT testing results. Investigating Out of specification (OOS) test results. Trouble shooting instrumentation malfunctions. High problem-solving skill, thinking out of the box, innovative approaches to roadblocks. Attendance at ACS Short Courses and Certificates for Short Courses online. Standing, sitting, reading, writing, reasoning/analyzing, and social interaction. Frequent carrying and lifting 0-10 pounds, repetitive hand movement, reading, writing, reasoning/analyzing, and social interaction. Occasional carrying and lifting 10-30 pounds, standing/walking, bending/twisting, pushing/pulling, reaching above shoulder, and calculating. WORK ENVIRONMENT: (The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.) 100% inside work (Production Lab/Floor) FLSA Status: Non-Exempt Grade 7

Job DescriptionHeadquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! August Bioservices is looking for an Analytical Development team member that is passionate and driven regarding his/her work. August Bio desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. The Analytical Chemist I & II position, reporting to the Analytical Chemistry Supervisor, will operate under minimal supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development.Responsibilities Performs routine laboratory testing and duties Performs laboratory investigations in support of testing Troubleshoots analytical equipment Accurately documents all necessary and relevant information in a clear and concise manner per cGMP requirements Responsible in the development of analytical chemistry procedures to determine the identity, purity, stability, and other characteristics of samples that are analyzed Author and execute method validation protocols Author method validation reports Requirements Bachelor's Degree in chemistry, biology, or related science 2+ years of pharmaceutical experience or equivalent. Self-starter and ability to work independently Strong written/verbal communication and presentation skills Able to work flexible schedules on a short notice Ability to be a team player/work well with others Shifts 2nd shift: 3:00pm - 11:30pm, Monday - Friday 3rd shift: 11:00 - 7:30am, Monday - Friday At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment. We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team! August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

USAntibiotics, the only U.S. manufacturer of Amoxicillin products, is part of the Jackson Healthcare family of companies. We're always looking to add new talent to our teams, and we value diverse professionals who have strong leadership skills, align with our culture, and are committed to excellence. POSITION SUMMARY: Provide specialized technical support within the Quality Assurance Laboratory as assigned. Provide leadership/training to less experienced staff, as assigned to assure efficient and valid analytical laboratory support the Bristol site. Assist with supervisory duties in the absence of Management (including review and approval of analytical data per cGMPs and regulatory requirements). Perform analytical testing of all sample types as assigned. Assist with development and validation of chemical assays. Lead installation, validation and troubleshooting new and existing equipment, including automated systems, as assigned. Assist Management in improving efficiency and compliance status of laboratories. Roles & Responsibilities: Perform technical duties in specialized area or function as leader in absence of management, as assigned. Assist laboratory supervisors with tasks, as needed Perform efficient and reliable analytical tests following validated procedures for a wide variety of methods and sample types as assigned Document all results in accordance with cGMPs and written procedures Trouble-shoot and solve problems with assays and equipment with little or no supervision. Report all observations Recommend changes to methods and operations as appropriate Interpret analytical results correctly, notifying Management promptly of both situations that indicate analytical issues and manufacturing or product issues Develop/implement appropriate corrective and preventative actions (CAPA) Maintain the QC laboratories to comply with cGMP and USAntibiotics' standards of safety, quality, and cleanliness Participate in analytical method validations or transfers as required Perform satisfactorily on all analyst qualification studies, indicating technical proficiency Plan, perform, and document non-routine tests (or special studies) and investigations under the direction of Manager Evaluate and utilize state-of-the-art equipment including automated systems and computerized systems to perform testing and meet the goal of improved assay performance, including reliability , cost and assay characteristics Maintain and improve proficiency of operations through training Write validation reports, analytical procedure SOPs and equipment SOPs as required Notify Management of any SOPs that may require revision and initiate change requests per written policy, providing sufficient evidence/documentation to support change request Conduct special studies in accordance with protocols and direction of management. Prepare well documented reports of results Carry out other departmental duties as deemed appropriate by supervisor/manager Broaden understanding of subtleties of the techniques utilized by keeping current with technical and professional literature, attending technical discussions both inside and outside the USAntibiotics' community Provide technical and professional expertise to less experienced staff in the laboratory Serve as technical resource during Regulatory inspections and internal audits as required. Also, conduct internal audits and self-inspections as required. Provide information to outside vendors and technical representatives in a professional manner Review (i.e., validate) and approve analytical results for other laboratory personnel as assigned Assist management in conducting analytical failure investigations, as required, following all procedures Responsible for calibrating and maintaining assigned laboratory equipment according to schedules and procedures, documenting all results Lead equipment qualifications, drafting protocols and summary reports, as directed by management Specialized area of responsibility as assigned: Analytical Methodology/Instrumentation Mastery LIMS SAP Compendial/Regulatory Expertise QUALIFICATIONS - EDUCATION, WORK EXPERIENCE, CERTIFICATIONS: BS/BA degree in Chemistry (or related science) or equivalent related analytical experience PREFERRED QUALIFICATIONS: Master's Degree in Chemistry (or related science) and/or approximately 7 years scientific work experience, which includes a specialized skill Previous pharmaceutical industry experience EXPERIENCE REQUIRED: Minimum of 5-10 years of analytical experience in pharmaceutical industry and/or other scientific experience Strong knowledge/experience of cGMPs in areas beyond QC laboratory KNOWLEDGE, SKILLS, AND ABILITIES: Demonstrated ability to perform a wide variety of chemical, instrumental, and chromatographic analyses Demonstrated mastery of skills at Chemist level and/or expertise in specific topic Advanced computer skills Advanced method development and trouble-shooting skills Thorough understanding of chemical theory on which test methodology is based with strong laboratory testing skills Appropriate interpersonal and leadership skills Advanced verbal and written communication skills Ability to prioritize and decide appropriate course of actions. Consistently notifies Management of possible compliance and technical issues and suggests/implements corrective actions Ability to handle multiple priorities efficiently and make/implement decisions Fully versed in cGMPs, FDA, and other regulatory agency requirements Ability to function independently on special projects and follow through to successful completion Ability to maintain confidentiality Ability to work in a team multi-disciplinary environment interacting on a professional level with peers, subordinate and senior personnel ACCOUNTABILITY: Assures that testing of products manufactured at the facility is performed per approved procedures and appropriate regulations and that lab operations conform to company standards for safety and performance Performs technical functions based on mastery of specialized topic, and advises/assists less experienced personnel in the laboratories Assures the quality of laboratory documentation, i.e., documentation is comprehensive and accurate Provides leadership in the laboratory in the absence of Management and make appropriate decisions regarding product release and quality Assists laboratory supervisors with duties, as needed COMPLEXITY: Serves as backup to management for routine lab operations and in planning laboratory investigations, determining validity of results and appropriate actions Advises in a technical role less experienced staff, notifying Management of problems/issues or additional training needs Performs statistical analysis as required for annual product reviews, special studies, investigations, etc. Also must use judgement to raise possible issues to upper management Initiates operational changes in laboratory, within constraints of policies and procedures to improve cGMP compliance, efficiency, cost, and performance Assures the integrity of analytical results/documentation generated Assists the Quality Assurance Department in meeting goals established TRAVEL REQUIREMENTS & WORKING CONDITIONS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job While performing the duties of this job, the employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel; write; type; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; and smell The employee must frequently lift and/or move up to 50 pounds Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. EEO Statement: We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected status under the law.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. This facility is Lilly's largest investment in manufacturing capacity and is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site, and the successful candidate will help to build the processes and systems to enable a successful startup into GMP manufacturing operations. Position Overview: The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. Responsibilities: * Understand the scientific principles required for manufacturing intermediates and bulk drug substances, including the interaction of the chemistry and equipment. * Execute technical projects (experimental, modeling and/or production data analysis) to improve process control, yield, purity, and/or productivity. * Provide technical support for preparation of relevant technical documents, as required, such as: technical reports, change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures, PFDs (Process Flow Documents), VMPs, etc. * Develop and monitor established metrics in real-time to assess process variability and capability. * Understand, justify and document the state of validation (process and cleaning) with data that evaluate the capability of the manufacturing process to meet its stated purpose. * Ensure that an accurate instruction set (tickets & procedures) and PFD describe the process as performed and the control strategy for the discrete manufacturing steps. * Ensure that experiments are well designed with clear objectives. * Ability to analyze data and ensure appropriate documentation. * Write technical reports and documents. Basic Requirements: * Bachelors in STEM Discipline (Chemistry preferred) * 3+ years of experience in cGMP manufacturing (pharmaceutical manufacturing experience preferred) Additional Preferences: * Demonstrated understanding of process chemistry * Demonstrated basic knowledge in small molecule, peptide, or oligonucleotide API Manufacturing. * Relevant industrial experience in any of the following discipline such as API Manufacturing, TS/MS (Technical Services/ Manufacturing Sciences), Quality Control, Quality Assurance, or Development. * Familiarity with cGMP manufacturing environment and terminology. * Excellent analytical, interpersonal, written and oral communication skills. * Ability to work on own initiative and as part of a Process Team consisting of a diverse group of management, production, science and engineering professionals. * Creativity to identify improvement opportunities and the tenacity/initiative to see them implemented. * Guidance/mentoring of others through processes. * Flexibility to meet business needs. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

WHO WE ARE Helena Agri-Enterprises, LLC is a leading full-service agronomic solutions provider that's been in business since 1957. Our first location was in West Helena, Arkansas hence the name "Helena". We now have 450+ locations nationwide and over 6,000 employees. Our corporate office is located in Collierville, Tennessee, a suburb outside of Memphis. Year after year we rank at the top nationally for volume and sales in our industry. There are many facets to our company including product development, sales, operations, precision technology and manufacturing just to name a few. ABOUT THE JOB The Formulation Chemist is responsible for performing a wide range of tests and research services required for the development, manufacturing and support of fertilizers as well as pesticides on fertilizer for both liquid and dry. This position is also very involved with quality control of raw materials and finished goods. This position is with Helena Products Group (HPG). HPG develops Helena's extensive portfolio of proprietary products that includes seven product categories covering both crop production and crop protection. HPG leads the industry in creating innovations and formulation technologies and operates out of a state-of-the-art research, development and training facility located in Memphis, TN. WHAT YOUR DAY WILL LOOK LIKE Bench tests physical properties of agriculture products, such as pH, density, contact angle, water content, surface tension, viscosity, particle size distribution, emulsion performances, flashpoint and refractive index testing. Performs other quality control tests and analyses. Collects data and keeps appropriate records on all testing. Reports results to leader in a timely manner. Screens pure products and diluted mixtures for compatibility and stability. Blends small batches of finished goods for use in testing. Maintains chemical inventory, instruments, equipment, glassware and laboratory spaces. Aids in development and implementation of new laboratory methods and protocols. Maintains physical and electronic document storage including Safety Data Sheets. Cleans glassware per Standard Operating Procedures (SOP) instructions. Performs evaluations of raw materials for sourcing approval. Interprets and maintains the reading of storage stability project samples weekly. Manufactures lab batches for field efficacy protocol trials. Proficient operation of bead mill and particle size analyzer equipment to determine product specifications are met. Responsible for data entry writing of SOPs in Filemaker Pro software. Assists in the GHS classifications of SDS generations. Writes certificates of analysis (COA) for production products when applicable. Attends vendor/supplier meetings as needed. Regularly attends product development/formulation development meetings internally. Assists in product quality notification complaint resolution. Visits manufacturing facilities for the quality control of new product production and/or troubleshooting production issues when needed. Assists in the determination of acceptable cleanout levels (ACLs) from product to product to support manufacturing. May be required to drive a company vehicle. Provides excellent customer service to all internal and external customers. Other work-related duties as assigned by your leader. Regular and reliable attendance is required. Follows all company policies and procedures. EDUCATION & EXPERIENCE Bachelor of Science degree in chemistry, biology, agriculture or related field is required. Five years of formulation development in agricultural formulations is required. SKILLS & QUALIFICATIONS General laboratory skills and critical thinking. Organizational, time management and record-keeping skills. Interpersonal and communication skills. Flexibility with changing objectives and priorities. Working knowledge of Microsoft Office, including OneDrive, Teams and OneNote, is required. Travel by various means up to 10% of the time is required . Ability to read, write and speak in English is required. Communicating in Spanish is a valuable skill at Helena. Valid U.S. drivers license is required to drive a company vehicle. Successful completion of a drug test and background check is required for all positions at Helena. WORK ENVIRONMENT & PHYSICAL ASPECTS OF THE JOB At Helena, safety is our highest priority. We seek out extensive safety measures and put them in place to minimize exposure to anything that could be potentially harmful to our employees. The work environment for this position is that of a typical plant/laboratory environment where the noise level is usually moderate to loud. In this position, you will regularly work near moving equipment/mechanical parts and could be exposed to fumes, airborne particles, chemical and biological hazards, vibrations and a risk of electrical shock. This position requires you to use your hands for many different tasks and to talk, hear, walk, sit, stand, (8 hours a day or more), lifting, carrying, pushing or pulling (up to and including 50lbs or more), reaching overhead (up to and including 25lbs), climbing, gripping, grasping and twisting using hands and wrists, bending and stooping for long periods of time, working below knee levels for short periods of time and working above shoulder level for short periods. BENEFITS AT HELENA Health, Dental & Vision Insurance STARTS THE SAME DAY YOU DO! Earn up to $3,000 in Reward Dollars from Helena for your Health Savings Account (HSA). Helena's robust 401(k) Savings Plan offers you a 100% company-match up to 5% starting on your first day. As your years of service with Helena increase, so does our company-match - up to 10% based on your contribution amount. Three-year vesting on company match with 1,000 hours of service. Access your earned pay between paydays through Earned Wage Access (EWA) with DailyPay. Up to 15 days paid time-off plus 9 paid holidays. Free Term Life Insurance at 1x your annual base pay - paid for by Helena at no cost to you. Free Short & Long-Term Disability. Up to 80 hours of paid Parental Leave. Education Assistance. And much more! For more detailed information about our benefits, visit helenacareers.com/benefits. STAY CONNECTED TO THE HELENA POWERHOUSE! Follow us on social @HelenaCareers or visit us at helenacareers.com. Helena supports individuals with disabilities, and reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Helena is an equal opportunity employer.

Descricão Quality Control II Buckman - Memphis, TN Location: Memphis, TNLanguage: EnglishTravel: up to 5% Buckman is a privately held, global specialty chemical company with headquarters in Memphis, TN, USA, committed to safeguarding the environment, maintaining safety in the workplace, and promoting sustainable development. Buckman delivers exceptional service and innovative solutions to our customers globally in the pulp and paper, leather, and water treatment sectors to help boost productivity, reduce risk, improve product quality, and provide a measurable return on investment. Ensure the delivery of accurate, timely, and compliant analytical data that supports product quality, regulatory standards, and cross-functional decision-making. Success in this role directly impacts product release timelines, operational efficiency, and customer satisfaction.Key Outcomes/ResponsibilitiesOutcome: Drive consistent and reliable product quality testing, recording, and compliance across manufacturing operations. Actions: Independently execute and validate quality tests using standardized procedures, ensuring precision, repeatability, and alignment with regulatory and internal benchmarks. Lead real-time data logging and compliance audits, proactively identifying gaps and driving corrective actions to uphold documentation integrity and operational excellence. Facilitate cross-functional communication and escalation protocols for non-conforming products, ensuring timely resolution and alignment with production and engineering teams. Demonstrate proficiency in QA/QC protocols, maintaining up-to-date knowledge of approved testing methodologies by product and material type, and contributing to continuous improvement initiatives. Outcome: Ensure consistent equipment reliability and precise calibration to support accurate testing, regulatory compliance, and uninterrupted lab operations. Actions: Maintain and execute preventive maintenance schedules to ensure equipment uptime and minimize operational disruptions. Perform and document precise calibrations in alignment with regulatory standards and internal quality protocols. Monitor equipment performance trends and proactively address reliability issues through root cause analysis and corrective actions. Collaborate with lab teams and vendors to resolve equipment issues quickly and ensure continuous support for testing operations. Outcome: Maintain best-in-class lab facility and material management principles Actions: Ensure lab cleanliness, equipment readiness, and compliance through routine inspections, preventive maintenance, and adherence to safety and regulatory standards. Implement efficient inventory and material management systems to maintain accurate stock levels, traceability, and minimize waste. Drive continuous improvement initiatives to optimize lab layout, workflows, and resource utilization for enhanced operational performance. Collaborate and train lab personnel to uphold best practices in facility care, material handling, and documentation Outcome: Data Management & System SupportActions: Ensure accurate and timely data entry, review, and reporting to support reliable test results and regulatory compliance. Maintain and troubleshoot Macroview, SAP and other lab systems to ensure uninterrupted data flow and system integrity. Implement data governance practices including version control, access management, and audit trail maintenance. Collaborate with IT and quality teams to support system upgrades, validations, and continuous improvement of digital workflows. Basic Qualifications Education Requirements: Bachelor's degree in chemical engineering or related chemistry Job Experience: 2-3 years Competencies Ensures Accountability - Holding self and others accountable to meet commitments Optimizes Work Processes - Knowing the most effective and efficient processes to get things done, with a focus on continuous improvement Communicates Effectively - Developing and delivering multi-mode communications that convey a clear understanding of the unique needs of different audiences Drives Results - Consistently achieving results, even under tough circumstances Situational Adaptability - Adapting approach and demeanor in real time to match the shifting demands of different situations We appreciate the interest of recruitment partners, but we are not engaging external agencies for this role. #LI-TF1#LI-Onsite

About Us: Remedy Labs is a leading hemp manufacturing company dedicated to delivering high-quality products. We are seeking a detail-oriented and motivated scientist to join our team and support our research and manufacturing processes. Job Description: At Remedy Labs, you will play a crucial role in ensuring the quality and consistency of our existing products, developing new molecules, and improving yields. You will be responsible for conducting experiments, analyzing samples, and maintaining accurate records to support our operations. This position requires experimental organic chemistry experience, strong attention to detail, analytical skills, and a commitment to maintaining high standards OR exceptional intelligence and desire to learn. Highly qualified applicants (process chemistry experience and/or advanced degrees) will be considered for roles with more responsibility and should indicate their qualifications in bold text at the top of their resume. If you have a non-traditional background that you believe would translate to success in a chemistry lab please surface your story in large bold font at the top of the resume you attach to this application. Key Responsibilities: Execute experiments in an organic chemistry lab. Operate and maintain laboratory/ industrial laboratory equipment, including calibration and troubleshooting. Conduct quality control checks and assist in identifying areas for improvement in the manufacturing process. Collaborate with production and quality assurance teams to address any issues related to product quality. Maintain a clean and organized laboratory environment, adhering to safety protocols and regulations. Qualifications: Organic chemistry wet laboratory experience. Strong attention to detail and ability to work with precision. Excellent organizational and time management skills. Good communication and teamwork abilities. Commitment to maintaining a clean and organized work space. Working Conditions: Full-time position, Monday to Friday, with occasional overtime as needed. Hours are flexible and self motivation and autonomy are required. Primarily laboratory-based work with some exposure to manufacturing areas. Use of personal protective equipment (PPE) as required. Remedy Labs is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Compensation: $20.00 - $50.00 per hour Our MissionEmpowering Entrepreneurs with the Future of Rare Cannabinoids. We are a science company dedicated to providing the next generation of cannabis-based innovations. The study and manufacturing of cannabis compounds demands precision. In collaboration with industry-leading scientists and research partners from around the world, we develop the highest quality cannabinoids for cultivators, extractors, agencies, brands & manufacturers at every point along the supply chain. Our Vision Polygon is redefining the future of rare cannabinoid ingredient brands through innovations and a tireless dedication to quality. Built on the promise of these powerful natural ingredients, coupled with the most advanced science and technology, we define the highest benchmark the industry has to offer. Why Polygon?Polygon stands at the intersection of the finest organic Hemp farms and game-changing product innovators. Our R&D process combines world-class science with deep market knowledge to find first in class product-market fits; light years ahead of the competition. Yes, science is at the heart of what we do, but our greatest skill is finding excellence - the best growers, processors, researchers, and strategic partners to realize the potential of this ancient plant - turning it into one of the most valuable products in the world.

About Us: Remedy Labs is a leading hemp manufacturing company dedicated to delivering high-quality products. We are seeking a detail-oriented and motivated scientist to join our team and support our research and manufacturing processes. Job Description: At Remedy Labs, you will play a crucial role in ensuring the quality and consistency of our existing products, developing new molecules, and improving yields. You will be responsible for conducting experiments, analyzing samples, and maintaining accurate records to support our operations. This position requires experimental organic chemistry experience, strong attention to detail, analytical skills, and a commitment to maintaining high standards OR exceptional intelligence and desire to learn. Highly qualified applicants (process chemistry experience and/or advanced degrees) will be considered for roles with more responsibility and should indicate their qualifications in bold text at the top of their resume. If you have a non-traditional background that you believe would translate to success in a chemistry lab please surface your story in large bold font at the top of the resume you attach to this application. Key Responsibilities: Execute experiments in an organic chemistry lab. Operate and maintain laboratory/ industrial laboratory equipment, including calibration and troubleshooting. Conduct quality control checks and assist in identifying areas for improvement in the manufacturing process. Collaborate with production and quality assurance teams to address any issues related to product quality. Maintain a clean and organized laboratory environment, adhering to safety protocols and regulations. Qualifications: Organic chemistry wet laboratory experience. Strong attention to detail and ability to work with precision. Excellent organizational and time management skills. Good communication and teamwork abilities. Commitment to maintaining a clean and organized work space. Working Conditions: Full-time position, Monday to Friday, with occasional overtime as needed. Hours are flexible and self motivation and autonomy are required. Primarily laboratory-based work with some exposure to manufacturing areas. Use of personal protective equipment (PPE) as required. Remedy Labs is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Analytical Lab Tech Permanent About Heraeus Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead. About Heraeus Precious Metals With more than 350 years of experience in precious metals processing, Heraeus Precious Metals is the world's leading provider of innovative products and services, such as precious metals trading and recycling. Our products are used in a wide range of industries, for example to reduce climate killers such as nitrous oxide and methane and in the form of pharmaceutical ingredients for the treatment of cancer. Our innovative strength is driven by our 3,000 employees in more than 15 countries, who work passionately with our partners to develop pioneering and sustainable solutions. We are aware of our responsibility towards people and the environment and have set ourselves ambitious CO₂ targets. Sustainability is at the heart of all our business activities. Analytical Lab Technician The Analytical Lab Technician produces accurate and timely analysis of specified samples using the defined methods and procedures in order to support the company's sales, material management and production efforts. Your Role and Responsibilities: Performs analyses according to assigned written procedures, manages several concurrent analyses as required, and strives to exceed accuracy and performance measures as provided by company management. Closely examines sample quality and labeling and brings any deviation to the attention of Supervisor/Manager and suggests course of action. Prepares and reviews assay in specified form to be approved by Supervisor/Manager. Review equipment calibration status and correct as needed. Review laboratory data for completeness and accuracy. Perform/Support Method Development Activities Participates in shift change over and communicates the status of all analyses and needed work. Participate in and assist in generating method, equipment, quality, procedure and other training as provided by the laboratory manager. What is required for this role: High school diplomia required. Degree or certificate in chemistry is preferred but not required. Wet Chemistry Laboratory: Experience in wet chemical analysis and precious metals analysis preferred. Experience in general preparation and instrumental methods such as ICP, ICP-MS, Acid/Base Titrations, and XRF preferred. Ability to effectively communicate (orally and in writing) with all levels of the organization. The ability to understand concepts involving statistics, probabilities and formula manipulation and perform basic calculations on volume, mass, atomic percentages, weight percentages, density, molecular weight of alloys and compounds and charge weights. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; balance; stoop, kneel, crouch or crawl; talk or hear; taste or smell. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Curious? Apply now! We look forward to receiving your documents by reference code 58254 via our online application portal - even if you don't meet all the requirements, but have good reasons why you are still the right fit for this role! Any further questions? Our Recruiting Team, Heraeus Precious Metals, is happy to assist you by email: [[cust_RecTeam]]. Or visit us at jobs.heraeus.com.

Chemical Technician for a Data Center-Clarksville, TN A Water treatment Chemical Technician will be responsible for working at a customer's data center in the Clarksville, TN, area. The Chemical Technician will solve customer water treatment concerns, perform water treatment lab work, commission new piping and system assets, and troubleshoot water treatment and control equipment at a customer's massive data center. As a Technician, you will receive an industry competitive salary, expenses, and benefits. In addition, ample technical support is provided along with continuous training. Compensation is based upon experience and the ability to succeed. $55,000 to $70,000 first year base for a qualified candidate. Plus a year end bonus! We hire with a focus that favors the committed employee both in terms of overall compensation and growth opportunities. We have designed our compensation package accordingly. Benefits include a corporate 401k, health, dental, vision, and life insurance. Garratt-Callahan (wwwgarrattcallahan.com) is family friendly, profitable, stable, and fiercely private. No layoffs in 100+ years. No ownership change in 100+ years. 75+ straight years of profitability. We have operations from Asia, to the Caribbean, and in every state in the USA. Let's talk. Job Responsibilities: Solve customers' water problems. Treat industrial cooling towers to keep them energy efficient and environmentally friendly. Perform detailed water testing & analyses at a data center. Help deliver on customer KPIs and promote Garratt-Callahan solutions including proprietary chemical blends, equipment, & monitoring technology. Commission newly installed assets and control equipment. Reports directly to the Site Manager. Keep our existing customers happy and safe. About Garratt-Callahan: Garratt-Callahan is a US based private 100+ year old, nationwide water treatment chemical company. Garratt-Callahan *********************** treats industrial boilers and cooling towers to keep them energy efficient and environmentally friendly with one of the most advanced product lines in the industry. We are registered to ISO 9001:2015 and sell an industry leading line of “green" solutions, G-C GreenTech. We are headquartered in Burlingame, California. G-C is family owned, profitable, and expanding. We have five chemical plants in the USA, sales people in every state, and operations in Asia, the Pacific, and the Caribbean. Benefits: We offer a competitive benefit package which includes medical, dental, vision, AD&D, LT, and 401k. First year compensation $55,000 to $70,000 plus bonus, depending on experience. A car allowance. Advanced training, and a clear career path. Family friendly, flexible hours. A huge benefit of working for Garratt-Callahan is our stability and low turnover. No Layoffs in our 100+ year history. G-C is a profitable company. The last year that G-C did not turn a profit was during World War 2. To Apply, please log on to : ************************************************************************************************************************ Id=19000101_000001&job Id=557124&source=CC2&lang=en_US Thank you for considering Garratt-Callahan Company. Garratt-Callahan is an EEO/AAE employer. Minorities, women, veterans and individuals with disabilities are encouraged to apply. Requirements : You will be a successful applicant if you have a technical degree such as Chemistry, Chemical Engineering, Biology, Mechanical Engineering, Paper Science, or Water Resources. You must have a 4 year technical degree in the sciences to qualify for this position. A successful applicant must have experience or interest in learning advanced water treatment technologies. A successful applicant must be detail-oriented, adhere to safety protocols, and be able to lift 50 pounds wearing PPE in all weather conditions. One year technical sales, or an internship related to water treatment chemicals is preferred, but we are willing to train and mentor. Outside industrial sales experience is a plus. You must live in or near Clarksville, TN, area, and be familiar with the industrial marketplace of the area. Additional Preferred Qualifications: • Familiarity With Industrial Cooling Towers • Knowledge and Proficiency with Lab Procedures, Water Equipment, & Water Chemistry • Ability to Provide Virtual Presentations to Group • Experience Working in a Team Setting as a Collaborative Partner NOTE: Garratt-Callahan does not sponsor work visas. No recruiters please. If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at ************. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. This phone number is only for disability assistance. When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan. Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants. Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. The “Equal Employment Opportunity is the Law” poster is available at:**************************************************************** Garratt-Callahan Company's reaffirmation of Equal Employment/Affirmative Action Statement************************************************************************ Key Words: Chemistry, chemicals, scientific, science, salesperson, salesman, saleswoman, outside sales, technical sales, account representative, account executive, territory sales, territory manager, district sales, district manager, field engineer, field service, AE, sales engineer, data center, chemical engineer, chemist, mechanical engineer, biologist, biology, microbiology, nalco, ecolab, us water, veolia, Suez, ge water, chemtreat, drew industrial, solenis, chem-aqua, kurita, evoqua, fremont, water treatment, boilers, cooling towers, waste water, pumps, equipment, chillers, polymers, biocides, data center, Clarksville, TN, Nashville, TN.

I have a Special Chemistry Med Tech role available near Cane Ridge, Tennessee! Details - Full-time and permanent - Shift: Days - Opportunities for growth - Full, comprehensive benefits package (PTO, health insurance, etc.) Requirements - College degree - ASCP cert - Prior experience, including special chemistry Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751! You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min. REF#LM5029

is for a fast-paced production environment. involves physical testing of tile products and analytical testing of raw materials. The ideal candidate can learn the SOPs and can operate with minimal supervision. Typical hours are defined on a shift basis. However, overtime and schedule changes may be required as work must sync with production schedules and available staffing. Initial training would be on the day shift. The position reports to the Quality Supervisor. Requirements: Adhere to all safety rules and report any circumstances that are unsafe or that could lead to an unsafe condition. Clearly communicate any time off (paid or unpaid) to Supervisor. Responsible for being prompt and adhering to designated work hours and breaks. Able to lift 60 lbs. Experience with Microsoft Office is strongly preferred. Mathematics: addition, subtraction, & division. Ability to compose emails and attach files from PC. Good color vision. Ability to read spec sheets, measure products, and detect changes in critical values. Strictly follow SOPs and Testing Methods. Ask questions when unsure about the task. Clear and proactive communication with other team members. Actions based on data. Previous experience in QA/QC is a plus. Must be able to work night shift.

Permanent About Heraeus Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead. About Heraeus Precious Metals With more than 350 years of experience in precious metals processing, Heraeus Precious Metals is the world's leading provider of innovative products and services, such as precious metals trading and recycling. Our products are used in a wide range of industries, for example to reduce climate killers such as nitrous oxide and methane and in the form of pharmaceutical ingredients for the treatment of cancer. Our innovative strength is driven by our 3,000 employees in more than 15 countries, who work passionately with our partners to develop pioneering and sustainable solutions. We are aware of our responsibility towards people and the environment and have set ourselves ambitious CO₂ targets. Sustainability is at the heart of all our business activities. Analytical Lab Technician The Analytical Lab Technician produces accurate and timely analysis of specified samples using the defined methods and procedures in order to support the company's sales, material management and production efforts. Your Role and Responsibilities: * Performs analyses according to assigned written procedures, manages several concurrent analyses as required, and strives to exceed accuracy and performance measures as provided by company management. * Closely examines sample quality and labeling and brings any deviation to the attention of Supervisor/Manager and suggests course of action. * Prepares and reviews assay in specified form to be approved by Supervisor/Manager. * Review equipment calibration status and correct as needed. * Review laboratory data for completeness and accuracy. * Perform/Support Method Development Activities * Participates in shift change over and communicates the status of all analyses and needed work. * Participate in and assist in generating method, equipment, quality, procedure and other training as provided by the laboratory manager. What is required for this role: * High school diplomia required. Degree or certificate in chemistry is preferred but not required. * Wet Chemistry Laboratory: Experience in wet chemical analysis and precious metals analysis preferred. * Experience in general preparation and instrumental methods such as ICP, ICP-MS, Acid/Base Titrations, and XRF preferred. * Ability to effectively communicate (orally and in writing) with all levels of the organization. * The ability to understand concepts involving statistics, probabilities and formula manipulation and perform basic calculations on volume, mass, atomic percentages, weight percentages, density, molecular weight of alloys and compounds and charge weights. * While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; balance; stoop, kneel, crouch or crawl; talk or hear; taste or smell. * Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Curious? Apply now! We look forward to receiving your documents by reference code 58254 via our online application portal - even if you don't meet all the requirements, but have good reasons why you are still the right fit for this role! Any further questions? Our Recruiting Team, Heraeus Precious Metals, is happy to assist you by email: [[cust_RecTeam]]. Or visit us at jobs.heraeus.com. ReqID: 58254

Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! August Bioservices is looking for an Analytical Development team member that is passionate and driven regarding his/her work. August Bio desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. The Analytical Chemist I & II position, reporting to the Analytical Chemistry Supervisor, will operate under minimal supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development.Responsibilities Performs routine laboratory testing and duties Performs laboratory investigations in support of testing Troubleshoots analytical equipment Accurately documents all necessary and relevant information in a clear and concise manner per cGMP requirements Responsible in the development of analytical chemistry procedures to determine the identity, purity, stability, and other characteristics of samples that are analyzed Author and execute method validation protocols Author method validation reports Requirements Bachelor's Degree in chemistry, biology, or related science 2+ years of pharmaceutical experience or equivalent. Self-starter and ability to work independently Strong written/verbal communication and presentation skills Able to work flexible schedules on a short notice Ability to be a team player/work well with others Shifts 2nd shift: 3:00pm - 11:30pm, Monday - Friday 3rd shift: 11:00 - 7:30am, Monday - Friday At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment. We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team! August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.