Science jobs in IN

Job Description Contractor will prepare and analyze samples for drugs of abuse and antibiotics in blood, urine and wastewater using LC-MS/MS and LC-QTOF. Purpose of Position/Summary: Incumbent serves as a junior level chemist in the Chemistry Laboratory of the I Chemistry Laboratories. Incumbent prepares and analyzes samples for opioids and other novel psychoactive substances in human specimen (Blood, urine and serum) and wastewater. Other range of contaminants include antibiotics, Radionuclides, Metals, and Pesticides. Qualifications Incumbent shall have at least a bachelors degree in chemical or physical science from an accredited college or university. Incumbent shall have a minimum of 2 years of experience as an analytical chemist. Essential Duties/Responsibilities : Performs highly complex chemical analysis on environmental, food or clinical matrices to determine the level of contaminants or toxic substances using sophisticated instrumentation in compliance with EPA, FDA, or CLIA requirements. Adheres to Quality Assurance guidelines. Maintains proficiency and technical expertise by passing Proficiency Testing (PT) samples. Maintains assigned instrumentation in working order; performs preventative maintenance and repair on laboratory equipment. Completes all required paperwork; maintains instrument logbook, prepares technical reports and updates standard operating procedures (SOPs). Maintains a safe and uncluttered work area. Trains and cross trains on other analytical procedures within the laboratory. Assists the supervisor by performing related tasks as assigned. Job Requirements: Technical knowledge of and ability to operate highly complex laboratory equipment such as LC/MS/MS, LC/QTOF and GC/MS/MS. Familiarity with Sciex equipment such as QTRAP 6500+ and X500QTOF preferred. Ability to communicate effectively with others both within and outside of the laboratory. Broad knowledge of good laboratory practices (GLP) and good automated laboratory practices (GALP). Broad knowledge of principles and practices of analytical, organic and inorganic chemistry with subsequent experience during the last 2 years. Specialized knowledge of related scientific areas such as information systems, physics, and statistics. Practical knowledge of laboratory safety and biosafety. Extensive knowledge of appropriate state and federal laws, rules, regulations, and policies relative to the specialty area such as EPA, FDA, DEA, ISO 17025, CLIA. Ability to design analytical techniques and develop new methods of analysis. Ability to assist with epidemiological and/or statistical reports from data compiled on a daily, weekly, monthly or annual basis. Supervisory Responsibilities/Direct Reports: Not applicable. Difficulty of Work: Incumbent is engaged in scientific analyses that demand accuracy and demonstrated proficiency in applying laboratory analytical skills to problem solving. Projects involve many complex variables of great intricacy, and the chemist is often called upon to analyze unusual sample matrices. Work requires considerable use of analytical judgment and technical knowledge in order to draw accurate, logical conclusions. Incumbent may be required to testify in judicial proceedings as an expert witness for the . Errors in work could adversely affect the health, safety, and well-being of the public, coworkers, or the incumbent. Responsibility: Incumbent works under minimal supervision as a subject matter expert. Technical assistance is occasionally sought if expertise outside the incumbents specialized area is needed. Work is reviewed and evaluated upon completion for general technical accuracy; however, tasks are performed independently. Incumbents work has a substantial impact on the control and identification of opioids and other substances used for public health surveillance. Personal Work Relationships: Incumbent works with the supervisor, other State Department of Health employees, and representatives from the other state, local, and federal agencies to receive or provide assistance or work for solutions to common problems concerning analytical problems/techniques or interpretation of federal requirements. Physical Effort: Incumbent must be able to handle and prepare clinical specimens. Working Conditions: Incumbent works in a laboratory environment. Hazards include compressed gasses, flammable materials and chemicals which may be poisons or carcinogens/teratogens. Biohazards are also present. Appropriate safety precautions are always required.

Job DescriptionSalary: $62K-$80K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation. Cogent Scientific offers competitive pay (with relocation package when applicable), attractive benefits, and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values: Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharmaceutical Purification Chemist. Job duties include, but are not limited to, the following: • Purify small molecule organic samples using reversed-phase chromatography on milligram to multi-gram scale., • Thorough knowledge of preparative/semi-preparative chromatography and instrumentation required., • Utilize LC-MS systems to identify collection fractions., • Select an appropriate purification technique for unique mixtures., • Communicate with synthetic chemists regarding purification requirements and issues., • Help maintain a safe, organized, and productive lab. Job requirements include, but are not limited to: • BS - Chemistry or related field with 3-5 years of industry experience OR MS-Chemistry with 1-3 years of industry experience (preferably pharma)., • Preparative reverse phase (RP) LC experience required., • Familiarity with Agilent HPLCs and ChemStation software would be helpful., • Experience using Teledyne ISCO chromatography systems preferred., • Excellent communication skills verbal and written., • Works well both as a team and as an individual., • Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.

Job Description Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow. As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage— premiums either paid by Superior or highly subsidized—so you and your family can access great benefits with minimal cost. You’ll also join a supportive team, where experienced coworkers help you learn, grow, and succeed from day one. At Superior, you get more than a job—you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to team success. Superior is currently seeking an experienced Quality Control Chemist for our Indianapolis, IN location. This is a Monday through Friday position with working hours 8am-5pm. The position will perform quality control testing on incoming and outgoing products using the following instrumentation: Gas Chromatograph, Karl Fischer, viscometer, etc. The successful candidate will: • Possess strong problem-solving skills and initiative, • Work well under pressure and handle multiple tasks effectively and efficiently, • Display exceptional organizational skills and ability to prioritize work assignments, • Demonstrate ability to work in teams with members from various disciplines, • 4-year degree required (chemistry/biology/science), • Prior quality control experience (preferred), • Familiar with analytical equipment – specifically, GC, KF, viscometer We hire based on character as well as experience! EOE including disability/veteran/drug free

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Analyzes samples and/or develops/validates methodologies using HPLC and or GC for various compounds and components in compliance with SOPs and regulatory agency guidelines. Essential Duties and Responsibilities: • Demonstrates and promotes the company vision, • Regular attendance and punctuality, • Applies GMP/GLP in all areas of responsibility, as appropriate, • Organizes and conducts routine analyses for compounds using HPLC, LCMS, G independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines, • Documents work and maintains study documentation and laboratory records, • Independently able to use and perform basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while learning to perform routine and non-routine maintenance, • Provides input and participates in project meetings, • Performs peer review and QC review of data, • Performs assigned workload on a daily basis and effectively completes multiple assignments., • Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members., • Maintains a clean and safe laboratory work environment, • Understands data generated, and history of methods., • Recognizes deviations from normal results and inform Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems., • Identifies problems independently., • Able to adapt to new procedures or particular needs as directed., • Able to identify critical steps in an assay., • Leads process improvement initiatives., • Completes all required training courses., • Trains and assists less experienced staff, • May assist in optimizing and validating methods for a variety of matrices, • Knowledge of departmental procedures and policies, • Viewed as a resource within their team, • Conducts all activities in a safe and efficient manner, • Performs other duties as assignedQualifications, • Bachelor’s Degree in relevant field (Laboratory experience may be substituted for degree), • 1+ years of experience preferred, • Ability to learn new tasks, • Ability to think critically and solve problems quickly and efficiently, • May work with potentially hazardous substances and/or radio labeled materials, • Mandatory immunizations and screening as required, • Expected to understand the process for handling hazardous wastes and receive on-the-job training for handling specific waste types in their job area, • Will be exposed to food allergens (ex. Milk, tree nuts, peanuts, fish, shellfish, etc.), • Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top., • Work requires use of PPE (personal protective equipment), • Overtime and weekend work as required, • Will be exposed to potential food allergens Additional Information What we offer: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Job Description • Perform analytical testing of medium to high complexity on drug substance/drug product using instrumentation including, but not limited to, compendial testing (e.g. description, EP color/clarity, VOI, osmolality), pH, HIAC, MFI, HPLC, UPLC, icIEF, GC, TOC, Karl Fischer, FTIR, UV, LC/MS, and NMR., • Initiate Trackwise events and participate in conducting investigations, • Execute method qualifications, • Document test results in notebooks and reports, • Perform technique training with new analystsQualifications The ideal candidate would possess: • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies, • Bachelor’s or M.S. degree with a science concentration (chemistry, biology, or related fields) with at least 2 years of related industry experience, • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply, • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace ®. We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: • Health benefits available Day 1, • 401k available Day 1, • 10+ paid holidays/year, • Free HAZWOPER training and certification, • Overtime opportunities, • Ability to be cross-trained into different roles Job Description CDL A or B Sign-on $3,000. Performs various assigned tasks and physical labor to ensure proper off-site treatment and disposal of customers’ hazardous waste materials in accordance with environmentally responsible and cost-effective practices and Clean Earth policies, practices, and procedures. Primary Responsibilities (Essential Functions): PRINCIPAL DUTIES AND RESPONSIBILITIES: • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations. • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. • Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures. • May require obtaining and maintaining a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations. • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies, • Performs other duties as assigned. Qualifications Preferred Qualifications: EDUCATION/CREDENTIALS: Entry Level Associates Degree(Preferred Bachelor of Science) MEASURES OF PERFORMANCE Completion of the following curriculum: • 40-hour OSHA HAZWOPER (29 CFR 1910.120), • Acquisition of Commercial Driver’ s License (B or C) with Hazmat Endorsement, • Clean Earth Lab Pack I Training – (24 hours), • RCRA/DOT refresher course, • Department of Transportation, • Lab Pack definitions and procedures, • Lab pack Field Program, • Introduction to High Hazardous Cylinder Assessment course, • Customer Interactions, • Waste Management Methods, • On-Site Expectations, • Manifest/ LDR Completion, • Health & Safety course(s), • Customer Approach, • 40 hours Depack Experience, • Forklift Training Additional Information Clean Earth offers competitive benefits, including health, dental and vision insurance, life insurance and disability plans, as well as a 401k with company matching. Together, we work hard, we succeed through industry know-how, safety, and sustainable growth, and we recognize a job well done. Knowledge is power and at Clean Earth, we support the continuing education and training of each team member. Every team member is encouraged to learn and grow with the company through various educational channels that are well-suited for their career path at Clean Earth. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Harsco Clean Earth’s website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Contact Kayla Wallace, Senior Recruiter at 414-388-6933 and Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. Please call only for disability application.

Job Description WHO WE ARE We are a company where people matter. We are family driven. We are financially strong. And we are looking for problem-solvers to join our growing team. BENEFITS • Up to 10% Retirement Contribution, • $600 per Year Wellness Incentive, • Two Weeks Starting Paid Time Off QC Chemist OPPORTUNITY The primary purpose of this position is to perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions. This position may also provide technical support to operations and sales. Hours are for this position are Sunday-Monday 7am -7:30pm and Tuesday- Wednesday from 7am-7:30pm. As QC Chemist, primary responsibilities include: • Perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions., • Record and maintain analysis/records accurately, neatly, legibly and completely., • Prioritize daily laboratory activities to meet production schedules., • Perform instrument maintenance, calibrations, quality control checks, solution preparations, and solution standardizations., • Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues., • Maintain a clean and neat laboratory at all times., • Adhere to all safety SOPPs., • Initiate corrective actions on identified non-capable procedures or practices., • Maintain and properly store sample retains., • Communicate to supervisor concerns about standard laboratory procedures, operational problems, quality trends, etc., • Maintain a professional attitude and demeanor at all times, treat others with courtesy and respect, and respond to all requests in a professional manner., • Promote complete customer satisfaction through quality and service to both internal and external customers., • All staff members are responsible for reporting food safety problems to their supervisor or the SQF Practitioner upon observation of a known or potential issue., • Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers, • Perform all duties outlined in relevant SOPs and all other duties to be assigned., • Bachelor's Degree in Chemistry or related field is required., • Must have good communication and interpersonal skills, including the ability to read, write, and speak in English., • Proficiency in computer skills and good working knowledge with all MS Office applications., • Ability to accurately transfer written and verbal information and documentation and enter data into existing computer system., • Must be self-motivated and able to work independently as well as in a group setting., • Able to apply mathematical and problem solving skills for resolution., • Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers., • Participate in RCRA, regulatory, health & safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant., • Regular attendance is essential., • Perform all duties outlined in relevant SOPs and all other duties to be assigned., • Work with other staff members to maintain workload balances. Provide back-up support as necessary. Benefits and perks include 401k and profit sharing, medical/dental/vision/life insurance, paid time off, tuition reimbursement, adoption assistance, legal services insurance, scholarship awards for children of employees, summer picnic, community giving events, free family wellness coaching including nutritionist and fitness coach. WHY HYDRITE? Watch this Why Hydrite video to find out: WANT TO STAY CONNECTED? FIND US ON SOCIAL MEDIA • LinkedIn: linkedin.com/company/hydrite-chemical-co-, • Facebook: facebook.com/hydrite Privacy Notice for California Residents:

Job Description MC Labs is growing and we have exciting opportunities available for analytical chemists! If you are a recent graduate in the chemical or biological sciences or have industrial experience already, we would love to hear from you. Due to large growth in the pharmaceutical testing sector, we are aggressively seeking new chemists wanting a challenge and a great place to learn and grow. Some of the advantages of working at MC Labs include: • -Flexible Work Schedules (optional 4-day work weeks available), • -Highly Competitive Pay, • -Sign-On and Retention Bonuses, • -Industry leading Paid-Time-Off Program, • -Paid holidays, • -Continued education in the Pharmaceutical Sciences, • -401K Savings with Company Match, • -Comprehensive Benefits Package (Health, Dental, Vision) Job Title: Analytical Chemist Job Description: Perform Chemical, Analysis on a variety of sample types (pharmaceutical intermediates and finished goods, raw materials, food additives, etc.) using the latest in laboratory and software technology. General responsibilities include maintaining a clean and safe working environment and adhering to laboratory procedures and policies in a cGMP laboratory. Essential Duties Include: • Perform analysis utilizing a variety of laboratory equipment and procedures that may include Wet Chemistry, HPLC, GC, UV-VIS, KF, FTIR, pH, and TLC., • Maintenance of a clean and safe working area., • Execute Method Validation Protocols and Method Technical Transfer Protocols, • Document laboratory data using Good Documentation Practices utilizing an Electronic Laboratory Notebook, • Perform Data Analysis as Required by Analytical Method including data package write up and submission to Quality for approval., • May author data reports for development studies as required., • Must be motivated and able to work independently in a dynamic laboratory environment., • Able to troubleshoot and maintain laboratory equipment as required., • Good documentation skills are required., • Must have a strong mathematic and analytical aptitude., • B.S. in Chemistry/Biology, • Must be motivated and able to work independently in a dynamic laboratory environment., • Able to troubleshoot and maintain laboratory equipment as required., • Good documentation skills are required., • B.S. in Chemistry/Biology, • 0 – 5 Years of experience in an industrial laboratory setting

Job Description WHO WE ARE We are a company where people matter. We are family driven. We are financially strong. And we are looking for problem-solvers to join our growing team. BENEFITS • Up to 10% Retirement Contribution, • $1.50/hr shift premium!, • $600 per Year Wellness Incentive, • Two Weeks Starting Paid Time Off QC Chemist The primary purpose of this position is to perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions. This position may also provide technical support to operations and sales. Hours are for this position are Wednesday 2am-6am, and Thursday- Saturday from 7pm-7:30am. Training will be done on 1st shift. As QC Chemist, primary responsibilities include: • Perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions., • Record and maintain analysis/records accurately, neatly, legibly and completely., • Prioritize daily laboratory activities to meet production schedules., • Perform instrument maintenance, calibrations, quality control checks, solution preparations, and solution standardizations., • Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues., • Maintain a clean and neat laboratory at all times., • Adhere to all safety SOPPs., • Initiate corrective actions on identified non-capable procedures or practices., • Maintain and properly store sample retains., • Communicate to supervisor concerns about standard laboratory procedures, operational problems, quality trends, etc., • Maintain a professional attitude and demeanor at all times, treat others with courtesy and respect, and respond to all requests in a professional manner., • Promote complete customer satisfaction through quality and service to both internal and external customers., • All staff members are responsible for reporting food safety problems to their supervisor or the SQF Practitioner upon observation of a known or potential issue., • Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers, • Perform all duties outlined in relevant SOPs and all other duties to be assigned., • Bachelor's Degree in Chemistry or related field is required., • Must have good communication and interpersonal skills, including the ability to read, write, and speak in English., • Proficiency in computer skills and good working knowledge with all MS Office applications., • Ability to accurately transfer written and verbal information and documentation and enter data into existing computer system., • Must be self-motivated and able to work independently as well as in a group setting., • Able to apply mathematical and problem solving skills for resolution., • Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers., • Participate in RCRA, regulatory, health & safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant., • Regular attendance is essential., • Perform all duties outlined in relevant SOPs and all other duties to be assigned., • Work with other staff members to maintain workload balances. Provide back-up support as necessary. Benefits and perks include 401k and profit sharing, medical/dental/vision/life insurance, paid time off, tuition reimbursement, adoption assistance, legal services insurance, scholarship awards for children of employees, summer picnic, community giving events, free family wellness coaching including nutritionist and fitness coach. WHY HYDRITE? Watch this Why Hydrite video to find out: WANT TO STAY CONNECTED? FIND US ON SOCIAL MEDIA • LinkedIn: linkedin.com/company/hydrite-chemical-co-, • Facebook: facebook.com/hydrite Privacy Notice for California Residents:

Job DescriptionSenior Analytical Chemist - Method Development Tri-Pac, Inc., a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced Senior Analytical Chemist for immediate addition to our fast growing team. This position is in South Bend, Indiana (Onsite) Job Description: Senior Analytical Chemist - Method Development maintains a working knowledge of all Tri-Pac procedures, customer procedures and requirements, and follows Good Manufacturing Processes (GMP) and GLP. This individual must have good interpersonal skills with a collaborative team attitude that is customer focused and quality driven. Responsibilities: • Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV, IR, titration) of analysis for excipients, new chemical entities, drug products and stability samples., • Independently perform method evaluation/development/validation/verification and troubleshooting instruments and improvement of processes., • Support Cleaning Validation method development and sample testing., • Interpret data and make recommendations to management for improvement or potential concerns., • Compare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirements., • Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation., • Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations., • Independently author standard operating procedures, analytical testing procedures, batch release testing forms, and create document templates for use by junior team members., • Create report templates and/or enter data into established reports/templates or software-based systems., • Review routine laboratory experiments for accuracy and provide guidance to junior team members to ensure future compliance., • Identify and recommend opportunities for improved efficiencies, internal/external client service and teamwork within the analytical group., • Serve as a point of contact for laboratory testing support and provide updates to laboratory supervision and/or client., • With supervision, support the scheduling and planning of internal/external client project work to ensure the highest levels of efficiency and quality standards are met., • Support the development of a quality environment by driving and monitoring quality standards within the team., • Become a resident expert in the use of LIMS (perform supervisory sign-off for electronic reports) and other software-based systems., • Serve as a method troubleshooting resource to identify and document critical factors that affect method performance and assist peers in resolving method issues in a timely, cost-effective manner., • Assist laboratory management with the preparation and execution of laboratory investigations/deviations and CAPA., • Mentor and train new laboratory team members.Education and/or Experience:, • Minimum bachelor’s degree in Chemistry, Pharmacy, or another related field; 4-7 years related experience., • Experience with Medical Devices and/or OTC consumer products., • Lab Instrumentation including GC, HPLC, FTIR., • GMP, GLP, LIMS. yswoGqHhkQ

Job Description Research and Development ( R &D )Chemist Tri-Pac, Inc. a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced Research and Development ( R &D ) Chemist for immediate addition to our fast growing team. Job Description: The R&D Chemist is responsible for all steps of formula development from ideation to final formulation. Primary responsibilities will be the innovation of new products, technology transfer and cost savings. He/she will demonstrate formulation and innovation skills in Personal Care, Cosmetics and Over-the-Counter products. The R&D Chemist will be proficient with analytical and numerical skills and able to perform basic mathematical calculations in various units of measurement and able to navigate concepts such as fractions, percentages, and ratios. He/she must have a strong attention to detail, capable of efficiently communicating verbally and through writing, produce and share reports, demonstrate excellent organizational skills be able to perform physically demanding activities such as moving and lifting equipment and standing for extended periods of time. Responsibilities: • Formulate product prototypes and evaluate them for chemical and physical properties, performance, and stability., • Develop new formulations for different personal care products, cosmetics, and OTC’s., • Improve current product formulations., • Research product formulations and properties of raw materials., • Provide and prepare samples for biological laboratory and field testing for efficacy and safety., • Initiate, develop, and create innovative products to expand the R&D formulation library and enhance customer presentations., • Establish product specifications and procedures as required for R & D projects., • Support scale-ups from prototype to commercial manufacture and following Good Manufacturing Practices (GMP)., • Support technical service for operations and consumer relations., • Conduct research and field evaluations on new products., • Develop new products and improve functioning of existing products., • Provide technical assistance and supervisory support within laboratory, and documentation to Compounding, Production, Documentation, and Scheduling Departments., • Coordinate research and development activities within all organizational departments., • Develop reports and documents detailing project processes, results, and conclusions., • Maintain accurate records, notebooks of analysis and work performed., • Comply with all Tri-Pac Safety requirements, GMP/GLP, and customer requirements., • Support scheduling and testing of R&D stability samples., • Support shipping samples to external lab for testing., • BS or MS Degree in Chemistry or Biosciences or related degree, • Minimum 2 years’ experience in cosmetic formulation/product development or related field. OTC/Drug formulation preferred. Competitive Salary/ Pay & Packages, Vacations, Insurance, 401K, Life Insurance, Disability (Long term/ Short term) and Continuous Training. Work where you are HAPPY! Tri-Pac, Inc. also recognizes the importance of continuing education and offers Education Assistance to our employees to encourage continued personal development and growth. Thank you for your interest and consideration of a career with Tri-Pac, Inc. Tri-Pac, Inc. is an Equal Employment Opportunity / Affirmative Action Employer To Staffing & Recruitment Agencies: Our Company does not accept unsolicited CV's or applications from agencies. We are not responsible for any fees related to unsolicited CV's or applications and explicitly reserve its right to contact candidates presented in such unsolicited CV or application. Powered by JazzHR eXiHhRAyh2

We are seeking an experienced and detail-oriented Senior Analytical Chemist to join our client’s team and support critical pharmaceutical development projects. This onsite, contract-to-hire position, based near Brownstown, IN, focuses on performing advanced laboratory testing and method development for raw materials, packaging components, in-process samples, and finished products. The role plays a key part in ensuring compliance with cGMP standards while driving innovation in analytical testing and method validation. Compensation: • $38-$47/hour based on experience Work Schedule: • Monday through Friday, 8:30am – 5:30pm Key Responsibilities of the Senior Analytical Chemist: • Perform routine and complex chemical and physical tests on raw materials, active pharmaceutical ingredients (APIs), packaging, in-process, and finished products, • Utilize advanced techniques including HPLC, GC, dissolution, Karl Fischer titration, wet chemistry, and particle size analysis, • Develop and validate analytical test methods in alignment with ICH, FDA, and USP requirements with minimal supervision, • Conduct analytical research to evaluate new raw materials, packaging materials, and reference standards, • Draft and revise SOPs for laboratory processes and ensure compliance with regulatory guidelines, • Prepare technical documents to support regulatory submissions (IND, NDA, ANDA), • Troubleshoot laboratory methods and instrumentation, recommending and implementing improvements, • Provide peer review of analytical data and ensure accuracy of laboratory records, • Train and mentor junior chemists on instrumentation, methodology, and best practices, • Support method transfers and contribute technical insight for the purchase of new laboratory equipment, • Collaborate with cross-functional teams to ensure testing and reporting timelines are met Qualifications and Skills for the Senior Analytical Chemist: • Bachelor’s degree in Chemistry or related field required; advanced degree preferred, • 8–12 years of experience in pharmaceutical product analysis within a cGMP-regulated laboratory, • Strong expertise in method development, method validation, and analytical instrumentation (HPLC, GC, dissolution, wet chemistry, ICP-MS, particle size analysis), • In-depth knowledge of cGMP, FDA, ICH, and USP/NF guidelines, • Proven ability to write and edit technical documentation and regulatory reports, • Skilled in troubleshooting laboratory instrumentation and analytical methods, • Proficiency in Microsoft Word and Excel, LIMS, and Chromatography Data Systems, • Excellent communication skills with the ability to lead projects and mentor junior analysts, • Strong organizational, problem-solving, and time management abilities Why Join Us? This opportunity provides the chance to work on complex, cutting-edge projects within a collaborative pharmaceutical laboratory environment. You’ll play a critical role in developing analytical methods that directly impact drug product quality, while being part of a team that values technical expertise, mentorship, and professional growth. About Us: Contemporary Staffing Solutions (CSS) is a trusted leader in providing contract, temporary, temp-to-hire, and direct hire staffing solutions. With decades of experience, we’ve grown from a staffing agency to a nationwide provider of workforce management solutions. Our niche recruitment expertise spans Accounting & Finance, Call Center & Office Support, Human Resources, Sales & Marketing, and Information Technology. Explore more about CSS and how we connect great talent with exceptional opportunities by visiting .

Job Responsibilities: • Perform accurate and timely testing of routine lab samples in compliance with GMP and safety protocols., • Assist with LCMS and HPLC analysis of materials, ensuring reliable and precise results., • Support the preparation, processing, and characterization of samples for research and development activities., • Operate and maintain laboratory instruments for sample characterization, ensuring efficient and accurate data collection., • Contribute to the qualification of new active ingredients and raw materials, including assisting with shelf-life extension studies for existing products., • Adhere to established laboratory safety standards, ensuring a safe and compliant working environment., • Communicate data, findings, and recommendations effectively to team members and cross-functional stakeholders. Qualifications: • Bachelor's degree in Chemistry, Chemical Engineering, Biochemistry, or a related scientific field., • Minimum of 0-2 years of experience in a research or manufacturing/research laboratory environment., • Experience with laboratory equipment and techniques, such as HPLC, LCMS sample preparation, and characterization methods., • Familiarity with formulation design or development is a plus., • Strong attention to detail, with the ability to follow protocols and guidelines precisely., • Excellent communication skills, both verbal and written., • Ability to work independently while also being an effective team player.

Job Title: Environmental Field Chemist (Entry Level) Location: Indianapolis, IN Starting Pay: $22/hr Contact to Hire - 9 months or sooner • Extensive training and advancement program including pay raises, • Open to recent graduates (2025) Our client, who is one of the largest environmental services firms in North America is looking for Environmental Specialist to join their renowned team of professionals. They provide leading institutions in the higher education, life sciences, healthcare, and industrial sectors with diverse services and advice to assist them with compliance management. As an Environmental Specialist you will support our clients by managing their hazardous waste programs & projects, utilizing state & federal regulations. This is a labor-intensive role that requires a high-level of technical aptitude and the ability to deliver high-level customer service Essential responsibilities and duties: Technical • Completion of on-boarding and Safety Training Development Program, • Safety equipment inspections, • Hazardous waste inspections, • Perform and document environmental health and safety (EHS) audits for clients, • Regularly preparing chemical and biological waste for shipment and disposal, including creation of all federal/state waste documents and managing the paperwork for the material, • Following any applicable state and federal regulations [Resource Conservation and Recovery Act (RCRA) & Department of Transportation (DOT) regulations], • Develop understanding of OSHA regulations as well as Health and Safety practices, • Monthly on-call responsibilities as part of our Emergency Response team Hands-on: • Material handling (e.g. transportation of materials within client sites as well as from client sites to transfer and/or end disposal facilities), • Safe handling of hazardous waste containers on client sites, as well as loading/unloading of waste from vehicles, • Packaging and prepping of hazardous waste for shipment, • Spill response measures, including assessment of the spills and potentially leading the cleanup efforts, • Requires you to work 40+ hours per week and overtime is frequently required Customer service: • Professional attitude, high energy, and high-level communication skills required when dealing directly with client representatives, • High level of expertise (e.g. state/federal regulations, EHS standards, waste management procedures, etc.), • Train clients on proper chemical safety and hazardous waste management, • Attending client operations meetings, • Training of new team member(s) Qualifications: • BS/BA in Environmental Science or Business-related degree or relative Military experience preferred, • Valid driver’s license, • Ability to work as a member of a team as well as an individual