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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 • Perform non-routine analytical activities by independently developing and characterizing stability indicating methods for early phase pharmaceutical small to medium molecules with pre-set timelines using instrumentation such as, but not limited to, UPLC/HPLC, Dissolution, GC, Thermogravimetric DSC/TGA, and KF titration, • Participate in technical discussions with project leads to recommend alternatives, research new methods/techniques and discuss potential solutions to problems., • Plan critical laboratory experiments to investigate aberrant results, determine root cause and recommend action plan, • Write Standard Operating Procedures (SOPs), assist in generating technical reports, prepare data for presentations/technical discussions and transfer methods internally and externally, • Prepare method protocols, & technical reports for characterization of analytical methods based on separation techniques (HPLC, UPLC, GC), Spectro-analytical technique (Ultraviolet-Visible Spectrophotometry) and dissolution testing, • Assist and mentor junior level scientists on analytical techniques and troubleshooting issues., • Ensure project deliverables are scientifically accurate and meet timeline expectations, • Comply with all laboratory safety guidelines including Personal Protective Equipments (PPEs), • Maintain general cleanliness of the lab, including personal bench space and common use areasQualifications The ideal candidate would possess: • Deep understanding of analytical sciences, drug development process, GMP/GLP requirements, and pharmaceutical industry trends, • Previous experience in pharmaceutical oral solid dosage & parenteral drug product analytical testing, • Good knowledge of three main pharmacopoeias (Japanese; JP, US; USP and European; Ph. Eur.) and ICH guidelines related to method development and validation, • Experience in developing pharmaceutical small molecules analytical chemistry methods for dissolution multi-media screening and analyzing data using compendial methods, • Understanding of experimentation and data analysis using Empower software, • Excellent project management skills; Ability to communicate complex scientific findings/recommendations and project resource requirements (material, manpower, time, etc.), and elevate relevant issues to project lead and line-management, • Excellent communication (oral and written), attention to detail, effective problem-solving and decision-making skills, • 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, • Experience in exploration and application of innovative technologies/approaches to analytical development activities, • Experience with the transfer of analytical technologies, • Ability to drive performance by tracking and managing key performance indicators using internal and external metrics, • Ability to prioritize complex workloads and manage changing priorities, • Bachelor's, Master's, or Doctorate degree with a science concentration (chemistry, biology, or related fields) with at least 4 years of related industry experience, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information • Position is full-time, 8:00 am- 5:00 pm Overtime as needed., • 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 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 • 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 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 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 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.

The individual selected will be based at the central IU Health Pathology Laboratory (IUHPL) in Indianapolis, which houses an automated clinical chemistry core laboratory providing testing for general chemistry and special chemistry including toxicology. This position is expected to have a major impa

Job Responsibilities: • Perform qualitative and quantitative chemical analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and titrations., • Prepare and standardize reagents, solutions, and buffers., • Conduct testing on raw materials, intermediates, and finished products according to approved methods and SOPs., • Document all testing activities clearly and accurately in compliance with cGMP and ALCOA+ principles., • Interpret and evaluate analytical data, ensuring results meet established specifications., • Participate in method validation, equipment calibration, and troubleshooting as needed., • Maintain laboratory equipment and ensure proper functioning through routine maintenance and calibration., • Assist in investigations of OOS (Out of Specification), OOT (Out of Trend), and deviations., • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field., • Minimum 2 years of hands-on experience in a QC laboratory within the pharmaceutical or biotech industry., • Proficient in analytical techniques (e.g., HPLC, GC) and good laboratory practices., • Solid understanding of cGMP, USP/EP, and FDA regulatory requirements.

The QC Chemist will support all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compl

The Company is seeking a Vice President of Marketing Data Science to provide strategic leadership in the intersection of digital marketing, data science, AI, and measurement. Vice President of Marketing Data Science. Applicants for the Vice President of Marketing Data Science position at the company

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AI PhD Discovery Data Science Internship. PhD student with at least three years of completed graduate work in Statistics, Computer Science, Electrical and Computer Engineering, Operations Research, Mathematics/Applied Math, or closely related field.

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Gpac, a 30+ years recruitment company, is partnered with a well-established company in the mechanical industry.We are currently seeking a highly experienced HVAC/Piping Project Manager for our client, a large Mechanical Contractor known for its great employee tenure.This is an amazing opportunity fo

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My client is the leading General Contractor in Indianapolis, specializing in large-scale commercial construction projects.They place a strong emphasis on safety, employing full-time safety professionals and implementing proven practices that utilize both leading and lagging indicators to continuousl

Since 1953, Ferguson has been a source of quality supplies for a variety of industries.Together We Build Better infrastructure, better homes and better businesses.We exist to make our customers' complex projects simple, successful, and sustainable.We proactively solve problems, adapt and grow to con

My client specializes in light industrial and manufacturing projects in the Indianapolis market.This tight-knit organization is family-owned and growing rapidly, with a full project pipeline of $30-50M properties over the next year.They are looking for a Project Manager to join their team and help g

Product Deployment Project Manager.At Calumet we deliver innovative specialty products trusted by companies across the globe.We are the foundation to everyday essential products that help millions of people live and thrive.We are headquartered in Indianapolis and have numerous production locations i

Join American Structurepoint and become part of a team that goes the extra mile for our clients and communities.We live by our values - respect, staff development, results and family.Our team is encouraged to explore new ideas and turn our clients' dreams into reality.With exceptional benefits, trai

Project Manager - Water Business - Indianapolis.Black & Veatch is a leading employee-owned global engineering, procurement, consulting and construction company.Consistently recognized as "Best Companies to Work For" and "Best Employers for Diversity.One of the biggest Water & Wastewater Civil Design

Determine the scheduling of different phases of a project based on established deadlines.Negotiate contracts with architects, vendors, contractors and other workers.Secure building permits and licenses and delivery of materials and equipment to construction sites.Monitor construction progress, inclu

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Licensing Analyst/Business Admin.Begin a fulfilling career with the State of Indiana by joining one of the largest employers in the state, offering a range of opportunities across 60+ agencies.At the state, you'll find competitive compensation, a robust benefits package, and a commitment to work-lif

Project Manager Special Projects.My client is one of the best known GCs in Indianapolis.They already have a pipeline over $450M for the next two years with some exciting projects in the area.They are a self perform GC with great benefits! Apply today!.Lead construction projects and supervise the con

Assume duties of the classroom teacher in accordance with school district lesson plans, school rules, and Kelly policies.This includes: Leading instruction in the classroom by conducting the teachers existing lesson plans Instructing students Substitute Teacher, Teacher, Substitute, Tow, Staffing.

My client is a well-established general contractor based in Indianapolis, known for delivering high-quality commercial and industrial projects.They specialize in construction management, general contracting, and design-build services across sectors like retail, multifamily, healthcare, and education

Assume duties of the district employee in accordance with school district lesson plans, school rules, and Kelly policies - Empower students to learn, and encourage classroom participation - For long-term teacher assignments, it may be requir Substitute Teacher, Teacher, School, Substitute, Tow, Educ

GEO Academies is a national, non-profit network of open-enrollment, public charter schools committed to empowering students to accelerate their academic pathways, advance their social mobility, and achieve their career and lifelong goals.Our innovative and award-winning K-16 GEO Academies Model begi