Research and development technician jobs in Zionsville, IN - 247 jobs

Indianapolis, IN $24/HR The Analytical R&D Team is seeking a detail-oriented and motivated Chemist. In this role, you will support scientists in day-to-day laboratory activities related to method development, non-GLP and GLP validations, and sample analysis. This position is ideal for someone who is eager to learn, values collaboration, and is committed to maintaining high standards of data quality and safety. Chemist Responsibilities: Assist ARD scientists with sample weighing, preparation, and analysis of active ingredients, intermediates, impurities, and formulated products for both quantitative and qualitative purposes Support laboratory experiments for non-GLP and GLP method validation as needed Learn and operate analytical instrumentation, including HPLC, GC, LC/GC/MS, and more. Perform routine instrument maintenance and troubleshoot issues when they arise Process analytical data and document experimental procedures and results in a timely and accurate manner to ensure data integrity Collaborate effectively with scientists and other stakeholders; adjust priorities to support urgent projects when necessary Work independently when appropriate and demonstrate strong problem-solving abilities Adhere to all Corteva EHS&S policies and demonstrate a strong commitment to laboratory safety Chemist Qualifications: Bachelor's degree in Chemistry or a related scientific field Familiarity or strong understanding of analytical chemistry techniques preferred Excellent written and verbal communication skills Willingness to learn continuously and follow all safety protocols

This role can sit anywhere in the US as long as it is near an Accenture Corporate Office We are: Looking to be part of a transformational digital engineering and manufacturing practice? How about an opportunity to help world-class clients solve their biggest challenges and create products and services that customers love - quickly, efficiently and sustainably? Industry X combines Accenture's powerful digital capabilities with deep engineering and manufacturing expertise. We use the power of data and digital to help our clients reimagine the products they make, and how they make them. By connecting engineering and manufacturing operations every step of the way - from how products are designed and engineered, sourced and supplied, manufactured, to how they are serviced and renewed, we help them achieve greater productivity, drive growth and meet their sustainability commitments. Find out more about Industry X. You are: A ambitious Manufacturing Systems (MES) Specialist ready to take on new challenges. As industries head towards Manufacturing and Factory Digitalization, MES stand in the center of manufacturing excellence. The Work: * Lead in the design, development, documentation, and implementation of Körber PAS-X Manufacturing Execution Systems (MES) * Design/Author/Develop/Configure Electronic Batch Records (EBR) * Implement MES solutions and integrate with ERP and control equipment * Documentation of MES configuration and validation of EBRs * Work closely with business management and users to strategically define the needs and design solutions that add value * Document and analyze the information needs of the business and ensure appropriate solutions are delivered according to GxP standards * Respond to requests for client proposals * Manage and develop client relationships Job Requirements: * Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements. Qualification Here's What You Need: * A minimum of 2 years of experience with Körber PAS-X MES solutions in a highly automated Life Sciences manufacturing environment * Bachelor's Degree or equivalent (minimum 3 years work experience). If Associate's Degree, must have equivalent minimum 6 years work experience Set Yourself Apart: * Knowledge of FDA and GMP guidelines * Strong written and oral communication skills * Ability to work in a team-oriented, collaborative environment * Ability to facilitate meetings and follow up with resulting action items * Understanding of Life Sciences validation processes * Working knowledge of software Development Life Cycle (SDLC) and support methodologies Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. Role Location Hourly Salary Range California $30.67 to $98.94 Cleveland $28.41 to $79.13 Colorado $30.67 to $85.48 District of Columbia $32.69 to $91.01 Illinois $28.41 to $85.48 Maryland $30.67 to $85.48 Massachusetts $30.67 to $91.01 Minnesota $30.67 to $85.48 New York/New Jersey $28.41 to $98.94 Washington $32.69 to $91.01 #LI-NA-FY25 Locations

SpectronRx is a rapidly growing Contract Development and Manufacturing Organization (CDMO) based in Indianapolis, IN, with additional locations in South Bend and Bunker Hill, IN, Danbury, CT and Europe. We are seeking an experienced R&D, Technician to join our growing company. The R&D, Technician will ensure the quality built into our products. ESSENTIAL FUNCTIONS Wet Chemistry testing including pH, Osmolality, Immunoreactivity Fraction (IRF) testing. Prepare buffers, mobile phase, and linearity sets for testing. Take inventory and maintain ordering. Maintain clean laboratory environment by performing waste management. Train on instrumentation such as High Performance Liquid Chromatography (HPLC), Ion Chromatography (IC), etc. Gather data and reports for other SpectronRx employees. Provide support of product data/documentation to SpectronRx customers. Write and manage any out specification or deviation events. Performs other related duties as assigned. KNOWLEDGE-SKILLS-ABILITIES Physical Ability - Must be able to lift up to 40 pounds. Customer and Personal Service - Knowledge of principles and processes for providing customer and personal services. This includes customer needs assessment, meeting quality standards for services, and evaluation of customer satisfaction. Active Listening - Giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. • Speaking - Talking to others to convey information effectively. • Critical Thinking - Using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. • Time Management - Managing one's own time and the time of others. • Active Learning - Understanding the implications of new information for both current and future problem-solving and decision-making. • Coordination - Adjusting actions in relation to others' actions. • Oral Comprehension - The ability to listen to and understand information and ideas presented through spoken words and sentences. • Oral Expression - The ability to communicate information and ideas in speaking so others will understand. • Written Comprehension - The ability to read and understand information and ideas presented in writing. • Written Expression - The ability to communicate information and ideas in writing so others will understand. Deductive Reasoning - The ability to apply general rules to specific problems to produce answers that make sense. TRAVEL • Regular travel is minimal REQUIRED EDUCATION AND EXPERIENCE Associate's Degree or equivalent Excellent Time Management Must have a strong background in analytical chemistry and instrumentation. Able to work well individually and in a group Excellent organizational skills and attention to detail. Continual learner and has a curiosity for science Must have the flexibility to work various shifts/rotate schedules as required Thorough understanding of project management. Excellent organizational skills and attention to detail. PREFERRED EDUCATION AND EXPERIENCE Bachelor's Degree in Science related field such as Chemistry, Biology or Biochemistry 2+ years experience in a laboratory environment, GMP preferred. Experience with ICP-OES, IC or electrochemistry a plus. Radiochemistry experience preferred, but not required. • Ability to train and be trained ADDITIONAL REQUIREMENTS • Valid Indiana driver's license • Pass a Background Check. ADDITIONAL INFORMATION/BENEFITS Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. We recognize that people come with a wealth of experience and talent beyond just the technical requirements of the job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and excellence; therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. We are an equal opportunity employer. Qualified applicants shall be considered for all positions without regard to race, color, sex, religion, national origin, age, disability, veteran status, or any other status protected by federal, state or local law. Refusal to submit to testing will result in disqualification of further employment consideration.

**About ETS:** ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 75 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL , TOEIC , GRE and Praxis tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide. The Associate R&D Data Scientist contributes to the planning, development, and execution of data science analyses for research and development projects within the ETS Research Institute. This role focuses on applying advanced data science, statistics, machine learning, and AI to make inferences and/or predictions from data. The position requires expertise in modern frameworks and cloud computing environments to support innovative research in educational measurement and assessment. **Primary Responsibilities** _Technical Responsibilties:_ Data Management and Analysis + Collect, preprocess, and manage structured and unstructured data from diverse sources, ensuring data quality and integrity. + Perform exploratory data analysis to identify trends, patterns, and actionable insights. Model Development and Evaluation + Design, implement, and validate predictive models and machine-learning algorithms using frameworks such as PyTorch/TensorFlow, and scikit-learn. + Experiment with large language models and generative AI techniques (e.g., working with large language model APIs, prompt engineering) to support innovative research. Deployment and Scalability + Develop and maintain pipelines for model deployment in cloud computing environments (e.g., AWS, Azure) to ensure scalability and reproducibility. _Research and Collaboration_ + Collaborate with scientists and cross-functional research teams to align data science efforts with program objectives + Contribute to technical reports, presentations, and publications that disseminate research findings. + Communicate complex technical concepts clearly to both technical and non-technical stakeholders. \#LI-MM1 \#Remote + Demonstrable proficiency and experience in Python and/or R for data analysis and modeling. + Hands-on experience with PyTorch/TensorFlow, Scikit-learn, and other machine learning frameworks. + Familiarity with generative AI methods and their practical applications. + Strong understanding of statistical methods, experimental design, and data visualization. + Ability to work in cloud computing environments (e.g., AWS) for model deployment and data processing. + Excellent problem-solving skills and adaptability to evolving research priorities. + Effective written and verbal communication skills for collaborative research environments. + Exceptional attention to detail, ensuring accuracy and reliability in data analysis, modeling, and reporting. **Education:** Master's degree in Data Science, Computer Science, Statistics, or a related quantitative field; or equivalent combination of education and experience. **ETS is mission driven and action oriented** + We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning. + We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth! + As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you! + The base salary range advertised represents the low and high end of the anticipated salary range for this position. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. The base pay is only one aspect of the Total Rewards Package that will be offered to the successful candidate. **ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.**

Description & Requirements The Federal Tax Specialty brings a forward-thinking approach to strategic tax advisory, offering tailored solutions that go far beyond compliance. With deep expertise in federal tax law, they deliver value-driven planning, proactive risk management, and innovative strategies aligned with each client's objectives. Their multidisciplinary approach empowers businesses to optimize tax positions, manage costs effectively, and capitalize on growth opportunities. What You Will Do: * Manage R&D tax credit consulting services for a diverse portfolio of clients, including Fortune 500 corporations, middle-market companies, privately held businesses, and start-ups. * Oversee multi-disciplinary engagement teams, providing strategic direction and subject matter expertise to ensure high-quality outcomes. * Manage all phases of R&D credit engagements-from initial scoping and proposal development through execution, client communication, and final deliverables-while ensuring alignment with client objectives and timelines. * Interpret and apply complex R&D tax credit statutes, regulations, and case law to support defensible credit positions. * Direct the collection and analysis of technical and financial documentation to identify and substantiate qualified research activities. * Review and validate research credit calculations and ensure accuracy and compliance with applicable tax laws. * Oversee the preparation of comprehensive technical reports and supporting documentation to substantiate R&D tax credit claims. * Guide the development and review of detailed project narratives that align with IRS and state-specific requirements. * Supervise, mentor, and develop staff by delegating responsibilities aligned with their skill levels and providing timely feedback and coaching. * Conduct and lead client site visits and interviews to uncover qualifying R&D activities and enhance client relationships. * Contribute to practice growth by identifying new opportunities, supporting business development efforts, and aligning with the team's strategic goals. Minimum Qualifications: * Bachelor's Degree in Accounting, Finance, Engineering, or a related field * 4.5+ years of experience in public accounting or corporate tax * Experience with Research & Development (R&D) Tax Credit Projects * Current and valid CPA, EA, JD, or LLM credential * Proficient in Microsoft Office Suite Preferred Qualifications: * Master's Degree in Accounting, Taxation, or a related field #LI-OAK, #LI-IND, #LI-CLTSP, #LI-HOU #LI-SS1 Illinois Wage Transparency Pursuant to Illinois' Equal Pay Act, the salary range displayed is for the Illinois market. The salary for this role will be based on the experience, education, and skill set of the individual for the position. Non-exempt/hourly positions will be eligible for time and half pay for employees that work over 40 hours in a workweek. Benefits are eligibility-based and could include group health plan benefits, 401(K), bonuses, profit-sharing contributions, flexible time off, and parental leave. For more information on benefits, please visit **************************************** Forvis Mazars reserves the right to make changes to the salary range based on business needs. IL Minimum Salary (USD) $ 80000 IL Maximum Salary (USD) $ 140000

Scheduling Daily Activities: Schedule daily activities to maintain customer satisfaction, internal satisfaction, and efficient use of equipment, under the direction of the Sr. Director of R&D. Reporting Progress: Report the progress of R&D activities to Applied Management. Maintaining R&D Facilities and Equipment: Ensure R&D facilities and equipment are updated and maintained properly. Evaluating New Projects: Assist in the evaluation of new projects prior to and during development as details become known, in conjunction with the Sr. Director of R&D and other Applied Laboratory departments. Balancing Department Needs: Balance the needs of the R&D department, business development, and the customer. Communicating Project Progress: Communicate project progress, needs, and concerns (both written reports and verbal) with clients and Applied management. Directing R&D Personnel: Direct R&D personnel in a professional and efficient manner. Leading Efficiency Efforts: Lead a sustained effort with the R&D team to be a more efficient and effective partner to other departments and customers. Utilizing Personnel Resources: Ensure that each personnel resource is utilized to its fullest potential given the tasks at hand. Communicating Needs: Communicate the needs of R&D with management and R&D personnel. Experience 5-8 years of pharmaceutical industry experience required. 3-5 years of laboratory management experience in R&D required. You really stick to 7am - 4 pm Mon - Friday and rarely have overtime and don't take work home. Skills: balance,customer satisfaction,project,management,overtime,d,other,efficiency improvement,customer,r,project management,projects,r&d evaluation,communication,team leadership,facility management

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

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. Job Description Performing biochemical testing on proteins and antibodies including, but not limited to: CE, IC, HPLC, SEC, SDS-PAGE, UV, Protein A titer Prepare reagents, samples and standards according to procedures Documenting test results in electronic notebook systems Demonstrates strong client service skills, teamwork, and collaboration Proactively plans and multitasks to maximize productivity Perform laboratory maintenance and housekeeping as assigned Performs other duties as assigned Qualifications Preferred Qualifications Good work habits (organized, efficient, careful, safety-conscious, accurate) Excellent communication (oral and written) with attention to detail Function under a high stress level Ability to work independently and as part of a team in a lab environment Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Interact with others in a positive and professional manner Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. Minimum Qualifications Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration At least 3 months related laboratory experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday - Friday 8am to 5 pm - overtime as required. May be required to respond to off-shift operational issues. Tasks require repetitive motion and standing for long periods of time. #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today! Your Role: Associate Scientist - Technical Services & Manufacturing Sciences (TS/MS) As a Scientist on the TS/MS team at Elanco's Technology Center in Indianapolis, you will support the optimization and advancement of bacterial and mammalian cell culture manufacturing processes. In this role, you'll be responsible for executing lab-scale models, analyzing experimental data, identifying process improvements, and collaborating across functions to support Elanco's diverse pharmaceutical and biotech product portfolio. Your Responsibilities: Design, execute, and analyze lab-scale experiments to model large-scale fermentation and cell culture processes, using engineering and microbiological principles to generate actionable data that supports process optimization and troubleshooting Lead and manage small-scale laboratory projects, ensuring experiments are properly designed with clear objectives, timelines, and documentation in laboratory notebooks and technical reports Drive process improvement initiatives by monitoring process trends, performing data mining using control systems and data historians, and identifying optimization opportunities through technical investigations and collaboration with senior scientists Provide scientific support for manufacturing processes, including oversight of mammalian and bacterial culture (e.g., E. coli, Salmonella), guidance on scale-up strategies, and troubleshooting deviations or yield issues Communicate technical findings and recommendations through formal presentations, summary reports, and participation in department technical reviews, while also contributing to a culture of safety and scientific rigor in the lab What You Need to Succeed (minimum qualifications): Education: Bachelor's or Master's Degree in Biology, Molecular Biology, Microbiology, Engineering, or a related scientific discipline Required Experience: Demonstrated laboratory experience in designing and conducting experiments; ability to interpret biological and process data with strong mechanical aptitude Top Skills: Strong communication and problem-solving skills; ability to prioritize tasks and work effectively in both team-based and independent settings What will give you a competitive edge (preferred qualifications): Hands-on experience with bacterial and/or mammalian cell culture systems and the operation of bioreactors or fermenters Experience with experimental design, data interpretation, and use of basic statistical tools for biological process analysis Proficiency in Microsoft Office and basic statistical software; ability to document and present scientific results clearly Flexibility to adapt to evolving project needs and the ability to work cross-functionally with R&D, manufacturing, and quality teams Growth mindset with a desire for ongoing scientific and professional development Additional Information: Location: Elanco Technology Center - Indianapolis, IN May involve working with hazardous or biologically active materials, occasional exposure to high noise levels, and interaction with large-scale lab equipment Some weekend or off-hours work may be required during peak periods Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: Multiple relocation packages Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) 8-week parental leave 9 Employee Resource Groups Annual bonus offering Flexible work arrangements Up to 6% 401K matching Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

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 * Cell culture supporting cell line generation - passaging cells, banking, expression studies (shake flask/bioreactor studies) * Plate Screening - whole cell 96 well plate formats, hit picking/consolidation, antibody capture * Equipment experience - cell counters, metabolite analyzers, titer measurement, liquid handlers * Phenotypic suitability assays, flow cytometry analysis, and software analysis and reports * Imaging automation and data mining * Overall general lab support - order media/materials, restocking supplies, eLN documentation Qualifications * At least 1 year experience in the lab setting * Strong aseptic technique * Strong computer, scientific, and organizational skills * Excellent communication (oral and written) and attention to detail * Experience in molecular and cell biology lab techniques * 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 * Proficiency in IT related skills such as Microsoft excel, word, PowerPoint etc Additional Information * Position is full-time, Monday - Friday 8am to 5 pm.Potential overtime and weekend work as needed * Tasks require repetitive motion and standing for long periods of time. * May be required to respond to off-shift operational issues. * 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 Purpose: - The Product Development Specialist at KYB Americas Corporation is responsible for driving the development and enhancement of innovative automotive products. This role involves collaborating with cross-functional teams to ensure that products meet market demands and align with the company's strategic objectives. Key Responsibilities: - Conduct market research to identify consumer needs and emerging trends in the automotive industry. - Collaborate with engineering, design, and marketing teams to conceptualize and develop new products. - Manage the product development lifecycle from ideation to launch, ensuring timely and cost-effective delivery. - Evaluate product performance and gather feedback to inform future product enhancements. - Prepare and present product proposals and progress reports to senior management. - Maintain up-to-date knowledge of industry standards and regulatory requirements to ensure compliance. - Coordinate with suppliers and vendors to source materials and components for product development. - Support the sales and marketing teams with product knowledge and technical expertise. - Monitor competitive products and strategies to identify opportunities for differentiation and innovation. Qualifications Purpose of Position/Summary: The Product Development Specialist supports the creation, evaluation, and maintenance of KYB products through detailed technical analysis and cross-functional collaboration. This position assists in ordering, tracking, and validating components, performing fitment checks, and ensuring that all specifications meet internal and industry standards. The Product Development Specialist works closely with procurement, engineering, and suppliers to resolve issues, support prototype testing, and prepare documentation for new product launches. Additionally, this role provides technical support to customers, consumers, and internal teams responding to inquiries and assisting with requests. Over time, this position will expand to include catalog and data management responsibilities to improve accuracy and efficiency across product lines. Essential Duties/Responsibilities : Support product development projects by ordering, tracking, and evaluating OE samples for fitment validation and performance verification. Perform fitment checks and assist with prototype builds to ensure accuracy, consistency, and compliance with specifications. Review supplier drawings and technical documentation to confirm dimensional accuracy and alignment with internal standards before production approval. Prepare unification reports to consolidate applications, reduce redundancies, and improve catalog accuracy. Coordinate with Procurement, Project Coordinators, and suppliers to resolve issues that delay product launches or production. Assist in creating documentation and reports required for new product approvals and launches. Provide technical support to customers, distributors, and internal teams. Identify recurring technical issues or catalog gaps and communicate findings to improve product data accuracy. Maintain organized records of development activities, test results, and supplier communications to support traceability and quality assurance. Collaborate with cross-functional teams to align product specifications, timelines, and launch readiness. Support the preparation of data and materials for internal and external communications related to new products. Perform other duties as assigned by the Product Manager or immediate supervisor as needed. Job Requirements: An associate degree in a technical, mechanical, or business-related field is preferred. Equivalent hands-on experience in automotive, manufacturing, or product support environments will also be considered. Prior experience in product development, catalog management, or technical support is highly desirable. Candidates must be proficient in Microsoft Office applications, particularly Excel, and capable of organizing and analyzing data accurately. The ability to read and interpret technical drawings is required. Knowledge of coil springs, suspension systems, or automotive components is strongly preferred. Successful candidates will demonstrate attention to detail, strong problem-solving skills, and clear communication across departments and with external partners. A proactive attitude, willingness to learn, and commitment to teamwork are essential. Technology Requirements: Must be proficient with computers, software and devices that utilize: Microsoft Office applications, with strong Excel and data organization skills. CAD viewing or modeling software for reviewing technical drawings and verifying specifications. File management systems and shared data platforms used to track development progress and maintain documentation. Email, video conferencing, and collaboration tools for clear communication across departments and with external partners. Photo and video tools for documenting prototypes, assemblies, and fitment checks. Online research tools used for verifying applications, catalog data, or cross-references. Supervisory Responsibilities/Direct Reports: None Difficulty of Work: The position of Product Development Specialist requires strong technical aptitude and attention to detail when working with components, drawings, and supplier documentation. This role involves coordinating with internal teams to ensure accurate fitment, proper specifications, and timely project execution. Clear communication and problem-solving are essential for addressing technical challenges, managing data accuracy, and supporting customers and distributors with product information. Responsibility: The Product Development Specialist works with moderate autonomy within the Product Department and is expected to manage assigned projects from initial sample review through production release with appropriate oversight. The position requires collaboration with multiple departments and external suppliers to gather feedback and resolve issues at each stage of development. The role is supported by the Product Manager and contributes directly to the accuracy, quality, and success of new product launches. Personal Work Relationships: The Product Development Specialist collaborates closely with the Product, Procurement, and Engineering teams and frequently interacts with suppliers, warehouse personnel, and customers to support product validation and development activities. The role also involves working with technicians and service shops during fitment checks, requiring clear communication and professionalism in diverse environments. Building and maintaining cooperative relationships across departments and with external partners is essential to ensuring smooth project execution and accurate technical results. Physical Effort: This position involves a combination of office and physical work. Approximately half of the time is spent at a computer performing data analysis, documentation, and communication tasks. The remaining time is spent handling components, conducting fitment checks, and evaluating samples in the warehouse or field settings. The role requires standing, walking, bending, reaching, and lifting or moving items up to 50 pounds with or without reasonable accommodation. Travel to mechanic shops or partner facilities is required for measurements, fitment testing, and related technical tasks. Working Conditions: The Product Development Specialist splits time between office, warehouse, and field environments. Work may include exposure to varying temperatures, noise, and mechanical equipment while performing fitment checks or product testing. Travel to off-site locations such as mechanic shops or customer facilities is required.

The High Energy Physics Group at Purdue University has an opening for an outstanding, passionate and driven postdoctoral research associate to work on an applied nuclear research project. The main focus of the position is the analysis of data collected with photon spectrometer detectors recording nuclear collisions. The expected candidate has strong experience in ML/AI to facilitate the development of a framework to search for unknown and not yet discovered transitions in such spectra. There is an option to also work on the CMS experiment for a fraction of the time, and/or detector R&D for future colliders. On the CMS side, the Purdue group has extensive involvement in many aspects of CMS, including detector operations, upgrade, software, and physics analysis. The group is deeply involved in detector upgrade projects using a center of excellence for composite manufacturing and simulation for detector support mechanics and cooling, as well as an in-house facility to design, develop and build silicon detectors. At Purdue we also operate a Tier-2 computer center, providing resources for data analysis both locally and as part of the CMS computing Grid. The position offers exciting possibilities in the analysis of the new 13.6 TeV collision data towards quantum tomography of top quarks. The selected candidate will work in this exciting new area of top quark physics, coupled into precision measurements to search for new physics. The successful candidate is expected to take on a leadership role in the physics analysis efforts within the top group. The candidate has ample opportunity to have a substantial involvement in the ongoing R&D efforts related to HL-LHC upgrades, and more importantly, towards future colliders. Cutting-edge machine learning developments for classical and quantum computational platforms are pursued in the group to benefit particle physics and beyond. Experience Candidates should have a Ph.D. in experimental particle physics, excellent data analysis, computing and programming skills and the ability to carry out an independent research program. Prior experience with Machine Learning, and nuclear physics, as well as CMS will be weighted preferably and existing experience with silicon detectors is an advantage. Application Process The position is available starting immediately and applications will be considered until the position is filled. The appointment is initially for one year and renewable annually, subject to mutual satisfaction. Salary range: $55,000 - $60,000 depending on the experience. The position will be based in West Lafayette, IN, although travel to other locations is expected for a number of short trips per year and/or extended periods of time. Applications should include a curriculum vitae, a list of publications, a description of research interests (2 pages), and three letters of recommendation. Complete applications will be considered immediately. For information about the position, please contact Prof. Andreas Jung (***************** ). Contact: Jung, Andreas (*****************) Letters of Reference should be sent to: ***************** Apply now Posting Start Date: 12/18/24

Supports Sustainability Services onsite program, including manual labor associated with chemical handling, lab pack duties, drum movements within the facility, drum bulking, drum crushing, assisting when extra personnel are needed and other duties as assigned. This is a support position focused on hazardous and non-hazardous waste related projects 7:00 a.m. - 4:00 p.m. M-F Essential Duties and Responsibilities To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Other minor duties may be assigned. Ensure waste types are properly segregated, regulatory shipment windows are met, proper container labeling is adhered to, good housekeeping is maintained and accurate tracking logs are kept. Identify best practices that assist customers in reducing waste volumes, increasing operational efficiencies, identifying optimal equipment usage and generating cost savings. Segregate, label, mark and package waste materials in a safe and compliant manner. Collect, pour, transfer, consolidate, repackage and package solid, liquid and sludge material. Perform labor intensive activities such as container or drum collection, drum bulking, sorting trash for recyclables and loading of trucks. Transfer waste into containers of different size. Provide labor support at 90-Day Hazardous Waste Pad, when applicable. May provide support or direction to less experienced Technicians. Wears required personal protective equipment. Participates and cooperates in safety process, including following written procedures, attending required training and scheduled meetings. Immediately reports any unsafe conditions, incidents, injuries or property damage to supervisor. Follows Environmental and Quality Management System (ISO 14001/9001) policy, procedures and operational controls related to job responsibilities. Maintains compliance with applicable environmental, safety and transportation regulations (EPA, OSHA and DOT). Supervisory Responsibilities This job has no supervisory duties. Qualifications The requirements listed below are representative of the qualifications necessary to perform the job. Education and Experience Education: Bachelors Degree (accredited) Experience: None required (in addition to education requirement). Certificates, Licenses, Registrations or Other Requirements RCRA and DOT regulatory compliance experience preferred. Ability to pass a respirator FIT test Valid Drivers License Ability to obtain a medical card & CDL within 6 months Labpacking experience preferred 40-hour HAZWOPER certification (or equivalent) or the ability to obtain such within 30 days of employment. Manifesting hazardous and non-hazardous waste experience preferred. Pre-assignment and/or pre-hire customer-specific drug and/or alcohol testing may be required by certain customer-contract requirements. Such testing may include urinalysis, oral swab, drug hair follicle testing and/or alcohol testing. Other Knowledge, Skills or Abilities Required Must be able to work independently with little direction, and as a member of a team. Work Environment Listed below are key points regarding environmental demands and work environment of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job. Required to use motor coordination with finger dexterity (such as keyboarding, machine operation, etc.) most of the work day; Required to exert physical effort in handling objects up to 50 pounds most of the work day; Required to be exposed to physical occupational risks (such as cuts, burns, exposure to chemicals, etc.) most of the work day; Required to be exposed to physical environment which involves dirt, odors, noise, weather extremes or similar elements most of the workday; Benefits At Waste Management, each eligible employee receives a competitive total compensation package including Medical, Dental, Vision, Life Insurance and Short Term Disability. As well as a Stock Purchase Plan, Company match on 401K, and more! Our employees also receive Paid Vacation, Holidays, and Personal Days. Please note that benefits may vary by site. If this sounds like the opportunity that you have been looking for, please click "Apply.

At Corteva Agriscience, you will help us grow what's next. No matter your role, you will be part of a team that is building the future of agriculture - leading breakthroughs in the innovation and application of science and technology that will better the lives of people all over the world and fuel the progress of humankind. Corteva Agriscience has the responsibility to develop new active ingredients and new formulated products that are competitive with the current and future market conditions. The individual in the Formulation Scientist position will create and develop novel formulations and delivery systems for new and existing agricultural active ingredients. The individual will collaborate with other functions in Corteva R&D to explore and test novel delivery concepts through proof-of-concept studies, translate these concepts into practice, and advance successful technologies and product ideas through the stage-gate pipeline toward business case development and commercialization. The individual will also provide SME (subject matter expertise) and support necessary in technology transfer, product registration, and process scale up for these concepts. This individual should be skilled in the conception and development of formulations for the agricultural, pharmaceutical, personal care or related industries. What You'll Do: * Exploration, proof of concept, and development of novel formulation and delivery system technologies and concepts for new and registered agricultural active ingredients * Collaboration with other functions across the company to deliver maximum success, such as analytical R&D, process development, application technology, biology, regulatory, operations and commercial teams * Collaboration with external companies or universities to evaluate novel and promising technologies for Ag applications * Staying abreast of new discoveries and technologies in the area of formulation and delivery system technologies * Intellectual property (IP) capture and research report writing and presentation * Compliance with laboratory safety procedures Other responsibilities include: * Under minimal guidance of senior colleagues, develops hypotheses, plans, and executes effective experiments, generates reproducible data, interprets results, and modifies hypotheses appropriately. * Leads the investigation of product quality concerns / issues and troubleshooting of product quality issues at plant level, conducts rework evaluations and provides recommendations to the plant. * Consistently applies sound scientific methods to solve technical problems. * Develops understanding of customer needs through discussion with sales and marketing groups and works towards meeting the needs. * Develops an understanding of competitors and key competitive technologies. Uses knowledge of the strengths and weaknesses of competitive products to identify opportunities for competitive product positioning What Skills You Need: * Demonstrated competence in the area of formulation technology (including colloids, interfacial phenomena, rheology, solids processing etc.). * Prior experience in research or manufacturing/engineering is desirable. * Ability to work independently and drive projects to completion. * Strong interpersonal and leadership skills * Ability to successfully partner with team members and stakeholders (sales, marketing, R&D, regulatory, product stewards, etc.) from multiple backgrounds. * Excellent verbal and written communication skills. Ability to persuade/influence others of the value of Corteva technology. Ability to clearly articulate the value of technology when talking with customers. * Working knowledge of formulation design & development and product registration process. Education * BS/MS/PhD in Chemistry, Chemical Engineering, Material Science, or related fields. #LI-BB1 Benefits - How We'll Support You: * Numerous development opportunities offered to build your skills * Be part of a company with a higher purpose and contribute to making the world a better place * Health benefits for you and your family on your first day of employment * Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays * Excellent parental leave which includes a minimum of 16 weeks for mother and father * Future planning with our competitive retirement savings plan and tuition reimbursement program * Learn more about our total rewards package here - Corteva Benefits * Check out life at Corteva! ************************************* Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team. Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

This role will be a key member of the INCOG Quality Control laboratory team who has a passion for learning, collaborating, and contributing to the success of our clients. The Method Transfer Scientist will be dedicated to the success of the Quality Control team, resulting in the production of the highest quality products for our clients. The Method Transfer Scientist will work closely with Quality Control leadership and will develop and lead the program for performing method transfer for analytical and/or microbiological assays from client laboratories into the INCOG QC Laboratories. The Method Transfer Scientist will be committed to operating with a Quality Mindset in every aspect of their role, including attention to detail, on time delivery, and efficiency. Essential Job Functions: * Lead the development and implementation of the INCOG QC Method Transfer program for both analytical and microbiological assays. * Perform assessments of both incoming client methods and compendial test methods for raw materials, container/closures, API/BDS, in-process, and finished products for suitability with existing INCOG laboratory capabilities to identify if additional chemicals or instruments are required. * Partner with customers to develop, review, approve, and execute method transfer into the chemistry and/or microbiology laboratory. * Collaborate with the Quality Team on building laboratory safety program to ensure a safe and quality-minded environment for all personnel working in the laboratory. * Holds self and others accountable for rigorous scientific and quality work standards. * Advocate for clients by collaborating cross-functionally to schedule microbiological sampling, testing, instruments, and personnel to meet customer needs and timelines. * Maintain a constant state of safety and inspection-readiness in the QC laboratories. Use knowledge of quality principles, cGLPs, cGMPs, and regulatory standards to act as a key point-of-contact for regulatory agencies during inspections and audits. * Support laboratory investigations using troubleshooting tools to identify errors, and exercise rapid decision making to implement corrective actions during OOS/OOT and other non-conformance events. * Utilize various paper and automated systems to manage local QC and site policies, procedures, and technical reports throughout document lifecycles including authoring, reviewing, approving, and retiring. Special Job Requirements: * Be available to participate in client meetings that may go outside of standard business hours (Monday-Friday 8 AM-5 PM) * Use applied statistics to analyze and track test results to identify sources of variability and error in laboratory and manufacturing processes. Use data trends to apply a systematic approach to resolve technical issues, prevent errors, identify improvement opportunities, and implement continuous improvement plans. * Maintain regulatory intelligence on the regulatory landscape, policies, and pharmaceutical industry trends through continuous education, networking, literature, trade organizations, etc. * Be available to support routine QC testing for raw materials, API/BDS, container/closures, in-process, finished products, and environmental monitoring as needed, even on alternate shifts. * 5+ years of microbiology, chemistry, or other related experience in GMP manufacturing/GMP QC testing of pharmaceuticals. * Experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control, particularly related to method development and method transfer. * Experience with using laboratory instrumentation from pH/conductivity meters, osmometers, and density meters to more complicated systems used for UHPLC/HPLC, GC, CE, and ic IEF analysis. * Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, OpenLab CDS, ChemStation, etc.). * Ability to author scientifically sound SOPs, Work Instructions, Transfer Protocols and Summary Reports. * B.S./B.A. in Biology, Microbiology, Biochemistry, or Chemistry Additional Preferences: * Prior leadership experience in GMP QC laboratories supporting pharmaceuticals. Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

This role will be a key member of the INCOG Quality Control laboratory team who has a passion for learning, collaborating, and contributing to the success of our clients. The Method Transfer Scientist will be dedicated to the success of the Quality Control team, resulting in the production of the highest quality products for our clients. The Method Transfer Scientist will work closely with Quality Control leadership and will develop and lead the program for performing method transfer for analytical and/or microbiological assays from client laboratories into the INCOG QC Laboratories. The Method Transfer Scientist will be committed to operating with a Quality Mindset in every aspect of their role, including attention to detail, on time delivery, and efficiency. Essential Job Functions: Lead the development and implementation of the INCOG QC Method Transfer program for both analytical and microbiological assays. Perform assessments of both incoming client methods and compendial test methods for raw materials, container/closures, API/BDS, in-process, and finished products for suitability with existing INCOG laboratory capabilities to identify if additional chemicals or instruments are required. Partner with customers to develop, review, approve, and execute method transfer into the chemistry and/or microbiology laboratory. Collaborate with the Quality Team on building laboratory safety program to ensure a safe and quality-minded environment for all personnel working in the laboratory. Holds self and others accountable for rigorous scientific and quality work standards. Advocate for clients by collaborating cross-functionally to schedule microbiological sampling, testing, instruments, and personnel to meet customer needs and timelines. Maintain a constant state of safety and inspection-readiness in the QC laboratories. Use knowledge of quality principles, cGLPs, cGMPs, and regulatory standards to act as a key point-of-contact for regulatory agencies during inspections and audits. Support laboratory investigations using troubleshooting tools to identify errors, and exercise rapid decision making to implement corrective actions during OOS/OOT and other non-conformance events. Utilize various paper and automated systems to manage local QC and site policies, procedures, and technical reports throughout document lifecycles including authoring, reviewing, approving, and retiring. Special Job Requirements: Be available to participate in client meetings that may go outside of standard business hours (Monday-Friday 8 AM-5 PM) Use applied statistics to analyze and track test results to identify sources of variability and error in laboratory and manufacturing processes. Use data trends to apply a systematic approach to resolve technical issues, prevent errors, identify improvement opportunities, and implement continuous improvement plans. Maintain regulatory intelligence on the regulatory landscape, policies, and pharmaceutical industry trends through continuous education, networking, literature, trade organizations, etc. Be available to support routine QC testing for raw materials, API/BDS, container/closures, in-process, finished products, and environmental monitoring as needed, even on alternate shifts. 5+ years of microbiology, chemistry, or other related experience in GMP manufacturing/GMP QC testing of pharmaceuticals. Experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control, particularly related to method development and method transfer. Experience with using laboratory instrumentation from pH/conductivity meters, osmometers, and density meters to more complicated systems used for UHPLC/HPLC, GC, CE, and ic IEF analysis. Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, OpenLab CDS, ChemStation, etc.). Ability to author scientifically sound SOPs, Work Instructions, Transfer Protocols and Summary Reports. B.S./B.A. in Biology, Microbiology, Biochemistry, or Chemistry Additional Preferences: Prior leadership experience in GMP QC laboratories supporting pharmaceuticals. Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

Job Description We at ELIQUENT are looking for an experienced QC Analytical Method Development Scientist to immediately join our ELIQUENT Engineering team. The Analytical Method Development Scientist supports pharmaceutical product development by designing, developing, optimizing, and validating analytical methods used for characterization, in-process control, release testing, and stability studies. This role ensures all analytical work complies with GMP/GLP requirements and ICH guidelines. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Develop and optimize analytical methods for small-molecule drug substances, drug products, excipients, and in-process samples. • Utilize pharma-relevant techniques such as HPLC/UPLC, GC, LC-MS, dissolution testing, UV-Vis, FTIR, and compendial methods. • Assess method performance (e.g., selectivity, sensitivity, linearity, robustness) and generate scientifically sound rationale for method conditions. • Troubleshoot analytical methods and instrumentation issues to ensure reliable performance in a GMP setting. • Design and execute validation protocols with any of the following 21 CFR Part 212, USP /, ICH Q2(R2), and FDA guidance. • Prepare method validation reports, risk assessments, and technical justifications. • Perform statistical analysis of method performance using pharma-appropriate tools. • Maintain accurate and compliant GMP documentation consistent with ALCOA+ principles. • Assist with the development of method SOPs. • Participate in project teams to ensure analytical readiness for clinical and commercial production. • Participate in failure investigations, root cause analyses, and CAPA activities involving analytical methods or results. QUALIFICATIONS AND REQUIREMENTS: • Bachelor's in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field. • 3-7+ years of experience in pharmaceutical analytical development, method validation, or QC in a GMP-regulated environment. • Experience supporting PET/SPECT radiotracers, sterile injectables, or radioactive drug products is preferred but not required. • Strong hands-on experience with HPLC/UPLC, GC, LC-MS, UV-Vis, FTIR, dissolution, and compendial methods. • Knowledge of 21 CFR Part 212, 21 CFR Part 211, USP, and ICH guidelines • Familiarity with Empower and GMP documentation systems. • Strong analytical problem-solving skills. • Excellent technical writing and communication abilities. • Ability to manage multiple development projects and work independently in a fast-paced pharma environment. WORK ENVIRONMENT: • Primarily laboratory-based with routine use of analytical instrumentation. • Requires adherence to GMP, safety procedures, and PPE requirements. • Occasional flexibility needed to support project deadlines and analytical troubleshooting What We Offer: Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience. Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment. Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance. Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.

Job Title: R&D Process EngineerJob Description The R&D Process Engineer will be responsible for evaluating, developing, and implementing processes for the pre-separation, separation, and post-separation of rare earth materials. This role involves ensuring safety compliance, developing standard and emergency operating procedures, transitioning technology from pilot to commercial scale, and leading maintenance and commissioning activities. Responsibilities * Evaluate existing and alternative technologies for pre-separation and post-separation processing of rare earth materials using patented processes. * Perform process hazard analyses associated with chemical processes and implement required personnel and environmental safety protocols to ensure compliance with local, state, and federal standards. * Lead the development of standard operating procedures and emergency procedures for rare earth material pre-separation, separation, and post-separation processes, with the support of the Plant Operations department. * Determine the appropriate 'freeze' point of the rare earth material technology platform to transition from pilot scale operations to commercial scale operations. * Support the engineering of commercial scale processes with the assistance of a Process Consultant and potentially a third-party engineering partner. * Lead the development of commissioning procedures for rare earth material pre-separation, separation, and post-separation processes, with the support of the Research & Development department. Essential Skills * Bachelor's degree in Chemical Engineering, Materials Science, or a related field. * 5 years of experience in chemical process engineering. * Experience with stimulation software, particularly Aspen software. Additional Skills & Qualifications * Experience within the rare earth materials, chemical, or related industries. * Knowledge of chromatophy. Work Environment This position is onsite with working hours from 9 AM to 5 PM. The company currently has about 22 people, making it a part of one of the newest and fastest-growing companies in North America. Job Type & Location This is a Permanent position based out of Noblesville, IN. Pay and Benefits The pay range for this position is $120000.00 - $135000.00/yr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Noblesville,IN. Application Deadline This position is anticipated to close on Jan 26, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description Perform accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executing well defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of process development/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conducted and documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems. The first two weeks will be trained during the day Monday - Friday 6AM to 5:45PM. Additional Information All your information will be kept confidential according to EEO guidelines.