Research and development technician jobs in Bloomington, IN - 124 jobs

Austin, IN Direct Hire Hybrid $90k with potential to earn more depending on experience As a Regulatory Labeling Scientist, you will play a key role in guaranteeing that all products meet FDA, USDA, and third-party labeling requirements, while collaborating cross-functionally to support accurate and timely product labeling across the organization. Position Summary: The Regulatory Labeling Scientist supports the R&D Manager and Label Regulatory Specialist in the development, review, and management of product labeling. This includes ensuring ingredient and recipe compliance, maintaining SAP label data, and supporting certification and audit processes. Key Responsibilities: Ingredient & Recipe Compliance: Review ingredients and recipes to ensure compliance with all applicable regulations. Interpret and apply FDA and USDA labeling rules and standards. Label Development & Management: Create and manage Nutrition Facts Panels and ingredient statements. Ensure label accuracy for health and wellness claims and standards of identity. Maintain and update label data within SAP PLM systems. Customer & Certification Support: Collaborate with customers on label artwork, specifications, and approvals. Manage USDA submissions and third-party certifications (Organic QAI, Non-GMO, Kosher OU). Support customer label changes using SAP Engineering Change Management. Cross-Functional Collaboration: Work closely with Food Safety, QA, Purchasing, and Operations teams. Assist with audits and regulatory filings to maintain compliance readiness. Regulatory Leadership & Improvement: Research and interpret evolving food labeling regulations. Develop documentation such as white papers and position statements. Drive continuous improvement in regulatory processes and data accuracy. Qualifications & Skills: Bachelor's degree in Food Science, Biology, Chemistry, Nutrition, or related field. 2-5 years of experience in Regulatory Affairs, QA, or Food Safety within the food industry. Strong understanding of FDA, USDA, HACCP, and food labeling regulations. Proficiency in Microsoft Office and ERP systems (SAP preferred). Excellent communication, analytical, and project management skills. Strong interpersonal and cross-functional collaboration abilities. Highly organized and able to manage multiple priorities in a fast-paced environment. Ability to travel as needed. Physical Requirements: Ability to stand and walk for extended periods (8-12 hours). Must be able to lift up to 50 lbs and push/pull up to 100 lbs with assistance. Ability to bend, stoop, climb, and perform manual handling tasks as needed. Comfortable working in varying temperature environments (hot, cold, humid). Must wear required PPE (hairnets, gloves, goggles, etc.).

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

The Department of Biology is a large, unified department with strong undergraduate degrees, nationally ranked graduate programs, and world-class research spanning the breadth of biological questions and experimental systems - from ecosystems to microbiology and developmental biology, from evolution to cell biology, from molecular biology to systems biology, bioinformatics, and genomics. It is always an exciting time for Biology - enormous advances in global genome analysis coupled with unprecedented developments in interdisciplinary research have made the 21st century the “Century of Biology”. For more information about the department, you can find it here: About: Department of Biology: Indiana University Bloomington . Indiana University is an equal opportunity employer and provider of ADA services and prohibits discrimination in hiring. See Indiana University Notice of Non-Discrimination here which includes contact information. The Department of Biology at Indiana University Bloomington invites applications for Visiting Research Associate position under the supervision of Dr. Chris Smith ( Home | Chris Smith). Our new lab in Evolution, Ecology, and Behavior investigates machine learning approaches for population genetics. Our research integrates custom neural architecture design, simulations, and publicly available genomic datasets to develop new inference methods. The Research Associate will serve as a scientific programmer, creating or testing deep learning models for genomics, exploring new techniques related to spatial simulations, or other topics discussed with the PI.

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

Description: Our Company Big Red Liquors has been serving Indiana for over 50 years! We seek to offer incredible selection, vast product knowledge and superior customer service as a resource in the communities we serve. When you step into a Big Red Liquors store, we hope you'll be not only surprised, but amazed, by our selection, knowledge, and willingness to go above & beyond for our loyal customers. We really take pride in the history and culture of consuming responsibly! Wine Manager Summary A Wine Manager is responsible for establishing and maintaining guest services, oversees and is accountable for the operation of the Wine Department ensuring maximum sales and profitability through merchandise, inventory, and expense control. Essential Functions & Responsibilities: Ensure each guest receives outstanding guest service by providing a guest friendly environment which includes greeting and acknowledging every guest, maintaining outstanding standards, solid product knowledge and all other components of guest service. Analyze and measure business trends; develop and implement plans to maximize sales and meet or exceed goals and objectives. Ensure appropriate merchandise stock levels, presentations; signing, and assortment in the Wine Department; coordinating with Corporate Merchandising & Marketing Wine Department to do so. Ensure compliance with all policies and procedures through regular store management and staff meetings, store walk-through and audits, etc. Train and develop Wine Sales Associates. Requirements: Qualifications, Education & Experience: Must be 21 years of age or older High School Diploma or equivalent required Two years of management experience preferred Strong Knowledge of wine necessary Three years or more experience in retail or on-premise setting CSW Certification an advantage CSW Certification required to maintain position Excellent communication and interpersonal skills Provide an extremely high level of customer service MS Office knowledge required Ability to work in a fast pace setting Organized with a great attention to detail Self-Motivated Demonstrated reliability and punctuality Physical Requirements: Regularly required to talk or hear Frequently required to stand, walk, bend, kneel, stoop, crouch, crawl and climb Regularly lift and or move objects up to 50 pounds Vision abilities include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus Travel: Minimal travel is expected for this position Additional Eligibility Qualifications: Must maintain Indiana State Employee Permit Must maintain Indiana State Approved Server Training Certification This job description indicates in general the nature and levels of work, knowledge, skills, abilities, and other essential functions (as covered under the Americans with Disabilities Act) expected of an incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of an incumbent. An incumbent may be asked to perform other duties as required.

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.

The Packaging Engineer 2 uses their experienced in medical device packaging to design and develop solutions for new and modified products. This includes supporting product design, verification testing, regulatory compliance, process validation and manufacturing line establishment. A Packaging Engineer 2 leads packaging activities with a cross-functional team including SBU Product Management, Regulatory Affairs, Operations, Quality Assurance, Clinical Affairs, and other Engineering personnel. Responsibilities Apply packaging design principles from the Medical Device/Pharma field to develop packaging designs that meet company, customer and industry standards. Works with suppliers to spec and acquire packaging materials. Coordinate distribution simulation and packaging testing. Develop and maintain department standards in packaging. Ability to lead multiple projects to successful completion with tight time lines and critical deliverables. Ensure compliance of equipment and packaging designs with company quality system. Coordinate or perform verification and validation testing of packaging designs and manufacturing methods. Write and maintain appropriate documentation per the company quality system. Evaluate issues with existing packaging and implement corrective actions. Must work and interact effectively and professionally with and for others throughout various levels of the global organization. Must strictly adhere to safety requirements. Maintain regular and punctual attendance. Must maintain company quality and quantity standards. Must have effective communication skills and ability to work in a collaborative and independent work situations and environments with minimal supervision. Ability to remain calm and receptive in fast paced situations. Qualifications Qualification/ Educational Requirements: Bachelor's degree in Mechanical Engineering, Packaging Science or closely related field and 3 years experience; or experience of such kind and amount as to provide a comparable background Experience with medical packaging materials (Tyvek, PE/PET films, PETG trays, etc.) Experience with environmental and regulatory requirements and standards that relate to medical packaging design and testing (i.e. ASTM F1886, F88, F2096, D4169, and ISO 11607) Physical Requirements: Works under general office environmental conditions. Sitting for extended periods, utilizes close visual acuity for working with computers, equipment, etc. Researches and designs using standard computer equipment. The employee is frequently required to stand; walk; use hands to grasp, feel or touch; reach with hands and arms; climb or balance; stoop; kneel; crouch; or crawl; and talk; or hear. Moderate exposure to noise level in the work environment that is moderate to occasionally loud. Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements under the ADA.

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.

The Packaging Engineer 2 uses their experienced in medical device packaging to design and develop solutions for new and modified products. This includes supporting product design, verification testing, regulatory compliance, process validation and manufacturing line establishment. A Packaging Engineer 2 leads packaging activities with a cross-functional team including SBU Product Management, Regulatory Affairs, Operations, Quality Assurance, Clinical Affairs, and other Engineering personnel. Responsibilities * Apply packaging design principles from the Medical Device/Pharma field to develop packaging designs that meet company, customer and industry standards. * Works with suppliers to spec and acquire packaging materials. * Coordinate distribution simulation and packaging testing. * Develop and maintain department standards in packaging. * Ability to lead multiple projects to successful completion with tight time lines and critical deliverables. * Ensure compliance of equipment and packaging designs with company quality system. * Coordinate or perform verification and validation testing of packaging designs and manufacturing methods. * Write and maintain appropriate documentation per the company quality system. * Evaluate issues with existing packaging and implement corrective actions. * Must work and interact effectively and professionally with and for others throughout various levels of the global organization. * Must strictly adhere to safety requirements. * Maintain regular and punctual attendance. * Must maintain company quality and quantity standards. * Must have effective communication skills and ability to work in a collaborative and independent work situations and environments with minimal supervision. * Ability to remain calm and receptive in fast paced situations. Qualifications Qualification/ Educational Requirements: * Bachelor's degree in Mechanical Engineering, Packaging Science or closely related field and 3 years experience; or experience of such kind and amount as to provide a comparable background * Experience with medical packaging materials (Tyvek, PE/PET films, PETG trays, etc.) * Experience with environmental and regulatory requirements and standards that relate to medical packaging design and testing (i.e. ASTM F1886, F88, F2096, D4169, and ISO 11607) Physical Requirements: * Works under general office environmental conditions. * Sitting for extended periods, utilizes close visual acuity for working with computers, equipment, etc. * Researches and designs using standard computer equipment. * The employee is frequently required to stand; walk; use hands to grasp, feel or touch; reach with hands and arms; climb or balance; stoop; kneel; crouch; or crawl; and talk; or hear. * Moderate exposure to noise level in the work environment that is moderate to occasionally loud. * Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements under the ADA.

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.

Salary: commensurate Site I.D.: 140820 The Ross-Carlisle Group has a rewarding opportunity for a Sr. R&D Engineer who is either local to Indianapolis or willing to relocate him/herself at his/her own expense to Indianapolis. Requirements: MS or foreign equiv. in Electrical or Mechanical Engineering or closely related field; at least 3-yr exp. .; strong ability in C/C++, embedded software development, DAQ and fluid theory; background in Fluid Dynamic or Hydraulic. Qualifications Responsibilities: Develop Intelligent Sensor firmware using C/C++ & Windows testing software using VB.net & customer test machines; code HMI software using LabVIEW & machine control software using PLC; conduct research & development on new features & productions. Full Time. Additional Information All your information will be kept confidential according to EEO guidelines.

Indiana University Department of Psychological and Brain Sciences in Bloomington, Indiana invites applications for a full-time Research Associate. Responsibilities include designing, planning, executing, and analyzing experiments with mice investigating the consequences of perinatal cannabis use, training undergraduate students, preparing reports, and presenting experimental results to scientific communities. Basic Qualifications: PhD in neuroscience or related field and at least three years of post-doctoral experience. Interested candidates should review the application requirements and submit their application at *********************************************** Questions about the position should be addressed to ***************. Applications received by May 6, 2024 will receive full consideration. The anticipated start date for this position is August 1, 2024.

Our Company Big Red Liquors has been serving Indiana for over 50 years! We seek to offer incredible selection, vast product knowledge and superior customer service as a resource in the communities we serve. When you step into a Big Red Liquors store, we hope you'll be not only surprised, but amazed, by our selection, knowledge, and willingness to go above & beyond for our loyal customers. We really take pride in the history and culture of consuming responsibly! Wine Manager Summary A Wine Manager is responsible for establishing and maintaining guest services, oversees and is accountable for the operation of the Wine Department ensuring maximum sales and profitability through merchandise, inventory, and expense control. Essential Functions & Responsibilities: Ensure each guest receives outstanding guest service by providing a guest friendly environment which includes greeting and acknowledging every guest, maintaining outstanding standards, solid product knowledge and all other components of guest service. Analyze and measure business trends; develop and implement plans to maximize sales and meet or exceed goals and objectives. Ensure appropriate merchandise stock levels, presentations; signing, and assortment in the Wine Department; coordinating with Corporate Merchandising & Marketing Wine Department to do so. Ensure compliance with all policies and procedures through regular store management and staff meetings, store walk-through and audits, etc. Train and develop Wine Sales Associates. Requirements Qualifications, Education & Experience: Must be 21 years of age or older High School Diploma or equivalent required Two years of management experience preferred Strong Knowledge of wine necessary Three years or more experience in retail or on-premise setting CSW Certification an advantage CSW Certification required to maintain position Excellent communication and interpersonal skills Provide an extremely high level of customer service MS Office knowledge required Ability to work in a fast pace setting Organized with a great attention to detail Self-Motivated Demonstrated reliability and punctuality Physical Requirements: Regularly required to talk or hear Frequently required to stand, walk, bend, kneel, stoop, crouch, crawl and climb Regularly lift and or move objects up to 50 pounds Vision abilities include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus Travel: Minimal travel is expected for this position Additional Eligibility Qualifications: Must maintain Indiana State Employee Permit Must maintain Indiana State Approved Server Training Certification This job description indicates in general the nature and levels of work, knowledge, skills, abilities, and other essential functions (as covered under the Americans with Disabilities Act) expected of an incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of an incumbent. An incumbent may be asked to perform other duties as required.

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 Indianpolis, 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.

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.

Salary: commensurate Site I.D.: 140820 The Ross-Carlisle Group has a rewarding opportunity for a Sr. R&D Engineer who is either local to Indianapolis or willing to relocate him/herself at his/her own expense to Indianapolis. Requirements: MS or foreign equiv. in Electrical or Mechanical Engineering or closely related field; at least 3-yr exp. .; strong ability in C/C++, embedded software development, DAQ and fluid theory; background in Fluid Dynamic or Hydraulic. Qualifications Responsibilities: Develop Intelligent Sensor firmware using C/C++ & Windows testing software using VB.net & customer test machines; code HMI software using LabVIEW & machine control software using PLC; conduct research & development on new features & productions. Full Time. Additional InformationAll your information will be kept confidential according to EEO guidelines.

The Department of Biology is a large, unified department with strong undergraduate degrees, nationally-ranked graduate programs, and world-class research spanning the breadth of biological questions and experimental systems - from ecosystems to microbiology and developmental biology, from evolution to cell biology, from molecular biology to systems biology, bioinformatics, and genomics. For more information about the department, see ************************ The Saltz Lab in the Department of Biology at Indiana University (saltzlab.com), Bloomington is seeking a Research Associate/Lab manager. Our department is a large, unified department with world-class research spanning all levels of biological organization and diverse experimental systems. Our lab in Evolution, Ecology, and Behavior investigates the evolutionary processes that shape behavior and its variation. We use sophisticated behavioral experiments and statistical analysis alongside other tools, focusing on fruit flies ( Drosophila melanogaster ) as a model system. The main goal for this position is to conduct research investigating genetic and genomic links between social preference, social dynamics, and the development of aggressive behavior in males. The ideal candidate will be passionate about science and have exceptional organizational and time-management skills, and attention to detail. This is a great position for a recent college graduate interested in obtaining research experience before moving on to graduate school or something else. I view it as an important part of my job to mentor you towards your next career step(s). Core job duties include: (1) rearing large numbers of fruit flies and measuring their behavior and/or preserving them for genetic analysis. (2) Supervising and mentoring undergraduate and other contributors to the project (3) Supporting our research compliance associated documentation. (3) Management and analysis of large datasets. (4) Learning, conducting and teaching other lab members our key research protocols. Other general responsibilities include: coordinating shared resources in the lab, managing general lab operations, troubleshooting problems, and participating in lab meetings.

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 evaluations and laboratory testing on primary container-closure components and system, critical secondary packaging, and shipping systems utilizing mechanical testing equipment, dimension measurement instruments, and container closure integrity testing systems Execute methods, collect data, and document results in lab notebooks and LIMS Participate in the development of laboratory test methods or equipment to ensure reliability and accuracy of results Interact with colleagues in other groups on a routine basis Ensure all activities follow established safety standards, regulatory requirements and Good Manufacturing Procedures (GMP) Qualifications Bachelor's in science, engineering, or technology, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) At least 4-10 years of related laboratory experience 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.