Associate scientist jobs in Noblesville, IN

Job Responsibilities: Develop, evaluate, and optimize the QC method transfer program for both analytical and microbiological assays. Assess incoming client methods and compendial test methods for raw materials, container/closures, APIs, in-process samples, and finished products, determining suitability with existing laboratory capabilities and identifying any additional instrumentation or reagents required. Collaborate with clients and internal teams to plan, review, approve, and execute method transfers into the laboratory. Work closely with the Quality team to maintain and enhance laboratory safety programs and promote a quality-driven culture. Maintain rigorous scientific and quality standards, ensuring accuracy, reproducibility, and compliance in all laboratory activities. Coordinate resources, scheduling, and logistics to support client testing needs, including microbiological sampling, laboratory instruments, and personnel availability. Ensure laboratory readiness for inspections, audits, and regulatory compliance by applying knowledge of cGMP, cGLP, and other regulatory standards. Lead and support investigations for out-of-specification (OOS), out-of-trend (OOT), and other non-conformance events using troubleshooting and corrective action processes. Manage laboratory documentation and technical records throughout their lifecycle, including authoring, reviewing, approving, and retiring procedures and reports, utilizing both manual and automated systems. Qualifications: Bachelor's degree in Biology, Microbiology, Biochemistry, or related field. 5+ years of experience in microbiology or related roles within GMP manufacturing or QC laboratory testing. Practical experience implementing FDA, EMA, and other regulatory authority expectations for QC, particularly regarding method development and method transfer. Proficiency with laboratory instrumentation and automated data management systems (e.g., LIMS, JMP, Minitab).

The QC Chemist will support all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compliance with GMP regulation, procedures, and product specifications Key Responsibilities: Finished Product testing, Environmental Monitoring and Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations and manage these quality incidents as per procedures. Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions. Participation in assigned qualification/validation activities, as necessary. Responsible for successful on time completion of required training curricula comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications, Testing and specifications, and other relevant training including HSE for the specific role. Prepares applicable documents, forms, and records such as analytical batch records and follows Good Documentation Practices. Support internal and external Audits and Inspections, as required. Essential Requirements: Education: Bachelors' degree required in relevant Scientific discipline (e.g Chemistry, Microbiology). Minimum of 3-year experience in cGMP or aseptic environment required. Knowledge of cGMP regulations and FDA guidance applicable to Quality Control for product and Environmental Monitoring testing, as well as Aseptic techniques. Practical experience with Microbiology method verification and routine testing practices, EM Monitoring and basic knowledge of method/equipment validation principle and methodologies preferred HPLC knowledge is required. Ability to interpret analytical data and convert into technical documentation.

• There is an opportunity at Client for a scientist to serve as Analytical Lab Technician in the Regulatory Analytical Sciences Team within Global Regulatory Sciences R&D. Primary Responsibilities Assists in the receiving, weighing and extraction of samples within a study to support product registration and to develop biologically active research chemicals. Supports laboratory testing and data generation as outlined by the principal investigators for the Regulatory Analytical Sciences residue studies. Support experimental lab routine operations such as sample shipments, sample receiving, sample weighing, consumable ordering, etc. Prioritize daily work activities to meet timelines. Interact regularly with LIMS (Laboratory Information Management System) and with an assortment of automated equipment such as liquid handlers. Follow specific protocols to perform routine lab support tasks including the following: Solution preparation Sample processing Sample aliquotting Sample extraction Equipment and assay maintenance Operate laboratory instrumentation, including balances, genogrinders, centrifuges, gas chromatographs, high performance liquid chromatographs, and mass spectrometers. Interface with instrument/equipment owners and the Lab Operations team to maintain system performance and minimize downtime. Complies with all laboratory safety procedures, GLP Standards, and all other study-specific or pertinent regulatory agency requirements Documents activities in the required manner. Maintenance of neat, accurate, and complete records. As needed, follow Good Laboratory Procedures (GLP) and prepare related support documentation. Required Qualifications: Minimum of an Associate Degree in a science related field, BS preferred. General knowledge of chemistry. An understanding of computers and laboratory techniques is desirable. Ability to conduct research and provide high-quality, finalized data in a fast-paced, time sensitive environment. Preferred Qualifications: Experience with quantitative weighings, extractions and sample clean-up techniques from various complex agricultural matrices. Quantitative LC-MS/MS analytical experience in small molecules. An understanding of GLP regulations. Excellent interpersonal skills. Must be able to effectively interact with a diverse group of customers, peers, and R&D regulatory and residue experts

In a world of possibilities, pursue one with endless opportunities. Imagine Next! At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what's possible. Job Description: Parsons is now hiring a Wetland Scientist for our rapidly expanding portfolio of environmental projects! Parsons extensive experience in this field combined with your wetland science knowledge will propel your career forward. We need our Wetland Scientists at this level to apply experience and increasing proficiency in the use of technical theories, practices, and company policies. In this role you will lead a group to conduct wetland delineations/waters investigations and prepare Waters of the U.S. Reports and associated permits. What You'll Be Doing: * This position is responsible for conducting waters investigation, including wetland delineations; preparing Waters of the U.S./State Reports; preparing and obtaining permits from state, local, and federal regulatory agencies; researching and screening alternative project approaches with respect to environmental impacts; and coordinating with clients, agencies and other stakeholders with respect to potential environmental impacts of proposed projects. * Serves as a recognized expert in field of practice. * Provides advice and counsel regarding regulatory compliance issues. * Performs other responsibilities associated with this position as may be appropriate. What Qualifications You'll Bring: * Bachelor's or Master's degree in biology, ecology, or related field * 5 or more years of directly related work experience (Indiana & INDOT specific experience) * Professional Wetland Scientist (PWS) Certification is preferred but not required * National Environmental Policy Act (NEPA) knowledge is preferred * Proficiency in utilizing PC and various software packages typically used in environmental assignments is required Security Clearance Requirement: None This position is part of our Critical Infrastructure team. For more than 80 years, our experts have designed and delivered the critical infrastructure that connects and protects communities around the world. We work in collaborative teams, both within the company and with our partners and customers, to plan, design, build, and modernize infrastructure. We take special pride in projects and solutions that improve communities as well as people's quality of life by promoting economic growth, enhancing mobility, and increasing sustainability and resiliency. Powered by our people, we provide the imagination necessary to support our customers' visions-and to help them see what's next! Salary Range: $72,900.00 - $127,600.00 We value our employees and want our employees to take care of their overall wellbeing, which is why we offer best-in-class benefits such as medical, dental, vision, paid time off, Employee Stock Ownership Plan (ESOP), 401(k), life insurance, flexible work schedules, and holidays to fit your busy lifestyle! Parsons is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status. We truly invest and care about our employee's wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest-APPLY TODAY! Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to ************************************************

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 a cutting edge facility for the manufacture of new modalities including Gene Therapy. At Lebanon, Indiana, this facility will be Lilly's most technically advanced manufacturing site focused on the delivery of the next wave of innovative products at Lilly. It will include next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety and quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to design, commission and start up the facility for both clinical and commercial supply. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up. The TS/MS team will own all areas of technology transfer, process validation, and process stewardship. Position Description: Bioprocess - Technical Services/Manufacturing Scientist (TS/MS) role is responsible for providing technical support for the development, implementation, and technical transfer of compliant manufacturing of gene therapy drug substance for clinical and commercial manufacture. The successful candidate will be required to build deep technical expertise in their area of responsibility (including in-depth knowledge of the science behind the molecule and the process), have strong working skills on the manufacturing equipment set and control systems, and consistently demonstrate strong data-driven decision-making and problem-solving capabilities. They may also work to ensure that the process is in-control, capable, compliant, and maintained in a validated state through continual monitoring and may play a role in by implementing new technologies and process improvements in the manufacturing environment. Key Objectives/Deliverables Have an in-depth knowledge of the science behind the molecule and the processes. Understand the process control strategy for gene therapy products Provide technical support for all start-up TS/MS activities (e.g., NPI, tech transfer, process validation, process stewardship and improvement) Ownership and technical stewardship of bioprocess and provide technical expertise during Root Cause Analysis for deviations and Impact Assessments for changes Work as part of cross-functional teams, and establish partnerships with applicable functions, operations, and development to understand interface between the science/engineering with the operations on the floor and bring deep technical expertise to the team Be able to assess whether the process is in control and capable of meeting its stated purpose and is in a constant state of validation Identify process improvements and participate in implementation of Lean manufacturing initiatives Prepare, review, approve, and provide technical support for preparation of relevant technical documents, as required, such as: change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, process description documents and annual reports Support and/or lead TS/MS technical projects to ensure a successful start-up, improve process control, yield, product quality and/or productivity. Implement process changes and improvements through the technical agenda Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability Serve as technical interface external to the Lebanon site Provide audit support, as needed Work within or lead cross-functional teams in a positive fashion to implement TS/MS objectives and deliver on business plan and quality objectives. Ensure a safe working environment through compliance with safety rules and improve safety culture by actively participating in safety-related activities Basic Requirements: Bachelor's in Biochemical Engineering, Chemical Engineering, Biotechnology, Biochemistry or related quantitative field 3+ years of experience in cGMP manufacturing, specifically within Operations, Validation, TS/MS, or Engineering Additional Preferences: Have an in-depth knowledge of the science behind the molecule and the processes on mRNA/LNP drug substance manufacturing. Understand the process control strategy for mRNA/LNP mediated gene therapy products Experience and understanding of technical challenges with mRNA as a therapeutic modality is required Experience with mRNA/LNP formulation Experience with QC assays in line with product CQAs including variability Strong interpersonal and teamwork skills Strong self-management and organizational skills Strong oral and written communication skills that demonstrate an ability to effectively (clearly, succinctly) communicate with all levels of the organization Experience with data trending and analysis Ability to analyze complex data and solve problems Demonstrated successful membership/leadership of cross-functional teams 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. 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 The successful candidate will possess the experience or develop the skills to: Prepare and analyze different LC-MS samples (including biological samples) according to applicable Standard Operating Procedures (SOPs) Assist in the development of bioanalytical methods using LC-MS platforms. Accurately document experimental procedures and results in electronic lab notebook (eLN) and other systems as appropriate. Qualifications BS in analytical chemistry, physical science, or a related field. Demonstrated proficiency in a laboratory setting Works effectively with others in a team setting Strong hands-on experimental skills and attention to detail Strong analytical and time/task management skills Additional skills and experience that will be beneficial: Experience with biological sample preparation and peptide analysis using LC and mass spectrometry is highly desirable Experience on Waters HPLC and Q-TOF instrument is beneficial Technical proficiency in operation and troubleshooting of analytical instrumentation including chromatography and mass spectrometry Additional Information Position is Monday-Friday 8:00am - 5:00pm overtime as needed. Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Cogent Scientific, an insourced contract research organization in Indianapolis, is looking for the right people to accomplish our Mission: partnering in the global effort to improve lives through innovative science with an experienced workforce. We typically hire scientists with the following backgrounds: * BS/MS - Chemistry, Biochemistry, Organic Chemistry, Molecular Biology and related fields. * Industrial experience in pharma/biotech arenas. * Laboratory skills sets such as: organic synthesis, purification and formulation; analytical chemistry utilizing LC, LC/MS, wet chemistry techniques; molecular biology using PCR, cell culture, Western blot. * Team players who embody our Core Values: C lient Focused: We only succeed when our clients succeed. O utstanding: We deliver meticulous results through outstanding performance. G ood: We act ethically and morally. E mployee-Centric: We honor and support our employees. N imble: We are prepared to adapt in an ever-changing industry. T eam-Oriented: We collaborate with each other and with our clients. If you do not see a job posted on our employment page that fills your skills and experience, feel free to upload your information and resume here. We are continually growing and look forward to working with you soon!

Your responsibilities will include: * Design and develop nanoparticle conjugation methods for high-sensitivity assays * Optimize protocols for nanoparticle functionalization, including iron oxide and colloidal gold * Implement bioconjugation strategies like PEGylation, biotinylation, and covalent coupling with antibodies, antigens, nucleic acids, and small molecules * Troubleshoot and improve bioconjugation processes to enhance stability, sensitivity, and specificity * Collaborate with product development and scale-up teams to ensure consistent performance in nanoparticle assays * Maintain detailed experiment records, contribute to reports, and share insights with the team Must have: * Ph.D/MsC. in Biochemistry, Chemistry, Materials Science, or a related field, focused on nanoparticle bioconjugation with 5+ years of industrial experience * Strong expertise in nanoparticle surface modification and functionalization * Hands-on experience with various conjugation chemistries, including thiol, amine, acid, azide, and other click chemistries * Proven success in developing particle-based immunoassays, like ELISA and lateral flow * Solid background in analytical methods for characterizing nanoparticles * Ability to work effectively as part of a cross-functional team Nice to have: * Experience with scaling nanoparticle products for FDA-regulated markets. * Background in developing in vitro diagnostic assays, especially in oncology applications

Job Details BANGS IN - Fishers, IN Full Time 4 Year Degree None Day ManufacturingDescription Who We Are Ott Scientific The Ott Scientific family of companies comprises Polysciences, Bangs Laboratories, and Ethos Biosciences. Together, we bring the whole of our experience with best-in-class facilities and scientific, technical, analytical, and manufacturing capabilities to serve customers around the globe. We deliver highly specialized products and services that support scientific discovery and innovations. Bangs Laboratories Bangs Laboratories experience in microsphere synthesis and fine particle analysis have established us as a leading manufacturer of polymer, silica and magnetic microspheres for diagnostic, research, and flow cytometry applications. We also manufacture many specialty products to support validation and QC programs for analytical instruments, including a broad portfolio of fluorescent, count, size, and cell viability standards. This position is responsible for all aspects of the timely and quality-focused production of Bangs Laboratories' products. In addition, this position may be involved in research and development of new products, or application support. Production Receive relevant job requests and maintain them in appropriate software Monitor inventory of lab reagents and supplies; submit requests as appropriate Produce established products, following current ISO procedures Perform preliminary QC testing prior to release to Materials Dept. Write / update ISO documents as necessary. Periodically evaluate the quality of finished goods. Evaluate alternate raw material suppliers and new raw material lots. Integrate newly developed products into the manufacturing system. Scale-up processes as required. Train personnel on laboratory procedures. Assist with technical service, trouble shooting and applications support as necessary. Investigate and recommend equipment replacement / addition. Present periodic internal mini-seminars on technical topics as needed. Can participate in product development projects as a team member. Maintain laboratory work area. Maintain equipment. Qualifications This position requires a Bachelor of Science degree, or equivalent, in chemistry, chemical engineering, or a related scientific field as well as general, broad-based understanding of scientific principles. Successful applicants will have hands-on laboratory experience with kilo-lab experience as a big plus. The person filling this position must be self-motivated and organized, with good interpersonal and written skills. Product and application-specific training will be provided. What We Offer Culture Great people Peer to Peer Recognition Broader, hands-on work experience Clean and Modern Equipment & Labs Fun company events Competitive Wages & Generous Year-end Bonus Comprehensive Benefits 4 Medical PPO Medical Plans with Telemedicine, Rx, & Vision 2 Dental Plans Healthcare, Dependent care, & Commuter Flexible Spending Accounts 401(k) with company match Financial Health & Wellness w/1:1 Coaching Basic & Supplemental Life Insurance Accident, Hospital Indemnity, & Critical Illness Paid Time Off Short & Long-term Disability 9 Paid Holidays Must have legal authorization to work in the US and will not require sponsorship. Bangs Laboratories is an equal opportunity employer. Drug-free workplace. Tobacco-free work site. Bangs Laboratories does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need. Equal access to programs, services, and employment is available to all persons. Those applicants requiring reasonable accommodation to the application process and/or interview process should notify a representative of the Human Resources Department.

Corteva Agriscience has an exciting opportunity for a Associate Formulation Scientist in Indianapolis, IN. The incumbent will provide technical support in the Formulations Development laboratory through hands-on experimentation and problem-solving for research problems that are well defined. Key Responsibilities: Provides technical support to the formulation development scientists through the preparation of formulation samples and testing of formulation samples for physical properties. Prepares formulation samples with minimum supervision using standard processing equipment such as bead mills, high shear mixers, air jet mills, blenders etc. Independently evaluates formulation samples for physical / chemical properties and is proficient in the use of laboratory instruments such as laser diffraction particle size analyzers, rheometers, density meters, pH meters etc. Maintains laboratory equipment and instruments in good working order. Reports, discusses and provides solutions for any issues related to the Lab equipment. Prepares formulation samples for field trials. Keeps the raw materials inventory updated, ensures samples are labeled in compliance with EH&S requirements and disposes of materials with expired shelf-life. Maintains laboratory notebook and accurately documents all experiments and results. Communicates project status in a timely fashion and immediately raises any issues to the project owner. Maintains a high housekeeping standard in the laboratory. Supports sample shipping in the importation and exportation of experimental samples and raw materials. Understands and follows appropriate EH&S standards, policies and procedures applicable to their job. Leads by example in the area of safety behaviors by promoting safe work habits. Required Qualifications No prior experience required, but technical experience in academia or industry is a plus Capable of taking action and resolving issues independently. Performs duties with minimal supervision, actively demonstrates accountability by providing recommendations and or thorough analysis of options for issues/solutions. Proficient in tools used within the work process. Education B.Sc. degree in Chemistry or related fields. 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.

Explore research careers and be a part of something bigger as an Operations Scientist I in our Bioanalytical Lab in Indianapolis, IN! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. As a Operations Scientist I in Bioanalytical Services you will be part of a cohesive team and conduct routine analysis on biological and chemical samples in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines for multiple studies. The ideal candidate for an Immunochemistry Operations Scientist would demonstrate the following: Resiliency to failure Ability to handle multiple projects in various stages at once Ability to handle a fast paced environment GLP Documentation skills and/or knowledge Organized and detailed communication Duties and Responsibilities: Conduct ELISA assays independently at least four days per week Communicate with project managers, lead scientists, and supervisor on projects daily/weekly Provide detailed sample analysis and inventory updates to project managers and lead scientists to ensure projects meet agreed upon timelines Order reagents for projects as needed Document work and maintain study documentation and laboratory records. Assist in writing text for reports, methods or protocols. Assist in setting up and performing method development and validation of various analytes in a variety of matrices. Set up, operate and perform routine and non-routine maintenance on general equipment. Attend and participate in project meetings. Perform QC review of data. Plan assigned workload on a daily basis and effectively schedule multiple assignments. Support process improvement initiatives. Maintain a clean and safe laboratory work environment. Participate in client visits as needed. Education/Qualifications/Experience: Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Relevant Bioanalytical experience may be substituted for education Ability to perform basic computer skills (e.g., Word, Excel) 1-2 years related or relevant laboratory experience required Familiar with the use of standard laboratory equipment (e.g., balances, pipettes, centrifuges) Experience with analytical instrumentation Knowledgeable on a variety of study types, analysis procedures and methodology Able to effectively communicate, both verbally and in writing Application Window 9/12 thru 9/26/25 Pay Range $22 - $27.00 per hour Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

HIRING NOW: Analytical Chemist | ICP Specialist INTERVIEWS AVAILABLE THIS WEEK Interested in this role? Reach out directly to ***************************** or CALL ************ with an updated resume to apply (HIRING NOW) * Located In Fishers* Description Job Title: Analytical Chemist - ICP-OES/MS Specialist for Advanced Materials Position Overview We're seeking an experienced Analytical Chemist with specialized expertise in ICP-OES and ICP-MS to support precision analysis in advanced materials purification. This role plays a critical part in optimizing separation workflows and ensuring ultra-trace elemental accuracy across experimental and production-scale operations. The successful candidate will contribute to method development, quality assurance, and data-driven process refinement in a dynamic, innovation-focused lab environment. Responsibilities: Operate and maintain ICP-OES/MS instrumentation for multi-element and trace-level analysis of complex samples. Develop and validate analytical protocols for diverse sample types including powders, solutions, and solid residues. Perform acid digestion and fusion techniques tailored to high-solid and refractory materials. Quantify impurities and elemental recoveries to support purification and product qualification efforts. Collaborate with process engineers and scientists to provide analytical insights for system design and performance tuning. Address spectral and matrix interferences using advanced techniques such as collision/reaction cells and internal standards. Maintain calibration logs, SOPs, and QA documentation aligned with laboratory accreditation standards. Drive continuous improvement in analytical workflows, including automation and integration with digital systems. Train junior staff in sample prep, instrument use, and safety protocols. Prepare technical reports and data summaries for internal reviews and external stakeholders. Qualifications Required: Bachelor's degree in Analytical Chemistry, Geochemistry, Materials Science, or a related field. 1-2 years of hands-on experience with ICP-OES/MS in a materials, chemical, or metallurgical setting. Proven ability to analyze trace metals in complex matrices. Familiarity with hydrometallurgical processes such as leaching, precipitation, and solvent extraction. Proficiency with instrument software and data systems (e.g., Qtegra or similar). Strong documentation and troubleshooting skills. Preferred: Advanced degree (M.S. or Ph.D.) in a relevant discipline. Experience with rare-earth elements, battery metals, or high-purity oxide analysis. Knowledge of complementary analytical tools and techniques. Exposure to pilot-scale or scale-up operations. Skills Chemistry, Analytical chemistry, ICP, ICP OES, ICP MS, Hplc, Laboratory, Gmp, Quality control, Wet chemistry, Chemical, Method validation, Gas chromatography, Chromatography, Gcms, Gc-ms Top Skills Details Chemistry,Analytical chemistry,ICP,ICP OES,ICP MS Additional Skills & Qualifications Qualifications Required: Bachelor's degree in Analytical Chemistry, Geochemistry, Materials Science, or a related field. 1-2 years of hands-on experience with ICP-OES/MS in a materials, chemical, or metallurgical setting. Proven ability to analyze trace metals in complex matrices. Familiarity with hydrometallurgical processes such as leaching, precipitation, and solvent extraction. Proficiency with instrument software and data systems (e.g., Qtegra or similar). Strong documentation and troubleshooting skills. Preferred: Advanced degree (M.S. or Ph.D.) in a relevant discipline. Experience with rare-earth elements, battery metals, or high-purity oxide analysis. Knowledge of complementary analytical tools and techniques. Exposure to pilot-scale or scale-up operations. Experience Level Expert Level INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: I am scheduling interviews for this position ASAP and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Max Richey HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to mrichey@actalentservices. com or CALL ************ Job Type & Location This is a Contract to Hire position based out of Fishers, IN. Pay and Benefits The pay range for this position is $40.00 - $48.00/hr. 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 Fishers,IN. Application Deadline This position is anticipated to close on Dec 12, 2025. 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.

Starting at $13 per hour!!! The Retail Associate assists the store management team in reaching the operational goals of the site by functioning in various capacities within the retail location. The titles of the various jobs the Retail Associate may be called upon to learn and work include: Cashier, Textiles or Wares Producer, Donation Door Attendant, eCommerce Producer, e-Books Producer, and Rack or Cart Runner. Example Duties and Activities Cashier: Rings up customer orders, maintains a balanced drawer, and follows all cash handling procedures and protocols. Provides general information about Goodwill programs to educate customers and answer questions. Directs all higher-level questions to the appropriate associate or manager. Maintains cleanliness of the sales floor (purge, size, run racks, and merchandise). Textiles or Wares Producer: Sorts product to identify quality and value (checks for holes, missing buttons, defective zippers, or stains and cleans as needed) and properly barbs, tags, and hangs textiles or wares. Sort textiles (curating for quality). Produces 100 items per hour for wares/85 items per hour for textiles adhering to Goodwill's pricing standards and updating daily production tracking sheet. Occasionally uses a pallet jack and regularly uses a conveyor belt. Donation Door Attendant: Accepts donations from customers and maintains a clean and clear donation door. Quickly and accurately sorts products and distributes them to appropriate areas. Maintains an efficient working area by ensuring the backroom is clean and organized (all boxes labeled, everything in its place, and a place for everything). Loads and unloads trucks as needed and regularly uses heavy equipment, including a pallet jack, double stacker, floor scrubber, and hydraulic lift. eCommerce Producer: Develops a keen eye to identify and secure items of value for ClickGoodwill. Stays informed of the market value of merchandise through eBay and other Internet shopping sites to properly tag, itemize, and secure items in totes for ClickGoodwill and educates team of eCommerce high ticket items. Properly, efficiently and carefully pack curated products onto pallets, wraps, and ships totes to ClickGoodwill to meet the store budget regarding totes shipped per week. e-Books Producer: Scans books received by the store and decides what is sent to ClickGoodwill or displayed at the store location to meet the store budget. Prints inventory sheets and packs, seals, and ships totes for ClickGoodwill. Identifies top sellers and manages a clean, organized, in-store sales-effective display. Rack and Cart Runner: Checks each rack/cart to ensure quality and value. Properly sizes, merchandises, and purges the sales floor. Maintains a clean and orderly sales floor, puts away carts, and stocks shelves. Runs one textile rack/wares cart per 15 minutes and updates daily production tracking sheet. Required Competencies Degree and Credential Requirements- NONE! We value candidates who can demonstrate capability and articulate how prior experiences will help them contribute. We believe in continuous learning and professional development. Customer Focus - Has the ability to see, comprehend and relate with customers in an impartial, unbiased yet effective and balanced manner; builds and maintains customer satisfaction with the products and services offered by the organization; provides excellent service to internal and external customers. Teamwork - Works well with others and makes valued contributions to the outputs of others in order to assist the team or project to achieve the required outputs. Ethical - Adheres to procedures and protocol, including maintaining confidentiality in passwords, logging on and off procedures, and adherence to Goodwill's values. Attention to Detail - Attends to details and pursues quality in accomplishing tasks, including safety awareness. Time Management - Manages one's own time and the time of others effectively. Preferred Competencies Technical Knowledge - Has familiarity with computers and relevant software including basic computer and Internet navigation skills. Communication Skills - Articulates thoughts and expresses ideas effectively using oral, written, visual and non-verbal communication skills, as well as listening skills to comprehend customers' needs. Delivers information in person, in writing, and in a digital world. Mathematical Aptitude - Develops and applies mathematical thinking in order to solve a range of problems in everyday situations. Critical Thinking - Uses judgment and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems. Other Requirements Reasonable accommodations may be made to enable people with disabilities to perform essential job functions. Hard to Very Hard Physical Work - Is able to spend time in excess of 8 hours sitting, standing, walking, stooping, kneeling, and crouching. Uses hands to grasp, carry, feel, or touch products and machinery. Has the ability to move and lift 10-50 pounds. Can manage frequent exposure to moderate noise and temperature variations. Benefits: If you are hired on full-time or eventually move to full-time status, our full-time employees may participate in a comprehensive benefits program that includes: Continuing education and leadership development as well as tuition reimbursement Discount programs including 20% discount off Goodwill retail stores immediately upon hire Comprehensive health plan Generous paid time off (PTO) and paid holidays Sabbatical and parental leaves Life, dental and vision insurance Short- and long-term disability plans Nationally recognized preventive health and wellness program Section 125 pretax health spending account, dependent care spending account, and premiums Retirement planning options with generous company % match Free mental health support services with up to 15 free counseling sessions for you and your family members Free nurse health coaching services on-site Daily pay options available Mission and Values: click here Goodwill of Central and Southern Indiana is an EEO Employer/Vet/Disabled Retail1

The QC Chemist will support all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compliance with GMP regulations, procedures, and product specifications. Key Responsibilities: Compendia experience (USP, EP, BP, JP, CP). Finished Product testing, Environmental Monitoring, Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations, and manage these quality incidents as per procedures. Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow-up and implementation, and Change Control management, including procedure and form revisions. Participation in assigned qualification/validation activities, as necessary. Responsible for the successful on-time completion of required training curricula comprising the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications, Testing and specifications, and other relevant training, including HSE for the specific role. Prepares applicable documents, forms, and records such as analytical batch records, and follows Good Documentation Practices. Support internal and external Audits and Inspections, as required. Essential Requirements: Education: Bachelor's degree required in a relevant Scientific discipline (e.g, Chemistry, Microbiology). A minimum of 2-3 years of experience in a cGMP or aseptic environment is required. Knowledge of cGMP regulations and FDA guidance applicable to Quality Control for product and Environmental Monitoring testing, as well as Aseptic techniques. Practical experience with Microbiology method verification and routine testing practices, EM Monitoring, and basic knowledge of method/equipment validation principles and methodologies preferred; HPLC knowledge is required. Ability to interpret analytical data and convert it into technical documentation. Basic knowledge and understanding of aseptic principles and techniques, Quality Control Sampling, Quality Control (QC Testing), and General HSE knowledge.

Responsibilities: Assist in the preparation, setup, and daily operation of biological experiments. Perform routine laboratory techniques such as sample collection, microscopy, culturing, buffer preparation, staining procedures, and basic molecular assays (PCR, gel electrophoresis, DNA/RNA extraction). Prepare reagents, solutions, and media according to established laboratory protocols. Maintain and calibrate laboratory equipment-including centrifuges, incubators, microscopes, biosafety cabinets, and spectrophotometers-following institutional and lab-specific guidelines. Accurately record experimental procedures, data, and observations in lab notebooks or electronic systems to support reproducibility and publication-quality research. Follow academic lab safety standards, including proper handling of biological samples, chemical reagents, and shared equipment, while helping maintain an organized and contamination-free workspace. Help analyze, review, and validate experimental results; report any unexpected outcomes or technical issues to supervising researchers. Contribute to general lab operations by monitoring inventory, preparing supply orders, and restocking reagents and consumables. Qualifications: Bachelor's degree in Biology, Biochemistry, Molecular Biology, Microbiology, or a related life science field, or equivalent academic laboratory experience. Working knowledge of standard biological research techniques and academic lab practices. Strong attention to detail and ability to follow experimental protocols accurately to ensure data reproducibility. Organizational and multitasking skills to support multiple research projects simultaneously. Familiarity with common research tools such as micropipettes, microscopes, PCR instruments, centrifuges, and spectrophotometers. Effective written and verbal communication skills, including maintaining clear lab notes and discussing results with supervising researchers. Basic computer proficiency for data entry, spreadsheet management, and literature searches.

Job DescriptionSalary: Cogent Scientific, an insourced contract research organization in Indianapolis, is looking for the right people to accomplish our Mission: partnering in the global effort to improve lives through innovative science with an experienced workforce. We typically hire scientists with the following backgrounds: * BS/MS - Chemistry, Biochemistry, Organic Chemistry, Molecular Biology and related fields. * Industrial experience in pharma/biotech arenas. * Laboratory skills sets such as: organic synthesis, purification and formulation; analytical chemistry utilizing LC, LC/MS, wet chemistry techniques; molecular biology using PCR, cell culture, Western blot. * Team players who embody our Core Values: C lient Focused: We only succeed when our clients succeed. O utstanding: We deliver meticulous results through outstanding performance. G ood: We act ethically and morally. E mployee-Centric: We honor and support our employees. N imble: We are prepared to adapt in an ever-changing industry. T eam-Oriented: We collaborate with each other and with our clients. If you do not see a job posted on our employment page that fills your skills and experience, feel free to upload your information and resume here. We are continually growing and look forward to working with you soon!

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. The Visiting Scientist Fellowship is a one-year postgraduate program that introduces participants to various medical, commercial, clinical development, project management, health outcomes, and regulatory aspects of the pharmaceutical industry. It is designed to train professionals for a career in the pharmaceutical industry by allowing them hands-on experience with the drug development process. The visiting scientist fellow is assigned to one department yet has continuous contact with other functional areas. Interviews for these positions will begin in October 2025 with an anticipated start date in June or July of 2026. We anticipate offering the following positions: Market Access: Insights and New Product Planning Cardiometabolic Health (CMH) Market Access Lilly Value & Access - Value and Transformation Business Development Oncology New Product Planning Health Outcomes and Medical Engagement Health Outcomes Liaison For more information regarding these positions or for the most up to date listing of our positions, please visit our website Visiting Scientist | Lilly Basic Qualifications PharmD, MD, relevant PhD and/or Master's degree Completion of required degree by June 2026 but not earlier than May 2023 Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor the following work authorization or visas for this role: F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1. Additional Skills/Preferences Strong interpersonal and communication skills Strong leadership, decision-making, and critical thinking skills A demonstrated ability to learn quickly 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 $205,500 - $301,400 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. 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 Responsibilities include, but are not limited to, the following: Perform routine analytical testing of medium to high complexity drug substance/drug product and/or method verification/characterization using instrumentation including, but not limited to, HPLC, GC, UV spectrophotometer, dissolution apparatus, pH meter, water activity meter, Karl Fischer titrators. Participate in conducting investigations Document test results in notebooks and reports Qualifications The ideal candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Proficiency in IT-related skills such as Microsoft Excel, Word, PowerPoint, etc Basic Minimum Qualifications: Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration, At least 4+ years of related laboratory experience Additional Information Position is full-time, Monday - Friday 8am to 5 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.

Starting at $11 per hour!!! The Retail Associate assists the store management team in reaching the operational goals of the site by functioning in various capacities within the retail location. The titles of the various jobs the Retail Associate may be called upon to learn and work include: Cashier, Textiles or Wares Producer, Donation Door Attendant, eCommerce Producer, e-Books Producer, and Rack or Cart Runner. Example Duties and Activities Cashier: Rings up customer orders, maintains a balanced drawer, and follows all cash handling procedures and protocols. Provides general information about Goodwill programs to educate customers and answer questions. Directs all higher-level questions to the appropriate associate or manager. Maintains cleanliness of the sales floor (purge, size, run racks, and merchandise). Textiles or Wares Producer: Sorts product to identify quality and value (checks for holes, missing buttons, defective zippers, or stains and cleans as needed) and properly barbs, tags, and hangs textiles or wares. Sort textiles (curating for quality). Produces 100 items per hour for wares/85 items per hour for textiles adhering to Goodwill's pricing standards and updating daily production tracking sheet. Occasionally uses a pallet jack and regularly uses a conveyor belt. Donation Door Attendant: Accepts donations from customers and maintains a clean and clear donation door. Quickly and accurately sorts products and distributes them to appropriate areas. Maintains an efficient working area by ensuring the backroom is clean and organized (all boxes labeled, everything in its place, and a place for everything). Loads and unloads trucks as needed and regularly uses heavy equipment, including a pallet jack, double stacker, floor scrubber, and hydraulic lift. eCommerce Producer: Develops a keen eye to identify and secure items of value for ClickGoodwill. Stays informed of the market value of merchandise through eBay and other Internet shopping sites to properly tag, itemize, and secure items in totes for ClickGoodwill and educates team of eCommerce high ticket items. Properly, efficiently and carefully pack curated products onto pallets, wraps, and ships totes to ClickGoodwill to meet the store budget regarding totes shipped per week. e-Books Producer: Scans books received by the store and decides what is sent to ClickGoodwill or displayed at the store location to meet the store budget. Prints inventory sheets and packs, seals, and ships totes for ClickGoodwill. Identifies top sellers and manages a clean, organized, in-store sales-effective display. Rack and Cart Runner: Checks each rack/cart to ensure quality and value. Properly sizes, merchandises, and purges the sales floor. Maintains a clean and orderly sales floor, puts away carts, and stocks shelves. Runs one textile rack/wares cart per 15 minutes and updates daily production tracking sheet. Required Competencies Degree and Credential Requirements- NONE! We value candidates who can demonstrate capability and articulate how prior experiences will help them contribute. We believe in continuous learning and professional development. Customer Focus - Has the ability to see, comprehend and relate with customers in an impartial, unbiased yet effective and balanced manner; builds and maintains customer satisfaction with the products and services offered by the organization; provides excellent service to internal and external customers. Teamwork - Works well with others and makes valued contributions to the outputs of others in order to assist the team or project to achieve the required outputs. Ethical - Adheres to procedures and protocol, including maintaining confidentiality in passwords, logging on and off procedures, and adherence to Goodwill's values. Attention to Detail - Attends to details and pursues quality in accomplishing tasks, including safety awareness. Time Management - Manages one's own time and the time of others effectively. Preferred Competencies Technical Knowledge - Has familiarity with computers and relevant software including basic computer and Internet navigation skills. Communication Skills - Articulates thoughts and expresses ideas effectively using oral, written, visual and non-verbal communication skills, as well as listening skills to comprehend customers' needs. Delivers information in person, in writing, and in a digital world. Mathematical Aptitude - Develops and applies mathematical thinking in order to solve a range of problems in everyday situations. Critical Thinking - Uses judgment and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems. Other Requirements Reasonable accommodations may be made to enable people with disabilities to perform essential job functions. Hard to Very Hard Physical Work - Is able to spend time in excess of 8 hours sitting, standing, walking, stooping, kneeling, and crouching. Uses hands to grasp, carry, feel, or touch products and machinery. Has the ability to move and lift 10-50 pounds. Can manage frequent exposure to moderate noise and temperature variations. Benefits: Goodwill offers a competitive package of benefits even for part-time employment that includes: Corporate wellness program that includes: an Employee Assistance Program (EAP), health coaching and wellness discounts (Weight Watchers, YMCA, etc.) Discount programs for phone carriers (Verizon, AT&T, etc.) and 20% discount off Goodwill retail stores immediately upon hire Financial education programs- credit union membership and access to online workshops Daily pay options available Mission and Values: click here Goodwill of Central and Southern Indiana is an EEO Employer/Vet/Disabled Retail1