Microbiologist jobs in Indianapolis, IN

Work for Indiana Begin a fulfilling career with the State of Indiana by joining one of the largest employers in the state, offering a range of opportunities across 60+ agencies. At the state, you'll find competitive compensation, a robust benefits package and a commitment to work-life balance. Most importantly, you'll have the chance to make a real and measurable impact on the lives of Hoosiers across Indiana. About the Indiana Department of Health (IDOH): The Indiana Department of Health's mission is to promote, protect, and improve the health and safety of all Hoosiers so that they can reach their optimal health regardless of where they live, learn, work, or play. Role Overview: The Microbiologist's role in Method Development will be responsible for the implementation, validation, and SOP generation for new methods being brought into our laboratory. They will assist with developing new assays, new technologies, and troubleshooting existing assays. This position will also play a large role in our genomic sequencing and analysis. The position is located at the Indiana Department of Health laboratory and has no travel requirements. Salary Statement: The salary for this position traditionally starts at $53,222.00 but may be commensurate with education or work experience. A Day in the Life: The essential functions of this role are as follows: * Conduct procedures of clinical specimens and/or reference samples/food samples/environmental samples for serological analysis or isolation and identification of micro-organisms or their antigens/nucleic acids. * Evaluate, interpret, and validate laboratory results and reports findings to the submitter. * Organize and plan identification schemes for examination of organisms not fitting regular schemes. * Evaluate quality control checks on laboratory methods, materials, and equipment. * Coordinate the preparation of media, reagents, stains, supplies and other materials used in the transport, examination, and analysis process. * Prepare epidemiological and statistical reports from data compiled on a daily, weekly, monthly, or annual basis. * Development, preparation and updating of procedural manuals on methods, instrumentation, and quality assurance. * Participate in training programs as a planner or instructor at workshops and conferences for private and public laboratory personnel. * Initiate special research projects designed to test and improve microbiological methods and procedures. * Participate in testing evaluation of new products used in clinical/reference laboratory work. * Work with local laboratories and other health department staff to ensure their use of adequate materials, techniques, methods, and procedures. * May appear at legal proceedings as an expert witness. The job profile is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Other duties, responsibilities and activities may change or be assigned at any time with or without notice. This position is exempt from overtime compensation for additional work hours which may be required to complete essential functions or other assigned work. Exempt employees may work more than 75 hours in a pay period without additional compensation and must report a minimum of 75 hours per pay period of work hours and/or paid leave taken to receive their base biweekly salary. What You'll Need for Success: You must meet the following requirements to be considered for employment: * A four (4) year degree (B.S. or B.A.) in a biological, chemical, or physical science. If the position will be working in an area that falls under CLIA-regulation, degree must meet the degree requirements for CLIA high-complexity testing personnel. * Two (2) years of testing experience that is relevant to the hiring area. * Thorough knowledge of the principles, theories and practices of microbiology and related sub-specialties. * Ability to meet requirements for personnel certification as a general supervisor pursuant to the Clinical Laboratory Improvement Act of 1988. * Thorough knowledge of, and the ability to apply, accepted or unprecedented laboratory problems. * Broad knowledge of, and ability to use, complex and specialized technical/scientific equipment and automated techniques of analysis. * Broad knowledge of laboratory safety practices and principles. * Specialized knowledge of state and federal laws, rules, regulations, and policies concerning the program area. * Ability to satisfactorily participate in proficiency testing programs. * Ability to compile, analyzes, evaluate and present laboratory data to physicians, veterinarians, public health staff and professional organizations. * Able to perform essential functions with or without reasonable accommodation. Supervisory Responsibilities/Direct Reports: This role may be utilized in a supervisory capacity based on agency needs. Benefits of Employment with the State of Indiana: The State of Indiana offers a comprehensive benefit package for full-time employees which includes: * Three (3) medical plan options (including RX coverage) as well as vision and dental plans * Wellness Rewards Program: Complete wellness activities to earn gift card rewards * Health savings account, which includes bi-weekly state contribution * Deferred compensation 457(b) account (similar to 401(k) plan) with employer match * Two (2) fully-funded pension plan options * A robust, comprehensive program of leave policies covering a variety of employee needs, including but not limited to: * 150 hours of paid New Parent Leave and up to eight weeks of paid Childbirth Recovery Leave for eligible mothers * Up to 15 hours of paid community service leave * Combined 180 hours of paid vacation, personal, and sick leave time off * 12 paid holidays, 14 on election years * Education Reimbursement Program * Group life insurance * Referral Bonus program * Employee assistance program that allows for covered behavioral health visits * Qualified employer for the Public Service Loan Forgiveness Program * Free Parking for most positions * Free LinkedIn Learning access Equal Employment Opportunity: The State of Indiana is an Equal Opportunity Employer and is committed to recruiting, selecting, developing, and promoting employees based on individual ability and job performance. Reasonable accommodations may be available to enable individuals with disabilities to complete the application and interview process as well as perform the essential functions of a role. If you require reasonable accommodations to complete this application, you can request assistance by contacting the Indiana State Personnel Department at ***************. Current Employee? Click here to apply.

Job Details Shifts: day Medical benefits-eligible first of the month following 28 days of employment. All other benefits-eligible first of the month following 90 days of employment. Benefits: 401(k) Dental insurance Health insurance Paid time off Employee Discount Vision insurance Position Overview: The Microbiologist is responsible for monitoring and qualitative/quantitative testing of process and product attributes to ensure food safety and food quality. Ensure compliance with all applicable regulations. Compliance with all applicable standards such as Safe Quality Foods (SQF), Third party audits, Kosher, and Organic requirements. Interpretation of testing results to release of product that has met specifications. Process documentation for non-conforming product and communicate information to plant management. Language Skills: English proficiency required. Spanish is a plus. Supervisory Responsibilities: None. Amount of Travel Involved: None. Essential Duties and Responsibilities: Follow all safety procedures and work as safe as possible at all times. Maintain Good Manufacturing Practices (GMP's). Maintain Good Laboratory Practices (GLP's). Daily operation of equipment which includes Autoclave, Air Sampler, and all other related equipment. Responsible for microbiological testing/documentation of finished product, water, swabs, ingredient and or other material as needed. Interpret the results and retest/report abnormalities as needed; Generate standard report of results. Standardizes equipment prior to use, ensures reagents and other materials are available. Performs analysis on products to ensure compliance to customer and regulatory agency guidelines. Ensures that all products not meeting microbiological specification is communicated to QA Manager for further review. Ensure that all-pertinent analytical results into the data collections system on a timely basis, immediately informs supervision of any deviations. Review, creates, maintains, files, and scan logs, charts, finished goods/ingredients/packaging microbiological results and other reports. Manage the laboratory operations, maintain lab equipment and supplies. Maintain lab equipment and order supplies. Release products that have met microbiological specification in ILS. Conduct work processes with the use of chemicals. Evaluate the physical properties of ingredients and products. Train Analytical Technician, QA Lead, on plating, reading, documenting, filing, and scanning microbiological sampling and results. Provide management with microbiological expertise as needed. Create Certificate of Analysis (COA) and submit microbiological results to customers. Other duties as assigned at discretion of management Maintain a positive work atmosphere and interaction with customers, co-workers, and management. Regular and punctual attendance. Work scheduled shift, weekends, and extended hours as required. To perform this job successfully, must be able to perform each fundamental task listed above satisfactorily. Experience for Success: Must be accurate and precise in testing procedures. Must possess strong oral and written communication skills. Must be able to read, write and interpret documents such as, procedure manuals. Must have the ability to read, comprehend and follow technical instructions. Ability to effectively present information in one-on-one and small group situations to customers, clients and other employees of the organization. Must be able to speak and understand English fluently. Must have the ability to apply commonsense understanding to carry out detailed and involved written or oral instructions. Must have the ability to calculate figures and amounts such as proportions, percentages, averages, and ratios. Must have the ability to prioritize and organize. Must demonstrate superb decision-making ability to determine best course of action in assessing test results. Must possess strong computer skills. Education and/or Experience: Bachelor of Science degree in Microbiology Biology, or Food Science, required. Two years of laboratory with microbiology and chemistry experience required. Or equivalent combination of education and experience. At least 1 year in a food or beverage production environment preferred. Experienced with MS Office (Word and Excel) required. Behaviors & Competencies: Upholds mental, spiritual and physical safety Asks for and provides feedback Holds self and others accountable Supportive and collaborative of team members Participates in self-development and encourages the development of those who report/to him or her and peers Demonstrates flexibility and desire for growth Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to sit; use hands to finger, handle or feel and reach with hands and arms. The employee is frequently required to stand; walk and stoop, kneel, crouch or squat. The employee must regularly lift, pull and/or move up to 10 pounds, frequently lift, pull and/or move up to 25 pounds and occasionally lift, pull and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate but may be exposed to loud noises from production equipment. The employee is occasionally exposed to fumes or airborne particles; toxic or caustic chemicals; extreme cold and extreme heat. Manna Beverages is an equal opportunity employer-----M/F/D/V

Job Description Job Details Shifts: day Medical benefits-eligible first of the month following 28 days of employment. All other benefits-eligible first of the month following 90 days of employment. Benefits: 401(k) Dental insurance Health insurance Paid time off Employee Discount Vision insurance Position Overview: The Microbiologist is responsible for monitoring and qualitative/quantitative testing of process and product attributes to ensure food safety and food quality. Ensure compliance with all applicable regulations. Compliance with all applicable standards such as Safe Quality Foods (SQF), Third party audits, Kosher, and Organic requirements. Interpretation of testing results to release of product that has met specifications. Process documentation for non-conforming product and communicate information to plant management. Language Skills: English proficiency required. Spanish is a plus. Supervisory Responsibilities: None. Amount of Travel Involved: None. Essential Duties and Responsibilities: Follow all safety procedures and work as safe as possible at all times. Maintain Good Manufacturing Practices (GMP's). Maintain Good Laboratory Practices (GLP's). Daily operation of equipment which includes Autoclave, Air Sampler, and all other related equipment. Responsible for microbiological testing/documentation of finished product, water, swabs, ingredient and or other material as needed. Interpret the results and retest/report abnormalities as needed; Generate standard report of results. Standardizes equipment prior to use, ensures reagents and other materials are available. Performs analysis on products to ensure compliance to customer and regulatory agency guidelines. Ensures that all products not meeting microbiological specification is communicated to QA Manager for further review. Ensure that all-pertinent analytical results into the data collections system on a timely basis, immediately informs supervision of any deviations. Review, creates, maintains, files, and scan logs, charts, finished goods/ingredients/packaging microbiological results and other reports. Manage the laboratory operations, maintain lab equipment and supplies. Maintain lab equipment and order supplies. Release products that have met microbiological specification in ILS. Conduct work processes with the use of chemicals. Evaluate the physical properties of ingredients and products. Train Analytical Technician, QA Lead, on plating, reading, documenting, filing, and scanning microbiological sampling and results. Provide management with microbiological expertise as needed. Create Certificate of Analysis (COA) and submit microbiological results to customers. Other duties as assigned at discretion of management Maintain a positive work atmosphere and interaction with customers, co-workers, and management. Regular and punctual attendance. Work scheduled shift, weekends, and extended hours as required. To perform this job successfully, must be able to perform each fundamental task listed above satisfactorily. Experience for Success: Must be accurate and precise in testing procedures. Must possess strong oral and written communication skills. Must be able to read, write and interpret documents such as, procedure manuals. Must have the ability to read, comprehend and follow technical instructions. Ability to effectively present information in one-on-one and small group situations to customers, clients and other employees of the organization. Must be able to speak and understand English fluently. Must have the ability to apply commonsense understanding to carry out detailed and involved written or oral instructions. Must have the ability to calculate figures and amounts such as proportions, percentages, averages, and ratios. Must have the ability to prioritize and organize. Must demonstrate superb decision-making ability to determine best course of action in assessing test results. Must possess strong computer skills. Education and/or Experience: Bachelor of Science degree in Microbiology Biology, or Food Science, required. Two years of laboratory with microbiology and chemistry experience required. Or equivalent combination of education and experience. At least 1 year in a food or beverage production environment preferred. Experienced with MS Office (Word and Excel) required. Behaviors & Competencies: Upholds mental, spiritual and physical safety Asks for and provides feedback Holds self and others accountable Supportive and collaborative of team members Participates in self-development and encourages the development of those who report/to him or her and peers Demonstrates flexibility and desire for growth Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to sit; use hands to finger, handle or feel and reach with hands and arms. The employee is frequently required to stand; walk and stoop, kneel, crouch or squat. The employee must regularly lift, pull and/or move up to 10 pounds, frequently lift, pull and/or move up to 25 pounds and occasionally lift, pull and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate but may be exposed to loud noises from production equipment. The employee is occasionally exposed to fumes or airborne particles; toxic or caustic chemicals; extreme cold and extreme heat. Manna Beverages is an equal opportunity employer-----M/F/D/V

Indianapolis, IN 9 Months Contract About the Job: As the Microbiologist, you are responsible for coordinating and performing tests for SARS-CoV-2 and other targets of public health concern in wastewater and water samples. Duties include sample examination and analyses, recording, interpreting, and result reporting of test results. You are responsible for completing all required Quality Control, compliance with all certification requirements, and maintaining all required safety standards. Work hours are Monday - Friday, 7.5 hour day. A Day in the Life: The essential functions of this role are as follows: • Conduct wastewater sample concentration, RNA extraction and PCR molecular testing. • Maintain laboratory record system of submitted samples. • Evaluate, interpret, and validate laboratory results. • Conduct quality control checks on laboratory methods, materials, and equipment. • Assists with preparation of reports from data compiled. • Participate in evaluation of new products used in environmental laboratory work. The job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee. Other duties, responsibilities and activities may change or be assigned at any time. Reasonable accommodations may be made to enable individuals with disabilities to interview and to perform the essential functions of this role. What You'll Need for Success: • Four (4) year degree (B.S. or B.A.) in a biological science. • Experience performing RNA/DNA extraction and PCR testing is required. • Extensive knowledge of the principles, theories, and practices of molecular testing. • Specialized knowledge of current molecular scientific methods and testing procedures. • Specialized knowledge of and ability to use a full range of molecular and standard technical equipment • Ability to compile, analyze, evaluate, and prepare laboratory reports. • Extensive knowledge of laboratory safety practices and principles. • Aware of state and federal laws, rules, regulations, and policies concerning the program area. • Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships. • Ability to satisfactorily participate in proficiency testing programs.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: You will help ensure our manufacturing areas are meeting all pharmaceutical standards, including our aseptic environment. You will assist with collecting samples on critical utilities such as nitrogen, process air and the sites' water systems. You will help with performing media fills including qualification and release in support of the environmental monitoring program. You will help with maintaining equipment and adhering to the sites Environmental Health and Safety program. You will assist with routine lab-related tasks and ensuring your work area is tidy to support audit readiness and bring issues to supervision immediately for escalations. You will also support QC in-process testing as a backup for weekend work. Shift: Thursday - Sunday 7am - 5:30pm Who You Are: Minimum Qualifications: * High School Diploma or GED. * 1+ years of experience with biology or sterile pharmaceutical manufacturing. Preferred Qualifications: * Bachelor's Degree in Biology, Immunology, Biochemistry or other Science or Medical discipline. Pay Range for this position: $24 - $38 / hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

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. **Responsibilities:** + The Sr. Principal Associate - Lab Informatics -LabVantage LIMS/LES Program is part of a team of informatics professionals who work closely with Tech@Lilly to identify, develop, validate, deploy, maintain, and defend globally owned, GMP compliant, informatics applications throughout their lifecycle. They represent the needs and interest of the business areas they support, and act as their voice and advocate. + This position will focus on being the subject matter expert for LIMS/LES Systems by championing standardization of business processes, workflows, master data, and procedures globally to enable manufacturing sites and quality control labs to deliver world class performance. The candidate must consider the impacts of additional business processes that work with LIMS/LES such as other manufacturing and automation systems. + The Sr. Principal Associate - Lab Informatics -LabVantage LIMS/LES Program is responsible for business processes owned, delivered, and maintained by the Quality Control function, including Test Execution, Data Documentation, Instrument Data Collection, Lab Inventory/Consumable Management, Equipment/Instrument Management, Lab Data Integrity, Data Review, and associated Test Automation and/or Master Data Management. Business Requirements and Processes: + Collaborate with business SMEs and stakeholders to define, develop and refine new business processes that promote the effective use of current and NextGen LIMS/LES applications. + Develop and document Standard Operating Procedures (SOPs) for the application. + Identify areas for improvement, propose, network, and implement + potential solutions. + Support deployment activities by guiding the sites on the "to be" processes on the NexGen solutions. + Partner with third party application experts to find solutions to set up processes in the system or resolve issues. + Advocate for users and stakeholders across the organization throughout requirements gathering and refinement of future release schedules. Develop, Validate, and Implement systems and solutions: + Identifying, refining, and standardizing global business requirements and business specific system configuration items, providing business input and guidance for system design decisions. + Develop testing protocols and associated test scripts, authoring/editing validation deliverables, and execution/review of business-related validation test scripts. + Participate in the execution of User Acceptance Testing (UAT) to ensure the application meets business requirements and quality standards. + Document rational of business decisions to enable efficient progress, review, and historical reference. Master Data: + Knowledge in LIMS/LES master data and collaborate with the Global Data Stewards in the architecture of method built. + Experienced in the master data elements related with instrument connectivity Training: + Partner with global training representatives and third-party professional services teams to develop and maintain training materials. + Work closely with global and local training professionals and third-party providers throughout this process to ensure effective delivery of the training regimen to site personnel. Support Team Participation and Issue Resolution: + Provide ongoing support for LabVantage application including the reporting, management, and resolution of support issues. + Coaching and mentoring of system users, sharing key learning and standard processes to the global LabVantage community to increase their system knowledge, and the identification of transferrable work processes between sites. Inspection Support: + The candidate will be part of the team that will provide answers to questions from inspections, audits, and other formal and informal assessments that impact globally owned applications and their associated workflows. **Basic Requirements** + Bachelor's Degree in STEM field (Science, Technology, Engineering, Mathematics), preference in Chemistry, Biology, Chemical Engineering, or Pharmacy + 5+ years of laboratory experience Additional Skills + Experience working in/with GMP laboratories + Strong scientific background + Clear understanding of quality laboratory issues and activities + Experience in defining and improving business processes + Knowledge of cGMP and quality systems + Proficient in quality documentation, control processes, and data integrity principles. + Proven work with computer systems and their adaptability to existing business processes. + Extensive knowledge of analytical methods, laboratory documentation and control processes. + Knowledge of product release processes. + Experience in defining and improving business processes **Additional Information** + This position will require occasional travel 20-30% to manufacturing sites, development laboratories, and application vendors. Individual must be willing to visit laboratory and manufacturing sites involving unique PPE and/or gowning requirements. + This role is primarily on-site, with the flexibility to work from home 4 days per month. We believe in providing a balanced work environment that supports both collaboration and individual productivity. 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 $63,000 - $162,800 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

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. Responsibilities: * The Sr. Principal Associate - Lab Informatics -LabVantage LIMS/LES Program is part of a team of informatics professionals who work closely with Tech@Lilly to identify, develop, validate, deploy, maintain, and defend globally owned, GMP compliant, informatics applications throughout their lifecycle. They represent the needs and interest of the business areas they support, and act as their voice and advocate. * This position will focus on being the subject matter expert for LIMS/LES Systems by championing standardization of business processes, workflows, master data, and procedures globally to enable manufacturing sites and quality control labs to deliver world class performance. The candidate must consider the impacts of additional business processes that work with LIMS/LES such as other manufacturing and automation systems. * The Sr. Principal Associate - Lab Informatics -LabVantage LIMS/LES Program is responsible for business processes owned, delivered, and maintained by the Quality Control function, including Test Execution, Data Documentation, Instrument Data Collection, Lab Inventory/Consumable Management, Equipment/Instrument Management, Lab Data Integrity, Data Review, and associated Test Automation and/or Master Data Management. Business Requirements and Processes: * Collaborate with business SMEs and stakeholders to define, develop and refine new business processes that promote the effective use of current and NextGen LIMS/LES applications. * Develop and document Standard Operating Procedures (SOPs) for the application. * Identify areas for improvement, propose, network, and implement * potential solutions. * Support deployment activities by guiding the sites on the "to be" processes on the NexGen solutions. * Partner with third party application experts to find solutions to set up processes in the system or resolve issues. * Advocate for users and stakeholders across the organization throughout requirements gathering and refinement of future release schedules. Develop, Validate, and Implement systems and solutions: * Identifying, refining, and standardizing global business requirements and business specific system configuration items, providing business input and guidance for system design decisions. * Develop testing protocols and associated test scripts, authoring/editing validation deliverables, and execution/review of business-related validation test scripts. * Participate in the execution of User Acceptance Testing (UAT) to ensure the application meets business requirements and quality standards. * Document rational of business decisions to enable efficient progress, review, and historical reference. Master Data: * Knowledge in LIMS/LES master data and collaborate with the Global Data Stewards in the architecture of method built. * Experienced in the master data elements related with instrument connectivity Training: * Partner with global training representatives and third-party professional services teams to develop and maintain training materials. * Work closely with global and local training professionals and third-party providers throughout this process to ensure effective delivery of the training regimen to site personnel. Support Team Participation and Issue Resolution: * Provide ongoing support for LabVantage application including the reporting, management, and resolution of support issues. * Coaching and mentoring of system users, sharing key learning and standard processes to the global LabVantage community to increase their system knowledge, and the identification of transferrable work processes between sites. Inspection Support: * The candidate will be part of the team that will provide answers to questions from inspections, audits, and other formal and informal assessments that impact globally owned applications and their associated workflows. Basic Requirements * Bachelor's Degree in STEM field (Science, Technology, Engineering, Mathematics), preference in Chemistry, Biology, Chemical Engineering, or Pharmacy * 5+ years of laboratory experience Additional Skills * Experience working in/with GMP laboratories * Strong scientific background * Clear understanding of quality laboratory issues and activities * Experience in defining and improving business processes * Knowledge of cGMP and quality systems * Proficient in quality documentation, control processes, and data integrity principles. * Proven work with computer systems and their adaptability to existing business processes. * Extensive knowledge of analytical methods, laboratory documentation and control processes. * Knowledge of product release processes. * Experience in defining and improving business processes Additional Information * This position will require occasional travel 20-30% to manufacturing sites, development laboratories, and application vendors. Individual must be willing to visit laboratory and manufacturing sites involving unique PPE and/or gowning requirements. * This role is primarily on-site, with the flexibility to work from home 4 days per month. We believe in providing a balanced work environment that supports both collaboration and individual productivity. 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 $63,000 - $162,800 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

The Quality Control Senior Microbiologist will work closely with the full Quality Control team, Quality Assurance and Manufacturing to develop and execute the microbiological testing of a wide variety of materials critical to and inclusive of the parenteral drug product manufacturing process. Such testing includes, but is not limited to: Bioburden, Endotoxin, Sterility, Hold-Time Studies, Hypothesis Testing, and Environmental/Utilities Monitoring. The Senior Microbiologist will be committed to operating with a Quality Mindset in every aspect of their role, including attention to detail, on time delivery, and efficiency. They will generate, participate in, SME for, and review process critical Quality Events (Laboratory Investigations, CAPAs, Deviations, Continuous Improvements etc.). The Quality Control Senior Microbiologist will demonstrate an ability to define problems, propose solutions, collect data, establish facts, and draw valid conclusions. It is critical to have excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences. The Senior Microbiologist will exemplify excellent interpersonal skills and be capable of developing productive cross-functional relationships within the company. They will thrive in a dynamic, fast paced team environment but can also work autonomously with strong self-management and organizational skills. Additionally, the Microbiologist will possess a demonstrated ability to influence positive outcome within the QC Microbiology team and take ownership of processes/systems. Essential Job Functions: Participate as a key player in establishing and improving the QC Microbiology Laboratory team. Perform and improve testing including, at a minimum, sterility, endotoxin, and bioburden. Testing will be performed on Drug Products (API, BDP, FIP, and AI), excipients, and in-process materials. Develop, improve, and participate in a robust Environmental and Utilities Monitoring program. Hold self and others accountable for rigorous scientific and quality work standards. Perform microbiological testing required to support a state-of-the-art aseptic drug product manufacturing facility. Utilize various paper and automated systems to manage local QC and site policies, procedures, and technical reports throughout document lifecycles including authoring, reviewing, approving, and retiring. Generate, review, own, and complete Quality Events efficiently and to a high degree of accuracy. Interpersonal Focus Train fellow QC personnel on instruments, processes, and assays when cross-training or new employee training is needed. Assist in the professional support and development of QC Microbiology Technicians within the QC lab. Be team oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed. Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by co-workers for accuracy and alignment with procedures. Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured and released. View constructive criticism and critiques to work and documentation as opportunities to improve themselves and the quality of the department; can also give feedback in a constructive manner. Special Job Requirements: B.S. in Science (Biology, Microbiology, Biochemistry etc) 3+ experience with microbiological testing. High proficiency level in performing bioburden, endotoxin and sterility testing. Ability to evaluate, troubleshoot, and investigate testing results as they apply to the pharmaceutical process. Possesses an excellent working knowledge of regulatory guidance (FDA, EP, JP etc). Exceptional computer skills and data management both digital and manual. Additional Preferences: Advanced microbiology specific degree. 4+ years of experience in GMP biopharma industry in an aseptic drug product QC laboratory role. Experience with Kaizen, Six Sigma, and/or Lean principles. Experience in an isolator-based aseptic drug product manufacturing facility. Project Management experience Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

Certified Lab Scientist Are you a detail-oriented lab professional ready to take the next step in your career? A trusted and well-respected healthcare facility in Fort Wayne, Indiana is looking for a Certified Lab Scientist to join its clinical laboratory team. This is a full-time, on-site opportunity with a sign-on bonus available for eligible candidates. About the Role As a Certified Lab Scientist, you'll play a vital role in the delivery of high-quality diagnostic testing. You'll ensure that patient results are accurate, timely, and in compliance with laboratory standards. Beyond testing, you'll contribute to equipment maintenance, staff training, and ongoing quality improvement initiatives. Key Responsibilities: Perform a wide range of clinical laboratory tests with accuracy and efficiency Maintain, calibrate, and troubleshoot laboratory instruments Assist with validation and implementation of new tests or equipment Provide training and guidance to fellow lab team members Support inspection readiness and maintain regulatory compliance Participate in lab-based committees and continuous improvement projects Why This Role Stands Out Sign-on bonus available for eligible hires Be part of a collaborative and well-equipped lab team Work in a supportive, patient-centered environment Opportunities for professional growth and leadership involvement Contribute to a culture of excellence and continuous improvement in care 12-hour day shift

You got game? You got spring in your step? You want the best job in the world! And schedules that work with you, not against you? That's right, we live to beat the rush and make it possible to make, bake or take pizzas during the hungry hours of the day and night, part or full time. You'll have plenty of time left over for school, hanging with your friends, or whatever. Sound good? Even if you just need a second job for some extra cash, Domino's Pizza is the perfect place for you. We are searching for qualified Assistant Managers with personality and people skills. We're growing so fast it's hard to keep up, and that means Domino's has lots of ways for you to grow (if that's what you want), perhaps to management, perhaps beyond. Whether it's your hobby, main-gig, or supplemental job, drop us a line. We're bound to have just the thing for you. ADVANCEMENT Many of our team members began their careers as delivery drivers and today are successful Domino's franchise owners. From customer service representative to management, General Manager to Manager Corporate Operations or Franchisee, our stores offer a world of opportunity. DIVERSITY Our mission is to recognize, appreciate, value and utilize the unique talents and contributions of all individuals. To create an environment where all team members, because of their differences, can reach their highest potential. SUMMARY STATEMENT We take pride in our team members and our team members take pride in Domino's Pizza! Being the best pizza delivery company in the world requires exceptional team members working together. At Domino's Pizza, our people come first! Job Description This position will be actively training to become a store General Manager. Start your career today! Assistant Managers are responsible for cost controls, inventory control, cash control, and customer relations while they are working a shift. What we offer: A safe, rewarding, and fast paced working environment Competitive hourly rate Training with an industry leading brand Excellent career opportunities Awesome discounts on menu items! What we're looking for in our Assistant Managers: Prior leadership experience preferred Assist with basic operations procedures Experience in employee development Ability to demonstrate team member and food safety protocols Excellent customer service skills Ability to operate and troubleshoot technology Qualifications As this is a leadership position in the store, you will need to have flexible, full time (40 hours) availability. This position will be responsible for opening and/or closing the store as needed. Must be at least 18 years of age. Possess great interpersonal skills Additional Information All your information will be kept confidential according to EEO guidelines. This job posting is for a position in a store owned and operated by an independent franchisee, not Domino's Pizza LLC, Domino's Pizza Franchising LLC, or Domino's Pizza, Inc. (“Domino's Corporate”). This means, among other things, that the independent franchisee is alone responsible for and will independently make all decisions concerning employment matters for the store, including those relating to hiring, firing, discipline, supervision, compensation and benefits, staffing, and scheduling. Domino's will not receive a copy of any application you submit for this job posting and will not have any control over whether you receive an interview and/or are ultimately hired. Further, Domino's does not control and is not responsible for the employment policies and practices of independent franchisees. If you are hired for this job posting, the independent franchisee will be your only employer, and you will not be an employee of Domino's.

Job Details Indianapolis - Indianapolis, INResearch Assistant II (Lab) The Research Assistant II (Lab) will be responsible for assisting the clinical research staff in conducting clinical research trials and assisting in the pre-screening process. DUTIES & RESPONSIBILITIES Completing DMCR-required training, including GCP and IATA. Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols. Assisting in the collection and recording of patient data per Sponsor requirements via the respective EDC system. Timely and accurately assist in collection, management, and shipment of subjects' samples, and/or specimens Completing Sponsor-required training prior to study-start, including, but not limited to Sponsor-provided and IRB-approved protocol All amendments Investigator Brochure Sponsor-specified EDC and/or IVRS This includes completing the above-mentioned training prior to any study-related procedures being conducted on that said protocol should the RA be added to a protocol post-study start. Maintaining clear, concise, accurate, and legible records. Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s). Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s). Assisting in the compilation and organization of all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable. Assisting in the creation of source documents for their assigned protocols at their respective site(s). Conducting patient visits. Assisting in reporting Adverse and Serious Adverse Events to the appropriate authorities per Sponsor. Assisting in addressing and resolving issues from internal/external audits and monitoring letters for all assigned protocols at their respective site(s) in a timely manner. Assists with all other aspects of the study and conducts as needed. Assist the lab team in conducting EKG/ECGs. Assist the lab team in blood drawing and lab processing. Able to manually take patient blood pressure. Assists in conducting rapid clinical tests. Any other matters as assigned by management. KNOWLEDGE & EXPERIENCE Education: High school diploma or equivalent required Experience: 1-2+ years experience in the clinical field Credentials: Phlebotomist certificate preferred Medical Assistant Certification preferred Knowledge & Skills: Knowledge of medical terminology required Must be detail-oriented and demonstrate attention to detail Excellent customer service skills Excellent computer skills Patient-centric focus. Strong organizational and time-management skills. Able to work in a fast-paced environment ensuring limited oversights.

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.

We are seeking a self-motivated Chemistry Lab Technician to join our Lab Operations team. In this role you will assist in laboratory confirmatory analysis of biological fluids including urine, oral fluid (saliva) or hair specimens. This role is also responsible for operating, maintaining and troubleshooting various Auto Chemistry instrumentation. Shift: 03:00 - 11:30pm Salary: $20.00 per hour Primary Responsibilities Loads, prepares and extracts specimens using various Auto-Chem Instrumentation. Assist in instrument calibration, QC review, and initial analytical review. Prepare reagents and buffers as needed. Assists with maintaining an adequate inventory of laboratory supplies. Responsible for all record keeping associated with specimen preparation, including following chain of custody handling guidelines and storage requirements. Conducts safe work practices according to safety protocols, PPE requirements and decontamination procedures. Responsible to maintain all safeguards as it pertains to Protected health information (PHI). Qualifications Bachelor's degree in a science field (Chemistry, Biochemistry, Biology, Microbiology, Pre-med (Biomed), required. Experience as a lab technician, preferred utilizing LCMS equipment. Data entry skills via a keyboard (alpha and numeric) required. Strong eye-hand coordination. Ability to handle a high-volume environment while maintaining the highest level of quality, required. Physical demands required to perform critical tasks in this role include standing for long periods of time, lifting up to 25lbs, bending and carrying. Benefits Cordant supports our employees by providing a comprehensive benefits package to eligible staff (per state regulations) that includes: Medical, Dental, Vision Insurance, Flexible Spending Accounts (FSA), Health Savings Accounts (HSA) Paid Time Off (PTO) accruing on day 1, Volunteer Time Off (VTO), Paid Holidays, 401(k) with Company Match, Employee Assistance Program (EAP), Short Term and Long-Term Disability (STD/LTD) and Company Paid Basic Life Insurance. #LAB123

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. Why join Team Simtra? Because we: Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways. Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health. This role: The Research Associate II role is responsible for independently managing analytical method development, validation and transfer projects for internal and external clients. They are also responsible for supporting formulation development projects for internal or external clients. This role reports to the Research Scientist II and is 100% onsite at the Bloomington, Indiana facility. The responsibilities: Independently plan and execute a series of design and/or technical projects (small and large molecules) that may or may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines from early pre-formulation/formulation development to technical transfer of established formulations and processes in manufacturing operations Lead the evaluation, selection, and adaptation of new technologies and techniques to accomplish business objectives, such as quality and cycle-time May provide training to other employees within the department or plant Routinely provide advice and assistance to team members regarding unique problems Provide responsive customer service to external customers and internal project managers Support department Enterprise Management System (EMS) and Quality Assurance initiatives Devise new approaches to complex formulation and process development problems through adaptations and modifications of standard technical principles and incorporate new methods and technologies for improving existing or new products/processes Maintain current knowledge of relevant quality and regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities Develop an in-depth knowledge and understanding of Good Manufacturing Practices (GMP) and related regulations and guidance Act as an Analytical Instrument Subject Matter Expert and support instrument validations and/or periodic review validations Contribute to technical feasibility analysis of complex research and analytical method concepts Evaluate results relative to product requirements, definitions and/or program goals Required qualifications: BS degree in Chemistry, Biochemistry, Pharmaceutical Science or related scientific discipline required 2+ years of laboratory experience (MS or PhD in Chemistry, Biochemistry, Pharmaceutical Science, or related scientific discipline in lieu of laboratory experience) Expertise in fundamentals of freeze-drying, including characterization of formulations intended to be freeze-dried and characterization of lyophilized solids Experience in chromatography, spectroscopy and other analytical methods (i.e. HPLC, CE, ELISA, UV, FTIR, etc.) Good scientific technique in a corporate laboratory setting Strong written and oral communication skills with the ability to interact with external and internal stakeholders Advanced proficiency in Microsoft Office Suite (Word, Excel, and Outlook) Experience with following software and/or programs: Minitab, JMP, or Python Knowledge and/or ability to use Enterprise software (i.e., JDE, Veeva, Trackwise, etc.) Physical / safety requirements: Duties may require overtime work, including nights and weekends Position requires sitting for long hours, but may involve walking or standing for periods of time Practice safe laboratory practices In return, you'll be eligible for [1]: Day One Benefits Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance Spouse Life Insurance Child Life Insurance Short and Long-Term Disability Insurance 401(k) Retirement Savings Plan with Company Match Time Off Program Paid Holidays Paid Time Off Paid Parental Leave and more Adoption Reimbursement Program Education Assistance Program Employee Assistance Program Community and Volunteer Service Program Employee Ownership Plan Additional Benefits Voluntary Insurance Benefits Vision Coverage Accident Critical Illness Hospital Indemnity Insurance Identity Theft Protection Legal and more Onsite Campus Amenities Workout Facility Cafeteria Credit Union [1] Current benefit offerings are in effect through 12/31/25 Disclaimer This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. Equal Employment Opportunity Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: **********************************

Pay: $23.50/hour On-site in Indianapolis. In this role you will: Conduct wastewater sample concentration, RNA extraction and PCR molecular testing. Maintain laboratory record system of submitted samples. Evaluate, interpret, and validate laboratory results. Conduct quality control checks on laboratory methods, materials, and equipment. Assists with preparation of reports from data compiled. Participate in evaluation of new products used in

• Four (4) year degree (B.S. or B.A.) in a biological science. • Experience performing RNA/DNA extraction and PCR testing is required. • Extensive knowledge of the principles, theories, and practices of molecular testing. • Specialized knowledge of current molecular scientific methods and testing procedures. • Specialized knowledge of and ability to use a full range of molecular and standard technical equipment • Ability to compile, analyze, evaluate, and prepare laboratory reports. • Extensive knowledge of laboratory safety practices and principles. • Aware of state and federal laws, rules, regulations, and policies concerning the program area. • Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships. • Ability to satisfactorily participate in proficiency testing programs.

General Managers are responsible for overseeing the daily operations of a single Domino's store. General Managers provide overall leadership and supervision over operations, and are accountable for achieving operational standards, food safety, profitability, and creating an inclusive and engaged environment. What we offer: A safe, rewarding and fast-paced working environment Competitive salary, bonus eligibility, and benefits package We pride ourselves in the benefits we offer our full-time store team members: medical, dental, vision; 401(k) with up to 5% company match, education assistance, employee stock purchase program, paid time off, parental leave, mental health, and family support service Full training with an industry-leading brand Excellent career opportunities Awesome discounts on menu items What we're looking for: Minimum of one year of prior General Manager experience in a fast-paced service environment Understand and demonstrate basic operations procedures and cost management capabilities Experience in recruiting, retaining and developing multiple employees Ability to lead and promote team member and food safety protocols Excellent customer service skills Ability to operate and troubleshoot technology (POS, ATS, etc.) Valid driver's license with safe driving record meeting company standards preferred Minimum job requirements(see the Job Description for full details): Must be at least 18 years of age Additional Information At Domino's, we are a brand of honesty, transparency and accountability and we want exceptional people like you to join our team! We have continued to prove we “Put our People First” by making sure our work environment is safe and provides stability for you as a team member. The brand continues to deliver the “Power of Possible” to local Domino's store owners, 90% of which started as delivery drivers and pizza makers in our stores!

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.

Microbiologist for Water Micro Lab coordinating and performing tests for SARS-CoV-2 and other targets of public health concern in wastewater and water samples. About the Job: As the Microbiologist, you are responsible for coordinating and performing tests for SARS-CoV-2 and other targets of public health concern in wastewater and water samples. Duties include sample examination and analyses, recording, interpreting, and result reporting of test results. You are responsible for completing all required Quality Control, compliance with all certification requirements, and maintaining all required safety standards. A Day in the Life: The essential functions of this role are as follows: •Conduct wastewater sample concentration, RNA extraction and PCR molecular testing. •Maintain laboratory record system of submitted samples. •Evaluate, interpret, and validate laboratory results. •Conduct quality control checks on laboratory methods, materials, and equipment. •Assists with preparation of reports from data compiled. •Participate in evaluation of new products used in environmental laboratory work. The job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee. Other duties, responsibilities and activities may change or be assigned at any time. Reasonable accommodations may be made to enable individuals with disabilities to interview and to perform the essential functions of this role. What You'll Need for Success: •Four (4) year degree (B.S. or B.A.) in a biological science. •Experience performing RNA/DNA extraction and PCR testing is required. •Extensive knowledge of the principles, theories, and practices of molecular testing. •Specialized knowledge of current molecular scientific methods and testing procedures. •Specialized knowledge of and ability to use a full range of molecular and standard technical equipment •Ability to compile, analyze, evaluate, and prepare laboratory reports. •Extensive knowledge of laboratory safety practices and principles. •Aware of state and federal laws, rules, regulations, and policies concerning the program area. •Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships. •Ability to satisfactorily participate in proficiency testing programs.