Quality Control Analyst Jobs in Beech Grove, IN

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. RayzeBio is seeking a Quality Control Supervisor, reporting to the Sr. Manager of Quality Control. The position will oversee quality control testing activities related to radiopharmaceuticals. This role will involve managing a team of QC chemists, ensuring compliance with regulatory and QA system requirements, and maintaining high standards of quality for radiopharmaceutical product release. The Quality Control Supervisor will also ensure laboratory personnel comply with Environmental Health and Radiation safety standards within daily laboratory operations. The position will be located at RayzeBio's manufacturing plant, in Indianapolis, IN. Job Responsibilities: Team Management Supervise and mentor a team of QC Chemists. Assign tasks and prioritize workload to ensure timely completion of Quality Control activities, including release of drug product and isotopes in an on-time and right first time manner. Foster a positive and collaborative work environment within the lab and with external stakeholders both within the site and outside the side. Work with Management and Planning to schedule workflow and projects across the Quality Control team. Continuous Improvement Participate in method transfer activities from CMO or internal research facility to the production and QC teams, ensuring accuracy and reliability of data. Identify other opportunities for process improvements and implement changes to increase quality and efficiency within the Quality Control laboratoroies. Provide continuous improvement suggestions for analysis as novel radiopharmaceuticals move through regulatory stages to commercialization. Release of product and other studies Perform analyses of validated/verified methods to support novel RayzeBio Radiopharmaceuticals, raw materials, and components when required. Collaborate with Manager and/or Reviewer to ensure all documentation for release is reviewed. Work with Manager and/or Investigation Write to ensure any discrepancies are resolved in a timely manner. Quality Assurance/Regulatory Compliance Assist in the routine calibration and maintenance of laboratory equipment. Ensure schedule compliance to ensure GMP readiness. Work with Quality Assurance and Management to implement internal audits. Participate in troubleshooting of issues and implement corrective actions to improve quality processes as a result of investigations or internal audits. Develop and maintain appropriate documentation, particularly data analysis and team KPI's. Work with RSO and QA to ensure compliance with GMP regulations, safety guidelines, and quality standards (FDA, USP, NRC, EP, and other regulatory agencies as needed). Assist in the reviewing of Standard Operating Procedures and other documents Weekend work, early starts, or late ending times may be required. Up to 10% of travel may be required. Education and Experience: BS in chemistry or related field with 9+ years of experience in pharmaceutical field OR MS in chemistry or related field with 7+ years of experience in pharmaceutical field. Experience testing in a quality control chemistry lab. Preferred Education and Experience: Experience in radiopharmaceutical field Experience handling radioactive materials Skills: Highly motivated and organized professional with the ability to work independently or in a team environment. Multi-disciplined scientist with GMP experience Experience with root cause techniques such as 6 M's, 5 Why's, fishbone, or similar preferred. Very personable with strong communication skills Ability to multi-task and prioritize work based on multiple work-flows. Good organizational skills are required. Work with multiple computer systems, including Microsoft Office, and chromatography systems. Excellent professional ethics, integrity, and ability to maintain confidential information. Physical Demands: While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 40 pounds. Specific vision abilities required by this job include close vision and distance vision. This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials . Work Environment The noise level in the work environment is usually moderate. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to ************************** . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: ********************************************* Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY Lead qualification and procedures, perform laboratory techniques related to viral vector production and analytics following cGMP testing guidelines. Basic laboratory techniques include materials ordering, sample organization and sample shipping, sample receiving, solution preparation, media, molecular biology techniques, aseptic cell culture techniques, and general laboratory maintenance. The position requires working independently, but also under the supervision of experienced lab personnel in quality control. ESSENTIAL JOB FUNCTIONS Lead qualification side by side with the Analytical Development team to qualify reliable methods for QC testing Perform hands-on laboratory procedures related to viral vector production and characterization Evaluate new technologies for testing of cell and gene based therapies Order, organize, and maintain lab reagent material stocks Assist with organization and testing of samples Assist with managing outsource sample shipping and receiving Maintain cGMP documentation of processing activities Perform routine lab maintenance and maintenance of laboratory equipment Train new staff members and fellow hourly employees in designated processes Comply with all established policies, SOPs, and cGMP guidelines Participate actively in SOP establishment and revisions in coordination with supervisor and Quality Assurance Participate in method qualification and validation activities SPECIAL JOB REQUIREMENTS Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned KNOWLEDGE, SKILLS AND EXPERIENCE EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BS or higher degree in Biology, Biochemistry, Molecular Biology, or similar field Essential ON-THE-JOB EXPERIENCE 3+ years of relevant industry experience in QC, R&D, product development, or operations Essential SKILLS / ABILITIES Excellent computer, verbal, and written communication skills Essential Experience with laboratory techniques including cell culture, cell-based assays, qPCR, dd PCR, flow cytometry, ELISA, and/or biostatistical analysis Essential PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock Occasionally exposed to extremely loud noise levels Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required Movement Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl Lifting Frequently lift and/or move up to 10 pounds Occasionally lift and/or move up to 50 pounds Vision Frequently utilize close vision and the ability to adjust focus Communication Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. Resilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S BENEFITS Paid vacation days, amount based on tenure Paid sick time 9 observed holidays + 1 floating holiday + 1 volunteer day 401(k) plan with company match up to 6% of salary, vested immediately Share Appreciation Rights Choice of several healthcare plans FSA and HSA programs Dental & vision care Employer-paid basic term life/personal accident insurance Voluntary disability, universal life/personal accident insurance Accidental Death & Dismemberment (AD&D) Insurance ADDITIONAL DETAILS Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time. This position requires a criminal background check. Genezen is an Equal Opportunity Employer. Genezen participates in EVerify. Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas. Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live. Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY Lead qualification and procedures, perform laboratory techniques related to viral vector production and analytics following cGMP testing guidelines. Basic laboratory techniques include materials ordering, sample organization and sample shipping, sample receiving, solution preparation, media, molecular biology techniques, aseptic cell culture techniques, and general laboratory maintenance. The position requires working independently, but also under the supervision of experienced lab personnel in quality control. ESSENTIAL JOB FUNCTIONS Lead qualification side by side with the Analytical Development team to qualify reliable methods for QC testing Perform hands-on laboratory procedures related to viral vector production and characterization Evaluate new technologies for testing of cell and gene based therapies Order, organize, and maintain lab reagent material stocks Assist with organization and testing of samples Assist with managing outsource sample shipping and receiving Maintain cGMP documentation of processing activities Perform routine lab maintenance and maintenance of laboratory equipment Train new staff members and fellow hourly employees in designated processes Comply with all established policies, SOPs, and cGMP guidelines Participate actively in SOP establishment and revisions in coordination with supervisor and Quality Assurance Participate in method qualification and validation activities SPECIAL JOB REQUIREMENTS Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned KNOWLEDGE, SKILLS AND EXPERIENCE EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BS or higher degree in Biology, Biochemistry, Molecular Biology, or similar field Essential ON-THE-JOB EXPERIENCE 3+ years of relevant industry experience in QC, R&D, product development, or operations Essential SKILLS / ABILITIES Excellent computer, verbal, and written communication skills Essential Experience with laboratory techniques including cell culture, cell-based assays, qPCR, dd PCR, flow cytometry, ELISA, and/or biostatistical analysis Essential PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock Occasionally exposed to extremely loud noise levels Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required Movement Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl Lifting Frequently lift and/or move up to 10 pounds Occasionally lift and/or move up to 50 pounds Vision Frequently utilize close vision and the ability to adjust focus Communication Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. Resilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S BENEFITS Paid vacation days, amount based on tenure Paid sick time 9 observed holidays + 1 floating holiday + 1 volunteer day 401(k) plan with company match up to 6% of salary, vested immediately Share Appreciation Rights Choice of several healthcare plans FSA and HSA programs Dental & vision care Employer-paid basic term life/personal accident insurance Voluntary disability, universal life/personal accident insurance Accidental Death & Dismemberment (AD&D) Insurance ADDITIONAL DETAILS Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time. This position requires a criminal background check. Genezen is an Equal Opportunity Employer. Genezen participates in EVerify. Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas. Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live. Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

** As the Quality Control Specialist II your key responsibilities will include the performance of AML/CFT, OFAC, and Fraud quality control (QC) tests/inspections to ensure that alert reviews and case investigations are appropriately completed and suspicious activity is filed in accordance with regulatory requirements and agency guidelines. You will also support the identification, escalation and timely mitigation of compliance and operational risks in alignment with the First Internet Bank and its FinTech Partners Enhanced Due Diligence (EDD), alert and case investigation, suspicious activity reporting (SAR) filing policies, procedures and regulatory requirements. You will serve as oversight of the appropriate execution of substantive money laundering, economic sanctions and fraud compliance risk detection, prevention, and reporting practices. **What You Will Do:** - Ensure that First Internet Bank and its FinTech Partners maintain AML/CFT and OFAC standards and procedures, and recommend changes and/or alternatives for process improvements. - Review alerts and cases completed/closed by the AML/CFT, OFAC, and Fraud Analysts to ensure that the appropriate decisions/recommendations have been made according to First Internet Bank and its FinTech Partners standards, the appropriate supporting documentation for decision is made by an AML/CFT, OFAC, and Fraud Analyst is appropriately supported and documented. - Evaluate completed AML/CFT, OFAC, and Fraud work and evaluate KYC/KYCC profiles to ensure that they meet regulatory requirements as well as adhere to First Internet Bank and its FinTech Partners policies and procedures. - Communicate any errors/discrepancies found to the appropriate management to ensure that corrective action is taken, additional training provided. - Generate related reports, including findings and trends to management. - Maintain knowledge of developments in the area of Fraud, OFAC and anti-money laundering, including FinCEN and OCC requirements relating to AML/CFT and the USA PATRIOT Act. - Maintain QC standards and procedures, including risk-based standards for compliance testing, and recordkeeping for quality control findings accurately and in a timely manner. - Perform other duties as assigned. **What Were Looking For:** - A Bachelors Degree or equivalent experience in AML/CFT/OFAC and Fraud compliance in the financial services industry required - A minimum of two years of previous investigative experience or oversight with specific emphasis on OFAC, AML, BSA or prior audit and/or quality control experience in the banking industry is required. - Must be able to demonstrate knowledge of OFAC, USA Patriot Act, Bank Secrecy Act (BSA), and Anti-Money Laundering (AML) regulatory requirements. - Ability to work independently and in collaboration with others. - Ability to provide timely and excellent service to both internal and external customers. - Proven attention to detail. - Strong PC skills required, along with the ability to quickly learn new systems. **Working Conditions/Demands:** - Professional office setting. - Primarily sedentary position requiring long periods of time working at a computer. - Must be able to move throughout the office and buildings to obtain or relay information. - Must be able to perform the essential functions of the position with or without reasonable accommodation. **Who Are We?** Were not just another bank and were not looking for just another employee. Since 1999, First Internet Bank has been dedicated to finding a better way to bank and doing things that have never been done before. Yes, we really were the first state-charted, FDIC insured bank to operate entirely online and we have been leading the way ever since. We seek the game changers, the innovatorsthose who challenge the status quo because change really is the only constant. Ready to join a team of imaginative, driven individuals like you? Its your career, you deserve to imagine more. Keep reading, we think you will like you what see.

Job Title: Quality Assurance Associate GENERAL JOB DESCRIPTION Were looking for Quality Assurance Associates in our Fulfillment Center to inspect and ensure that all ingredients and all items in boxes meet required quality standards. MAJOR DUTIES AND RESPONSIBILITIES Objectives of this Role Assist Specialist with Gold Standard and table set up Audit tables on a continuous basis (each table at least once per hour) Audit bins of finished product continuously (each table at least once per hour, each automated prep at least once every 15 minutes) Document all audits in Quality Tool Suite Notify Specialist and Quality Auditor of any issues Attend monthly refresher trainings with Quality team Speak with Quality during start up communications Assist Specialist with calling the line and ensuring accuracy Audit pack lines on a continuous basis (at least twice per hour) Audit finished boxes continuously (at least three boxes per hour) Document all audits in Quality Tool Suite Notify Specialist and Quality Auditor of any issues Attend monthly refresher trainings with Quality team Speak with Quality during start up communications QUALIFICATIONS FOR THE JOB Skills and Requirements Clear and concise communicator, verbal and written. Ability to work calmly and effectively under pressure. Ability to work in fast-paced, deadline-oriented environment. Flexible availability; we work night and weekend shifts. Must be able to lift up to 49 pounds repetitively with or without reasonable accommodation Must be able to handle exposure to temperatures that range from freezing to sub-freezing (coolers, freezers, etc.) Must be able to stand/walk for up to 10-12 hours with or without reasonable accommodation Must be willing and able to frequently push, pull, squat, bend, and reach with or without reasonable accommodation Experience / Education 1-2 years experience in a food production or warehouse environment

The Chemical Production Scientist will perform tasks associated with the production of PTS chemical solutions in a dynamic fast paced GMP manufacturing environment. This position requires chemistry knowledge, attention to detail, and excellent communication. The chemist may be required to provide support by maintaining inventory and solution preparation. Responsible for compounding chemical solutions, impregnating membranes, and slitting membranes to company quality standards. Candidate must be able to quickly learn and integrate into existing workflows; possess strong oral and written communication capabilities; demonstrate excellent collaboration & interpersonal skills; and be adept at problem solving in a fast-paced environment. ESSENTIAL DUTIES AND RESPONSIBILITIES Compounding chemical solutions Impregnation of membranes with chemical solutions Slitting of membranes to appropriate width per BOM Monitoring and maintaining raw material and in-process inventory Operation of general lab equipment: - Eppendorf, Volumetric and Serological Pipettes - Analytical Balances - pH meter - Conductivity meter Cleaning and maintenance of parts and equipment for use in laboratory, tunnel, and slitting Provides Operation support to R&D and Quality Acts as Proxy for Chemical Production Supervisor Assists production personnel to facilitate completion of schedule Performs MAS transactions QUALIFICATIONS This position may require irregular and extended hours of work, so the individual must be able to work flexible hours. Individual must be able to lift approximately 25 lbs. Individual must be able to sit for extended periods of time when needed. Ability to use various hand tools to setup slitting equipment. Ability to follow written and verbal instructions. Must be detail oriented. EDUCATION and/or EXPERIENCE Bachelor's degree in a scientific discipline Previous experience in chemical compounding production preferred Previous laboratory or Quality Control experience Previous experience in the medical device industry or other FDA regulated industry Or, equivalent combination of education and experience WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This position works in a typical laboratory environment. Lab coat, safety glasses, and gloves are required when performing activities within the laboratory environment. Ability to sit for prolonged periods of time, handling, typing, talking, listening, requiring clear near and midrange vision in connection with performing essential functions. EQUAL OPPORTUNITY EMPLOYER: PTS Diagnostics is an Equal Opportunity and E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability, or other characteristics protected under local, state or federal law. QUALITY COMMITMENT This position requires compliance to applicable quality system and regulatory requirements. This individual adopts a “quality in everything we do” approach to all aspects of the execution of responsibilities of this position. Through vigilance, this individual remains alert to any potential compliance situations, and must report such observations to managers and the Head of Quality. STATEMENT of OTHER DUTIES DISCLAIMER This job description in no way states or implies that these are the only duties to be performed by this employee. This employee will be required to follow any other instructions and to perform any other duties requested by their supervisor.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Perform biochemical testing on proteins and antibodies including, but not limited to, CE, IC, HPLC, SEC, SDS-PAGE, UV, Protein A titer, ELISA, and Particulates · Enter data into LIMS · Ability to work independently and as part of a team in a GMP environment · 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, 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 Minimum Qualifications: · Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) · At least 2 years related laboratory experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information The schedule for this position will consist of four, ten hour night shifts, starting at 6PM. This will be on a rotating schedule (Monday-Thursday or Wednesday-Saturday). Employees will alternate between these two schedules so that everyone will have a chance to have Saturdays off. Training will take place on day-shift for roughly one month, Monday-Friday from 8AM-5PM. Night shift employees will receive a 10% shift differential. 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Asphalt Research Chemist** The Asphalt Research Chemist is responsible for working with the Heritage Construction +Materials team to develop new products, modifiers, and additives for the asphalt binder industry using a focused approached to both laboratory and field testing. The asphalt research chemist conceptualizes and develops to then produce and test asphalt products, modifiers, and additives in a timely manner. This involves the testing of research samples and field samples, innovative and creative thinking, analyzing data, and problem solving. **Key Accountabilities/Responsibilities** - Follow industry-standard preparation and testing protocol and quality control guidelines - Record and organize information from a variety of sources accurately - Communicate effectively with all members of the asphalt binder and emulsion team, The Heritage Research Group and other internal and external partners - Use a variety of equipment at high temperature to effectively prepare samples - Prepare and test specimens according to industry standards and specifications - Evaluate and analyze test results and provide input for further improvement - Generate and review technical reports, internal and external presentations - Participate in the design and execution of field trials and asphalt plant trials - Perform literature reviews of ongoing asphalt binder related research - Assist in general maintenance and calibration of all laboratory equipment - Represent HRG at various internal and external technical meetings. - Troubleshoot asphalt binder issues with company plant personnel and quality control representatives. **Required Qualifications** - Bachelor's degree in chemistry or related science is preferred - 5+ years experience related work experience required - Experience in performing asphalt binder laboratory testing - Outstanding organizational, problem solving, and creative thinking skills - Capable of managing time and easily able to perform multiple tasks concurrently - Effective communication skills with both internal and external stakeholders - Ability to respond proactively to needs or issues - Ability to read, understand, and follow ASTM, AASHTO, D.O.T., county, etc. testing methods **About The Heritage Group** The Heritage Group (THG) is a privately held portfolio of companies focused on creating long-term value by building world-class businesses. Under four generations of family ownership, we employ thousands of people around the world, with operations across North America, Europe, and China, in the core industries of Environmental and Remediation, Specialty Chemicals and Fuel Products, and Construction and Materials. Driven by innovation and research, our in-house RandD team, Heritage Research Group, specializes in helping our diverse set of companies evolve and adapt to a changing marketplace by providing cutting-edge solutions and exploring new opportunities in its state-of-the-art facility. And while acquisitions, partnerships, internal expansion, and startups may be our cornerstone, we're a family company at heart-aiming to build long-term relationships with our customers, vendors, and partners so that we can turn big challenges into even bigger opportunities to make a difference in the world. ***The Heritage Group welcomes the diverse backgrounds, experiences, and perspectives of all to work together to accomplish our goals*** For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website. ********************************************************

Description Why Thompson Thrift?At Thompson Thrift, we're reshaping communities through real estate development, property management, leasing, and construction management. Our legacy spans Thompson Thrift Residential, Thompson Thrift Construction, and Thompson Thrift Commercial, all rooted in our core values of excellence, leadership, and service. We're committed to enhancing lives, one project at a time. Your Role as Quality Control InspectorThompson Thrift Construction is seeking a Quality Control Inspector. This role reports to the Quality Control Manager. The position is responsible for managing, inspecting, and performing quality control responsibilities for all projects while assisting Project Superintendents in ensuring compliance with Thompson Thrift Construction (TTC) standards. The position is based out of our Indianapolis or Terre Haute, Indiana. The candidate can also be based out of Atlanta, GA. This position will require weekly travel to construction job sites across the U.S. Key Responsibilities & Duties Inspection Oversight: Perform field inspections to ensure compliance with project documents and TTC standards throughout project progression. Plan Analysis: Review project drawings and specifications to identify intended construction methods. Checklist Management: Monitor and track the completion of project checklists. Training & Mentorship: Provide onsite support and training to field staff regarding company standards and quality control checklists. Issue Resolution: Assist with resolving defective product installations by subcontractors or TTC personnel. Reporting: Document site observations and create detailed reports using Procore software. Collaboration: Conduct one-on-one reviews of inspection results with Project Superintendents after each site visit. Trend Analysis: Perform and report on trends observed during inspections. Our Ideal Candidate for this Role Education: High school diploma or equivalent required; Associate's degree preferred. Experience: Multiple years of construction experience demonstrating mastery of position requirements. Skills: Advanced knowledge of construction methods, ability to read and understand construction drawings/specifications, and proficiency with basic computer tools. Competencies: Strong problem-solving, analytical, organizational, and time-management skills. Must be a team player with excellent communication abilities and capable of managing multiple projects concurrently. Physical Requirements & Work Environment Physical Demands: Ability to climb permanent/temporary stairs, ladders, and construction hoists. Navigate uneven surfaces, mud, ruts, and other construction conditions. Frequent use of hands to handle objects, tools, or controls, and perform activities like climbing, balancing, stooping, kneeling, or crawling. Ability to lift and/or move up to 50 pounds. Specific vision requirements include close vision, peripheral vision, depth perception, and the ability to adjust focus. Work Environment: Regularly exposed to moving mechanical parts, high places, airborne particles, weather conditions, and electrical hazards. Noise levels range from moderate to very loud, depending on the construction site. Schedule and Travel Work Schedule: Monday - Friday, 8:00 a.m. - 5:00 p.m. Travel Requirements: Weekly travel required to construction job sites across the U.S.

Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Analyst on our BioAnalytical Lab Operations team in Indianapolis, IN. Great opportunity for new graduates, too! The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday. Other duties include: - Document work and maintain study documentation and laboratory records. - Use laboratory equipment appropriate for assigned tasks. - Attends and participates in project meetings. - Perform QC review of data. - Recognize deviations from normal results and informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data. - Plan assigned workload on a daily basis and effectively schedule multiple assignments. - Contributes to a cohesive team environment. Plans individual workload in coordination with team members. - Supports process improvement initiatives. - Maintains a clean and safe laboratory work environment. - Performs other related duties as assigned. - Learns to interact with internal clients. Qualifications: - Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Experience may be substituted. - Familiar with the use of standard laboratory equipment. - Basic knowledge of computers and software programs. 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: As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.

Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Analyst on our BioAnalytical Lab Operations team in Indianapolis, IN. Great opportunity for new graduates, too! The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday. Other duties include: * Document work and maintain study documentation and laboratory records. * Use laboratory equipment appropriate for assigned tasks. * Attends and participates in project meetings. * Perform QC review of data. * Recognize deviations from normal results and informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data. * Plan assigned workload on a daily basis and effectively schedule multiple assignments. * Contributes to a cohesive team environment. Plans individual workload in coordination with team members. - Supports process improvement initiatives. - Maintains a clean and safe laboratory work environment. * Performs other related duties as assigned. * Learns to interact with internal clients. Qualifications: * Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Experience may be substituted. * Familiar with the use of standard laboratory equipment. * Basic knowledge of computers and software programs. 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: As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.

Expand Show Other Jobs Job Saved Formulations Lab Technician-Study Tech Dose Formulations Labcorp Details **Posted:** 19-Nov-24 **Type:** Full-time **Internal Number:** 2435345 **Labcorp BioPharma-** We give everything our all -because everything we do has the potential to change lives. **Formulations Lab Technician-Study Tech Dose Formulations -Greenfield Indian** a $22 per hour minimum with 5% shift premium and .50 increase at 6 months. Day shift hours-4-10 hour days once fully trained Preparing formulations for research studies that are evaluating the safety, effectiveness of new drugs and/or chemicals used on crops. Common duties include preparing laboratory reagents, vehicles, diets, solution/suspensions, and capsules according to study protocols. Extensive training provided! In this position your work matters! You will be joining Labcorp Drug Development mission to delivering healthcare breakthroughs. Candidates looking for a career in laboratory and research. Prior lab experience in any field including pharmacy, research, manufacturing, medical, is preferred but not required. Ability to follow standard procedures, documentation and willingness to take ownership for your work Ability to plan your assigned workload on a daily basis and deliver on multiple assignments throughout your work day. **Work hours** Training work hours will be 8:00am-4:30pm Monday-Friday for approximately 1-2 months. Once training is completed this position offers a 4-day work week!! Work hours are Sunday-Wednesday OR Wednesday-Saturday 6:00am-4:30pm. No late nights! A career where your work connects to improving the lives and health of people and animals around the world. A great work culture where the company is investing in growing your career. Extensive training to ensure your success and investment in growing your skills. $22 ($23.10when working 6:00am-3:30pm). Full time position with outstanding benefits that begin the first of the month 24 days of PTO the first year with outstanding growth potential **Education/Experience/Qualifications** We are open to a variety of backgrounds, the most common being candidates with a BS degree in Chemistry, Biology or other related fields. Candidates BS, AS or 2+ years of college in a related field and prior laboratory work experience in research, manufacturing, pharma, food science, or other fields are encouraged to apply. Prior work experience may qualify in lieu of a degree. **Benefits:****.** **Labcorp is proud to be an Equal Opportunity Employer:** As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. **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 or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our . About Clear and confident health care decisions begin with questions. At Labcorp, we're constantly in pursuit of answers. With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you're a patient, provider, researcher or in the pharmaceutical industry, we're here for you. More than 70,000 employees strong, we serve clients in more than 100 countries. Labcorp (NYSE: LH) reported revenue of $14 billion in FY 2020. *******************************************************************************************************

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 Sterility Assurance Validation Associate I is responsible for the management and the execution of project and system qualifications, and validation confirmations including equipment and processes. The Validation Associate I ensures compliance that meets worldwide regulatory agency requirements, internal company standards/best practices and current industry practices. This position is 100% onsite at the Bloomington facility and reports to the Sr. Technical Services Validation Manager. The responsibilities: * Document (protocols, SOPs, summary reports) new processes and update existing processes where vital that will be reviewed by clients, corporate and regulatory auditors * Conduct development studies on critical equipment * Owns and onboards new client projects, including the relevant validations on syringe lines * Serve as line owner, conducting gap assessments and determining validation approaches when onboarding new projects * Collaborates directly with client representatives * Owns non-conformance investigations (NCR) * Owns corrective and preventive actions (CAPA) * Owns change control management tasks (CCM) * Participates in client audits and provides rationale / justification for practices with aid from senior team member / management Responds to audit observations and owns deliverables * Subject matter expert for up to 3 processes, technologies or process equipment * Owns, plans interventions and leads syringe line media fills and has full ownership through closure of the summary * Owns & drives value improvement projects (VIP) to realize savings * Become trained and perform semi-annual HEPA filter certification testing (integrity testing, velocity testing, visible smoke testing) Required qualifications: * BS degree in science related field with laboratory experience or High School diploma/GED with a minimum of 6 years related experience within a pharmaceutical, biotechnology or related industry including responsibilities comparable to this position (e.g., technical writing, audit experience, project lead, authoring and performing studies, etc.) * Microsoft Office Suite (Word, Excel, Outlook) intermediate proficiency * Ability to use enterprise software (JDE, BPLM, Pilgrim, Trackwise, Ellab Valsuite Pro, etc.) * Critical thinking and problem-solving skills * High initiative and ability to deal with ambiguity * Skills to interact professionally and collaboratively with the client representatives * Good writing skills - including technical writing * Strong oral and written communication - including communication with external clients Physical / safety requirements: * Ability to meet Grade A and B gowning requirements. * Ability to lift 50 lbs. * Must be able to climb and work from ladders. * Duties will require some overtime work, including nights and weekends * Position requires standing for long hours, but may involve walking or sitting for periods of time 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 * 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 12/31/24 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. EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: ********************************************************************************

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 Sterility Assurance Validation Associate I is responsible for the management and the execution of project and system qualifications, and validation confirmations including equipment and processes. The Validation Associate I ensures compliance that meets worldwide regulatory agency requirements, internal company standards/best practices and current industry practices. This position is 100% onsite at the Bloomington facility and reports to the Sr. Technical Services Validation Manager. The responsibilities: Document (protocols, SOPs, summary reports) new processes and update existing processes where vital that will be reviewed by clients, corporate and regulatory auditors Conduct development studies on critical equipment Owns and onboards new client projects, including the relevant validations on syringe lines Serve as line owner, conducting gap assessments and determining validation approaches when onboarding new projects Collaborates directly with client representatives Owns non-conformance investigations (NCR) Owns corrective and preventive actions (CAPA) Owns change control management tasks (CCM) Participates in client audits and provides rationale / justification for practices with aid from senior team member / management Responds to audit observations and owns deliverables Subject matter expert for up to 3 processes, technologies or process equipment Owns, plans interventions and leads syringe line media fills and has full ownership through closure of the summary Owns & drives value improvement projects (VIP) to realize savings Become trained and perform semi-annual HEPA filter certification testing (integrity testing, velocity testing, visible smoke testing) Required qualifications: BS degree in science related field with laboratory experience or High School diploma/GED with a minimum of 6 years related experience within a pharmaceutical, biotechnology or related industry including responsibilities comparable to this position (e.g., technical writing, audit experience, project lead, authoring and performing studies, etc.) Microsoft Office Suite (Word, Excel, Outlook) intermediate proficiency Ability to use enterprise software (JDE, BPLM, Pilgrim, Trackwise, Ellab Valsuite Pro, etc.) Critical thinking and problem-solving skills High initiative and ability to deal with ambiguity Skills to interact professionally and collaboratively with the client representatives Good writing skills - including technical writing Strong oral and written communication - including communication with external clients Physical / safety requirements: Ability to meet Grade A and B gowning requirements. Ability to lift 50 lbs. Must be able to climb and work from ladders. Duties will require some overtime work, including nights and weekends Position requires standing for long hours, but may involve walking or sitting for periods of time 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 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 12/31/24 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. EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: ********************************************************************************

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. Position Brand Description: The Chemist - QC - IAPI performs accurate and timely testing of routine and investigative lab samples in accordance with appropriate GMP and safety guidelines. The Chemist - QC - IAPI also participates in second person verification (SPV) of analytical data, laboratory investigations, equipment calibrations and maintenance by executing well-defined protocols and procedures. The Chemist - QC - IAPI identifies, communicates, and owns opportunities for improvement within the lab. The Chemist - QC - IAPI utilizes technical skills to perform in-depth problem solving, proactively identify opportunities for continuous improvement, and complete thorough investigations of atypical data and results. Outcomes of these activities including results, conclusions, and action plans and/or technical documents. The position is also responsible for technical mentoring of laboratory staff and sharing technical information and best practices within the work group and across plant sites. The Chemist - QC - IAPI participates and influences the technical agenda of the plant or corporation. Key Objectives/Deliverables: Sample Analysis and Reporting Accurately and safely perform analytical test methods or related support activities (such as Forensic Investigations) as per procedures or protocols and reviews that results conform to standards. Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards, and GMP requirements. Recognizes when a deviation from procedures has occurred and initiates an investigation. Verify (SPV) analytical data of other analysts within the lab as required. Continuous Improvement Initiatives Identifies and communicates opportunities for improvement initiatives in daily work activities. Troubleshoot equipment and methods as required. Lab Operations One in this position will have a primary work schedule from Thursday to Monday to provide weekend support for the raw materials testing and investigational support team. Training and mentoring others within lab, where applicable Executes notification to management when required by procedures or standards. Understand the scientific principles required for manufacturing and testing of intermediates and bulk drug substances, including the interaction of the chemistry and equipment. Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess analytical vs. process variability and capability. Provide technical support to non-routine (e.g., deviation) investigations. Support production floor operations through change proposals, investigations, and deviation root cause analysis. Maintain and improve quality systems including method remediation. Participate in self-assessments and regulatory agency inspections. Ensure that the laboratory meets internal and external quality and supply commitments. Basic Requirements: Bachelor's degree in a science related field Experience and knowledge of cGMP requirements in API manufacturing. Additional Preferences: Demonstrated strong problem solving and analytical thinking skills. Understanding of statistical tools and analysis Excellent interpersonal skills and networking skills Experience in QA, QC, Manufacturing, Tech Services, or Regulatory Affairs Demonstrated strong written and verbal communications skills. Strong attention to detail Ability to organize and prioritize multiple tasks. Other Information: Must complete applicable Learning Plan Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE. This position may require 24-hour coverage and will require one to be on call. This position will primarily support weekend work and will require holiday work to support business needs. Tasks may require repetitive motion and standing for extended periods of time, and one must be able to lift at least twenty pounds. 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 an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. #WeAreLilly

** **Read about how we use , along with our and**** ** (Contractor) Senior Quality Control Technician** Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium' honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward' represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team. ****Summary of Position**** Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. May supervise the work of others and coordinate instrumentation use and completion of laboratory testing. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Work Schedule: Monday - Friday 8-4:30pm ****Essential Functions**** * Ensure a safe and quality working environment through training, awareness, and compliance to Safety/Quality guidelines and SOPs. * Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.). * Ensure the maintenance of their department, premises, and equipment. * Ensure that all necessary training is carried out to perform all the assigned tasks confidently and consistently. * Perform all work in compliance with site safety and radiation protection guidelines. * Collaborate with other team members to ensure that quality tasks are performed in a timely manner. * Must demonstrate flexibility in adjusting to changing priorities and schedules. * Attend mandatory trainings as required by site regulatory requirements and management. * Assist with investigations by providing testing results and communication of practice(s). * Assist in the training and development of employees. * Manage inventory of laboratory supplies. * Perform other general duties associated with the position as required by supervision. ****Requirements**** * Associate Degree in life science or a related field or completion of 4 college-level life science courses required. Bachelor Degree in life science or a related field preferred. Work experience is considered in lieu of degree. * Three or more years of relevant experience required. * Proficient in the use of several of the following laboratory instruments: Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, Autotitrator, HPLC, GC, IC, ICP, Flame AA, TOC, Conductivity meter. * Ability to work independently and with others to accomplish goals and priorities. * Flexibility and teamwork skills. * High level of energy and regular, consistent attendance. **Working Conditions:** * Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels. * Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment. * Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury. * Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed. * May be required to sit or stand for long periods of 8+ hours a day while performing duties. * Must possess good hand-eye coordination; close attention to detail is required. * Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants. * Willingness to complete safety training within allotted timeframes, and work in a team-based environment. * Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require. ****Competencies**** ANALYZE + ADAPT COMMUNICATE EFFECTIVELY DEVELOP SELF + OTHERS INTERNAL/EXTERNAL CUSTOMER-FOCUSED RESULTS-DRIVEN **Disclaimer** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. **Equal Opportunity Employer** Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. **Job Segment:** Medical Technologist, Instrumentation, Maintenance, Compliance, QC, Healthcare, Engineering, Manufacturing, Legal, Quality

** As the Quality Control Analyst, your key responsibilities will include the performance of AML/CFT, OFAC, and Fraud quality control (QC) tests/inspections to ensure that alert reviews and case investigations are appropriately completed and suspicious activity is filed in accordance with regulatory requirements and agency guidelines. You will also support the identification, escalation and timely mitigation of compliance and operational risks in alignment with the First Internet Bank and its FinTech Partners' Enhanced Due Diligence (EDD), alert and case investigation, suspicious activity reporting (SAR) filing policies, procedures and regulatory requirements. You will serve as oversight of the appropriate execution of substantive money laundering, economic sanctions and fraud compliance risk detection, prevention, and reporting practices. **What You Will Do:** * Ensure that First Internet Bank and its FinTech Partners maintain AML/CFT and OFAC standards and procedures, and recommend changes and/or alternatives for process improvements. * Review alerts and cases completed/closed by the AML/CFT, OFAC, and Fraud Analysts to ensure that the appropriate decisions/recommendations have been made according to First Internet Bank and its FinTech Partners standards, the appropriate supporting documentation for decision is made by an AML/CFT, OFAC, and Fraud Analyst is appropriately supported and documented. * Evaluate completed AML/CFT, OFAC, and Fraud work and evaluate KYC/KYCC profiles to ensure that they meet regulatory requirements as well as adhere to First Internet Bank and its FinTech Partners policies and procedures. * Communicate any errors/discrepancies found to the appropriate management to ensure that corrective action is taken, additional training provided. * Generate related reports, including findings and trends to management. * Maintain knowledge of developments in the area of Fraud, OFAC and anti-money laundering, including FinCEN and OCC requirements relating to AML/CFT and the USA PATRIOT Act. * Maintain QC standards and procedures, including risk-based standards for compliance testing, and recordkeeping for quality control findings accurately and in a timely manner. * Perform other duties as assigned. **What We're Looking For:** * A Bachelor's Degree or equivalent experience in AML/CFT/OFAC and Fraud compliance in the financial services industry required * A minimum of two years of previous investigative experience or oversight with specific emphasis on OFAC, AML, BSA or prior audit and/or quality control experience in the banking industry is required. * Must be able to demonstrate knowledge of OFAC, USA Patriot Act, Bank Secrecy Act (BSA), and Anti-Money Laundering (AML) regulatory requirements. * Ability to work independently and in collaboration with others. * Ability to provide timely and excellent service to both internal and external customers. * Proven attention to detail. * Strong PC skills required, along with the ability to quickly learn new systems. **Working Conditions/Demands:** * Professional office setting. * Primarily sedentary position requiring long periods of time working at a computer. * Must be able to move throughout the office and buildings to obtain or relay information. * Must be able to perform the essential functions of the position with or without reasonable accommodation. We're not just another bank and we're not looking for just another employee. Since 1999, First Internet Bank has been dedicated to finding a better way to bank and doing things that have never been done before. Yes, we really were the first state-charted, FDIC insured bank to operate entirely online and we have been leading the way ever since. **Our benefits package includes the following and so much more:** * Medical Dental, Vision Insurance * 401(k) Retirement Plan with Generous Match * Tuition Reimbursement * 3 Weeks Paid Vacation Plus Paid Holidays * Paid Volunteer Time * Business Apparel Allowance Equal Opportunity Employer - Women, Minorities, Veterans and Individuals with Disabilities If you are a California resident, you may be entitled to certain rights regarding your personal information. Additional information about our data collection practices and location specific notices is available on our privacy policy. Click to read more. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c). Click to read more.

Category Lab Operations Location Greenfield, Indiana, United States of America **Job Id :** 2435345 Job Type Full-Time **Remote:** No JOB DESCRIPTION **Labcorp BioPharma-** We give everything our all -because everything we do has the potential to change lives. **Formulations Lab Technician-Study Tech Dose Formulations -Greenfield Indian** a $22 per hour minimum with 5% shift premium and .50 increase at 6 months. Day shift hours-4-10 hour days once fully trained Preparing formulations for research studies that are evaluating the safety, effectiveness of new drugs and/or chemicals used on crops. Common duties include preparing laboratory reagents, vehicles, diets, solution/suspensions, and capsules according to study protocols. Extensive training provided! In this position your work matters! You will be joining Labcorp Drug Development mission to delivering healthcare breakthroughs. Candidates looking for a career in laboratory and research. Prior lab experience in any field including pharmacy, research, manufacturing, medical, is preferred but not required. Ability to follow standard procedures, documentation and willingness to take ownership for your work Ability to plan your assigned workload on a daily basis and deliver on multiple assignments throughout your work day. **Work hours** Training work hours will be 8:00am-4:30pm Monday-Friday for approximately 1-2 months. Once training is completed this position offers a 4-day work week!! Work hours are Sunday-Wednesday OR Wednesday-Saturday 6:00am-4:30pm. No late nights! A career where your work connects to improving the lives and health of people and animals around the world. A great work culture where the company is investing in growing your career. Extensive training to ensure your success and investment in growing your skills. $22 ($23.10when working 6:00am-3:30pm). Full time position with outstanding benefits that begin the first of the month 24 days of PTO the first year with outstanding growth potential **Education/Experience/Qualifications** We are open to a variety of backgrounds, the most common being candidates with a BS degree in Chemistry, Biology or other related fields. Candidates BS, AS or 2+ years of college in a related field and prior laboratory work experience in research, manufacturing, pharma, food science, or other fields are encouraged to apply. Prior work experience may qualify in lieu of a degree. **Benefits:** All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please **.** **Labcorp is proud to be an Equal Opportunity Employer:** As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. **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 or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our . **Our U.S. Personal Choice Benefits** We believe improving health and lives starts from within. Learn about our comprehensive U.S. Personal Choice Benefits program, including wellness tools and resources. Live your healthiest life We offer a range of medical, dental and vision plans as well as life insurance and short-/long-term disability coverage. As a U.S. employee, you are automatically enrolled in our No Charge Laboratory Testing program. Promote inclusion and diversity Employee Resource Groups (ERGs) are an important part of our culture. Through our ERGs our employees build career development skills, experience developmental opportunities and partner with volunteer organizations to strengthen our bond with communities. Invest in your wellbeing We offer solutions for maintaining mental health, including live and personal wellness coaching, free premium mental health app access and an Employee Assistance Program which provides 24/7 confidential guidance from professional advisors. Location Greenfield, Indiana, United States of America Category Lab Operations Location Madison, Wisconsin, United States of America Category Lab Operations Location Greenfield, Indiana, United States of America Category Lab Operations Location Birmingham, Alabama, United States of America Category Lab Operations Location Madison, Wisconsin, United States of America Category Lab Operations Location Greenfield, Indiana, United States of America Category Lab Operations Location Burlington, North Carolina, United States of America Category Lab Operations Location Madison, Wisconsin, United States of America Category Lab Operations Location Burlington, North Carolina, United States of America Category Lab Operations Location Terre Haute, Indiana, United States of America Category Lab Operations We are seeking Histology Professionals to join the Labcorp team where we are dedicated to providing the highest quality medical laboratory services. Come work in our Pathology laboratory located in... Location Indianapolis, Indiana, United States of America Category Lab Operations Job Summary. The individual will independently provide support to the bioanalytical laboratory and facilitate the successful conduct of studies. These statements are intended to describe the genera... Location Logansport, Indiana, United States of America Category Lab Operations Location Greenfield, Indiana, United States of America Category Lab Operations Location Waukesha, Wisconsin, United States of America Category Lab Operations

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 Chemist in the DC In-Process Laboratory performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. This individual completes second person verification of others results and also assists in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by performing well-defined protocols and procedures. The Chemist shares technical information and best practice within plant sites or group. Responsibilities: Verify (SPV) analytical data of other analysts within the lab as requested. Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformance to procedures, standards and protocols and/or real-time recognition of aberrant data and results. Perform data entry and review work ensuring accuracy in accordance with laboratory procedures, standards and GMP requirements. May perform comprehensive review of data for release of data from the laboratory. Recognizes when a deviation from procedures, etc has occurred and initiates and participates in a Root Cause Investigation. Performs investigations for deviations. Troubleshoot equipment and methods as required. Assist in improvement of quality systems by crafting or revising worksheets and other lab documentation systems. Evaluates and communicates opportunities for improvement initiatives in daily work activities. Contribute to development of PQEs. Reviews SOPs for executable as written. Shares technical information and best practice within plant sites or group. Write protocols for non-routine testing or validation with appropriate guidance. Develops equipment qualification protocols with appropriate guidance. Perform routine equipment calibrations or maintenance through execution of well- defined protocols. Follow and implement safety standards. Handles notification to management when required by procedures or standards. Initiate change controls and deviations. Train and mentoring others. Develop training materials. Basic Qualifications: Bachelor degree required, preferably in Chemistry. 1+ year experience in a GMP analytical chemistry lab required. Additional Skills: Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals. Proficiency with computer systems including Microsoft Office products, LIMS (list other lab systems), etc. Ability to working in a lab environment including wearing appropriate PPE and other safety required equipment and considerations. Demonstrated strong math and documentation skills. Demonstrated strong oral and written communication and interpersonal interaction skills. Other Information: Work schedule: 10 Hour Nights (Monday-Thursday or Tuesday-Friday) Rotating On-Call Weekend Coverage May be required to have a company phone off shift and respond to operational issues. Minimal travel required. Applicant will work in various areas within the Parenteral Plant. Some allergens are present in the parenteral plant. Mobility requirements and exposure to allergens should be considered when applying for this position Tasks may require repetitive motion (e.g., keyboarding). Post-offer testing exam may be required. 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 an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. #WeAreLilly