Quality control analyst jobs in Indianapolis, IN

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

Title: Environmental Monitoring Technician Temp to perm potential 6am/8am start time - 8 hours a day Monday-Friday 3 positions on first shift Aseptic Technique/comfortable in clean rooms entry level microbiologist water collection GDP willingness to learn Background Qualifications: High School diploma required as minimum. Associates degree and/or related certification in Microbiological Sciences highly preferred. Experience with aseptic technique and/or working in aseptic environments. Ability to gown aseptically for Manufacturing and Aseptic Filling areas. As persons in this role are engaged in sampling and environmental monitoring during open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body. Working hours will require flexibility with available work hours. Sufficient mobility to work in manufacturing processing areas is required. Major Position Activities & Responsibilities: Environmental monitoring of the aseptic area during production fills or weekly monitoring Must immediately notify supervisor if affected by infectious disease or open lesions on body, as individuals are not permitted to enter manufacturing areas or handle product if these conditions exist. Water collection and testing of WFI, Clean Steam, and the Deionized Water Performs media fill qualification and release in support of environmental monitoring program. Perform sampling activities in support of environmental investigations Maintenance of the cleanliness of the microbiology laboratory area, refrigerators, and incubators Handling of wastes including hazardous wastes. Attendance at mandatory annual hazardous waste training meeting(s). Demonstration of competency in training by passing test(s) administered by the company or consultant providing such training. Responsible for adhering to the Environmental, Health and Safety program. Performs special projects and other duties as assigned. As a part of the employees job requirements, the employee may be required to handle wastes including hazardous wastes. The employee must attend mandatory annual hazardous waste training meeting(s) and show a competency in that training by passing test(s) administered by the company or consultant providing such training.

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 Description: The Lilly Industrial Hygiene (IH) Lab provides trace analytical services for the company's global Industrial Hygiene (IH) community. The primary mission of the IH Lab is to develop and validate monitoring methods for active pharmaceutical ingredients (APIs) coming from the clinical development pipeline, followed by providing analytical analyses using these methods on IH samples collected by Lilly's IHs across the globe. Monitoring methods typically include air sampling methods for personnel exposure characterization, swab methods, and may also include air and water monitoring methods and sample analysis for environmental evaluations. Lab staff work closely with site Industrial Hygienists to provide routine analysis of samples taken in the development and manufacturing space in support of employee exposure assessment, and they coordinate all 3rd party analytical needs including external data review, release and archiving results into Lilly's global industrial hygiene electronic platform. Also, lab staff provide creative technical solutions and project support for emerging needs as identified by the global IH community. Key Objectives/Deliverables Partner with internal customers and external lab vendors to efficiently meet business needs. Develop and validate air and surface monitoring methods, including sampling media. Conduct laboratory analysis of active pharmaceutical ingredient (API) samples collected globally. Coordinate sample analysis with third party laboratories and conduct a review of results before releasing to internal customers. Calculate, document, and report study results via established laboratory programs and procedures such as electronic notebooks and company software application. Peer review and approve laboratory data. Research and support the solution of key technical, operational, or business problems, as needed. Organize and/or conduct laboratory inspections and support resolution of observations or areas for improvements. Support benchmarking and maintain awareness of analytical sciences, pharmaceutical industry trends and challenges, new monitoring devices, and techniques to drive continuous improvement in laboratory services. Minimum Requirements: B.S. in Chemistry, Biochemistry or closely related field of study 3+ years of experience in analytical chemistry (Liquid and gas chromatography analytical method development experience). Additional Preferences: Mass spectrometry experience Experience in ISO 17025 accredited laboratory Industrial Hygiene Chemist Certification Experience in GMP lab operations and Lean Coursework or experience in industrial hygiene or environmental sampling Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

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

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

QC Lab Method Scripter needs 2+ years experience QC Lab Method Scripter requires: Bachelor's degree in a scientific field, computer science, or related area. Strong analytical and problem-solving skills. Proficiency in Microsoft Word. Ability to read and write formulas in Microsoft Excel Experience with computer scripting or programming in any language is desirable. Prior experience in a GMP laboratory environment is highly desirable. Basic understanding of XML and its applications in data structuring is beneficial. Prior experience with analytical instrumentation highly preferred Must understand basic window file/folder structure architecture Must translate requirements in Analytical Methods to scripted code for semi-automated execution by laboratory personnel QC Lab Method Scripter duties: We are seeking a detail-oriented and technically skilled individual to join our team as a Quality Control Laboratory Method Scripter. Develop and write scripts to translate paper-based laboratory methods into an electronic laboratory notebook. Review, revise, and rigorously test method scripts, including data parsing, to ensure reliability. Develop techniques to read and process data from scientific testing equipment into the electronic laboratory notebook. Collaborate with laboratory personnel and other teams to meet laboratory processes and data integrity requirements. Develop and write scripts to translate paper-based laboratory methods into an electronic laboratory notebook. Review, revise, and rigorously test method scripts, including data parsing, to ensure reliability. Develop techniques to read and process data from scientific testing equipment into the electronic laboratory notebook. Collaborate with laboratory personnel and other teams to meet laboratory processes and data integrity requirements. Convert paper-based laboratory methods into digital formats for an electronic laboratory notebook (ELN).

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

Knauf Insulation North America is the world's fastest-growing insulation manufacturer. We are wholly committed to the conservation of the environment while also sustainably developing and manufacturing a comprehensive line of acoustical fiberglass insulation for residential, commercial, industrial, marine, OEM and metal building applications, using post-consumer recycled materials. We welcome passionate and creative individuals who thrive in an entrepreneurial, collaborative and ever-changing environment. We know how important your health, wellbeing, and financial strength is to you. To support you, we provide affordable benefits for you and your family members. "Supporting all aspects of the individual - self, health, wealth and community” Our benefits include: Offsite free clinic Medical, Dental, Vision - starting on day one! Virtual Medical Services 401(k) Retirement Plan (earn 100% matching on your first 6% and fully vested day one) Paid parental leave Company paid life insurance Vacation time to enjoy getting away Tuition Reimbursement Employee Assistance Program (EAP) Plus, more! Growth opportunities available! Apply online or contact us to hear why our employees appreciate being part of the Knauf family! About the Role: We are seeking a detail-oriented and motivated Analytical Lab Technician to join our team. In this role, you will be responsible for conducting laboratory tests on raw materials, certifying finished products, and performing requested laboratory analyses. You will also ensure the proper maintenance and cleaning of laboratory instruments while adhering to all company safety requirements and policies. This position plays a critical role in supporting our commitment to quality, innovation, and employee engagement. Responsibilities Perform laboratory analysis on a variety of materials, including batch raw materials, glass, chemicals, and glass mineral wool final products. Conduct tests to certify finished products and ensure compliance with quality standards. Analyze data and prepare detailed technical reports to support decision-making processes. Maintain and clean laboratory instruments to ensure optimal performance and accuracy. Follow and actively participate in all company safety requirements, policies, and related documentation. Assist Innovation team members with laboratory testing and other tasks as requested. Leadership and Culture: Drives the highest levels of employee retention and engagement to ensure a sustainable and motivated workforce. Foster a culture of innovation, collaboration, and accountability within the organization. Promote an environment of inclusion, ensuring all employees feel valued and empowered to contribute positively to the company. Qualifications Education: Bachelor's or Associate's degree in Chemistry, Geology, Environment Science, Engineering or similar field Experience: Analytical and/or Inorganic lab experience, preferred Knowledge, Skills, and Abilities: Proficient in Microsoft Excel and/or other data analysis software. Knowledge of X-Ray Fluorescence (XRF), preferred. Strong analytical and problem-solving skills. Experience in laboratory testing and data analysis. Familiarity with laboratory instruments and their maintenance. Commitment to safety and adherence to company policies. Excellent communication and teamwork abilities. Why Join Us? At Knauf, we are committed to fostering a workplace that values innovation, collaboration, and inclusion. As an Analytical Lab Technician, you will have the opportunity to contribute to our mission of delivering high-quality products while working in an environment that supports your professional growth and development. It is the policy of Knauf Insulation to provide equal employment opportunities to all qualified persons without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status or any other protected characteristic prohibited by applicable law.

Donaldson is committed to solving the world's most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities. Position Summary: The Quality Control Inspector is responsible for verifying product quality, conducting inspections and tests, and documenting results to ensure compliance with internal and external requirements. This role actively participates in problem-solving, root cause analysis, and continuous improvement efforts across the organization. Role Responsibilities: * Perform inspections and testing of products to ensure compliance with specifications and quality standards. * Read and interpret blueprints, engineering drawings, and bills of materials. * Document inspection results, including Certificates of Conformance and other quality records. * Investigate customer complaints and product returns, and implement containment measures. * Participate in root cause analysis and develop corrective and preventive actions. * Calibrate and maintain standard measuring equipment (gauges, calipers, tooling). * Support the Production Part Approval Process (PPAP) and ISO 9001 requirements. * Resolve nonconforming material using company resources and procedures. * Collaborate with production, engineering, and management to drive continuous improvement. * Adhere to all EHS and PPE policies while maintaining a safe and positive work environment. Minimum Qualifications: * High school diploma or GED with at least 1 year of quality control experience. * Knowledge of ISO 9001 or similar quality standards and quality techniques (e.g., SPC, PPAP). * Strong communication skills and proficiency with Microsoft Office. * Ability to work independently and in a fast-paced, team-oriented environment, including off-shifts or extended hours as needed. Preferred Qualifications: * Associate's degree or technical certification in quality, manufacturing, or related field. * 2+ years of quality control experience in a manufacturing environment. * Experience with ISO 9001 audits, SPC, PPAP, and root cause analysis. * Proficient with dimensional measurement tools, calibration, and interpreting blueprints. * Strong problem-solving skills with ability to support continuous improvement in a fast-paced environment. Immigration Sponsorship Not Available: * Donaldson will not offer immigration sponsorship or assume sponsorship of an employment visa for this position. * International relocation or remote work arrangements outside of the U.S. will not be considered. Keywords: Quality Assurance, Inspection, ISO9001 Equal Opportunity Employer, including Disability and Veterans Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States. Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers. These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process. Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address. If you have any questions about the legitimacy of an employment opportunity, please reach out to ******************************* to verify that the communication is from Donaldson. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

The Quality Control Technician is responsible for inspecting and testing raw materials and finished products to ensure they meet required levels of quality and industry regulations. This position performs quality tests, inspection checks, and communicates test results to their Quality Supervisor. Essential Functions/Key Deliverables Take measurements and samples according to the control/sampling plan (e.g., lacquer weights and distribution, visual can inspection, bar code and QR code inspection, abrasion testing, mobility testing, etc.) Conduct tests using high-tech measurement equipment (Torus, Versatile, Sencon) and interface with quality control reporting system Monitoring and testing of critical control points (CCPs) Monitor the quality of products on the line and at specific production stages and provide support and feedback to production team members Provide final approval for finished goods Contain out-of-spec finished goods per containment guidelines and report to supervisor Create and analyze quality reports Communicate quality status and progress to all team members Collaborate with all plant teams and areas to ensure the highest quality Ensure compliance with BRCGS Understanding of HARA Perform any other duty reasonable corresponding with the role Knowledge/Skills/Experience Specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus High attention to detail Ability to communicate with and influence others Ability drive for root cause identification and corrective actions Ability to run reports and analyze data Familiarity with basic and sophisticated measurement devices Proficient in Microsoft Office Products CAN DO attitude, ability to work in a highly collaborative team environment, and a desire to WIN Physical Demands N (Not Applicable) Activity is not applicable to this position. O (Occasionally) Position requires this activity up to 33% of the time (0 - 2.5+ hrs/day) F (Frequently) Position requires this activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day) C (Constantly) Position requires this activity more than 66% of the time (5.5+ hrs/day) Lift/Carry 10 lbs or less F 11-25 lbs O 25-50+ lb- O Push/Pull 10 lbs or less F 11-25 lbs O 25-50+ lb- O Stand C Walk C Sit O Manually Manipulate O Reach Outward O Reach Above Shoulder O Climb O Crawl O Squat or Kneel O Bend O Other Physical Requirements Vision (Near, Distance, Color, Peripheral, Depth) Sense of Sound - Ability to understand conversational speaking Sense of Touch Ability to wear Personal Protective Equipment (PPE) - per safety guidelines Mobility to cover expansive manufacturing environment Work Environment Ability to work in an environment that can become very hot (temperature) depending on the weather. Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. If you are a current CANPACK employee, please apply through your Workday account. CANPACK Group is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, age, sex, sexual orientation, gender identity, national origin, disability, or any other characteristic protected by law or not related to job requirements, unless such distinction is required by law.

TempToFT Job Summary: Develops systems and documentation for specific programs that ensure that products and services provided meet all contractual and program quality requirements. Essential Functions and Basic Duties: 1. Reviews the program quality performance to provide analysis and obtains corrective actions where necessary. 2. Provides interface and support to customer quality concerns to facilitate responsiveness to customers. 3. Provides technical and advisory support to the prototype area to ensure the development of products in a manner that produces a quality system and documentation which will provide adherence to customer requirements. 4. Dispositions discrepant material in a manner that ensures product quality and adherence to program requirements. 5. Performs program-specific tasks as required (e.g., customer-required First Article Inspection, Qualification Test Failure Analysis, etc.) to ensure compliance to individual requirements. 6. Reviews all design drawings and changes, operation sheets, process procedures, test procedures, procurement documents, and quality manuals, and inspection analyses to ensure that the divisions' and customers quality requirements are met on assigned products, programs, areas, and functions. 7. Provides support to his or her assigned operation group including visual aids and inspection analyses and includes a key role serving as “referee” in making “accept” or “reject” decisions. 8. Provides support to the Design Engineering group on engineering hardware, to the Customer Service Department on the analysis of hardware returned from the field, and to the Purchasing group for procurements. 9. Reviews quality trends based on quality data system information and interaction with inspectors and production personnel, and participates in generation and implementation of defect-reduction programs for his or her assigned product or program. 10. Assists in identifying the root causes of the problem and instituting corrective action such as changes to operation sheets, generation of Engineering Change Requests, installation of fixtures, changes in workstations, changes to inspection analyses and changes to process procedures. 11. Evaluates discrepant hardware in accordance with quality requirements, and determines its disposition or referral to the Purchasing Department. 12. Interacts with representatives from a variety of functional groups, including design engineering, manufacturing engineering, purchasing, and all production and inspection personnel in the assigned product or program area, as well as within the Product assurance Department. 13. Provides recommendations to improve procedures that apply to quality and other functions, such as configuration management and operations functions. 14. Reviews quality trends to prevent or reduce defects, determine problem causes, and initiate actions to correct them, convincing others of the validity of potential solutions.

Title: Environmental Monitoring Technician Temp to perm potential 10am/12pm start time - 8 hours a day Monday-Friday Shift differential: 7% 3 positions on first shift Aseptic Technique/comfortable in clean rooms entry level microbiologist water collection GDP willingness to learn Background Qualifications: High School diploma required as minimum. Associates degree and/or related certification in Microbiological Sciences highly preferred. Experience with aseptic technique and/or working in aseptic environments. Ability to gown aseptically for Manufacturing and Aseptic Filling areas. As persons in this role are engaged in sampling and environmental monitoring during open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body. Working hours will require flexibility with available work hours. Sufficient mobility to work in manufacturing processing areas is required. Major Position Activities & Responsibilities: Environmental monitoring of the aseptic area during production fills or weekly monitoring Must immediately notify supervisor if affected by infectious disease or open lesions on body, as individuals are not permitted to enter manufacturing areas or handle product if these conditions exist. Water collection and testing of WFI, Clean Steam, and the Deionized Water Performs media fill qualification and release in support of environmental monitoring program. Perform sampling activities in support of environmental investigations Maintenance of the cleanliness of the microbiology laboratory area, refrigerators, and incubators Handling of wastes including hazardous wastes. Attendance at mandatory annual hazardous waste training meeting(s). Demonstration of competency in training by passing test(s) administered by the company or consultant providing such training. Responsible for adhering to the Environmental, Health and Safety program. Performs special projects and other duties as assigned. As a part of the employees job requirements, the employee may be required to handle wastes including hazardous wastes. The employee must attend mandatory annual hazardous waste training meeting(s) and show a competency in that training by passing test(s) administered by the company or consultant providing such training.

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Job Description Perform biochemical testing on proteins including, but not limited to, TOC, IC, HPLC, UV, Spectroscopy, Wet chemistry- pH, Nitrates and Conductivity testing 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 a related major) At least 2 years of related laboratory experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday - Friday 8am to 5 pm 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 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Quality Control Laboratory Method Scripter needs 3+ years experience Quality Control Laboratory Method Scripter requires: Bachelor's degree in a scientific field, computer science, or related area. Strong analytical and problem-solving skills. Proficiency in Microsoft Word. - Ability to read and write formulas in Microsoft Excel. Experience with computer scripting or programming in any language is desirable. Prior experience in a GMP laboratory environment is highly desirable. Basic understanding of XML and its applications in data structuring is beneficial Quality Control Laboratory Method Scripter duties: Script analytical methods into the electronic laboratory execution system (LES), Convert paper-based laboratory methods into digital formats for an electronic laboratory notebook (ELN). Enhance the efficiency and accuracy of our quality control processes. Develop and write scripts to translate paper-based laboratory methods into an electronic laboratory notebook. Review, revise, and rigorously test method scripts, including data parsing, to ensure reliability. Develop techniques to read and process data from scientific testing equipment into the electronic laboratory notebook.

INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients. The QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory. This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence. Strict adherence to Good Documentation Practices (GDP) is required as Good Manufacturing Practice (GMP) testing is performed. Excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences is critical in this role. The QC Chemist will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, clients, suppliers, and partners. The QC Chemist will thrive in a team environment but can also work autonomously with strong self-management and organizational skills. Essential Job Functions: * Perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods as well as special testing deemed necessary by protocols * Assist in sampling and testing of incoming materials requiring QC testing as needed * Create/revise SOPs and other relevant documents related to laboratory equipment and/or processes * Participate in the completion of laboratory investigations/deviations and provide SME support where needed * Perform basic troubleshooting activities with respect to methods/assays, equipment malfunctions, and investigations (Deviations and OOS) * Execute routine laboratory work orders for maintenance and non-critical calibrations * Perform minor preventative maintenance on QC laboratory instrumentation as needed using written SOPs or assist vendors with access to systems/materials when vendor performs maintenance * Execute day-to-day tasks within the laboratory including sample inventory disposition/disposal, consumables ordering/inventory, preparing instruments for testing, and laboratory waste management * Assist in the control and management of laboratory waste in cooperation with relevant EH&S standards * Assist in the development and execution of protocols for method transfers, method validations, stability studies, cleaning validations, and any other special testing required from the Quality Control Chemistry laboratory * Support internal and external customers to ensure proper and timely execution of all aspects of the clinical/commercial analytical method life cycle across clients * Conduct periodic reviews of analytical test procedures and SOPs as required * Review and approve analytical testing procedures and protocols as needed * Assist in training fellow QC and Development personnel on instruments and assays when cross-training is needed * Assist in the professional support and development of QC Chemistry Technician staff within the QC laboratory * Be team-oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed * Set deadlines and prioritize work for self, group members, and support groups involved * Review/approve work performed by coworkers for accuracy and alignment with procedures * Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured, and released * Identify, evaluate, and implement continuous business process improvements Special Job Requirements: * This position will support primarily third shift (11:00pm-7:30am) * Bachelor's Degree in Science (Chemistry or Biochemistry) * Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience * High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements * Excellent working knowledge, understanding, and experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control * Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.) Additional Preferences: * Experience with Continuous Improvement, Six Sigma, and/or Lean principles * Experience with building processes and procedures * Experience in performing testing and/or characterization of biologic (monoclonal antibody, enzyme) and small molecule (peptide, mRNA) products * Experience performing container closure integrity testing (CCIT) Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients. The QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory. This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence. Strict adherence to Good Documentation Practices (GDP) is required as Good Manufacturing Practice (GMP) testing is performed. Excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences is critical in this role. The QC Chemist will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, clients, suppliers, and partners. The QC Chemist will thrive in a team environment but can also work autonomously with strong self-management and organizational skills. Essential Job Functions: Perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods as well as special testing deemed necessary by protocols Assist in sampling and testing of incoming materials requiring QC testing as needed Create/revise SOPs and other relevant documents related to laboratory equipment and/or processes Participate in the completion of laboratory investigations/deviations and provide SME support where needed Perform basic troubleshooting activities with respect to methods/assays, equipment malfunctions, and investigations (Deviations and OOS) Execute routine laboratory work orders for maintenance and non-critical calibrations Perform minor preventative maintenance on QC laboratory instrumentation as needed using written SOPs or assist vendors with access to systems/materials when vendor performs maintenance Execute day-to-day tasks within the laboratory including sample inventory disposition/disposal, consumables ordering/inventory, preparing instruments for testing, and laboratory waste management Assist in the control and management of laboratory waste in cooperation with relevant EH&S standards Assist in the development and execution of protocols for method transfers, method validations, stability studies, cleaning validations, and any other special testing required from the Quality Control Chemistry laboratory Support internal and external customers to ensure proper and timely execution of all aspects of the clinical/commercial analytical method life cycle across clients Conduct periodic reviews of analytical test procedures and SOPs as required Review and approve analytical testing procedures and protocols as needed Assist in training fellow QC and Development personnel on instruments and assays when cross-training is needed Assist in the professional support and development of QC Chemistry Technician staff within the QC laboratory Be team-oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed Set deadlines and prioritize work for self, group members, and support groups involved Review/approve work performed by coworkers for accuracy and alignment with procedures Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured, and released Identify, evaluate, and implement continuous business process improvements Special Job Requirements: This position will support primarily third shift (11:00pm-7:30am) Bachelor's Degree in Science (Chemistry or Biochemistry) Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements Excellent working knowledge, understanding, and experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.) Additional Preferences: Experience with Continuous Improvement, Six Sigma, and/or Lean principles Experience with building processes and procedures Experience in performing testing and/or characterization of biologic (monoclonal antibody, enzyme) and small molecule (peptide, mRNA) products Experience performing container closure integrity testing (CCIT) Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

Knauf Insulation North America is the world's fastest-growing insulation manufacturer. We are wholly committed to the conservation of the environment while also sustainably developing and manufacturing a comprehensive line of acoustical fiberglass insulation for residential, commercial, industrial, marine, OEM and metal building applications, using post-consumer recycled materials. We welcome passionate and creative individuals who thrive in an entrepreneurial, collaborative and ever-changing environment. We know how important your health, wellbeing, and financial strength is to you. To support you, we provide affordable benefits for you and your family members. "Supporting all aspects of the individual - self, health, wealth and community” Our benefits include: Offsite free clinic Medical, Dental, Vision - starting on day one! Virtual Medical Services 401(k) Retirement Plan (earn 100% matching on your first 6% and fully vested day one) Paid parental leave Company paid life insurance Vacation time to enjoy getting away Tuition Reimbursement Employee Assistance Program (EAP) Plus, more! Growth opportunities available! Apply online or contact us to hear why our employees appreciate being part of the Knauf family! About the Role: We are seeking a detail-oriented and motivated Analytical Lab Technician to join our team. In this role, you will be responsible for conducting laboratory tests on raw materials, certifying finished products, and performing requested laboratory analyses. You will also ensure the proper maintenance and cleaning of laboratory instruments while adhering to all company safety requirements and policies. This position plays a critical role in supporting our commitment to quality, innovation, and employee engagement. Responsibilities Perform laboratory analysis on a variety of materials, including batch raw materials, glass, chemicals, and glass mineral wool final products. Conduct tests to certify finished products and ensure compliance with quality standards. Analyze data and prepare detailed technical reports to support decision-making processes. Maintain and clean laboratory instruments to ensure optimal performance and accuracy. Follow and actively participate in all company safety requirements, policies, and related documentation. Assist Innovation team members with laboratory testing and other tasks as requested. Leadership and Culture: Drives the highest levels of employee retention and engagement to ensure a sustainable and motivated workforce. Foster a culture of innovation, collaboration, and accountability within the organization. Promote an environment of inclusion, ensuring all employees feel valued and empowered to contribute positively to the company. Qualifications Education: Bachelor's or Associate's degree in Chemistry, Geology, Environment Science, Engineering or similar field Experience: Analytical and/or Inorganic lab experience, preferred Knowledge, Skills, and Abilities: Proficient in Microsoft Excel and/or other data analysis software. Knowledge of X-Ray Fluorescence (XRF), preferred. Strong analytical and problem-solving skills. Experience in laboratory testing and data analysis. Familiarity with laboratory instruments and their maintenance. Commitment to safety and adherence to company policies. Excellent communication and teamwork abilities. Why Join Us? At Knauf, we are committed to fostering a workplace that values innovation, collaboration, and inclusion. As an Analytical Lab Technician, you will have the opportunity to contribute to our mission of delivering high-quality products while working in an environment that supports your professional growth and development. It is the policy of Knauf Insulation to provide equal employment opportunities to all qualified persons without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status or any other protected characteristic prohibited by applicable law. Not ready to apply? Connect with us for general consideration.

Donaldson is committed to solving the world's most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities. Position Summary: The Quality Control Inspector is responsible for verifying product quality, conducting inspections and tests, and documenting results to ensure compliance with internal and external requirements. This role actively participates in problem-solving, root cause analysis, and continuous improvement efforts across the organization. Role Responsibilities: Perform inspections and testing of products to ensure compliance with specifications and quality standards. Read and interpret blueprints, engineering drawings, and bills of materials. Document inspection results, including Certificates of Conformance and other quality records. Investigate customer complaints and product returns, and implement containment measures. Participate in root cause analysis and develop corrective and preventive actions. Calibrate and maintain standard measuring equipment (gauges, calipers, tooling). Support the Production Part Approval Process (PPAP) and ISO 9001 requirements. Resolve nonconforming material using company resources and procedures. Collaborate with production, engineering, and management to drive continuous improvement. Adhere to all EHS and PPE policies while maintaining a safe and positive work environment. Minimum Qualifications: High school diploma or GED with at least 1 year of quality control experience. Knowledge of ISO 9001 or similar quality standards and quality techniques (e.g., SPC, PPAP). Strong communication skills and proficiency with Microsoft Office. Ability to work independently and in a fast-paced, team-oriented environment, including off-shifts or extended hours as needed. Preferred Qualifications: Associate's degree or technical certification in quality, manufacturing, or related field. 2+ years of quality control experience in a manufacturing environment. Experience with ISO 9001 audits, SPC, PPAP, and root cause analysis. Proficient with dimensional measurement tools, calibration, and interpreting blueprints. Strong problem-solving skills with ability to support continuous improvement in a fast-paced environment. Immigration Sponsorship Not Available: · Donaldson will not offer immigration sponsorship or assume sponsorship of an employment visa for this position. · International relocation or remote work arrangements outside of the U.S. will not be considered. Keywords: Quality Assurance, Inspection, ISO9001 Equal Opportunity Employer, including Disability and Veterans Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States. Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers. These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process. Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address. If you have any questions about the legitimacy of an employment opportunity, please reach out to ******************************* to verify that the communication is from Donaldson. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

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 Job Summary The position will be responsible for performing analytical testing on raw materials, intermediates, finished products, and to ensure compliance of all product quality attributes as defined in approved specifications. The incumbent will also participate in investigations (CAPA) and Deviation investigations when appropriate. This role will provide the opportunity to work within laboratory setting, giving exposure to different types of analysis. The successful candidate will have experience working within a GMP/GDP environment and possess excellent communication skills. Responsibilities: • Performing sample preparation and various analytical test procedures including chromatography (HPLC), spectroscopy (UV-Vis & IR), electrochemistry (pH, ORP, and conductivity), acid-base titrations, aliquoting, filtering, centrifuging, pipetting, and various other laboratory techniques. • Assisting in maintaining laboratory equipment, keeping accurate records, generating reports, and providing technical assistance to other departments. • Participating in Deviation investigations as needed. • Ensuring data integrity through good documentation practices. • Utilizing various software applications for data management and documentation purposes. • Other duties as assigned. Qualifications Minimum Qualifications: • Bachelor's degree in Chemistry or related field with at least 1 year of relevant industrial experience preferred. • Experience with HPLCs and basic wet chemistry • Knowledge of cGMPs and regulatory requirements. • Strong communication skills. • Ability to troubleshoot and problem-solve. • Ability to collaborate effectively across multiple disciplines. • Ability to generate reports and communicate results. • Basic computer skills. Preferred Qualifications: Experience with Empower Experience with Smartlab and Darwin Additional Information Position is Monday-Friday 8:00am - 5:00pm overtime as needed. Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.