Quality assurance technician jobs in Bloomington, IN - 589 jobs

Driven by Vision | Industrial-Strength Construction| Powered by Passion Are you looking to work for a successful, stable, and growing company that rewards employees with annual bonuses and exceptional benefits? BMWC is an industrial construction company seeking a Site Quality Inspector to join the Quality Team. This crucial position allows you to contribute to the delivery of large-scale industrial construction projects. You will be part of a top-performing project team and report to an expert in the industry. This position regularly interacts with project managers, project engineers, site supervisors, and company operations leaders. RESPONSIBILITIES As a Site Quality Inspector, you will: Be responsible for inspecting all site welds and ensuring compliance with governing guidelines. Stop and report all unsafe conditions and acts. Understand the governing construction codes. Understand the inspection and test plan requirements applicable to the work scope. Ensure welders are qualified for the welding being performed. Inspect the welds, assigns numbers for the weld map, create weld logs. Perform all aspects of Hydro-test and Turnover Package maintenance. Utilize punch lists to identify incomplete items and present to supervision. Compile all appropriate documents in the turnover package. REQUIREMENTS AND QUALIFICATIONS Minimum of 2 years professional experience with piping inspection Turnover package creation Experience with at least one of the following: Heat Maps, Weld Maps, Hydro Packages Certified Welding Inspector with AWS or similar Knowledge of ASME codes and applications Has administered weld tests, as required Ability to manage multiple tasks simultaneously in a constantly changing environment Proficiency with Microsoft Office; Excel, WORD, Outlook, and technical aptitude to learn new systems BENEFITS Competitive Pay with Bonus PTO and paid holidays 401K/Profit Sharing with company match Medical, Dental and Vision Insurance Life, AD&D and Disability benefits Pet Insurance Tuition Reimbursement Paid Volunteer Time Off ABOUT US BMWC tackles the world's toughest and most daunting industrial construction challenges. Our work encompasses an array of industrial sectors, including aerospace, chemical, electric power, food and beverage, oil and gas, pharmaceutical and biotechnology, and semiconductor. As one of the premier specialty construction companies in the country, our employees enjoy a focus on growth and development, work/life balance, and one of the best safety records in the industry. We are 100% management-owned, making our employees' development and advancement paramount to our success.

Join a Global Leader in Workforce Solutions - Net2Source Inc. Who We Are Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 32 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision-Right Talent. Right Time. Right Place. Right Price. Position: Laboratory Technician Payrate: $19-$20/hr. on W2 Location: Indianapolis IN Duration: 12+ Months (Possible Extension) Key Responsibilities: Prepare media, sterilize equipment using autoclave, and clean/rinse glassware Handle plant material: tagging, moving, inoculating, and harvesting Safely handle and apply research chemicals (fungicides, etc.) while wearing proper PPE, including PAPR (Powered Air-Purifying Respirator) Maintain lab and greenhouse cleanliness, manage waste, and stock supplies Assist with routine test setups and fungal culture preparation/inoculation Requirements: Background in Biology, Plant Pathology, or related field (preferred) 1-2 years of relevant lab/greenhouse experience can substitute for a degree Knowledge of plant science and handling fungal cultures Strong work ethic, attention to detail, and ability to work independently and in a small team Comfortable wearing PAPR and handling chemicals (OSHA Respirator Medical Evaluation required) Why Work With Us? We believe in more than just jobs-we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition America's Most Honored Businesses (Top 10%) Fastest-Growing Staffing Firm by Staffing Industry Analysts INC 5000 List for Eight Consecutive Years

*Lab EHR Technologist Contract Opportunity* Our client is seeking 1-2 experienced Med Tech-level professional to provide on-site operational support for the Roche Sysmex project. This role is non-technical and focuses on lab operations, not Epic or technical build activities. Candidates must have direct experience with Roche lab operations and/or Sysmex Caresphere, with familiarity in Navify middleware. *Responsibilities/Experience Needed*: -Support high-volume lab testing and ensure accurate sample processing through Roche Sysmex systems. -Validate results in Cerner and maintain proper documentation. -Provide on-site assistance during go-lives, including potential off-hours and extended (>40 hours) support. -Collaborate with lab teams to manage workflow and troubleshoot operational issues. -Travel extensively across Indiana, primarily central and southern regions, with overnight stays as needed. *Job Type & Location* This is a Contract position based out of Indianapolis, IN. *Pay and Benefits*The pay range for this position is $40.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) *Workplace Type*This is a fully onsite position in Indianapolis,IN. *Application Deadline*This position is anticipated to close on Jan 26, 2026. h4>About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Quality matters. People matter. YOU matter. Join Brulin as a Quality Assurance Technician and make a real impact. Inspect, improve and innovate with a team that values excellence. In this role, the Quality Assurance Technician ensures all incoming raw materials, bulk tankers, staged materials, batch production, filling operations, finished goods, and shipments meet established quality and regulatory requirements. This position acts as the on-the-floor QA authority for manufacturing, providing verification, documentation, troubleshooting, and continuous improvement support. The role is critical in preventing mislabeling, cross-contamination, off-spec product releases, and shipment errors while ensuring traceability from raw materials, to batching, to finished goods, and final shipment. CORE RESPONSIBILITIES Incoming Raw Material Quality Assurance Verify raw materials against PO and internal specifications. Review supplier COAs and conduct/assist in required QC tests (pH, SG, viscosity, color, actives %, appearance). Ensure incoming materials are correctly processed through our ERP following internal SOP's. Collect/store retain samples per SOP. Tanker Receiving Oversight: Validate seal integrity, documentation, cleanliness, and material identity. Perform in-line or pre-transfer QC (SG, pH, clarity, contamination checks). Record receiving logs; release or quarantine materials. Initiate/assist in supplier nonconformance reports as needed. Batch Manufacturing Quality Assurance Review batch tickets for completeness, accuracy, and proper WO/BOM alignment. Confirm staging accuracy: correct raw materials, correct internal lots, label placement. Verify equipment readiness (tank ID, cleanliness, hoses, pumps, rinsing, calibration). Conduct or assist in-process testing (pH, SG/density, viscosity, appearance, solids). Manage batch retain samples and post-filtering to storage verification. Fill Line QA Confirm proper line rinsing, dedicated hose usage, and filtration setup. Conduct fill-weight/volume checks at established SOP frequencies (start/middle/end). Verify correct lot assignment and LP/traceability linkage. Oversee changeovers: cleaning logs, rinse logs, line-flush confirmation. Reject/document any off-spec packaging or filling defects. Post-Fill & Shipping QA (100% Audit) Perform 100% audits post-fill before finished goods move to inventory/shipping. Confirm palletization, packaging, labeling, and LP/WO/date label accuracy. Conduct final visual inspection before pallet release. Validate BOL and shipping documents for accuracy. Documentation, ISO Compliance & Continuous Improvement Maintain batch records, QA logs, retains, and calibration documentation. Support ISO 9001/14001 programs and internal audits. Update and improve SOPs related to batching, filling, raw material receiving, and QC testing. Provide operator training on quality-critical checkpoints. Demonstrates awareness and competency relevant to both the Environmental Management System (EMS) and the Quality Management System (QMS), including but not limited to policies, objectives, and compliance obligations related to International Organization for Standardization (ISO) systems. Industry-Relevant Competencies Quality Systems & Compliance Inspection, Auditing & Verification Documentation & Data Integrity Safety & Environmental Awareness

As a Quality Control Technician - 3rd Shift, you will receive samples from production and perform various testing depending on customer specifications. You will document the data and approve or reject product based on testing results. You will work onsite at our Liquid Production Plant in Brazil, IN and you will report to a Quality Supervisor. This shift is 11:00pm to 7:00am Sunday night through Friday morning. Benefits: PPG Offers excellent Benefits including medical, dental, vision, disability, life, 401k, PTO, family leave, continuing education, and Opportunities for Growth! Main Responsibilities: Perform various scientific testing to evaluate the quality of in-process materials and finished goods Compile, interpret, and document data from the testing process to confirm compliance with established quality standards Keep basic laboratory housekeeping May be responsible for establishing specifications and writing standard operating procedures Qualifications: High School Diploma or GED required, Chemistry courses helpful 1+ year of experience Data entry, basic math and reading, and basic computer skills required (Word, Excel, etc), experience with Oracle a plus Experience with ISO 9001 helpful Ability to lift up to 50lbs, sit, stand, bend, twist, kneel #LI-Onsite About us: Here at PPG we make it happen, and we seek candidates of the highest integrity who share our values, with the commitment and drive to strive today to do better than yesterday - everyday. PPG: WE PROTECT AND BEAUTIFY THE WORLD™ Through leadership in innovation, sustainability and color, PPG helps customers in industrial, transportation, consumer products, and construction markets and aftermarkets to enhance more surfaces in more ways than does any other company. To learn more, visit *********** and follow @ PPG on Twitter. The PPG Way Every single day at PPG: We partner with customers to create mutual value. We are "One PPG" to the world. We trust our people every day, in every way. We make it happen. We run it like we own it. We do better today than yesterday - everyday. PPG provides equal opportunity to all candidates and employees. We offer an opportunity to grow and develop your career in an environment that provides a fulfilling workplace for employees, creates an environment for continuous learning, and embraces the ideas and diversity of others. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status, sexual orientation, gender identity or expression. If you need assistance to complete your application due to a disability, please email ******************. PPG values your feedback on our recruiting process. We encourage you to visit Glassdoor.com and provide feedback on the process, so that we can do better today than yesterday. Benefits will be discussed with you by your recruiter during the hiring process. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

Why Choose Us? Novolex is a leading manufacturer of food, beverage, and specialty packaging that supports multiple industries including foodservice, restaurant delivery and carryout, food processing, grocery and retail, and industrial sectors. Novolex manufacturing and sourcing expertise spans a diverse range of substrates including resin, paper, molded fiber, aluminum and more. We provide customers a broad array of stock and customized solutions with 120 product categories, 250 brands and over 39,000 SKUs. Our Sustainability Commitment The Novolex sustainability vision is built upon three pillars: our products, our operations and our people. Each is critically important to our growth and future as a business. These pillars form the foundation of our company-wide commitment to sustainability, helping us achieve our ambitious goals through our wide-ranging initiatives. Job Description Compensation: * $17.75-$23.00 Shift Available * 7pm-7am ($1.50 Shift Diff) How You'll Perform the Role: * Responsible for the testing of products and recording data • Notifying management of non-conforming material• Prepare daily quality/product reporting • Perform safety and quality audits• Record and save data in company database• Ensure all company safety standards are being utilized What We Need From You * High School diploma or equivalent.• Eligible to work in the United States.• Successful completion of pre-employment background and drug screen.• Work overtime as required.• Satisfactorily completes training courses as determined by management.• Ability perform the essential functions of the job with or without accommodation.• The commitment to stay safe and to continue to learn and develop.• Satisfactorily completes training courses as determined by management. Company Benefits What You'll Get From Us Benefits With safety as our top priority and a commitment to employee well-being an important focus, we offer comprehensive and competitive benefits that include medical, dental and vision insurance as well as a variety of other well-being resources focused on mental, physical and financial health. Specific benefits and well-being programs may vary depending on where you work. Community Engagement At Novolex, giving back to the local communities that support us is important. Our Focused Giving Program prioritizes support for organizations whose missions promote sustainability initiatives or address food and hunger needs. We also encourage facility level support of activities in the communities where our employees live and work. Training and Development We offer constant opportunities for advancement. From skills development to advanced education programs, training and development programs and courses are available through MyLearning. Programs include company and industry training curricula, support for formal education through the Tuition Reimbursement Program, and a Learning Management System that supports and enhances employee skills at all levels of the organization. Novolex is committed to providing equal employment opportunity in all employment practices, including but not limited to selection, hiring, promotion, transfer, and compensation to all qualified applicants and employees without regard to age, race, color, national origin, sex, pregnancy, sexual orientation, gender identity, religion, handicap or disability, genetics, citizenship status, service member or veteran status, or any other category protected by federal, state, or local law. Any individual who, because of his or her disability, needs an accommodation in connection with an aspect of the Company's application process should contact my **********************. Responsibilities Compensation: - $17.75-$23.00 Shift Available - 7pm-7am ($1.50 Shift Diff) How You'll Perform the Role: •Responsible for the testing of products and recording data •Notifying management of non-conforming material •Prepare daily quality/product reporting •Perform safety and quality audits •Record and save data in company database •Ensure all company safety standards are being utilized What We Need From You •High School diploma or equivalent. •Eligible to work in the United States. •Successful completion of pre-employment background and drug screen. •Work overtime as required. •Satisfactorily completes training courses as determined by management. •Ability perform the essential functions of the job with or without accommodation. •The commitment to stay safe and to continue to learn and develop. •Satisfactorily completes training courses as determined by management.

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 QA Representative - Floor Support team member provides daily oversight, assistance, and guidance to issues within Parenteral Visual Inspection such as deviation investigations, change control proposals, procedure / batch record revisions, validations, batch disposition, commissioning, and qualification activities. The QA Representative position is essential for maintaining GMP compliance and providing support during preparation for Pre-Approval / General Inspections by various regulatory agencies. Responsibilities: Lead, mentor, and coach Operations and support personnel on quality matters. Ensure regular presence in visual inspection operational areas to monitor GMP programs and quality systems. Collaborate cross-functionally as a core member of a manufacturing process team. Assess and triage deviations that occur within the local process team. Work with Lilly support groups and external partners to resolve or provide advice on product related issues Participate in self-led inspections and provide support during internal / external regulatory inspections. Effectively review and / or redline documents to ensure quality attributes are met (i.e., deviations, procedures, technical studies, validation protocols, change controls, and engineering documents) Support project and process improvement initiatives for plant Process Teams. Basic Requirements: Bachelor's degree in STEM related field, Engineering degree preferred. Additional Skills/Preferences: Previous experience in GMP production environments or Quality Control Laboratories Knowledge and understanding of manufacturing processes and Quality Systems Proven ability to work independently or as part of a team to resolve an issue Strong attention to detail Strong oral and written communication and interpersonal skills Demonstrated decision making and problem-solving skills Technical writing skills Additional Information: Travel: Less than 10% Shift information: Day shift Monday-Friday. May be required to respond to operational issues outside of core business hours / days Overtime may be required Position location: LTC-South Applicant may 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. 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 - $148,500 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

The Quality Assurance Technician performs a variety of quality control tests/inspections at various stages of the process to ensure products are manufactured to conform with all customer and company food safety and quality specifications. Job Responsibilities Enter results of product evaluations and production checks into the computer database, using Microsoft Excel; analyze the data using charts, graphs and statistics, report trends to the QA Supervisor; Publish reports based on the production data and non-compliance to specifications or standards; Collect ingredient samples for analysis, conduct tests, initial and file raw material COA's and report any results out of specification; Conduct laboratory tests using equipment (but not limited to) weigh scales, measurement tools, pH meters, moisture analyzer, yeast gassing test, product scoring evaluations; Clean and maintain laboratory equipment; Perform line process audits for conformance to Standard Operating Procedure (SOP); Conduct process audits and line checks to ensure the manufacturing process is conforming to customer specifications; Examine and document line inspections for compliance to standard operating procedures; Sample product, learn how to prepare samples and conduct bake tests of products, and report a finished product evaluation; Verify production sheets are complete and accurate; review, coach, train staff as needed. Assist in training production employees on properly conducting tests or product sampling; Place non-conforming product on QA Hold; Oversee Hold product to ensure proper disposition is adhered to: Conduct Hazard Analysis Critical Control line verifications; Participate in plant self-inspections auditing Good Manufacturing Practices; Perform daily flour tailings check; Perform weekly scale and thermometer calibration checks; Continuously strives to improve processes to eliminate waste; Leads and contributes to the efforts of Continuous Improvement Teams; Share with relevant staff daily shift recaps, communicate opportunities for improvement or observations Perform other required tasks as assigned. Job Requirements High School Diploma required; Preferred 2-year degree in laboratory science, food technology or related field experience in food quality assurance role(s); Demonstrated knowledge of statistics, SPC fundamentals and laboratory skills; Working knowledge of GMPs, HACCP, Food Safety, SQF requirement; Solid computer proficiency in Microsoft applications such as Excel, Word, and PowerPoint; Excellent verbal, written and presentation communication skills; Ability to function and contribute in a team environment; Bakery or other food industry training is a plus; Regular and predictable attendance.

1st shift (0700 - 1530) Mon to Fri Must have previous isolator experience. This is a mid-level position in the aseptic filling groupwithin the Manufacturing department. It utilizes those with experience and the training needed tomanufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through anumber of job functions and be required to demonstrate increasing skill levels while demonstrating leadershipcapabilities. Major Position Activities & Responsibilities: Become certified for entry into the GMP cleanroom spaceto be able to perform sanitization, stock/replenish supplies, equipment set up,and all related aseptic filling operations. Execute aseptic fill processes using batch records and SOPs. Responsible for verifying the calibration of all relatedequipment and sanitization of supplies to support production. Increasing level of competency in the manufacturing areaprocedures. Assigned job duties will include Aseptic and clean room areas,Component Preparation, Capping, and Packaging. Learn the functions necessary to work in the fill suite.This will include the operation of the associated equipment. Ability to perform tasks with minimal supervisordirection. Provide training of new team members. Able to understand the manufacturing schedule andcoordinate tasks to achieve the schedule. Provide floor leadership in the absence of supervisor or PT3 technicians. Transport and/or dispose of hazardous chemicals. Perform all other duties as assigned. Must immediately notify supervisor if affected byinfectious disease or open lesions on body, as individuals are not permitted toenter manufacturing areas or handle product if these conditions exist. Scope: This position has no direct reports. Background Qualifications: High school diploma or the equivalent. College coursework preferred Minimum 3-5 years including relative aseptic fillingexperience in a cGMP pharmaceutical manufacturing facility. Must possess working knowledge and understanding of GMPcompliance regulations. Must possess knowledge and experience in the asepticfilling process along with equipment cleaning, preparation and assembly.Experience in stopper prep, capping and packaging preferred. As persons in this role are engaged in the openmanufacture of medicinal products, individuals must not be affected by aninfectious disease nor have open lesions on any exposed surface of the body. Must be able to comprehend and follow detailed proceduralinstructions in written and verbal form. Must possess adequate working knowledge of arithmeticfunctions to accurately perform or check calculations required in the productdocumentation. While performing the duties of this job, the employee isregularly required to use their hands and arms. The employee is frequentlyrequired to stand. The employee is occasionally required to sit; walk; stoop,kneel, bend, crouch, or crawl, talk or hear. The employee must regularly liftand /or move up to 10 pounds, frequently lift and/or move up to 50 pounds.Specific vision abilities required by this job include close vision, distancevision, color vision and peripheral vision. Must possess fluent English (written and verbal) skillsin order to read, comprehend, and communicate GMP compliance documentation aswell as Standard Operating Procedures. Computer skills in Microsoft Office such as Word and Excel are a plus.

:** Crown Equipment Corporation, one of the world's largest lift truck manufacturers, offers local support on a global scale with more than 15 manufacturing facilities worldwide and more than 500 retail locations in over 80 countries. Our global sales and service network provides our customers with a local resource for a wide variety of quality material handling equipment, fleet management solutions, warehouse products and support services to meet their needs anytime, anywhere. **Job Posting External** **Primary Responsibilities** + Responsible for the daily tactical quality support of manufacturing components/processes and assembly processes/outputs. + Implement containment actions for non-conformances ensuring impact to production is minimal. + Participate in quality assurance audits. + Maintain/update quality control documents. + Utilize basic inspection equipment and blueprint reading. + Assist in the evaluation and disposition of non-conforming product. + Provide metrics and input for the Quality function to other departments. + Review and verify corrective actions for effectiveness to prevent reoccurrences **Qualifications** + A two-year college degree and/or ASQ Certification as a Quality Technician preferred. + Three to five years' experience in quality and/or manufacturing related fields desirable. + Must have good problem solving skills. + Working knowledge of advanced mathematics, including statistical techniques, SPC, Capability Analysis and Gage R+R is required. + Must be able to apply quality tools for continuous improvement (FMEA). + Must know basic inspection and testing concepts, how to read blueprints and GD+T information. Must possess good communication skills - both verbal and written. + Must possess the ability to work effectively and maintain a professional composure with other employees. + Requires understanding of basic PC computer application skills, including database, spreadsheets and word-processing. **Work Authorization:** Crown will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future, are not eligible for hire. No agency calls please. **Compensation and Benefits:** Crown offers an excellent wage and benefits package for full-time employees including Health/Dental/Vision/Prescription Drug Plan, Flexible Benefits Plan, 401K Retirement Savings Plan, Life and Disability Benefits, Paid Parental Leave, Paid Holidays, Paid Vacation, Tuition Reimbursement, and much more. EOE Veterans/Disabilities

We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there's nowhere like RSM. At RSM, interns work with large and small companies in various industries. They develop strong working relationships with clients built on understanding their businesses and challenges. Interns work on multiple team engagements each year, including several pieces of any particular assignment - not just one part. Working in a mutually respectful team environment helps our associates perform at their best and integrate their career with their personal life. Examples of the candidate's responsibilities include: Understanding clients' needs and expectations, their business and industry, accounting and control systems, employees, company values and industry-related GAAP and GAAS issues Developing an understanding of the RSM audit approach and tools Assessing risks and evaluating the client's internal control structure Performing substantive tests and tests of internal controls to identify and resolve accounting or reporting issues Drafting financial statements under prescribed formats Basic Qualifications: 90 credit hours completed Working towards B.A. / B.S. degree or equivalent from accredited university Accounting major Travel to assigned client locations is required. Must have access to and ability to arrange for use of reliable modes of transportation to those locations A minimum 3.0 GPA is preferred At RSM, we offer a competitive benefits and compensation package for all our people. We offer flexibility in your schedule, empowering you to balance life's demands, while also maintaining your ability to serve clients. Learn more about our total rewards at ************************************************** All applicants will receive consideration for employment as RSM does not tolerate discrimination and/or harassment based on race; color; creed; sincerely held religious beliefs, practices or observances; sex (including pregnancy or disabilities related to nursing); gender; sexual orientation; HIV Status; national origin; ancestry; familial or marital status; age; physical or mental disability; citizenship; political affiliation; medical condition (including family and medical leave); domestic violence victim status; past, current or prospective service in the US uniformed service; US Military/Veteran status; pre-disposing genetic characteristics or any other characteristic protected under applicable federal, state or local law. Accommodation for applicants with disabilities is available upon request in connection with the recruitment process and/or employment/partnership. RSM is committed to providing equal opportunity and reasonable accommodation for people with disabilities. If you require a reasonable accommodation to complete an application, interview, or otherwise participate in the recruiting process, please call us at ************ or send us an email at *****************. RSM does not intend to hire entry-level candidates who require sponsorship now or in the future. This includes individuals who will one day request or require RSM to file or complete immigration-related forms or prepare letters on their behalf in order for them to obtain or continue their work authorization. RSM will consider for employment qualified applicants with arrest or conviction records. For those living in California or applying to a position in California, please click here for additional information. At RSM, an employee's pay at any point in their career is intended to reflect their experiences, performance, and skills for their current role. The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including, but not limited to, education, skills, work experience, certifications, location, etc. As such, pay for the successful candidate(s) could fall anywhere within the stated range. Compensation Range: $30 - $35 per hour

Job Description Job Details Shifts: 6 pm - 6:30 am on a 2/2/3 schedule Medical benefits-eligible first of the month following 28 days of employment. All other benefits-eligible first of the month following 90 days of employment. Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Position Overview: The Quality Assurance Technician conducts quality assurance audits of beverage production products assuring company and customer standards are maintained and product integrity is preserved. Ensure compliance with all applicable regulations. Compliance with applicable standards such as FSMA, Safe Quality Foods (SQF), third party audits, Kosher, and Organic requirements. Consults with management to resolve quality, production, and efficiency problems. Functions as an information resource to various departments when special and critical quality issues occur. Language Skills: English proficiency required. Spanish is a plus. Supervisory Responsibilities: None. Amount of Travel Involved: None. Essential Duties and Responsibilities: Follow all safety procedures and work as safe as possible at all times. Maintain Good Manufacturing Practices (GMP's). Daily operation of equipment which includes Refractometer, pH Meter, Densitometer, Timer, Water bath, Calibrated Thermometer, Zahm Nogel, NoScale, High-Performance Liquid Chromatography (HPLC,) and all other related equipment. Standardizes equipment prior to use, ensures reagents and other materials are available. Performs analysis on products to ensure compliance to customer and regulatory agency guidelines. Performs processing system (line checks) on a timely basis to ensure compliance to specifications. Collect and stores retention samples. Provide production assistance in product audits. Ensures that all products not meeting specified attributes are segregated and held for further review and disposition. Quality testing of temperature of finished product. Ensure that all-pertinent analytical results are entered into the data collections system in a timely basis, immediately informs supervision of any deviations. Review inventory of lab materials and reagents at close of shift to ensure subsequent shifts have adequate supplies. Passes on pertinent information to the following shift. Perform hold and disposition of out of grade product. Provide training to QA Technicians. Participate in Quality System audits. Conduct qualitative and quantitative testing of beverages, syrups, and raw materials through production process. Analyze syrup beverage and/or water attributes. Audit container rinsers, air blowers, filters, and coders to ensure proper operation standards are met. Conducts tests for allergens. Conduct packaging audits and quality inspection of products during production runs and final finished products. Determines or verifies Brix, Acid, Asorbic Acid, pH, Flavor and/or Color of products. Verifies or determines fill levels and weight of products. Perform caffeine, sorbic acid, and benzoic acid testing of products. Participate and contribute to the Quality Management System Programs including Food Safety. Perform cleaning tasks during the shift, at the end of the shift and at shutdowns. Keep work area clean at all times. Conduct swabbing and Allergan Control Test ( ATP) swab. Participate in Safety inspections. Other duties as assigned at the discretion of management. Maintain a positive work atmosphere and interaction with customers, co-workers, and management. Regular and punctual attendance. Work scheduled shift, weekends, and extended hours as required. To perform this job successfully, must be able to perform each fundamental task listed above satisfactorily. Experience for Success: Ability to read, analyze, and interpret general business periodicals, professional journals, and technical procedures. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, and customers. Mathematical skills, ability to calculate figures and amounts such as proportions, percentages, averages, ratios, circumference, and volume. Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several variables. Demonstrates attention to detail, a professional attitude, and produces accurate work product. Familiarity with lab safety and handling of hazardous materials. Good written and verbal communication skills. Adapts to changes in the work environment. Have a strong work ethic and be able to work independently as well as working in a team. Ability to prioritize, multi-task, and adhere to deadlines. Must be proactive. Must have a cooperative attitude. Must have the ability to follow-up. Familiar with Microsoft Excel and Word. Must be able to work in a fast-paced environment. Education and/or Experience: High School Degree, General Education Degree (G.E.D.) or Equivalent., required Bachelor's Degree in Science related field preferred. 1-year relevant experience preferably in Production or Manufacturing environment, preferred Or the equivalent combination of education and experience. Food or Beverage industry experience is a plus. Behaviors & Competencies: Upholds mental, spiritual and physical safety Asks for and provides feedback Holds self and others accountable Supportive and collaborative of team members Participates in self-development and encourages the development of those who report/to him or her and peers Demonstrates flexibility and desire for growth Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to sit; use hands to finger, handle or feel and reach with hands and arms. The employee is frequently required to stand; walk and stoop, kneel, or squat. The employee must regularly lift, pull and/or move up to 10 pounds, frequently lift, pull and/or move up to 25 pounds and occasionally lift, pull and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. Manna Beverages & Ventures is an equal opportunity employer-----M/F/D/V 6 pm - 6:30 am 2/2/3 schedule

Job Details Shifts: 6 pm - 6:30 am on a 2/2/3 schedule Medical benefits-eligible first of the month following 28 days of employment. All other benefits-eligible first of the month following 90 days of employment. Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Position Overview : The Quality Assurance Technician conducts quality assurance audits of beverage production products assuring company and customer standards are maintained and product integrity is preserved. Ensure compliance with all applicable regulations. Compliance with applicable standards such as FSMA, Safe Quality Foods (SQF), third party audits, Kosher, and Organic requirements. Consults with management to resolve quality, production, and efficiency problems. Functions as an information resource to various departments when special and critical quality issues occur. Language Skills: English proficiency required. Spanish is a plus. Supervisory Responsibilities: None. Amount of Travel Involved : None. Essential Duties and Responsibilities : Follow all safety procedures and work as safe as possible at all times. Maintain Good Manufacturing Practices (GMP's). Daily operation of equipment which includes Refractometer, pH Meter, Densitometer, Timer, Water bath, Calibrated Thermometer, Zahm Nogel, NoScale, High-Performance Liquid Chromatography (HPLC,) and all other related equipment. Standardizes equipment prior to use, ensures reagents and other materials are available. Performs analysis on products to ensure compliance to customer and regulatory agency guidelines. Performs processing system (line checks) on a timely basis to ensure compliance to specifications. Collect and stores retention samples. Provide production assistance in product audits. Ensures that all products not meeting specified attributes are segregated and held for further review and disposition. Quality testing of temperature of finished product. Ensure that all-pertinent analytical results are entered into the data collections system in a timely basis, immediately informs supervision of any deviations. Review inventory of lab materials and reagents at close of shift to ensure subsequent shifts have adequate supplies. Passes on pertinent information to the following shift. Perform hold and disposition of out of grade product. Provide training to QA Technicians. Participate in Quality System audits. Conduct qualitative and quantitative testing of beverages, syrups, and raw materials through production process. Analyze syrup beverage and/or water attributes. Audit container rinsers, air blowers, filters, and coders to ensure proper operation standards are met. Conducts tests for allergens. Conduct packaging audits and quality inspection of products during production runs and final finished products. Determines or verifies Brix, Acid, Asorbic Acid, pH, Flavor and/or Color of products. Verifies or determines fill levels and weight of products. Perform caffeine, sorbic acid, and benzoic acid testing of products. Participate and contribute to the Quality Management System Programs including Food Safety. Perform cleaning tasks during the shift, at the end of the shift and at shutdowns. Keep work area clean at all times. Conduct swabbing and Allergan Control Test ( ATP) swab. Participate in Safety inspections. Other duties as assigned at the discretion of management. Maintain a positive work atmosphere and interaction with customers, co-workers, and management. Regular and punctual attendance. Work scheduled shift, weekends, and extended hours as required. To perform this job successfully, must be able to perform each fundamental task listed above satisfactorily. Experience for Success: Ability to read, analyze, and interpret general business periodicals, professional journals, and technical procedures. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, and customers. Mathematical skills, ability to calculate figures and amounts such as proportions, percentages, averages, ratios, circumference, and volume. Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several variables. Demonstrates attention to detail, a professional attitude, and produces accurate work product. Familiarity with lab safety and handling of hazardous materials. Good written and verbal communication skills. Adapts to changes in the work environment. Have a strong work ethic and be able to work independently as well as working in a team. Ability to prioritize, multi-task, and adhere to deadlines. Must be proactive. Must have a cooperative attitude. Must have the ability to follow-up. Familiar with Microsoft Excel and Word. Must be able to work in a fast-paced environment. Education and/or Experience: High School Degree, General Education Degree (G.E.D.) or Equivalent., required Bachelor's Degree in Science related field preferred. 1-year relevant experience preferably in Production or Manufacturing environment, preferred Or the equivalent combination of education and experience. Food or Beverage industry experience is a plus. Behaviors & Competencies: Upholds mental, spiritual and physical safety Asks for and provides feedback Holds self and others accountable Supportive and collaborative of team members Participates in self-development and encourages the development of those who report/to him or her and peers Demonstrates flexibility and desire for growth Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to sit; use hands to finger, handle or feel and reach with hands and arms. The employee is frequently required to stand; walk and stoop, kneel, or squat. The employee must regularly lift, pull and/or move up to 10 pounds, frequently lift, pull and/or move up to 25 pounds and occasionally lift, pull and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. Manna Beverages & Ventures is an equal opportunity employer-----M/F/D/V

Pay: $33/hr Set-up and calibrate equpment for operation and testing to specifications May adjust filler and labeler equipment with proper parts and settings for products to be portioned Assemble containers and components for portioning process. Assure they are correct Conduct housekeeping tasks following set-up (including disinfection and autoclaving, as required) to assure cleanliness of assembled equipment Sign in for bulk containers and lot number verification to paperwork Order and stock necessary supplies to suppport operations Portion materials into containers under safe production conditions Assemble and don required safety equipment specified by protocol Follow-up on inventory shortages Verfiy quantities for accuracy (cases vs box vs EA) Set up, operate, and troubleshoot all automated labeling and bagging equipment Check and update mainframe systems and SAP as required Maintain records for accountability and procedure traceability Document all data for traceability of bulk and components Record all tests, measurements and calibrations required during operations Record all calculations and conversions necessary to process paperwork Clean and maintain equipment/work area to assure product integrity Clean packaging equipment, test equipment, tools-disassembling if required Clean workstations and restock all materials storage areas. Document cleaning on area/hood cleaning log Process Improvement Shares ideas for improvement including common sense ways to save money Participates in testing and implementation of changes Wear the appropriate personal protective equipment inclusive of steel-tied safety shoes Maintain, clean, and keep safe all work areas and equipment Maintain personal protective equipment Take necessary steps to assure we provide our customers with the highest quality possible Immediately report any situation that could compromise safety or quality Miscellaneous duties and tasks as assigned Exemplary attendance and adherence to schedule BASIC QUALIFICATIONSEducation: HS Diploma, GED or HSED required Desirable: College course work in chemistry or 6 months previous experience weighing chemicals is preferred Knowledge and Skills: Basic math-including metrics and conversions, knowledge of safety rules, FMP, SOP's, UOP's, mechanical inclination, eye-hand coordination, communication skills, legible lhandwriting, mechanical skills, teamwork, problem solving, able to train others, ability to use hand and air tools, pumps, and an electronic scale and to operate material handling equipment. Ability to identify problems, ability to read instructions and understand oral and written instructions.

**_What Quality Assurance contributes to Cardinal Health_** Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Assurance develops and implements a compliant and cost-effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and procedures and ensures that all products and services are properly reviewed for quality and documented. **_Job Summary_** + Reports to Manager, Quality Assurance. + QA Principal Specialist is responsible for ensuring quality standards and procedures are followed and will oversee quality monitoring and assurance to ensure that all products manufactured are of the highest quality possible. Inspection and quality assurance activities to meet specifications and quality standards for variety of in-process and finished products. + Authorized to inspect products to ensure the required quality standards are met. **_Responsibilities_** + Inspecting and sampling of product throughout the manufacturing process. + Establish and maintain quality control procedures. + Assist in determining types of tests to be performed as well as documentation and reporting requirements. + Interact regularly with manufacturing and service functions to establish quality standards for raw material, work in process, and finished products. + Champion Quality, GMP compliance and EHS/Radiation Safety practices. + Develop and lead GMP/GDP training of all employees. Follows/ mentors GDP/GMP requirements. + Actively partner with plant management and personnel in troubleshooting quality deficiencies and implement corrective measures to eliminate quality problems. + Assists in the release of the final product in compliance with applicable regulations (FDA, EU, etc.) and marketing authorizations. + Responsible for the review and dispositioning of incoming raw materials and components. + Assures quality events are complete and accurate and resolved in a timely manner that meets the expectations of applicable quality agreements. Responsible for approval of minor Quality Events. + Ability to network across business and functional units to achieve positive outcomes. + Able to challenge, appropriately, the design, conduct, and reporting of GMP activities including metrics and annual reporting. In that context, has the knowledge of the production process of the product. + Understands technical/release product issues and evaluate their potential impact on product quality and compliance. + Provides ideas for continuous improvement of the GMP Quality Management System. + Escalates complex issues to management in a timely manner. + Prioritizes and ensures work is delivered in an efficient way. + Performs other job duties as assigned. **_Qualifications_** + Bachelor's degree in related field, or equivalent work experience, preferred. Advanced Degree may be preferred + 4-8 years' experience in related field, preferred **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives + Completes work independently receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **Anticipated salary range:** $79,700 - $113,800 **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 2/1/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

**Quality Technician Indianapolis (onsite)** **_Come join a team that makes a difference here and around the world!_** **_Peerless Pump Company, an Indianapolis based subsidiary of Grundfos_** _,_ is seeking an experienced **Quality Technician** to join its Quality Assurance team. Founded in 1923, Peerless Pump Company is a US-based manufacturer of horizontal and vertical centrifugal pumps for fire, industrial, and municipal applications. With pump installations in 145 countries, Peerless is globally recognized for engineering tough, reliable, and versatile pump solutions with extensive flow and pressure capabilities. From our production facilities in Indianapolis and Houston to our service centers in Lubbock and Fresno, Peerless pumps are designed to protect people and property from fire and to bring water where it's needed most. Our product quality is second to none, but it's our people who've made us Peerless for over 100 years. Our legacy of innovation is fueled by attracting, training, and retaining employees from diverse backgrounds. With competitive benefits and a strong emphasis on development, growth, and innovation, Peerless employees come seeking a job but stay to build a career. **What is the job about?** The Quality Technician is responsible for Quality Control support of products, processes, and assistance with Continuous Improvement programs. This position reports directly to the 1st shift Quality Supervisor and will operate daily out of the **Indianapolis, IN** facility (primarily Mon-Fri). **_Relocation for this position cannot be supported and qualified candidates must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future. Sponsorship is not available for applicants for US Work visa status for this opportunity (no sponsorship is available for H-1B, L-1, TN, O-1, E-3, H-1B1, F-1, J-1, OPT, CPT or any other employment-based visa._** The salary range for this position is $53,575.00-$72,883.00. Individual pay will be determined based on market location and the candidate's profile. The range listed is just one component of Peerless/Grundfos's total compensation and benefits package for employees. Total compensation includes paid time off, paid holidays, merit increases, bonuses, and employee stock purchase programs, etc. Peerless/Grundfos salary rates are benchmarked and reflect the target for new hire salaries for the position in Indianapolis, Indiana. **_Your main responsibilities:_** + Provide Shop Support for incoming parts, assembly and establish root cause; + Process Quality Transactions. + Operate Coordinate Measurement Machines (CMM), use hand gauges, go/no go tooling to determine part compliance to company drawings. + Quality planning, including the establishment and maintenance of procedures for quality related tasks and processes; contribute to Material Review Board meetings. + Assist in problem-solving efforts both internal and external facilities. + Develop and implement quality systems for new products, parts including inspection and layout. + Communicate directly with suppliers for disposition of material and to process vendor corrective actions requests; + Work with suppliers to achieve capable products and processes. + Perform work, promote teamwork and communicate in conjunction with our culture and corporate standards (Safety/Environmental, Quality, Continuous Improvement, Communication, Internal Controls, etc.) + Occasionally perform Quality System audits (internal & external) **_Key Success Factors_** Computer competency with Microsoft Office Suite, digital pictures, and e-mail. Practical knowledge of using Coordinate Measurement Machines (CMM) **Your background** **_We imagine that you have:_** + High School Diploma, GED/HSE/HiSET or equivalent *required + Associate's degree in Engineering/Science *much preferred. + 3-5 years of Quality Measurement Inspection experience *much preferred + Operating experience using CALYPSO software on Zeiss Contura CMM desired. *much preferred + Veterans with MOS experience related are strongly encouraged to apply. *much preferred + **_Competencies_** + Team Player a must with strong communication, organizational, and written skills. + Strong blueprint reading skills including GD&T and proficient with measuring equipment. + Knowledge: Process improvement techniques. + This position requires the incumbent to stand for extended periods of time, frequently grasp tools, bend, stoop, crouch, twist, reach, stand, and walk when performing duties. + Able to work in non-climate controlled factory and lab environment. **What's in it for you?** **What are your goals?** Here at Peerless it's our mission to enable you develop and fulfil your aspirations, both career and personal. You'll find that your fresh ideas will be welcomed and make a difference in how we conduct our business. **_In addition, your day-to-day benefits as a regular, full-time employees include:_** + 5 paid holidays; paid time off for volunteering; up to 20 paid vacation days a year accrued by date of hire. + Competitive medical, dental, and vision plans; 401(k)-match program. + Annual bonuses, parental support, engaging team buildings. + Diverse, inclusive environment with employee-led forums offering colleagues a safe place to connect and share openly. + Long-term career development with regular dialogue, as well as continuous learning and development opportunities. + Access to the modern Grundfos Academy to pursue further both personal and professional development. + Diverse, inclusive environment with employee-led forums offering colleagues a safe place to connect and share openly. **_Do you want to learn more?_** If you have questions or would like to know more about this position, please contact Recruiter at ************************ If this job sounds interesting, please send your resume and cover letter by clicking " **Apply** ". **_We look forward to hearing from you._** If you would like to dig deeper into the Peerless universe, please visit us and check out why our employees are Peerless. **I am PEERLESS!** **_Peerless participates in E-verify and is an Affirmative Action, Equal Opportunity Employer. All positions subject to post offer drug screening and background checks._** Peerless needs and welcomes professional people from all corners and backgrounds by providing equal employment opportunities for all applicants and employees and prohibits discrimination and harassment of any type. Employment decisions at Peerless and Grundfos are based on business needs, job requirements, and individual qualifications without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. All qualified applicants are encouraged to apply. Learn more about your rights as an applicant and pay transparency. Accommodations are available for applicants with disabilities. Information at a Glance **Job details** Workplace: Onsite Position Job Location: Indianapolis, Indiana, United States Contract Type: Full-Time Employment Type: Regular

For over 65 years, pharmaceutical and biotech companies have partnered with Simtra BioPharma Solutions (Simtra) to bring their sterile injectable products to market. Simtra is a world-class Contract Development Manufacturing Organization with facilities in Indiana, US and Halle/Westfalen, Germany. We offer a wide-range of delivery systems including prefilled-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, at Simtra, there is a strong emphasis on quality and continuous improvement. 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. In addition to unmatched expertise and experience, we offer a uniquely collaborative approach. Clients look to Simtra as an extension of their own companies. It is very rewarding industry to work in. Our teams are driven to help clients scale, innovate, and bring-life changing medicines to patients worldwide. Your role at Simtra BioPharma Solutions: The Incoming Quality Control Technician plays a vital role in the safety of patients and overall success of the manufacturing process by inspecting the incoming products and raw materials under the supervision of the Quality Lead. The working hours for this role are Monday-Friday 7:00am-3:30pm. What you'll do: Perform a variety of physical, functional testing, and inspection analysis on components that support the company's quality manufacturing program Sample raw material and components for inspection, QC analysis, and sample requests Perform raw material verification on incoming material used in production Operate and maintain a variety of laboratory equipment Maintain a good attendance record Perform existing procedures with recommendations for improved efficiency Write, review, and revise SOP's when needed. Write coherent and complete reports Maintain an accurate and up-to-date training history Train others on skills required Act as a role model for the laboratory Strong team player and willingness to help others Ability to work independently with minimal supervision What you'll bring: A High School Diploma or GED equivalent Previous QC and/or QA experience preferred Excellent Documentation Skills Excellent Communication Skills Computer Skills including word and excel Organizational and Detail Oriented skills Physical / Safety Requirements Must wear appropriate PPE as required for various manufacturing areas when applicable. Must be able to gown qualify for Grade A/B areas when applicable. Duties will require overtime work, including scheduled weekend shifts Use of hands and fingers to manipulate office equipment is required Position requires standing for long hours but may require sitting for periods of time. #IND-USOPS Equal Employment Opportunity Simtra is 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: ********************************************************************************

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

Description & Requirements In today's dynamic regulatory environment, public companies must uphold the highest standards of financial integrity and IT risk management. As an SEC Auditor, you will play a critical role in ensuring compliance with SEC regulations by performing financial statement and IT audits. You will help clients identify and manage business and technology risks, strengthen internal controls, and support the integrity of financial reporting What You Will Do: * Execute integrated audits of financial statements and IT systems for SEC registrants, ensuring compliance with PCAOB and SEC standards. * Perform audit testing on financial statement accounts such as cash, accounts payable, and fixed assets. * Assess and test internal controls over financial reporting (ICFR), including IT general controls (ITGCs) and application controls, in accordance with SOX 404 requirements. * Conduct walkthroughs and substantive testing of financial statement accounts, disclosures, and related IT processes. * Evaluate the design and operating effectiveness of IT controls for applications, databases, operating systems, networks, and reporting tools. * Collaborate with client teams to understand business processes, IT environments, and control frameworks; obtain audit evidence; and analyze testing results. * Draft audit findings, management letter comments, and recommendations for remediation. * Participate in discussions with clients and leadership regarding audit results and emerging risks. * Stay informed on SEC, PCAOB, and IT risk trends impacting clients. * Deliver an exceptional client experience through timely and responsive communication. Minimum Qualifications: * Bachelor's degree in a related field, preferably in Management Information Systems or Computer Science. * Eligibility to sit for the CPA exam, meeting educational requirements as defined by the applicable state board of accountancy. * Proficiency in Microsoft Office Suite. * Ability to travel for client engagements and internal meetings, including overnight stays. Preferred Qualifications: * Masters degree in a related field, preferably in Management Information Systems or Computer Science. * Prior experience or internships in public accounting with exposure to SEC or IT audits. * Eligibility to sit for the CISA exam or CISA certification. #LI-IND #LI-JB1