Quality control analyst jobs in Duluth, MN

Quality Control Active Cabinet OBJECTIVE: Responsible for quality control of Active Cabinets. Ensures cabinets and related components meet company and customer quality standards throughout the entire production process. Ensures electrical safety in the Active Cabinet Test Area is to OSHA and company standards. Develops and documents the Corrective action process utilizing root cause analysis and troubleshooting techniques. Supports the calibration of all test equipment utilized for the Active Cabinet production process. POSITION RESPONSIBILITIES Active Cabinet Test Skilled in interpreting technical drawings, blueprints, and quality specifications to guide and meet project requirements. Knowledge working with 240V AC and -48V DC power systems to turn up cabinets for test. Follow process instructions and quality guidelines to complete Functional Test of Active Cabinets. Supporting internal and external audits to ensure compliance with company, industry standards (e.g., ISO), and relevant safety regulations. Actively participating in problem-solving activities, root cause analysis, and continuous improvement efforts to address and resolve recurring quality issues. Utilize various measuring devices to perform routine measurements and tests. Troubleshoot and correct Test Failures. Document Test Failures and Train Assembly Technicians on Test Failure modes. Learn simple coding to develop Functional Test programs/procedures for new Active Cabinets. Ability to work independently and accept work direction from Manufacturing Engineer Team, Leads, Supervisor and co-workers. Performs electro-mechanical assembly when needed. Collaborate with trainers to support the onboarding and retraining of employees to quality standards and procedures. Assist in building active cabinets when there is no quality testing to conduct. Quality Focus Inspects finished cabinets to ensure they comply with quality specifications and technical drawings/blueprints. Perform tests and use special equipment to ensure package and product quality Operate all manufacturing equipment efficiently and safely, related to Active Cabinets production Maintaining detailed and accurate records of all inspections, test results, and quality data. Identifying defects or non-conformances and reporting findings to production teams, supervisors, and management. Follow process guidelines and expedite quality concerns to management Demonstrate flexibility and prioritization of work orders Work with production/maintenance as necessary to support Active Cabinet department Following Standard of Operations Procedures (SOP s) and WIO s Inspect, test, or measure materials or products being produced Utilize correct measuring tools for product build and quality inspections. Accept or reject finished items according to quality standards and guidelines Remove all products and materials that fail to meet specifications Monitor quality standards for all manufactured products Record the results of inspections through test reports. Report inspection and test data Detailed focused to identify flaws and/or deviations from design specifications Ensure clean work area through good housekeeping practices throughout shift Assess and verify the accuracy and functional statues of measuring equipment. Proficiency in quality control and corrective action, non-conforming products, processes, and equipment. COMPETENCIES: Initiative: Dealing with situations and issues proactively and persistently, seizing opportunities that arise. Brings issues to the attention of appropriate personnel as needed Offers ideas or suggests modified approaches to address current situations or issues. Undertakes straightforward tasks that go beyond the job's routine demands (e.g., helps others when own work is completed), without being prompted. Problem Solving: Identifying problems and the solutions to them. Identifies alternate solutions, considering applicable precedents. Identifies optimal solutions based on weighing the advantages and disadvantages of alternative approaches. Evaluates the effectiveness and efficiency of solutions after implementation. Attention to Detail: Working in a conscientious, consistent and thorough manner. Seeks out others to check or review own work for accuracy and completeness. Verifies assumptions and information before accepting them. Review all relevant information or aspects of a situation before taking action or making a decision. Teamwork: Working collaboratively with others to achieve organizational goals. Initiates collaboration with others. Assumes additional responsibilities to facilitate the achievement of team goals. Seeking input from other team members on matters that affect them. POSITION REQUIREMENTS: Three plus years of Quality Control experience or relevant experience preferred Five plus years of manufacturing, or light electrical assembly is preferred Strong attention to detail Ability to identify colors, and strong eye-hand coordination. Operating testing instruments preferred General assembly experience, Basic electric testing concept Ability to work with a wide variety of part sizes and weights Extensive dexterity and hand, wrist, and arm movement Ability to work in a fast-paced environment. Ability to read and understand written instructions, basic arithmetic skill and electrical schematics. Strong communication and problem-solving skills. Intermediate skill level in both Microsoft Office Suites and computer navigation Continuous improvement mindset, Lean Sig Sigma training, yellow belt preferred. Change Management mindset Safety mindset Role requires standing or walking for extended periods of time Able to lift up to 50 lbs. Forklift Certified, is a plus BENEFITS for full time: Comprehensive Medical, Dental, and Vision benefits. 100% company paid Short-term and Long-term disability insurance coverage. 100% company paid Basic Life and Accidental Death and Dismemberment (AD&D) insurance coverage. 100% company paid Business Travel Accident (BTA) insurance. 100% company paid Employee Assistance Program (EAP). Additional voluntary benefits are offered. 401K plan: Maximum match is 4.5% of the first 6% of contribution. Employee Stock Purchase Plan: Clearfield's Time Off Policy includes Personal Time Off (PTO) beginning at three weeks annually. PTO is accrued on the first of the month starting on day of hire. In addition, nine paid holidays per year. Hourly Salary Range: Starting rate $ 26.00 per hour, Retention Bonus, and Semi-Annual Production Bonus An Offer of employment will be extended at a level consistent with the experience and qualifications of the candidate. This information reflects the anticipated salary range for this position at the time of posting. The salary range may be modified in the future and actual compensation may vary from the posting based on various factors such as geographic location, work experience, education and/or skill level.

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. AUDIT ASSOCIATE At RSM, associates work with large and small companies in various industries. They develop strong working relationships with clients built on understanding their businesses and challenges. Associates 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: Minimum B.A / B.S. degree or equivalent from an accredited university by the time employment commences 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 Ability to travel up to 25% A minimum 3.0 GPA is preferred Preferred Qualifications: Excellent written and verbal communication skills Strong computer skills, including MS Office Ability to work as an effective member of a team Motivated to work in a fast-paced environment Client focused Ability to multitask 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 in accordance with the requirements of applicable law, including but not limited to, the California Fair Chance Act, the Los Angeles Fair Chance Initiative for Hiring Ordinance, the Los Angeles County Fair Chance Ordinance for Employers, and the San Francisco Fair Chance Ordinance. For additional information regarding RSM's background check process, including information about job duties that necessitate the use of one or more types of background checks, click here. 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: $61,600 - $73,500

What we offer Starting pay at $29.43 per hour Benefits begin 30 days after hire INSERT BONUS HERE Ask about our Hourly Bonus Program Fully customizable medical plans (HRA, HSA, FSA), 5 different carrier choices + Prescription (Rx) card Full suite of additional plans: vision, dental, life, disability, adoption/family planning reimbursement, childcare, parental leave LiveWell lifestyle/well-being discount and rewards program (for example, $50 subsidy for fitness tracker) 401(k) matching + extra 3% freebie company contribution Employee Perks include FREE Product & Swag Business Resource Groups (BRGs) Award-winning Ownerversity learning & development resource library Employee Assistance Program (EAP) for mental health support Location New Ulm, Minnesota - Home of VELVEETA Work Schedule Monday - Friday work week, 2nd shift/Afternoons Essential Functions & Responsibilities The Senior Rotating Analyst is responsible for all finished product testing. Occasionally may also be responsible for blender testing, blender standardization, problem solving and in process testing. Works from brief verbal and complex written instructions and is expected to exercise individual judgment and resolve questions independently in a timely manner. When 1 to 2 lines are running, Analysts work alone - therefore they must exercise good judgment with all aspects of in process and finished product testing when issues arise. Rotating Analysts are expected to work between areas and help out when needed. Must have good written and oral communications skills. Work requires mathematical skills including fractions, decimals and knowledge of personal computers. Work is expected to meet the high standards of Kraft Heinz, AOAC and legal parameters. Must be able to perform sensitive adjustments of complex controls requiring skill in fine tuning of the process variables. Job Responsibilities: Regular Moisture/Finished Product Testing: Performs five-hour vacuum moisture tests or NIR moisture test on every hourly sample for every product run daily. Responsible for all accurate recording of data and documenting out of standard results. Performs recheck testing on all samples out of standard and special samples. Calculates all results by use of personal computers and makes decisions accordingly. Performs moisture and fat tests on raw material cheese as requested by supervisor. Responsible for cleaning, labeling and preparation utensils and equipment. Responsible for cleaning and maintaining work area at all times. Responsible for performing pH tests on hourly samples, as specifications require. Accountable for all retests and monitoring of equipment. Responsible for performing extraneous tests as required on finished product and raw materials. Projects as requested by supervisors. Fat Testing: Performed tests, requires safety awareness at all times due to the chemicals being worked with. Safety eye wear, apron and gloves are mandatory in this area. Performs fat tests on samples as required by specifications. Performs fat tests on blender samples on an as needed basis. Responsible for all special fat testing required on natural cheese samples. Performs fat testing on ingredients and liquid loads as specifications require. Accountable for all data entry, calculating and recording of fat results. Accountable for any data that is out of standard and must be retested and/or special samples received. Responsible for knowledge of all fat testing procedures, techniques and methods as prescribed by Kraft Heinz, AOAC and legal standards. Salt and Lactose Testing: Preforms tests on samples as required by specifications. Accountable for all data entry, calculating and recording of all Salt and Lactose results. Accountable for any data that is out of standard and must be retested and /or special samples received. Responsible for knowledge of the procedures, techniques and methods as prescribed by Kraft Heinz, AOAC and legal standards. Responsible for all critical control point checks performed in areas. Responsible for cleaning and maintaining work area and equipment at all times. Rapids Area: When required, responsible for accurate testing of blend samples for moisture and fat on a timely basis. Methods used include NIR, vacuum oven and Roccal Method. Concise and quick decisions must be made based on these results. Responsible for solving blender errors/problems using G40 personal computer. Responsible for activating, adding and deleting liquid load data in the G40 for proper blender standardization. Responsible for maintaining and operating the G40 back up and special standardization programs on the personal computer. Prepares in process testing tools for each blender standardization. Maintains an ample supply of folded, numbered and weighed foils daily. Responsible for knowledge of all methods, techniques and procedures according to Kraft Heinz, AOAC and legal standards. Responsible for maintaining and cleaning work area at all times. Hot Tests/In-Process Testing: When required, performs in-process testing on certain blenders on a timely basis. Accountable for all decisions made for corrections at the cooker to adhere to 100% compliance for every product. Timely decision making skills are utilized. Utilizes various methods for testing including a vacuum oven and NIR units. Performs in process testing on wet mix and liquid loads. Responsible for additions and data reporting. Personal computers and mathematical skills are used to compute data. Utilizes a personal computer for computing calculations on all vacuum tests. Responsible for an in-process test on certain blenders of standardized product. Communicates correction/additions to the cook room cooks. Responsible for checking all corrections. Responsible for knowledge of proper methods, techniques and procedures according to Kraft Heinz, AOAC and legal standards. Accountable for maintaining and cleaning of work area at all times. Responsible for all critical control point checks performed in areas. Responsibilities: Work on programs and other requests. Record cooker steam out results and grade the steam out pads. Test standardized cream, cream whey and WPC as required by the specifications and record results. When needed, performs blender checks as required. Involves retesting blender samples for moisture and fat. Responsible for the salvage of blender, moisture, fat, NIR, naturals and raw material samples. Miscellaneous testing required on ingredients as to adhere to the specifications. Preparation of solutions for miscellaneous testing (pepsin, acid pH). Responsible for cleaning five-hour ovens centrifuge, grading room buckets, fat bottles, beakers, moisture pans and all other lab dishes and glassware. Prepares fat (Roccal) solution and fills acid bottles. Monitoring and cleaning of water bath and acid dispensers. Monitor the hazardous waste that is produced by some of the testing and dispose of it properly. Responsible for air exposures and swabs for start-up, qualifications and regular production. Responsible for entering COA results into SAP for incoming ingredients. Responsible for net content scale and weight verifications. Maintenance: Responsible for all thermometer checks in the Laboratory. (Primary, secondary and calibration thermometers) for start-up. Responsible for all balance and scale calibrations in Laboratory for start-up. General Requirements: Computer skills, operating knowledge of SAP, Quality Suites, Excel, demonstrated math skills (including decimals, fractions, divisions) and decision-making skills. Person must be willing to train in other areas of the Lab (Special Testing, Bacti, etc.) or take upgrading when offered. Safety: Follow all OSHA and safety procedures. Working with acids, heat and glassware are a safety hazard. Knowledge of proper treatment, response, and care and preventative measures required. Equipment Operated: Primarily responsible for the safe and efficient operation of NIR units, G40, 6500, personal computers, vacuum ovens, centrifuges, water baths and scales. Value of Material: Lack of responsible decision making skills and inattention to required duties may result in substantial monetary losses, delays or inconveniences. The results not are readily detectable until 10-20 hours later. Lifting Requirements: Moderate - Lifting requires handling materials up to 20 lbs. frequently or less and up to 45 lbs. infrequently. Working Conditions: Fair - Standing throughout the shift required of several job areas. Hazards are present when working with Laboratory testing reagents and disposals. Work may be a fast pace and hectic; therefore, cautions and common sense must be exercise. Exposure to noise and unfavorable working conditions (such as wet slippery floors) at times. Training: The Senior Rotating Analyst will have a three phase training period; 30 days, 3 months and 6 months. An evaluation will be done after each phase. The successful Senior Lab Analyst will be able to demonstrate the following competencies throughout each phase of training: 30 days Decision making skills Technical aptitude Math and computer skills 3 months Effective communications skills Dependability Analytical skills 6 months Self-confidence Team working skills Versatility This job description is not designed to cover or contain all duties or responsibilities that are required of the role. Duties or responsibilities may change or be added with or without notice. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #INDMFGH Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family's needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families. You'll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example: Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments Social - Paid Time Off, Company Holidays, Leave of Absence, Recognition, Training Emotional - Employee Assistance Program , Wellbeing Programs, Family Support Programs Financial - 401k, Life, Accidental Death & Dismemberment, Disability Location(s) New Ulm Plant Kraft Heinz is an Equal Opportunity Employer that prohibits discrimination or harassment of any type. All qualified applicants are considered for employment without regard to race, color, national origin, age, sex, sexual orientation, gender, gender identity or expression, disability status, protected veteran status, or any other characteristic protected by law. Applicants who require an accommodation to participate in the job application or hiring process should contact ***********************.

Salary range: $78,000-$102,000 Full time, Exempt The Quality Control Scientist provides technical expertise to research and develop new, or improve existing analytical processes to evaluate oncolytic viral and viral vector based therapeutics, pipeline assets, and to improve overall efficiency in QC processes towards commercialization. Key responsibilities include performing and supporting analytical testing, method development and validation, and quality control (QC) release activities in compliance with cGMP and regulatory standards. The QC Scientist will work closely with internal teams to ensure the timely release of materials, intermediates, and final products used in various phases of drug pipeline. Supervisory Responsibilities None Duties and Responsibilities Method Development and Product Testing * Perform GMP testing of various sample types, which may include raw materials, in-process samples, cell banks, viruses/viral vectors, and final drug products using molecular, biochemical, and/or cell-based analytical methods. * Execute assays including qPCR/dPCR, flow cytometry, ELISA, infectivity/titer assays, vector genome copy number determination, potency assays, and detection of production contaminants * Support method development, qualification, validation, and transfer for novel analytical methods specific to various biologic/cell and gene therapy platforms. * Participate in stability studies, and trending of analytical data to ensure product consistency and compliance. * Review and interpret analytical data, ensuring data integrity and alignment with specifications, SOPs, and regulatory requirements. * Support investigations of deviations, OOS/OOT results, and implementation of CAPAs. * Author, review, and revise controlled documents, including test methods, protocols, reports, and SOPs. * Collaborate with QA, Manufacturing, Process Development, and Regulatory teams to support product release and regulatory filings (e.g., IND, BLA, IMPD). * Maintain laboratory equipment and ensure calibration, qualification, and preventive maintenance activities are completed as required. * Uphold GMP compliance, data integrity, and safety practices in a dynamic, fast-paced environment. * Additional duties as assigned Education and Experience * Advanced degree (Ph.D. and/or relevant degree highly desirable) and 2+ years of related work experience, or a Bachelor's degree with 5+ years of related work experience * Minimum of 1 year working in biologics drug product role with a good understanding of working with a defined QMS and assay qualification. * Experience with setting up, supporting, and troubleshooting multiple pieces of drug product analytical equipment. * Experience with advanced QC techniques, including qPCR/dPCR, flow cytometry, potency assays, and/or ELISA. * Experience conducting process characterization, analysis and development with minimal supervision. * Knowledge of ICH Q2(R2), FDA/EMA regulations for ATMPs, and cGMP testing principles. * Excellent analytical, documentation, and communication skills. Physical Requirements * Prolonged periods of standing at laboratory benches. * Prolonged periods of sitting at a desk and working on a computer. * Must be able to lift up to 15 pounds at times. Benefits * Group Healthcare Plan, including company paid dental and vision. * Short- and long-term disability, life and AD&G insurance. * Simple IRA with employer match * Educational assistance program * Holiday and PTO

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Sign on Bonus $5000 if hired. Your Role: In this role your tasks will include, but are not limited to: * Produce chemicals (including existing items, new products, and custom requests) while actively ensuring quality specifications are met for all final products. * Set up and operate production equipment, run necessary analytical tests, and ensure the functioning of all related systems. * Accurately document all production results, observations, and deviations as defined by department guidelines, and create/maintain calibration logs and training records. * Review, suggest changes, and approve protocols, and serve on committees focused on improving departmental and company performance (safety, quality, inventory, output, costs). * Independently recheck results for out-of-specification issues, select and implement alternative test methods, and coordinate with management for assistance when necessary. * Lead small production groups, manage shift changeovers, train new employees, and assist in cross-training current staff to maintain knowledge parity. * Assist the supervisor by helping with scheduling duties, assigning tasks, ensuring completion, and leading the department during the supervisor's absence. * Maintain an exemplary attendance record and schedule adherence, demonstrating the ability to work independently and accurately in a fast-paced environment. * Shift/Hours: 12-hour night shift, 6:00 PM - 6:30 AM - 2/2/3 schedule (M/T on, W/R off, F/S/S on, M/T off, W/R on, F/S/S off, repeat). Physical Attributes: * Wear appropriate PPE. * Lift up to 50 lbs. * Use close vision, distance vision, color vision, peripheral vision, depth vision and adjust focus. * Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, or crouch for long periods of time. Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biology, Chemical Engineering, Electrical Engineering, or other Life Science or Engineering discipline. OR * High School Diploma or GED and 4+ years of work experience in a chemical production, laboratory or chemical engineering role. Preferred Qualifications: * Experience with ISO and quality systems. * Ability to read and understand written protocols. * Strong problem solving and equipment troubleshooting skills. * Strong oral and written communication skills. * Advanced knowledge of chemistry and math. * Strong mechanical and technical aptitude. * Experience with ISO and quality systems. * Experience operating a forklift. RSREMD Pay Range for this position: $27/hr - $46/hr The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

The R&D Technician assists the Ravin and Centerpoint Product Managers in the testing, evaluation, and set up of new products. This position is in Superior, WI. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform product testing following established procedures. Accurately document product assessment and testing. Identify and conduct root cause analysis of product failure. Maintains a clean and organized work area to facilitate product testing. Review CAD drawings. Access prototype assembly for potential production assembly challenges. Create Standard Operating Procedures (SOPs) for the production team. Proficiency in MS Office (Word, Excel) Maintain a clean, organized, and safe work environment by adhering to safety procedures and regulations Keeps a positive attitude and good work ethic for other employees to emulate Follow detailed instructions, processes, and procedures Comply with policies, guidelines, intellectual property, and regulatory requirements Report problems with quality, processes, equipment, and materials to Management Communicate effectively with Management, Engineering, and Quality Assurance. Any other duties as assigned JOB RELATIONSHIPS: This position will report to the Product Managers. Position requires the ability to work effectively with other disciplines including Design Engineers, Marketing, Sales, Manufacturing Operations, Purchasing, QA, Customer Service and Warranty. ESSENTIAL DUTIES AND RESPONSIBILITIES: Follow detailed assembly instructions (SOP's), processes and procedures Comply with policies, guidelines, and regulatory requirements Report problems with quality, processes, equipment, and materials to Management in timely manner Maintain a clean and organized work area to facilitate manufacturing functions PHYSICAL DEMANDS: The R&D Technician may be subject to standing long hours with repeated bending, lifting (20-50 pounds) and squatting. The R&D Technician must be adept at fine motor skill manipulation with both hands. In addition, the Level I Production Assembler must write, speak, and understand English. Reasonable accommodations may be made for individuals with disabilities to perform the physical demands and essential functions of this position.

Work Arrangement: Hybrid or In-office A Day in the Life A typical day as an Assurance Associate in the Mankato office is performing audit, review, and compilation procedures for clients. Works with all phases of client engagements including workpaper, financial statement, and audit report preparation. Assists with planning and scheduling engagements. The role may also include the following: * Participates in client engagement meetings to determine timelines and objectives of an audit. * Performs audit, review, and compilation procedures for clients. * Analyzes and prepares trial balances, complex financial statements and audit reports using audit software programs, Word, and Excel. * Performs schedule computations of accruals, property, and equipment, calculates depreciation expenses and long-term debt schedules for clients. * Reconciles accounting information to control accounts. * Assists with financial analysis upon completion of fieldwork to improve client internal controls and accounting procedures. * Assists in proofing financial statements and other accounting documents. * Maintains awareness of general business trends and issues and applies that knowledge to client issues and solutions. * Performs field work at client locations as necessary. * Attends training seminars, professional development, and networking events. * Ensures timely and accurate performance on assigned projects. * Maintains compliance with project budgets, turnaround times, and deadlines. Who You Are * Bachelor's degree in accounting required. * 2-3 years of experience auditing in a public accounting setting. * Valid Certified Public Accountant license or working towards obtaining CPA license preferred. * Knowledge of auditing standards and accounting principles. * Demonstrates critical and analytical thinking skills. * Ability to communicate clearly in writing and verbally. * Ability to work on multiple projects and meet deadlines by setting priorities with work projects. * Ability to establish and maintain effective working relationships with co-workers and clients. * Proficient with computers, Microsoft Office (Word and Excel) and use of various software packages. Must be authorized to work in the United States now or in the future without visa sponsorship. Making an Impact Together People join Eide Bailly for the opportunities and stay because of the culture. At Eide Bailly, we've built a collaborative workplace based on integrity, authenticity, and support for one another. You'll find opportunities for education and career growth, a team dedicated to your success, and benefits that put your family's needs first. Hear what our employees have to say about working at Eide Bailly. Compensation $64,000 - $70,000. Our compensation philosophy emphasizes competitive and equitable pay. Eide Bailly complies with all local/state regulations regarding displaying ranges. Final compensation decisions are dependent upon factors such as geography, experience, education, skills, and internal equity. Benefits Beyond base compensation, Eide Bailly provides benefits such as: generous paid time off, comprehensive medical, dental, and vision insurance, 401(k) profit sharing, life and disability insurance, lifestyle spending account, certification incentives, education assistance, and a referral program. Next Steps We'll be in touch! If you look like the right fit for our position, one of our recruiters will be reaching out to schedule a phone interview with you to learn more about your career interests and goals. In the meantime, we encourage you to learn more about us on Facebook, Twitter, Instagram, LinkedIn or our About Us page. For extra assistance in your job search journey, explore -a complimentary external tool that offers career exploration, resume workshops, interview prep and other professional development options. Eide Bailly LLP is proud to be an affirmative action/equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, or any other status protected under local, state or federal laws. #LI-KP1 #LI-HYBRID

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Method Development Chemist Location: Minneapolis, MN Duration: 3+ months (Possibility of extension) local candidate needed - Minneapolis, MN. REQUIRED: Top 3 must haves: Chromatography experience analytical lavatory experience Seasoned HPLC chemist. Job Roles & Responsibilities 3 months contract position performing method development on GPC methodology. Perform and document laboratory work. Review and approve test records. Participate in the validation of the new GPC test method Basic Qualifications and Experience EDUCATION - Minimum BS in Chemistry or related scientific degrees EXPERIENCE - Minimum 1 year in a regulated industry environment with a Bachelor's Degree in Chemistry. Minimum 3 years of hands on experience operating HPLC Performing chemistry and/or material properties testing in a high throughput laboratory Documenting work accurately and completely Ability to use common software including MS Word, MS Excel, Powerpoint Self-motivated, able to plan/execute work tasks independently Critical thinking skills Safely handle chemical and hazardous materials Preferred Skills and Experience Prior experience and knowledge of materials properties and GPC testing Experience working with laboratory data management system Experience working with Empower chromatography software Additional Information · We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 Email id - seema @irionline.com| www.irionline.com LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row

The Analytical Chemist provides technical support to the laboratory team, developing equipment, processes, and procedures used by technicians to test products in compliance with ISO 17025, NADCAP, and AS9100 management systems. Key Responsibilities Develop, validate, and improve analytical equipment, test methods, and practices to ensure high-quality and timely test results. Maintain open communication with managers and other functions regarding workflow, issues, and improvement opportunities. Plan and select tests required on materials; document test methods and practices for lab staff. Author technical reports, project updates, and overviews, possibly including papers and patent applications. Participate in improvement projects and problem-solving teams. Requirements Preferred: Four-year degree in physics, chemistry, or engineering. Minimum: High school diploma, technical school, or GED plus 10+ years of relevant analytical experience. Mass Spectroscopy experience preferred. Ability to perform advanced mathematical equations relevant to chemistry. Proficient in computers and software (Microsoft Office, MiniTab, SAP). Strong decision-making skills, able to act decisively with limited input. Familiarity with LIMS systems and data entry accuracy. Job Type & Location This is a Contract to Hire position based out of Milwaukee, WI. Pay and Benefits The pay range for this position is $29.50 - $29.50/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 Milwaukee,WI. Application Deadline This position is anticipated to close on Dec 19, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary of Objective: This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management Essential Duties and Responsibilities: Perform routine analytical testing of samples supporting incoming raw materials, in-process production, finished product release, long term stability and validation samples. Assist in deviation investigation, out-of-specification or aberrant results and process changes Assist in authoring and/or review of GMP documentation including test methods, protocols, reports and raw data Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals with support Logging and tracking of samples and chemicals. Order chemicals and laboratory supplies as needed Documents/peer reviews laboratory work using laboratory notebooks/worksheets. Documentation must be detailed, timely and in compliance with cGMP/GDP requirements May participate in communication between PCI, clients, and analytical testing vendors to support activities including release testing, analytical methods transfer, qualification, validation and implementation Performs routine data generation and problem solving Other duties, as assigned Special Demands: Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear Ability to sit or stand for prolong periods of time Must be able to walk and drive between locations Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves Must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly Must be able to occasionally lift and/or move up to 50 pounds Comfortable with working/handling of hazardous materials Work Environment: Works closely with quality assurance and quality control staff in performing varied work procedures and activities. Interacts with Operations staff. Qualifications: 0-3 years relevant Analytical Chemistry experience, preferably in Quality Control Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study General knowledge of analytical techniques using instruments such as: UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer and Osmometer is preferred Excellent organizational skills and ability to document technical data Excellent interpersonal skills and the ability to communicate well orally and in writing to all levels of the organization Ability to multi-task in a dynamic environment with changing priorities Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment. #LI-LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Hentzen is a unique company in today's world. Since our founding in 1923, we've remained an independent, privately held organization committed to being a leader in the development and manufacturing of high-performance coatings. Our success is built on a foundation of innovation, dedication, and service-to both our customers and our employees. With over 100 years of experience, Hentzen has earned recognition as a technology leader and trusted partner in the aerospace, defense, and industrial markets. Our ability to custom-engineer advanced coatings tailored to meet the specific and challenging requirements of our customers sets us apart. This innovation comes to life in our state-of-the-art facilities, where our talented employees are empowered to solve complex problems through creativity and collaboration. If you're looking to join a company known for its technical excellence, employee commitment, and customer focus, Hentzen offers a rewarding and challenging opportunity to learn, grow, and make a meaningful impact. DEVELOPMENT CHEMIST - DEFENSE M-F: 1 st Shift The Development Chemist - Defense is responsible for the formulation, research, and development of new products in the defense market. DESCRIPTION OF ESSENTIAL DUTIES: Develop new products for defense customers per their requirements. Develop products and solve technical issues with a relatively minor amount of direction. Exercise wide discretion when solving challenges. Provide technical assistance for existing accounts. Build knowledge of analytical methods for solving problems. Train production and quality control personnel. Work with production personnel to solve problems. Exhibit demonstrated decision-making abilities. Plan activities for support personnel. Reduce or rework distressed products on hand to reduce inventory. As part of the housekeeping procedures, the employee may be involved with the disposal of hazardous waste. The initial training of how to properly dispose of hazardous waste will be performed by the Environmental and Safety department or the department supervisor. Annual training of the same will be performed by the EHS department. Perform other miscellaneous duties as assigned. QUALIFICATION REQUIREMENTS: Education level strongly preferred: Bachelor's degree in chemistry or related field. Experience level preferred: One to three years in a manufacturing or industrial setting, preferably in coatings or chemical environment. Ability to receive and provide instructions in a positive manner. Ability to read, understand and apply complex mathematical calculations. Exemplify core values, i.e., Integrity, Loyalty, Passion, Commitment, and Respect. Must be a high energy, results driven individual with excellent communication, computer, and decision-making skills. Ability to work independently, in a fast-paced team environment, with the proactive problem-solving skills and work ethic necessary for timely completion of projects. Excellent computer skills (Microsoft Office - Word, Excel, Outlook), ERP system and other office machinery. Ability to travel up to 10% of time. WORK ENVIRONMENT: While performing the duties of this job, the employee is frequently required to talk and/or hear, stand, and/or walk, use hands to finger, handle or touch objects or controls, and move from place to place. The employee is regularly required to sit, balance, stoop, and occasionally reach above shoulders. The employee occasionally must use foot/feet to operate machinery, climb, or balance and reach above the shoulders. The employee may regularly lift and/or move up to 65 lbs. Personal Protection Equipment is required during various processes in the production area. Safety shoes, glasses, and flame-retardant uniforms are required in the production area. Respirators and ear plugs may be required when performing certain production activities. Please send resume to: Hentzen Coatings, Inc. Attn: Human Resources 6937 W. Mill Road Milwaukee, WI 53218 or APPLY ONLINE AT: Hentzen Career Center Hentzen Coatings, Inc. is an Equal Opportunity Employer, including Veterans and Individuals with Disabilities. *************** All candidates are subject to post-offer testing: including a job-related pre-employment physical, drug screen, and background check. 1st Shift

Generates data and provides research in support of professional activities and is also responsible for the coordination of the physician/advanced practice clinician quality program throughout Essentia Health. Responsible to abstract, aggregate, and analyze data and clinical indicators from the electronic medical record to be used in centralized functions for hospital and clinic peer review, Focused Professional Practice Evaluation (FPPE), and Ongoing Professional Practice Evaluation (OPPE). Provides oversight and recommendations for the development of monitoring processes of physician/APC practice quality, bylaw, accreditation, and regulatory compliance. Assists in the operations of the medical staff to facilitate their functions and may act as a resource and liaison between the medical staff, hospital personnel, clinic personnel, and administration. **Education Qualifications:** **Required Education:** + Associate degree **Required Qualifications:** + 2 years of experience in a support role utilizing Microsoft/Windows based products, preferably in a healthcare setting + Must be proficient in the use of Microsoft Office products and other office software + Experience with electronic patient/medical record, or Epic preferred Employee Benefits at Essentia Health: At Essentia Health, we're committed to supporting your well-being, growth, and work-life balance. Our comprehensive benefits include medical, dental, vision, life, and disability insurance, along with supplemental options to fit your needs. We offer a 401(k) plan with employer contributions to help you plan for the future, and we invest in your professional development through training, tuition reimbursement, and educational programs. To help you thrive both at work and at home, we provide flexible scheduling, generous time off, and wellness resources focused on your physical, mental, and emotional health. Please note that benefit eligibility may vary. For full details, refer to your benefit summary or contact our HR Service Center at **************. **Job Location:** Business Service Center **Shift Rotation:** Day Rotation (United States of America) **Shift Start/End:** / **Hours Per Pay Period:** **Compensation Range:** **Union:** **FTE:** 0 **Weekends:** **Call Obligations:** **Sign On Bonus:** It is our policy to afford EEO to all individuals, regardless of race, religion, color, sex, pregnancy, gender identity, national origin, age, disability, family medical history, genetic information, sexual orientation, marital status, military service or veteran status, culture, socio-economic status, status with regard to public assistance, and other factors not related to qualifications, including employees or applicants who inquire about, discuss, or disclose their compensation or the compensation of other employees or applicants, or membership or activity in a local human rights commission, or any other category as defined by law.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your Role R&D Sterility Assurance has an exciting Microbiology Laboratory Technician III opportunity to start your career. You will work with a growing, high energy, knowledgeable team and work on R&D projects including innovation and new product development activities. This could also be an opportunity to develop your career through engagement with other functions such as Manufacturing, Quality and other R&D locations. The Oakdale Laboratory Technician III will report to the Oakdale, MN Microbiology Lab Manager and be responsible for performing daily functions of the microbiology lab to support testing. This includes, but not limited to, supporting testing and following instructions of senior microbiologists, maintaining lab equipment, making media and facilitating testing as directed by the manager. What you'll be doing Assist experienced Microbiologists in the design, development, and building of test protocols and monitoring strategies, appropriate with experience level. Make and record observations, perform simple calculations. Collect and prepare technical data for evaluation. Proficient with data entry and computer applications. Experience in a Micro Lab either in medical devices , pharmaceutical or other industrial setting, and background in aseptic techniques preferred. Perform routine microbiology processes and procedures using aseptic techniques and Good Laboratory Practices (GLP). Obtains and tests samples for bioburden testing. Performs monthly environmental settle plates. Performs microbial testing according to established test methods. Performs gram stain and LPCB staining. Completes testing projects from beginning to end. Maintains supply arrival, COA, labeling and inventory. Responsible for shipping samples for testing at a contract laboratory. Accountable for shipping equipment for maintenance and in-house equipment calibrations and those done by outside contractors. Maintains laboratory cleanliness, housekeeping chores and cleaning glassware. Accurately label samples. Follow guidelines when recording data. Accurately calculate, interpret, and report results. Accurately maintain laboratory data and logs using electronic lab notebook. Demonstrate flexibility, i.e. willingly take on new tasks. Collaborate in cross-functional teams. Follow designated work schedule. Accept and act upon supervisory directions. What you'll bring Associate degree in microbiology or similar field preferred or combination of education and/or work experience. Basic knowledge of microbiology and laboratory concepts and techniques. Basic knowledge of computer applications. Vantive is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. We understand compensation is an important factor as you consider the next step in your career. At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $68,000-102,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Vantive This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive's 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive's US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive 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. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

We are seeking an experienced, detail-oriented Quality Control Chemist to add to our 2nd-shift team. The ideal candidate has a strong background in chemistry and thrives in a fast-paced and team-oriented laboratory environment. QC Chemist Hours: Approximately 2p - 1a, Monday - Thursday, some occasional work outside of normal schedule may be required. Reports to: Quality Manager Summary: The QC Chemist will support the manufacturing process by performing laboratory analysis of raw materials, intermediate blends, and finished goods. The QC Chemist will have strong complex instrumentation knowledge and support calibration and maintenance of lab instruments, as well as assisting in the transfer of customer test methods as necessary. Responsibilities: · Follow standard operating procedures and quality directives as outline by the IKI Quality Manual. · Perform raw material, intermediate blend, and finished product testing to ensure quality on all manufactured goods. · Prioritize workload and schedule testing to align with production and distribution plans. · Support the transfer of customer test methods, as needed. · Assist in the development and review of standard operating procedures for laboratory equipment, instruments, and processes. · Complete the required preventative maintenance on lab instruments and equipment, as necessary. · Document all test results in written and electronic format where appropriate. · Assist in the training of other lab personnel on laboratory instruments and new test methods. · Perform other duties as assigned. Required Skills & Abilities: · Attention to detail and thoroughness. · Ability to thrive in a fast-paced environment. · Maintain clean and organized workspace. · Effective prioritization and self-motivation skills. · Ability to read, interpret, and correlate data. · Excellent math skills and familiarity with MS Office suite, especially Excel. · Ability to communicate effectively cross-functionally. Education & Experience: · B.S. in chemistry, or similar discipline, required. · Minimum of 3 years of lab experience required. · Experience with HPLC, GC, pH, UV-vis, FTIR, Karl Fisher, and other wet chemistry techniques required. · Experience with HPLC, GC, and general analytical test method development and transfer highly preferred. · Experience with microbial testing and/or procedures is highly preferred. · Experience with contract manufacturing and testing preferred. Work Environment: Laboratory environment with exposure to chemicals. Proper PPE must be worn, and safety precautions must be followed. Physical Demands: Stands 75%, sits 25%, occasional lifting up to 50 lbs.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. $5000 Sign On Bonus if Hired. Your Role: * Perform operations to meet quality expectations throughout the manufacturing process. * Perform routine assays, processes and/or unit operations. * Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). * Provide complete and accurate records consistent with quality guidelines. Participate in quality audits. * Ensure all applicable logbooks have been filled out completely. * Improve processes through application of scientific knowledge, experience, and principles while in compliance with change control procedures. Identify opportunities for process improvement. * Assist with training. * Work in both a large-scale process environment and a glass lab environment. * Shift/Hours: 12-hour night shift, 6:00 PM - 6:30 AM - 2/2/3 schedule (M/T on, W/R off, F/S/S on, M/T off, W/R on, F/S/S off, repeat). Physical Attributes: * Wear appropriate PPE. * Lift up to 50 lbs. Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biology, Chemical Engineering, Electrical Engineering, or other Life Science or Engineering discipline. OR * High School Diploma or GED and 4+ years of work experience in a chemical production, laboratory or chemical engineering role. Preferred Qualifications: * Strong chemistry and math skills. * Experience with chemical production on the glassware scale. * Experience with laboratory instruments and production equipment. * Experience in an independent chemistry research lab or industrial experience. * Experience with process techniques and unit operations. * Experience in analytical techniques and equipment. * Experience with safe chemical handling methods. * Strong verbal and written communication skills. RSREMD RSREMD Pay Range for this position: $27/hr - $46hr The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Salary range: $90,000 - $119,000 Full time, Exempt The Quality Control Senior Scientist position is expected to manage a small group of quality control (QC) personnel and provide team oversight in the analytical and technical aspects of QC testing programs supporting oncolytic viral and viral vector-based therapeutics. Other initiatives may include making modifications to existing assays to improve overall efficiency and progress in drug phase pipeline. Key responsibilities include deep technical understanding of the assays, participation in investigations, regulatory support, and mentorship within the QC organization. Supervisory Responsibilities Expectations to supervise ≤ 5 FTE, including planning of daily schedules to align with testing needs. Make-up of team will be organized into key specialized areas pertaining to either Biochemical/Protein Assays, Molecular Assays, or Cell-Based/Potency Assays. Duties and Responsibilities * Supervise personnel involved with GMP testing of various sample types, which may include raw materials, in-process samples, cell banks, viruses/viral vectors, and final drug products using molecular, biochemical, and/or cell-based analytical methods. * Serve as technical lead for assays which may include qPCR/dPCR, flow cytometry, ELISA, infectivity/titer assays, vector genome copy number determination, potency assays, and detection of contaminants, or coordination for send-out testing. * Lead initiatives in method development, qualification, validation, and transfer for novel analytical methods specific to various biologic/cell and gene therapy platforms. * Lead initiatives in stability studies, and trending of analytical data to ensure product consistency and compliance. * Review and interpret analytical data, ensuring data integrity and alignment with specifications, SOPs, and regulatory requirements. * Serve as primary investigator of deviations, OOS/OOT results, and implementation of CAPAs. * Mentor QC Analysts and Scientists in analytical techniques and GMP practices * Additional duties as assigned. Education and Experience * Advanced degree (Ph.D. and/or relevant degree highly desirable) and 4+ years of related work experience, or a Bachelor's degree with 9+ years of related work experience * Minimum of 3 years working in biologics drug product role with a good understanding of working with a defined QMS and assay qualification. * Experience with setting up, supporting, and troubleshooting multiple pieces of drug product analytical equipment. * Proven expertise in at least one area of cell-based potency, molecular, and/or biochemical/protein assays. * Experience conducting process characterization, analysis and development with minimal supervision. * Knowledge of ICH Q2(R2), FDA/EMA regulations for ATMPs, and cGMP testing principles. * Excellent analytical, documentation, and communication skills. Physical Requirements * Prolonged periods of standing at laboratory benches. * Prolonged periods of sitting at a desk and working on a computer. * Must be able to lift up to 15 pounds at times. Benefits * Group Healthcare Plan, including company paid dental and vision. * Short- and long-term disability, life and AD&G insurance. * Simple IRA with employer match * Educational assistance program * Holiday and PTO

Boehringer Ingelheim Animal Health is currently seeking an innovative, tech savvy Intern to join our Commercial Quality team located at our Duluth, GA US headquarters. As an intern, you will learn basic quality principles while performing critical process evaluations. The mission of this internship will be to streamline a critical quality process which contributes to the continuity of the US Animal Health Commercial Supply Chain. As an intern at Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. Duties & Responsibilities Assist Subject Matter Experts in core quality tasks associated with release of batches to the US market, deviation management, and complaint management Evaluate a core quality process and use BI digital tools (i.e. Tableau, Power BI, Dashboards, Excel, DocuSign) to streamline the process Develop and execute quality culture initiatives to spread Quality Culture across the US AH Commercial business Requirements Must be a current undergraduate, graduate or advanced degree student in good academic standing. Student must be enrolled at an accredited college or university for the duration of the internship. Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred. Major or minor in related field of internship. Undergraduate students must have completed at least 12 credit hours at current college or university. Graduate and advanced degree students must have completed at least 9 credit hours at current college or university. Desired Skills, Experience and Abilities Advanced skills in Excel, Dashboards, and/or Power BI Strong organization skills Proficient in MS PowerPoint Excellent written and verbal communication Eligibility Requirements: Must be legally authorized to work in the United States without restriction. Must be willing to take a drug test and post-offer physical (if required). Must be 18 years of age or older.

The Analytical Chemist provides technical support to the laboratory team, developing equipment, processes, and procedures used by technicians to test products in compliance with ISO 17025, NADCAP, and AS9100 management systems. Key Responsibilities Develop, validate, and improve analytical equipment, test methods, and practices to ensure high-quality and timely test results. Maintain open communication with managers and other functions regarding workflow, issues, and improvement opportunities. Plan and select tests required on materials; document test methods and practices for lab staff. Author technical reports, project updates, and overviews, possibly including papers and patent applications. Participate in improvement projects and problem-solving teams. Requirements Preferred: Four-year degree in physics, chemistry, or engineering. Minimum: High school diploma, technical school, or GED plus 10+ years of relevant analytical experience. Mass Spectroscopy experience preferred. Ability to perform advanced mathematical equations relevant to chemistry. Proficient in computers and software (Microsoft Office, MiniTab, SAP). Strong decision-making skills, able to act decisively with limited input. Familiarity with LIMS systems and data entry accuracy. Job Type & Location This is a Contract to Hire position based out of Milwaukee, WI. Pay and Benefits The pay range for this position is $29.50 - $29.50/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 Milwaukee,WI. Application Deadline This position is anticipated to close on Dec 19, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Description Hentzen is a unique company in today's world. Since our founding in 1923, we've remained an independent, privately held organization committed to being a leader in the development and manufacturing of high-performance coatings. Our success is built on a foundation of innovation, dedication, and service-to both our customers and our employees. With over 100 years of experience, Hentzen has earned recognition as a technology leader and trusted partner in the aerospace, defense, and industrial markets. Our ability to custom-engineer advanced coatings tailored to meet the specific and challenging requirements of our customers sets us apart. This innovation comes to life in our state-of-the-art facilities, where our talented employees are empowered to solve complex problems through creativity and collaboration. If you're looking to join a company known for its technical excellence, employee commitment, and customer focus, Hentzen offers a rewarding and challenging opportunity to learn, grow, and make a meaningful impact. DEVELOPMENT CHEMIST - DEFENSE M-F: 1st Shift The Development Chemist - Defense is responsible for the formulation, research, and development of new products in the defense market. DESCRIPTION OF ESSENTIAL DUTIES: Develop new products for defense customers per their requirements. Develop products and solve technical issues with a relatively minor amount of direction. Exercise wide discretion when solving challenges. Provide technical assistance for existing accounts. Build knowledge of analytical methods for solving problems. Train production and quality control personnel. Work with production personnel to solve problems. Exhibit demonstrated decision-making abilities. Plan activities for support personnel. Reduce or rework distressed products on hand to reduce inventory. As part of the housekeeping procedures, the employee may be involved with the disposal of hazardous waste. The initial training of how to properly dispose of hazardous waste will be performed by the Environmental and Safety department or the department supervisor. Annual training of the same will be performed by the EHS department. Perform other miscellaneous duties as assigned. QUALIFICATION REQUIREMENTS: Education level strongly preferred: Bachelor's degree in chemistry or related field. Experience level preferred: One to three years in a manufacturing or industrial setting, preferably in coatings or chemical environment. Ability to receive and provide instructions in a positive manner. Ability to read, understand and apply complex mathematical calculations. Exemplify core values, i.e., Integrity, Loyalty, Passion, Commitment, and Respect. Must be a high energy, results driven individual with excellent communication, computer, and decision-making skills. Ability to work independently, in a fast-paced team environment, with the proactive problem-solving skills and work ethic necessary for timely completion of projects. Excellent computer skills (Microsoft Office - Word, Excel, Outlook), ERP system and other office machinery. Ability to travel up to 10% of time. WORK ENVIRONMENT: While performing the duties of this job, the employee is frequently required to talk and/or hear, stand, and/or walk, use hands to finger, handle or touch objects or controls, and move from place to place. The employee is regularly required to sit, balance, stoop, and occasionally reach above shoulders. The employee occasionally must use foot/feet to operate machinery, climb, or balance and reach above the shoulders. The employee may regularly lift and/or move up to 65 lbs. Personal Protection Equipment is required during various processes in the production area. Safety shoes, glasses, and flame-retardant uniforms are required in the production area. Respirators and ear plugs may be required when performing certain production activities. Please send resume to: Hentzen Coatings, Inc. Attn: Human Resources 6937 W. Mill Road Milwaukee, WI 53218 or APPLY ONLINE AT: Hentzen Career Center Hentzen Coatings, Inc. is an Equal Opportunity Employer, including Veterans and Individuals with Disabilities. *************** All candidates are subject to post-offer testing: including a job-related pre-employment physical, drug screen, and background check. 1st Shift