Quality control analyst jobs in Madison, WI - 78 jobs

Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated Scientist to support Manufacturing (MFG), Quality Control (QC), and equipment oversight within our Operations team. This individual will assist in MFG and QC of reagents and consumables utilized with our Elephas platform. This individual will support equipment preventative maintenance (PM) and calibrations (CAL) ensuring documentation is maintained in the computerized maintenance management system (CMMS). The individual will work closely with the lead scientists, technical transfer team, R&D, Quality, and Operations to ensure successful production and release of products into inventory and management of all equipment onsite. This role will utilize appropriate inhouse systems and tools to execute the production runs based on sales and operating plans (S&OP) and will work closely with outside vendors to complete all PMs and CALs where needed. This candidate will be self-motivated to learn, and comfortable in a fast-paced and highly collaborative environment. Essential Duties and Responsibilities * Assist in labeling, manufacturing, dispensing, and quality control of Elephas products * Partner with lead scientists and technical transfer team to execute manufacturing, analytical testing methods, and quality control assays for production and release of the products to inventory * Support scaling activities for manufacture of reagents, consumables, and testing methods * Follow protocols, procedures, and work instructions to support manufacturing and quality control capabilities in compliance with RUO, GMPs, FDA 21 CFR 820, and ISO13485 guidelines * Draft and review Standard Operating Procedures (SOPs) and related manufacturing process documentation as required aligned with the Quality Management System (QMS) * Assist in troubleshooting production and quality control related performance issues and out of specifications working closely with senior scientists to identify root cause and develop process improvements to reduce and mitigate risk * Support CAPAs, non-conformances, deviations, and investigations with Quality partners and Operations leaders to drive action and mitigations going forward * Follow proper lab processes and documentation including equipment use and safety practices * Comfortable working with biological and chemical materials, and instrumentation * Execute PMs and CALs as required working with outside vendors or internal employees to ensure proper documentation and completion of records and tracking in the CMMS * Support onboarding of new equipment assets into lab spaces Education/Experience/Skills * Bachelor's degree in Life Sciences field or related discipline * Computer proficiency of Microsoft Office Suite * Strong attention to detail * Ability to problem solve with good analytical skills * Excellent verbal and written communication skills We offer our employees competitive compensation and benefits, including paid time off, health insurance, life insurance, flexible spending accounts, a 401(k) plan, and stock options. DISCLAIMER The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

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. This position will have responsibility for supporting activities in the QC Sample Management group, which includes use of material control procedures and specification documents, raw material sampling & inspection, participation in the coordination of testing with internal and external resources, and collection of data and material certificates for review by QA. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. Review all incoming material receipt packets to assess testing needs Schedule and perform sampling of raw materials across the PCI Madison, WI Sites Request quotes and purchase orders for testing performed externally Assist with regular communications with 3 rd party labs performing external testing Complete and submit all applicable sample submission paperwork to the appropriate testing labs Escalate testing failure or safety concerns to management in a timely fashion Assist in deviation, out-of-specification or aberrant result investigations, as needed Assist with the writing and revision of cGMP documents and Raw Material Specifications documents to meet industry standards Assist with reviewing testing results to ensure accuracy and compliance. Perform routine cleaning of sampling facilities Routinely perform aseptic sampling inside a Biological Safety Cabinet Perform dimensional inspections on packaging components Perform routine data generation and problem solving Order/restock laboratory and office supplies, as needed. Complete assigned training in a timely fashion Special 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. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions. Must be able to walk and drive between local sites Must be able to physically wear laboratory protective attire and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves Must be comfortable working with and handling hazardous materials in safety cabinets Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Laboratory, manufacturing, warehouse Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 0-3 years relevant business experience Proficient in MS Office. Must have strong attention to detail as well as ability to work in a cross-functional team environment Professional interpersonal skills and the ability to communicate well orally and in in writing Ability to multi-task in a dynamic environment with changing priorities Ability to work independently as well as on a team, with limited supervisory oversight Master Control experience a plus cGMP experience a plus 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.

Benefits: * 401(k) * Bonus based on performance * Flexible schedule * Training & development Doping Control Officer I or II (DCO I or DCO II) USADA is seeking a dedicated and driven person to help our organization fulfill its mission to "Stand with athletes to champion their right to clean sport, inspire true and healthy sport, and promote the integrity of sport." This is an incredibly exciting time to join Team USADA, as we continue to grow our Anti-Doping program and work to support major international competitions such as the Olympic and Paralympic Games in 2026 (Milan), and 2028 (Los Angeles). New team members will have the chance to help ensure USADA is well-positioned in the near and long term for these opportunities as we look to the future with our efforts to protect clean athletes. With the 2028 Games on domestic soil, there will also be opportunities and growth potential over the years for USADA team members to underpin the organizing committee's commitment to a clean Games. REPORTS TO: DC Ops Manager & Asst Manager FLSA: Non-Exempt SUPERVISES: N/A Last revised: July 2025 LOCATION: Madison, WI (Must reside w/in 50 miles) Anticipated # of Tests/Year: 10-15 JOB SUMMARY: Responsible for sample collection from athletes. Tasks performed by the Doping Control Officer (DCO) include preparation for, execution of and post-collection administration as it relates to Doping Control both at events and in the out-of-competition setting. DCOs are the field facing representatives of USADA. The primary objective of the DCO is to conduct Doping Control throughout the United States, under direction of the Doping Control Operations team, for Olympic, Paralympic, and Client Services testing teams, in support of USADA's mission and vision. The DCO works with the HQ team to uphold USADA's goals of creating and maintaining a fair and healthy environment for all athletes. The role will include both local and national travel to conduct Doping Control assignments. The following job expectations, responsibilities, and qualifications apply to both the DCO I and DCO II positions, however, in order to qualify for a DCO II level, one must have a valid phlebotomy credential in good standing, as further outlined below. A DCO II is able to serve as a doping control officer that can draw blood. RESPONSIBILITIES: * Conduct sample collection sessions in support of the testing programs for the Olympic/Paralympic, and Client Services testing teams, as well as on behalf of other agencies, when requested by USADA. * Accept, plan and manage doping control assignments, in accordance with the minimum requirements of the WADA/International Standards, and any minimum criteria established by USADA. * Execute logistics aspects as they relate to the doping control process to facilitate successful completion of missions. * Conduct doping control, including processing of Samples, in accordance with USADA's protocols and procedures, and in accordance with the WADA Code/International Standards. * Recruit and onboard independent contractors to serve in the capacity of a Chaperone*. *(Chaperones may be required in the event the athlete is a minor and/or if the gender of the DCO is not the same as the gender of the athlete being tested) * Witness sample collection or overseeing the witnessing of the sample collection process. * Travel (car, plane, train etc.) to various locations to perform sample collections (by the most economical route). * Ensure accurate documentation/completion of the doping control process. * Ship and submit processed Samples to the specified WADA certified laboratory. * Assist in the onboarding and training of new doping control officers. * Accountable to the most current version(s) of the DCO Manual, sample collection. documentation and other training resources. * Participate in DCO evaluation and support program, continuing education and re-accreditation. * Ensure adequate control of document, record and sample collection equipment. * Schedule and manage all travel, as well as associated expense reports. * Provide witness testimony in Legal cases, such as whereabout failures, other Anti-Doping Rule Violations. * Enforce infection control processes at all times that you are working with equipment or athletes. GENERAL: * Maintain confidentiality at all times. * Have no affiliation with sample collection organizations outside of USADA. * Keep USADA aware of issues in the field and/or any conflicts of interest. * Recommend necessary updates and revisions to USADA protocol and procedures as related to Doping Control. * Projects and other duties, as assigned. REQUIRED QUALIFICATIONS: Skills: * Excellent oral and written communication skills. * Excellent organizational skills and attention to detail. * Demonstrated high proficiency in utilizing technology such as tablets, multiple software platforms, and various applications. Demonstrated ability to: * Make decisions in accordance with USADA's protocol and procedures. * Multitask and work accurately under pressure. * Interact with internal and external customers professionally and in line with USADA's values. * Travel, possibly at short notice, to conduct test assignments. * Work flexible hours, as needed. * Access the internet for daily communication. * Values integrity, respect, and justice among internal and external constituents. * Perform effectively and collaboratively in a team environment. * Meet deadlines and operate with limited supervision. * Stand, bend and lift 50 pounds, on a regular basis. Certification: * Successful completion of all USADA certification/recertification requirements. * Pass bi-annual written and practical exams. * Attend DCO training sessions, meetings, conferences. * Valid Driver's License in good standing with state requirements where you reside. * Must be fully vaccinated against COVID-19. DCO II Additional Requirements: * *National Phlebotomy certification from one of the following accredited agencies: * ACA- American Certification Agency (certified on/after July 2003) * AMT -American Medical Technologists (certified on/after April, 2003) * ASCP - American Society of Clinical Pathology (certified on/after June, 2003) * NHA- National Healthcareer Association (certified on/after February 2005) * NCCT/MMCI- National Center for Competency Testing (certified on/after February 2003) * Applicants who are certified before the above dates must re-take the certifying examination. A more advanced, applicable credential such as RN, NP or PA will satisfy this requirement. * CPT I & II in California are acceptable credentials as they require successful completion of a national exam by one of the certifying bodies outlined above. * In addition to a current national certification, individuals will be required to ensure compliance with state specific phlebotomy training requirements for the state in which they reside. * At least 3 years phlebotomy experience, preferred. Additional Certification(s): * Obtain SafeSport Certification (post-offer) DESIRED QUALIFICATIONS: * Work experience in Allied Health Professions w/certification and/or License (Athletic Trainer, Physical Therapist, Registered Nurse, Paramedics, etc.) COMPENSATION & TIME COMMITMENT: * Compensation is on a per-test basis(piece rate) for out-of-competition (OOC) missions, with compensation typically ranging from $130 to $180 per test dependent on the test parameters. OOC test sessions can vary in length, but generally take 1 to 2 hours for successful completion. * In Competition (event) testing is paid at a daily flat rate, typically at $250 per day. * Onboarding is anticipated to begin in December/January with a more significant time commitment up front for training. Expect a time commitment of 24-30 hours of time during the first 60 days of onboarding. After that it should only be 2-3 hours of training and updates per quarter, plus the necessary time to complete test assignments.

Interested in contributing to improving and saving lives? Eurofins Food Chemistry Madison is growing and we're looking for amazing team members to join us. In 2021 we moved into a brand new ISO 17025 accredited laboratory in Madison, WI designed to conduct food chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies. We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! Job Description Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Organizes, conducts and evaluates analytical results and testing independently in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines. Documents work, maintains study documentation and laboratory records. Independently sets-up, maintains, operates, and performs routine and non-routine maintenance on laboratory equipment and software, including problem identification and resolution. Leads project meetings, plans, monitors and guides project work, Performs peer review and QC review of data, Performs assigned workload on a daily basis and effectively completes multiple assignments. Promotes and contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members and plans team workload in coordination with supervisors or managers Maintains a clean and safe laboratory work environment Understands data generated, and history of methods. Recognizes deviations from normal results and informs Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and drives corrective action of problems. Identifies problems and performs modifications in test methods or procedures. Helps develop new procedures as needed or directed. Understands chemistry of all steps of multiple assays. Initiates, drives, implements and directs others in process improvement initiatives. Completes all required training courses. Trains, mentors, and assists less experienced staff. Sets up and performs optimization, and validation of various analytes in a variety of matrices, and assists in method development. Participates / leads client visits as needed, and communicates technical information. Evaluates data for incorporation into written reports. Writes reports, methods, protocols, and SOPs, and evaluates suggestions for modifications to test methods and procedures. Knowledge of departmental procedures and policies. May assist in modifications to these procedures and policies. Effectively plans and utilizes personnel and resources for timely completion of assigned projects. Drives the assessment and qualification of new equipment and instrumentation as appropriate. Assures technical staff compliance to SOPs and other regulatory agency guidelines. Viewed as a resource across EFII. Transfers, sets up and performs complex analyses using unfamiliar or new methods, utilizing EFII resources including scientific guidance as needed. Designs and independently conducts tests for chemistry projects and provide initial analysis. Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. BS/BA degree in science plus at least 5+ years of previous laboratory experience. Relevant experience may be substituted for education. Experience with use and troubleshooting of analytical equipment. Basic knowledge of computers and software programs. Familiar with the use of standard laboratory equipment. Effective communication (verbal and written), presentation and interpersonal skills. Ability to learn new tasks Ability to think critically and solve problems quickly and efficiently Additional Information Expected to understand the process for handling hazardous wastes and receive on-the-job training for handling specific waste types in their job area. · Work requires use of PPE (personal protective equipment). · Work requires some standing and sitting for long periods of time. · Work may require lifting of weights of up to 40 lbs. · Overtime, weekend and holiday work as required. · May include second shift work. · Will be exposed to potential food allergens. What we offer: As an employer, we're keen to look after our people with as much dedication as they look after our patients. That's why we offer competitive salaries, excellent training and exceptional career prospects. We're a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career. Your data: As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position This position is within the Quality Control structure, under the Quality Organization. A Senior Scientist I, Quality Control will support the analytical testing of Environmental monitoring samples, pharmaceutical raw materials, in process manufacturing samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Senior Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Senior Scientist I is expected to be proficient in several analytical techniques and will be capable of making independent scientific decisions. The position also requires the ability to lead and mentor co-workers. This position reports to QC Laboratory Management. Responsibilities Fully knowledgeable of cGMP requirements and ICH guidelines Works independently to meet project timelines and deliverables with minimal supervision to no supervision Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures Proficient with various analytical instrumentation theory and practice Executes training requirements for assigned SOPs and participates in department specific training modules. Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation as Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization Performs analyses in a timely and efficient manner to support ongoing prioritized studies Works closely with other department personnel for efficient project execution and timely/accurate deliverables while building a relationship with respect and communication Trains and mentors co-workers (analysts) Shows initiative and interest in mastering new techniques and tests Ability to track/trend data and interpret degrative changes to the product on stability Uses stability tracking software as a repository generated results (data entry, review and approval). Owns and leads scientific technical discussions and brainstorming sessions Identifies and troubleshoots analytical method issues with instrumentation, general chemistry, test methodology and sample product Communicates laboratory testing issues or challenges to laboratory management Maintains a clear, concise, and accurate notebook Performs technical data review on data acquired by other QC analysts as applicable Drafts technical documents such as COAs, investigations, deviations, and CAPAs Possesses excellent written and verbal communication skills Embraces cGMP and ICH requirements for all associated work Works cooperatively in a team environment Demonstrates a high attention to detail Calibration, maintenance, and troubleshooting of analytical equipment with little to no guidance from management Routinely makes sound, scientific decisions independently and serves as a back-up to Laboratory Management Demonstrates enduring flexibility and understanding with changing Requirements: M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience Fully knowledgeable of cGMP and ICH laboratory requirements and operations Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices Wisconsin pay range $90,000-$108,000 USD Arrowhead provides competitive salaries and an excellent benefit package. 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The Quality Control Chemist plays a crucial role in supporting manufacturing by conducting laboratory analysis of raw materials, intermediate blends, and finished products. This analysis is performed using wet chemistry techniques such as pH measurement, UV-Vis spectroscopy, FTIR, and titration, along with advanced instrumentation including HPLC and GC. Responsibilities + Follow standard operating procedures to ensure quality control. + Conduct quality testing and document results accurately. + Maintain and calibrate laboratory instruments regularly. + Assist with the transfer of test methods. + Train personnel on equipment usage and testing methods. Essential Skills + Bachelor's Degree in Chemistry + Minimum of 3 years of laboratory experience + Proficiency in HPLC, GC, pH measurement, UV-Vis spectroscopy, FTIR, and other wet chemistry techniques Additional Skills & Qualifications + Experience in HPLC, GC, and analytical test method development and transfer + Familiarity with microbial testing and procedures + Experience in contract manufacturing and testing Work Environment The position is based in a laboratory environment requiring adherence to safety protocols. Proper PPE including safety glasses, gloves, lab coat, and ear plugs will be provided and must be worn at all times. The role involves 75% standing, 25% sitting, and occasional lifting of up to 25 lbs. The work schedule is 2nd shift, Monday to Thursday, from 2pm to 1am, consisting of four 10-hour shifts. Occasional weekend work or overtime may be required. Initial training will require some first shift hours. Job Type & Location This is a Permanent position based out of Edgerton, WI. Pay and Benefits The pay range for this position is $62400.00 - $62400.00/yr. Medical, dental, vision, 401K Workplace Type This is a fully onsite position in Edgerton,WI. Application Deadline This position is anticipated to close on Jan 26, 2026. 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.

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.

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.

Urgently Hiring! 2nd Shift Quality Control Hours: 2pm-10pm (Mon-Fri) Pay: $17 Get Hired! Advance Services is hiring motivated workers to join our team with a leading plastics manufacturer in the Janesville area! We're offering competitive pay at $17 an hour, advancement opportunities, and great training. Job Duties: Read and comprehend instructions on the Quality Requirements Sheet Review and comprehend instructions on part drawings Inspect and approve existing products(visual, functional, and dimensional) Carton and pallet inspections Approve and sign-off on pallet transfers Record visual, functional, and dimensional inspections of products Complete required paperwork for red tagging non conforming materials and nonconforming finished product Perform audits and/or sorting of nonconforming finished product Setup and operate testing equipment Assist with training for new hire auditors Carry out special projects assigned Requirements: High School Diploma or GED Minimum 1-2 years of quality control/assurance experience; manufacturing environment preferred Strong computer skills (Word, Excel, Powerpoint, etc.) Ability to read and understand blueprints Excellent oral and written communication skills Strong attention to detail Data driven Self- Motivated Why work for Advance Services, Inc. Advance Services is for and about people; we are your employment specialists. Enjoy our easy application process. You NEVER pay a fee! Weekly pay. Fun Safety and attendance incentives. Health Benefits to keep you and your family healthy. Great Referral Incentives. Advance Services partners with the top companies in the area! Apply Now! #TK2 Advance Services is an equal opportunity employer

Our client operates within the solar energy industry, and their products are manufactured in a state-of-the-art automatic production facility using sophisticated machinery. These products are assembled with high-precision, fully automatic equipment. Position Summary: The Quality Control Coordinator is responsible for ensuring the adherence to established standard operating procedures by inspecting frames produced in an aluminum or metal products manufacturing environment. They assist in the development and implementation of quality control policies, perform verification and calibration of measuring devices, and maintain documentation of all productions. The technician communicates with production line workers, schedules and reports audits to management, and participates in investigations and corrective actions for nonconformities. Key Requirements: High school and/or college diploma in a technical discipline or equivalent combination of education and experience Minimum of 2 years of related experience in quality control, ideally in an aluminum or metal products manufacturing environment. Knowledge of QA manuals and practices regarding manufacturing, certification, marking and stamping requirements applicable to products Knowledge of relevant codes and standards (ISO 9001, etc.) Superior organization and time management skills. Proficient spoken and written English. Demonstrated Competencies: Positive influential leadership ability to lead and manage a team to achieve production objectives for the plant. Proficiency in Microsoft Office and quality management systems. Excellent communication, interpersonal, and public speaking skills. Excellent decision-making and problem-solving skills. Strong organizational skills. Key Responsibilities: Inspect the produced frames in accordance with established standard operating procedures. Support the development and implementation of quality control policies and procedures required for internal standards. Perform verification and calibration of measuring devices. Investigate outcomes and recommend changes if needed. Maintain a documentation of all productions at the plant and on site. Maintain communication with the production line workers to ensure accuracy. Communicate audit schedules and report audit results to management. Participate in investigations and complete root cause analyses and implement corrective actions in case of nonconformities. Salary Base range: $45,000.00 - $55,000.00 Our client is an equal opportunity employer that is committed to diversity and inclusion in the workplace. They prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, or any other protected characteristic as outlined by federal, state, or local laws.

Primary Duties and Responsibilities: Perform testing and measurement of products to ensure compliance with Orchid Monroe, LLC and customer requirements. Conduct in-house calibration of instruments, maintain calibration schedules, and accurately document results in the calibration system and on instruments. Inspect and test incoming raw materials and components, including dimensional, chemical, and soft-magnetic properties. Perform internal product audits and ensure audit findings are addressed appropriately. Operate and maintain specialized testing equipment such as fluoroscopy machines, Epstein testers, and humidity chambers. Conduct customer-specific testing (e.g., phosphate thickness via XRF) in accordance with customer specifications. Properly document, contain, and control all non-conforming products, ensuring timely resolution. Maintain quality documentation and records in compliance with ISO/IATF requirements. Support PPAP submissions, engineering changes, and the validation of gauges and Control Plans/QRRs. Provide quality support to manufacturing operations, assisting in root cause analysis, problem-solving, and corrective/preventive actions. Participate in continuous improvement activities to enhance processes, reduce waste, and improve product reliability. Ensure the laboratory environment and equipment meet operational and cleanliness standards. Analyze and interpret test data, including statistical calculations (cpk, ppk, standard deviations, trends, etc.), and communicate results in clear, concise reports or presentations. Enforce compliance with safety regulations and promote a culture of workplace safety. Execute quality checks per Control Plans/QRRs and document objective evidence. Stop production if processes produce nonconforming product or waste. Validate gauges, initiate recalls when calibration issues are found, and ensure corrective actions. Control and quarantine nonconforming product, escalating to supervision and Quality Assurance as necessary. Maintain current knowledge of quality documentation, requesting updates or revisions when appropriate. Perform other related duties as assigned by supervision. Qualifications: Education & Experience: Associate's Degree in Quality, Engineering Technology, or related field; or equivalent work experience. Minimum of five (5) years of quality assurance experience in a manufacturing environment, preferably in metrology. ASQ Certified Quality Technician (CQT) strongly preferred. Technical Skills: Proficient in operating manual and DCC/CMM systems and vision measuring systems. Strong ability to interpret engineering drawings, with emphasis on GD&T and 3D datum structures. Advanced data analysis skills using Microsoft Excel or equivalent tools (e.g., cpk, ppk, SPC analysis). Solid math skills applicable to measurement, SPC, GD&T, and MSA. Knowledge of ISO 9001:2015 and IATF 16949:2016 standards. Communication Skills: Ability to read, write, and interpret technical content in English. Strong verbal and written communication skills for cross-functional collaboration. Other Requirements: Physical ability to work safely in a manufacturing and lab environment (standing, kneeling, lifting product, vision acuity for inspection, etc.). Work distribution: Lab (40%), Manufacturing Floor (20%), Desk/Computer (40%). Diversity & Inclusion Statement UPG Electrical is an equal opportunity employer committed to a diverse and inclusive workforce.

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary Verification of procured materials, sub-assemblies, finished products and processes to the companies Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Essential Functions Inspect measure and/or test material to established methods and standards. Utilize various inspection tools, such as Vision System, Verniers, Micrometers, Rulers, Oscilloscopes, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. Document inspection and test results according to established procedures. Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. Process returned material to established procedures. Read and interpret documentation such as Standard Operating Procedures (SOP), schematics, technical drawings, PDAs and ECOs. Interface with other functions and departments as required. Required/Preferred Education and Experience High School Diploma Or equivalent. required 1-3 years experience in a related position. required Knowledge, Skills and Abilities Good written and oral communication skills. Ability to read specifications, procedures and engineering drawings. Familiar with use of mechanical and electronic test equipment. IPC-A-61OD for Incoming Inspection, preferred. Basic computer skills: Microsoft Office, Oracle and MES. Physical Demands Ability to lift up to 50 lbs. ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. The hourly pay rate for this position is: $20.00 to $20.00 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Scientist, Quality position is responsible for the cGMP analytical laboratory analysis review in the Quality Control department of MilliporeSigma. Analysis may consist of all/some of the following: incoming raw material analysis, in-process testing, final product analysis, stability, reference standard requalification, method validation/qualification, cleaning, and environmental monitoring to support Quality Control activities at the Madison and Verona sites. Analysis includes techniques specific to, but not limited to: HPLC, GC, KF, DSC, TGA, IR, MS, NMR and LC-MS among other tests and instruments. Other responsibilities may include initiation and review of deviations, OOS/OOT's, change controls, and CAPA's. Additionally, participation in process improvement initiatives, working in a team environment, maintaining a clean and safe work area, and supporting the department in maintaining the laboratory in an audit ready state are other duties. * Analyze complex cGMP data using sound scientific rationale to identify root causes and implement effective CAPAs with minimal oversight. * Perform in-depth analytical data review in support of QC, ensuring accuracy, integrity, and compliance with ALCOA+ principles. * Prioritize and coordinate in-process testing reviews with manufacturing and laboratory teams to minimize downtime. * Author and manage complex deviations, investigations, change controls, CAPAs, and OOS/OOT activities, communicating status to stakeholders. * Review and support method development, validation, transfers, product changeovers, and ICP-MS testing for routine QC analysis. * Maintain audit-ready laboratory operations, including safety, housekeeping, reagent management, waste disposal, and equipment qualification review (IQ/OQ/PV). * Provide peer review, technical documentation, and training support for laboratory staff while upholding data integrity and "right first time" principles. * Collaborate cross-functionally to manage projects and timelines while ensuring compliance with ICH Q7, 21 CFR Parts 11/210/211, and applicable regulatory standards. Physical Attributes: * Work in analytical testing lab with hazardous and toxic chemicals. Who You Are Minimum Qualifications: * Bachelors Degree in Chemistry, Biology, or other Life Science discipline. * 5+ years experience in a GLP or cGMP analytical laboratory environment Preferred Qualifications: * Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7. * Excellent written and verbal communication skills, as well as good documentation practices and attention to detail. * Knowledge and understanding of analytical chemistry techniques listed above in the 'your role'. (HPLC, GC, KF, DSC, TGA, IR, MS, NMR and LC-MS) * Experience in reviewing GMP technical data from the analytical chemistry technique listed above in the 'your role'. * Adequate technical writing skills to author reports, training memos and operating procedures. Pay Range for this position: $70,000-$109,200 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!

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.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Quality Control Intern will support quality operations at Arrowhead Pharmaceuticals by assisting with raw materials supplier qualification and analytical method verification activities. This internship offers hands-on experience in a GMP laboratory environment while contributing to critical quality processes that support manufacturing timelines. The intern will work alongside QC analysts to execute testing, documentation, and verification activities that ensure raw materials meet quality and regulatory standards. This is an 11-week Summer Internship Program paying $21.00 per hour and requires full-time, onsite work five days per week at the designated location. Responsibilities Read and understand QC raw materials programs, procedures, and associated documentation. Observe and shadow trainers during QC raw materials testing procedures. Perform and execute QC raw materials procedures and documentation under the guidance of trained QC personnel. Assist with supplier qualification activities, including: Execution of analytical testing Sourcing required supplies and materials Drafting and supporting review/approval of reports Assist with analytical test method verification for raw materials, including execution of analyses, sourcing of supplies, and documentation support. Maintain accurate and compliant records in accordance with GMP and QC standards. Follow all laboratory safety, quality, and compliance requirements. Requirements Currently enrolled student at an accredited university or college, with a minimum of two years completed toward a degree in Chemistry, Biochemistry, or a related scientific discipline. Understanding of laboratory environments and interest in analytical testing and method verification. Interest in learning and applying a variety of laboratory instrumentation and techniques. Excellent verbal and written communication skills, including comfort presenting in group settings. Strong problem-solving and organizational skills. Proficiency in Microsoft Office applications. Preferred Prior experience in a QC, analytical, or laboratory setting. Familiarity with raw material testing, analytical methods, or supplier qualification processes. Interest in pursuing a career in Quality, Analytical Chemistry, or Pharmaceutical Sciences. Wisconsin pay range $9,240-$9,240 USD Arrowhead provides competitive salaries and an excellent benefit package. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

The Quality Control Chemist plays a crucial role in supporting manufacturing by conducting laboratory analysis of raw materials, intermediate blends, and finished products. This analysis is performed using wet chemistry techniques such as pH measurement, UV-Vis spectroscopy, FTIR, and titration, along with advanced instrumentation including HPLC and GC. Responsibilities * Follow standard operating procedures to ensure quality control. * Conduct quality testing and document results accurately. * Maintain and calibrate laboratory instruments regularly. * Assist with the transfer of test methods. * Train personnel on equipment usage and testing methods. Essential Skills * Bachelor's Degree in Chemistry * Minimum of 3 years of laboratory experience * Proficiency in HPLC, GC, pH measurement, UV-Vis spectroscopy, FTIR, and other wet chemistry techniques Additional Skills & Qualifications * Experience in HPLC, GC, and analytical test method development and transfer * Familiarity with microbial testing and procedures * Experience in contract manufacturing and testing Work Environment The position is based in a laboratory environment requiring adherence to safety protocols. Proper PPE including safety glasses, gloves, lab coat, and ear plugs will be provided and must be worn at all times. The role involves 75% standing, 25% sitting, and occasional lifting of up to 25 lbs. The work schedule is 2nd shift, Monday to Thursday, from 2pm to 1am, consisting of four 10-hour shifts. Occasional weekend work or overtime may be required. Initial training will require some first shift hours. Job Type & Location This is a Permanent position based out of Edgerton, WI. Pay and Benefits The pay range for this position is $62400.00 - $62400.00/yr. Medical, dental, vision, 401K Workplace Type This is a fully onsite position in Edgerton,WI. Application Deadline This position is anticipated to close on Jan 26, 2026. 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.

We are seeking a diligent and detail-oriented individual to contribute to our quality team! This is a 2nd shift position with standard hours of 2:30pm-1am Monday-Thursday and occasional Friday OT shifts from 2:30pm-12am. Pay starting at $20.25 per hour, plus $2.00 shift premium.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: MilliporeSigma is seeking a skilled and motivated Analytical Chemist with expertise in Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to support a multidisciplinary CDMO center in Madison/Verona WI. The successful candidate will be responsible for conducting advanced chemical analyses, developing, transferring, and validating analytical methods, and ensuring the accuracy and reliability of test results. The Quality Scientist position, like all positions at SAFC, will require a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties. * Conduct qualitative and quantitative analyses using ICP-MS and microwave digestion, ensuring compliance with cGMP standards with minimal oversight. * Develop, optimize, and validate analytical methods for trace element analysis while maintaining accurate documentation of procedures. * Perform analytical testing of cGMP materials, guaranteeing data accuracy and quality through proper laboratory techniques while managing tight project deadlines. * Maintain and troubleshoot ICP-MS and digestion instruments, conducting performance verifications and operational qualifications as needed. * Collaborate with cross-functional teams on research and development projects, providing technical support and training to junior staff. * Document and investigate out-of-specification (OOS) and out-of-trend (OOT) results, applying critical thinking to identify root causes and corrective actions. * Ensure laboratory safety and cleanliness, managing supplies and housekeeping tasks to maintain an audit-ready environment. * Author and revise standard operating procedures (SOPs) in compliance with regulatory requirements, supporting data integrity initiatives. Physical Attributes: Ability to work in analytical testing lab with hazardous and toxic chemicals. Who You Are Minimum Qualifications: * Bachelor's Degree in Chemistry, Biology, or other Life Sciences discipline. * 3+ years experience in a cGMP analytical laboratory environment * 2+ years experience operating and maintaining ICP-MS instrumentation (ideally with the Agilent 7800/7850/7900/8900 or similar) with the subsequent data acquisition/processing software (ideally MassHunter 5.2 or similar) and microwave digestors Preferred Qualifications: * Thorough understanding of 21 CFR Part 11, 210 and 211, and ICH Q7. * Excellent written and verbal communication skills, as well as excellent documentation practices and attention to detail. * Knowledge and understanding of analytical chemistry. * Adequate technical writing skills to author reports and operating procedures. * Strong team player and willing to adapt to changes / be flexible * Proven problem-solving skills and attention to detail. Pay Range for this position:$70,000-$112,000. 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!

Job Title: Quality Control ChemistJob Description The Quality Control Chemist plays a crucial role in supporting manufacturing by conducting laboratory analysis of raw materials, intermediate blends, and finished products. This analysis is performed using wet chemistry techniques such as pH measurement, UV-Vis spectroscopy, FTIR, and titration, along with advanced instrumentation including HPLC and GC. Responsibilities + Follow standard operating procedures to ensure quality control. + Conduct quality testing and document results accurately. + Maintain and calibrate laboratory instruments regularly. + Assist with the transfer of test methods. + Train personnel on equipment usage and testing methods. Essential Skills + Bachelor's Degree in Chemistry + Minimum of 3 years of laboratory experience + Proficiency in HPLC, GC, pH measurement, UV-Vis spectroscopy, FTIR, and other wet chemistry techniques Additional Skills & Qualifications + Experience in HPLC, GC, and analytical test method development and transfer + Familiarity with microbial testing and procedures + Experience in contract manufacturing and testing Work Environment The position is based in a laboratory environment requiring adherence to safety protocols. Proper PPE including safety glasses, gloves, lab coat, and ear plugs will be provided and must be worn at all times. The role involves 75% standing, 25% sitting, and occasional lifting of up to 25 lbs. The work schedule is 2nd shift, Monday to Thursday, from 2pm to 1am, consisting of four 10-hour shifts. Occasional weekend work or overtime may be required. Initial training will require some first shift hours. Job Type & Location This is a Permanent position based out of Janesville, WI. Pay and Benefits The pay range for this position is $62400.00 - $62400.00/yr. Medical, dental, vision, 401K Workplace Type This is a fully onsite position in Janesville,WI. Application Deadline This position is anticipated to close on Jan 21, 2026. 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.