Chemist jobs in Madison, WI - 52 jobs

Current Employees: If you are currently employed at any of the Universities of Wisconsin, log in to Workday to apply through the internal application process. The Clinical Chemistry service provides professional and scientific direction for over 3 million tests annually in laboratories of the University of Wisconsin Hospitals and Clinics system. Services include automated chemistry and immunoassay, toxicology and therapeutic drug monitoring and blood gas systems, point of care and emergency department testing. The successful applicant will have expertise in test development, method validation, clinical interpretation of laboratory results, laboratory information systems and automation, consultation with physicians, experience in quality control and quality assurance, and hands-on experience and knowledge in the interpretation and development in the ever-widening field of molecular diagnostics, genomics, and proteomics. Areas of responsibility within chemistry and broader laboratory management will be assigned according to the successful applicants' experience and professional goals in coordination with other chemistry faculty. Applicants for this position will be considered for the following titles, Assistant Professor (CHS), Associate Professor (CHS), Professor (CHS). The title is determined by the experience and qualifications of the finalist. Key Job Responsibilities: Participate in administrative and committee work to support the clinical and scholarly missions of UW Health and the School of Medicine and Public Health. An essential part of these duties will be working in a collegial relationship with other faculty members. Teach medical students, residents, and fellows. Department: School of Medicine and Public Health, Department of Pathology & Laboratory Medicine The Department of Pathology and Laboratory Medicine is dedicated to the highest quality patient care, cutting-edge and impactful research, and teaching the next generation of pathologists and scientists. We emphasize a healthy work-life balance and provide a supportive work environment committed to the growth and advancement of our members. Our vibrant clinical department integrates anatomic pathology, laboratory medicine, teaching, and a robust research enterprise, and serves the UW, American Family Children's, VA, and other Madison hospitals. Our basic science and translational research programs have made fundamental discoveries in cell and stem cell biology, immunology, neuroscience, and infectious disease. Opportunities in education include a T32-funded PhD graduate program, pathology resident and fellowship programs, and both medical school and undergraduate curricula. Madison, often rated as one of the best places to live in America, is built on an isthmus, surrounded by lakes. The city, campus, green spaces and urban areas are blended to create a place unlike any other. Compensation: Negotiable, 12 month Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits. For more information, refer to the campus benefits webpage and the SMPH Academic Staff Benefits Flyer. Required Qualifications: Expertise in a subspecialty area such as molecular pathology, informatics, pharmacogenomics, toxicology, chemistry or pediatric clinical chemistry is preferred. Candidates must be board eligible or certified by the American Board of Clinical Chemistry with experience in basic and select specialty chemistry, blood gases, and point of care testing. Preferred Qualifications: For an appointment at Associate Professor or Professor rank on CHS Track, candidates will meet criteria established by the department and as outlined in the School of Medicine and Public Health guidelines for promotion or appointment to Associate or Professor on the CHS Track. Education: PhD Required How to Apply: For the best experience completing your application, we recommend using Chrome or Firefox as your web browser. To apply for this position, select either “I am a current employee” or “I am not a current employee” under Apply Now. You will then be prompted to upload your application materials. Important: The application has only one attachment field. Upload all required documents in that field, either as a single combined file or as multiple files in the same upload area. Upload required documents: Cover letter Resume List of contact information for three (3) references, including your current/most recent supervisor. References will not be contacted without prior notice. Your cover letter should address how your training and experience align with the required and preferred qualifications listed above. Application reviewers will rely on these written materials to determine which applicants move forward in the process. References will be requested from final candidates. All applicants will be notified once the search concludes and a candidate is selected The deadline for assuring full consideration is February 6, 2026; however, the position will remain open and applications may be considered until the position is filled. The department will not be able to support a request for a J-1 waiver. If you choose to pursue a waiver and apply for our position, neither the UW nor UWMF will reimburse you for your legal or waiver fees. Contact Information: Tia Seguin, *******************, ************ Institutional Statement on Diversity: Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals. The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world. The University of Wisconsin-Madison is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, national origin, age, pregnancy, disability, or status as a protected veteran and other bases as defined by federal regulations and UW System policies. We promote excellence by acknowledging skills and expertise from all backgrounds and encourage all qualified individuals to apply. For more information regarding applicant and employee rights and to view federal and state required postings, visit the Human Resources Workplace Poster website. To request a disability or pregnancy-related accommodation for any step in the hiring process (e.g., application, interview, pre-employment testing, etc.), please contact the Divisional Disability Representative (DDR) in the division you are applying to. Please make your request as soon as possible to help the university respond most effectively to you. Employment may require a criminal background check. It may also require your references to answer questions regarding misconduct, including sexual violence and sexual harassment. The University of Wisconsin System will not reveal the identities of applicants who request confidentiality in writing, except that the identity of the successful candidate will be released. See Wis. Stat. sec. 19.36(7). The Annual Security and Fire Safety Report contains current campus safety and disciplinary policies, crime statistics for the previous 3 calendar years, and on-campus student housing fire safety policies and fire statistics for the previous 3 calendar years. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.

Join our Regulated BioAnalytical Team as an Analyst where you will engage in cutting-edge biological extractions and analytical processes. This role is perfect for those who thrive in a structured environment and enjoy the challenge of working with advanced laboratory equipment. Responsibilities * Run biological extractions on samples such as urine, blood, and plasma. * Focus initially on wet lab extractions before transitioning to LC-MS (HPLC-Mass Spec) after six months. * Operate robotics for liquid handling. * Utilize laboratory equipment including balances, pH meters, and pipettes. * Work with eWorkbook software, with each chemist having access to a tablet. * Adhere to GLP regulations and protocols. Essential Skills * Bachelor's degree in Chemistry, Biochemistry, Biology, Microbiology, or related Life Science field. * 1+ year of chemistry education or undergraduate research experience with pipettes and solution preparation. * Experience with HPLC, LC-MS, or Mass Spec is highly desirable. * Strong attention to detail and communication skills. * Ability to work well in a team and under pressure. Additional Skills & Qualifications * 2-3 years of relevant experience for mid-level candidates. * Experience in food service or client-facing roles is advantageous for handling a fast-paced environment and meeting deadlines. * Proven ability to multitask and take ownership of work, recognizing and correcting errors. Work Environment Work in a lab setting as part of the Bioanalytical team, which consists of approximately 100 employees. The environment is highly focused on laboratory tasks, providing a collaborative and structured atmosphere. Job Type & Location This is a Contract to Hire position based out of Madison, WI. Pay and Benefits The pay range for this position is $24.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Madison,WI. Application Deadline This position is anticipated to close on Jan 30, 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 looking to fill a **Scientist 3 -** **Third Shift** **Analytical Chemist Pilot Plant** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ** . This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **Description** The Scientist III **Third Shift** - Analytical Chemist Pilot Plant operates and maintains a myriad of analytical instrumentation and other duties as assigned by the client. **Responsibilities** + Experience in routine and real-time testing for high-performance liquid chromatography (HPLC), gas chromatography (GC), ultraviolet (UV) spectroscopy, infrared (IR) spectroscopy, titrations, Karl Fischer (KF) testing, and other wet chemistry methods + Experience in HPLC and GC is required with an interest in expanding the knowledge and background in method development and optimization, validation, data analysis, and sample preparation techniques + Routine use of modern analytical techniques such as HPLC, GC, KF, ultraviolet-visible spectroscopy (UV-VIS), and IR spectroscopy + Comfortable working in a cGMP environment; knowledgeable in various GMP analytical activities, such as documentation procedures, abiding by relevant department SOPs and generation and second scientist review of GMP data + Experience with automated liquid handling systems (Tecan) for high throughput testing + Experience with a myriad of software platforms used in the compilation, processing, and reporting of data, such as Waters Empower, Relational Laboratory Information Management System (RLIMS), Lab X, etc. **Qualifications** + BA/BS (3-5 yrs.) of relevant experience in n chemistry or a related discipline testing lab + MS (1-2 yrs.) of relevant experience in chemistry or a related discipline testing lab **Desired Skills and Experience** + Effective organizational, multi-tasking, and oral/written communications skills + Ability to work under pressure and provide reliable results with quick turnarounds + Consistently deliver high quality and fully compliant results and interact with a diverse customer base daily + Proficient in written and spoken English, is required **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.) Job Description Position: Entry Level Biochemist/Scientist I Location: Middleton, Wisconsin Details: Full time, fully onsite This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: As an Entry Level Biochemist, you will use innovative technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Essential Functions: Trains on routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds with periodic direct supervision. Over time progresses to more complex techniques/procedures and performs analysis on a variety formulations and/or biological matrices. Completes all laboratory documentation in clear and accurate language and according to SOP and GLPs. Reviews and compiles results from assignments and makes initial determination on acceptability per SOP acceptance criteria. Problem solves with assistance pertaining to extraction and/or instrumentation problems. Performs work assignments accurately, and in a timely and safe manner. Manages QC responsibilities with minimal/no supervisor input. Communicates project status to project leader. Builds an understanding of QA processes and manages responsibilities with decreasing supervisor or QA input. Keys to Success: Education Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification Experience Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0-2 years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines Knowledge of applicable regulatory authority, compendia and ICH guidelines Demonstrates excellent manual dexterity skills, allowing for precise and accurate work. Exhibits strong written and oral communication skills, facilitating effective communication within the team and with stakeholders. Displays exceptional time management and project management skills, ensuring efficient completion of tasks. Proven problem-solving and troubleshooting abilities, enabling the identification and resolution of issues. Capable of cross-training on sample preparation techniques with another laboratory group, enhancing versatility and collaboration. Thrives in a collaborative work environment, actively contributing to a cohesive and productive team. To demonstrate behaviors which align to the 4i Values of Thermo Fisher Working Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds. Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. *This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

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 Responsibilities include, but are not limited to, the following: Applies GMP/ GLP in all areas of responsibility, as appropriate Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines Learns how to document work and maintains study documentation and laboratory records Learns how to use laboratory equipment and software appropriate for assigned tasks Attends and participates in project meetings Learns to perform peer review of data Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members Performs other related duties as assigned The ideal candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team Self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) Authorization to work in the United States indefinitely without restriction or sponsorship May work with potentially hazardous materials Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) Overtime and weekend work as required Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top Work requires use of PPE (personal protective equipment) Reside within a commutable distance to Madison, WI lab Additional Information 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.

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 Responsibilities include, but are not limited to, the following: Applies GMP/ GLP in all areas of responsibility, as appropriate Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines Learns how to document work and maintains study documentation and laboratory records Learns how to use laboratory equipment and software appropriate for assigned tasks Attends and participates in project meetings Learns to perform peer review of data Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members Performs other related duties as assigned The ideal candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team Self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) Authorization to work in the United States indefinitely without restriction or sponsorship May work with potentially hazardous materials Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) Overtime and weekend work as required Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top Work requires use of PPE (personal protective equipment) Reside within a commutable distance to Madison, WI lab Additional Information 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.

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 Responsibilities include, but are not limited to, the following: * Applies GMP/ GLP in all areas of responsibility, as appropriate * Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines * Learns how to document work and maintains study documentation and laboratory records * Learns how to use laboratory equipment and software appropriate for assigned tasks * Attends and participates in project meetings * Learns to perform peer review of data * Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments * Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members * Performs other related duties as assigned The ideal candidate would possess: * Strong computer, scientific, and organizational skills * Excellent communication (oral and written) and attention to detail * Ability to work independently and as part of a team * Self-motivation, adaptability, and a positive attitude * Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies * Reside within a commutable distance to Madison, WI Qualifications * Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) * Authorization to work in the United States indefinitely without restriction or sponsorship * May work with potentially hazardous materials * Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) * Overtime and weekend work as required * Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top * Work requires use of PPE (personal protective equipment) Additional Information 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.

LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Our high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality and range. Our tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to: bring new diagnostics and therapies to market; progress research and development; optimize food production; and continuously monitor and enhance the quality of food, the environment and consumer products. Job Description The Associate Scientist II, Production is responsible for the manufacture of site product within one or more portfolios in a cost-effective manner and in compliance with appropriate quality and safety standards. This role supports departmental success by following approved operational protocols, using good documentation practices, escalating process variances, and helping to maintain a clean and safe work environment. This position is also expected to support or participate in process improvement activities, quality investigations, and operational excellence (OE) initiatives. To perform this job successfully, an individual must be able to capably perform each of the following essential duties: Contribute to operations teams performing manufacturing, quality control, and production maintenance activities in a manner consistent with the company quality and safety standards Assist in the fermentation and purification of recombinant proteins from different expression systems In accordance with designated procedures and work instructions, prepare and operate chromatography systems, dialysis/TFF operations, and reagent preparation Support and follow production protocols geared towards robust and cost-effective supply of molecular biology product and NGS proteins Process, record, and analyze data following approved protocols and using good documentation practices Identify and escalate events that deviate from normal operations Support process improvements, nonconformance reporting, investigations, and corrective/preventative actions as assigned Effectively communicate results to immediate team, and other stakeholders as directed Maintain cleanliness and orderliness of operational area and work environment Conscientiously learn and diligently follow the requirements of the site's quality management system Adhere to company Personal Protection Equipment (PPE) policy Perform other duties as required, or assigned by management, to meet business needs Qualifications Bachelor's degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.)-or applicable industry experience Prior experience operating standard laboratory equipment (e.g. pH meters, conductivity meters, pipettes) Ability to follow standard operating procedures (SOP's) and/or manufacturing protocols Familiarity with standard biological and analytical techniques, including PCR, SDS-PAGE, and western blotting Prior experience with manual or automated chromatography systems or processes (e.g., AKTA platform) Proven ability to effectively communicate work results, including technical data, to colleagues Working knowledge of Microsoft Office, including Word, Excel, and PowerPoint Desired Knowledge & Qualifications: Prior experience performing fermentation, protein production and purification in an industrial setting Prior experience performing operations on the AKTA platform and executing depth-filtration and Tangential Flow Filtration operations Experience with functional testing (PCR, LAMP, etc.) Experience with bacteria fermentation Additional Information About LGC: LGC is a leading, global life science tools company, providing critically important components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality, and range. Our values PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT Equal opportunities LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. Short listing, interviewing and selection will always be carried out without regard these factors. For more information about LGC, please visit our website **************** #scienceforasaferworld

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. 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.

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!

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 Associate Manufacturing Scientist I (third shift) will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations. 3rd shift work hours are 10 pm - 8:30 am and includes a 15% shift differential. Responsibilities Follow batch records, SOPs, and work instructions to detail Document all operations in batch records and notebooks Comply with GMP protocols Assist other chemists within the CMC group during synthesis and chromatography of oligonucleotides including: Reagent solution preparation Column Packing Mobile phase preparation Fraction collection Operate TFF to desalt purified RNA solutions Operate a lyophilizer and package solid drug substance Execute processes as part of a team to ensure production timelines are kept and quality product is produced Maintain a clean work space Maintain safety by wearing required personal protective equipment Requirements BS or MS in chemistry, biochemistry, engineering, or related scientific field Entry level to 3 years experience in a similar position Good verbal and written communication skills Ability to work in a team environment Ability to pay attention to detail Preferred Experience working in a GMP setting with controlled documentation Wisconsin pay range $70,000-$83,000 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

About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role The Associate Scientist - Dairy Applications applies scientific and engineering principles to research and develop new dairy products or improve existing ones. This role spans concept development, specification, product commercialization, and production. The position requires strong technical expertise, creativity, and collaboration with cross-functional teams to deliver innovative solutions for Kerry's customers. Key responsibilities * Conduct research on new dairy products and improve existing formulations. * Develop new and improved methods for food processing, production, quality control, and packaging. * Respond to internal and external customer requests from concept through troubleshooting and commercialization. * Participate in ideation and brainstorming sessions. * Develop gold standards in collaboration with Culinary and Subject Matter Experts. * Perform competitive product matching and formulation optimization. * Execute projects from concept to commercialization, ensuring compliance with internal processes. * Troubleshoot customer processes and provide technical support. * Act as a strong customer-facing team member, delivering technical and culinary presentations. * Collaborate with sales and culinary representatives during customer calls. * Work with cross-functional teams to optimize Kerry's strengths and deliver superior taste and nutrition experiences. * Document research notes to develop and protect intellectual property. * Study methods to improve food quality (flavor, color, texture, nutritional value, convenience, and microbiological composition). * Complete project requests within required timelines. * Employ efficient time management and multitasking skills. * Assist customers with technical issues as they arise. * Taste and smell chemicals, flavors, and food products as part of sensory evaluation. * Stand for extended periods in a laboratory setting and lift required weights. * Communicate effectively through verbal and written channels. Qualifications and skills Education * BS/MS in Food Science or related scientific field. Technical Skills * Strong background in food chemistry, sensory science, microbiology, food packaging systems, and food engineering. * Experience in product development and food processing technology. * Knowledge of statistical process control and data analysis. * Internship or prior experience in a related field preferred. The pay range for this position is $75,602.00 - $123,432.00 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, and internal equity. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance, and tuition reimbursement. This job posting is anticipated to expire on Jan 30th, 2026. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at Know Your Rights Workplace Discrimination is Illegal (dol.gov).

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

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.

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 Responsibilities include, but are not limited to, the following: Applies GMP/ GLP in all areas of responsibility, as appropriate Learns to conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines Learns how to document work and maintains study documentation and laboratory records Learns how to use laboratory equipment and software appropriate for assigned tasks Attends and participates in project meetings Learns to perform peer review of data Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members Performs other related duties as assigned The ideal candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team Self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Reside within a commutable distance to Madison, WI Qualifications Bachelor's Degree in relevant field (laboratory experience may be substituted for a degree) Authorization to work in the United States indefinitely without restriction or sponsorship May work with potentially hazardous materials Will be exposed to potential food allergens (ex: milk, tree nuts, peanuts, fish, shellfish, etc) Overtime and weekend work as required Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top Work requires use of PPE (personal protective equipment) Additional Information 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.

LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Our high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality and range. Our tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to: bring new diagnostics and therapies to market; progress research and development; optimize food production; and continuously monitor and enhance the quality of food, the environment and consumer products. Job Description The Associate Scientist II, Production is responsible for the manufacture of site product within one or more portfolios in a cost-effective manner and in compliance with appropriate quality and safety standards. This role supports departmental success by following approved operational protocols, using good documentation practices, escalating process variances, and helping to maintain a clean and safe work environment. This position is also expected to support or participate in process improvement activities, quality investigations, and operational excellence (OE) initiatives. To perform this job successfully, an individual must be able to capably perform each of the following essential duties: Contribute to operations teams performing manufacturing, quality control, and production maintenance activities in a manner consistent with the company quality and safety standards Assist in the fermentation and purification of recombinant proteins from different expression systems In accordance with designated procedures and work instructions, prepare and operate chromatography systems, dialysis/TFF operations, and reagent preparation Support and follow production protocols geared towards robust and cost-effective supply of molecular biology product and NGS proteins Process, record, and analyze data following approved protocols and using good documentation practices Identify and escalate events that deviate from normal operations Support process improvements, nonconformance reporting, investigations, and corrective/preventative actions as assigned Effectively communicate results to immediate team, and other stakeholders as directed Maintain cleanliness and orderliness of operational area and work environment Conscientiously learn and diligently follow the requirements of the site's quality management system Adhere to company Personal Protection Equipment (PPE) policy Perform other duties as required, or assigned by management, to meet business needs Qualifications Bachelor's degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.)-or applicable industry experience Prior experience operating standard laboratory equipment (e.g. pH meters, conductivity meters, pipettes) Ability to follow standard operating procedures (SOP's) and/or manufacturing protocols Familiarity with standard biological and analytical techniques, including PCR, SDS-PAGE, and western blotting Prior experience with manual or automated chromatography systems or processes (e.g., AKTA platform) Proven ability to effectively communicate work results, including technical data, to colleagues Working knowledge of Microsoft Office, including Word, Excel, and PowerPoint Desired Knowledge & Qualifications: Prior experience performing fermentation, protein production and purification in an industrial setting Prior experience performing operations on the AKTA platform and executing depth-filtration and Tangential Flow Filtration operations Experience with functional testing (PCR, LAMP, etc.) Experience with bacteria fermentation Additional Information About LGC: LGC is a leading, global life science tools company, providing critically important components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality, and range. Our values PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT Equal opportunities LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. Short listing, interviewing and selection will always be carried out without regard these factors. For more information about LGC, please visit our website **************** #scienceforasaferworld

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 Associate Manufacturing Scientist I (second shift) will assist in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations. 2 nd shift work hours are 1pm - 11:30pm and includes a 10% shift differential. Responsibilities Follow batch records, SOPs, and work instructions to detail Document all operations in batch records and notebooks Comply with GMP protocols Assist other chemists within the CMC group during synthesis and chromatography of oligonucleotides including: Reagent solution preparation Column Packing Mobile phase preparation Fraction collection Operate TFF to desalt purified RNA solutions Operate a lyophilizer and package solid drug substance Execute processes as part of a team to ensure production timelines are kept and quality product is produced Maintain a clean work space Maintain safety by wearing required personal protective equipment Requirements: Bachelor's degree in chemistry, biochemistry, engineering, or related scientific field Experience working in a GMP setting and controlled documentation Good verbal and written communication skills Ability to work in a team environment Ability to pay attention to detail Wisconsin pay range $63,000-$73,000 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