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Patent Agent - Biotechnology Our client is a major Am law 100 firm, seeking a Patent Agent for its IP Chemical, Biotech and Pharmaceutical Practice in Boston, Madison, Milwaukee, New York, San Diego, San Francisco, Silicon Valley, or Washington, DC. The salary for this position is between $125k to $200k. Qualifications • 2-5 years of patent counseling experience, including preparation and prosecution experience. Law firm experience is strongly preferred., • Experience drafting and prosecuting domestic and international patent applications., • Experience preparing patent opinions preferred., • PhD in the biotechnology field (i.e. Molecular Biology, Immunology, or Genetics), Chemistry, or a related field., • Excellent legal writing and research skills, academics, and written and oral communication skills., • All candidates must be authorized to work in the U.S. About Us Marina Sirras & Associates LLC is a boutique legal recruiting firm committed to connecting exceptional legal talent with top-tier law firms and in-house legal departments nationwide. With decades of experience and a personalized, relationship-driven approach, we take pride in understanding the unique needs of both our clients and candidates. We are a proud member of the National Association of Legal Search Consultants (NALSC) and strictly adhere to the NALSC Code of Ethics. Marina Sirras, our founder, is a former President and Chairperson of the organization, reflecting our longstanding commitment to integrity and professionalism in legal recruiting. To learn more about our team and services, please visit us at ___.

Position Title: Lab Tech III Work Location: Madison, WI 53701 Assignment Duration: 12 Months (possible extension) Work Arrangement: Onsite Position Summary: To support the daily operations of the peptide array synthesis lab by performing essential laboratory duties, including reagent preparation, inventory management, and maintenance of lab equipment-to ensure accurate, efficient, and safe operations that drive innovation and advance scientific programs. Key Responsibilities: Prepare and handle samples, reagents, and laboratory equipment to assist in instrument setup. Wash laboratory dishes and clean instrumentation as part of routine maintenance. Maintain laboratory cleanliness following established SOPs. Participate in inventory management, ordering, and stocking of laboratory supplies and consumables. Participate in hazardous waste bulking and disposal following established SOPs. Other duties of a similar nature as assigned by supervisor / manager. Qualifications & Experience: • Bachelor of Science degree in a relevant field (e.g., Biology, Chemistry, Biochemistry)., • Experience with laboratory techniques and equipment (can be from coursework, internships, or previous employment)., • Strong attention to detail, organization, and communication skills., • Completing initial and ongoing required training and following established standard operating procedures (SOPs) are essential to safely performing duties., • Ability to work independently and as part of a team., • Ability to routinely lift 50 lbs. as required for laboratory duties.

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 purpose of this position is to provide quality assurance support to programs utilizing contract development, manufacturing, and testing organizations. The incumbent will review vendor documentation and perform lot disposition per applicable quality agreements as well as capture quality data and generate metrics for vendors. The incumbent will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development programs at Arrowhead Pharmaceuticals, Inc. Responsibilities • Interact with personnel companywide to obtain the necessary information and details to provide quality assurance support of development, clinical, and commercial programs., • Review and approve vendor generated documentation, including but not limited to, master and executed batch records, testing records, certificates of analysis (CoA), labels, protocols, and reports., • Perform lot disposition and generate certificates of compliance (CoC) as necessary., • Collaborate with vendors on quality events and non-conformances as outlined in the applicable quality agreement., • Review and release of completed manufacturing batch documentation including Quality Control data and issuance of Certificates of Analysis., • Organization and control of quality, compliance, and project related documentation., • Maintain knowledge of current compliance expectations and regulations pertaining to drug development, • Collaborate with, and provide quality support for, other departments (QC, Project Management, Toxicology, Clinical Operations, Supply Chain, etc.), • Participate in meetings with vendors and external organizations as the QA team representative., • Other duties consistent with the position as assigned from time to time., • Assist with tracking vendor quality metrics; notify QA management of any performance issues., • Assist with preparation, update, review, and routing of Arrowhead procedural documents., • Draft, review, and approve standard operating procedures (SOP) and work instructions (WI) as needed., • 8 years of quality assurance experience in a pharmaceutical development company and/or contract manufacturing organization., • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry, • Working knowledge of drug GMP regulations, as well as ICH/FDA guidance documents., • Excellent written and verbal communication skills and ability to communicate with internal and external parties., • Highly motivated team player willing to contribute to a growing pharmaceutical organization., • Ability to work independently with minimal supervision and as well as manage priorities within a fast-paced environment., • Previous experience with quality systems supporting drug-device combination products per 21 CFR Part 3 and medical devices QSR per 21 CFR Part 820/ISO 13485 is preferred. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionCompany Description 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, • 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 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

Job Description Company Overview: Oakhouse Bakery is committed to producing high-quality, safe, and delicious products that our customers love. As we continue to grow, we are looking for dedicated team members who share our passion for excellence. We take pride in maintaining rigorous food safety and quality standards to ensure that every product we create meets the highest levels of consumer trust. General Function: The Quality Assurance Technician plays a vital role in maintaining the safety, quality, and consistency of the products created at Oakhouse Bakery. The QA tech is responsible for conducting various tests and inspections on raw materials, in-process product, and finished goods to ensure compliance with established food safety, quality, and regulatory standards. The QA lab tech works closely with mixing, packaging, and warehouse teams to support operations and to identify and address any quality or food safety issues, ensuring resolution and contributing to the overall success of the bakery’s operations. Reports to: Regulatory Compliance Coordinator Positions Supervised: None Key Responsibilities: • Promote Safety First: Promote a culture of safety throughout the facility, ensuring all activities prioritize employee well-being., • Policy Adherence: Strictly follow and reinforce Oakhouse Bakery's food safety, quality, and Good Manufacturing Practices (GMP) policies., • Cross-Departmental Support: Collaborate with production, warehouse, and maintenance teams on quality and food safety matters., • Laboratory Analyses: Perform routine laboratory tests on raw materials, in-process products, and finished goods to ensure compliance with food safety, quality, and regulatory standards., • Program Maintenance: Support the maintenance and adherence to Oakhouse Bakery’s food safety, regulatory, Gluten-Free, Organic, and Non-GMO programs, under the guidance of FSQA leadership., • Inspections: Conduct routine GMP and food safety inspections, identifying non-conformance events and opportunities for improvement., • Label Management: Print and verify product labels to ensure accuracy and compliance., • Chemical Monitoring: Check and maintain sanitation chemical titrations to meet safety standards., • Equipment Calibration: Calibrate lab equipment and record results accurately to ensure consistent product quality., • Process Checks: Perform in-line process checks and verifications, including setting up and adjusting metal detectors, weight checks, and x-rays., • Sanitation Validation: Conduct sanitation swab validations as needed to verify cleanliness and safety., • Ingredient Verification: Verify ingredients are staged properly to ensure they meet quality and food safety standards., • Education: Highschool diploma or equivalent is required; college degree in biology, microbiology, chemistry, food science, or a related discipline is strongly desired., • Experience: Prior experience in food manufacturing is desired, with a strong preference for candidates with experience in quality assurance and food safety., • Communication Skills: Effective communication skills are essential, with bilingual Spanish/English abilities strongly desired., • Work Ethic: Must have a strong work ethic and ability to self-supervise and motivate., • Safety: Consistently work safely and promote a safety-first environment., • GMP and Policy Enforcement: Adhere to and enforce all GMPs and food safety policies with integrity., • Process Control: Empowered to stop any process for safety, food safety, or quality reasons., • Policy Enforcement: Responsible for enforcing all company policies and procedures and reporting any safety, food safety, or quality issues to the FSQA Manager.

Job DescriptionQA Validation Manager Scientific Protein Laboratories (SPL) Waunakee, WI | On-site | Biopharmaceutical Manufacturing Lead validation. Shape quality. Make an impact in life-saving biologics. Scientific Protein Laboratories (SPL) is a global leader in biopharmaceutical manufacturing, supporting the production of critical therapies that improve and save lives worldwide. As we continue to expand our capabilities, we’re seeking a QA Validation Manager to lead enterprise-level validation programs across our Waunakee, WI site. This is a high-visibility leadership role for a validation expert who thrives in regulated environments, enjoys cross-functional collaboration, and wants to influence how validation is done, not just maintain the status quo.What You’ll Do As the QA Validation Manager, you’ll provide strategic and hands-on leadership across all major validation disciplines, ensuring SPL’s validation programs meet the highest standards of quality, compliance, and efficiency. • Lead and oversee equipment, process, cleaning, and computerized systems validation within a biologics drug substance manufacturing environment, • Own and maintain the Master Validation Plan (MVP) and validation governance framework, • Develop and execute risk-based validation strategies aligned with cGMP, 21 CFR Part 11, and global regulatory expectations, • Review and approve validation protocols, reports, change controls, deviations, and CAPAs, • Partner closely with Manufacturing, Engineering, Quality, IT, and Regulatory teams to ensure seamless integration of validation activities, • Serve as a subject matter expert during audits, inspections, and regulatory interactions, • Lead continuous improvement initiatives to modernize validation processes and documentation, • Support technology transfer, scale-up, and new product introductions, • Mentor and develop validation team members while managing resources and budgetsWhat Success Looks Like, • Validation programs are inspection-ready, compliant, and efficient, • Cross-functional teams view you as a trusted technical and quality leader, • Validation strategies evolve with regulatory expectations and industry best practices, • Bachelor’s degree in Pharmacy, Pharmaceutical Engineering, Biology, Chemistry, or a related scientific field, • 5+ years of validation experience in a regulated pharmaceutical or biologics environment, • At least 2 years of people leadership or management experience, • Deep expertise across multiple validation disciplines, • Strong knowledge of cGMP and regulatory compliance requirementsPreferred, • Master’s degree or higher, • 10+ years of validation experience in biologics or complex manufacturing environmentsWhy Join SPL?, • Meaningful work supporting life-saving biologically based therapeutics used worldwide, • Competitive compensation package including base salary and recognition programs, • 401(k) with company match to support your long-term financial goals, • Generous paid time off (PTO) and paid holidays, • Career development and leadership growth opportunities within a global biopharmaceutical organization, • Collaborative, science-driven culture that values integrity, accountability, and continuous improvement, • High quality of life in Waunakee, WI! A growing community just outside Madison with excellent schools and outdoor recreation, • If you’re a validation leader ready to take ownership, influence quality strategy, and work on products that truly matter, SPL wants to hear from you. SPL is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. We Make it Easy Founded in 1901, MRA is a nonprofit employer association that serves more than 4,000 employers, covering more than one million employees. As one of the largest employer associations in the nation, MRA helps its member organizations thrive by offering the most comprehensive assortment of HR services, information, education, and resources to help build successful workplaces and a powerful workforce. We partner with these companies working directly with their HR department and leadership to hire their talent. We are a direct line to the company, not an agency recruiter. Powered by JazzHR iKQ46kYcMB

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 purpose of this position is to provide Quality Assurance support for Arrowhead Pharmaceuticals' raw materials program. As a member of the Supplier Quality team, this role supports raw material supplier qualification, material risk assessment, specification development, and change control activities to ensure compliance with GMP and applicable regulatory requirements. The position also assists with the collection, analysis, and generation of supplier performance metrics to support ongoing monitoring and continuous improvement. This role requires regular interaction with internal cross-functional stakeholders as well as external organizations to support pre-clinical, clinical, and commercial manufacturing programs Responsibilities • Assist with raw material lifecycle management including, but not limited to, drafting, editing, reviewing, and approving raw material specifications, reviewing raw material qualification protocols and reports, and ensuring compliance with periodic requalification cycles, in collaboration with internal functional teams, • Perform risk assessments for raw materials (e.g., impact to product quality, patient safety, and regulatory compliance)., • Advise Supplier Quality Audits team with supplier qualification and requalification as needed, • Support maintenance of the ASL by providing and entering qualification information into the eQMS, • Collaborate with raw material suppliers to resolve quality issues, documentation discrepancies, and non-conformances per internal procedures., • Review Supplier Change Notifications and assess impact on product quality., • Initiate and manage change controls related to raw materials, • Manage Supplier Corrective Action Requests (SCARs) per internal procedures and applicable quality agreements., • Support deviation investigations, CAPAs, and root cause analyses involving material issues., • Provide quality oversight during material onboarding and lifecycle management, • Request and review supporting documentation for raw material qualifications from suppliers including, but not limited to, production records, certificates of analysis (CoA), certificates of conformance (CoC), BSE/TSE statements, etc., • Scan and upload executed documents to the EDMS, properly categorize within the system, and route for verification/approval., • Assist with the preparation, update, review, and routing of Arrowhead procedural documents., • Track and trend raw material-related quality metrics, • BS/BA in Chemistry, Biology, Biochemistry, or related scientific field is preferred., • Minimum of 5+ years of Quality Assurance experience in a GMP-regulated biotech or pharmaceutical manufacturing environment, with an emphasis on raw material release, Supplier Quality, and/or material qualification activities., • Prior experience with use of an Electronic Document Management System (EDMS) in a regulated environment., • Prior experience with use of an Enterprise Resource Planning (ERP) software in a regulated environment., • Working knowledge of ICH Q3, Q8, Q9, Q10, and Q11., • Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office applications, and SmartSheet., • Excellent interpersonal, verbal, and written communication skills., • Ability to consistently communicate with external parties in a professional manner., • Ability to follow company procedures, work instructions, and policies., • Excellent attention to detail and organizational skills. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionSalary: Are you ready tolaunch your career in environmental serviceswith a dynamic, employee-owned team? Join Ruekert & Mielke, Inc. and gain hands-on experience working onmunicipal, civil, agricultural, or water resources projects that make a real impact in local communities. Were seeking enthusiastic student interns who are eager to learn, contribute, and grow in a supportive environment. As an intern, youll participate in environmental field work, perform desktop analysis, and support regulatory compliance efforts whilecollaboratingwith engineers, scientists, and ecologists on projects that improve water quality and community infrastructure. Your work will directly support project success and our mission of building better communities. Experience the benefits of a culture that values learning, mentorship, and professional growth. Apply now for a May to August internship and jumpstart your engineering career! What Youll Gain • Practical experience on real-world environmental and water resources projects, • Supportive, team-oriented culture focused on mentorship and professional development, • Exposure to a variety of project types, including municipal stormwater, watershed planning, and natural resource assessments, • Opportunities to work alongside engineers, scientists, biologists, and GIS professionals Goals & Responsibilities This position includes, but is not limited to, the following duties and responsibilities: • Conduct desktop-level environmental screening and research using websites, technical resources, historic water quality data, watershed information, prior studies, stream characterization, and agency guidance documents., • Utilize GIS and mapping resources to evaluate wetlands, floodplains, waterways, soils, environmental corridors, and cultural or historic resources., • Perform water quality sampling, including NR 151 infiltration testing and illicit discharge detection and elimination (IDDE) outfall inspections., • Participate in field inspections and site visits to evaluate outfalls, stream conditions, erosion control practices, streambank stabilization sites, wetlands, habitat conditions, invasive species, and stormwater facilities., • Utilize mobile field technology (GPS, tablets, Survey123, ArcGIS, or similar tools) to collect and document environmental field data., • Collect accurate field data and prepare sampling reports, datasheets, photo logs, narratives, and electronic reporting forms., • Assist with preparation of site-specific and watershed-based studies, including municipal stormwater management, TMDL support, watershed planning, pollutant trading, and adaptive management efforts. Qualifications & Skills The ideal candidate for this position will possess the following education, experience, and abilities: • Pursuing an Associates, Bachelors, or Masters degree in Environmental Science, Environmental Studies, Biology, Ecology, Natural Resources, Water Resources, or a related field, • Strong work ethic, attention to detail, and willingness to learn, • Comfortable working outdoors in various weather conditions, • Ability to collaborate and communicate with project managers and team members to ensure project success, • Basic math skills for measurements and estimations, • Valid drivers license and insured, reliable transportation About Us Ruekert & Mielke, Inc. is a 100% employee-owned civil engineering firm that has been empowering clients and employee owners to thrive since 1946. Together with our family of firms, Axiom Consultants and Outland Design, we tackle engineering challenges for a diverse set of clients across multiple sectors including government, agriculture, and real estate. Our team of engineers, environmental scientists, and technology experts work as an extension of our clients, offering exceptional planning, design, and construction management services. Combining experience, vision, and innovative technology, R/M serves as a trusted infrastructure ally to help make community possible. Visit learn more. Learn how you can make community possible as an employee owner at R/M!Watch Video

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 Serve as a key contributor to the Quality Management System (QMS) by supporting the management and execution of comprehensive internal and external audit programs. This position requires expertise in quality management systems and regulatory compliance to ensure audit activities are executed in accordance with global GxP regulations, company policies, and industry standards. This role plays an integral part in upholding Arrowhead Pharmaceutical's commitment to patient safety, product quality, and regulatory compliance by partnering with cross-functional teams, external collaborators, and regulatory authorities to drive continuous improvement and maintain a culture of compliance and quality. Responsibilities: • Develop, implement, and maintain a comprehensive internal audit program covering applicable company objectives and global GxP requirements including GMP (FDA, EMA, ICH, MHRA, etc.), ICH guidelines, and ISO standards across Arrowhead facilities and operations., • Create risk-based audit plans and schedules and maintain oversight of planning, coordination, and execution per the established audit plans., • Prepare and issue comprehensive audit reports that clearly identify compliance gaps, systemic risks, and areas for improvement., • Coordinate and support regulatory inspections by FDA, EMA, and other health authorities, ensuring inspection readiness and effective responses to regulatory queries., • Conduct inspection readiness assessments and mock inspections to prepare facilities and teams for regulatory scrutiny., • Communicate audit findings to applicable quality leadership and facilitate timely escalation and resolution., • Coordinate audit response activities and maintain oversight to ensure regulatory compliance and effective follow-up through to closure., • Coordinate with cross-functional teams to implement process improvements and preventive measures based on audit observations., • Oversee corrective and preventive actions (CAPAs) CAPA activities resulting from internal audits and external inspections to ensure timely and effective closure., • Track audit findings, trends, and metrics to identify systematic issues and opportunities for improvements initiatives., • Mentor and train other team members on audit methodologies and best practices., • Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Chemistry, Biology, or related discipline., • 5 years in Quality Assurance or GxP-regulated operations (pharmaceutical, biotechnology, or related industry)., • Strong knowledge of GxP regulations and global compliance expectations., • Deep expertise and understanding of quality management systems, auditing principles, and risk identification and mitigation., • Excellent interpersonal and communication skills, with the ability to influence and work within a matrixed environment, • Strong critical thinking, problem-solving, and conflict resolution capabilities. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionJob Title: LCMS Lead ScientistJob Description As an LC-MS Lead Scientist, you will oversee studies, ensuring that methods are ready, validated, executed, and documented to meet regulatory requirements. You will not work in the lab but will review data, act as the primary scientific point of contact, and coach team members while coordinating with internal and external stakeholders. Responsibilities • Oversee bioanalytical study work of moderate complexity., • Sign off on reports and review/approve raw data., • Act as the primary scientific point of contact for studies., • Coordinate across internal and external stakeholders., • Provide scientific guidance and mentoring to team members., • Ensure methods meet regulatory requirements and are documented appropriately., • Engage with regulators for clinical or pre-clinical studies.Essential Skills, • B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.)., • 2-5 years of experience working on LCMS., • Experience as a BioA Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector., • Proven data review/approval skills and method validation readiness., • Experience with Sciex Mass Spec and other analysis software., • Familiarity with GLP or GCP regulations.Additional Skills & Qualifications, • Experience with Nautilus and Analyst software., • Knowledge of ICH or 28BMV regulatory guidance protocols., • Familiarity with FDA internal standards. Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care FSA Disability Plan Short Term Disability (STD) Long Term Disability (LTD) Life and Accidental Death and Dismemberment (AD&D) Insurance Plans Basic Life Optional Life Dependent Life Optional AD&D Employee Stock Purchase Plan (ESPP) Workplace Type This is a hybrid position in Madison,WI. Application Deadline This position is anticipated to close on Apr 1, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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 This position will be primarily responsible for leading technical transfer activities to support manufacturing readiness. This includes writing and developing GMP batch records, methods, and other necessary documentation to ensure effective process transfer between process development and manufacturing groups. They will assist with writing and updating SOPs and technical documents pertaining to GMP operations. The position is also responsible for coordinating process transfer activities for new and existing programs across cross-functional teams. Responsibilities • Work between process development and manufacturing scientists to create and maintain production batch records and process documentation for new and existing programs., • Facilitate cross-functional coordination and input to document new methods, • Manage project timelines and provide project milestone updates to internal team members, • Identify and implement best practices and process improvements to technical transfer activities and documentation, • Lead deviation investigations and implement appropriate corrective action as necessary., • Contribute to the compilation of master data, • Write SOPs pertaining to GMP production., • Perform reviews of executed batch records, • Work with different departments to achieve project readiness goals, • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry, • 3 years working in a GMP setting with a minimum of 1 year of experience in a technical writer or technical transfer position, • Proficient experience working with controlled documentation, • Experience with internal CAPA investigations, • Proficient project management skills, • Ability to collaborate with and coordinate cross-functional teams, • Proficiency with Microsoft Suite applications (Word, Excel), • High attention to detail, • 5+ year's GMP experience and 3+ years tech transfer experience. Wisconsin pay range $84,000—$100,000 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

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 purpose of this position is to provide quality assurance support to programs utilizing contract development, manufacturing, and testing organizations. The incumbent will review vendor documentation and perform lot disposition per applicable quality agreements as well as capture quality data and generate metrics for vendors. The incumbent will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development programs at Arrowhead Pharmaceuticals, Inc. Responsibilities • Interact with personnel companywide to obtain the necessary information and details to provide quality assurance support of development, clinical, and commercial programs., • Review and approve vendor generated documentation, including but not limited to, master and executed batch records, testing records, certificates of analysis (CoA), labels, protocols, and reports., • Collaborate with vendors on quality events and non-conformances as outlined in the applicable quality agreement., • Perform lot disposition and generate certificates of compliance (CoC) as necessary., • Assist with tracking vendor quality metrics; notify QA management of any performance issues., • Assist with preparation, update, review, and routing of Arrowhead procedural documents., • Scan and upload executed documents to the EDMS, properly categorize within the system, and route for verification/approval., • Draft, review, and approve standard operating procedures (SOP) and work instructions (WI) as needed., • 5 years of quality assurance experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization., • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry, • Working knowledge of GMP, GCP, and/or GLP regulations as well as ICH and FDA guidance documents., • Excellent interpersonal, verbal, and written communication skills., • Ability to consistently communicate with external parties in a professional manner., • Ability to follow company procedures, work instructions, and policies., • Excellent attention to detail and organizational skills., • Prior experience with use of an electronic document management system in a regulated environment All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionSalary: Summary Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated Associate Scientist to join our team. Responsibilities will scale with experience and educational level. Applicants should be comfortable in a fast-paced and highly collaborative environment. The successful candidate will be a highly detailed and clear communicator who will contribute to the development, optimization, and validation of Elephas cancer diagnostics platform. Essential Duties and Responsibilities • Handle live biological specimens safely and free from contamination in tissue culture, • Process live and fixed biological specimens, • Operate and maintain laboratory equipment, • Communicate with various stakeholders regarding instrument performance and process bottlenecks, • Adhere to all safety protocols, • Keep accurate and timely records in electronic laboratory notebooks, • Perform operations to meet quality expectations in a regulated environment, • General lab maintenance as needed Education/Experience/Skills • Bachelors degree in lab technology, instrumentation, biology or related field is preferred but not required, if relevant work experience is applicable, • Familiarity with laboratory instruments and production equipment, • Experience in safe tissue handling methods 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.

Job DescriptionSalary: Summary Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated Associate Scientist to join our team. Responsibilities will scale with experience and educational level. Applicants should be comfortable in a fast-paced and highly collaborative environment. The successful candidate will be a highly detailed and clear communicator who will contribute to the development, optimization, and validation of Elephas cancer diagnostics platform. Essential Duties and Responsibilities • Handle live biological specimens safely and free from contamination in tissue culture, • Process live and fixed biological specimens, • Operate and maintain laboratory equipment, • Communicate with various stakeholders regarding instrument performance and process bottlenecks, • Adhere to all safety protocols, • Keep accurate and timely records in electronic laboratory notebooks, • Perform operations to meet quality expectations in a regulated environment, • General lab maintenance as needed Education/Experience/Skills • Bachelors degree in lab technology, instrumentation, biology or related field is preferred but not required, if relevant work experience is applicable, • Familiarity with laboratory instruments and production equipment, • Experience in safe tissue handling methods 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.

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 We are seeking a highly skilled and motivated Process Validation Engineer with a strong background in Good Manufacturing Practices (GMP) to join our team. This individual will be responsible for drafting, reviewing, and overseeing the execution of process and cleaning validation documentation. The ideal candidate will have a minimum of 8 years of experience in GMP validation or related fields, with at least 3 years of GMP manufacturing experience preferred. Responsibilities • Draft and review process validation and cleaning validation protocols and reports, ensuring compliance with GMP regulations., • Oversee and manage the execution of manufacturing validation activities, ensuring timelines and quality standards are met., • Collaborate with cross-functional teams to ensure validation strategies align with production requirements and regulatory guidelines., • Provide technical support to manufacturing during validation and qualification activities., • Identify and assess risks, proposing corrective actions and improvements to enhance validation processes., • Ensure compliance with all applicable regulatory requirements, including FDA, EMA, and ICH guidelines., • Review and approve validation data and documentation to ensure accuracy and regulatory compliance., • Participate in audits and inspections, providing validation documentation and responding to inquiries from regulatory agencies., • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry., • 8 years of experience in GMP validation or a related field., • Knowledge of process and cleaning validation activities, including test methods, execution, and data analysis., • Excellent technical writing skills with high attention to detail., • Excellent problem-solving skills and attention to detail., • Strong written and verbal communication skills to effectively interact with internal teams, management, and regulatory bodies., • Experience with regulatory submissions and/or inspections., • Ability to work across teams., • Experience in drafting and reviewing validation protocols and reports., • Strong understanding of GMP regulations, validation principles, and industry best practices., • 3 years of GMP manufacturing experience, • Six Sigma or Lean certifications Wisconsin pay range $90,000—$120,000 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

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 purpose of this position within the Quality Assurance department is to support on-going development programs for preclinical, clinical, and commercial drug candidates at Arrowhead. A key function of the position will involve review of manufacturing batch records, analytical data and reports, and associated documents within the Quality Assurance department and will also support general quality systems related to current Good Manufacturing Practices (cGMP) within the organization. The Specialist II is expected to interact with multiple internal departments. Responsibilities • Interact with representatives from other departments, including manufacturing, QC, and Analytical Development, to obtain the necessary information for review of documentation., • Review and approve analytical testing data and final reports from internal and external sources with minimal supervision., • Review and approve manufacturing batch records, forms, and associated testing with minimal supervision., • Perform room releases as required., • Perform QA on the floor as required., • Assist with investigations and deviations as appropriate with minimal supervision., • Organization and control of project related documentation., • Issue, review, and reconcile controlled forms., • Review, verify, and reconcile labels., • Scan and upload executed documents to the EDMS, properly categorize within the system, and route for verification/approval., • Maintain knowledge of current compliance expectations and regulations pertaining to drug development., • Assist with Good Documentation Practices, GMP, and data integrity training as needed., • BS/BA in Chemistry, Biology, Biochemistry, or related scientific field is preferred., • 3 years of Quality Assurance experience in a GMP-regulated biotech or pharmaceutical manufacturing environment, • Experience with quality systems supporting GMP regulations (21 CFR Parts 11, 210, 211, and EU GMP, including Annex 11 and 15)., • Competent knowledge of and ability to use Microsoft Word, Excel, and Smartsheet. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description About Asahi Beer USA: Asahi Beer USA is a premium beverage business headquartered in the U.S., with a focus on building and expanding a portfolio of super premium brands including Asahi Super Dry and Twisted Shotz. As part of Asahi Europe & International, the global arm of Asahi Group Holdings, the U.S. team plays a strategic role in shaping the future of Asahi’s international portfolio through consumer-led innovation and agile market execution. With access to global brands, insights, and capabilities, and supported by Octopi Brewing— a leading production facility based in Wisconsin — Asahi Beer USA combines local agility with global scale to deliver high-quality, distinctive products to U.S. consumers and drive growth across the RTD and beer categories. Available Shift: Friday-Sunday, 6am-6pm Total pay includes $20/hr base + a weekend day shift premium of $5.75/hr. The base pay for this role may vary based on experience. Job Summary: The Quality Assurance (QA) Technician will perform checks and tests to maintain quality throughout the plant and in all processes. They will perform physical, chemical, and microbiological tests, sample product from several points during production, manage the documentation and data associated with those tests/samples, and maintain equipment associated with those checks. Primary Responsibilities: • Daily sampling and testing of in-process and finished product, including, but not limited to: Alcohol by Volume, Apparent Extract, Bitterness, Can Seam Analysis, Carbonation, Color, Diacetyl by Gas Chromatography, Microbial Analysis by qPCR, Microbial Analysis by Spread Plate, Pour Plate, Membrane Filtration, etc., Oxygen Content, Package Integrity, pH, Sensory Analysis, Total Acidity, Yeast Counts and Viability., • Documenting test results, confirming that results meet specifications defined by client and legal requirements, and implementing product holds as necessary., • Working with production, liquid processing, and warehouse to ensure finished product meets all quality and food safety requirements, • Organizing, transcribing, trending, interpreting, and summarizing analytical data for historical reference, sharing with internal stakeholders, and uploading to client shared drives., • Communicating results with brewing, cellaring, batching, and packaging team members to ensure all departments are running smoothly., • Cleaning, calibration, and maintenance of various testing equipment., • Creating and editing new and existing standard operating procedures (SOPs)., • Working with the Quality Manager and other department heads to guarantee that client needs and expectations are met., • Maintaining a clean and organized work environment. Including regular inventorying of consumables, reagents, media, and other materials., • Performing other related duties as assigned. About Our Team: We are looking for energetic candidates to grow with us at Asahi Beer USA. As we complete our current expansion, we will increase the output of our state-of-the-art production and brewing facilities. Qualified individuals are detail-oriented, collaborative, growth-focused, and self-motivated. Our team is a community; we are open, informal and laid back, but also hard working and respectful of others. You should be as well. Qualified and interested individuals should please submit their letter of intention and resume. Compensation varies based on experience. Health insurance, dental, vision, paid time off, 401k and other extra perks. We are an equal opportunity employer. Offers of employment at Asahi Beer USA are contingent upon clear results of a thorough background check. Background checks will be conducted on all final candidates, as deemed necessary. Required Skills/Abilities: • Strong attention to detail and organization., • Strong interpersonal and customer service skills, including excellent verbal and written communication., • Time management skills with a proven ability to prioritize tasks and meet deadlines., • Ability to function well in a fast-paced environment., • Familiarity with lab procedures including, but not limited to, pipetting, titrating, pH measurement, and GC sample prep., • Understanding and appreciation of aseptic technique., • Ability to utilize all five senses to inspect quality., • Flexibility with working hours., • Ability to maintain confidentiality with business related information., • Adhere to all PPE and GMP requirements., • Maintain a clean, safe, and organized work environment., • Ability to lift 55lbs and move 165lb as needed., • High school diploma required. Associate’s or Bachelor’s degree in Food Science, Applied Science, Chemistry, Biology, Biochemistry, Biotechnology, Environmental Science, or a similar field is a plus., • Prior quality assurance and/or laboratory experience is preferred. Brewing and/or beverage packaging experience is a plus., • Familiarity with common quality control and lab terminology. Compensation details: 25.75-25.75 Hourly Wage PI14eedcbb7423-25405-40124208

Work Location: Madison, Wisconsin Shift: Department: LS-SC-UYWQFB QC Release, VOA Hiring Manager: Abel Madrigal This information is for internals only. Please do not share outside of the organization. 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. \n • Analyze complex cGMP data using sound scientific rationale to identify root causes and implement effective CAPAs with minimal oversight.\n, • Perform in-depth analytical data review in support of QC, ensuring accuracy, integrity, and compliance with ALCOA+ principles.\n, • Prioritize and coordinate in-process testing reviews with manufacturing and laboratory teams to minimize downtime.\n, • Author and manage complex deviations, investigations, change controls, CAPAs, and OOS/OOT activities, communicating status to stakeholders.\n, • Review and support method development, validation, transfers, product changeovers, and ICP-MS testing for routine QC analysis.\n, • Maintain audit-ready laboratory operations, including safety, housekeeping, reagent management, waste disposal, and equipment qualification review (IQ/OQ/PV).\n, • Provide peer review, technical documentation, and training support for laboratory staff while upholding data integrity and "right first time" principles.\n, • Collaborate cross-functionally to manage projects and timelines while ensuring compliance with ICH Q7, 21 CFR Parts 11/210/211, and applicable regulatory standards.\n\n Physical Attributes: • Work in analytical testing lab with hazardous and toxic chemicals.\n Who You Are Minimum Qualifications: \n • Bachelors Degree in Chemistry, Biology, or other Life Science discipline.\n, • 5+ years experience in a GLP or cGMP analytical laboratory environment\n\n Preferred Qualifications: \n • Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7.\n, • Excellent written and verbal communication skills, as well as good documentation practices and attention to detail.\n, • Knowledge and understanding of analytical chemistry techniques listed above in the 'your role'. (HPLC, GC, KF, DSC, TGA, IR, MS, NMR and LC-MS)\n, • Experience in reviewing GMP technical data from the analytical chemistry technique listed above in the 'your role'.\n, • Adequate technical writing skills to author reports, training memos and operating procedures.\n\n 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. The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

JOB OBJECTIVE: Responsible for activities related to customer internal validations for the Genetic Identity Business Unit. Ensure alignment between departmental objectives and corporate activities and initiatives for delivery of validation support to our customers. Reinforce customer advocacy throughout the organization. Ideal candidates are located in Europe/Middle East. CORE DUTIES: 1. Present validation programs on Genetic Identity Business Unit products, instrument platforms utilizing Promega chemistries, and related applications to customers (internal and external) worldwide., 2. Provide expert technical solutions to customers in multiple stages of the validation (pre-validation consultation, laboratory validation work, or post-validation training). Support methods include telephone, e-mail, or visits to customer labs., 3. Perform data analysis and/ or laboratory work to fulfill the Statement of Work requirements for validation service engagements., 4. Attend and give presentations at local, national, and international meetings and seminars on the Genetic Identity Business Unit products primarily in the forensic field., 5. Assist in the design, analysis and publication of developmental validations in white papers and peer-reviewed journals, reinforcing Promega's industry credibility and customer confidence., 6. Promote interdepartmental communications by acting as liaison between GI marketing and other groups including, but not limited to, GI R&D, Technical Services, Technical Training, Complaint Investigation, Scientific Applications Services, and Scientific Communications., 7. Produce and maintain an archive of validation material that would facilitate the development of specific validation programs as the need arises. This includes, but is not limited to, tests, electronic files, videos, and Internet presentations., 8. Monitor and report competitor activities, technical developments, and trends., 9. Maintain pertinent customer contact information within the CRM system., 10. Perform data analysis and/ or laboratory work to identify root cause of customer technical issue, prepare for workshop or training, evaluate a new Promega product, or evaluate a competitor's product., 11. Review marketing material for technical accuracy, including Profiles in DNA (publication), European GI team Identity, product brochures, communication to customers in compliance with ISO requirements, and other technical documents as they occur., 12. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others., 13. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work., 14. Understands and complies with ethical, legal and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. M.S. degree in molecular biology (or equivalent) with 3 or more years' relevant forensic experience or B.S degree in molecular biology (or equivalent) with 5 or more years' experience in a forensics laboratory., 2. Experience with fluorescent detection, DNA sequencing or CE platforms with the ability to troubleshoot and train others on their use. Emphasis is on PCR and CE instrumentation and related software, including real-time analysis and use of CE instruments for genotyping., 3. Excellent communication and listening skills, both verbal and written., 4. Proven strong presentation skills in small or large audiences., 5. Ability to travel extensively both domestically and internationally - averaging 30% of the time., 6. Ability to maintain a safe and clean laboratory environment., 7. Ability to work independently with minimal supervision and with other team members in a cooperative manner., 8. Ability to troubleshoot technical questions from customers and provide information to the customer in a timely, helpful, courteous, and professional manner., 9. Demonstrated proficiency in digital tools and technology, including Microsoft applications and mobile platforms, with the ability to adapt and leverage emerging technologies, such as artificial intelligence, to improve efficiency, automation, and collaboration. PREFERRED QUALIFICATIONS: 1. Prior forensic validation experience in genetic identity related areas or molecular biology., 2. Ability to troubleshoot most applications related to Promega's complete product line. PHYSICAL DEMANDS: 1. Ability to work with computer equipment frequently., 2. Ability to frequently and accurately communicate with customers via digital communication tools., 3. Ability to use scientific instruments and to wear personal protective equipment (lab coat, goggles, gloves, etc.)., 5. Ability to remain stationary at a laboratory bench for extended periods, including with biological and fume hoods., 6. Ability to move and position laboratory materials up to 25 pounds., 7. Ability to travel for training or validation support, which may include long flights and adjusting to new time zones. At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.

Job Locations US-MN | US-IA | US-IL | US-WI ID 2026-18892 Job Function Service & Support Bruker is enabling scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Bruker's high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nano analysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. Today, worldwide more than +11000 employees are working on this permanent challenge at over 90 locations on all continents. Bruker continues to build upon its extensive range of products and solutions, its broad base of installed systems and a strong reputation among its customers. Being one of the world's leading analytical instrumentation companies, Bruker is strongly committed to further fully meeting its customers' needs as well as continuing to develop state-of-the-art technologies and innovative solutions for today's analytical questions. The Bruker Microbiology Applications Specialist supports all microbiology platforms and associated products within the Microbiology and Diagnostics Division. The Bruker MALDI and IR Biotyper Systems are revolutionary products which utilize mass and infrared spectrometry to produce rapid, accurate and cost-effective microorganism identifications and typing. The Microbiology Applications Specialist is responsible for managing the technical success at all Bruker M&D accounts in the assigned geographic region. This position will be based in the Central West MAS Territory covering Minnesota, Iowa, Illinois, and Wisconsin. Independently schedule and conduct on-site and factory-based application trainings for new and current customers for all MALDI and IR Biotyper protocols. • Proactively contact current customers quarterly to provide product and service information, product updates and to resolve any current customer issues. This may include but is not limited to new product launch information, software updates, library updates, hardware or software troubleshooting, and basic or advanced Biotyper training needs., • Work cooperatively with Service and Sales Team to drive consumable product adoption., • Independently maintain contact and strong relationships with users in respective region., • Communicate with the field sales teams to relay pertinent information regarding current and future customers. This information can include but is not limited to product requirements and interest and customer support satisfaction., • Attend local workshops, trade shows, congresses, or seminars according to the needs of the region as well as provide seminars and talks to promote Bruker M&D line of products., • Adhere to company policies for expense control and meeting expense budgets, • Provide monthly lead generations and customer training metrics to the MAS Manager., • Bachelor's degree in microbiology, Bacteriology, or similar., • 2+ years of experience in a microbiology laboratory., • First-hand knowledge of the one of the following microbiology disciplines: clinical, food, pharma, environmental, or veterinary microbiology laboratory., • Ability to effectively communicate and train others on technical workflows., • Provide superior customer service with timely, accurate, and clear responses to customers' needs., • Ability to present company products and services to laboratory personnel., • Ability to work with internal partners (sales, service, support, marketing) to provide outstanding customer service and product satisfaction., • Strong verbal, written, and technical presentation skills, including MS Office with advanced Excel applications proficiency., • Ability to independently manage multiple tasks and deliverables., • Occasional lifting of up to 50 pounds., • Able to manipulate small hand tools., • Working knowledge of Sales Force CRM., • Strong knowledge of microbiology coupled with an energetic personality and strong customer focus., • Regular domestic travel up to 70%., • Ability to travel on a routine basis and maintain a current Passport/ VISA as required for international travel. Occasional weekend travel will be required. The MAS must plan and execute individual travel per company travel guidelines and within expense budget objectives. At Bruker, the base salary is part of our total compensation. The estimated base salary range for this full-time position is between $86,400.00 and $153,500.00 and provides an opportunity to progress as you grow and develop within a role. The base salary for the role will depend on several job-related factors, including, but not limited to, education, training, experience, the geographic location of the successful candidate, skills, competencies, job-related knowledge, and travel requirements for this position. Full-time employees may also be eligible for a performance-related incentive in addition to a full range of benefits, including 401(k) with company match, an employee stock purchase plan, medical and dental plans, life insurance, short-term and long-term disability insurance, employee assistance program and paid time off including vacation, sick time and holidays, and more. Bruker is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, and other protected characteristics. Certain positions at Bruker require compliance with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions.

OUR TEAM: The Nucleic Acids Technology group at Promega consists of highly experienced and dedicated scientists. The group focus is developing high quality products for amplification related workflows across multiple technologies and disciplines including Life Sciences and Diagnostics. YOUR ROLE: As Sr Research Scientist 1 you would be involved in the scientific leadership of the company, i.e. management, mentoring, consensus building and/or act as technical expert in multiple areas of specialization. Apply scientific leadership to individual R&D Projects. Demonstrate the ability to execute and champion innovative research. Formulate an overall project strategy for experimental design in the context of experimental results and scientific literature. CORE DUTIES: 1. Design, develop, and validate amplification assays and platform workflows for diverse applications including absolute quantification and rare target detection; troubleshoot complex amplification challenges., 2. Apply AI/ML tools, machine learning algorithms, and advanced data analytics to qPCR, dPCR, NGS and molecular biology datasets to extract biological insights, identify novel assay modalities, and develop predictive models for assay performance optimization., 3. Leverage NGS knowledge to support sequencing-related initiatives and integrate qPCR, dPCR and NGS capabilities within multi-omics workflows., 4. Work independently and collaboratively to create novel product concepts, experimental strategies, and applications for nucleic acid amplification technologies., 5. Collaborate across interdisciplinary teams-including bioinformatics scientists, data science groups, and commercial and product development teams-to accelerate assay innovation and computational integration., 6. Communicate findings effectively through scientific reports, presentations, and cross-functional discussions., 7. Provide scientific mentorship to junior scientists and contribute to building a collaborative, innovative team environment., 8. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others., 9. Embraces and is open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work., 10. Understands and complies with ethical, legal, and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. PhD (or equivalent) in Molecular Biology, Biochemistry, Genomics, Computational Biology, Bioinformatics, Biostatistics, or a related discipline, with demonstrated ability to bridge experimental and analytical domains., 2. 2-5+ years of postdoctoral or industry experience applying experimental and/or computational approaches to nucleic acid technologies, assay development, or molecular biology research., 3. Demonstrated hands-on expertise in PCR-based technologies (PCR, qPCR, RT-qPCR) and assay design, including experience with multiparametric readouts., 4. Experience with NGS methodologies (DNA and/or RNA sequencing), with demonstrated application preferred., 5. Demonstrated ability to apply computational approaches-such as machine learning, statistical modeling, predictive simulations, or AI-driven analysis-to molecular biology or assay datasets., 6. Strong quantitative and problem-solving skills, with the ability to bridge computational and experimental domains., 7. Strong written and verbal communication skills, with the ability to collaborate effectively across scientific and commercial teams. PHYSICAL DEMANDS: 1. Ability to remain stationary at a laboratory bench or computer for extended periods., 2. Ability to operate and use laboratory equipment, prepare reagents, and assemble experimental systems., 3. Ability to position oneself in low positions (e.g., accessing freezers or lab equipment)., 4. Ability to move objects up to 20 pounds., 5. Ability to transport materials between laboratories and buildings. At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.

We're looking for someone available for 40 hours per week for a minimum of 6 months (ideal timeline: one semester through the following summer, or ideally a full year). We understand the realities of student schedules and have successfully worked with interns on essential coursework, particularly courses offered on longer cycles. If you're juggling school and this internship, let's talk about what's realistic. Who We're Looking For • Current students or recent graduates in biotech, chemistry, biology, or related fields, • MATC biotech program graduates especially encouraged to apply, • Strong interest in protein science or hands-on lab work, • Ability to commit to a structured schedule while being flexible where possible JOB OBJECTIVE: Apply fermentation and protein purification principles and methods to tasks which support the ongoing production, projects, and responsibilities of the Fermentation and Protein Purification departments. CORE DUTIES: 1. Production and project assistant - assist with routine production, projects, assays, and maintenance as required in Fermentation and Protein Purification production labs., 2. Be part of a team preparing for assay validation. Includes execution of repetitive automated assays. Reagent preparation and dispensing., 3. Additional duties as assigned., 4. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others., 5. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work., 6. Understands and complies with ethical, legal and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. Pursuing a technical degree in Biotechnology., 2. At least 2 semesters towards associate degree in Biotechnology., 3. Excellent organization, communications, and planning skills., 4. Able to work full time (40hr/week) Monday-Friday 7:00am - 3:30pm, approximately. PREFERRED QUALIFICATIONS: 1. Desire to develop hands-on skills to pursue career in industrial biotechnology., 2. Excellent written and verbal communications skills., 3. Ability to work with a variety of team members. PHYSICAL DEMANDS: 1. Ability to work in a lab environment with chemical, biological materials., 2. Ability to work in a lab environment with automated equipment., 3. Ability to work in a lab with radioactivity., 4. Ability to work in an office environment utilizing a computer workstation., 5. Ability to move 50 pounds., 6. Ability to wear appropriate person protection equipment (minimally safety glasses and lab coat). At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.

Job Summary Are you passionate about handson laboratory experience and excited to contribute to innovative probiotic research? IFF is a global leader in flavors, fragrances, food ingredients and health & biosciences. We deliver sustainable innovations that elevate everyday products. Our Health & Biosciencesbusiness unit channels our passion for nature and bioscience into sustainable, lifeenhancing technologies that power innovative solutions across healthcare, food, consumer and industrial markets. This coopis based on-site in Madison, Wisconsin (United States). Be part of a motivated, collaborative and growthorientedteam where together we can achieve greatness and make a real impact. Your potential is our inspiration. * Support daily laboratory operations, including media preparation for enumeration. * Operate autoclave equipment and conduct glassware washing and sterilization. * Assist in maintaining shared laboratory spaces, including restocking supplies. * Perform microbiological and molecular methods to support probiotic research. * Contribute to experiments investigating probiotic applications in supplements and food products. * Develop an understanding of internal IFF probiotic R&D projects. * Participate in rolespecific training and development sessions. * Collaborate with experienced research associates and scientists. * Ensure compliance with lab safety policies, procedures, and good laboratory practices. * Currently enrolled as a fulltime student at an accredited college or university. * Sophomore or above in a bachelor's program, or firstyear student in a master's program. * Pursuing a degree in Microbiology, Food Microbiology, Food Science, Biology or a related field. * GPA of 3.0 or higher preferred. * Experience with Microsoft Office Suite (especially Excel) and SharePoint. * Ability to work according to the coop schedule structure: * A minimum of 16 hours/week but up to Fulltime (40 hours/week) during the summer, and * A minimum of 16 hours/weekduring the academic term, following a set schedule. * Authorization to work in the U.S. without restrictions. * Strong interpersonal skills and leadership experience (e.g., community service). * Prior laboratory experience (academic or industry). * Strong ability to independently coordinate and prioritize work. * Experience working on research, customerfacing, or regulatoryrelated projects. * Fulltime opportunity during summer months. * Handson experience in an innovative industrial R&D laboratory. * Exposure to cuttingedge probiotic research and realworld application. * Opportunity to collaborate with highly skilled scientists and research associates. * Development and learning opportunities within a global industry leader. * We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit ___ to learn more

We are seeking Biology tutors and teachers in Madison.

Clinical Biostatistics** - Statistical analysis planning across endpoint types (binary, continuous, time-to-event) - Multiplicity-adjusted hypothesis testing and sample size determination - Subgroup and heterogeneous treatment effect analyses with appropriate false discovery controls - Handling of e

Minimum Qualifications** - Native-level fluency in Spanish (written), specifically native to the United States (Spanish-speaking), Spain, Chile, or Mexico - Strong reading and writing proficiency in English - BS or BA in Biology / Physics / Chemistry - Familiarity with undergraduate-level biology /

Mercor is hiring experienced Mathematics, Biology, Chemistry, and Physics professionals** to support a variety of high-impact research collaborations with leading AI labs.

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 purpose of this position is to provide quality assurance support for the Supplier Quality Management program. This person supports the qualification, monitoring, and ongoing oversight of suppliers, contract manufacturers, and service providers to ensure compliance with company quality standards and applicable global GxP regulations. This role plays a key part in maintaining supplier compliance and managing quality events related to externally sourced materials and services used in pharmaceutical development and commercialization. This person will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development as well as commercial programs at Arrowhead Pharmaceuticals, Inc. Responsibilities • Support supplier qualification, requalification, and ongoing monitoring activities for raw material suppliers, CMOs, contract laboratories, packaging vendors, and service providers., • Assist with supplier risk assessments and ensure documentation is current and compliant., • Collaborate with stakeholders and suppliers, as needed, on quality events and non-conformances and issue supplier corrective action requests, as outlined in the applicable quality agreements, • Assist with maintenance of approved supplier lists and supplier quality records., • Review and assess supplier change notifications for quality and regulatory impact., • Ensure timely and accurate documentation within the Quality Management System (QMS)., • Track and trend supplier performance metrics (e.g., deviations, on-time CAPA closure, audit findings)., • Identify recurring issues and support continuous improvement initiatives., • Assist with preparation, update, review, and routing of Arrowhead procedural documents., • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry is preferred, • 3 years of quality assurance experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization with an emphasis on Supplier Quality., • Prior experience with use of an electronic document management system in a regulated environment., • Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office programs, and Smartsheet., • Excellent interpersonal, verbal, and written communication skills., • Ability to consistently communicate with external parties in a professional manner., • Ability to follow company procedures, work instructions, and policies., • Excellent attention to detail and organizational skills. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description About Deibel Laboratories At Deibel Laboratories, our mission is to safeguard lives through accurate food safety testing. With multiple locations across the U.S., we pride ourselves on our scientific expertise, client partnerships, and culture of quality and integrity. Our lab location in Madison, WI is hiring a full-time, Autoclave Technician/Lab Aide (40 hours/week). Deibel Laboratories is seeking a dependable and detail-oriented Autoclave Technician to support our mission of protecting public health through food safety testing. This role is critical in managing sterilization processes and ensuring laboratory equipment and supplies are prepared safely and efficiently. The position requires physical strength, resilience in small and hot spaces, mechanical aptitude, and the ability to work in an environment with strong odors common to microbiological testing. Candidates with construction or hands-on trade experience are strongly encouraged to apply, as the role involves regular equipment upkeep and physically demanding tasks. We offer a competitive salary based upon knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option. Check out our website at . Compensation: Starting hourly rates at $18 - $21 D.O.E. Schedule: Wednesday - Sunday 11am - 7:30pm(Close) - Autoclave Tech • Key Responsibilities • Operate, monitor, and maintain autoclaves for sterilization of glassware, waste, and laboratory equipment., • Safely push, pull, and maneuver loads up to 250 pounds (e.g., autoclave carts, waste containers)., • Work effectively in limited space environment and areas with elevated heat during sterilization cycles., • Maintain accurate logs, batch records, and inventory related to autoclave processes., • Perform routine maintenance and cleaning of autoclaves and support upkeep of related equipment., • Apply construction or mechanical skills to support troubleshooting, repair, and workspace upkeep., • Follow all safety, biohazard, and chemical handling procedures., • Support lab operations through routine cleaning, stocking, and equipment upkeep. • Required Qualifications • High school diploma or equivalent (associate degree or technical training in biology, chemistry, or trades preferred)., • Ability to safely push, pull, and maneuver up to 250 pounds., • Comfortable working in confined spaces and high-heat conditions., • Must not be sensitive to strong odors associated with laboratory testing., • Strong attention to detail and ability to follow SOPs., • Reliable, punctual, and able to work independently or as part of a team., • Previous laboratory or manufacturing experience., • Experience operating autoclaves or similar sterilization equipment., • Familiarity with GLP (Good Laboratory Practices) and food safety testing environments., • Exposure to hot, humid, and small spaces when handling autoclave equipment., • Regular interaction with chemicals, biohazardous materials, and laboratory odors. *Prior experience in a bakery, restaurants, barista, steam sterilizers, sanitation, and/or dish washing are a plus. We will train you!