Danaher jobs in Fargo, ND - 21 jobs

At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences. Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Job Summary The primary function of this role is to provide Quality and compliance leadership and direct supervision for in-process reviews of manufacturing, packaging, labeling, laboratory operations, technical services, storage, distribution, and quality systems at Aldevron. This individual will support and execute company directives, policies, processes, and procedures in support of this objective. Additionally, the OQA Supervisor (2nd Shift) will help resolve any quality issues on areas of oversight that impact manufacturing delays and successfully address complex problems or development and implementation of robust preventative or corrective actions to enhance overall operational reviews. This position is 2nd shift. Job Responsibilities Manage, train, develop, and mentor a team of OQA professionals while providing technical input and justification for release or rejection of OQA reviews Provides ‘on-the-floor' Quality oversight of manufacturing, inspection, packaging, labeling, warehousing, and provides timely input to enable compliant and timely operations Serves as the Subject Matter Expert (SME) in assessing the impact of excursions and deviations that occur during operations Performs “real time” batch record review on the floor to reduce or eliminate errors and improve Right First Time (RFT) Supports a program to ensure timely batch record review, resolution of batch-related investigations and review of laboratory test results, to enable a smooth release of finished product Collaborate with internal partners in other parts of Quality Assurance (QA), Quality Control (QC), Technical Operations, manufacturing , and Supply Chain to resolve issues Manages reviewed and in-process documentation necessary for in-process releases including solution preparations, in-process QC testing and SOPs Qualifications 3+ years of relevant experience in a quality position, required 2+ years of that experience in a lead, supervisory or managerial position Direct experience with regulatory or internal audits and inspections Bachelor of Science preferred. Life science related field preferred or equivalent experience. 5% travel Additional Skills Experience in process understanding as it pertains to cGMP manufacturing Comprehensive understanding of cGMP manufacturing expectations Exposure to regulatory agency inspections or other types of audits (e.g. FDA, notified bodies, ISO, etc.). #LI-LCS Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System which makes everything possible. The CSV Specialist is responsible for taking an active role in Aldevron's realization of continuous improvement and operational excellence through digital technology, while maintaining quality and a state of regulatory compliance. CSV Specialists will use science-based critical thinking to ensure new and existing computerized systems are implemented and operated in compliance with Good Manufacturing Practices. CSV Specialists will regularly collaborate with all stakeholders in a system/project and will be responsible for generating documented evidence which provides assurance that our computerized systems function reliably and are fit for their intended use. This position reports to the Computer Systems Validation Manager and is part of the IT Team located in Fargo, ND and will be an on-site role. In this role, you will have the opportunity to: * Contribute to risk assessments and management processes; support QMS functions including Deviations, Change Control, and CAPA. * Author, review, and/or contribute to User Requirements, Configuration, and Functional Specifications; develop and execute Qualification protocols and other testing activities. * Perform lifecycle tasks such as periodic reviews, change management, and system decommissioning. The essential requirements of the job include: * Associate's degree in engineering, biology, computer science, mathematics, or related discipline and 2+ years in a technical role (e.g., Engineering, IT, lab work); or equivalent combination of education and experience. * Experience in Validation, GxP quality systems, software quality, biomanufacturing, or related fields (may substitute for degree); basic understanding of GMP regulatory requirements. * Professional communication and technical writing; proficiency with computer hardware/software for business functions It would be a plus if you also possess previous experience in: * Familiarity (operation, commissioning, and/or design) with any of: computerized chemical/biological manufacturing systems, enterprise software platforms (ERP, eQMS, LIMS), computerized analytical instruments * Demonstrated proficiency in science-based critical thinking and risk management Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. #L1-WT1 Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Want to build a stronger, more sustainable future and cultivate your career? Join Cargill's global team of 155,000 employees who are committed to safe, responsible, and sustainable ways to nourish the world. This position is in Cargill's food ingredients and bio-industrial business, where we anticipate trends around taste, nutrition, and safety to innovate and provide solutions to manufacturers, retailers, and foodservice companies. Job Type: Full Time Shift(s) Available: Rotating Compensation: $28.10/hr Sign on Bonus: $3000 New, easy-to-apply options are available for this role: chat with our recruiting assistant Ana at careers.cargill.com or text CargillJobs to 60196. Benefits Information: * Medical, Dental, Vision, and Prescription Drug Insurance * Health and Wellness Incentives * Paid Vacation and Holidays * 401(k) with Cargill matching contributions * Flexible Spending Accounts (FSAs) * Short-Term Disability and Life Insurance * Employee Assistance Program (EAP) * Tuition Reimbursement * Employee Discounts A Typical Work Day May Include: * Executing processes and operating all equipment of a designated area to maintain a dynamic and continuous process flow such as collecting and processing samples * Monitor tank levels, product temperatures and pressures, including observing readings on computers and field instruments, documenting key readings and information and making appropriate adjustments * Troubleshoot and operate equipment & instrumentation efficiently and perform routine maintenance. * Unloading raw materials, loading finished products (trucks, railcars, etc.) and controlling inventory to meet both internal and external customer needs * Open communication with peers and management to promote a teamwork focused environment as well as developing and participating in individual/group skill development training * Operate mobile equipment such as forklifts, mobile lifts, and railcar movers as necessary * Moving, dumping and unloading ingredients in railcars/trucks * Operate standard maintenance tools such as power tools, basic hand tools, electric tools, etc. * Understanding and adhering to all safety trainings, food safety, sanitation, hygiene and environmental policies and procedures * Interfacing with customers and carriers of our products * Other duties as assigned What You Will Need: * Must be eligible to work in the United States without visa sponsorship * Must be 18 years or older * Ability to work in varied indoor and outdoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE) including a respirator * Ability to perform physical job duties which may include bending, lifting up to 50lbs, kneeling, climbing, crawling, and twisting, with or without reasonable accommodation * Ability to work in elevated areas (4 feet and above) * Ability to understand and communicate in English (verbal/written) * Ability to work overtime including weekends, holidays, or different shifts * Basic use of computer What Will Put You Ahead: * Experience operating mobile equipment such as forklifts, loaders, etc. * High school diploma/GED or a minimum of two years equivalent work experience * Experience with SAP or a Computerized Maintenance Management System (CMMS) * Experience working in a production lab, analyzing samples, and collecting data * Prior experience in production-related work * Basic experience troubleshooting various mechanical components and systems Considered candidates will receive a phone call from a (952) area code. Please note that this position does not include relocation reimbursement. Equal Opportunity Employer, including Disability/Vet To apply using chat/text, please click Apply Now button OR use this link to create a login to apply.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System which makes everything possible. This position is part of the RG Receiving and Logistics Specialist located in Fargo at the A1 location and will be on-site . At Aldevron , w e combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Research Grade Manufacturing Support Department and report to the RG Manufacturing Support Manager responsible for supply chain functions for the A1 Advance Campus. In this role, you will have the opportunity to: + Responsible for receiving, storing, and inventory control of inbound shipments. + Package material for shipment according to established SOP's Complete foreign and domestic waybills . + Performs cycle counts to verify record accuracy and audit stocking levels. The essential requirements of the job include: + Must have a high school diploma or GED + At least 2-years experience in a supply chain (Warehouse, receiving etc.). + Computer knowledge. ERP experience is a plus. It would be a plus if you also possess previous experience in: + Experience receiving and shipping sensitive items . Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's (*********************************** 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System (************************************************************ which makes everything possible. The Senior Validation Engineer, Process Validation role is responsible providing expertise, guidance, and maintenance of the Validation programs across biological Critical Starting Materials, Drug Substances, and Drug Products manufactured at Aldevron's Fargo, ND site. As the subject matter expert in validation, this position leads the development, execution, and implementation of validation, practices, policy, and procedures. This position reports to the VP, Global Technical Operations and is part of the Technical Operations Department located in Fargo, ND and will be an on-site role. In this role, you will have the opportunity to: + Design, execute, and oversee validation documents supporting process characterization and validation spanning biological critical starting materials, drug substance, and drug product + Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design + Develop and implement validation policies and procedures based on current regulations and industry standards + Provide subject matter expertise during client and regulatory audits, kaizen and workshop events, and manufacturing support + Help resolve quality issues and CAPA's leading lab investigations, risk assessments, root cause analysis, and developing implementation plans The essential requirements of the job include: + Bachelor's degree in Engineering or Scientific field (preferably Chemical, Biology, or Microbiology) with 5+ years of experience or MS degree with 3+ years of experience. + PhD in Engineering or Scientific field with 2+ years of experience. + Experience in process development, engineering, and process validation required. Experience working in CDMO environment is a plus + Experience using statistical, risk assessment, and process improvement tools Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role + 10% travel to support routine inspections, audits, and customer projects It would be a plus if you also possess previous experience in: + Working knowledge of current industry critical starting material, drug substance, and drug product regulatory guidelines Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info (**************************************************************************************** . #LI-KP1 Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .

Cargill's size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way. Cargill is a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials - from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill. This position is in Cargill's agricultural supply chain business. We sit at the heart of the supply chain, partnering with farmers and customers to source, make and deliver essential products. Job Purpose and Impact The Director, Crush Management will provide strategic operational guidance and direction for all production and operating facility with moderate presence with a moderate degree of complexity. In this role, you will oversee and hold operating facilities accountable to standards for safety, quality, operational effectiveness, and financial performance. Key Accountabilities Implement and monitor employee and product safety and environmental compliance program standards and goals for a most complex plant. Accountable for all internal and external operating and regulatory procedures on employee and product safety including strategic and tactical execution in alignment with corporate environment, health and safety and food safety, quality and regulatory functions as well as government regulations. Monitor general operations and maintenance of plant equipment and executes on operational priorities for a most complex plant or multiple plants and monitors operations and quality management deliverables to ensure customer, product and quality standards requirements are met within specifications. Prepares, administers and controls capital and operating budgets for a most complex plant to achieve short and medium term financial performance objectives set by the business and ensure accountability for meeting and controlling operating expenses and established targets. Accountable for the overall operational management of a most complex plant to implement operational efficiency improvements including standardization of plant information manufacturing systems, quality control, safety, production reliability excellence and maintenance and operators best practices. Develop plans and deliver results in a fast-changing business or regulatory environment, while leading and developing a team of experienced professionals and supervisors, coaching and making decisions related to talent management hiring, performance and disciplinary actions. You will also collaborate with managers and supervisors in your organization to ensure staff selections align with current and future needs. Other duties as assigned #LI-KP1 Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience Minimum of six years of related work experience Ability to travel up to 10% Preferred Qualifications Three years of supervisory experience Digital fluency and acumen Reliability and asset management experience Safety and quality ownership experience Budgeting and operations planning experience Additional Details • Location: ND-West Fargo; Relocation support may be provided • Schedule is Monday - Friday typically from 7am to 4pm. There are also some events that might need to work on the weekends and rotational on-call. • The business will not sponsor applicants for work visas for this position At Cargill we put people first. As part of your overall rewards, we offer a comprehensive benefit program including medical and/or other benefits dependent on the position offered and hours worked. Visit: *************************************************************** learn more (subject to certain collective bargaining agreements for Union positions). Equal Opportunity Employer, including Disability/Vet.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System which makes everything possible. The Technical Project Manager (TPM) II is responsible for managing the development elements of biomanufacturing projects in support of client programs and services. This position reports to the Manager of Technical Project Management and is part of the Project Management team located in Fargo, North Dakota, and will be an on-site role. In this role, you will be expected to: Oversee complex biomanufacturing projects utilizing department standards and tools. Work collaboratively with the Project Managers, internal stakeholders, Program Managers, and clients while maintaining the project timeline data, communicating project status updates, managing project changes, ensuring timely achievement of key milestones, and tracking and driving the completion of action items and project deliverables. Proactively identify potential obstacles and work alongside cross-functional teams to develop and execute effective solutions. Resolve conflicts and remove roadblocks with internal and external stakeholders in a constructive manner to preserve and strengthen professional relationships. The essential requirements of the job include: Bachelor's degree or higher in Biological Sciences, Chemistry, or a related discipline. Prefer 3-5 years of experience in method development, method validation, quality control, biomanufacturing validation, process development, or technology transfer, ideally pertaining to nucleic acids. Proven experience successfully leading relevant departments and/or managing complex projects with both waterfall and agile methodologies. Proficiency in tools: SmartSheet, OneNote, Excel, and Outlook. Excellent written and verbal communication skills, with strong facilitation and presentation capabilities. Travel, Motor Vehicle Record & Physical/Environment Requirements: Must have a valid driver's license with an acceptable driving record. This role could require travel of 10%+ It would be a plus if you also possess previous experience in: CDMO environment Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. #LI-ND19 #thisisbelonging #thebestteamisdiverse Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's (*********************************** 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System (************************************************************ which makes everything possible. The Manager, Metrology is responsible for performing preventive maintenance and repairs on equipment and systems (e.g., mechanical, electrical), evaluating and recommending equipment improvements to improve availability, capability and yield. Performs equipment failure analyses (including preventive and unscheduled maintenance), troubleshoots and diagnoses equipment problems, prepares technical reports to document equipment modifications and equipment maintenance procedures This position reports to the Sr. Manager, Facilities and is part of the Operations Team located in Fargo, ND and will be an on-site role. In this role, you will have the opportunity to: + Develop calibration methods and techniques based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements + Develop and maintain Standard Operating Procedures (SOPs), equipment records and qualification records + Work with support departments to obtain user requirements for equipment/utility, assist in the vendor review, instrument demonstrations/evaluations and final vendor selection process + Lead team of metrology technicians, inclusive of hiring, development of associates, and performance management as needed. + Responsible for hands-on calibration, supervisory functions, maintenance, troubleshooting, conducting investigations and repair on a variety of equipment/utilities in such a manner to have minimal interruptions within the manufacturing schedule + Manage the identification, purchase, scheduling and administration of appropriate service contracts and calibration vendors + Investigate Out of Tolerance results The essential requirements of the job include: + Associates or Bachelors degree preferred + 5+ years experience in metrology, + Prior experience leading teams preferred + Experience in a GMP or regulated industry, preferred It would be a plus if you also possess previous experience in: + Experience with CAPAs, Change Controls, and writing SOPS Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info (**************************************************************************************** . This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Our team at Integrated DNA Technologies (IDT), is united by a commitment to collaboration and scientific excellence, building on a strong foundation of innovation, expertise, and reliability. Guided by our vision to help researchers rapidly move from the lab to life-changing advances, we work closely with global partners to accelerate progress and genomics breakthroughs across fields like cancer, infectious disease, rare genetic disorders, and more. At IDT, you'll be part of a culture rooted in continuous learning and improvement-where your growth fuels our mission to accelerate the pace of genomics and helps shape a healthier, brighter future for all. Learn about the Danaher Business System which makes everything possible. The Global EHS Manager is responsible for driving adherence to standard work and ensuring consistent implementation of Environment, Health & Safety programs across global operations. This role delivers measurable impact by reducing incidents and improving compliance through leadership and operational excellence. This position reports to the Director of EHS, is part of a multi-site and operating company Environment, Health & Safety Team and will be an on-site role at one of the IDT or Aldevron locations. In this role, you will have the opportunity to: * Drive adherence to standard work across global Environment, Health & Safety (EHS) programs to ensure consistent and effective safety practices. * Implement and monitor compliance with EHS policies and procedures, maintaining high standards of safety and regulatory alignment. * Lead global initiatives aimed at reducing incidents and improving overall safety performance throughout the organization. * Collaborate with regional teams to ensure alignment with global EHS standards and facilitate the sharing of best practices. * Provide leadership and guidance to EHS teams worldwide, supporting operational excellence and a proactive safety culture. The essential requirements of the job include * Bachelor's degree in Environmental Science, Occupational Health & Safety, Engineering, or related field * 5+ years of proven leadership in environmental and safety compliance within a manufacturing environment, with a strong track record of driving result and experience in EHS management within global operations * Proven expertise in implementing standard work and DBS methodologies * Proficiency in EHS management systems and reporting tools and knowledge of global regulatory requirements and compliance frameworks * Strong communicator, both written and verbal, and can lead training, investigations, and cross-functional collaboration with clarity and confidence. * Able to lead, motivate, and partner with global and regional teams to elevate safety and environmental standards Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role * Ability to travel as required (up to 20%, including overnight stays) It would be a plus if you also possess previous experience in: * Professional certification in EHS or related discipline * Experience with Danaher Business System (DBS) or similar continuous improvement frameworks IDT, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. The annual salary range for this role is 114,000 to 130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Sr. Manager Analytical Method Validation At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences. Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. The Sr. Manager Analytical Method Validation position is responsible for leading Aldevron's analytical method validation program to ensure robust, compliant, and scientifically sound methods for plasmid DNA, mRNA, and related biologics. This role oversees method development support, validation, transfer, and lifecycle management in alignment with global regulatory requirements This position reports to the Sr. Director Quality Control and is part of the Quality Regulatory Affairs department located in Fargo, ND and will be an on-site role. In this role, you will have the opportunity to: + Oversee Aldevron's Method Validation program and personnel, ensuring compliance with established SOPs for analytical method qualification, validation, transfer, and lifecycle management. + Provide leadership and mentorship to validation teams, fostering a high-performance culture through coaching, development, and effective performance management. + Direct and oversee multiple validation projects simultaneously, ensuring timely execution, resource allocation, and alignment with organizational priorities. + Ensure strong interaction with multiple groups to facilitate appropriate resource allocation and scheduling of method validation and transfer activities. + Serve as the subject matter expert for inspections and audits; defend validation strategies and ensure compliance with data integrity standards. + Approve validation documentation and monitor method performance trends to ensure compliance and reliability. + Lead structured problem-solving and continuous improvement initiatives using visual management and standard work principles to optimize method performance and maintain lifecycle control. The essential requirements of the job include: + Bachelor's degree in Analytical Chemistry, Biochemistry, Molecular Biology, or related field (Master's or PhD preferred). + 8+ years in GMP biopharma/biotech analytical development/validation + 5+ years of proven leadership experience managing teams in a GMP environment + Comprehensive understanding of global regulatory expectations for analytical methods in GMP environments, including principles for validation, verification, and lifecycle management It would be a plus if you also possess previous experience in: + Experience driving continuous improvement initiatives using data analytics to enhance method performance, reduce variability, and improve efficiency. + Experience in developing, implementing, and maintaining key departmental metrics to monitor performance, drive accountability, and support continuous improvement initiatives. #LI-GC1 Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .

At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences. Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Job Summary The primary function of this role is to provide Quality and compliance leadership and direct supervision for in-process reviews of manufacturing, packaging, labeling, laboratory operations, technical services, storage, distribution, and quality systems at Aldevron. This individual will support and execute company directives, policies, processes, and procedures in support of this objective. Additionally, the OQA Supervisor (2nd Shift) will help resolve any quality issues on areas of oversight that impact manufacturing delays and successfully address complex problems or development and implementation of robust preventative or corrective actions to enhance overall operational reviews. This position is 2nd shift. Job Responsibilities * Manage, train, develop, and mentor a team of OQA professionals while providing technical input and justification for release or rejection of OQA reviews * Provides 'on-the-floor' Quality oversight of manufacturing, inspection, packaging, labeling, warehousing, and provides timely input to enable compliant and timely operations * Serves as the Subject Matter Expert (SME) in assessing the impact of excursions and deviations that occur during operations * Performs "real time" batch record review on the floor to reduce or eliminate errors and improve Right First Time (RFT) * Supports a program to ensure timely batch record review, resolution of batch-related investigations and review of laboratory test results, to enable a smooth release of finished product * Collaborate with internal partners in other parts of Quality Assurance (QA), Quality Control (QC), Technical Operations, manufacturing , and Supply Chain to resolve issues * Manages reviewed and in-process documentation necessary for in-process releases including solution preparations, in-process QC testing and SOPs Qualifications * 3+ years of relevant experience in a quality position, required * 2+ years of that experience in a lead, supervisory or managerial position * Direct experience with regulatory or internal audits and inspections * Bachelor of Science preferred. * Life science related field preferred or equivalent experience. * 5% travel Additional Skills * Experience in process understanding as it pertains to cGMP manufacturing * Comprehensive understanding of cGMP manufacturing expectations * Exposure to regulatory agency inspections or other types of audits (e.g. FDA, notified bodies, ISO, etc.). #LI-LCS Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Want to build a stronger, more sustainable future and cultivate your career? Join Cargill's global team of 155,000 employees who are committed to safe, responsible, and sustainable ways to nourish the world. This position is in Cargill's food ingredients and bio-industrial business, where we anticipate trends around taste, nutrition, and safety to innovate and provide solutions to manufacturers, retailers, and foodservice companies. **Job Type:** Full Time **Shift(s) Available:** Rotating **Compensation:** $28.10/hr **Sign on Bonus** : $3000 **New, easy-to-apply options are available for this role: chat with our recruiting assistant Ana at careers.cargill.com or text CargillJobs to 60196.** **Benefits Information:** + Medical, Dental, Vision, and Prescription Drug Insurance + Health and Wellness Incentives + Paid Vacation and Holidays + 401(k) with Cargill matching contributions + Flexible Spending Accounts (FSAs) + Short-Term Disability and Life Insurance + Employee Assistance Program (EAP) + Tuition Reimbursement + Employee Discounts **A Typical Work Day May Include:** + Executing processes and operating all equipment of a designated area to maintain a dynamic and continuous process flow such as collecting and processing samples + Monitor tank levels, product temperatures and pressures, including observing readings on computers and field instruments, documenting key readings and information and making appropriate adjustments + Troubleshoot and operate equipment & instrumentation efficiently and perform routine maintenance. + Unloading raw materials, loading finished products (trucks, railcars, etc.) and controlling inventory to meet both internal and external customer needs + Open communication with peers and management to promote a teamwork focused environment as well as developing and participating in individual/group skill development training + Operate mobile equipment such as forklifts, mobile lifts, and railcar movers as necessary + Moving, dumping and unloading ingredients in railcars/trucks + Operate standard maintenance tools such as power tools, basic hand tools, electric tools, etc. + Understanding and adhering to all safety trainings, food safety, sanitation, hygiene and environmental policies and procedures + Interfacing with customers and carriers of our products + Other duties as assigned **What You Will Need:** + Must be eligible to work in the United States without visa sponsorship + Must be 18 years or older + Ability to work in varied indoor and outdoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE) including a respirator + Ability to perform physical job duties which may include bending, lifting up to 50lbs, kneeling, climbing, crawling, and twisting, with or without reasonable accommodation + Ability to work in elevated areas (4 feet and above) + Ability to understand and communicate in English (verbal/written) + Ability to work overtime including weekends, holidays, or different shifts + Basic use of computer **What Will Put You Ahead:** + Experience operating mobile equipment such as forklifts, loaders, etc. + High school diploma/GED or a minimum of two years equivalent work experience + Experience with SAP or a Computerized Maintenance Management System (CMMS) + Experience working in a production lab, analyzing samples, and collecting data + Prior experience in production-related work + Basic experience troubleshooting various mechanical components and systems Considered candidates will receive a phone call from a (952) area code. Please note that this position does not include relocation reimbursement. Equal Opportunity Employer, including Disability/Vet To apply using chat/text, please click Apply Now button OR use this link (*********************************************************** Id=319291&company=cargill&locale=en\_US) to create a login to apply.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System which makes everything possible. This position is part of the RG Receiving and Logistics Specialist located in Fargo at the A1 location and will be on-site. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Research Grade Manufacturing Support Department and report to the RG Manufacturing Support Manager responsible for supply chain functions for the A1 Advance Campus. In this role, you will have the opportunity to: Responsible for receiving, storing, and inventory control of inbound shipments. Package material for shipment according to established SOP's Complete foreign and domestic waybills. Performs cycle counts to verify record accuracy and audit stocking levels. The essential requirements of the job include: Must have a high school diploma or GED At least 2-years experience in a supply chain (Warehouse, receiving etc.). Computer knowledge. ERP experience is a plus. It would be a plus if you also possess previous experience in: Experience receiving and shipping sensitive items. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System which makes everything possible. The Senior Validation Engineer, Process Validation role is responsible providing expertise, guidance, and maintenance of the Validation programs across biological Critical Starting Materials, Drug Substances, and Drug Products manufactured at Aldevron's Fargo, ND site. As the subject matter expert in validation, this position leads the development, execution, and implementation of validation, practices, policy, and procedures. This position reports to the VP, Global Technical Operations and is part of the Technical Operations Department located in Fargo, ND and will be an on-site role. In this role, you will have the opportunity to: Design, execute, and oversee validation documents supporting process characterization and validation spanning biological critical starting materials, drug substance, and drug product Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design Develop and implement validation policies and procedures based on current regulations and industry standards Provide subject matter expertise during client and regulatory audits, kaizen and workshop events, and manufacturing support Help resolve quality issues and CAPA's leading lab investigations, risk assessments, root cause analysis, and developing implementation plans The essential requirements of the job include: Bachelor's degree in Engineering or Scientific field (preferably Chemical, Biology, or Microbiology) with 5+ years of experience or MS degree with 3+ years of experience. PhD in Engineering or Scientific field with 2+ years of experience. Experience in process development, engineering, and process validation required. Experience working in CDMO environment is a plus Experience using statistical, risk assessment, and process improvement tools Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role 10% travel to support routine inspections, audits, and customer projects It would be a plus if you also possess previous experience in: Working knowledge of current industry critical starting material, drug substance, and drug product regulatory guidelines Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. #LI-KP1 Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher Business System which makes everything possible. The Manager, Metrology is responsible for performing preventive maintenance and repairs on equipment and systems (e.g., mechanical, electrical), evaluating and recommending equipment improvements to improve availability, capability and yield. Performs equipment failure analyses (including preventive and unscheduled maintenance), troubleshoots and diagnoses equipment problems, prepares technical reports to document equipment modifications and equipment maintenance procedures This position reports to the Sr. Manager, Facilities and is part of the Operations Team located in Fargo, ND and will be an on-site role. In this role, you will have the opportunity to: Develop calibration methods and techniques based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements Develop and maintain Standard Operating Procedures (SOPs), equipment records and qualification records Work with support departments to obtain user requirements for equipment/utility, assist in the vendor review, instrument demonstrations/evaluations and final vendor selection process Lead team of metrology technicians, inclusive of hiring, development of associates, and performance management as needed. Responsible for hands-on calibration, supervisory functions, maintenance, troubleshooting, conducting investigations and repair on a variety of equipment/utilities in such a manner to have minimal interruptions within the manufacturing schedule Manage the identification, purchase, scheduling and administration of appropriate service contracts and calibration vendors Investigate Out of Tolerance results The essential requirements of the job include: Associates or Bachelors degree preferred 5+ years experience in metrology, Prior experience leading teams preferred Experience in a GMP or regulated industry, preferred It would be a plus if you also possess previous experience in: Experience with CAPAs, Change Controls, and writing SOPS Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's (*********************************** 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Our team at Integrated DNA Technologies (IDT), is united by a commitment to collaboration and scientific excellence, building on a strong foundation of innovation, expertise, and reliability. Guided by our vision to help researchers rapidly move from the lab to life-changing advances, we work closely with global partners to accelerate progress and genomics breakthroughs across fields like cancer, infectious disease, rare genetic disorders, and more. At IDT, you'll be part of a culture rooted in continuous learning and improvement-where your growth fuels our mission to accelerate the pace of genomics and helps shape a healthier, brighter future for all. Learn about the Danaher Business System (************************************************************ which makes everything possible. The Global EHS Manager is responsible for driving adherence to standard work and ensuring consistent implementation of Environment, Health & Safety programs across global operations. This role delivers measurable impact by reducing incidents and improving compliance through leadership and operational excellence. This position reports to the Director of EHS, is part of a multi-site and operating company Environment, Health & Safety Team and will be an on-site role at one of the IDT or Aldevron locations. In this role, you will have the opportunity to: + Drive adherence to standard work across global Environment, Health & Safety (EHS) programs to ensure consistent and effective safety practices. + Implement and monitor compliance with EHS policies and procedures, maintaining high standards of safety and regulatory alignment. + Lead global initiatives aimed at reducing incidents and improving overall safety performance throughout the organization. + Collaborate with regional teams to ensure alignment with global EHS standards and facilitate the sharing of best practices. + Provide leadership and guidance to EHS teams worldwide, supporting operational excellence and a proactive safety culture. The essential requirements of the job include + Bachelor's degree in Environmental Science, Occupational Health & Safety, Engineering, or related field + 5+ years of proven leadership in environmental and safety compliance within a manufacturing environment, with a strong track record of driving result and experience in EHS management within global operations + Proven expertise in implementing standard work and DBS methodologies + Proficiency in EHS management systems and reporting tools and knowledge of global regulatory requirements and compliance frameworks + Strong communicator, both written and verbal, and can lead training, investigations, and cross-functional collaboration with clarity and confidence. + Able to lead, motivate, and partner with global and regional teams to elevate safety and environmental standards Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role + Ability to travel as required (up to 20%, including overnight stays) It would be a plus if you also possess previous experience in: + Professional certification in EHS or related discipline + Experience with Danaher Business System (DBS) or similar continuous improvement frameworks IDT, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info (**************************************************************************************** . The annual salary range for this role is 114,000 to 130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .

Want to build a stronger, more sustainable future and cultivate your career? Join Cargill's global team of 155,000 employees who are committed to safe, responsible, and sustainable ways to nourish the world. This position is in Cargill's food ingredients and bio-industrial business, where we anticipate trends around taste, nutrition, and safety to innovate and provide solutions to manufacturers, retailers, and foodservice companies. Job Type: Full Time Shift(s) Available: Rotating Compensation: $28.10/hr Sign on Bonus: $3000 New, easy-to-apply options are available for this role: chat with our recruiting assistant Ana at careers.cargill.com or text CargillJobs to 60196. Benefits Information: Medical, Dental, Vision, and Prescription Drug Insurance Health and Wellness Incentives Paid Vacation and Holidays 401(k) with Cargill matching contributions Flexible Spending Accounts (FSAs) Short-Term Disability and Life Insurance Employee Assistance Program (EAP) Tuition Reimbursement Employee Discounts A Typical Work Day May Include: Executing processes and operating all equipment of a designated area to maintain a dynamic and continuous process flow such as collecting and processing samples Monitor tank levels, product temperatures and pressures, including observing readings on computers and field instruments, documenting key readings and information and making appropriate adjustments Troubleshoot and operate equipment & instrumentation efficiently and perform routine maintenance. Unloading raw materials, loading finished products (trucks, railcars, etc.) and controlling inventory to meet both internal and external customer needs Open communication with peers and management to promote a teamwork focused environment as well as developing and participating in individual/group skill development training Operate mobile equipment such as forklifts, mobile lifts, and railcar movers as necessary Moving, dumping and unloading ingredients in railcars/trucks Operate standard maintenance tools such as power tools, basic hand tools, electric tools, etc. Understanding and adhering to all safety trainings, food safety, sanitation, hygiene and environmental policies and procedures Interfacing with customers and carriers of our products Other duties as assigned What You Will Need: Must be eligible to work in the United States without visa sponsorship Must be 18 years or older Ability to work in varied indoor and outdoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE) including a respirator Ability to perform physical job duties which may include bending, lifting up to 50lbs, kneeling, climbing, crawling, and twisting, with or without reasonable accommodation Ability to work in elevated areas (4 feet and above) Ability to understand and communicate in English (verbal/written) Ability to work overtime including weekends, holidays, or different shifts Basic use of computer What Will Put You Ahead: Experience operating mobile equipment such as forklifts, loaders, etc. High school diploma/GED or a minimum of two years equivalent work experience Experience with SAP or a Computerized Maintenance Management System (CMMS) Experience working in a production lab, analyzing samples, and collecting data Prior experience in production-related work Basic experience troubleshooting various mechanical components and systems Considered candidates will receive a phone call from a (952) area code. Please note that this position does not include relocation reimbursement. Equal Opportunity Employer, including Disability/Vet

Cargill's size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way. Cargill is a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials - from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill. This position is in Cargill's agricultural supply chain business. We sit at the heart of the supply chain, partnering with farmers and customers to source, make and deliver essential products. **Job Purpose and Impact** The Director, Crush Management will provide strategic operational guidance and direction for all production and operating facility with moderate presence with a moderate degree of complexity. In this role, you will oversee and hold operating facilities accountable to standards for safety, quality, operational effectiveness, and financial performance. **Key Accountabilities** + Implement and monitor employee and product safety and environmental compliance program standards and goals for a most complex plant. + Accountable for all internal and external operating and regulatory procedures on employee and product safety including strategic and tactical execution in alignment with corporate environment, health and safety and food safety, quality and regulatory functions as well as government regulations. + Monitor general operations and maintenance of plant equipment and executes on operational priorities for a most complex plant or multiple plants and monitors operations and quality management deliverables to ensure customer, product and quality standards requirements are met within specifications. + Prepares, administers and controls capital and operating budgets for a most complex plant to achieve short and medium term financial performance objectives set by the business and ensure accountability for meeting and controlling operating expenses and established targets. + Accountable for the overall operational management of a most complex plant to implement operational efficiency improvements including standardization of plant information manufacturing systems, quality control, safety, production reliability excellence and maintenance and operators best practices. + Develop plans and deliver results in a fast-changing business or regulatory environment, while leading and developing a team of experienced professionals and supervisors, coaching and making decisions related to talent management hiring, performance and disciplinary actions. You will also collaborate with managers and supervisors in your organization to ensure staff selections align with current and future needs. + Other duties as assigned \#LI-KP1 **Qualifications** **Minimum Qualifications** + Bachelor's degree in a related field or equivalent experience + Minimum of six years of related work experience + Ability to travel up to 10% **Preferred Qualifications** + Three years of supervisory experience + Digital fluency and acumen + Reliability and asset management experience + Safety and quality ownership experience + Budgeting and operations planning experience **Additional Details** - Location: ND-West Fargo; Relocation support may be provided - Schedule is Monday - Friday typically from 7am to 4pm. There are also some events that might need to work on the weekends and rotational on-call. - The business will not sponsor applicants for work visas for this position At Cargill we put people first. As part of your overall rewards, we offer a comprehensive benefit program including medical and/or other benefits dependent on the position offered and hours worked. Visit: *************************************************************** learn more (subject to certain collective bargaining agreements for Union positions). Equal Opportunity Employer, including Disability/Vet.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: Medical Affairs Group Job Sub Function: Professional Medical Education Job Category: People Leader All Job Posting Locations: Albuquerque, New Mexico, United States of America, Albuquerque, New Mexico, United States of America, Anchorage, Alaska, United States, Atlanta, Georgia, United States, Baton Rouge, Louisiana, United States, Boise, Idaho, United States, Boston, Massachusetts, United States of America, Burlington, Vermont, United States, Camden, New Jersey, United States, Cedar Rapids, Iowa, United States, Charleston, South Carolina, United States, Charleston, West Virginia, United States, Charlotte, North Carolina, United States, Charlottesville, Virginia, United States, Chicago, Illinois, United States, Columbia, Maryland, United States, Columbus, Ohio, United States, Dallas, Texas, United States, Denver, Colorado, United States, Detroit, Michigan, United States, Fargo, North Dakota, United States, Gulfport, Mississippi, United States, Helena, Montana, United States, Honolulu, Hawaii, United States, Indianapolis, Indiana, United States {+ 23 more} Job Description: Johnson & Johnson MedTech - Neurovascular division is currently seeking a Senior Manager of Professional Education. This is a remote role within the United States. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. This role also requires up to 60% overnight travel. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/. Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at *******************/medtech/ Position Summary: As the Senior Manager, Professional Education (US), you will be instrumental in creating strategic training initiatives that ensure the safe and effective use of J&J Neurovascular products. Reporting directly to the Director of Education, you will oversee a dynamic team of managers and specialists, collaborating with multiple cross-functional partners including Marketing, Medical Affairs, Clinical Teams, Regulatory Affairs, and Sales Leadership. Your leadership will drive the design, execution, and continuous improvement of a comprehensive educational curriculum targeting healthcare providers - from physicians and residents to allied health professionals such as NPs, PAs, RNs, and RTs. You will establish strong, consultative relationships with our KOL faculty, leaning on their expertise to elevate our training programs, driving creativity to be best in class and including the newest and next technologies. The Senior Manager-US Professional Education is primarily aligned to the US, but must be cognizant of the global strategy, and may be consulted for regional business needs. Key Responsibilities: * Design and execute all aspects of Professional Education programs to ensure the safe and effective use of JNJ MedTech Neurovascular products and technology. * Collaborate with cross-functional business partners and key stakeholders to develop and execute impactful educational programs that support the US Business Plan, in conjunction with New Product Introductions (NPI) Launch Excellence (LEX) Reviews. * Maintain oversight of Professional Education discretionary budget with manager and Finance partners, inclusive of Team T&E and sample product forecast. * Stay current on company products instructions for use (IFU), best practices and technical troubleshooting, as well as relevant scientific clinical literature and new product information. * Keep current of the competitive market, treatment trends, technology, competitors, treatment guidelines and new regulations. * Identify and develop strong relationships with KOL faculty and oversee all consulting HCP & Facility agreements, Faculty Time Records, Faculty Payments, and execution of all planned training programs and activities. * Evaluate and implement innovative training modalities, which meet the needs of the learner, i.e. web-based applications and technology-based tools, AI platform, AR/VR, Telementoring, * Maintain the required training documents that fulfill the FDA training commitment for TRUFILL n-BCA Liquid Embolic System and Enterprise Vascular Reconstruction Device with Clinical Affairs, Regulatory, and Legal teams. * Oversee development and progressive learning stages of the Johnson & Johnson Institute comprehensive and scalable curriculum for Fellows, Residents, and Allied Health Professionals * Operate under limited supervision and in strict adherence to applicable company guidelines on Regulatory, Health, Safety, and Environmental practices. * Align with established project and management processes, instruction design standards and processes, and corporate brand style and standards, including compliance requirements. Qualifications: Required: * Bachelor's degree is required. * Minimum of ten (10) years of relevant business experience (Professional or Commercial Education, Marketing, Sales, and Clinical. * Minimum of three (3) years of experience working in organizational learning or a Professional or Commercial Education environment. * Ability to effectively communicate with customers (physicians) and internal stakeholders with demonstrated presentation skills and written communication skills, as well as solid organizational and time management abilities. * Ability to champion product concepts and promote change through indirect influence. * Ability to work independently, requiring limited oversight. * Ability to collaborate well with cross-functional partners. * Ability to provide solutions to complex problems to enhance customer experience. * Previous People Leader/Management experience. * Proficient with Microsoft Outlook, Teams, SharePoint, Excel, PowerPoint, and ZOOM Preferred: * Neurovascular experience is strongly preferred. * Current or previous experience launching new products. * Comprehension of Health Care Compliance guidelines. * This position is to be remote field based within the continental United States and may have up to 50% overnight travel in the US. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (********************************) or contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: The anticipated base pay range for this position is : $137,000 - $235,750 Additional Description for Pay Transparency: The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company's long-term incentive program. Employees are eligible for the following time off benefits: Vacation - up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year Holiday pay, including Floating Holidays - up to 13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Additional information can be found through the link below. *********************************************