Research and development technician jobs in Sioux Falls, SD - 604 jobs

R&D Laboratory Technician Pay Rate:$20-30/HR The R&D Laboratory Technician will support the Maize Transformation team within Crop Transformation Systems in Biotechnology/Trait Discovery and Optimization. This role is responsible for executing laboratory procedures to generate high-quality transgenic and genome-edited plants in support of trait discovery, trait optimization, and product development programs. Responsibilities Perform crop transformation activities, including preparation of explants, plant transformation procedures, sub-culturing tissue during the selection process Follow all standard operating procedures (SOPs) to ensure quality, consistency, and regulatory compliance. Maintain accurate and complete electronic and legal laboratory notebook documentation. Summarize experimental results, identify trends, and recommend opportunities for process improvement. Organize and manage daily laboratory workflows to meet project timelines and deliverables. Perform all laboratory work in accordance with safety, ergonomic, and regulatory standards. Collaborate effectively within a team-oriented research environment and contribute to shared goals. Qualifications Associate's or Bachelor's degree in Biology, Biotechnology, Plant Science, Molecular Biology, or a related scientific field. Previous laboratory experience in plant tissue culture, biotechnology, or a research laboratory environment preferred. Familiarity with aseptic techniques, SOP-driven lab environments, and documentation practices. Strong attention to detail with the ability to accurately document experimental procedures and results. Effective communication and organizational skills. Ability to manage multiple tasks and meet deadlines in a fast-paced research setting. Demonstrated teamwork skills with a positive, proactive attitude.

Medica is a nonprofit health plan with more than a million members that serves communities in Minnesota, Nebraska, Wisconsin, Missouri, and beyond. We deliver personalized health care experiences and partner closely with providers to ensure members are genuinely cared for. We're a team that owns our work with accountability, makes data-driven decisions, embraces continuous learning, and celebrates collaboration - because success is a team sport. It's our mission to be there in the moments that matter most for our members and employees. Join us in creating a community of connected care, where coordinated, quality service is the norm and every member feels valued. Defining problems, conducting and narrowing research, analyzing criteria, finding, analyzing and applying solutions. Performs other duties as assigned. Key Accountabilities Work with Lead Developers on implementation of changes related to our ecosystem surrounding Health Share product by Intersystems Develop and maintain interfaces using Health Share IRIS and ObjectScript Interpretation and implementation of data transformations and mappings using HL7, CDA/CCD, FHIR, JSON. XML. Resolve integration issues, configuration and other changes through Health Share toolset High level understanding of Interoperability standards Document technical specifications, workflows and test plans Support continuous improvement through automation and best practices. Required Qualifications Bachelor's degree or equivalent experience in related field 5 years of work experience beyond degree Role requirements: 3+ years of experience with InterSystems HealthShare, or IRIS. Strong ObjectScript programming skills. Proficiency in healthcare data standards (HL7, FHIR, CDA, C-CDA). Experience with integration protocols (MLLP, REST, SOAP, SFTP). Solid understanding of SQL and relational databases. Familiarity with healthcare compliance (HIPAA) and interoperability concepts. Preferred Qualifications Experience with EMR/EHR systems (Epic, Cerner, etc.). Knowledge of cloud platforms (AWS, Azure, GCP). InterSystems certification (HL7 Interface Specialist or similar). This position is an Office role, which requires an employee to work onsite, on average, 3 days per week. We are open to candidates located near one of the following office locations: Minnetonka, MN, or Madison, WI. The full salary grade for this position is $102,100 - $175,100. While the full salary grade is provided, the typical hiring salary range for this role is expected to be between $102,100 - $138,605. Annual salary range placement will depend on a variety of factors including, but not limited to, education, work experience, applicable certifications and/or licensure, the position's scope and responsibility, internal pay equity and external market salary data. In addition to base compensation, this position may be eligible for incentive plan compensation in addition to base salary. Medica offers a generous total rewards package that includes competitive medical, dental, vision, PTO, Holidays, paid volunteer time off, 401K contributions, caregiver services and many other benefits to support our employees. The compensation and benefits information is provided as of the date of this posting. Medica's compensation and benefits are subject to change at any time, with or without notice, subject to applicable law. Eligibility to work in the US: Medica does not offer work visa sponsorship for this role. All candidates must be legally authorized to work in the United States at the time of application. Employment is contingent on verification of identity and eligibility to work in the United States. We are an Equal Opportunity employer, where all qualified candidates receive consideration for employment indiscriminate of race, religion, ethnicity, national origin, citizenship, gender, gender identity, sexual orientation, age, veteran status, disability, genetic information, or any other protected characteristic. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

The Senior Food Scientist will lead technical projects that support Karlsburger Foods' strategic business goals, including new product development, product optimization, cost savings, quality improvement, and troubleshooting. This role will focus on a range of product forms including dry powders, broths concentrate, stocks concentrate, sauces, and gravies. The ideal candidate is a self-starter with deep experience in savory product development and commercialization, especially in powdered and concentrated formats. Essential Functions and Responsibilities: Lead new product development projects with emphasis on dry powders, soup/broth bases, and seasoning blends. Optimize existing powdered, liquid and paste products for quality, shelf-life, and cost. Execute plant trials, product validations, and troubleshooting in both dry and wet processing environments. Maintain accurate and detailed technical documentation, including formulations, batching instructions, and product specifications. Participate in sensory panels and lead evaluations for taste, appearance, and texture. Serve as a technical resource for powder blending, ingredient functionality, and processing parameters to operations and sales. Partner with supply chain, operations, and procurement to support scale-up and identify alternative ingredients. Apply food science principles to support sensory performance and commercializability. Ensure formulations meet food safety, regulatory, and labeling requirements. Manage multiple projects concurrently, delivering on time and within scope. Other Duties and Responsibilities: Contribute to ideation and concept development for new powdered and liquid product formats. Collaborate with culinary, QA, and sales teams to align technical execution with customer needs. Mentor junior scientists and support continuous improvement in lab and pilot operations. Required Qualifications: Bachelor's degree in food science or a related field (Master's preferred). 9-10 years of food product development experience, with at least 3+ years focused on powdered food systems and or food bases. Proven track record leading projects from benchtop through commercialization. Strong formulation and process development skills, especially with food bases and/or powders. Hands-on experience in pilot and manufacturing environments. Strong communication, organization, and leadership skills. Self-starter who takes initiative, works well cross-functionally, and thrives in a fast-paced setting. Tools and Technology: Microsoft Office Suite (Excel, Outlook, Word, PowerPoint). Specification and PLM systems. Lab and pilot-scale powder blending equipment. Moisture analyzers, sieves, and sensory evaluation tools. Preferred Qualifications: Experience with savory product building blocks including bases, bouillons, seasonings, and dry mixes. Knowledge of powder flow, agglomeration, and moisture control in dry blends. Familiarity with aseptic, retort, and spray drying processes. Experience collaborating with chefs or other culinary professionals. Experience with GMP, HACCP, SQF, and FDA labeling standards. Experience with products requiring Organic, Kosher, NON GMO, GAP certifications. Physical Requirements: Stand and work at lab bench or pilot area for extended periods. Use hands to operate blending and lab equipment. Lift and carry containers of powder ingredients (up to 25 lbs.). Occasional travel to support trials or customer meetings (up to 20%).

This Quality Control Scientist III serves as a vital influencer within the Biologics Quality Control team, shaping the team's approach to quality, compliance, and animal care through expertise and example. In this role, the colleague performs essential product release testing and maintains the highest standards in laboratory animal care, consistently demonstrating best practices and attention to detail. Daily contributions from the colleague help elevate the team's proficiency by sharing knowledge, offering guidance on routine challenges, and providing training to peers. By assisting the team leader with testing coordination and animal distribution, the colleague helps streamline operations and fosters a collaborative, solutions-focused atmosphere. Position Responsibilities: Conduct potency, identity, inactivation, and extraneous agent testing on antigen stocks and final product vaccines using both egg-based and tissue culture methodologies, adhering to strict aseptic techniques, and operating independently without supervision. Perform essential product release safety and potency testing in accordance with regulatory and company standards. Maintain the highest standards of laboratory animal care, consistently demonstrating best practices and ethical responsibility in accordance with IACUC, AAALAC, and other regulatory guidelines. Accurately record laboratory observations and test results, recognizing and reporting deviations promptly. Offer support and guidance on laboratory challenges, helping troubleshoot, and resolve routing issues. Monitor and maintain optimal inventory levels of laboratory supplies and equipment to ensure uninterrupted workflow and compliance with operational standards. Support the upkeep, cleanliness, and routine maintenance of laboratory facilities to promote a safe, organized, and regulatory-compliant working environment. Assist the team leader with coordinating testing schedules and animal distribution to optimize workflow. Foster a collaborative, solutions-focused atmosphere and encourage continuous improvement and ethical standards within the department. Assist with writing and reviewing Animal Usage Protocols (AUPs) to ensure compliance with IACUC guidelines. Contribute to the onboarding and performance training of new team members by providing technical guidance, sharing best practices, and supporting skill development to ensure effective integration into laboratory operations. Help revise departmental methods and protocols, including animal usage procedures and change controls. Participate in laboratory investigations when necessary. Education and Experience: BS/BA plus 2 years' experience OR AA plus 5-7 years' experience. Animal care and handling experience Experienced with the following software programs: Word, Excel, and PowerPoint Strong technical writing skills Knowledge of USDA, EU, and Animal Welfare Act guidelines Experience with maintenance, ordering, testing, and other company-based programs Willingness to positively embrace change and flexibility in adjusting to changing priorities Strong attention to detail, ability to work well independently and as a part of a team, and to work effectively with people at all levels within the organization Trouble-shooting skills Technical Requirements: Proficient in Microsoft Word, Excel, and PowerPoint, with the ability to leverage advanced features for data analysis, reporting, and presentation development. Strong attention to detail, ability to work well independently and as a part of a team, and to work effectively with people at all levels within the organization. Proactively seeks out opportunities for improvements and takes action with minimal direction. Applies problem solving skills in a team environment. High level of understanding of multiple technologies and/or assays within the workgroup. Proficiency of 90% of the testing within the workgroup. Physical Requirements: Must be able to walk, sit, or stand for long periods of time. Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently. Must be able to work scheduled 40 hours with the ability to work overtime as needed. Must be able to work weekends as needed. Frequent lifting and carrying of 5 to 25 lbs. Regular reaching, bending, stooping, and twisting. Repetitive motion and substantial movement of the wrists, hands, and/or fingers. Ability to grasp and manipulate objects like pipettors, flasks, and bottles. Flexibility to cover rotating weekend duties. Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Must Haves: 1-3 years of hands-on microbiology lab experience (academic or industry).. Ability to accurately record and organize experimental results. Experience preparing media, plating samples, and maintaining a clean lab environment. Basic proficiency in Excel for data entry and simple graphing. Nice to Haves: Experience in food or beverage quality labs. Familiarity with PetriFilm products or similar microbiological testing methods. Knowledge of cGMP / ISO standards and SOP compliance. Responsibilities: Perform microbiological testing to validate manufacturing changes for PetriFilm products. Prepare reagents, media, and samples for experiments. Record and summarize experimental results for review. Support continuous improvement initiatives and troubleshoot experimental issues. Maintain calibrated equipment and ensure proper documentation in technical notebooks. Execute and maintain SOPs to meet regulatory requirements. Day-to-Day: Insight Global is seeking three Microbiology Lab Technicians to support the PetriFilm Manufacturing Transition Project. These roles will be 90% hands-on lab work and 10% basic data processing, working closely with senior team members to ensure product quality and consistency during a critical manufacturing move. Candidates will work full-time on-site in Oakdale, MN, assisting with sample preparation, plating, and accurate record-keeping. Ideal candidates will have experience in food safety or quality labs and be comfortable working in a fast-paced environment.

We're seeking an Engineering Technician support the design, planning, and execution of electric utility projects in Davenport, IA . In this role, you'll help ensure electric transmission and distribution work orders are accurately designed, properly constructed, and fully documented-supporting safe, reliable service for residential, commercial, and industrial customers. You'll collaborate with engineering staff, electricians, contractors, and customers while balancing office-based design work with hands-on field inspections. Responsibilities Design, plan, and prepare work orders for construction, maintenance, and modification of electric transmission and distribution systems Review work orders for accuracy, completeness, and compliance with utility standards Conduct field visits to gather data, stake routes, and inspect work in progress Ensure completed work is accurately reflected in drawings, GIS maps, and maintenance systems Assist in scheduling and coordinating transmission and distribution projects; serve as project lead when assigned Develop line designs and cost estimates for maintenance and small capital projects (Level II) Work with customers and contractors on job sales, including cost estimates, material lists, and drawings Monitor construction activities and approve customer billings Respond to customer questions or concerns and communicate utility policies Support preventive maintenance programs and generate corrective work orders as needed Collaborate with electricians, residential customers, and commercial customers on electrical and lighting service design Qualifications Associate's degree or equivalent combination of education and experience Engineering Technician I: Entry-level; utility experience preferred Experience with electric transmission and distribution systems strongly preferred Familiarity with overhead and underground electrical systems and utility equipment Working knowledge of applicable codes and standards (NESC, NEC, NFPA, OSHA) Valid driver's license and ability to perform field work in all weather conditions Preferred Skills Experience using GIS software (Esri ArcGIS preferred) - required for Level II Familiarity with computerized maintenance management systems (CMMS) Strong written and verbal communication skills Ability to read and interpret drawings, schematics, and technical documentation Solid problem-solving and organizational skills Project management experience (required for Level II, preferred for Level I) Basic proficiency with Microsoft Word and Excel Comfort working around high-voltage environments

Working at Freudenberg: We will wow your world! Responsibilities: Assist in the development and maintenance of the engineering bill of material (BOM) Assist in development and implementation of new processes, technologies or tooling needed to build products. Assist in identifying/developing/qualifying fixture for manufacturing processes. Assist in the creation and maintenance of tool files. Support engineering studies and data analysis. Fabricate or assist in fabrication of units for prototypes and engineering builds. Assist in setup and performing design verification and process validation. Assist with drafting and executing protocols within all areas of Product Development such as Design, Process Development and Design Assurance. Work with engineers to specify, procure and commission equipment and procure material. Manage product development materials to help maintain traceability and quantities. Execute inspections of components and devices. Qualifications: Associate Degree in a technical area is preferred Years of experience required depends on level of seniority Demonstrated mechanical aptitude Experience performing tedious processes, building prototypes and working with small parts Basic statistical skills Basic SolidWorks skills is a plus Demonstrated ability in Microsoft Word and Excel Continue to learn and utilize new skills related to typical product development capabilities Ability to utilize metrology equipment such as calipers, micrometers etc.. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Medical LLC

Come join our great work culture with excellent career growth opportunities! Kawasaki Motors Manufacturing Corp., U.S.A seeks a full-time Research and Development Technician at our Consumer Products manufacturing facility in Lincoln, NE. Apply now at KawasakiCareers.com Please note: Sponsorship for employment visa status for these positions is unavailable. Applicants requiring sponsorship for employment visa status now or in the future will not be considered. Responsibilities of R&D Technician can include: * Perform support to R&D Development * Assist in scheduling testing to meet development schedules * Analyze, compile, evaluate, and present data in an organized fashion * Develop and/or prepare schematics, designs, tooling, specifications, and parts lists * Interpret engineering drawings, schematic diagrams or formulas and confers with management or engineering staff to determine quality, reliability and testing standards * Prepare graphs or charts of data, test reports, test standards, or enter data into computer for analysis * Assist in vehicle or accessory design, development, part installation, fitment checking and scheduling * Set up and perform destructive and nondestructive tests on materials, parts or products to measure performance, life or material characteristics * Set up and operate a variety of testing equipment, improvising hook-up and equipment modifications as necessary to test, adjust, align, calibrate, and modify circuitry, components, and systems or subsystems Qualifications for R&D Technician: * Associate's Degree in a technical field or equivalent combination of education and experience * Able to acquire PIT qualification / Valid drivers' license if operating licensed vehicles * Ability to read, understand and accurately follow engineering orders, quality procedures, and operating instructions * Must be able to display appropriate proficiency with computers and computer applications * Experience with applying and interpreting symbols and information from prints, work instructions, drawings, schematics and other relevant technical documents preferred Perks for R&D Technician: * Great work culture with career growth potential * Excellent benefits package including medical, vision, dental, 401(k), and many more * Paid holidays and flexible spending account available * Employee discount for purchase of company products * Company fitness center and wellness program available * Uniforms, lockers, and uniform laundry available * Educational and relocation reimbursements available Mission: Kawasaki, working as one for the good of the planet. We are the Kawasaki Group, a global technology leader with diverse integrated strengths. We create new value for a better environment and a brighter future for generations to come. We value each of our employees and support efforts to use their talents and abilities in full. We respect diversity and strive to build a workplace in which all employees can live up to their full potential. Kawasaki Motors Manufacturing Corp., U.S.A. is an Equal Opportunity Employer who complies with all Federal, State and Local laws prohibiting discrimination in employment.

Syngenta Seeds is one of the world's largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs. Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is headquartered in the United States. Job Description The Production Technician Sr. Independently performs and oversees a broad range of plant activities to support in the distribution of high-quality seed to our clients and customers. Duties: Operate and have expertise of all equipment and systems within the site. Including, running, and operating the conditioning tower. Drive Forklifts, operate pallet wraps, support systems such as conditioning, packaging, and treating. Lead field activities and process of planting, field observations, harvest, and data collection. Troubleshoot equipment issues when incidents or breakdowns occur, in addition to routine maintenance. Responsible for supporting, training, and mentoring new Production Technicians. Create and update training material related to all production technician processes and procedures. Maintain and ensure compliance with site HSE protocols and Syngenta HSE policies and code of conduct. Responsible for shift change hand off and facilitating production meetings. Provide support and troubleshoot process order tracking, administrative procedures, maintenance orders and production information leveraging data systems (SAP, SMMS, WMS). Responsible for developing metrics to create visual boards/data dashboards to drive teamwork and support data-driven decisions. Log non-conformities in the system and supporting root cause analysis on issues; Support site escalation process on issues / non-conformities. Demonstrate adherence and educate peers to the company's Quality Management System (QMS) standards. Maintain compliance with site HSE protocols, local /legal compliance, Syngenta HSE policies and employee code of conduct. Qualifications 5+ years of relevant experience. Limited knowledge of SAP. Advanced knowledge of relevant production software (SCADA). Able to perform manual labor tasks, such as bending, lifting, and standing for extended periods. Ability to lift, push, pull up to 70 pounds. Ability to effectively work in assigned areas of plant, such as warehouse, packaging, treating. Additional Information What We Offer: A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs. Full Benefit Package (Medical, Dental & Vision) that starts your first day. 401k plan with company match, Profit Sharing & Retirement Savings Contribution. Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits. Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: ******************************************* Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. WL2A #LI-ONSITE #LI-KR1

Job Description HiFyve is hiring a Senior R&D Chemist in the Personal Care/Cosmetics industry in Minneapolis, MN OR Miami, FL! Salary: $90K - $110K Shift: Days Job Summary: HiFyve is hiring a Senior R&D Chemist to lead formulation and development of personal care, cosmetic, and OTC products (including lip balms and sunscreens). This role owns projects end-to-end-from concept through scale-up-while collaborating cross-functionally and interfacing directly with customers. Key Responsibilities: Lead formulation projects from concept to commercialization Develop, optimize, and scale formulations; troubleshoot production issues Set product specifications and write compounding procedures Oversee pilot batches, stability testing, and documentation Partner with QC, Operations, Sales, and Regulatory Communicate technical, regulatory, and performance details to customers Identify cost-reduction opportunities and source raw materials Mentor and train lab staff; maintain compliant lab documentation Stay current on formulation trends, ingredients, and market gaps Knowledge, Skills, and Abilities: BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field 8+ years of hands-on formulation experience in personal care/cosmetics OR - Advanced degree with 6+ years' experience Strong knowledge of FDA regulations and cGMPs Advanced formulation and scale-up expertise Excellent communication, leadership, and project management skills Master's degree (Prefered) 10+ years of formulation experience (Preferred) If you are interested, please apply.

A Senior Research and Development Chemist is an experienced researcher/formulator who combines technical knowledge and innovation when formulating a variety of personal care products, cosmetics and OTC (lip balms and sunscreens) from concept to finished product based on customers' requests. Shows the ability to look at different brands' gaps and develop products based on those gaps or customer specification. The Senior R&D Chemist II demonstrates strong leadership and communication skills that are utilized within the organization and with external customers. Requirements Responsibilities Responsible for initiating project concepts, developing objectives, planning and assigning priorities, and completing multiple projects under minimal supervision. Independently investigate/resolve research problems/scale up issues. Ability to communicate with customers on technical aspects as well as regulatory and performance. Utilize and follow relevant legal requirements, regulations and product development standards. Determine and perform appropriate cost reductions (raw materials). Scale-up of approved formulations, to include identification of critical process variables. Ability to troubleshoot production issues and address batch variations. Set product specifications and write compounding procedures. Supervise and coordinate pilot batches. Provide paperwork for new formula and new raw materials to operations. Provide specifications and other information to QC to receive and test new ingredients and finished goods. Test stabilities and monitor testing statuses. Research product formulations and properties and interactions of raw materials. Vendor research for raw materials. Compose and check ingredient lists, QQs and artwork Interpret results of laboratory findings and assess risks involved in new products and communicate findings to sales and upper management. Remain up to date and current on trends in the retail market and trends on formulations materials, ingredients, etc. Training and supervising lab staff (permanent and temporary). Notebook documentation Other duties as assigned. Required Skills/Abilities Working knowledge of laboratory equipment set-up and operation, common laboratory techniques and safe chemical handling Advanced formulation skills and technical knowledge Thorough understanding of FDA regulations and cGMP's Excellent written, verbal and interpersonal communication skills High level of initiative, innovation, critical thinking and problem-solving skills Ability to work cross-functionally & at all levels within the organization including senior leadership Ability to prioritize multiple responsibilities and manage deadlines accordingly. Communicate effectively and professionally with clients and vendors Exceptional attention to detail and high level of accuracy & organization Ability to work as part of a team and excel independently in fast-paced environment Ability to adapt quickly to changing policies and procedures Demonstrated leadership skills Proficient with Microsoft Office Required Education and Experience BS in Chemistry, Cosmetic Science, Physical Chemistry, Chemical Engineering or related sciences with 8+ years of formulating personal care products -OR- advanced degree in cosmetic chemistry and more than 6 years' experience. Preferred Education and Experience Master's Degree in Chemistry, Cosmetic Science, Chemical Engineering or related field 10+ years of experience in formulation of personal care products EEO Statement Bell International Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Salary Description $90k/yr - $110k/yr

Trystar is at the forefront of advancing power solutions, charged and driven by a committed, dynamic team, tackling complex challenges, and creating innovative solutions. We're looking for motivated, driven, and talented individuals eager to be part of the future of power. Safety and integrity aren't just buzzwords, they are the north star guiding us as we aspire to wow our customers every day. We've created power solutions that are not only durable and unique but are also the result of exciting teamwork from every corner of our organization. Individually and collectively, every team member at Trystar plays for each other and strives to deliver unmatched value and 100% accuracy to our customers every single day. Our cutting-edge headquarters is in Faribault, MN, a facility that is partially solar- and wind-powered by our own microgrid! You'll find that we're also pushing boundaries across the country at our additional facilities in Troy, MI; Houston, TX; Merrimack, NH; Burnsville, MN; and Charolette, NC. Trystar's team members are our most important asset, we are in search of a Senior Production Technician who will train and guide our teams to meet/exceed customer expectations & achieve strategic and aspirational growth plans while following our values & guiding principles. The Senior Production Technician is a skilled and organized professional responsible for the training of the department's team members, daily operations, and utilizing Epicor MRP (Material Requirements Planning) system for efficient resource planning and inventory control. They play a pivotal role in ensuring the timely and cost-effective fabrication of components and assemblies while maintaining high-quality standards. In this role you will get to lead a team of production associates to execute production, improve and implement effective manufacturing processes, utilize concepts of lean & 6 sigma to drive a culture of safety, quality, and continuous improvement, while working to achieve key performance metrics and meeting/exceeding customer expectations. This position reports directly to the Production Supervisor. We are looking for people who believe in our guiding principles and values of: Safety - We believe everyone should leave Trystar facilities in the same or better condition than when they arrived. Integrity - We're honest, transparent, and committed to doing what's right. Customer focus - We have relentless focus on our customers and their success. Right with speed - We use good judgement, make thoughtful decisions quickly, and execute them with purpose and intensity. Play for each other - We're a team. We show up for each other and we know that through teamwork we achieve greatness. Champion change - We know adaptation and improvement are requirements to survive and to thrive. Enjoy the journey - We create an environment where our team feels appreciated and has fun along the way. In this role you will get to: Production Oversight: Train and lead the production team members, providing direction and support to achieve production targets and quality objectives. Epicor MRP Utilization: Utilize the Epicor MRP system to plan and schedule production activities, ensuring optimized resource utilization and timely delivery of products. Production Schedule: Train to a comprehensive production schedule based on customer orders, sales forecasts, and material availability, ensuring on-time delivery of fabricated components. Quality Control: Monitor and train to the assembly/fabrication process to ensure compliance with engineering specifications and quality standards. Equipment Maintenance: Coordinate with maintenance personnel to ensure proper upkeep and functioning of equipment, minimizing downtime and delays. Safety Compliance: Enforce safety protocols and best practices to maintain a safe working environment for fabrication personnel. Be accountable for operating a safe working environment for all employees, including leading by example, on-the-spot rectification of safety hazards, and timely incident reporting. Process Improvement: Continuously evaluate processes and procedures, seeking opportunities for improvement in efficiency, productivity, and cost-effectiveness. Implement and create work instructions where applicable. Reporting: Generate regular production reports and performance metrics to assess productivity, track KPIs, and identify areas for improvement. Create a culture of accountability and empowerment in the production environment. Guide production team to ensure effective cross-training for the production workforce, including backups from other areas, to assure a continuously operating and smooth-running department. Recognize employees for results & behaviors that support our values & principles that lead to customer satisfaction. Be accountable to the Production Supervisor for performance of the department shift around metrics covering Safety, Quality, Delivery, Cost, Inventory, and People. Be a change agent within the department, driving continuous improvement and elimination of waste. Develop knowledge of products, processes, equipment, and quality standards to develop/update standard work procedures and cross train department production employees. Instill and maintain a positive can-do team atmosphere within the department; hold regular team meetings, assigning team members tasks, and coordinating support services needed outside the team. Utilize the Tier Accountability Meetings and Team Improvement Boards to ensure results. Escalate major issues and opportunities to Production Supervisors with proposed solutions and participate in execution of follow-on actions. Be responsible for all aspects of managing the department shift to include developing, coaching & mentoring production team members, ensure that team input is used to thoroughly evaluate decisions, to be rapidly implemented. Facilitate and support the identification, selection, and prioritization of process improvement projects. Job Requirements: BASIC QUALIFICATIONS High School Diploma or 2 years of leadership experience in a manufacturing environment. Associate or bachelor's degree in engineering, manufacturing, or a related field is preferred. Equivalent technical education and relevant experience may be considered. Basic knowledge of electrical, mechanical assembly, and/or fabrication. Computer literacy, including MS Word, Excel, and MRP transactions (Epicor preferred). Understanding of safety protocols and the ability to enforce safety standards. Ability to work department shift hours and relevant overtime. PREFERRED QUALIFICATIONS Proficiency in using MRP systems for production planning, material management, and resource allocation. Strong understanding of fabrication processes, equipment, and material requirements. Demonstrated and effective leadership style, with a positive and proactive approach to supervision with a proven ability to build high performing teams. Excellent people skills with a proven ability in supervising, coaching, and training employees. Analytical and problem-solving abilities to optimize production schedules and address challenges. Excellent communication and interpersonal skills to facilitate collaboration among different departments and team members. Ability to develop Team Leads & front-line employees to grow their skills and achieve desired metrics. Ability to adapt & thrive in a fast-paced/high growth work environment. Familiarity with project management tools to track production progress, team tasks, and deadlines, ensuring effective communication and collaboration within the fabrication department. Knowledge of data analysis and visualization tools to create insightful reports and dashboards for monitoring production performance, identifying trends, and making data-driven decisions to improve fabrication processes. Bilingual (English and Spanish) Benefits: 401 (k) with company match Medical Insurance Dental Insurance Vision Insurance Disability Insurance PTO Sick Time Employee Appreciation Time Paid Holidays Trystar is an Equal Opportunity Employer and is committed to creating a diverse and inclusive environment. We consider all applicants for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, age, disability, marital status, veteran status, or any other characteristic protected by law. We are committed to providing equal opportunities for all individuals and to fostering a workplace that values diversity, equity, and inclusion.

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

Responsibilities + Transfer and reformat SOPs related to immunoassay development. + Utilize existing documentation to integrate into new SOP templates. + Ensure quality assurance through data entry and document accuracy. + Engage in formulation processes including weighing materials and measuring pH. + Support documentation projects related to site transfer Essential Skills + Formulation + Laboratory skills + Chemistry + GMP experience + Data entry + Quality assurance expertise Additional Skills & Qualifications + Bachelor's degree in life science (chemistry, biology, biochemistry, microbiology). + 6+ months of experience in a GMP environment. + 6+ months of experience writing SOPs. + Experience in production formulation including weighing materials and using a spectrophotometer. + 3+ months of experience with immunoassay manufacturing. + Knowledge of writing CAPAs, supplier notifications, and change orders. + Familiarity with inventory management systems. Work Environment This position is a full-time, desk-based role, operating Monday through Friday on the first shift with start times between 6 am and 9 am for an 8.5-hour workday. The team has recently undergone reorganization and focuses on new product introduction, site transfer projects, CAPAs, maintenance requests, and supplier notifications. Job Type & Location This is a Contract position based out of Chaska, MN. Pay and Benefits The pay range for this position is $28.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Chaska,MN. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Title: Senior Production Technician Department: Operations Reports to: Director of Manufacturing Pay Range: $50,000.00 to $80,000.00 Salary - based on experience Full-Time, Monday-Friday, 40 hours/week About Elucent Medical: Elucent Medical is a medical device company focused on developing surgical navigation technologies, particularly for cancer surgery, to improve patient outcomes through precision and efficacy. The company's solutions are designed to transform traditional surgical instruments into "smart" tools, enhancing surgical precision and patient outcomes. Job Summary: The Senior Production Technician will investigate and conduct root cause failure mode analysis on the Elucent navigation system, which consists of an electromechanical chassis, computer, display, and an electrical patient pad. This will require understanding assembly drawings, electrical schematics manufacturing procedures, as well as the ability to trace the interaction of software programming with hardware functionality. This will also require using equipment such as soldering equipment, electrical test equipment (oscilloscope, multi-meter), vision systems, and standard mechanical tools for assembly. Supervisory Responsibilities: None. Job Responsibilities: Investigation and identification of root cause for non-conforming systems. Evaluation of returned capital assets for potential repairs and necessary upgrades as part of the depot service repair activities. Assist manufacturing engineering with process improvements, fixture development, and equipment maintenance and validations. Provide overflow capacity for standard production activities by assisting with capital asset builds, production release testing, and crating for shipment. Assist with experimentation and evaluation of new designs, processes, and software revisions. Qualifications Education and Experience: 5+ years of Production Technician experience. GED of HS diploma, preferred Associates or Technical degree Medical device experience required. Electrical experience required. Extensive solder experience required. Startup, small business experience preferred. Required Skills/Abilities: Ability to work independently to troubleshoot non-conforming capital systems and sub-components. Identify root cause failure modes. Self-starter who can thrive in a fast-paced environment. Creative troubleshooting with minimal guidance from engineering. Physical Requirements / Work Conditions: Lift 55 lbs, stand 4 hrs. Light Manufacturing. Elucent Medical Benefits, Culture and Work Environment At Elucent Medical, we prioritize our employees' well-being by providing comprehensive benefits including comprehensive health insurance, a generous retirement savings plan with company matching, flexible work arrangements, generous paid time off, and ongoing professional development opportunities, ensuring a fulfilling and balanced work life. Fulltime Employees are provided: 401(k) 401(k) matching (4%) Dental insurance Health insurance Vision insurance Paid Holidays Paid Vacation Days Paid Sick Days Short Term Disability Long Term Disability Life Insurance Pet Insurance Employee Assistance Programs Affirmative Action / EEO Statement Elucent Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Assist the GFP southeast area fisheries management team with fisheries management, fisheries research, aquatic habitat, aquatic access and aquatic invasive species activities on southeastern South Dakota waters. Duties include fish spawning and stocking operations, fish population sampling, fishing access improvement, assisting with research studies, data entry, lab work, aquatic invasive species outreach, and equipment maintenance. General Requirements : Valid driver's license, the ability to perform strenuous physical labor, and the ability to work nights and weekends. Knowledge, Skills, and Abilities : Operation and maintenance of boats, motors, and trailers, basic vehicle and equipment maintenance, knowledge of fisheries management principles and techniques, fish identification and basic computer operation. Please note this is a temporary or seasonal, non-benefited position, exempt from civil service. How to Apply: Applicants have the option to fill out the online application: ************************************************************************************ or The State of South Dakota Seasonal/Temporary Application form and email or mail it to the address listed below. Applications can be emailed or mailed to: Email to: ************************* Or mail to: Dave Lucchesi 4500 S Oxbow Ave Sioux Falls, SD 57106-4114 *Seasonal positions can be filled prior to the closing date.* #LI-Onsite AN EQUAL OPPORTUNITY EMPLOYER

**Be visionary** Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. **Job Description** **Purpose Statement** **:** The Chemist position is a laboratory position for a chemist, lab technician degreed person with 0 to 5 years industrial experience. The position includes performing various laboratory duties, such as experimentation, testing, sales support, engineering support, and manufacturing support. **Results Expected** **:** 1. Designs, develops, and performs chemical techniques for separation procedures. Develops methods for testing sample introductions for Inductively Coupled Optical Emmision Spectrometers. 2. Evaluate and test Isco instruments and critical components. 3. Communicates in a clear and concise manner, through and written reports, the results of assigned tasks. 4. Practices safe and environmentally sound laboratory techniques. 5. Maintains secrecy of confidential and sensitive information by observing all procedures regarding securing and transmitting privileged information. 6. Collaborates and communicates effectively with other departments as a team member of projects. 7. Responsible for general laboratory maintenance including supply ordering and cleanup. 8. Responsible for other duties assigned by the Separations Laboratory Manager that are within the knowledge level of a college degreed chemistry major. **Job Specifications** **:** + Requires associate's degree in laboratory, Electronic, Industrial, Mechanical, Manufacturing or Engineering Technology or equivalent related schooling and experience. + Experience designing manufacturing support equipment and testing equipment required. + Should possess excellent communication skills, be able to work well with people, also able to work on multiple tasks simultaneously, have a proper sense of urgency to resolve problems that can significantly affect the company's financial performance + Experience with and knowledge of computers and programming is preferred. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

Requisition ID: 912465 Store #: WM0029 Optical Coating BPARK Position: Full-Time Total Rewards: Benefits/Incentive Information Since 1915, Walman Optical has served thousands of independent eye care professionals providing solutions for all of their optical needs. Our experienced and knowledgeable team helps businesses grow while providing quality eyewear and unmatched service for an exceptional patient experience. With us, you'll bring our most advanced technology and innovative products to our partners. As a division of Walman, our collective mission is to enrich the lives of our customers, employees and the communities we serve through better vision. Walman is part of EssilorLuxottica, a global leader in the design, manufacture and distribution of world-class vision care products, including iconic eyewear, advanced lens technology and cutting-edge digital solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn!GENERAL FUNCTION Responsible for all aspects of the Anti-Reflective (AR) Coating process to produce quality eyewear that meets customer standards. Primary responsibility is the daily operation and maintenance of the large-capacity AR coating machines and final quality inspection of outgoing lenses. The Sr Production Technician will be responsible for adhering to the company's quality and safety requirements during all operations. MAJOR DUTIES AND RESPONSIBILITIES Operate large-capacity AR coating machines. Perform daily and weekly maintenance of the vacuum coating chambers and equipment involved in the AR coating process. Keep a current and accurate log of all processes and maintenance for the machines. Perform all aspects of operation of the AR Coaters, including: Clean machine and make ready for operation. Inspect each lens for accuracy and any other defects present on lens surface. Log all scratches or other conditions found. Place lenses into appropriate tooling based on lens diameter and shape. Load lenses into AR coating machine and select correct recipe and chemicals for each different AR coating process. Perform all necessary parts change-outs and other maintenance items in a timely manner. Perform necessary quality testing on finished product. Perform final inspection on all batch coated lenses and ensure adherence to the cosmetic standards. Verify performance of coating runs and ensure coating meets desired specification. Perform troubleshooting of machine/equipment problems and work with supervisor to resolve issues. Pack completed work. Review rejected lenses and re-work or assign proper breakage codes. Sandblast machine parts as needed. Follow standard procedures while continually evaluating opportunities for improvement. Provide recommendations to improve processes to simplify jobs, eliminate non-value-added tasks and reduce costs. Effectively communicate with all levels of the organization to ensure understanding and the proper application of company policies, practices and procedures. Actively participate and engage in continuous improvement processes Maintain work area and common areas of department in a neat, clean, and organized condition. Understand and follow all company and manufacturer's policies and procedures and ensure compliance with all attendance & safety rules and regulations. Maintain confidentiality of all proprietary and HIPAA protected information. Willingly assist others as necessary to keep work current, meet deadlines or maintain an even workload. Cooperate with other employees and demonstrate a good attitude. Perform an acceptable quantity and quality of work on time as required. Provide proper training, work direction, and technical guidance for less experienced employees. Attends in-house or sponsored training meetings when necessary. Perform other duties as assigned. This position requires exposure to one or more hazardous substances/chemicals which requires safety training. BASIC QUALIFICATIONS High school diploma, GED or equivalent work experience 3+ years of manufacturing experience Ability to multi-task, orient to detail and operate in a fast-paced environment Ability to lift and/or move up to 50 pounds and lift up to 15 pounds above head. Specific vision abilities required by this job, including close vision. Pay Range: Starting Rate at $20/hour; more for experience This posting is for an existing vacancy within our business. Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. EssilorLuxottica complies with all applicable laws related to the application and hiring process. If you would like to provide feedback regarding an active job posting, or if you are an individual with a disability who would like to request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name, job id number, and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Nearest Major Market: Minneapolis Job Segment: Social Media, Marketing

The Production Technician Sr. Independently performs and oversees a broad range of plant activities to support in the distribution of high-quality seed to our clients and customers. * Operate and have expertise of all equipment and systems within the site. Including, running, and operating the conditioning tower. * Drive Forklifts, operate pallet wraps, support systems such as conditioning, packaging, and treating. * Lead field activities and process of planting, field observations, harvest, and data collection. * Troubleshoot equipment issues when incidents or breakdowns occur, in addition to routine maintenance. * Responsible for supporting, training, and mentoring new Production Technicians. * Create and update training material related to all production technician processes and procedures. * Maintain and ensure compliance with site HSE protocols and Syngenta HSE policies and code of conduct. * Responsible for shift change hand off and facilitating production meetings. * Provide support and troubleshoot process order tracking, administrative procedures, maintenance orders and production information leveraging data systems (SAP, SMMS, WMS). * Responsible for developing metrics to create visual boards/data dashboards to drive teamwork and support data-driven decisions. * Log non-conformities in the system and supporting root cause analysis on issues; Support site escalation process on issues / non-conformities. * Demonstrate adherence and educate peers to the company's Quality Management System (QMS) standards. * Maintain compliance with site HSE protocols, local /legal compliance, Syngenta HSE policies and employee code of conduct.