Research and development technician jobs in Lawrence, KS

Job DescriptionIndustrial Cybersecurity Consultant - SOC Operations (Extended Night-Shift) Location: Remote (must reside in Kansas City, MO) Training: Onsite in Kansas City, MOShift Options: Full-TimeNight Shift: Four 10-hour shifts, typically 6:00 PM - 4:00 AMPart-Time Night Shift: AvailableWeekend Coverage: Open to candidates willing to work weekends Position Overview The Industrial Cybersecurity Consultant will be an integral member of a Security Operations Center (SOC) team, responsible for both operational and consulting tasks. This role combines real-time security monitoring and incident response with project-based cybersecurity consulting. Key duties include triaging security events, providing recommendations through a case management system, and participating in client calls for incident response or escalation. In addition, the consultant will support ICS/OT security projects, vulnerability assessments, penetration testing, and compliance initiatives aligned with frameworks such as NIST CSF and RMF. Key Responsibilities Security Event Management Monitor and triage security events, analyze alerts, and prioritize incidents for remediation. Provide actionable recommendations through the case management system to ensure timely resolution. Participate in client calls for incident response or escalation as needed. Cybersecurity Consulting Execute planning, design, development, and implementation of technical controls, procedures, and policies associated with cybersecurity compliance and regulatory standards. Conduct network penetration tests and vulnerability assessments of IT and Operational Technology (OT) networks for compliance and security purposes. Perform detailed post-event analysis of unusual events and recommend procedural changes. Develop policies and procedures for secure process control network design, including technical recommendations for firewalls and other security controls. Compile technical documentation of network traffic and firewall services/solutions, including diagrams and explanations. Collaboration & Compliance Work with internal teams and client stakeholders to resolve technical issues and communicate implications effectively. Maintain confidentiality and security of all client and project information. Comply with all applicable policies and standards. Job Requirements Education: Bachelor's degree in Cybersecurity, Computer Science, Computer Engineering, Electrical Engineering, or related technical field. Experience: Minimum 3 years of related experience in cybersecurity operations and consulting. Certifications: Security+ preferred (other advanced certifications a plus). Technical Skills: Advanced knowledge of security principles and cybersecurity technologies. Experience with vulnerability assessments, penetration testing, and associated tools/techniques. Familiarity with cybersecurity controls (firewalls, access control, authentication, anti-virus/anti-malware, patching, logging). Knowledge of control systems used in utilities, manufacturing, oil & gas, transportation, smart buildings, and cities. Strong written and oral communication skills for client interaction and reporting. Ability to operate under pressure and meet tight deadlines in industrial, corporate, and government environments. Understanding of business principles and operational security practices specific to engineering/security consulting. Strong technical writing skills and knowledge of modern and legacy networking and telecommunications. Experience 2ith physical cabling for network communications and control system I/O. Other: Ability to obtain and maintain access to client sites, including applicable U.S. security clearances.

This position is responsible for supporting R&D activities of one or more product lines. The technician will conduct experiments, compile data results, and reactions in support of R&D Sustaining and New Product Developments. They will follow testing plans as laid out by R&D Chemists and Managers and record and report results in a detailed and thorough manner. This position may participate in special studies and be required to conduct testing and work outside of established standard operating procedures. Essential Duties: Conduct routine analytical tests to determine chemical, and physical properties of raw materials, process, and product samples. Manufactures samples and prototype formulations. Tests proposed formulations for performance, lifetime, and manufacturability and suggest modifications as warranted. Conducts competitive product testing, as required. Accurately and thoroughly recording and entering data into electronic systems and R&D lab notebooks. Reports progress on pending projects at regular timeframes. Act with strong listening and analytical skills to develop/maintain relationships and deliver results. Helps maintain laboratory equipment and assists with calibrations. Follows AS9100 Quality Management System as applies to R&D and as defined in the Quality System. Actively participates in company Safety Programs, as required, and practices safe work methods on a daily basis. Actively supports and participates in the site Laboratory Safety and Chemical Hygiene Program. Attends company sponsored training and outside seminars as required. Acts in accordance with company policies, procedures, and corporate ethics. Perform other duties as assigned. Education & Experience: B.S. degree in Chemistry, Chemical Engineering, Material Science, or related field from an accredited college or university. Proficient within Windows based environment. Experienced in Microsoft Office Suite software (Excel, Word, Power Point, Outlook). Experience working with ERP systems, particularly Microsoft Navision, a plus. Proficiency in using standard laboratory equipment. Experience following SOPs and GLPs. Experience working under ISO 9001/AS 9100 Quality Management environments a plus. Exposure to GHS and other regulatory requirements applicable to the supported product line(s) a plus. ITW is an equal opportunity employer. We value our colleagues' unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential. As an equal employment opportunity employer, ITW is committed to equal employment opportunity and fair treatment for employees, beginning with the hiring process and continuing through all aspects of the employment relationship. All qualified applicants will receive consideration for employment without regard to race, color, sex, gender identity, sexual orientation, religion, national origin, age, disability, protected Veteran status or any other characteristic protected by applicable federal, state, or local laws.

General Summary: Under limited supervision, responsible for working closely with our Sales Team and Customers to develop a wide variety of products. Benefits and Culture We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future. Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees. Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options. We strive to be your Employer of Choice. As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career. Visit our website to learn more about our competitive benefit programs - **************************************** Principle Duties and Responsibilities 1. Develops new production processes for new product development. 2. Streamlines current plant processes for maximum efficiency and continuous improvement. 3. Investigates and implements new and innovative packaging solutions. 4. Investigates and evaluates new equipment for the development of next generation products. 5. Collects and documents records on formulas, specifications, processes and packaging. 6. Coordinates and conducts test batches to develop new formulas, processes and specification in all Production facilities. 7. Involved in every stage of product cycle from ideation and Development to First Production and Launch. 8. Presents recommendations and solutions to Sales and Customer Service personnel. 9. Joins project teams at different site frequently without knowing team members in advance. Job Specifications 1. 5+ years product development or process engineering experience is preferred. 2. Bachelor's Degree in Food Science or a related field is preferred. 3. Knowledge of food and safety regulations is required 4. Experience using scientific methods within the food industry is required. 5. Excellent oral and written communication skills with great presentation and interpersonal skills. 6. Strong PC skills are required including Microsoft Excel, PowerPoint, and Word. 7. Experience in and be comfortable with a fast-paced environment of changing priorities, multiple project and short deadlines. Working Conditions 1. Office and Food laboratory environment and refrigerated food manufacturing plant. 2. The environment may be wet or dry and temperatures may range from 25°F to 110°F. 3. Frequent exposure to hazardous materials. 4. Requires walking and standing for long periods of time. 5. Some travel required. 6. Occasional lifting of up to 50 pounds. This position is eligible for a bonus based on company goals/performance. Recipe for Success Reser's is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries. Family owned and operated, Reser's has been a proud sponsor of good times at racetracks, picnics, BBQs, music festivals, and affordable family meals since 1950. Reser's family of brands include Reser's American Classics, Main St Bistro, Stonemill Kitchens, and more. With more than 4,500 employees, Reser's operates 14 facilities in the US, Mexico, and Canada and actively supports the communities it serves.

GENERAL STATEMENT OF RESPONSIBILITY: Coordinate the day-to-day activities of the Certifying Scientists and the specific duties associated with the hair testing department. Ensure the daily processing is conducted in an accurate and efficient manner, following guidelines and regulations. ESSENTIAL FUNCTIONS: * Manage team performance by evaluating, hiring, training, coaching, disciplining and motivating; initiating disciplinary action when appropriate. * Maintain teamwork schedules to ensure assignments to expedite work flow, operational coverage and staff coverage. * Establish and maintain department SOP's and ensure compliance. * Consult with MRO's and clients about drug test results. * Perform the duties of a Certifying Scientist when necessary. * Keep current with Federal Register, NLCP Guidance Documents, NRC requirements, CAP requirements, state requirements, etc. * Work with the QC department to resolve audit issues and ensure regulatory requirements are being met. * Ensure department meets production goals and expected turnaround time for samples. * Provide and maintain good communication with staff, other departments, and administration. * Carry out supervisory responsibilities in accordance with CRL's policies and applicable laws. * Maintain and protect the confidentiality of all CRL, CRL subsidiaries, legal entities and client information. * Be able to comply with all applicable federal, state, and local safety and health regulations that would apply to this job. * Be proactive in bringing ideas to Management's attention to improve productivity, service, quality, policies and procedures, cost savings, and utilization of company resources. * Continuously improve management skills through in-house training, self-study methods, and other available training resources. * Ensure concerns are raised to the appropriate level of management. * Keep work area neat and clean. Other duties as assigned. JOB QUALIFICATIONS: EDUCATION: A doctoral, master's, or bachelor's degree in medical technology, clinical laboratory, chemical, or biological science. EXPERIENCE: 4 years of pertinent laboratory experience. Must meet NYS Technical Supervisor requirements. SKILLS & ABILITIES: * Excellent interpersonal skills - positive, professional demeanor, attentive listener * Excellent verbal and written communication and documentation skills - spelling, grammar and proofreading * Strong working knowledge of MS office (MS Outlook, Word, Excel, PowerPoint) * Strong judgment/decision making skills * Ability to perform highly detailed work on multiple, concurrent task with constant interruptions and changing deadlines * Must be able to read, understand, and develop strong working knowledge of appropriate SOP's and other relevant information services. * Detail oriented * Strong analytical and organizational skills * Ability to work under pressure * Ability to be at work and on time * Ability and judgment to interact and communicate appropriately with other employees, clients and management PHYSICAL REQUIREMENTS: The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be available to enable qualified individuals with disabilities to perform the essential functions. The following physical attributes are required for this position: * Sitting for extended lengths of time * Close vision requirements due to computer work * Repetitive use of hands, fingers, wrists, and elbows for operating a computer and telephone * Light lifting, up to 10 pounds * The ability to discriminate between different colors visually is considered an essential function for the position. EQUIPMENT: PC and communications equipment OTHER: Overtime and weekend work as necessary according to workload and/or projects; occasional travel required. The employer shall, in its discretion, modify or adjust this position to meet the company's changing needs. This job description is not a contract and may be adjusted as deemed appropriate in the employer's sole discretion. * denotes essential job function An Equal Opportunity Employer Pay Range: $26.00 - $48.00 Benefits for Full Time Employees: * Medical, Dental, Vision * Life/AD&D * Supplemental Life/AD&D * Section 125 FSA Plan * 401(k) * Short and Long-Term Disability * Paid Time Off * Holidays * Tuition Reimbursement

Medical Research Associate - PRN - (Onsite) Lenexa, KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. What you will be doing * Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process. * You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures. * Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized. * Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort. Your profile * A strong command of both English and the host country's language is essential, enabling effective communication and collaboration. * A High School Diploma or G.E.D. qualification * If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you. * 1+ years of work experience in a medical or clinical field is preferred * If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage * Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Career Guidant, an internationally acclimed, trusted multi-faced orgiansation into Information Technology Custom Learning Services for Enterprises, Lateral Staffing Solutions, Information Technology Development & Consulting, Infrastructure & Facility Management Services and Technical Content development as core competencies. Our experienced professionals bring a wealth of industry knowledge to each client and operate in a manner that produces superior quality and outstanding results. Career Guidant proven and tested methodologies ensures client satisfaction being the primary objective. Committed to our core values of Client Satisfaction, Professionalism, Teamwork, Respect, and Integrity. Career Guidant with its large network of delivery centres,support offices and Partners across India, Asia Pacific, Middle East, Far East, Europe, USA has committed to render the best service to the client closely to ensure their operation continues to run smoothly. Our Mission "To build Customer satisfaction, and strive to provide complete Information Technology solution you need to stay ahead of your competition" If you have any queries about our services. Job Description Preferred • At least 1 year of experience with Ecommerce technologies • At least 1 year of experience in Demandware development with at least 1 full lifecycle Demandware implementations. • At least 2 years of experience in software development life cycle. • At least 2 years of experience in Project life cycle activities on development and maintenance projects. • At least 2 years of experience in Design and architecture review. • Ability to work in team in diverse/ multiple stakeholder environment • Analytical skills • Experience and desire to work in a Global delivery environment The job entails sitting as well as working at a computer for extended periods of time. Should be able to communicate by telephone, email or face to face. Travel may be required as per the job requirements Qualifications Basic • Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education. • At least 4 years of experience with Information Technology Additional Information Additional Information ** U.S. citizens and those authorized to work in the U.S. are encouraged to apply. We are unable to sponsor at this time. Note:- 1.This is a Full-Time Permanent job opportunity for you. 2.Only US Citizen, Green Card Holder and GC-EAD can apply. 3.No OPT-EAD & H1B Consultants please. 4.Please mention your Visa Status in your email or resume.

Research Associate (RA) Glass Lewis is a trusted ally to more than 1,300 investors globally who use our corporate governance research, custom policy recommendations, engagement services and tools, and industry-leading proxy vote management solution to help drive value across their governance activities. We also work with over 3,000 corporate issuer clients, providing research reports, thought leadership, customized voting policies, equity plan models, and opportunities for direct engagement on material governance and disclosure practices. Glass Lewis' industry-leading research and analysis covers more than 30,000 meetings each year across approximately 100 global markets. Our clients include many of the world's leading pension funds, mutual funds, and asset managers, collectively managing over $40 trillion in assets. We have teams located across the United States, Europe, and Asia-Pacific regions, giving us global reach with a local perspective on the most important governance issues. Founded in 2003, Glass Lewis is headquartered in San Francisco, California with additional offices in Kansas City, Missouri; London, U.K.; Paris, France; Limerick, Ireland; Karlsruhe, Germany; Stockholm, Sweden; Manila, Philippines; Toronto, Canada; Sydney, Australia; Timișoara, Romania; and Tokyo, Japan. Our team includes more than 400 full-time employees globally, over half of which are dedicated to research. For more information, please visit ******************* Position Details Contract Type: Full-time, temporary (~5 months from January/February 2026 - May/June 2026) Location: Kansas City, Missouri Work Model: Hybrid, 3 days per week in office Level: Entry-level Compensation: USD $1,906.25 semi-monthly (15th and last day of each month) Position Description Research Associates (“RAs”) work with Glass Lewis' research teams to produce unbiased, independent research (Proxy Papers). RA positions are separated into two areas of focus: Governance covers meeting proposals for board of director elections, committee memberships, environmental and social issues, skills matrices, auditor appointments, etc. Compensation covers meeting proposals for executive pay practices, incentive plans, pay-for-performance, etc. Glass Lewis is an equal opportunity employer in compliance with applicable state and federal laws. Accordingly, we take affirmative action to ensure that all employment and recruiting activities are conducted on a non-discriminatory basis without regard to race, color, religious creed, age, marital status, national origin, ancestry, sex, gender identity or expression, intellectual, mental, or physical disability, veteran status, or other characteristics protected by law. Requirements Bachelor's degree Strong English writing and editing skills Strong analytical research skills (emphasis on qualitative analysis) Able to quickly synthesize new information and apply to unique scenarios Thorough, accurate, organized and productive Able to work effectively under tight and overlapping deadlines Flexibility to navigate shifting priorities Desire to learn, with ability to receive and apply feedback Able to effectively communicate in a collaborative environment Genuine interest in areas of corporate law, economics, finance, public policy and governance is helpful Desire to work in a professional, fast-paced atmosphere with other bright people

8350 NW Roanridge Kansas City, MO 64151 < Back to search results This location is operated by an independent franchise owner. Benefits may vary by location. When applying, please note that current job availability is found by clicking the link to the franchise specific hiring website. Role Overview Chili's Managers are wired for hospitality! We're in the people business. So, we know how to make someone feel special, and our most successful Managers are passionate about connecting with Team Members and Guests. Our win-together atmosphere rewards teamwork, and a willingness to go above and beyond is always recognized and celebrated. For decades, Chili's has been known for our culture of fun. Simply put - we take our jobs seriously but not ourselves. Our Managers are hungry for top business results but also know how to have fun along the way. From leading the team through a high-energy shift to exceeding Guest expectations on every occasion to ensuring we meet our financial responsibilities, Managers are the critical link to making it all happen. Responsibilities * Ensure a great Guest experience * Role model and hold Team Members accountable to operational and quality standards * Identify root cause of issues while being self-reflective and holding yourself accountable first, showing vulnerability and transparency * Foster open communication between Team Members and Management * Influence Team Member behaviors by championing change and restaurant initiatives * Lead with heart and mind * Drive business results by utilizing Chili's systems to effectively control costs * Follow operational systems, such as our Manager Timeline and performing quality Line Checks * Hire, train, retain, and develop Team Members to take on larger roles * Drive Guest engagement within the four walls of the restaurant while developing relationships within the community * Understand and practice safe food handling procedures * Communicate and embody Chili's culture and Cultural Beliefs: Every Guest Counts, Food Perfection, Be Accountable, Play Restaurant About Us Chili's was born in Dallas, Texas in 1975. Since then, we've boldly claimed our place in the casual dining industry as the place to go for Big Mouth burgers, house smoked ribs, full on fajitas, and hand shaken margaritas! With a legacy deeply rooted in service, hospitality, and giving back, we are committed to delivering the best experience to every Guest, every day. About You * Dependable team player * Prefers to work in a fast-paced environment * Great multitasking skills

Hennesy Research Associates - a Kemin company is looking for an Associate Scientist with a strong focus on ELISA creation and development. Step into the heart of innovation as an ELISA Scientist, where your benchwork drives breakthroughs in veterinary medicine. You'll lead the charge in developing potency assays, crafting and executing ELISA protocols, and solving complex analytical puzzles that shape how the USDA evaluates product efficacy. This is more than R&D - it's your chance to define the science behind real-world impact. If you're passionate about precision, problem-solving, and pioneering research, this is where your expertise belongs. Join the Kemin Team and Transform Lives! We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet. We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet's natural resources, and protect the global food supply chain for generations to come. We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines. We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States. As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being: Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays. Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career. Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits. Service Opportunities: Make a positive impact with paid time off for volunteering in your community Responsibilities Independently conduct innovative scientific experiments and translate research into practical applications. Perform literature reviews and provide written summaries that are incorporated into strategy. Designing and executing enzyme-linked immunoassay (ELISA) potency assays. Independently develop and review SOP's, research protocols and research methods; design safety procedures. Independently perform advanced data analysis and review other's data to provide input and insight. Must keep detailed records of activities and prepare written documents including research reports and method protocols Independently, collect, interpret and document research data. Generate scientific publications for internal and external publication, with guidance and review. Prepare and present data analytics and research in multiple formats both internally and externally. Review internal publication across Kemin. Identify and participate in external research collaborations. Contribute to strategic planning process and customer meetings. Provides instruction and training to interns and junior staff. Ability to balance multiple projects, meet deadlines, meticulous record keeping skills, excellent oral and written communication skills, ability to work independently but also cooperate and work well with the entire R&D team. Other duties/projects as assigned Qualifications Education Bachelor's Degree in a scientific field with 7+ years of relevant experience Masters Degree or PhD in a scientific field with 3+ years of relevant experience is preferred Skilled at experimental design, sterile technique, data evaluation, project management, and problem solving. Experience in cell culture and sterile technique and knowledge of hybridoma based monoclonal antibody generation. Expertise in standard laboratory procedures such as ELISA and SoftMax Pro Software. Experience with the JESS automated western blot system. Must be able to work independently or on a team and have the ability to work in a fast-paced multidisciplinary environment. Excellent Scientific skills in experiment design and data collection, able to maintain instruments. Detail oriented, organized, prioritization skills and motivated by accomplishment. Ability to understand and perform advanced statistical analysis. Analytical lab skills with a strong scientific curiosity and innovative thinking. Fluent in English. Excellent written and oral communication skills with ability to present ideas effectively. Advanced computer knowledge (Word, Excel, Access, PowerPoint, etc.). A post-offer background check and drug screen is required. Additional pre-employment requirements may be necessary based on position. Kemin is an equal opportunity employer, and all reasonable accommodations will be considered. Kemin is a drug-free and tobacco-free campus. #LI-MP1

Thanks for your interest in Children's Mercy! Children's Mercy is in the heart of Kansas City - a metro abounding in cultural experiences, vibrant communities and thriving businesses. This is where our patients and families live, work and play. This is a community that has embraced our hospital and we strive to say thanks by giving back. As a leader in children's health, we engage in meaningful programs and partnerships throughout the region so that we can improve the lives of children beyond the walls of our hospital. Overview The Children's Mercy Research Institute is recruiting a Research Associate to join the Community Engaged Research Team in the department of Population Health. The Community Engaged Research Team works with interdisciplinary teams throughout Children's Mercy, and our academic affiliates (UMKC, KU, KUMC), patients, families, and community partners to promote engagement of community members and stakeholders in the design, implementation, and dissemination of research to advance health outcomes. Through technical consultations, trainings and large project collaborations, the Community Engaged Research Team applies expertise in community based participatory and community engaged research approaches. At Children's Mercy, we are committed to ensuring that everyone feels welcomed within our walls. A successful candidate for this position will join us as we strive to create a workplace that reflects the community we serve, as well as our core values of kindness, curiosity, inclusion, team and integrity. Additionally, it's important to us that we remain transparent with all potential job candidates. Because we value the safety of the patients and families we serve, as well as the Children's Mercy staff, we want to let you know that the seasonal influenza vaccine is a condition of employment for all employees in our organization. New employees must be willing to be vaccinated if found non-immune to measles, mumps, rubella (MMR) and chicken pox (varicella) and/or without evidence of tetanus, diphtheria, acellular pertussis (Tdap) vaccination since 2005. If you are selected for this position, you will be asked to supply your immunization records as proof of vaccination. If you and have any concerns about receiving these vaccines, medical and/or religious exemptions can be further discussed with Human Resources. Responsibilities Advising health professionals in community engaged research methods Coordinating meetings with members of the CMRI Community and Youth Research Advisory Boards and other patient, caregiver, and community partners Critically reviewing and/or contributing to grant proposals Drafting and reviewing IRB protocols Coordinating and contributing to Community Engaged Research workshops and training Contributing to manuscripts and presentations Qualifications Bachelor's Degree in Public Health, Psychology or Related Field and 5-7 years' with documented prior advanced education or training in laboratory techniques and methods requisite to conducting independent research or HS diploma, or equivalent, or Associates degree and 7 or more years experience may be accepted in lieu of a Bachelor's degree Demonstrated experience with research recruitment and data collection Skills in community engaged research approaches (e.g. generating research questions, coordinating with patient, caregiver, and community partners) Strong interpersonal and organizational skills Ability to work with interdisciplinary teams and community members Knowledge of social and behavioral theories as applied to the health sciences Strong writing skills Commitment to collaboration, shared decision making, and community centeredness Candidates with the following qualifications are strongly encouraged to apply: Spanish-language skills (QBS preferred) Benefits at Children's Mercy The benefits plans at Children's Mercy are one of many reasons we are recognized as one of the best places to work in Kansas City. Our plans are designed to meet the changing needs of our employees and their families. Learn more about Children's Mercy benefits. Starting Pay Our pay ranges are market competitive. The pay range for this job begins at $26.62/hr, but your offer will be determined based on your education and experience. EEO Employer/Disabled/Vet Children's Mercy hires individuals based on their job skills, expertise and ability to maintain professional relationships with fellow employees, patients, parents and visitors. A personal interview, formal education and training, previous work experience, references and a criminal background investigation all are factors used to select the best candidates. The hospital does not discriminate against prospective or current employees based on the race, color, religion, sex, national origin, age, disability, creed, genetic information, sexual orientation, gender identity or expression, ancestry or veteran status. A drug screen will be performed upon hire. Children's Mercy is smoke and tobacco free.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: Perform Quality Control activities in support of finished products, which includes testing of raw materials and serum. Perform testing according to approved procedures or compendia (such as USP, EP, ACS) following site quality and safety standards. Testing includes, but is not limited to, environmental monitoring, bioburden analysis, endotoxin testing, microbial limits testing, microbial identification, and growth promotion of microbiological media and reagents. Evaluate results against approved specifications, perform peer review of analytical data, and release data from QC in a timely manner to meet scheduled release dates. Typically performs routine assignments with little direction using existing procedures and practices that require some knowledge of concepts and specialized technical expertise within an analytical/scientific method or operational process. Accountable for the quality of own work. Receives clear instruction, guidance and direction from more senior level roles or even solves problems of low complexity independently by selecting solutions based on fact-based information. Work some weekends or holidays (as required by testing/business needs). Provide complete and accurate records consistent with quality guidelines and GDP requirements. Communicate the status of operations and bring deviations to the attention of the supervisor. Attention to detail. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal) and ensure equipment and work areas are maintained and clean. Take the necessary action to resolve any unsafe conditions. Who You Are Minimum Qualifications: * Bachelor's Degree in Biology, Chemistry, or other Life Sciences discipline Preferred Qualifications: * 1+ year of laboratory experience in a quality control lab * Good attention to detail * Knowledge of site Quality standards * Familiar with laboratory instruments and production equipment Pay Range for this position: $24-$44 per hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Medical Research Associate - PRN - (Onsite) Lenexa, KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. **What you will be doing** + Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process. + You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures. + Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized. + Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort. **Your profile** + A strong command of both English and the host country's language is essential, enabling effective communication and collaboration. + A High School Diploma or G.E.D. qualification + If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you. + 1+ years of work experience in a medical or clinical field is preferred + If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage + Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs. + Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. + Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. + Life assurance + Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (************************************* to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (****************************************************** Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (****************************************************** to apply

Hennesy Research Associates - a Kemin company is looking for an Associate Scientist with a strong focus on ELISA creation and development. Step into the heart of innovation as an ELISA Scientist, where your benchwork drives breakthroughs in veterinary medicine. You'll lead the charge in developing potency assays, crafting and executing ELISA protocols, and solving complex analytical puzzles that shape how the USDA evaluates product efficacy. This is more than R&D - it's your chance to define the science behind real-world impact. If you're passionate about precision, problem-solving, and pioneering research, this is where your expertise belongs. Join the Kemin Team and Transform Lives! We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet. We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet's natural resources, and protect the global food supply chain for generations to come. We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines. We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States. As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being: Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays. Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career. Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits. Service Opportunities: Make a positive impact with paid time off for volunteering in your community Responsibilities Independently conduct innovative scientific experiments and translate research into practical applications. Perform literature reviews and provide written summaries that are incorporated into strategy. Designing and executing enzyme-linked immunoassay (ELISA) potency assays. Independently develop and review SOP's, research protocols and research methods; design safety procedures. Independently perform advanced data analysis and review other's data to provide input and insight. Must keep detailed records of activities and prepare written documents including research reports and method protocols Independently, collect, interpret and document research data. Generate scientific publications for internal and external publication, with guidance and review. Prepare and present data analytics and research in multiple formats both internally and externally. Review internal publication across Kemin. Identify and participate in external research collaborations. Contribute to strategic planning process and customer meetings. Provides instruction and training to interns and junior staff. Ability to balance multiple projects, meet deadlines, meticulous record keeping skills, excellent oral and written communication skills, ability to work independently but also cooperate and work well with the entire R&D team. Other duties/projects as assigned Qualifications Education Bachelor's Degree in a scientific field with 7+ years of relevant experience Masters Degree or PhD in a scientific field with 3+ years of relevant experience is preferred Skilled at experimental design, sterile technique, data evaluation, project management, and problem solving. Experience in cell culture and sterile technique and knowledge of hybridoma based monoclonal antibody generation. Expertise in standard laboratory procedures such as ELISA and SoftMax Pro Software. Experience with the JESS automated western blot system. Must be able to work independently or on a team and have the ability to work in a fast-paced multidisciplinary environment. Excellent Scientific skills in experiment design and data collection, able to maintain instruments. Detail oriented, organized, prioritization skills and motivated by accomplishment. Ability to understand and perform advanced statistical analysis. Analytical lab skills with a strong scientific curiosity and innovative thinking. Fluent in English. Excellent written and oral communication skills with ability to present ideas effectively. Advanced computer knowledge (Word, Excel, Access, PowerPoint, etc.). A post-offer background check and drug screen is required. Additional pre-employment requirements may be necessary based on position. Kemin is an equal opportunity employer, and all reasonable accommodations will be considered. Kemin is a drug-free and tobacco-free campus. #LI-MP1

Performing critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what Associate Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you. When you work as an Associate Scientist on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, dd PCR and cell-based assays within a GLP (Good Laboratory Practice) environment laboratory environment. Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation. In this role, we will rely on you to: Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and dd PCR) and handling DNA/RNA Experience with procedures for the extraction and quantification of nucleic acids Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level Experience with cell culture is preferred Plan and carry out assigned experiments. Including method development, method validation, sample analysis, data calculation, interpretation & review, and troubleshooting Design experiments & evaluate outcomes versus current SOPs, protocols, and other relevant standards. Recommend appropriate course of action as necessary Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects Perform all aspects of the job in a way that supports the company brand, mission, vision, and values To qualify specifically for this role, you will have: Bachelor's, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 4 years' experience in a scientific laboratory environment Experience with design, method development, validation, and sample analysis Experience with GLP requirements and Good Documentation Practices (GDP) Manage material, equipment, and instrumentation Analyze and interpret data, prepare summary tables, and review raw data Assist with the preparation and review of SOPs, study plans, and reports Ability to multi-task and meet deadlines Excellent verbal and written communication and organizational skills Self-motivated and driven Flexible and adaptable - able to work independently and/or in a team environment Ability to troubleshoot and problem-solve - Critical Thinking (Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.) WHO YOU AREYou will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work. WHAT YOU'LL GETOur benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Learn more about the Benefits at KCAS Bio WHO WE AREWe are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another's growth. At KCAS Bio, we advance both great science AND great people. Learn more about what it is like to work at KCAS Bio KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to [email protected] or call ************ (for TTY assistance call 711) and ask for Human Resources. IND123We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description: Perform accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executing well defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of process development/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conducted and documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems. Request preferences / nice to haves: Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. Ability to troubleshoot problems and identify solutions. Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. Assist in addressing laboratory investigations within specified timeframe. Primary Position Responsibilities (major or daily tasks): Perform analytical and physical testing on in-process, finished product and stability samples. Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. Perform review and approval of analytical data. Maintain analytical methods in the laboratory in a state of validation. Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Qualifications Request preferences / nice to haves: Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. Ability to troubleshoot problems and identify solutions. Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. Assist in addressing laboratory investigations within specified timeframe. Additional Information All your information will be kept confidential according to EEO guidelines.

We are seeking a dedicated Quality Control Scientist to join our team in Lenexa, Kansas. This role focuses on ensuring the quality control of finished product testing, ensuring compliance with internal and external standards and guidelines. Friday to Monday - 07:00 AM To 05:30 PM Responsibilities + Review and maintain product compliance specifications and documentation control. + Perform and interpret microbiology testing, including growth promotion, biochemical, and AST. + Gain proficiency on all performance benches and document testing results to determine product disposition. + Maintain consistency in training and establish SOP criteria for inspection and testing. + Manage department equipment and request consumables as needed. + Monitor and ensure GMP compliance within the work environment. + Collaborate closely with the Quality Assurance department to maintain product quality. + Execute Stability Study testing in accordance with QA requirements. + Assist in maintaining standards in accordance with GMP and ISO regulations. Essential Skills + Minimum of 1-2 years of experience in related QC/QA or microbiology laboratory work. + Ability to manage tasks in an organized manner. + Effective communication skills across various departments regarding quality testing parameters. + Intermediate computer skills, preferably with Microsoft Word, Excel, and PowerPoint. + Experience working in SAP is a plus. + Adaptability and eagerness to learn new procedures while maintaining a scientific approach. Skills & Qualifications + Experience in quality control and microbiology. Job Type & Location This is a Contract position based out of Lenexa, KS. Pay and Benefits The pay range for this position is $20.00 - $20.00/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 Lenexa,KS. Application Deadline This position is anticipated to close on Dec 22, 2025. 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.

This role can sit anywhere in the US as long as it is near an Accenture Corporate Office We are: Looking to be part of a transformational digital engineering and manufacturing practice? How about an opportunity to help world-class clients solve their biggest challenges and create products and services that customers love - quickly, efficiently and sustainably? Industry X combines Accenture's powerful digital capabilities with deep engineering and manufacturing expertise. We use the power of data and digital to help our clients reimagine the products they make, and how they make them. By connecting engineering and manufacturing operations every step of the way - from how products are designed and engineered, sourced and supplied, manufactured, to how they are serviced and renewed, we help them achieve greater productivity, drive growth and meet their sustainability commitments. Find out more about Industry X. You are: A ambitious Manufacturing Systems (MES) Specialist ready to take on new challenges. As industries head towards Manufacturing and Factory Digitalization, MES stand in the center of manufacturing excellence. The Work: * Lead in the design, development, documentation, and implementation of Körber PAS-X Manufacturing Execution Systems (MES) * Design/Author/Develop/Configure Electronic Batch Records (EBR) * Implement MES solutions and integrate with ERP and control equipment * Documentation of MES configuration and validation of EBRs * Work closely with business management and users to strategically define the needs and design solutions that add value * Document and analyze the information needs of the business and ensure appropriate solutions are delivered according to GxP standards * Respond to requests for client proposals * Manage and develop client relationships Job Requirements: * Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements. Qualification Here's What You Need: * A minimum of 2 years of experience with Körber PAS-X MES solutions in a highly automated Life Sciences manufacturing environment * Bachelor's Degree or equivalent (minimum 3 years work experience). If Associate's Degree, must have equivalent minimum 6 years work experience Set Yourself Apart: * Knowledge of FDA and GMP guidelines * Strong written and oral communication skills * Ability to work in a team-oriented, collaborative environment * Ability to facilitate meetings and follow up with resulting action items * Understanding of Life Sciences validation processes * Working knowledge of software Development Life Cycle (SDLC) and support methodologies Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. Role Location Hourly Salary Range California $30.67 to $98.94 Cleveland $28.41 to $79.13 Colorado $30.67 to $85.48 District of Columbia $32.69 to $91.01 Illinois $28.41 to $85.48 Maryland $30.67 to $85.48 Massachusetts $30.67 to $91.01 Minnesota $30.67 to $85.48 New York/New Jersey $28.41 to $98.94 Washington $32.69 to $91.01 #LI-NA-FY25 Locations

General Summary: Under limited supervision, responsible for working closely with our Sales Team and Customers to develop a wide variety of products. Benefits and Culture We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future. Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees. Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options. We strive to be your Employer of Choice. As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career. Visit our website to learn more about our competitive benefit programs - **************************************** Principle Duties and Responsibilities 1. Develops new production processes for new product development. 2. Streamlines current plant processes for maximum efficiency and continuous improvement. 3. Investigates and implements new and innovative packaging solutions. 4. Investigates and evaluates new equipment for the development of next generation products. 5. Collects and documents records on formulas, specifications, processes and packaging. 6. Coordinates and conducts test batches to develop new formulas, processes and specification in all Production facilities. 7. Involved in every stage of product cycle from ideation and Development to First Production and Launch. 8. Presents recommendations and solutions to Sales and Customer Service personnel. 9. Joins project teams at different site frequently without knowing team members in advance. Job Specifications 1. 5+ years product development or process engineering experience is preferred. 2. Bachelor's Degree in Food Science or a related field is preferred. 3. Knowledge of food and safety regulations is required 4. Experience using scientific methods within the food industry is required. 5. Excellent oral and written communication skills with great presentation and interpersonal skills. 6. Strong PC skills are required including Microsoft Excel, PowerPoint, and Word. 7. Experience in and be comfortable with a fast-paced environment of changing priorities, multiple project and short deadlines. Working Conditions 1. Office and Food laboratory environment and refrigerated food manufacturing plant. 2. The environment may be wet or dry and temperatures may range from 25°F to 110°F. 3. Frequent exposure to hazardous materials. 4. Requires walking and standing for long periods of time. 5. Some travel required. 6. Occasional lifting of up to 50 pounds. This position is eligible for a bonus based on company goals/performance. Recipe for Success Reser's is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries. Family owned and operated, Reser's has been a proud sponsor of good times at racetracks, picnics, BBQs, music festivals, and affordable family meals since 1950. Reser's family of brands include Reser's American Classics, Main St Bistro, Stonemill Kitchens, and more. With more than 4,500 employees, Reser's operates 14 facilities in the US, Mexico, and Canada and actively supports the communities it serves.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description Job Title: Chemist Job ID : LLYJP00006309 Duration: 6+ Months (Possible Of Extension) Location: Overland Park, KS Job Details: QC Chemist position, they will be doing HPLC Analyses with possible dissolution testing. They will be working in a lab environment using GMP skills with a GC headspace, potentially could be running it. They will be an influx of testing required for the lab move which is requiring them to do comparative testing between the two spaces. There is a potential for hormone exposure so there is a respirator testing required. Perform accurate and timely testing of routine and some non-routine lab samples in accordance withappropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executingwell defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of processdevelopment/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conductedand documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems Requirements / have to haves not listed elsewhere Bachelor of Science in Chemistry or related field Request preferences / nice to haves • Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination Primary Position Responsibilities (major or daily tasks) • Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Qualifications Requirements / have to haves not listed elsewhere Bachelor of Science in Chemistry or related field Request preferences / nice to haves • Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination Primary Position Responsibilities (major or daily tasks) • Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Additional Information All your information will be kept confidential according to EEO guidelines.