Regulatory Affairs Specialist AxelonRegulatory Affairs SpecialistTopeka, KSUtilize Google Sheets to maintain trackers, manage logs, and ensure accurate, real-time visibility into the status of submissions. Use internal databases and digital tools (like SAP, AO Docs, and tracking systems) to maintain accurate compliance records.
NewSenior Regulatory Affairs Consultant (Program / Client Partnership Manager) ParexelSenior Regulatory Affairs Consultant (Program / Client Partnership Manager)Topeka, KSRemoteYou will play a key leadership role in managing midsize to large Regulatory Affairs outsourcing programs, partnering closely with clients and cross-functional teams to drive operational excellence, ensure delivery against regulatory objectives, and support the successful progression of development and commercial programs. Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team.
NewCompliance Analyst - Complaints & Regulatory Affairs Advisors ExcelCompliance Analyst - Complaints & Regulatory AffairsTopeka, KSThe Compliance Analyst plays a key role in maintaining Advisors Excel's regulatory standing by investigating/reviewing complaints, supporting regulatory exam readiness, and assisting with regulatory inquiries alongside the Compliance Director and Regulatory Counsel. What you'll do: Investigate complaints thoroughly - When a complaint comes in, you'll dig into what happened, gather the relevant documents and details, and work through the facts carefully to reach a fair and well-supported resolution.
Compliance Analyst - Complaints & Regulatory Affairs Advisors Excel LLCCompliance Analyst - Complaints & Regulatory AffairsTopeka, KSOverview: The Compliance Analyst plays a key role in maintaining Advisors Excel''s regulatory standing by investigating/reviewing complaints, supporting regulatory exam readiness, and assisting with regulatory inquiries alongside the Compliance Director and Regulatory Counsel. What you'll do: Investigate complaints thoroughly - When a complaint comes in, you''ll dig into what happened, gather the relevant documents and details, and work through the facts carefully to reach a fair and well-supported resolution.
NewSenior Manager, CMC Global Regulatory Affairs Otsuka America PharmaceuticalSenior Manager, CMC Global Regulatory AffairsTopeka, KSThe Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global regulatory strategies for CMC aspects of small molecule and biological/biotechnological products during late-stage development and throughout the commercial lifecycle. Develop and maintain collaborative relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs, Global Regulatory Strategy, Manufacturing facilities, Global Quality, Technical Operations, Business Development etc.] as well as affiliates, external partner companies, contract manufacturers, packagers and suppliers etc.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaKS$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
Regulatory Affairs Specialist Volt Information Sciences IncRegulatory Affairs SpecialistTopeka, KS$30–$35 / hourYou deserve a job you loveVolt is immediately hiring Regulatory Affairs Specialist in Topeka KSAs a Regulatory Affairs Specialist you will Be responsible for preparing and submitting accurate regulatory documentation to USDA and other agencies. Pay range offered to a successful candidate will be based on several factors including the candidates education work experience work location specific job duties certifications etc.
Regulatory Affairs Specialist TalentBurst, Inc.Regulatory Affairs SpecialistTopeka, KS$34.87 / hourData Tracking & Reporting: Utilize Google Sheets to maintain trackers, manage logs, and ensure accurate, real-time visibility into the status of submissions. System Management: Use internal databases and digital tools (like SAP, AO Docs, and tracking systems) to maintain accurate compliance records.
Senior Regulatory Affairs Manager Argenta LtdSenior Regulatory Affairs ManagerShawnee, KSRemoteRequirements: Bachelor's degree or equivalent experience in a scientific discipline, advanced degree (DVM, PhD, MS) is preferred 8+ years experience in veterinary regulatory and/or animal drug development Proven experience includes several of the following: CVM, E-Submitter, GLP, GCP, GMP, USDA, EPA, EMA Development and regulatory experience with food animal drugs is preferred but not required Good written and oral communication skills, and ability to work collaboratively within and across teams Results and bottom line oriented Excellent analytical skills and attention to detail Proven influence, negotiation and persuasion skills Defines and plans priorities well. About the role: Facilitates and supports the regulatory and drug development requirements of external clients and internal projects Effectively manage client and stakeholder expectations by providing timely, relevant, and accurate documents, assessments, reports and communications Demonstrates an awareness of current regulations, guidances, regulatory processes, and the animal drug development process, while maintaining a flexible and creative mindset to work through regulatory challenges Creates regulatory solutions to complex issues Provides client accurate expert regulatory advice on animal health product development Represent Argenta in industry associations (e.g.
Regulatory Affairs Specialist Apidel TechnologiesRegulatory Affairs SpecialistTopeka, KSContractorData Tracking & Reporting: Utilize Google Sheets to maintain trackers, manage logs, and ensure accurate, real-time visibility into the status of submissions. System Management: Use internal databases and digital tools (like SAP, AO Docs, and tracking systems) to maintain accurate compliance records.
Regulatory Affairs Specialist Axelon Services CorporationRegulatory Affairs SpecialistTopeka, KS$30 / hourUtilize Google Sheets to maintain trackers, manage logs, and ensure accurate, real-time visibility into the status of submissions. Use internal databases and digital tools (like SAP, AO Docs, and tracking systems) to maintain accurate compliance records.
Sr Director, Sci Affairs & Innovation Colgate-Palmolive CoSr Director, Sci Affairs & InnovationOverland Park, KS$245,000–$275,000 / yearThis role reports to the Global Chief Veterinary Officer and supports the execution of strategies that position Hill's as the most valuable partner, providing scientific evidence-based advancements in the field of nutrition that promotes Hill's product superiority, and demonstrating our commitment to transforming the lives of people and their pets. GPVA (Global Professional and Veterinary Affairs) plays an integral role in positioning Hill's in the global profession as a scientific, innovative and credible partner who is engaged in improving the health of dogs and cats, and in supporting the profession.
Sr Director, Sci Affairs & Innovation (Overland Park, KS, US) Colgate-Palmolive CompanySr Director, Sci Affairs & Innovation (Overland Park, KS, US)Overland Park, KS$245,000–$275,000 / yearThis role reports to the (Global) Chief Veterinary Officer and supports the execution of strategies that position Hill’s as the most valuable partner, providing scientific evidence-based advancements in the field of nutrition that promotes Hill’s product superiority, and demonstrating our commitment to transforming the lives of people and their pets. This role supports the execution of strategies that position Hill’s as the most valuable partner, providing scientific evidence-based advancements in the field of nutrition that promotes Hill’s product superiority, and demonstrating our commitment to transforming the lives of people and their pets.
Leader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsTopeka, KSRemote10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.
NewGovernment Affairs Administrative Coordinator Golf Course Superintendents Association of AmericaGovernment Affairs Administrative CoordinatorLawrence, KansasAbout GCSAA The Golf Course Superintendents Association of America (GCSAA), is a non-profit, membership-driven association with 21,000+ members in 78 countries and 95 employees whose mission is serving its members, advancing their profession and improving communities through the enjoyment, growth and vitality of the game of golf. Part-Time Government Affairs Administrative Coordinator GCSAA is seeking administrative support for the Government Affairs (G.A.) team assisting with the Grassroot Ambassador Program, GCSAA’s Political Action Committee (PAC), the Government Affairs Committee and G.A.’s two award programs.
Attorney - Manager of Legal Affairs QCHI/ LendNation Open CareerAttorney - Manager of Legal AffairsLenexa, KansasSuccess in this role will require strong legal research and analytical skills, sound judgment, the ability to evaluate statutory and regulatory requirements, often on tight timelines, and the ability to communicate practical, business-focused guidance to non-legal stakeholders in a clear and effective manner. The attorney in this role will help support the development, structure, and ongoing administration of financial products, while also advising business partners on legal and regulatory requirements that affect day-to-day operations and longer-term strategic initiatives.
Manager of Legal Affairs QCHIManager of Legal AffairsLenexa, KSSuccess in this role will require strong legal research and analytical skills, sound judgment, the ability to evaluate statutory and regulatory requirements, often on tight timelines, and the ability to communicate practical, business-focused guidance to non-legal stakeholders in a clear and effective manner. The attorney in this role will help support the development, structure, and ongoing administration of financial products, while also advising business partners on legal and regulatory requirements that affect day-to-day operations and longer-term strategic initiatives.
Regulatory Compliance Manager Argenta LtdRegulatory Compliance ManagerShawnee, KSIn-depth knowledge of FDA regulations, EU GMP, and ICH guidelines Strong understanding of cGMP requirements across dosage forms Experience with state licensing Experience with DEA Proven experience in regulatory inspection management and client-facing compliance reporting Ability to interpret regulatory requirements and translate into practical site-level compliance actions. The Compliance Manager partners closely with cross-functional teamsincluding Quality Assurance, Operations, Regulatory Affairs, and Client Services to ensure robust systems are in place andfunctioning effectively.
Regulatory Legal Assistant Advisors ExcelRegulatory Legal AssistantLenexa, KansasPosition: Compliance Analyst - Complaints & Regulatory Affairs Department: Compliance Reporting to: Compliance Director Location: Lenexa, KS/ Topeka, KS - Onsite Overview: The Compliance Analyst plays a key role in maintaining Advisors Excel's regulatory standing by investigating/reviewing complaints, supporting regulatory exam readiness, and assisting with regulatory inquiries alongside the Compliance Director and Regulatory Counsel. What you’ll do: Investigate complaints thoroughly - When a complaint comes in, you'll dig into what happened, gather the relevant documents and details, and work through the facts carefully to reach a fair and well-supported resolution.
Regulatory Compliance Engineer - North America Kalmar CorpRegulatory Compliance Engineer - North AmericaOttawa, KSWill be required to work closely with other TT RDE personnel, Project Managers, Business Development, Test & Validation, Sourcing, Production and Services groups worldwide. The company offers a wide range of industry shaping heavy material handling equipment and services to ports and terminals, distribution centres, manufacturing and heavy logistics.
Compliance Coordinator Stride, Inc.Compliance CoordinatorTopeka, KansasPrimary responsibilities include but are not limited to the submission of new and renewal applications, student performance data to various oversight agencies, maintaining point of contact information for oversight agencies, processing employment verifications, and distribution of internal compliance updates. The company partners with workforce organizations, healthcare providers, and academic institutions to help build talent pipelines and provide pathways to career advancement, including opportunities for articulated college credit.
Life Sciences Supply Chain and Operations - Supply Chain Planning Manager Accenture PlcLife Sciences Supply Chain and Operations - Supply Chain Planning ManagerOverland Park, KSAs part of working with clients you will help with several aspects of life sciences integrated planning including: Integrated Planning Strategy: Design and implement IBP/S&OP frameworks tailored to life sciences environments, accounting for regulatory release cycles, CMO/CDMO network complexity, and the distinct planning dynamics of biopharma and med tech product portfolios. Accenture is a leading solutions and services company that helps the world's leading enterprises reinvent by building their digital core and unleashing the power of AI to create value at speed across the enterprise, bringing together the talent of our approximately 786,000 people, our proprietary assets and platforms, and deep ecosystem relationships.
Medicaid & ACA Manager Blue Cross Blue Shield of KansasMedicaid & ACA ManagerTopeka, KansasThe Medicaid & ACA Manager supports the strategic and operational execution of Medicaid and Affordable Care Act (ACA) programs (individual and small group), serving as a critical operational, analytical, and coordination leader while partnering closely with the Director to translate strategy into disciplined execution. Monitor and interpret key ACA performance indicators (e.g., MLR, risk adjustment/coding capture, enrollment trends, utilization and cost drivers) and support ACA specific analyses related to morbidity shifts, affordability, benefit design, etc.
Vice President for Administration & Finance and Chief Financial Officer East Stroudsburg UniversityVice President for Administration & Finance and Chief Financial OfficerEmporia, KSThe position maintains strong relationships with internal stakeholders and external entities-including the Office of the Chancellor, Pennsylvania Department of General Services, legal counsel, regulatory agencies, and local municipalities-to ensure compliance with applicable laws and policies, facilitate efficient execution of capital and operational projects, and align institutional activities with broader system and governmental expectations. As a central member of the University's leadership team, the VPAF/CFO collaborates closely with academic and administrative leaders to advance institutional priorities, allocate resources strategically, and implement initiatives that support growth and sustainability.
Senior Licensing Engineer Deep Fission, IncSenior Licensing EngineerParsons, KSDeep Fission is seeking a Senior Licensing Engineer to lead regulatory planning and support for its advanced reactor development under the Department of Energy (DOE) authorization framework and subsequent NRC license approval. This role will translate regulatory requirements into actionable strategies for engineering execution, support preparation of licensing deliverables, and drive engagement with DOE and NRC regulators throughout the reactor design lifecycle.
Associate Director, Engineering Merck & Co IncAssociate Director, EngineeringDe Soto, KS$142,400–$224,100 / yearAs an Associate Director, Bioprocess Engineering, you will lead a team of technical professionals supporting regional vaccine technology transfer, post-transfer performance, and technical readiness across assigned processes and sites, while also providing technical support to a capital project to build a manufacturing facility. Required Skills: Bioprocess Engineering, Bioprocessing, Cell Culture Process Development, GMP Operations, Good Manufacturing Practices (GMP), Manufacturing Processes, Manufacturing Scale-Up, Pharmaceutical Manufacturing, Process Scale Up, Product Formulation, Technical Leadership, Technology Transfer, Technology Transfer Management, Vaccine Manufacturing.
Advanced Medical Support Assistant U.S. Department of Veterans AffairsAdvanced Medical Support AssistantWichita, KS$51,592–$67,069 / yearDuties include but are not limited to the following: Processes incoming patient secure messaging through My HealtheVet and coordinates with care team as appropriate; Participates in team huddles and team meetings to manage, plan, problem solve, and follow-up with patient care by sharing information and collaborating with the interdisciplinary team; Setting priorities and deadlines, adjusting the flow and sequencing of the work to meet team and patient needs; Identifies incomplete encounters and communicates findings to providers; as needed; Assists the team to reinforce the plan of care and self-help solutions; Enters appropriate information into the electronic record; Monitors pre-appointment information and/or requirements to assure readiness for patient visit/procedure; Manages patient systems to verify and validate accuracy and resolve issues; Evaluates patient information and clinic schedule lists to determine whether the patient requires an immediate appointment; Informs team members about shared patients (i.e., those who receive their care at multiple VA centers or those who receive care in the community). MSAs at this level develop and/or maintain effective and efficient communication with the patient, interdisciplinary (coordinated care delivery model teams), VA medical centers, and other agencies (e.g., assist with communications during the inpatient to outpatient discharge; communicate with non-VA medical facilities; prepare correspondence to notify patients of normal lab results; manages systems for follow-up care such as consults, tests, etc.
Director Utilization Management Blue Cross Blue Shield of KansasDirector Utilization ManagementTopeka, KansasThe Director serves as a clinical subject matter expert supporting quality care management, population health, behavioral health integration, and clinical strategy initiatives, while driving cross-functional collaboration within Medical Affairs and across the enterprise to advance organizational goals, member outcomes, and value-based care priorities. Provide strategic leadership and enterprise-wide operational oversight for utilization management programs across all lines of business, including prior authorization, concurrent and retrospective claims review, and appeals.
Nursing Assistant U.S. Department of Veterans AffairsNursing AssistantTopeka, KS$37,874–$61,837 / yearOne year of specialized experience as a NA or experience in another medical field (licensed practical nurse, health technician, hospital corpsman, etc.), performing technical and nursing skills requiring knowledge of the human physical and emotional states, therapeutic communication, and technical skills required for basic and intermediate treatments; OR, (b) Education. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.
Sr. Specialist, Quality Control Merck & Co IncSr. Specialist, Quality ControlDe Soto, KS$106,200–$167,200 / yearThe successful candidate will collaborate with cross‑functional teams (Analytical Tech Support, Manufacturing, Validation, Quality Control) to identify gaps and risks, implement appropriate controls, and drive continuous improvement to support the project. Specialist, Quality Control you will be part of a world-class team at our Center of Excellence in the Animal Health Corridor, contributing directly to the production of veterinary products that improve animal health and welfare globally.
Executive Director Brookdale Senior Living IncExecutive DirectorSalina, KSDemonstrates a high degree of financial acumen as it relates to community operations; works to meet or exceed budgeted revenue and profitability; and proactively creates plans to overcome unanticipated expenses or revenue shortfalls. Drives sales and marketing efforts in collaboration with community sales leader to meet or exceed occupancy or revenue targets by developing new business, generating leads, and building strategic relationships.
NewClinic Director Wichita Comprehensive Treatment CenterClinic DirectorWichita, KansasFull timeAcadia Healthcare's Comprehensive Treatment Centers (CTC) division operates 170+ CARF-accredited outpatient opioid treatment programs (OTPs) nationwide, serving patients undergoing treatment for opioid use disorder (OUD). Wichita Comprehensive Treatment Center (CTC) , located in Wichita, Kansas , is part of Acadia Healthcare’s nationwide network of Comprehensive Treatment Centers—the leading provider of medication-assisted treatment (MAT) for opioid use disorder (OUD).
Executive Director - Senior Living Brookdale Senior LivingExecutive Director - Senior LivingTopeka, KSFull timeDrives sales and marketing efforts in collaboration with the community sales leader to meet or exceed occupancy or revenue targets by developing new business, generating leads, and building strategic relationships. For assisted living or memory care communities, ensures collaborative relationship with community clinical leader to ensure community's care and services are appropriate to meet the needs of residents.
Clinic Director Acadia Healthcare Co IncClinic DirectorWichita, KSAcadia Healthcare''s Comprehensive Treatment Centers (CTC) division operates 170+ CARF-accredited outpatient opioid treatment programs (OTPs) nationwide, serving patients undergoing treatment for opioid use disorder (OUD). Wichita Comprehensive Treatment Center (CTC), located in Wichita, Kansas, is part of Acadia Healthcare's nationwide network of Comprehensive Treatment Centers-the leading provider of medication-assisted treatment (MAT) for opioid use disorder (OUD).
Medical Review Officer (MRO) Abbott LaboratoriesMedical Review Officer (MRO)Kansas City, KS$149,300–$298,700 / yearThe position directly supports management of the MRO-A team, nursing staff, and support personnel, and plays a key role in budget oversight, quality assurance, and stakeholder engagement (including regulatory agencies, internal leadership, and external partners). WHAT YOU'LL WORK ON: Leads and supports the management of physicians and cross-functional support staff within Medical Affairs, delivering occupational medicine and drug testing services.
Director, Engineering - Substation Quanta Infrastructure Solutions Group, LLCDirector, Engineering - SubstationOverland Park, KansasFull timeThe QISG team brings together Engineering, Safety, Quality, Material Procurement, QA/QC, Right-of-Way Acquisition, Scheduling, Environmental Planning, Permitting, Title and Land Management expertise that ensure outstanding results for our clients. What You'll Bring: Minimum of 15 years’ experience in the electric utility industry performing engineering related duties and/or management for high voltage electrical projects.
Director, Regional Marketing Lead (West Region) Ideaya Biosciences IncDirector, Regional Marketing Lead (West Region)KS$196,000–$242,000 / yearReporting into Commercial Strategy & Marketing, this field-based role will serve as a key commercial engagement partner responsible for developing relationships with priority thought leaders & academic centers, gathering actionable marketplace insights, supporting peer-to-peer education, and helping shape launch strategy in partnership with Marketing, Medical Affairs, Sales, Value & Access, and other cross-functional teams. The RML will play a critical role in helping IDEAYA transition to a commercial-stage organization by strengthening scientific engagement, supporting launch readiness activities, and building meaningful relationships with key stakeholders across academic and community oncology settings.
Thought Leader Liaison Ipsen SAThought Leader LiaisonKS$190,000–$225,000 / yearTo be successful: the TLL team members will build close working relationships with, but not limited to: National Sales Directors, Regional Business Directors, Neuroscience Specialty Representatives, Medical Science Liaisons, Marketing teams, and Value & Access teams to ensure alignment on broader business objectives in their assigned regions. The position focuses on building and maintaining strong relationships with established and emerging thought leaders, generating actionable market insights, and driving advocacy for Ipsen's Neuroscience portfolio across Adult Spasticity, Cervical Dystonia, Pediatric Spasticity, and future anticipated indications such as Migraine.
Thought Leader Liaison ImCheck Therapeutics SASThought Leader LiaisonKS$190,000–$225,000 / yearTo be successful: the TLL team members will build close working relationships with, but not limited to: National Sales Directors, Regional Business Directors, Neuroscience Specialty Representatives, Medical Science Liaisons, Marketing teams, and Value & Access teams to ensure alignment on broader business objectives in their assigned regions. The position focuses on building and maintaining strong relationships with established and emerging thought leaders, generating actionable market insights, and driving advocacy for Ipsen's Neuroscience portfolio across Adult Spasticity, Cervical Dystonia, Pediatric Spasticity, and future anticipated indications such as Migraine.
Immunology Business Director (HS) - Mid West Incyte CorpImmunology Business Director (HS) - Mid WestKSThrough the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia. The Immunology Business Director IBD will be accountable for translating brand strategy into disciplined field execution coaching and developing high-performing Therapeutic Specialists and delivering demand generation to support launch excellence and sustained growth.
Clinical Research Nurse Coordinator University of Kansas Medical CenterClinical Research Nurse CoordinatorKS$70,200–$105,300 / yearThe position provides professional nursing care and patient monitoring for clinical trials and works collaboratively with multidisciplinary teams, research personnel, and hospital staff to recruit, screen, educate, and support participants throughout the clinical study coordination process. Job Description Summary: The Clinical Research Nurse Coordinator in the Cancer Center manages clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
NewTechnical Project Manager Argenta LtdTechnical Project ManagerShawnee, KSLead end-to-end technology transfer projects for sterile products from originator sites or development into Argentas manufacturing network Develop and own detailed tech transfer plans including stage-gate milestones, risk registers, regulatory submission timelines, and batch scheduling Coordinate and track all transfer deliverables - process characterization, analytical method transfer, cleaning validation, process validation, and sterility assurance activities Drive readiness reviews (process, equipment, QA, regulatory) to ensure site and product launch readiness Proactively identify and resolve risks related to sterile process complexity, contamination control, and supply continuity. Manage a concurrent portfolio of sterile tech transfer and lifecycle programs, balancing scope, resource, and schedule across multiple clients and projects simultaneously Set and communicate clear priorities across the portfolio in alignment with business objectives, client commitments, and site capacity Identify and resolve cross-project dependencies, resource conflicts, and scheduling constraints in a proactive and structured manner Provide regular portfolio-level reporting to PMO leadership and senior stakeholders, with clear visibility of progress, risks, and decision points across all active programs.
Product Management Specialist III Thermo Fisher Scientific IncProduct Management Specialist IIILenexa, KSCapable of driving improvement in business performance, directing initiatives that deliver short-, medium- and long-term growth· Familiar with working in a global/international business environment· Strong analytical and problem-solving skills· Good listener with ability to influence across teams (without direct authority)· Willing and able to travel internationally (25-35% per annum), including overnight stays· Fluent in English, additional languages a plusWhat's in it for you:· Excellent career progression opportunities with a large and growing global employer· Competitive salary, plus annual incentive bonus· Full benefits package (specifics depend on country of hire). Bachelor's degree in Microbiology, Molecular Biology, Cellular Biology or similar requiredundefined· 2+ years experience within Microbiology - either as a scientist, salesperson, or marketeer· 2-3 years of experience in Marketing or Product Management of life science or technical products and services is considered a strong advantageKnowledge, Skills, Abilities· Able to capture sharp customer insights and translate into business and product strategy and actions.·
Administrative & Credentialing Coordinator The University of Kansas Health SystemAdministrative & Credentialing CoordinatorGreat Bend, KSAdministrative Responsibilities: Provides high-level administrative support by conducting research, preparing statistical reports, handling information requests, and performing clerical functions such as preparing correspondence, receiving visitors, arranging conference calls, and scheduling appointments. Demonstrates commitment to department and organization by remaining flexible to accommodate department needs in relation to work schedule; serves as a team player in all areas of TUKHS - Great Bend Campus and represents a positive role model for other employees.
Construction Technology Instructor Cowley Community CollegeConstruction Technology InstructorArkansas City, KSUnder the supervision of the Department Chair, the Construction Technology Instructor is responsible for the classes in the program and duties that include course approval, scheduling, recruiting, laboratory training, safety, presenting lecture material, providing constructive feedback to students and faculty, coordinating logistical matters, developing, assessing, verifying and coordinating student progress. Required Education and Experience: Minimum of an Associate's Degree in Carpentry or Construction and three years of experience in or directly related to the carpentry or construction industry, or a Bachelor's degree in Carpentry, Construction, or a closely related field from a regionally accredited educational institution, PLUS three years' industry or teaching experience is preferred.
Construction Technology Trainer (ADM3347) Hutchinson Community ClgConstruction Technology Trainer (ADM3347)Hutchinson, KSHeavy/indoor work environment; excellent verbal, written, and listen communication and organizational skills; ability and willingness to collaborate; ability to work independently; visual acuity to view a computer terminal; use appropriate judgment and apply tact and courtesy in difficult situations. Teach within a flexible training schedule including day and evening teaching assignments that may include alternative delivery systems such as online.
Senior Clinical Research Coordinator - Cancer Center University of Kansas Medical CenterSenior Clinical Research Coordinator - Cancer CenterKS$70,200–$105,300 / yearJob Description Summary: The Senior Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
Combustion Turbine / Renewables Engineer (Hutchinson) Evergy IncCombustion Turbine / Renewables Engineer (Hutchinson)Hutchinson, KS$83,600–$104,500 / yearThe candidate will direct and inspire a multidisciplinary team of internal and external professionals-including site management, engineering, procurement, project controls, regulatory affairs, real estate, vegetation management, legal, and administrative support-ensuring alignment from initial concept and strategic analysis through energization and final completion. Beyond execution, this candidate will act as the primary advocate for project interests, fostering collaboration and transparency through consistent, high-quality communication with a broad range of stakeholders, including executive leadership, regulatory bodies, community representatives, and industry partners.
Clinical Research Coordinator - Cancer Center University of Kansas Medical CenterClinical Research Coordinator - Cancer CenterKS$60,800–$91,200 / yearJob Description Summary: The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.
Combustion Turbine / Renewables Engineer (Emporia) Evergy IncCombustion Turbine / Renewables Engineer (Emporia)Emporia, KS$83,600–$104,500 / yearThe candidate will direct and inspire a multidisciplinary team of internal and external professionals-including site management, engineering, procurement, project controls, regulatory affairs, real estate, vegetation management, legal, and administrative support-ensuring alignment from initial concept and strategic analysis through energization and final completion. Beyond execution, this candidate will act as the primary advocate for project interests, fostering collaboration and transparency through consistent, high-quality communication with a broad range of stakeholders, including executive leadership, regulatory bodies, community representatives, and industry partners.