Senior Regulatory Affairs Manager Argenta GlobalSenior Regulatory Affairs ManagerShawnee, KSRemoteIdentify and pursue new regulatory consulting opportunities which may include meeting with new clients, traveling and speaking at professional meetings, networking in the industry and contributing to various publications. We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role.
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.
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, 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.
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.
Regional Manager, Google Cloud, Government Affairs and Public Policy Google LLCRegional Manager, Google Cloud, Government Affairs and Public PolicyKansas City, KSPartner with internal technical teams and external upstream and downstream stakeholder groups to advance technical infrastructure needs for our users and customers, ensuring a unified approach regarding economic, social, and environmental benefits of Google Cloud investments in new and existing markets. In this role, you will be involved in collaborating with Google Cloud and other internal teams to advance Google's Cloud business and technical infrastructure needs, leading government affairs and public policy matters within key state and local markets.
Associate Director, State and Local Government Affairs Black & Veatch Holding CoAssociate Director, State and Local Government AffairsOverland Park, KSAs the Associate Director, State and Local Government Affairs, you will have the opportunity to: Set strategy and conduct a government relations program in targeted states and with local governments in support of business development and sales efforts, project execution, payment issues, and Black and Veatchs growth strategies while adhering to budget and schedule. You'll work alongside teams solving complex challenges and turning ideas into solutions that perform in the real world-gaining hands-on experience across projects, technologies, and disciplines.
Government 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.
Global Medical Affairs Operations Manager MedelaGlobal Medical Affairs Operations ManagerWichita, KSThis role is a critical connector across Medical Affairs, Clinical, Sales, Marketing, and external healthcare partners to ensure successful delivery of scientific and educational programs that improve outcomes in maternity and neonatal care. This person will lead the execution of global Medical Affairs programs, educational initiatives, and real-world evidence activities supporting healthcare professionals and customers worldwide.
Regulatory Analyst, Sr ITC Great Plains LLCRegulatory Analyst, SrTopeka, KSSenior RTO Policy Analyst assumes an increasing amount of independence and personal responsibility for meeting the Company's strategic goals and business plan objectives, including ownership of discrete RTO or other regulatory issues and/or processes and increased engagement in written and verbal advocacy at the direction of the Manager of RTO Regulatory Strategy (SPP) ("Manager"). Supports Company advocacy efforts on RTO-related transmission policy issues by interacting with Company personnel, regulators, RTO stakeholders and staff, and customers with increasing autonomy and including ownership of discrete RTO or regulatory issues and/or processes as directed by the Manager.
Supply Chain Planning Life Sciences Manager Accenture PlcSupply Chain Planning Life Sciences 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.
QA Supervisor, Product Release Ceva Sante Animale SAQA Supervisor, Product ReleaseLenexa, KSWorking closely with Manufacturing, Quality Control, Regulatory Affairs, Supply Chain, and Warehouse Operations, the QA Supervisor supports the resolution of quality issues, promotes continuous improvement, and helps maintain inspection readiness and continuity of supply. Job Summary and Purpose: The QA Supervisor, Product Release is responsible for supervising and coordinating product release activities for Animal Health Biological vaccines, including documentation review, labeling verification, warehouse release operations, and final product disposition.
Life Sciences MedTech R&D, Management Consulting Senior Manager Accenture PlcLife Sciences MedTech R&D, Management Consulting Senior ManagerOverland Park, KSFrom strategy through execution, we help clients navigate regulatory complexity, accelerate product development timelines, and build the AI-enabled operating models that will define the next era of medical technology. We are looking for a commercially driven Senior Manager who can walk into a room with a Chief R&D Officer or VP of Innovation, earn their trust, and originate meaningful work - then lead a team to deliver it exceptionally.
NewSr. Manager, Quality & Compliance InfuSystem Holdings IncSr. Manager, Quality & ComplianceLenexa, KSInfuSystem provides the sale, rental, lease and associated supplies, including infusion pumps, nerve blocks for acute pain, nerve block catheters, postoperative pain pumps, central venous catheters, IV pumps, pole-mounted pumps, syringe pumps, enteral pumps, Huber needles, clean room supplies, IV extension tubing, pump tubing, ambulatory pumps, replacement pumps, disposable products, central venous access devices, closed system transfer devices, negative pressure wound therapy vacs, wound vac, and chemotherapy and oncology infusion pumps. Biomedical services include both on-site and depot preventive maintenance, repair and warranty services, ranging from equipment inspections to extensive repairs, including compression device systems, defibrillators, EKG machines, electrosurgical units, external pacemakers, humidifiers, infusion pumps, LCDs, light sources, modules, patient monitors, printers, pulse oximeters, telemetry transmitters and tourniquets - all completed to factory specifications.
NewSr. Manager, Quality & Compliance InfuSystem CareerSr. Manager, Quality & ComplianceLenexa, KansasInfuSystem provides the sale, rental, lease and associated supplies, including infusion pumps, nerve blocks for acute pain, nerve block catheters, postoperative pain pumps, central venous catheters, IV pumps, pole-mounted pumps, syringe pumps, enteral pumps, Huber needles, clean room supplies, IV extension tubing, pump tubing, ambulatory pumps, replacement pumps, disposable products, central venous access devices, closed system transfer devices, negative pressure wound therapy vacs, wound vac, and chemotherapy and oncology infusion pumps. Biomedical services include both on-site and depot preventive maintenance, repair and warranty services, ranging from equipment inspections to extensive repairs, including compression device systems, defibrillators, EKG machines, electrosurgical units, external pacemakers, humidifiers, infusion pumps, LCDs, light sources, modules, patient monitors, printers, pulse oximeters, telemetry transmitters and tourniquets – all completed to factory specifications.
Associate Director, Biologics New Product Commercialization Merck & Co IncAssociate Director, Biologics New Product CommercializationDe Soto, KS$142,400–$224,100 / yearThe Associate Director, Biologics New Product Commercialization for monoclonal antibodies (mAbs) is accountable for collaborating with technical SMEs in R&D and at manufacturing sites (internal and external) to transfer new veterinary mAb products from R&D into commercial manufacturing sites. Required Skills: External Manufacturing, Project Management, Project Management Execution, Strategic Planning, Technical Management, Technical Operations, Technical Projects, Technical Support, Technology Transfer Management.
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.
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.
General Engineering & Skilled Trade Expert GTT, LLCGeneral Engineering & Skilled Trade ExpertLenexa, KSRecognized by Forbes as one of the World's Best Employers and ranked 15th globally among top biotech and pharmaceutical employers by Science Magazine, this organization employs professionals across research and development, manufacturing, clinical operations, regulatory affairs, commercial strategy, and corporate functions. Demonstrated proficiency with Rockwell Automation / Allen-Bradley PLC platforms (ControlLogix, CompactLogix) and Studio 5000 / RSLogix 5000 programming software.