div class="content">About Streck: Streck is a Nebraska-based manufacturing company that makes a global impact by developing and distributing to labs worldwide.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information.
You will work cross‑functionally with functional and operating groups on regulatory topics impacting manufacturing operations, with primary responsibility for regulatory oversight of Conagra factories. When visiting these sites, the physical requirements below may apply: You may be required to walk around the facility, climb stairs/ladders, kneel, or perform repetitive tasks that require hand-eye coordination.
Compliance is promoted ensuring regulatory updates are evaluated, implemented and by performing monitoring to evaluate compliance with regulatory requirements required by, Centers for Medicare and Medicaid Services (CMS) and State Department of Health (DOH) regulations, and business requirements. Relevant previous work experience and knowledge of Department of Health (DOH) and Local Department of Social Services and Center for Medicare & Medicaid Services (CMS) regulations pertaining to managed care; etc.
The 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.
You will support the execution of processes and procedures and lead daily activities related to food safety, quality, and regulatory compliance while partnering cross‑functionally to strengthen food safety culture and supplier performance. When visiting these sites, the physical requirements below may apply: You may be required to walk around the facility, climb stairs/ladders, kneel, or perform repetitive tasks that require hand‑eye coordination.
Reporting to the Manager, Food Safety, Quality & Regulatory Affairs, you will support the Food Safety, Quality, and Regulatory Affairs organization by serving as a key liaison between internal manufacturing plants, external suppliers, contract manufacturers, and third‑party partners. You will focus on quality documentation management, data analysis, and external partner support while collaborating cross‑functionally with Research and Development, Procurement, Operations, and external partners to drive continuous improvement, regulatory compliance, and risk‑based decision making.
Lead and contribute to end-to-end delivery for Generis CARA and associated regulatory technology platforms - including requirements gathering, solution design, system configuration, content template development, and user acceptance testing. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
Participate in or lead cross-functional teams for site-to-site analytical method transfers: establish transfer plans, assess site readiness, and manage timelines, risks and deliverables with support from senior team members. Perform bench-level remediation across multiple test platforms, including live bacterial and virus titration/identification and ELISA for complex multivalent vaccines and in-process materials, working under guidance from senior team members.
p>US Analytical Technology Solutions (US-ATS) supports all Animal Health sites globally in analytical method development, improvement, validation, transfer as well as in all kinds of analytical investigations This position will lead and oversee all aspects of analytical life cycle management activities for in-line licensed products including collaboration with cross-functional teams to ensure that deviations are resolved in a timely manner, and that corrective actions are effectively implemented. Required Skills:
Analytical Problem Solving, Analytical Thinking, Assay, Biological Analysis, Biopharmaceutical Industry, Cross-Functional Teamwork, Root Cause Analysis (RCA), Root Cause Investigations, Technical Leadership.