Regulatory Affairs Manager Katalyst Healthcares & Life SciencesRegulatory Affairs ManagerDallas, TXMust be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts on complex projects. Demonstrated hands-on experience in preparing regulatory clearance/approvals for IVD products in the EU, USA, OUS; (Preferred experience: working experience with IVD submissions under IVDR Regulations is highly desirable).
NewManager, Regulatory Affairs FlightSafety International IncManager, Regulatory AffairsFort Worth, TXDocumented previous minimum experience within a FlightSafety International Learning Center of one to two (1-2) years at the Program Manager level; OR four (4) years minimum experience in similar positions within corporate/charter/airline or military organizations is required. Any offer of employment is contingent upon successful completion of required compliance reviews, including verification that the candidate is not prohibited from employment under U.S. economic sanctions programs administered by the U.S. Department of the Treasury's Office of Foreign Assets Control (OFAC).
NewManager, Regulatory Affairs (Fort Worth, TX, US, 76155) FlightSafety InternationalManager, Regulatory Affairs (Fort Worth, TX, US, 76155)Fort Worth, TXDocumented previous minimum experience within a FlightSafety International Learning Center of one to two (1-2) years at the Program Manager level; OR four (4) years minimum experience in similar positions within corporate/charter/airline or military organizations is required. Any offer of employment is contingent upon successful completion of required compliance reviews, including verification that the candidate is not prohibited from employment under U.S. economic sanctions programs administered by the U.S. Department of the Treasury’s Office of Foreign Assets Control (OFAC).
Regulatory Affairs Manager Karwell TechnologiesRegulatory Affairs ManagerDallas, TXMust be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts on complex projects. Demonstrated hands-on experience in preparing regulatory clearance/approvals for IVD products in the EU, USA, OUS; (Preferred experience: working experience with IVD submissions under IVDR Regulations is highly desirable).
Manager, Regulatory Affairs and Compliance Nordson CorpManager, Regulatory Affairs and ComplianceAllen, TXp>Prepares regulatory strategies and maintains submissions for U.S. and International markets, including but not limited to 510(k)s and Technical Files, to ensure timely approval of devices and continued regulatory support of marketed devices. A highly participative leader, responsible for the hands-on management and direction of regulatory and document control personnel and for implementing best practices, continuous improvement, and corrective/preventive actions as necessary.
Regulatory Manager Marmon Holdings IncRegulatory ManagerAddison, TXThe RM provides regulatory leadership and ensures compliance with all regulatory applications including submissions, managing departmental projects, creating, and reviewing labeling, interacting with governmental agencies, and directing and managing department employees. Oversee subordinates in the preparation, organization, coordination of content/data and ensure regulatory compliance for submission to the FDA or regulatory agencies (e.g., 510(k), PMA, MDD/MDR Technical Files/Design Dossiers, global registration applications, etc.).
Sr. Regulatory Affairs Manager Katalyst Healthcares & Life SciencesSr. Regulatory Affairs ManagerDallas, TXAssists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to QOL initiatives. Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.
Sr. Regulatory Affairs Manager Karwell TechnologiesSr. Regulatory Affairs ManagerDallas, TXAssists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to QOL initiatives. Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.
Legal Engineering Manager, In-House (Litigation/Regulatory) HarveyLegal Engineering Manager, In-House (Litigation/Regulatory)Dallas, TexasIn addition to managing and developing the team, you will work directly with strategic customers, help shape Harvey’s go-to-market approach, and partner cross-functionally with Product, Marketing, Enablement, and Engineering to improve how Harvey serves the legal industry. Qualified lawyer with 7+ PQE, including significant experience practicing litigation, regulatory, investigations, compliance, white-collar defense, enforcement, employment litigation, financial regulatory matters, government investigations, or other contentious legal work, including experience working in-house.
Legal Engineering Manager, In-House (Litigation/Regulatory) Counsel AI CorpLegal Engineering Manager, In-House (Litigation/Regulatory)Dallas, TX$315,000–$385,000 / yearIn addition to managing and developing the team, you will work directly with strategic customers, help shape Harvey's go-to-market approach, and partner cross-functionally with Product, Marketing, Enablement, and Engineering to improve how Harvey serves the legal industry. Qualified lawyer with 7+ PQE, including significant experience practicing litigation, regulatory, investigations, compliance, white-collar defense, enforcement, employment litigation, financial regulatory matters, government investigations, or other contentious legal work, including experience working in-house.
Research Regulatory Compliance Manager Methodist Health SystemResearch Regulatory Compliance ManagerDallas, TXOur reputation as an award-winning employer shows in the distinctions we've earned: • Great Place to Work Certified 2026-2027 • Glassdoor's Best Places to Work 2025 & 2026 • Glassdoor's Best Places to Work in Healthcare, Biotech & Pharma 2026 • TIME's Best Companies for Future Leaders 2025 & 2026 • Newsweek's America's Most Admired Workplaces 2026 • Glassdoor's Best-Led Companies 2025 • Fortune Best Workplaces in Health Care 2025 • Military Friendly Gold Employer 2025 • Becker's Hospital Review 150 Top Places to Work in Healthcare 2025 • Newsweek's Americas Greatest Workplaces 2025. Named one of the fastest-growing health systems in America by Modern Healthcare, Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others.
Regulatory Master, Regulatory Planning and Operations - Diagnostics Regulatory Affairs Agilent Technologies IncRegulatory Master, Regulatory Planning and Operations - Diagnostics Regulatory AffairsRemote Location, TXRemote$153,040–$239,125 / yearPartner within DRA and with key cross functional stakeholders (i.e. Quality, R&D, Supply Chain, MSAT, Manufacturing, Program Management, and Commercial) to support planning, workload forecasting, prioritization, and lifecycle strategies. S/he will be a key member of the DRA leadership team as well as the Global Regulatory Affairs (GRA) extended leadership team and serve as a key partner to the head of the department.
Compliance Manager - Regulatory Obligations Madison-DavisCompliance Manager - Regulatory ObligationsDallas / Fort Worth, TXThis role will focus on maintaining regulatory inventories, tracking regulatory developments, supporting compliance change initiatives, and ensuring regulatory requirements are appropriately reflected within policies, controls, and business processes. The successful candidate will work closely with Compliance, Legal, Risk, Audit, and business stakeholders to strengthen regulatory governance, improve traceability of obligations, and support enterprise compliance initiatives.
Senior Manager ? Bank Regulatory Compliance Officer Madison-DavisSenior Manager ? Bank Regulatory Compliance OfficerDallas, TXThe successful candidate will work closely with business leaders, Legal, Risk, Audit, and Compliance partners to strengthen regulatory frameworks, support remediation efforts, and ensure compliance programs remain aligned with evolving supervisory expectations. A global financial institution is seeking an experienced regulatory compliance professional to join a strategic Compliance Initiatives and Advisory team supporting wholesale banking and capital markets businesses.
Analyst, Regulatory Affairs Oscar HealthAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Analyst, Regulatory Affairs Oscar Health IncAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Senior Regulatory Affairs Program Lead - Mentor Worldwide, LLC Johnson & JohnsonSenior Regulatory Affairs Program Lead - Mentor Worldwide, LLCIrving, TXPurpose: The Senior Regulatory Affairs Program Lead is responsible for partnering with R&D, Life Cycle Management (LCM), Supply Chain, Quality Engineering, Global Strategic Marketing, and other key cross-functional leaders to develop and execute robust global regulatory strategies focused primarily on LCM guidance and projects for both of our manufacturing facilities. Required Skills: Preferred Skills: Analytical Reasoning, Business Writing, Coaching, Collaboration, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking.
Senior Director, Regulatory Affairs & Delegated Services | NantHealth NantHealth IncSenior Director, Regulatory Affairs & Delegated Services | NantHealthDallas, TXli>Partner with operations and technology teams to assess, design, and improve technical workflows that support delegated denials, appeals, and grievances processes, including intake, case routing, escalation paths, notices, queue management, documentation, audit trails, and reporting. Youll lead the design, implementation, and ongoing oversight of programs that ensure compliance with Medicare, Medicaid, Commercial, and state-specific regulatory requirements, with particular emphasis on audit readiness, delegated utilization management, denials, appeals, grievances, and physician licensing oversight.
Senior Specialist, Regulatory Affairs and Compliance Nordson CorpSenior Specialist, Regulatory Affairs and ComplianceAllen, TXAlternatively, will accept a Master's degree in Regulatory Affairs, Healthcare Policy, Healthcare Management, or related field and three (3) years of experience as a Senior Regulatory Affairs Specialist, International Regulatory Affairs Specialist, Regulatory Affairs Specialist, Regulatory Affairs Co-Ordinator, or related role where experience was gained, plus the special skills listed above. Requirements: Bachelor's degree in Regulatory Affairs, Healthcare Policy, Healthcare Management, or related field and five (5) years of experience as a Senior Regulatory Affairs Specialist, International Regulatory Affairs Specialist, Regulatory Affairs Specialist, Regulatory Affairs Co-Ordinator, or related role where experience was gained.
Senior Regulatory Affairs Analyst Keurig Dr Pepper IncSenior Regulatory Affairs AnalystFrisco, TX$76,400–$115,000 / yearThe analyst also monitors and interprets relevant government and technical information impacting our brands, develops finished-product regulatory specifications, and provides regulatory guidance to business partners and cross-functional project teams. By enabling compliant, science-based claims, labeling, and advertising, the function protects consumers and the business while supporting KDPs competitive edge.
Senior Regulatory Affairs Specialist Prosperity Workforce SolutionsSenior Regulatory Affairs SpecialistDallas, TexasThe Senior Regulatory Affairs Specialist is responsible for leading and executing regulatory activities to support compliance, product registrations, and lifecycle management activities across applicable markets. Review and approve labeling, packaging, artwork, instructions for use (IFUs), and related documentation to ensure compliance with applicable regulations and approved registrations.
Senior Compliance Analyst - Regulatory Exams Cetera Financial Group IncSenior Compliance Analyst - Regulatory ExamsDallas, TX$82,000–$117,000 / yearCetera Financial Group" refers to the network of independent retail firms encompassing, among others, Cetera Advisors LLC, Cetera Wealth Services LLC (f/k/a Cetera Advisor Networks), Cetera Investment Services LLC (marketed as Cetera Financial Institutions, or Cetera Investors. About Cetera Financial Group: Cetera Financial Group ("Cetera") is a leading network of independent retail broker-dealers empowering the delivery of objective financial advice to individuals, families and company retirement plans across the country through trusted financial advisors and financial institutions.
Quality & Regulatory Affairs Analyst University of Texas at ArlingtonQuality & Regulatory Affairs AnalystArlington, TXUniversity Information: The University of Texas at Arlington, UTA, is located in the heart of the Dallas-Fort Worth-Arlington metroplex, a vibrant and diverse metropolitan area that is home to over 7 million people, one of the fastest-growing tech economies in the United States, and a wide array of arts, entertainment, and cultural activities. The Quality & Regulatory Affairs Analyst Research Engineering Scientist Assoc V will deliver hands-on quality management and regulatory affairs solutions to a wide range of businesses including manufacturing, distribution, logistics, construction, healthcare, and government.
Director, Regulatory Affairs Argon Medical Devices IncDirector, Regulatory AffairsPlano, TexasFull timeActively communicate and collaborate with internal and external partners and across functions including Marketing, Commercial Regional Leaders, Engineering, R&D, Site Quality, Operations to support new product development and global registration strategy. This key leadership role involves developing and implementing regulatory strategies, mentoring teams and managing critical interactions with regulatory agencies across the globe.
Director, Regulatory Strategy (Pediatrics) - Remote Agios PharmaceuticalsDirector, Regulatory Strategy (Pediatrics) - RemoteDallas, TXRemote$183,549–$275,324 / yearThe current base salary range for this position is expected to be between $183,549 and $275,324 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. This individual will lead cross-functional teams in preparing and overseeing development of compliant, high quality, nonclinical and clinical global regulatory submissions to support development, registration, or life cycle management activities.
NewCoordinator, Regulatory Affairs - Onsite Roth Staffing CompaniesCoordinator, Regulatory Affairs - OnsiteFlower Mound, Texas$34.14–$34.14 / hourKey responsibilities include extracting and reconciling data from multiple systems, managing submissions to third-party compliance evidence providers, researching and responding to customer or sales-related compliance inquiries, revising compliance documentation, and supporting non-conformance investigations and corrective actions. The Product Environmental Compliance Coordinator (Contractor) supports the Endoscopy Division's Product Environmental Compliance program by helping ensure products meet global environmental regulations such as RoHS, REACH, POPs, WEEE, and California Proposition 65.
NewRegulatory Compliance Specialist The Hire SolutionRegulatory Compliance SpecialistDallas, TexasRemoteThe successful candidate will have experience working with regulatory documentation, supplier relationships, and supply chain processes, preferably within the chemical, personal care, cosmetic, pharmaceutical, or related industries. A growing specialty chemical distribution company is seeking a highly organized and detail-oriented Regulatory Affairs Specialist to join its team.
Regulatory Specialist 2 Marmon Holdings IncRegulatory Specialist 2Addison, TXMaintains working knowledge of the medical device regulations applicable to the devices being supported including, but not limited to, registration, classification, labeling, and post-market surveillance requirement through on-going education and training. Works with team members to conduct documentation reviews and change assessments including evaluation of effects of regulatory, design, and manufacturing changes, and helps determine required regulatory action e.g., submissions, notifications.
Manager, Clinical Science, Medical Affairs Danaher CorpManager, Clinical Science, Medical AffairsDallas, TXRemote$150,000–$170,000 / yearServe as a scientific expert and liaison to healthcare professionals, key opinion leaders, and internal stakeholders to facilitate clinical education, evidence exchange, and trusted relationships associated with off-label inquiries, third-party validation services, health hazard assessments, etc. This role will serve as a trusted scientific partner to internal/external stakeholders-including healthcare professionals, cross‑functional teams, and external collaborators - directly influencing product adoption, appropriate use, and long‑term market success.
Senior Project Manager, Clinical Risk Evaluation Abbott LaboratoriesSenior Project Manager, Clinical Risk EvaluationPlano, TX$78,000–$156,000 / yearFacilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers). The CRE Program Manager writes and manages risk evaluation files, performs risk analysis, manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables.
Senior Project Manager, Clinical Risk Evaluation AbbottSenior Project Manager, Clinical Risk EvaluationPlano, TexasFacilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers). The CRE Program Manager writes and manages risk evaluation files, performs risk analysis, manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables.
Maintenance Manager Pretium Packaging L.L.C.Maintenance ManagerCarrollton, TXPart timeJoin Pretium Packaging at our facility in Carrollton, Texas where you will take ownership of innovative molding and automation equipment while driving reliability, innovation, and continuous improvement. This position ensures the optimal performance, reliability, and safety of plant equipment, machinery, and infrastructure by leading a skilled maintenance team and implementing proactive, cost-effective maintenance programs.
Quality Manager StratAcuity Staffing Partners IncQuality ManagerMesquite, TX$95,000–$100,000 / yearIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. The employee is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; reading and proofreading for accuracy.
Life Sciences Supply Chain and Operations - Supply Chain Planning Manager Accenture PlcLife Sciences Supply Chain and Operations - Supply Chain Planning ManagerIrving, TXp>As 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.
Product Development Manager - Dog & Cat Regulated Products Central Garden & Pet CoProduct Development Manager - Dog & Cat Regulated ProductsDallas, TX$110,000–$140,000 / yearProvide technical support to Consumer Care, by assisting with responses to customer inquiries related to product efficacy, usage, and concerns, and develop accurate science-based guidance and leverage consumer feedback to inform continuous improvement, quality enhancements, and future product innovation. Central is home to a diversified portfolio of market-leading brands, including Amdro, Aqueon, Best Bully Sticks, Cadet, C&S, Farnam, Ferry-Morse, Kaytee, Nylabone, Pennington, Sevin, and Zocon.
Manager, Industry Solutions, Veeva Life Science Deloitte Touche Tohmatsu LtdManager, Industry Solutions, Veeva Life ScienceDallas, TX$144,200–$265,600 / yearThe wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. 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.
Kearney Healthcare & Life Sciences Practice Manager Pharma R&D Strategy A.T. Kearney IncKearney Healthcare & Life Sciences Practice Manager Pharma R&D StrategyTX$212,000–$235,000 / yearp>We are seeking experienced consultants with expertise across Pharma R&D, particularly those with a traditional consulting background advising biopharma clients on clinical development, drug development strategy, operating models, and R&D transformation initiatives. Advise clients on topics including clinical development strategy, drug development strategy, clinical operations, regulatory affairs, pharmacovigilance, clinical trial feasibility, and R&D operating models.
Maintenance Manager Pretium PackagingMaintenance ManagerCarrollton, TexasThis position ensures the optimal performance, reliability, and safety of plant equipment, machinery, and infrastructure by leading a skilled maintenance team and implementing proactive, cost-effective maintenance programs. Pretium Packaging, founded in 1992, is a leading supplier of injection-blow molded plastic containers, renowned for our commitment to superior quality, value, and customer service.
Life Science Veeva Senior Manager Deloitte Touche Tohmatsu LtdLife Science Veeva Senior ManagerDallas, TX$189,200–$372,900 / yearThe wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. 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.
DOT/TSA Program Manager FlightSafety International IncDOT/TSA Program ManagerFort Worth, TXProvide day-to-day guidance on the USDOT Drug and Alcohol Testing Program to all Drug Testing Site Coordinators (DTSC) and alternates, Human Resources (HR) representatives, Talent Acquisition employees, Flight Instructors, and Directors of Quality (DOQs). Associate degree (A.A.) from a two-year college or technical school preferred, or three (3) years related experience and/or training; or equivalent combination of education and experience; equivalency years' experience substitution must be in related field; plus.
Senior Manager/Manager, Compliance Testing Madison-DavisSenior Manager/Manager, Compliance TestingDallas / Fort Worth, TXThis role will be responsible for executing risk-based testing engagements, evaluating control effectiveness, identifying regulatory risks, and driving remediation efforts across a diverse portfolio of business lines. A global financial institution is seeking an experienced Compliance Testing professional to support and lead independent compliance reviews across capital markets, investment banking, and related financial services activities.
QA/RA Specialist - Pharmaceutical GLP/GMP Experience synergyQA/RA Specialist - Pharmaceutical GLP/GMP ExperienceDallas, TXThe specialist will be responsible for supporting the implementation, maintenance, and continuous improvement of quality and regulatory compliance systems to ensure adherence to FDA, EMA, and other regulatory requirements. Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry.
Managed Services Sr. Consultant Deloitte Touche Tohmatsu LtdManaged Services Sr. ConsultantTX$120,200–$140,000 / yearLead 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.
Kearney Healthcare & Life Sciences Practice Principal Pharma R&D Strategy A.T. Kearney IncKearney Healthcare & Life Sciences Practice Principal Pharma R&D StrategyTX$245,000–$270,000 / yearp>We are seeking experienced strategy consultants with deep expertise across Pharma R&D, particularly those with a traditional consulting background advising biopharma clients on clinical development, drug development strategy, operating models, and R&D transformation initiatives. You will work closely with senior clients and internal teams to develop strategic insights and deliver high-impact outcomes across complex pharmaceutical R&D and clinical development challenges.
Senior Hazmat Analyst Toyota Motor CorpSenior Hazmat AnalystPlano, TXReporting to the Hazmat Transportation & Compliance Manager, the person in this role will support the objective to develop and implement hazmat policies, programs, and training, ensuring Toyota's regulatory compliance and risk mitigation to avoid business interruptions. The primary responsibility of this role is to provide technical expertise in hazardous materials (hazmat) transportation compliance and management to support all Toyota Motor North America (TMNA) locations to meet or exceed regulatory requirements.
Food Safety Leader - DFW Central MarketFood Safety Leader - DFWDallas, TexasFull timeWorks closely with Central Market Managers, Quality Assurance Food Safety Managers; functions as a liaison for food safety communication, programs, and issues as directed. Familiarity with HACCP, Good Manufacturing Practices, Good Retail Practices, thermal processing, Code of Federal Regulations, FDA Food Code, Texas Retail Food Establishment rules, statistics, integrated pest management, and auditing practices - .
Director of IT Universal Diagnostics SLDirector of ITTXp>You will partner closely with Corporate Functions, Laboratory and Manufacturing Operations, Software Engineering, Bioinformatics, Quality Assurance, and Regulatory Affairs to ensure that IT systems and processes meet business needs while maintaining compliance with applicable regulatory requirements, including FDA, CAP/CLIA, ISO 13485, HIPAA, and GxP expectations. This role is responsible for the strategy, governance, and operational management of enterprise IT systems, infrastructure, cybersecurity, cloud platforms, workplace technology, and regulated IT systems supporting CLIA laboratory operations, medical device development, manufacturing activities, and quality systems.
Food Safety Leader - DFW H.E. Butt Grocery CoFood Safety Leader - DFWDallas, TXKey Responsibilities & Essential Functions: • Manages / executes food safety programs, including HACCP or HACCP-based programs as directed • Manages / conducts HACCP based food safety audits and assessments as required • Manages all food safety technology for the facility • Serves as Safe Quality Food (SQF) Practitioner • Assists in conducting facility plan review for food safety and sanitation compliance as directed • Leads response and follow up on any site pest control issues • Provides food safety expertise and support for emergency response events or crisis situations (e.g., power outages, hot water loss, natural disasters, pandemic response) • Provides input on food safety issues to other team members • Works closely with Central Market Managers, Quality Assurance Food Safety Managers; functions as a liaison for food safety communication, programs, and issues as directed • Provides support in administration and facilitation of the Certified Food Manager (CFM) training program for all Partners • Completes / maintains all required administrative reports accurately and on time • Provides communications support with state and local regulatory agencies, as assigned • Assists Regulatory Affairs in administration of / compliance with company recalls; focuses on 100% compliance on Class I recalls • Provides support for regulatory changes that would impact CM / H-E-B, as assigned • Assists with regulatory compliance issues at warehouse, transportation, distribution or store level as needed • Conducts investigations of complaints to protect CM / H-E-B liability and avoid negative customer perception • Serves as food safety liaison to state and local level regulatory agencies • Assists with development of VTAs, process documents, etc. Responsibilities Job Summary: As a Food Safety Leader, you'll oversee all food safety and food safety compliance for perishable, non-perishable, and food service departments.
Director of IT Universal DXDirector of ITDallas, TexasYou will partner closely with Corporate Functions, Laboratory and Manufacturing Operations, Software Engineering, Bioinformatics, Quality Assurance, and Regulatory Affairs to ensure that IT systems and processes meet business needs while maintaining compliance with applicable regulatory requirements, including FDA, CAP/CLIA, ISO 13485, HIPAA, and GxP expectations. This role is responsible for the strategy, governance, and operational management of enterprise IT systems, infrastructure, cybersecurity, cloud platforms, workplace technology, and regulated IT systems supporting CLIA laboratory operations, medical device development, manufacturing activities, and quality systems.
Food Safety Leader - DFW HEBFood Safety Leader - DFWDallas, TexasWorks closely with Central Market Managers, Quality Assurance Food Safety Managers; functions as a liaison for food safety communication, programs, and issues as directed. Familiarity with HACCP, Good Manufacturing Practices, Good Retail Practices, thermal processing, Code of Federal Regulations, FDA Food Code, Texas Retail Food Establishment rules, statistics, integrated pest management, and auditing practices - .