NewFamily Nurse Practitioner / Physician Assistant-Float Fast Pace HealthFamily Nurse Practitioner / Physician Assistant-FloatJasper, TXPosting Title: Family Nurse Practitioner / Physician Assistant-Float Overview: In a manner consistent and supportive of our values, the Provider is responsible for delivering high quality health care within Fast Pace Health’s scope of services while achieving optimum patient satisfaction. They must have the ability to respond quickly and accurately to changes in condition or response to treatment and is responsible for providing outstanding patient service within the clinic and through various virtual communication channels, while maintaining a compassionate and welcome atmosphere.
Sr. Associate II, Regulatory Affairs Strategy Alcon IncSr. Associate II, Regulatory Affairs StrategyFort Worth, TXIn this role, you will develop strong scientific and technical product knowledge and serve as a key resource to country Regulatory Affairs associates by providing regulatory guidance and information. 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 send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.
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.
Regulatory Affairs Associate EKF Diagnostics Holdings PlcRegulatory Affairs AssociateBoerne, TXEssential Functions, included but not limited to: Assist in monitoring implementation of new regulatory / legal requirements (including environmental legislation) in the relevant countries. Participate and assist in audits conducted by regulatory agencies, registrars, certifying bodies, and customers to include end-users, distributors, and other OEM customers, as applicable.
Manager, Regulatory Affairs and Compliance NordsonManager, Regulatory Affairs and ComplianceTexasPrepares 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.
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.
Sr. Manager, Regulatory Affairs Strategy Alcon IncSr. Manager, Regulatory Affairs StrategyFort Worth, TXAs a Senior Manager, Regulatory Affairs Strategy, you will lead regulatory compliance and strategy activities for Alcon's Intraocular Device portfolio, including intraocular lenses (IOLs), implantable glaucoma devices and associated delivery systems. This onsite position is based in Fort Worth, Texas (other on-site locations available) and plays a key role in enabling compliant, timely access to innovative devices across global markets.
Senior Regulatory Affairs Specialist EnovisSenior Regulatory Affairs SpecialistAustin, TexasWorking as part of a global RA function, the role will also support in sustainable regulatory activities such as management of post market surveillance activities on behalf of legal manufacturers, completing regulatory impact assessments for product changes and providing other regulatory SME support to the business as needed. We know that the power to create better – for our customers, our team members, and our shareholders – begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.
Senior Regulatory Affairs Specialist Enovis CorpSenior Regulatory Affairs SpecialistAustin, TXWorking as part of a global RA function, the role will also support in sustainable regulatory activities such as management of post market surveillance activities on behalf of legal manufacturers, completing regulatory impact assessments for product changes and providing other regulatory SME support to the business as needed. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.
Director, Clinical Research Regulatory Affairs University of Texas MD Anderson Cancer CenterDirector, Clinical Research Regulatory AffairsHouston, TXRemoteSuccessful completion of the LEADing Self Accelerate and/or LEADing Self Discover programs may substitute for one year of required supervisory or management experience Completion of both programs can be substituted for a maximum of two years of supervisory or management experience. Preferred: Demonstrated experience preparing and managing INDs and/or IDEs; familiarity with companion diagnostics and combination products is a plus, and an in-depth knowledge of FDA regulations, ICH guidelines, and GCP requirements, and an experience with EMA submissions.
Sr. Manager, Regulatory Affairs Strategy Alcon ResearchSr. Manager, Regulatory Affairs StrategyFort Worth, TexasAs a Senior Manager, Regulatory Affairs Strategy , you will lead regulatory compliance and strategy activities for Alcon’s Intraocular Device portfolio , including intraocular lenses (IOLs), implantable glaucoma devices and associated delivery systems. This onsite position is based in Fort Worth, Texas (other on-site locations available) and plays a key role in enabling compliant, timely access to innovative devices across global markets.
Regulatory Affairs Associate ARKRAY USA IncRegulatory Affairs AssociatePlano, TXSupport quality system activities as assigned, including audit support, validation/change control support, supplier activities, internal audit participation, and QMS compliance activities (FDA QMSR, ISO 13485, OSHA). Support product launch regulatory work such as Regulatory Master Plans, labeling program coordination, UDI/GUDID activities, facility registrations/device listings, import inspections/holds, and related documentation support.
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.
Associate Director, Regulatory Affairs Tonix PharmaceuticalsAssociate Director, Regulatory AffairsFort Worth, MarylandTonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. The Associate Director, Regulatory Affairs can work autonomously and will support all aspects of this process including early phase interactions with regulatory authorities (FDA and/or global), providing direction and actively participating in overall preparation of activities with cross-functional teams to advance the drug development program.
Manager - Regulatory Affairs (Remote) Caris Life SciencesManager - Regulatory Affairs (Remote)Boston, TexasRemotePrepares documents necessary for new product market clearance, approval, and continuance during product life cycle management that includes, but not limited to, 510Ks, IDEs, supplements, and technical files for CE marketing. Provide guidance to pharmaceutical partners and junior regulatory staff regarding regulatory requirements including indications of risk and approximate timing for approval for planning purposes.
Regulatory Affairs Specialist III, Animal Health Thermo Fisher ScientificRegulatory Affairs Specialist III, Animal HealthAustin, TexasWe provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. The Regulatory Affairs Specialist III will be responsible for defining and implementing regulatory strategy, providing regulatory guidance and support to product development teams for planning, design and development, and post-market surveillance and compliance activities.
NewManager, Regulatory Affairs - Clinical Research Baylor College of MedicineManager, Regulatory Affairs - Clinical ResearchHouston, TX$111,118–$130,000 / yearDirectly supervises Regulatory Affairs Associates and Senior Associates, including assigning and prioritizing workload, monitoring performance, and ensuring equitable distribution of study portfolios. Provides regulatory support for clinical protocols by coordinating submissions, reviewing regulatory content for completeness and compliance, and ensuring alignment with institutional requirements.
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.
Regulatory Affairs Specialist (Food Manufacturing) Dessert Holdings Inc.Regulatory Affairs Specialist (Food Manufacturing)Humble, TexasDessert Holdings is a collection of premium dessert companies and brands: The Original Cakerie, Lawler's Desserts, Atlanta Cheesecake Company, Steven Charles, Dianne's Fine Desserts, Kenny's Great Pies, and Willamette Valley Pie Company. Dessert Holdings is looking for a Regulatory Affairs Specialist to help administer Dessert Holdings' Regulatory Compliance Program, ensuring that packaging, specifications, and labeling meet regulatory requirements for the country of sale.
Senior Executive Assistant - Office of Legal and Regulatory Affairs University of Texas Medical Branch at GalvestonSenior Executive Assistant - Office of Legal and Regulatory AffairsGalveston, TXJob Summary: Directly supports and serves as an extension of the executive vice president, providing a broad range of highly responsible administrative services to guide the goals of the executive, the leadership team, the department, and the enterprise area, as well as the overall mission of the university. Works cooperatively and collaboratively with other executives and staff members to create a high-functioning team that sets and achieves goals.
Regulatory Affairs Specialist Cordialsa Usa IncRegulatory Affairs SpecialistThe Woodlands, TXThe ideal candidate has experience in the food or consumer packaged goods (CPG) industry, strong knowledge of North American regulatory frameworks, and the ability to collaborate effectively across cross-functional teams. This role will help ensure that products, labeling, and technical documentation comply with applicable regulatory requirements while supporting business growth and innovation initiatives.
NewDirector, 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.
Regulatory Affairs Associate - Clinical Research Baylor College of MedicineRegulatory Affairs Associate - Clinical ResearchHouston, TX$70,618–$83,080 / yearKnowledge and understanding of clinical research compliance, including OHRP, FDA and other federal regulations and requirements regarding human subjects research, including but not limited to GCPs and related ICH guidelines, informed consent, adverse event reporting and monitoring, and other human subjects research protection requirements. Acts as a liaison between institutional review committees, regulatory agencies and the investigators to ensure that protocols obtain applicable approvals, that protocol amendments are submitted appropriately and that annual renewals are obtained.
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).
NewSenior / Regulatory Affairs Consultant - Regulatory Labeling Strategist ParexelSenior / Regulatory Affairs Consultant - Regulatory Labeling StrategistAustin, TXRemoteAre you experienced in leading the strategy behind how life-changing therapies are communicated to the world, ensuring innovative products are supported by clear, compliant, and high-quality documentation that enables safe and effective use across global markets?. Parexel is seeking an experienced and highly motivated Global Regulatory Labeling Lead to provide strategic leadership and operational oversight for complex global labeling initiatives.
Regulatory Affairs Coordinator, Three locations: ( Portage MI, San Jose, Flower Mound Texas) Matlen Silver, Inc.Regulatory Affairs Coordinator, Three locations: ( Portage MI, San Jose, Flower Mound Texas)Flower Mound, TXJob overview: The Product Environmental Compliance Coordinator (Contractor) supports the Endoscopy Divisions Product Environmental Compliance program by helping ensure products meet global environmental regulations such as RoHS, REACH, POPs, WEEE, and California Proposition 65. This individual contributor role focuses on maintaining accurate compliance data, coordinating supplier outreach, supporting time-sensitive projects, and preparing reports that track progress and support decision-making.
Senior Regulatory Affairs Project Manager I, MILCON ICON Technology IncSenior Regulatory Affairs Project Manager I, MILCONAustin, TXReporting to the Regulatory Program Manager, youll execute public sector regulatory efforts, build critical relationships with government agencies, and expand the regulatory framework necessary to position ICONs 3D-printed construction technology as the governments construction technology of choice. Collaborate with internal technical teams - including testing, materials science, product engineering, and operations - to integrate federal regulatory requirements into product development; ensure validation efforts support approval pathways and resolve technical challenges that impact government acceptance.
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).
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaTX$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 Manager Electrolit USARegulatory Affairs ManagerHouston, TexasThis role maintains strong alignment with the Electrolit Global Regulatory Team to ensure consistency and best practices across markets and collaborates closely with internal and external legal counsel to address regulatory and legal matters. Operating cross-functionally across departments, the Regulatory Affairs Manager manages regulatory documentation, labeling compliance, advertising and serves as the primary liaison with regulatory authorities.
Senior Regulatory Affairs Manager Medtronic PlcSenior Regulatory Affairs ManagerFort Worth, TXThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Coordinator, Regulatory Affairs - Onsite Roth Staffing CompaniesCoordinator, Regulatory Affairs - OnsiteFlower Mound, Texas$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.
VP of Licensing and Regulatory Affairs Aalo AtomicsVP of Licensing and Regulatory AffairsAustin, TexasThe Vice President of Licensing and Regulatory Affairs is a critical executive role responsible for leading our regulatory strategy, establishing a clear pathway for technology approval, and driving complex nuclear licensing applications to completion. Drive licensing processes to completion, establishing rigorous execution frameworks, document control systems, and accountability across safety analysis, environmental reviews, and site permitting streams.
Director of Regulatory Affairs US FinTech | Supervisory & Licensing Governance MastarRecDirector of Regulatory Affairs US FinTech | Supervisory & Licensing GovernanceBleiblerville, TexasLeads engagement with federal and state regulators, manages licensing requirements, and oversees regulatory change management. • Multi-jurisdiction financial services exposure.
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.
Manager, Regulatory and Market Affairs Pattern Energy Group IncManager, Regulatory and Market AffairsHouston, TX$103,000–$138,000 / yearA key function of this role will be to identify, research, analyze, and synthesize the cross section of regulatory and wholesale market rules impacting Pattern's existing and planned assets in WECC, MISO, ERCOT, SPP, PJM and other priority markets as needed. Importantly, the role will support the coordination with expert consultants and internal SMEs to clearly and regularly identify and lead Pattern's engagement in regulatory and market design changes, develop Pattern's positions and execute on strategies to achieve desired objectives.
Director Regulatory and Government Affairs NextEra Energy IncDirector Regulatory and Government AffairsAustin, TXHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. Leaders in this role are responsible for directing timely preparation of accounting, financial, operating and statistical data required to support regulatory filings before the Florida Public Service Commission (FPSC) and the Federal Energy Regulatory Commission (FERC) and assure regulatory compliance.
Vice President, Quality Assurance & Regulatory Affairs | AirStrip NantHealth IncVice President, Quality Assurance & Regulatory Affairs | AirStripSan Antonio, TXThis is a highly visible executive role responsible for shaping regulatory strategy, strengthening external partnerships, and ensuring the organization maintains a scalable, efficient, and compliant quality infrastructure that supports innovation and growth. We provide mobile-first clinical surveillance and alarm communication management technology that unlocks siloed data from patient monitors and transforms it into contextually rich information easily accessible on mobile devices and the Web.
Coordinator, Regulatory Affairs - Skilled Apidel TechnologiesCoordinator, Regulatory Affairs - SkilledFlower Mound, TXContractorKey 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 Divisions Product Environmental Compliance program by helping ensure products meet global environmental regulations such as RoHS, REACH, POPs, WEEE, and California Proposition 65.
Director, Regulatory Affairs CMC Sionna Therapeutics IncDirector, Regulatory Affairs CMCAustin, TX$200,000–$240,000 / yearScientific Presentations. Scientific Literature.
NewDirector / Manager Tariffs and Regulatory Affairs Kinder MorganDirector / Manager Tariffs and Regulatory AffairsHOUSTON, TexasFull timeTo work with all Kinder Morgan products pipeline regulated assets (Calnev, Double Eagle, Hiland Crude (gathering), KM Crude and Condensate (KMCC), Products (SE) Pipe Line (PPL), Central Florida Pipeline (CFPL), and SFPP) plus Wink (CO2 group) in matters regarding Federal Energy Regulatory Commission (FERC) and state liquids pipeline regulations, in order to create and maintain tariff documents, set rates, adjust and defend rates (including the collection and organizing of pipeline volume and rate base data), and create and maintain tariff rules. • Teamwork/Cooperation: Works effectively with team/work group, as well as with other departments and/or outside contractors/agencies to accomplish organizational goals; takes action that respect the needs and contributions of others; takes responsibility for actively participating and contributing to team efforts; supports a team consensus or decision; acts as team facilitator when appropriate, promotes team concepts.
Regulatory Affairs Manager - Diabetes Care (on-site) Abbott LaboratoriesRegulatory Affairs Manager - Diabetes Care (on-site)Austin, TX$114,000–$228,000 / yearAs a member of the U.S. Regulatory Affairs management team, the successful candidate will lead and develop talent, shape regulatory strategy, and partner across functions to bring innovative products to market, whilst driving regulatory excellence for the manufacture, change management, and ongoing supply of the Libre portfolio. Drive and provide strategic guidance on FDA pathways, submissions, and interactions, including pre-submissions, 510(k), PMA, and post-market activities.
Open Rank - Clinical Faculty - Associate Dean for Faculty Affairs University of HoustonOpen Rank - Clinical Faculty - Associate Dean for Faculty AffairsTXReporting to the Dean, and in collaboration with the Vice or Associate Dean of Medical Education (V/ADME), the Associate Dean for Faculty Affairs (ADFA) provides strategic leadership for the full faculty life cycle across the College of Medicine, from workforce planning and recruitment to onboarding, development, advancement, support, and offboarding. Individuals conducting research in critical infrastructure areas (i.e., communication infrastructure systems, cybersecurity systems, electric grid, hazardous waste treatment systems, and/or water treatment facilities) are subject to regular review to ensure the security and integrity of the research is maintained.
NewDirector, Executive Operational Planning - Communications and Public Affairs USAADirector, Executive Operational Planning - Communications and Public AffairsSan Antonio, TX$127,310–$243,340 / yearAs a dedicated Director, Executive Operational Planning within Communications and Public Affairs team, you will lead a team responsible for guiding senior leadership in the prioritization and coordination of key deliverables and activities. What sets you apart: Exceptional executive-level written communication skills, with the ability to translate complex business strategies into clear, compelling narratives that drive alignment and decision-making among senior leaders.
Open Rank - Clinical Faculty - Associate Dean for Student Affairs University of HoustonOpen Rank - Clinical Faculty - Associate Dean for Student AffairsHouston, TXThis role leads the Office of Student Affairs and is responsible for student-centered programs and services, including academic advising, career advising, student wellness, registrar services, financial aid, and learning communities. Reporting to the Vice Dean for Education, The Associate Dean for Student Affairs provides strategic leadership and oversight for all aspects of the medical student experience, supporting student success across the continuum of medical education.
AVP Laboratory Affairs Baylor GeneticsAVP Laboratory AffairsHouston, TexasThe AVP Laboratory Affairs is a senior laboratory leadership role responsible for advancing laboratory governance, regulatory compliance, accreditation readiness, policy oversight, quality systems, and operational performance across Baylor Genetics’ high-complexity laboratory environment. This role provides enterprise-level oversight of laboratory KPIs, benchmark performance, risk identification, Non-Conforming Event (NCE) evaluation, root cause analysis (RCA), and corrective and preventive actions.
Environmental Affairs and Permitting Associate Repsol SAEnvironmental Affairs and Permitting AssociateHouston, TXJob Summary: Repsol Renewables North America is seeking an Environmental Affairs and Permitting Associate to join our dynamic team and support the Company's growing utility-scale wind, solar and energy storage projects across the U.S. This individual will utilize their academic background and experience to review, evaluate, and implement federal, state and local environmental regulatory requirements as they apply to Repsol projects. Key Responsibilities: The position will offer the opportunity to expand your knowledge of federal, state and local environmental regulations as they apply to major industrial energy projects, and to work with multi-disciplined project teams to: Assist with review and implement federal, state, and local regulatory permitting requirements as they apply to specific projects.
Director, State Affairs - Texas Humana IncDirector, State Affairs - TexasAustin, TXRemote$168,000–$231,000 / yearDemonstrated success developing and executing advocacy strategies at the state level, with significant, hands-on experience navigating the Texas landscape and a clear track record of achieving both short- and long-term policy or business objectives. Through our Humana insurance services and our CenterWell healthcare services, we make it easier for the millions of people we serve to achieve their best health - delivering the care and service they need, when they need it.
AVP Laboratory Affairs Baylor Miraca Genetics Laboratories LLCAVP Laboratory AffairsHouston, TXThe AVP Laboratory Affairs is a senior laboratory leadership role responsible for advancing laboratory governance, regulatory compliance, accreditation readiness, policy oversight, quality systems, and operational performance across Baylor Genetics' high-complexity laboratory environment. This role provides enterprise-level oversight of laboratory KPIs, benchmark performance, risk identification, Non-Conforming Event (NCE) evaluation, root cause analysis (RCA), and corrective and preventive actions.
AVP Laboratory Affairs Baylor Miraca Genetics Laboratories, LLCAVP Laboratory AffairsHouston, TXPart timeThe AVP Laboratory Affairs is a senior laboratory leadership role responsible for advancing laboratory governance, regulatory compliance, accreditation readiness, policy oversight, quality systems, and operational performance across Baylor Genetics’ high-complexity laboratory environment. This role provides enterprise-level oversight of laboratory KPIs, benchmark performance, risk identification, Non-Conforming Event (NCE) evaluation, root cause analysis (RCA), and corrective and preventive actions.