NewProperty Adjuster Specialist - Field Claims USAAProperty Adjuster Specialist - Field ClaimsKilleen, TXRemote$69,920–$133,620 / yearProactively manages assigned claims caseload comprised of complex damages that require commensurate knowledge and understanding of claims coverage including potential legal liability. 2 years of relevant property claims adjusting experience of moderate complexity losses that includes writing estimates, involving dwelling and structural damages.
NewLoan Sales Specialist OneMain FinancialLoan Sales SpecialistWharton, TXKey Word Tags Sales, Collections, Retail, Loan Sales, Customer Service, Customer Care, Business Development, New Grad, Newly Graduated, Entry level, Financial Sales, Management Development, Management Trainee, Finance, Full-time, Career, Benefits, Customer experience, Financial Representative, Credit, Leadership, Manager Trainee #OMHTF In our more than 1,300 community branches and across the U.S., team members help millions of customers solve critical financial needs, including debt consolidation, home and auto repairs, medical procedures and extending household budgets.
NewAffordable Housing Compliance Specialist Asset Living Corporate TeamAffordable Housing Compliance SpecialistLubbock, TXAsset Living's growing portfolio includes a multitude of properties across the country that span the multifamily, single-family home rentals, affordable housing, build-to-rent, active adult, and student housing divisions. Recognized as one of the nation's Best and Brightest Places to Work and ranked in the NMHC top 50 professionals, join Asset Living because of its reputation as the most trusted partner in real estate, workplace culture, and growth opportunities.
Clinical Quality Specialist University Medical Center of El PasoClinical Quality SpecialistEl Paso, TXThe Clinical Quality Specialist provides oversight of the professional practice evaluation process, including ongoing professional practice (OPPE) and focused professional practice (FPPE), for practitioners in the health system, including physicians and advanced practice professionals (APP). Reviews cases, interprets, evaluates, and reports data to improve quality and patient care outcomes using problem-solving skills to identify potential areas of improvement.
NewCoding Specialist PRN University HealthCoding Specialist PRNSAN ANTONIO, TXCandidate will also possess one of the following certifications: Registered Health Information Technician (RHIT), Registered Health Information Administrator, (RHIA), Certified Coding Specialist (CCS), or CPC (Certified Professional Coder). Codes inpatient, outpatient surgery and observation visits utilizing the ICD-9-CM and CPT coding classification systems.
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.
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.
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.
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.
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.
REGULATORY SPECIALIST - CRI Methodist Health SystemREGULATORY SPECIALIST - CRIDallas, TXYour Job Requirements: • Bachelor''s degree required; Master's degree preferred • CCRC or CCRP (preferred) • GCP certification (preferred) • 1 year of experience in a medical or clinical setting (required) • 1 year of experience in clinical research (required) • 1 year of experience in research regulatory affairs (required) • Strong proficiency using Microsoft Office products • Superior oral and written communication skills • Strong process orientation • Detail oriented, logical, and methodological approach to problem solving • Ability to provide vision and leadership. Your Job Responsibilities: • Communicate clearly and openly • Build relationships to promote a collaborative environment • Be accountable for your performance • Always look for ways to improve the patient experience • Take initiative for your professional growth • Be engaged and eager to build a winning team • Review clinical research protocols to determine logistical components of regulatory requirements • Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.
Regulatory Specialist - Cri Methodist Health SystemRegulatory Specialist - CriDallas, TexasYour Job Requirements: • Bachelor's degree required; Master’s degree preferred • CCRC or CCRP (preferred) • GCP certification (preferred) • 1 year of experience in a medical or clinical setting (required) • 1 year of experience in clinical research (required) • 1 year of experience in research regulatory affairs (required) • Strong proficiency using Microsoft Office products • Superior oral and written communication skills • Strong process orientation • Detail oriented, logical, and methodological approach to problem solving • Ability to provide vision and leadership. Your Job Responsibilities: • Communicate clearly and openly • Build relationships to promote a collaborative environment • Be accountable for your performance • Always look for ways to improve the patient experience • Take initiative for your professional growth • Be engaged and eager to build a winning team • Review clinical research protocols to determine logistical components of regulatory requirements • Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.
Regulatory 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 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 & Clinical Specialist LivaNova PlcRegulatory & Clinical SpecialistHouston, TXRemote$85,000–$95,000 / yearManage the overall development and approval process for assigned documents (CEP, CER, etc.) within timelines, including documentation generation, initiation of the review process, discussions on proposed revisions, and document completion in collaboration with other team members. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for "See Open Jobs" on https://www.livanova.com/en-us/careers , and check that all recruitment emails come from an @livanova.com email address.
Regulatory Specialist Witt O'Brien's Payroll ManagementRegulatory SpecialistHouston, TexasKnowledgeable about practices used to address clients’ unexpected emergencies, such as the National Incident Management System (NIMS), Incident Command System (ICS), crisis management, business continuity, and emergency response. A Compliance Services Regulatory Specialist is responsible for supporting Witt O’Brien’s clients nationally with a varying degree in environmental and emergency management regulatory programs.
Regulatory Compliance Specialist - Transplant Center Houston Methodist HospitalRegulatory Compliance Specialist - Transplant CenterHouston, TXAt Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating and performing study specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices (GCP) and all local, state, and federal laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Houston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval.
Regulatory Correspondence Specialist III NewRez LLCRegulatory Correspondence Specialist IIICoppell, TXRequires continuous learning and keeping up to date with the Regulations related to the Real Estate Settlement Procedures Act ("RESPA"), Truth in Lending Act ("TILA") the Fair Credit Reporting Act ("FCRA"), the Consumer Financial Protection Bureau ("CFPB"), and policies and procedures regarding Fraud/ID Theft. The Regulatory Correspondence Specialist III is adequately experienced to decipher the homeowner's complaint to the point of identifying the exact issues, identifying root cause, and determining corrective action and next steps.
Regulatory Compliance Specialist NSSRegulatory Compliance SpecialistHouston, TexasKnowledgeable about practices used to address clients’ unexpected emergencies, such as the National Incident Management System (NIMS), Incident Command System (ICS), crisis management, business continuity, and emergency response. A Compliance Services Regulatory Specialist is responsible for supporting Witt O’Brien’s clients nationally with a varying degree in environmental and emergency management regulatory programs.
Regulatory Specialist Texas Tech UniversityRegulatory SpecialistLubbock, TXNo The Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act is a federal statute requiring colleges and universities participating in federal financial aid programs to maintain and disclose campus crime statistics and security information. Team members also enjoy a variety of other perks, such as special membership rates at local gyms and golf courses, access to state-of-the-art software and facilities, and discounts on travel, technology, entertainment and more.
Sr Regulatory Compliance Specialist HMRISr Regulatory Compliance SpecialistTexasRegulatory Compliance Specialist position is responsible for leading, coordinating and performing study specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices (GCP) and all local, state, and federal laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities.
Regulatory Compliance Specialist HMRIRegulatory Compliance SpecialistTexasAt Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating and performing study specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices (GCP) and all local, state, and federal laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities.
Regulatory Compliance Specialist - Transplant Center HMRIRegulatory Compliance Specialist - Transplant CenterTexasAt Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating and performing study specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices (GCP) and all local, state, and federal laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities.
Regulatory Compliance Specialist CornerStone Professional PlacementRegulatory Compliance SpecialistFort Worth, TX$30–$34 / hourAdditionally, the specialist will collaborate with cross-functional teams to enhance operational systems, improve data quality, and drive process efficiencies across compliance-related programs. The Regulatory Compliance Specialist will partner closely with the Operations Senior Manager to support the execution, monitoring, and continuous improvement of compliance programs and operational processes.
Senior Regulatory Administration Specialist Victory Capital Holdings IncSenior Regulatory Administration SpecialistSan Antonio, TX$81,900–$96,360 / yearCoordinate with internal departments and external business partners to request, create, and prepare mutual fund regulatory documents (i.e., prospectus and statement of additional information disclosure) to be submitted to the Securities and Exchange Commission (SEC) or other regulatory bodies and agencies. This role oversees all aspects of board governance for 1940 Act mutual funds and manages the review, editing, maintenance, processing, and regulatory filing of fund documents, including prospectuses and statements of additional information.
NewSenior Client Delivery Specialist (Energy Regulatory Legal Assistant) Husch BlackwellSenior Client Delivery Specialist (Energy Regulatory Legal Assistant)Austin, TexasPrepares, edits, formats, and proofreads legal documents, correspondence, and presentations with a high degree of accuracy; manages version control, file organization, and secure document storage in compliance with firm policies; and facilitates the execution, filing, and distribution of legal documents. Reviews and routes incoming mail and fax communications; prepares and processes outgoing mail and faxes; arranges specialized mail or messenger services as required; and ensures attachments, exhibits, and enclosures are included.
Regulatory Docketing & Compliance Specialist Base Power IncRegulatory Docketing & Compliance SpecialistAustin, TX3+ years of regulatory experience at a utility, retail electric provider, alternative supplier, ISO/RTO, state commission, or regulatory consulting firm - with direct experience filing before state utility commissions. Regulatory Services works closely with Policy, Legal, and the operating teams that build and run Bases markets, keeping us clean with the regulators that govern every part of how Base delivers power.
Sr. Regulatory Compliance Specialist Mitsubishi Heavy Industries LtdSr. Regulatory Compliance SpecialistHouston, TXMHIA): For over 130 years Mitsubishi Heavy Industries (MHI) Group's innovative and integrated solutions have demonstrated our commitment to creating a positive social impact around the globe. Lead compliance investigations involving allegations of illegal, unethical, or improper conduct by employees or company representatives, including fact-finding, evidence review, and final reporting, in coordination with HR and Legal as needed.
NewTechnical and Regulatory Specialist Veolia Environnement SATechnical and Regulatory SpecialistBaytown, TXWhen needed, assist Technical Customer Advisors with creation of new direct approvals into Veolia or other 3rd party TSDFs, taking into consideration the best treatment options available as well as branch operational logistics to get the waste to the final intended TSDFs. Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country's largest private water operator and technology provider as well as hazardous waste and pollution treatment leader.
Oil & Gas Production / Regulatory Reporting Specialist IStick Capital ManagementOil & Gas Production / Regulatory Reporting SpecialistDallas, TexasPrepare and submit State and Federal Royalty Reports, including compliance with University Lands, Office of Natural Resources Revenue (ONRR), and other applicable agencies. Monitor and reconcile Oil and Gas Balancing, including production imbalances and partner allocations.
NewSenior Board Governance & Regulatory Filings Specialist Victory Capital ManagementSenior Board Governance & Regulatory Filings SpecialistSan Antonio, TXThe role reports to the Senior Manager of Board Governance in San Antonio, TX.You will coordinate with internal teams and external partners to ensure timely, accurate governance materials and filings, including annual questionnaires and sections of the prospectus.#J-18808-Ljbffr. Victory Capital Management is seeking a full‑time Senior Regulatory Administration Specialist to oversee board governance for mutual funds and manage regulatory filings and prospectus updates.
Regulatory Reporting Specialist, Responsible Minerals and Human Rights Compliance GoogleRegulatory Reporting Specialist, Responsible Minerals and Human Rights ComplianceAustin, TXAs the Responsible Minerals and Human Rights Compliance Regulatory Reporting Specialist, you will play a critical role in advancing our Responsible Minerals Program strategy, executing key initiatives across Alphabet and Google, and managing conflict minerals, anti-modern slavery, and human rights compliance and regulatory reporting obligations. You will work with a cross-functional set of stakeholders across Alphabet, including teams embedded in product areas responsible for operationalizing supplier responsibility and responsible minerals program efforts.
Senior Regulatory Compliance Specialist, Trust & Safety (Temporary - 6 month) Match Group IncSenior Regulatory Compliance Specialist, Trust & Safety (Temporary - 6 month)Dallas, TX$145,000–$180,000 / yearYou should be comfortable working independently with open-ended projects, and engaging with highly sensitive subject matter (with potential exposure to sensitive visual content) as part of the Trust & Safety team. Beyond documentation, we're looking for a hands-on changemaker who can identify the next steps needed to meet both the letter and spirit of evolving global regulatory requirements, and convey those next steps to product teams.
Sr Regulatory Product Compliance Specialist Motorola Solutions IncSr Regulatory Product Compliance SpecialistAllen, TX$98,100–$156,200 / yearRF: FCC Part 15 Subparts C, D, E, F, FCC Parts 22, 25, 90, 96, FCC RF Exposure Compliance, RSS-102, RSS-247, RSS-210, RSS-195, RSS-119, RSS-132, RSS-131, RSS-139, RSS-220, RSS-140, RSS-GEN, EN 300 328, EN 300 220, EN 300 440, EN 301 893, EN 301 908, EN 62479. Whether its helping firefighters see through smoke, enabling police officers to see around street corners, or reliably keeping the lights on in homes and businesses around the world, our work supports those who put their lives on the line to keep us safe.
Regulatory Compliance Specialist Texas Health and Human Services CommissionRegulatory Compliance SpecialistRICHMOND, TX$5,797.66–$9,508.25The position works with state office staff and center leadership to prepare for regulatory surveys, investigations, and other internal or external reviews; advises centers on regulatory readiness and citation responses, including plans of correction, plans of removal, and informal dispute resolutions; and analyzes data to identify risks, recommend improvements, and support sustained compliance. Gathers, organizes, correlates, and analyzes facts, data, reports, survey findings, plans of correction, monitoring results, and statewide trends to evaluate program performance and identify systemic issues affecting compliance, quality of services, active treatment, and health and safety of individuals served.
Regulatory Compliance Specialist WhiteWater MidstreamRegulatory Compliance SpecialistAustin, TexasCommunicate regularly with Operations and Engineering teams to address potential areas of risk, provide guidance and offer expertise on local or federal regulatory codes. Occasionally perform internal audits of site compliance activities and internal compliance programs and provide corrective measures where applicable.
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.).
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.
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. 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.
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).
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 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).
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.
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.
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.
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.
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.