Regional Director of Clinical and Regulatory Support (Post-Acute) Community Hospital CorporationRegional Director of Clinical and Regulatory Support (Post-Acute)Plano, TXFull timeUnder the supervision of the VP of Clinical Services for Post-Acute Services, the Regional Director of Clinical and Regulatory support: Supports clinical and quality initiatives for owned, managed, and consulting facilities by providing support to field CNO’s and DQMs; Serves as the infection control specialist for post-acute services and is responsible for developing, implementing and coordinating a consistent approach to infection prevention and control; Supports Regulatory compliance and provides regulatory support for owned, managed and consulting facilities; Serves as a lead for mock surveys; Serves as the Interim CNO and DQM roles when needed. Community Hospital Corporation (CHC), recently recognized as a 2026 Dallas Morning News Top Workplace and named to Becker’s list of 165 Top Places to Work in Healthcare, is seeking a Regional Director of Clinical and Regulatory Support for our Post-Acute hospitals.
NewCommercial Loan Closing Specialist CornerStone StaffingCommercial Loan Closing SpecialistDallas, TX$34–$43 / hourJoin a growing financial institution where your expertise in commercial loan operations will help ensure seamless closings, accurate funding, and exceptional service for both internal partners and clients. • Coordinate commercial loan closings by working with internal departments, legal counsel, title companies, and third-party vendors.
NewProperty Claims Adjuster Specialist - Field USAAProperty Claims Adjuster Specialist - FieldDallas, TX$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.
Licensed Pharmacy Benefits Specialist CornerStone StaffingLicensed Pharmacy Benefits SpecialistThe Colony, TX$22–$24 / hourAs a Pharmacy Benefits Support Specialist, you'll play an important role in helping patients and pharmacy partners navigate prescription benefit questions and claim-related concerns. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from CornerStone and its affiliates, and contracted partners.
NewPharmacy Benefits Support Specialist CornerStone StaffingPharmacy Benefits Support SpecialistThe Colony, TXThe Pharmacy Benefits Support Specialist provides accurate and timely assistance to patients and pharmacy partners regarding prescription benefits and claim-related questions. By applying for this position, you agree to receive calls, AI-generated calls, text messages, or emails from CornerStone and its affiliates and contracted partners.
NewCertified Pharmacy Support Specialist CornerStone StaffingCertified Pharmacy Support SpecialistThe Colony, TX$22–$24 / hourSuccess in this role comes from delivering compassionate support, maintaining accurate documentation, and ensuring every member receives a positive, seamless experience. Working closely with patients, healthcare providers, pharmacies, and assistance programs, you'll help remove barriers to prescription access while providing exceptional service throughout the process.
["Regulatory Affairs Specialist III","Regulatory Affairs Specialist III"] Cedent Life Talent["Regulatory Affairs Specialist III","Regulatory Affairs Specialist III"]PlanoThe Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices,software as a medical device, and de novo devices). Personal Attributes: Strong verbal and written communication skills, with the ability to articulate complex technical issues clearly and effectively to cross-functional teams and regulatory bodies.
Senior Regulatory Affairs Specialist EnovisSenior Regulatory Affairs SpecialistUSA, TXWorking as part of a global RA function, the role will also support in sustainable regulatory activities such as management of postmarket 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 Correspondence Specialist III","Regulatory Correspondence Specialist III"] NewRez LLC["Regulatory Correspondence Specialist III","Regulatory Correspondence Specialist III"]CoppellRequires 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 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.
NewREGULATORY 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 & Clinical Specialist LivaNova PlcRegulatory & Clinical SpecialistDallas, 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 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.
Clinical Research Regulatory Specialist Baylor Scott & White HealthClinical Research Regulatory SpecialistDallas, TXThis includes protocol revisions or amendments for new treatments, administrative changes, subject population changes, funding, recruitment, site changes, informed consent changes, or dual enrollment. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: Immediate eligibility for health and welfare benefits.
Regulatory & Clinical Specialist LivaNovaRegulatory & Clinical SpecialistDallas, 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 Compliance Exam Specialist Hankey Group ExternalRegulatory Compliance Exam SpecialistDallas, TexasWork closely with the Chief Compliance Officer and Regulatory Compliance Counsel to ensure that cited exceptions are in fact valid before developing and implementing a remediation/corrective action. In addition, the individual will be responsible for developing and implementing appropriate corrective actions to address deficiencies cited in federal regulatory and state examination reports.
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.
Midstream Regulatory And Compliance Specialist Matador Resources CompanyMidstream Regulatory And Compliance SpecialistDallas, TXThis role supports Matador's Midstream Regulatory Group by compiling data necessary to submit administrative filings required by the New Mexico Oil Conservation District (NMOCD) and other state and federal agencies regarding ongoing midstream operations, including gas gathering, gas processing, water gathering, water disposal and crude oil transportation. There is opportunity for this role to grow into a managerial position.
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.
NewRegulatory Affairs Expert - Remote YO AI LabsRegulatory Affairs Expert - RemoteDallas, TXRemoteThe role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content. We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation.
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.).
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, TexasNamed 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. The Research Regulatory Compliance Manager will work with Institutional Review Boards (IRBs), staff, sponsors, and investigators to achieve regulatory compliance related to the development, implementation, and management of IRB-approved clinical research across Methodist Health System and its affiliates.
Analyst, Regulatory Affairs Oscar Health InsuranceAnalyst, 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.
Manager, Regulatory Affairs And Compliance Nordson CorporationManager, Regulatory Affairs And ComplianceAllen, TXPrepares 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 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).
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.
Associate Director Regulatory Affairs - CMC Orano SAAssociate Director Regulatory Affairs - CMCPlano, TXRemotedata-css="[data-component="cookie-banner"] { --a-cookieBannerWidget-wrapper-color: #0000004D; --a-cookieBannerWidget-text-font-weight: 400; --a-cookieBannerWidget-text-text-decoration: none; --a-cookieBannerWidget-link-text-decoration: underline; --a-cookieBannerWidget-label-font-weight: 600; --a-cookieBannerWidget-label-text-decoration: none; --a-cookieBannerWidget-divider-border-style: solid; --a-cookieBannerWidget-text-margin-top: 0px; --a-cookieBannerWidget-text-margin-right: 0px; --a-cookieBannerWidget-text-margin-bottom: 0px; --a-cookieBannerWidget-text-margin-left: 0px; --a-cookieBannerWidget-text-padding-top: 0px; --a-cookieBannerWidget-text-padding-right: 0px; --a-cookieBannerWidget-text-padding-bottom: 0px; --a-cookieBannerWidget-text-padding-left: 0px; --a-cookieBannerWidget-divider-margin-top: 24px; --a-cookieBannerWidget-divider-margin-right: 0px; --a-cookieBannerWidget-divider-margin-bottom: 24px; --a-cookieBannerWidget-divider-margin-left: 0px; --a-cookieBannerWidget-divider-border-width: 1px; }">. Orano's activities in the U.S. include developing uranium enrichment facility in Oak Ridge, TN; packages and transportation of uranium & nuclear fuel assemblies; fabricating & installing used nuclear fuel dry storage canisters and casks, conducting pool-to-pad used nuclear fuel transfers; providing solutions to the National Labs and to the Dept of Energy; and supplying U.S. nuclear energy utilities with uranium, conversion, and enrichment services.
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 Counsel, Legislative & Regulatory Affairs Public StorageSenior Counsel, Legislative & Regulatory AffairsFrisco, TXThis individual will work closely with Legal, Operations, Compliance, Revenue Management, Marketing, Call Center, Insurance/Risk, and senior business leaders to monitor, interpret, and help shape legislative and regulatory developments affecting Public Storage and the self-storage industry. This role is well suited for someone who enjoys working across legal, business, and policy issues; can move comfortably between detail-oriented statutory analysis and executive-level guidance; and wants to help build a scalable legislative and regulatory affairs function for a national business.
Regulatory Affairs Coordinator RousselotRegulatory Affairs CoordinatorIrving, TXFull timeWeight and Force DemandsNoneOccasionally = up to 20%Frequently = 21% to 50%Constantly = at least 51%Up to 10 poundsUp to 25 pounds Up to 50 poundsUp to 100 poundsMore than 100 pounds Vision DemandsRequired No special vision requirementsClose vision (clear vision at 20 inches or less)Distance vision (Clear vision at 20 feet or more)Color vision (ability to identify and distinguish colors)Peripheral visionDepth perceptionAbility to adjust focus. The ability to competently perform all the essential duties of the position, with or without reasonable accommodation, demonstrated commitment to effective customer service delivery, integrity, and the ability to work productively as a member of a team or work group are basic requirements of all positions at Darling Ingredients.
NewExecutive Director, Regulatory Affairs Castle Biosciences IncExecutive Director, Regulatory AffairsFrisco, TXThe Executive Director combines strategic leadership with a hands-on approach, supporting product development, commercialization, lifecycle management, and regulatory submissions across U.S. and international markets. As the regulatory leader for a molecular diagnostics laboratory and medical device manufacturer, the Executive Director shapes and executes regulatory strategies and operations that support product development, commercialization, and ongoing compliance with regulatory requirements.
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.
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.
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.
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.
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.
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.
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.
NewRegional Director Of Clinical And Regulatory Support (Post-Acute) Community Hospital CorporationRegional Director Of Clinical And Regulatory Support (Post-Acute)Plano, TXUnder the supervision of the VP of Clinical Services for Post-Acute Services, the Regional Director of Clinical and Regulatory support: Supports clinical and quality initiatives for owned, managed, and consulting facilities by providing support to field CNO’s and DQMs; Serves as the infection control specialist for post-acute services and is responsible for developing, implementing and coordinating a consistent approach to infection prevention and control; Supports Regulatory compliance and provides regulatory support for owned, managed and consulting facilities; Serves as a lead for mock surveys; Serves as the Interim CNO and DQM roles when needed. Community Hospital Corporation (CHC), recently recognized as a 2026 Dallas Morning News Top Workplace and named to Becker’s list of 165 Top Places to Work in Healthcare, is seeking a Regional Director of Clinical and Regulatory Support for our Post-Acute hospitals.
Regional Director Of Clinical And Regulatory Support Community Hospital CorporationRegional Director Of Clinical And Regulatory SupportPlano, TXUnder the supervision of the VP of Clinical Services for Post-Acute Services, the Regional Director of Clinical and Regulatory support: Supports clinical and quality initiatives for owned, managed, and consulting facilities by providing support to field CNO’s and DQMs; Serves as the infection control specialist for post-acute services and is responsible for developing, implementing and coordinating a consistent approach to infection prevention and control; Supports Regulatory compliance and provides regulatory support for owned, managed and consulting facilities; Serves as a lead for mock surveys; Serves in interim CNO and DQM roles as requested by the VP Clinical Services; and. Community Hospital Corporation (CHC), recently recognized as a 2026 Dallas Morning News Top Workplace and named to Becker’s list of 165 Top Places to Work in Healthcare, is seeking a Regional Director of Clinical and Regulatory Support for our Post-Acute hospitals.
Consultant, Rates & Regulatory Black & Veatch Holding CoConsultant, Rates & RegulatoryDallas, TXRecognized by Glassdoor as a 2023 Top 100 place to work and winner of the Newsweek's 2023 America's Greatest Workplaces for Diversity, Black & Veatch allows you to lend your talent and perspective to humanity's biggest challenges in a flexible environment where you are empowered to grow and explore new possibilities. Black & Veatch's Infrastructure Advisory Business provides a portfolio of solutions focused on the asset lifecycle, including Asset Management & Operations & Maintenance, Infrastructure Technology, Cybersecurity Solutions, Planning, and Transactions.
Executive Director, Regulatory Management, Network Standards & Technology Transformation CVS Health CorpExecutive Director, Regulatory Management, Network Standards & Technology TransformationDallas, TX$131,500–$303,195 / yearThe candidate will be expected to have the following key attributes: 10+ years of progressive leadership experience in PBM, healthcare, pharmacy operations, regulatory compliance, technology, program management, or related healthcare disciplines. Partner with Legal, Compliance, Regulatory Affairs, Government Affairs, Finance, Digital, and Operations teams to evaluate business impacts, establish implementation strategies, and ensure timely execution.
QA/RA Specialist - Pharmaceutical GLP/GMP Experience synergyQA/RA Specialist - Pharmaceutical GLP/GMP ExperienceDallas, TexasThe 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.
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.
NewDocumentation Control Specialist Actalent IncDocumentation Control SpecialistDallas, TX$23–$25 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Compliance & Legal Specialist Lifespace CommunitiesCompliance & Legal SpecialistDallas, Texas$73,600–$101,200 / yearIf you're passionate about healthcare compliance, enjoy solving complex regulatory challenges, and want to make an impact beyond paperwork, this is an opportunity to build a meaningful career while helping protect residents, team members, and the organization. You'll be more than a compliance administrator, you'll become a trusted business partner helping shape compliance strategy, support investigations, coordinate audits, manage legal documentation, strengthen privacy initiatives, and foster an ethical culture across the organization.
Credential Specialist II Exceptional Healthcare Inc.Credential Specialist IIDALLAS, TXJob Responsibilities/Duties: Key Responsibilities Manage full-cycle credentialing and recredentialing processes for physicians across multiple hospital locations and states to ensure compliance with payors. Job Summary: The Credentialing Specialist II is responsible for managing the end-to-end credentialing and privileging process for physicians across a multi-state hospital system.
Legal Operations Specialist TalentRemedyLegal Operations SpecialistArlington, TexasPosition Overview: The Legal Operations Specialist is responsible for supporting compliance-related initiatives, including political law compliance, monitoring and tracking developments related to legal affairs, coordinating internal legal operations processes, and assisting with the implementation of association policies and procedures, as well as supporting the legal affairs team in day-to-day functions. Company Overview: A leading trade association representing some of the most recognized and trusted consumer brands, this organization plays a vital role in shaping the policies and conversations that impact products people rely on every day.
AI Data Governance Specialist Ampcus IncorporatedAI Data Governance SpecialistDallas, TXThis role will focus on ensuring data quality, compliance, lineage, and ethical AI practices while supporting scalable machine learning operations in a retail environment. We are seeking an experienced AI Data Governance Specialist to lead governance initiatives for AI/ML data across enterprise-scale platforms.