NewTerritory Operations Specialist (Overnight 7pm - 4am) Summit Pharmacy Solutions LLCTerritory Operations Specialist (Overnight 7pm - 4am)Saint Paul, MNThe TOS is responsible for managing the full driver lifecycle within their territory - recruiting, contracting, training, engaging and holding drivers accountable - while also serving as the primary operational escalation point for centralized dispatch during second shift and night hours. Account & Territory Knowledge: Maintain working familiarity with all accounts in the territory - SLAs, delivery windows, facility contacts, and escalation preferences - sufficient to support any account after hours without degrading service.
Medical Communication Specialist, Atlanta, GA UCBMedical Communication Specialist, Atlanta, GAAtlanta, GA$108,000–$141,000 / yearYou will serve as a trusted resource and subject matter expert, responding to medical inquiries, interpreting scientific literature and clinical data, and ensuring responses are balanced, compliant, and aligned with applicable regulations and company policies. We are looking for a Medical Communication Specialist who is scientifically curious, customer-focused, and compliance-minded to join us in our Epilepsy & Rare Syndromes US team, based in our Atlanta, GA headquarters.
REGULATORY SPECIALIST III - 64003616 Government of FloridaREGULATORY SPECIALIST III - 64003616TALLAHASSEE, FL$36,317.26–$38,000 / yearReview Osteopathic Physician, Osteopathic Resident Registration, Osteopathic Limited License, Osteopathic Expert Witness, Osteopathic Physician in an Area of Critical Need, Speech-Language Pathologist, Audiologist, Speech-Language Pathologist Assistant, Audiologist Assistant, Provisional Speech-Language Pathologist, Provisional Audiologist, Acupuncture, and military (VALOR, waiver) applications on the Initial Apps report to monitor the workflow and ensure processors are processing initial apps in less than ten days. The incumbent serves as the subject matter expert for Speech-Language Pathology and Audiology licensure and as a processor for Osteopathic Physician, Osteopathic Resident Registration, Osteopathic Limited License, Osteopathic Expert Witness, Osteopathic Physician in an Area of Critical Need, Speech-Language Pathologist, Audiologist, Speech-Language Pathologist Assistant, Audiologist Assistant, Provisional Speech-Language Pathologist, Provisional Audiologist, Acupuncture, and military (VALOR, waiver) applications.
Regulatory Affairs Manager, Companion Diagnostics F. Hoffmann-La Roche LtdRegulatory Affairs Manager, Companion DiagnosticsIndianapolis, IN$106,100–$197,000 / yearYou have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders.
Remote Regulatory Affairs contractor GlobalchannelmanagementRemote Regulatory Affairs contractorAtlanta, GeorgiaRemoteAuthor, compile and deliver a complete 510k submission, including preparation in FDA eSTAR format, Lead submission lifecycle activities, including: Acceptance Review support (RTA readiness). Conduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable) to ensure completeness, quality, and regulatory compliance.
Regulatory Affairs Manager, Companion Diagnostics RocheRegulatory Affairs Manager, Companion DiagnosticsIndianapolis, IndianaYou have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders.
NewAssociate Director / Director, Regulatory Affairs CMC ImmunomeAssociate Director / Director, Regulatory Affairs CMCBothell, WashingtonThis person will collaborate cross-functionally with teams including Technical Operations, Quality Assurance, Supply Chain Management, and Project Management to maintain alignment with regulatory CMC strategies and compliance requirements. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates.
Director / Senior Director of Regulatory Affairs PathosDirector / Senior Director of Regulatory AffairsNew YorkDirect IND lifecycle management experience: you have owned INDs from filing through amendment cycles, authored DSURs, prepared IB updates, and built FDA meeting packages as the primary author. That means authoring DSURs, preparing IB updates and IND amendments, building FDA meeting packages, managing ClinicalTrials.gov listings, and overseeing eCTD publishing.
Actuarial & Regulatory Filing Specialist Hankey Group ExternalActuarial & Regulatory Filing SpecialistLos Angeles, CaliforniaThis role is designed to bring much of the actuarial filing work currently outsourced in-house, enabling KnightBrook to manage routine CDI and TDI rate, rule, and form filings internally while leveraging external consultants only for specialized or large-scale projects. The ideal candidate will have direct experience preparing and managing California Department of Insurance (CDI) and Texas Department of Insurance (TDI) filings for personal auto and homeowners insurance products and be comfortable owning projects from actuarial analysis through regulatory approval.
Director, Regulatory Affairs – Global Regulatory Strategy Monte Rosa Therapeutics, IncDirector, Regulatory Affairs – Global Regulatory StrategyBoston, MassachusettsFull timeOverview: Monte Rosa Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our development programs, with a focus on immunology. Lead the preparation, submission, and maintenance of regulatory applications, including INDs, CTAs, marketing applications, Annual Reports, Orphan Drug Designation, Requests for Fast Track, and other regulatory documents.
Quality Assurance Document Control Specialist- Entry Level Thorne Research IncQuality Assurance Document Control Specialist- Entry LevelSummerville, SCThe Quality Assurance Document Control Specialist I supports Thorne''s Quality Management System (QMS) by maintaining the accuracy, integrity, and lifecycle of controlled documents and quality records. The ideal candidate is highly organized, detail-oriented, and committed to maintaining documentation accuracy, regulatory compliance, and continuous improvement within a regulated manufacturing environment.
Manager, 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.
NewSenior LOB Risk Specialist - Regulatory Reporting and Internal Controls The PNC Financial Services Group IncSenior LOB Risk Specialist - Regulatory Reporting and Internal ControlsPittsburgh, PAServe as the primary LOB contact to support and advise management in their effort to manage risk and controls effectively as they relate to FGO in-scope programs by understanding their LOB and bringing in FGO Reporting Risk subject matter expertise and process excellence. In addition, PNC generally provides the following paid time off, depending on your eligibility: maternity and/or parental leave; up to 11 paid holidays each year; 9 occasional absence days each year, unless otherwise required by law; between 15 to 25 vacation days each year, depending on career level; and years of service.
Traveling Recertification Specialist Pratum CompaniesTraveling Recertification SpecialistSterling/Dulles, VA, DCRemote$22–$26 / hourFull timeAlthough the Washington DC Metropolitan area, including Virginia and Maryland are primarily be where support is needed, such that reliable transportation for regional travel is a requirement , - This role will require travel nationwide to support third party management clients, as well as supporting Pratum's portfolio within the Washington DC Metropolitan area, including Virginia and Maryland are primarily be where support is needed, such that reliable transportation for regional travel is a requirement, overnight and multi-day travel to any state for operational coverage is a requirement of the role. This role is non-exempt and has an anticipated hourly pay range of $22-$26/hour (~$45k-54k annually) for a new employee depending on a number of relevant factors including individuals’ experience, qualifications, knowledge, skills, abilities, client/property or company budgetary limitations/guidelines, and other job-related company and market considerations.
Traveling Recertification Specialist (C&L - Affordable Housing Compliance) Pratum CompaniesTraveling Recertification Specialist (C&L - Affordable Housing Compliance)Gaithersburg, MDRemote$22–$26 / hourFull timeAlthough the Washington DC Metropolitan area, including Virginia and Maryland are primarily be where support is needed, such that reliable transportation for regional travel is a requirement , - This role will require travel nationwide to support third party management clients, as well as supporting Pratum's portfolio within the Washington DC Metropolitan area, including Virginia and Maryland are primarily be where support is needed, such that reliable transportation for regional travel is a requirement, overnight and multi-day travel to any state for operational coverage is a requirement of the role. This role is non-exempt and has an anticipated hourly pay range of $22-$26/hour (~$45k-54k annually) for a new employee depending on a number of relevant factors including individuals’ experience, qualifications, knowledge, skills, abilities, client/property or company budgetary limitations/guidelines, and other job-related company and market considerations.
NewAssoc Dir, Public Affairs & Policy (Neurology) Les Laboratoires Servier SASAssoc Dir, Public Affairs & Policy (Neurology)Washington, DCRemote$156,000–$185,000 / yearClearly and strategically articulate Servier's positions on assigned Neurology policy issues as the substantive policy lead, under supervision of Policy leadership and in coordination with Government Affairs for external advocacy strategy and the Oncology policy lead for cross-portfolio alignment. Represent Public Affairs and Policy as the Neurology policy subject matter expert to colleagues in US Market Access and other internal stakeholders on enterprise project teams, committees, etc., coordinating with the Oncology policy lead where issues span across the portfolio.
Regulatory and Litigation Counsel, Content Google LLCRegulatory and Litigation Counsel, ContentSan Francisco, CAGoogle is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting. Experience engaging with regulators, such as State Attorneys General, the Federal Trade Commission (FTC), Department of Justice (DoJ), and other content and media/consumer protection authorities.
NewCompliance Specialist – Regulatory / HR CFSCompliance Specialist – Regulatory / HRGaithersburg, MD$100,000–$125,000 / yearJoin a highly visible, enterprise-wide compliance role where you’ll partner directly with Legal and HR leadership to shape and strengthen regulatory strategy. You’d be working with a stable organization, in a collaborative work environment, which offers great benefits (100% healthcare for employee) and they work a hybrid schedule!
Education Specialist (COMPASS Program) Global Kids IncEducation Specialist (COMPASS Program)New York, NY$57,000–$65,000 / yearFull timeDirector for Academic Programs and Quality Assurance, the Education Specialist collaborates closely with school-based Program Directors and staff to plan and support staff in implementing engaging, developmentally appropriate programming for youth in grades K–8. Develop structured, engaging, culturally responsive, and developmentally appropriate scopes and sequences, lesson plans, and enrichment activities aligned with NYCPS and DYCD priority content areas, including: Social-Emotional Learning (SEL).
Mechatronics Specialist Company ConfidentialMechatronics SpecialistNorth Las Vegas, NVFull timeWe are seeking a Master Mechatronics Specialist with expertise in radio frequency utilization, Computer Numerical Control (CNC) machinery operation, multisystem integration, and the ability to fabricate custom/prototype Unmanned Aerial Vehicles (UAV)s. ● Documentation: Document aeronautical and electronic design and components research, collect and analyze radio frequencies in testing and performance environments.
Activity Specialist Global Kids IncActivity SpecialistNew York, NY$25–$30 / hourPart timeGlobal Kids, Inc. is seeking creative, hard-working, and passionate individuals who are experienced in youth development, academic support, global education, and social action, and are interested in working in New York City public Middle Schools. Hours/Wages/Benefits: Activity Specialists will be required to work September – June during after-school hours, plus additional hours of training, preparation, and follow-up time at a time to be scheduled with GK staff (typically between 2:00 pm -6:00 pm M-F, depending on the site placement).
Desktop Trade Floor Support Specialist Raas Info Solutions Pvt LtdDesktop Trade Floor Support SpecialistChicago, ILContractorThe position requires deep technical expertise, exceptional customer service, and superb communication skills to build strong relationships with business users and stakeholders at all levels, including Innovation & Engineering DWP (I&E). Maintain familiarity with office network topology, network closets, and demarcation points; assist with implementing fixes on network devices such as switches, routers, firewalls, wireless access points under remote guidance.
NewRegional Director of Clinical and Regulatory Support Community Hospital CorporationRegional Director of Clinical and Regulatory SupportPlano, 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 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.
Senior Accounting Specialist Kforce Inc.Senior Accounting SpecialistJacksonville, FL$59,075–$79,925Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. The ideal candidate is highly organized, detail-oriented, able to manage multiple priorities effectively, and capable of working independently while accurately following verbal instructions.
Quality & Regulatory Affairs AxelonQuality & Regulatory AffairsGlenview, ILInvestigate customer/consumer complaints using root cause analysis and work with department managers to determine necessary corrective and preventive actions. Provide technical information and evaluate regulatory compliance of products while adhering to internal policies and guidelines for exporting products.
Payroll Specialist Kforce Inc.Payroll SpecialistFenton, MO$50,000–$70,000Summary: This is an excellent opportunity to join a stable organization with a collaborative team environment where you'll play a key role in processing payroll, ensuring compliance, and supporting accounting operations. By clicking “Apply Today” you agree to receive calls, AI-generated calls, text messages or emails from Kforce and its affiliates, and service providers.
NewCommunications Specialist Kforce Inc.Communications SpecialistJuno Beach, FL$30–$34.25Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. By clicking “Apply Today” you agree to receive calls, AI-generated calls, text messages or emails from Kforce and its affiliates, and service providers.
Payroll and Benefits Specialist CFSPayroll and Benefits SpecialistSarasota, FL$70,000–$75,000 / yearProcess and audit bi-weekly payroll for 300 employees, including sales commission and bonuses with full ownership of accuracy and compliance. The Payroll and Benefits Specialist will serve as primary point of contact for payroll, benefits, HRIS, and leave-related inquiries.
NewPayroll Specialist CFSPayroll SpecialistSeattle, WAIf you’re a detail‑driven payroll professional ready to support a complex, high‑volume environment as a Payroll Specialist, this is a strong opportunity to join a well‑established organization with a North America workforce. You’ll play a key role in ensuring payroll is processed with speed, precision, and compliance while partnering closely with internal stakeholders.
NewAccounting Operations Specialist CFSAccounting Operations SpecialistPittsburgh, PA$55,000–$65,000 / yearYou'll join a supportive team where accuracy, collaboration, and exceptional member service are highly valued while enjoying outstanding benefits and long-term career stability. Review and process share draft exceptions while serving as a point of contact for member inquiries related to ACH and share draft services.
NewAccounting Specialist CFSAccounting SpecialistDayton, OHThis role is responsible for maintaining the general ledger, processing accounts payable, performing reconciliations, preparing journal entries, and assisting with month-end close. We are seeking a detail-oriented Accounting Specialist to support daily accounting operations and ensure the accuracy of financial records.
NewExport Compliance Specialist CFSExport Compliance SpecialistCleveland, OH$70,000–$90,000 / yearAnalyze transactions for export license applicability and manage the full export license lifecycle, including experience with SNAP-R and DECCS government application systems. Collaborate with engineering, operations, and other cross-functional teams to gather technical information needed for export classifications.
NewSr Medical Billing/Insurance Follow up Specialist CFSSr Medical Billing/Insurance Follow up SpecialistGreenwood, IN$45,000–$70,000 / yearKey Responsibilities for the Senior Medical Billing Specialist: • Manage end-to-end medical billing, including complex and high-dollar claims. Why This Opportunity Stands Out: • Operate at a higher level of the revenue cycle, managing claims from submission through final resolution.
NewLoan Servicing Specialist I Peoples Security Bank & Trust CompanyLoan Servicing Specialist IMoosic, PAWhile performing the essential job functions of this position, the employee is regularly required to sit, stand, talk, hear, walk, use hands and fingers, handle or feel objects, and reach with hands and arms. Peoples Security Bank & Trust Company is seeking a Loan Servicing Specialist to support the full lifecycle of our commercial, consumer, and real estate loan portfolios.
NewPer Diem / PRN Nurse RN - Clinical Document Improvement Specialist - $37-56 per hour United Health ServicesPer Diem / PRN Nurse RN - Clinical Document Improvement Specialist - $37-56 per hourBinghamton, NY$37–$56 / hourThe Clinical Documentation Improvement (CDI) Specialist-RN is a registered nurse responsible for performing concurrent and retrospective reviews of inpatient medical records to ensure complete, accurate, and compliant clinical documentation. This role works closely with providers, coders, and quality teams to clarify documentation and support accurate data capture for clinical, financial, and regulatory reporting.
NewVocational Educational Specialist LESCVocational Educational SpecialistCrotona Park, NY$50,000–$52,000 / yearWe offer excellent benefits including: Generous time off that includes 4 weeks of vacation Medical, Dental, and Vision Insurance Discounted Commuter benefits Life insurance & Long term disability Eligible for Federal Student Loan Repayment Program Training and other additional voluntary benefits To join our diverse team, please include a cover letter and salary requirements with your resume/application submission. Description: BASIC FUNCTION: To assist residents in obtaining necessary vocational skills, interests and work attitudes in order to secure employment/educational opportunities through face-to-face contacts in conjunction with inter-disciplinary team and service plan.
NewWealth Management Client Sales Specialist First Horizon BankWealth Management Client Sales SpecialistLafayette, LACoordinate and execute activities such as account paperwork fulfillment, account representative changes, and various project support • Fulfill financial advisor requests and resolve service-related issues and inquiries • Process tasks and resolve issues in a timely and accurate manner • Ensure adherence to compliance operating policies and procedures including maintaining confidentially and client privacy at all times • Maintain a focus on continuous improvement and provides feedback on system enhancements • Master technology to ensure it is being used to its full benefit. Essential Duties And Responsibilities • Under general supervision, provide overall support to management, advisors and other support staff including, operating the firms business process management system, maintaining appropriate files, monitoring multiple email inboxes, working with back office to ensure processing is completed, handling of inbound calls/requests when needed and all other facets of support activities assigned.
Principal Regulatory Affairs Specialist Elucent MedicalPrincipal Regulatory Affairs SpecialistEden Prairie, MinnesotaThe Principal Regulatory Affairs Specialist independently performs regulatory impact assessments for product design, manufacturing, labeling, software, process, supplier, and site changes; prepares technical documentation and regulatory submissions; supports implementation of regulatory pathways and strategies established by the Regulatory Affairs Director; and provides regulatory analysis to support product development, commercialization, change control, and post-market activities. Required: direct, hands-on experience preparing and supporting FDA 510(k)s for medical devices, including substantial equivalence documentation, submission compilation, FDA question responses, and clearance support.
Specialist Quality Assurance, Regulatory Affairs And Work Environment Management DBA: Zeiss GroupSpecialist Quality Assurance, Regulatory Affairs And Work Environment ManagementStockholm, METhe role Specialist Quality Assurance, Regulatory Affairs and Work Environment Management of will involve: Maintain, develop, and evaluate the ZEISS Nordics Quality Management System across all Nordic sites. In the Nordics, ZEISS has direct sales and service representation in all four countries and employs a network of Account Managers, Product and Applications Specialists and a strong Field Service team.
Senior Regulatory Affairs Specialist - Animal Health Cencora IncSenior Regulatory Affairs Specialist - Animal HealthPAYou will work closely with internal and client stakeholders across Regulatory Affairs, Quality, Manufacturing, Pharmacovigilance, Supply Chain, and Commercial teams to help ensure regulatory objectives are delivered efficiently and compliantly. This is an exciting opportunity for a regulatory professional who enjoys working across the full product lifecycle and partnering with cross-functional teams to deliver compliant, timely, and high-quality regulatory outcomes.
Senior Regulatory Affairs Specialist - Animal Health Cencora, Inc.Senior Regulatory Affairs Specialist - Animal HealthRemote, PARemoteYou will work closely with internal and client stakeholders across Regulatory Affairs, Quality, Manufacturing, Pharmacovigilance, Supply Chain, and Commercial teams to help ensure regulatory objectives are delivered efficiently and compliantly. This is an exciting opportunity for a regulatory professional who enjoys working across the full product lifecycle and partnering with cross-functional teams to deliver compliant, timely, and high-quality regulatory outcomes.
Regulatory Affairs Specialist CorDxRegulatory Affairs SpecialistAlpharetta, GAWith over 2000 employees across the world serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious diseases such as COVID-19, pregnancy, drug abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Sr. Regulatory Affairs Specialist Caldera Medical IncSr. Regulatory Affairs SpecialistWestlake Village, CADuties and Responsibilities: Prepare, review, and submit and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA, ANVISA, ANMAT, and other relevant regulatory bodies and/or Distributors. From developing and authoring regulatory submissions to providing critical input on cross-functional project teams you will ensure submissions are accurately prepared and comply with global regulations.
Regulatory Affairs Specialist V eTeam Inc.Regulatory Affairs Specialist VLake Forest, CAThe role involves setting or executing regulatory strategy, leading and managing as a strategist, ensuring local product registration, facilitating health registration approvals, and supporting the Senior Director during due diligence and integration activities for Business Development & Licensing projects. A self-starter, assertive leader who will be accountable for the end-to-end regulatory support for the anterior/posterior ophthalmologic products, including new products, sustaining legacy products, and improvements to the product lines.
Regulatory affairs specialist Karwell TechnologiesRegulatory affairs specialistMinneapolis, MNThe ideal candidate will possess deep knowledge of U.S. and international medical device regulations, strong analytical capabilities, and the ability to collaborate effectively across cross-functional teams to drive compliance and continuous improvement initiatives. This role is responsible for ensuring compliance with global regulatory requirements related to product incident reporting, corrective and preventive actions (CAPA), recalls, field actions, audits, and post-market surveillance activities.
Regulatory Affairs Specialist Patterson Companies IncRegulatory Affairs SpecialistSt Paul, MN$77,200–$100,333.33 / yearStrong verbal and written communications with ability to effectively communicate at specialist and line management levels in the organization; strong customer service-oriented skills. Ability to work effectively within a team and as an individual contributor in a fast-paced changing environment -- multi-tasks, prioritizes and meet deadlines in timely manner.
NewSenior Regulatory Affairs Specialist Intuitive Surgical IncSenior Regulatory Affairs SpecialistSunnyvale, CACertain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.
Regulatory Affairs Specialist, Cosmetics and OTC Personal Care, Growing Contract Manufacturer Pave TalentRegulatory Affairs Specialist, Cosmetics and OTC Personal Care, Growing Contract ManufacturerOttawa, Illinois2 to 4 years of Regulatory Affairs experience within cosmetics, personal care, or OTC manufacturing — beauty industry backgrounds strongly preferred; pharma-only or food backgrounds will not be considered. You will report to the Global Manager of Regulatory Affairs and serve as that person's key specialist, supporting compliance across a broad portfolio of cosmetic, personal care, and OTC drug products.
NewAssociate Specialist, Regulatory Affairs Operations TMTT Edwards LifesciencesAssociate Specialist, Regulatory Affairs Operations TMTTCalifornia$59,000–$83,000 / yearWorking in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs.