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.
Regulatory Affairs Specialist - Agriculture Hybrid BelcanRegulatory Affairs Specialist - Agriculture HybridChesterfield, MOHybrid position TASKS AND RESPONSIBILITIES: * Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products * Communicate with State regulatory agencies regarding submissions, approvals, renewals * Maintain and update regulatory databases and other internal tracking systems. * Scan regulatory and supporting documents, file in databases and/or mail to designated recipients REQUIRED: * BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience * Proficiency in the Microsoft Office suite * Database Management experience * Experience with document comparison tools is a plus.
Regulatory Affairs Specialist - Agriculture Remote BelcanRegulatory Affairs Specialist - Agriculture RemoteChesterfield, MORemoteRemote Position TASKS AND RESPONSIBILITIES: * Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA for crop protection products * Communicate with State regulatory agencies regarding submissions, approvals, renewals * Maintain and update regulatory databases and other internal tracking systems. * Scan regulatory and supporting documents, file in databases and/or mail to designated recipients REQUIRED: * BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience * Proficiency in the Microsoft Office suite * Database Management experience * Experience with document comparison tools is a plus.
Regulatory & Compliance Specialist CorDxRegulatory & Compliance SpecialistSan Diego, CA$90,000–$95,000 / yearWith over 2,100 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 disease such as COVID-19, pregnancy, drugs of 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.
Senior Regulatory Affairs Specialist - Manager Synaptic Medical LLCSenior Regulatory Affairs Specialist - ManagerCarlsbad, CAKey responsibilities: Lead the regulatory strategy for new product development and market entry, including 510(k), PMA, and CE Mark submissions. What we are looking for: Bachelor's degree in a scientific, engineering, or related field (RAC certification or advanced degree a plus).
Regulatory Specialist Globus Medical IncRegulatory SpecialistPAPosition Summary: The Regulatory Affairs Specialist assists with drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. Minimum of 2-5 years' experience in Regulatory Affairs in the medical device industry,, preferably within orthopedic medical devices; Experience in medical device development and registration of products.
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.
NewRegulatory Operations Specialist Caldera Medical IncRegulatory Operations SpecialistWestlake Village, CARequired Knowledge, Skills and Abilities: 1-3 years in regulatory operations, regulatory affairs, document control, quality, or a related medical device function - or a strong adjacent data/administrative role with regulatory exposure. Maintain the master registration matrix and renewal tracker (license/registration data, classifications, license holder, expiry dates, certificate links), updating weekly from RA Specialists, contractors, and ARs.
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.
Sr Extern Affairs Specialist - BGE Permitting ExelonSr Extern Affairs Specialist - BGE PermittingBALTIMORE, MDWe are a Fortune 200 company, 20,000 colleagues strong serving more than 10.7 million customers at six energy companies -- Atlantic City Electric (ACE), Baltimore Gas and Electric (BGE), Commonwealth Edison (ComEd), Delmarva Power & Light (DPL), PECO Energy Company (PECO), and Potomac Electric Power Company (Pepco). + Bachelor’s degree in political science, communications, business administration, and/or public relations AND 4-7 years related experience in governmental affairs, customer service, communications, or relevant utility experience OR, in lieu of a bachelor’s degree, 6-9 years relevant experience is required.
NewSupervisory Public Affairs Specialist U.S. Department of the InteriorSupervisory Public Affairs SpecialistWashington, DC$106,437–$138,370 / yearNOTE: Applicants claiming eligibility under VEOA or VRA, must submit a copy of your DD-214, "Certificate of Release or Discharge from Active Duty," (Member 4 copy is preferred), showing the dates of active duty, type of discharge, and character of service (must be honorable); OR acceptable proof of verification of your preference (i.e., official document, dated 1991 or later, from the Department of Veterans Affairs, or from a branch of the Armed Forces, certifying that the veterans total combined serviced-connected disability rating is 10% or more). NOTE: Applicants claiming eligibility based on 30% or more service connected disability, you are required to submit documentation that is indicated on the SF-15 as acceptable proof of verification of your preference (i.e., official document, dated 1991 or later, from the Department of Veterans Affairs, or from a branch of the Armed Forces, certifying that the veterans total combined serviced-connected disability rating is 30% or more.
Regulatory Specialist Science CorpRegulatory SpecialistAlameda, CA$140,000–$185,000 / yearThis role will drive global regulatory strategies for our medical device and biologic products, guide cross-functional teams through complex regulatory pathways, and ensure our innovative technology reaches patients safely and efficiently. Spearhead rapid response efforts to regulatory agency communications, including deficiency letters, requests for additional information, and pre-submission feedback; drafting clear, persuasive responses while managing tight turnaround time.
Senior Account Supervisor, Public & Government Affairs Daniel J. Edelman, Inc.Senior Account Supervisor, Public & Government AffairsWashington, DC$80,000–$120,000 / yearBring knowledge of, or strong interest in energy policy issues, including areas such as energy production, transmission, grid reliability, clean energy, permitting, infrastructure, manufacturing, climate, sustainability, and federal or state energy policy debates. An employee's pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, travel requirements, revenue-based metrics, any contractual agreements, and business or organizational needs.
Compliance Specialist - AZ - On Site Vensure Employer SolutionsCompliance Specialist - AZ - On SiteChandler, AZAssociate or bachelor's degree in Business Administration, Finance, Accounting, Law, Compliance, or related field (preferred) or related experience required or equivalent combination of experience, skills, education (including other relevant non-traditional degree programs, or job training programs) preferred. About UsVensure Employer Solutions is the largest privately held organization in the HR technology and service sector, providing a comprehensive portfolio of solutions, including HR/HCM technology, managed services, and global business process outsourcing (BPO).
New["Regulatory Affairs Analyst","Regulatory Affairs Analyst"] Careers Integrated Resources["Regulatory Affairs Analyst","Regulatory Affairs Analyst"]Baton RougePosition Summary: · Under the general direction of the Director of Compliance and Regulatory Affairs, the Regulatory Affairs Analyst assists in developing procedures to ensure regulatory compliance and foster open communication between the client and the Louisiana Department of Health and Hospitals (DHH). A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Engineering Specialist, Quality Fresenius Kabi AGEngineering Specialist, QualityNorth Andover, MA$160,000–$170,000 / yearStrengthen and maintain the QMS structure for design and software quality by defining workflows, templates, and governance for document control, change control, design reviews, DHF/DMR readiness, and inspection preparedness. • Position is eligible to participate in a bonus plan with a target of 15% of the base salary (include only if applicable to the grade level) • Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Labelling Specialist IconmaLabelling SpecialistCupertino, CA$62.16–$67.16 / hourParticipate in design and change control processes to update labelling related to new product developments product changes or regulatory updates. Responsibilities:Leads the Instructions for Use (IFU) creation and ensures compliance to global regulatory requirements, completes labeling reviews to verify compliance of labeling, and implements IFU with cross functional teams.
Labelling Specialist Iconma LLCLabelling SpecialistCupertino, CAParticipate in design and change control processes to update labelling related to new product developments product changes or regulatory updates. Responsibilities: Leads the Instructions for Use (IFU) creation and ensures compliance to global regulatory requirements, completes labeling reviews to verify compliance of labeling, and implements IFU with cross functional teams.
Documentation 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.
Labelling Specialist Pride GlobalLabelling SpecialistCupertino, CA$67.16–$67 / hourParticipate in design and change control processes to update labelling related to new product developments product changes or regulatory updates. • Leads the Instructions for Use (IFU) creation and ensures compliance to global regulatory requirements, completes labeling reviews to verify compliance of labeling, and implements IFU with cross functional teams.
Supervisory Inventory Management Specialist U.S. Department of Veterans AffairsSupervisory Inventory Management SpecialistLouisville, KY$74,678–$97,087 / yearSpecialized experience is defined as: planning, coordinating and executing an inventory and commodity management program; establishing procedures, overseeing and reviewing physical inventories and supply reconciliations; conducting data/information analysis for acquisition planning; planning and reviewing supply/inventory processes, functions and related systems; and exercising supervisory responsibilities to include planning, assigning and evaluating work and resolving complaints. Please use this checklist to make sure you have included other documents required for your application, such as a copy of your transcript (if using education to qualify), SF-50s (current/former Federal employees), documentation to support Veterans Preference claims, or ICTAP/CTAP documentation (for displaced Federal employees).
NewClinical Pharmacy Specialist (Gastroenterology and Hepatology) U.S. Department of Veterans AffairsClinical Pharmacy Specialist (Gastroenterology and Hepatology)Washington, DC$156,091–$202,921 / year2) Graduates of foreign pharmacy degree programs meet the educational requirement if the graduate can provide proof of achieving the Foreign Pharmacy Graduate Examination Commission (FPGEC) Certification, which includes passing the Foreign Pharmacy Graduate Equivalency Examination (FPGEE) and the Test of English as a Foreign Language Internet. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on a resume or during an interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.
Financial Administration Specialist U.S. Department of Veterans AffairsFinancial Administration SpecialistWashington, DC$97,582–$126,859 / yearSpecialized experience is defined as work that involves (1) Administering a fiscal program to include budgeting, reporting, and payment over a project or portion of a program; (2) Planning and conducting studies to forecast financial information; (3) Using automated accounting programs; and (4) Examining and auditing payment voucher while assessing compliance with applicable laws, regulations, policies and procedures. Evaluates total financial management accounting systems within a broad area of assignment by studying the accounts, reports, or procedural instructions and any legislative and program background pertaining to the accounts or operating program.
Supervisory Blind Rehabilitation Specialist U.S. Department of Veterans AffairsSupervisory Blind Rehabilitation SpecialistSan Juan, PR$89,508–$116,362 / yearIn addition to meeting the KSAs described at the GS-11 grade level, the candidate must demonstrate all the following KSAs: (a) Ability to plan, direct, mentor, and distribute work assignments to volunteers, assistants, interns, and/or Blind Rehabilitation Specialists at lower grade levels. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.
NewBiomedical Equipment Support Specialist (Information Systems) U.S. Department of Veterans AffairsBiomedical Equipment Support Specialist (Information Systems)Washington, DC$106,895–$138,967 / yearPhysical Requirements: Heavy lifting, 45 pounds and over; Heavy carrying, 45 pounds and over; Straight pulling (2 Hours); Pulling hand over hand (2 Hours); Pushing (2Hours); Reaching above shoulder; Use of fingers; Both hands required; Walking (4 Hours); Standing (4 Hours); Crawling (4 Hours); Kneeling (4 Hours); Repeated bending (4 Hours); Climbing (use of legs and arms); Both legs required; Ability for rapid mental ad muscular coordination simultaneously; Depth perception. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.
Vice President, Medical Affairs, Clinical Operations & Regulatory Affairs Dendreon CorporationVice President, Medical Affairs, Clinical Operations & Regulatory AffairsSeal Beach, CaliforniaThis executive role ensures alignment across scientific communications, product lifecycle management, clinical development, and regulatory strategy to support the successful development, approval, and commercialization of the company's products and contract manufacturing services (CMS) pipeline. Develop and maintain strategic relationships with physicians, investigators, Key Opinion Leaders (KOLs), healthcare providers, and scientific experts to support clinical development, evidence generation, product adoption, and medical education initiatives.
Staff Blind Rehabilitation Specialist U.S. Department of Veterans AffairsStaff Blind Rehabilitation SpecialistIL$79,533–$103,399 / yearIn addition to providing services to Veterans described at the GS-9 grade level, individuals at this level have duties that typically include the following: serving as a consultant to blind/low vision rehabilitation and other medical center staff in evaluating and treating Veterans in the specialty area; serving as a mentor to other therapists who are evaluating and treating Veterans in the content specialty or program area; serving as internship supervisor to students who are completing their supervised practice; and providing in-service and clinical training programs in the content specialty or program area. The West Palm Beach VA Medical Center provides health services to Veterans throughout South Florida and the Treasure Coast at its main facility in West Palm Beach and six contractor-operated community-based outpatient clinics in Boca Raton, Delray Beach, Fort Pierce, Okeechobee, Stuart and Vero Beach.
Labelling Specialist Pride Technologies LLCLabelling SpecialistCupertino, CAParticipate in design and change control processes to update labelling related to new product developments product changes or regulatory updates. Responsibilities: Leads the Instructions for Use (IFU) creation and ensures compliance to global regulatory requirements, completes labeling reviews to verify compliance of labeling, and implements IFU with cross functional teams.
Project Specialist I, Rates and Regulatory Affairs Liberty Utilities (Canada) Corp.Project Specialist I, Rates and Regulatory AffairsLondonderry, NHAssist with the discovery request process for regulatory proceedings, including assignment of discovery responses, preparation of electronic templates, coordination of responses and response review, and review, prepare and finalize discovery responses electronic form and hard copy as needed. Assist in managing the database for compliance filings and follow up with business leads to ensure timely and accurate submission of pertinent filings while ensuring accuracy of filings and adherence to applicable filing requirements.
Regulatory Affairs Specialist BetcoRegulatory Affairs SpecialistBowling Green, OHThe successful candidate will work independently and collaborate with cross-functional teams to lead small projects, evaluate product changes, maintain regulatory approvals, and manage regulatory databases. COMMUNICATIONS-ORAL AND WRITTEN: Is able to write and speak clearly and succinctly in a variety of communication settings and styles; can get messages across that have the desired effect.
Senior Regulatory Affairs Specialist IntegerSenior Regulatory Affairs SpecialistPlymouth, MN$113,025–$165,770 / yearBy living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success. Develops US and International regulatory strategies for product submissions, identifying needs for bench, animal and clinical testing.
New["Regulatory Affairs Assistant","Regulatory Affairs Assistant"] Apex Systems["Regulatory Affairs Assistant","Regulatory Affairs Assistant"]ConshohockenIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
NewSr Regulatory Affairs Specialist Globus MedicalSr Regulatory Affairs SpecialistAudubon, PennsylvaniaPrepares and maintains regulatory pre-market submissions and other pre-market filings to assist in acquiring appropriate commercial distribution clearances. Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements.
NewPayroll & Accounts Payable Specialist CFSPayroll & Accounts Payable SpecialistNorton Shores, MIAs the Payroll and Accounts Payable Specialist you'll manage payroll processing, support accounts payable, and collaborate closely with leadership to keep financial records accurate and timely. As the Payroll & Accounts Payable Specialist, you’ll be part of a team gearing up for meaningful growth, contributing to both day‑to‑day financial operations and long‑term process improvements.
NewPayroll Specialist II CFSPayroll Specialist IISchaumburg, IL$70,000–$75,000 / yearProcess payroll for union employees across multiple unions, job locations, and states while ensuring timely and accurate payments. Take ownership of payroll processing for union employees across multiple job sites and bargaining units, ensuring accuracy and compliance.
Regulatory Affairs Quality/Standards/Training Manager - Remote Roth Staffing CompaniesRegulatory Affairs Quality/Standards/Training Manager - RemoteAlameda, CaliforniaRemote$85–$93.68 / hourCollaborate with Quality Assurance and cross‑functional stakeholders to support health authority inspections across GPS and Regulatory Affairs, ensuring the RA function remains in a continuous state of inspection readiness. · Work with Regulatory Affairs Strategist, CRO and Clinical Operations to ensure the Trial Master File (TMF) and Veeva RIM is kept current and complete for Regulatory Affairs-related documents.
Study Startup Specialist Systimmune IncStudy Startup SpecialistPrinceton, NJ$70,000–$95,000 / yearThe Startup Study Specialist is responsible for the successful initiation of clinical trials by coordinating and executing all study start-up activities across assigned projects within a fast-paced startup environment. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
Associate Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking) CorDxAssociate Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking)San Diego, CAWith over 2,100 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 disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. The Associate Manager will work cross-functionally with internal teams and external partners to support product approvals and maintain regulatory compliance throughout the product lifecycle.
Senior Director, Program Management Siemens HealthineersSenior Director, Program ManagementTarrytown, NYFull timeExport Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”. Leading executive program governance by providing clear communication of program health, key milestones, risks, mitigation plans, dependencies, and critical decisions to Integrated Business Planning (IBP) governance teams and senior leadership.
Grant Reimbursement Specialist JobotGrant Reimbursement SpecialistOrlando, FL$20 / hourInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Excellent communication skills, both written and verbal, with the ability to effectively communicate complex financial information to a non-financial audience.
NewRadiology Technologist PRN St. David's North Austin Medical CenterRadiology Technologist PRNCedar Park, TXThe hospital also features the Texas Institute for Robotic Surgery , bariatric (weight loss) surgery, a Heart and Vascular Center, neurology and neurosurgery, a kidney transplant program, a Level IV Epilepsy Center, as well as inpatient and outpatient surgery and acute rehabilitation services for both inpatients and outpatients. This means it provides the highest level of care for pregnant and postpartum patients, especially those with serious or complex medical, surgical, or pregnancy-related conditions, including those at high risk for maternal morbidity or mortality.
Head Of US Regulatory Affairs Advertising And Promotion, Global Regulatory Affairs Viatris Inc.Head Of US Regulatory Affairs Advertising And Promotion, Global Regulatory AffairsWashington, DC$151,000–$314,000 / yearWith a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases. Serve as the primary contact with the FDA's Office of Prescription Drug Promotion (OPDP) within the U.S. Food and Drug Administration; lead submissions, risk mitigation strategies, and regulatory interactions including advisory comments, Form FDA 2253 submissions, and responses to regulatory enforcement actions.
Care Specialist/QMAP - The Commons White Logo Color BackgroundCare Specialist/QMAP - The CommonsGrand Junction, Colorado4. Promote and participate in positive customer relations by learning and using resident names; acknowledging residents and visitors; answering the phone as needed; having knowledge of the facility, where to direct people, and how to access resources; maintaining confidentiality; and demonstrating a positive attitude. Monitor the narcotic medications by counting all assigned narcotics prior to receiving control over the medication cart; conduct a narcotic count prior to giving control of the medication cart to any other individual.
Sr. SW Compliance Specialist – Regulatory Affairs & Design Assurance Meridian Bioscience, Inc.Sr. SW Compliance Specialist – Regulatory Affairs & Design AssuranceRemoteRemoteA minimum of 4–6 years of direct Regulatory Affairs, Design Assurance, Software Quality, or related regulated industry experience is required, including preparation of Pre-IDEs, 510(k) applications, EU Technical Files, Canadian Class II and III licenses, STED documentation, and/or software-enabled medical device regulatory submissions. Highly motivated, detail oriented, must have a constant awareness of customer requirements and must demonstrate an ability to make fact-driven decisions; maintain accurate and concise records, uphold regulatory and quality system requirements including 21 CFR Part 820, ISO 13485, EU IVDR (EU 2017/746), and applicable Canadian Medical Device Regulations.
NewAccounts Payable Specialist CFSAccounts Payable SpecialistColumbus, OH$50,000–$60,000 / yearThe Accounts Payable Specialist serves as a key liaison between program management and funding sources, ensuring compliance with grant regulations and accurate, timely financial reporting. Responding to vendor and internal staff inquiries related to grants and payments.
Echo Sonography Quality Coordinator SSM HealthEcho Sonography Quality CoordinatorFlorissant, MOFlexible Payment Options: our voluntary benefit offered through DailyPay offers eligible hourly team members instant access to their earned, unpaid base pay (fees may apply) before payday. American Registry of Magnetic Resonance Imaging Technologist (ARMRIT) - American Registry of Magnetic Resonance Imaging Technologists (ARMRIT).
Study Startup Specialist SystImmune, Inc.Study Startup SpecialistPrinceton, NJ$70,000–$95,000 / yearThe Startup Study Specialist is responsible for the successful initiation of clinical trials by coordinating and executing all study start-up activities across assigned projects within a fast-paced startup environment. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Director Regulatory Affairs Houston MethodistDirector Regulatory AffairsProvides comprehensive management oversight and regulatory guidance to move projects forward from basic laboratory research to regulated environments: Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), First in Human (FIH), early phase clinical trials. Ability to identify and understand issues, problems and opportunities, comparing data from different sources to draw conclusions; using effective approaches for choosing a course of action or developing appropriate solutions; taking action that is consistent with available facts, constraints and probable consequences.
Sr. SW Compliance Specialist - Regulatory Affairs & Design Assurance Meridian Bioscience IncSr. SW Compliance Specialist - Regulatory Affairs & Design AssuranceA minimum of 4-6 years of direct Regulatory Affairs, Design Assurance, Software Quality, or related regulated industry experience is required, including preparation of Pre-IDEs, 510(k) applications, EU Technical Files, Canadian Class II and III licenses, STED documentation, and/or software-enabled medical device regulatory submissions. Highly motivated, detail oriented, must have a constant awareness of customer requirements and must demonstrate an ability to make fact-driven decisions; maintain accurate and concise records, uphold regulatory and quality system requirements including 21 CFR Part 820, ISO 13485, EU IVDR (EU 2017/746), and applicable Canadian Medical Device Regulations.