Regulatory Affairs Director — MedTech Submissions
VitalConnect, Inc.
VitalConnect, Inc. is seeking an experienced Regulatory Affairs professional to lead submissions and maintain registrations for the U.S. and international markets. You will write and edit technical documents, maintain licenses and CE files, respond to authorities, and stay current with regulatory changes to ensure ongoing compliance. Requires a Bachelor’s in Engineering or Science and at least four years in medical device regulations, with strong communication and analytical skills. #J-18808-Ljbffr VitalConnect, Inc.
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Director — MedTech Submissions in California, MO vacancy
- Tarsus Pharmaceuticals, Inc. is seeking a Manager I, Regulatory Affairs Operations to support electronic submission management and dossier lifecycle activities from Irvine, CA. The role emphasizes content planning within Veeva Vault RIM, collaboration with publishing vendors...Suggested
- ...pharmaceutical company is hiring a Sr. Regulatory Specialist for a fully remote position.... ...Biomedical Science and expertise in regulatory affairs, particularly in IVD product development... ...teams, shape study designs, and prepare submission-ready documentation for FDA submissions....SuggestedRemote jobFlexible hours
$150k - $175k
Purpose Responsible for regulatory affairs activities such as regulatory submissions, registrations and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance and standards. Assist in creation and maintenance of regulatory files...Suggested$228k - $245k
A biotechnology company in Missouri is seeking a Director of Global Regulatory Affairs responsible for developing and executing regulatory strategies... ...in regulatory affairs and a strong track record of submissions. The position offers a competitive salary of $228,000 to...SuggestedRemote job$80 - $100 per hour
...80.00/hr - $100.00/hr Quality, Regulatory & R&D Staffing Expert | Contract... ...partnering with a scaling Class III MedTech business to hire a Senior Regulatory Affairs Specialist (Contractor). This is... ...is looking to complete first submissions and filings in 2026, which will...SuggestedHourly payPermanent employmentFull timeContract workFor contractorsRemote work- ...authoring protocols and analysis plans in support of RWE needs for the MedTech Cardiovascular franchise. Lead the synthesis of evidence from... ...learning algorithms. The position will report to the Senior Director, MT EPI-RWDS. Requirements A Doctor of Philosophy (PhD)...
$32.69 - $36.05 per hour
...business units are in compliance with state, federal, and local regulatory requirements. Will oversee and support within the timely... ...agencies, ensuring accuracy, completeness, and timeliness of submissions. Support and track agency insurance renewals, ensuring continuous...Hourly payFull timeContract workFor subcontractorWork at officeLocal areaRemote workMonday to FridayFlexible hoursShift workDay shiftThe Village Family Services, Inc.
California, MO3 days ago- Lead Engineering, Regulatory, Quality and Clinical Affairs Recruiter, Medical Device & Diagnostics at BioTalent and Investigo, part of The IN Group Position... ...will be responsible for overseeing global regulatory submissions and ensuring compliance for our diverse medical device...Full time
- Brief Description: The Senior Manager, Regulatory Affairs Global CMC will be responsible for managing registration and CMC regulatory support... ...and review of Module 2 and 3 CTD sections of regulatory submissions as assigned (INDs, IMPDs, CTAs, MAAs, NDAs, BLAs, meeting...Remote workWorldwide
- Direct message the job poster from GForce Life Sciences Senior Regulatory Affairs Manager 12-month Contract, Remote Must be able to work on a... ...clinical and nonclinical development programs. Regulatory Submissions and Related Activities Ensure that clinical and...Contract workRemote work
- ...in healthcare. Job Details Job Type: Full time Job Title: Regulatory Affairs Manager Location: Onsite - San Diego, CA Position Summary The... ...Affairs Manager will support the preparation, review, and submission of regulatory documentation for medical device products, ensuring...Full timeFlexible hours
- A leading recruitment firm is seeking a Regulatory Affairs Manager for their medical device portfolio. The successful candidate will oversee global regulatory submissions, ensure compliance with US FDA and European regulations, and develop regulatory strategies for both...Full time
$114k - $228k
Regulatory Affairs Manager - APAC - Diabetes Care (on-site) page is loaded## Regulatory Affairs Manager - APAC - Diabetes Care (on-site)locations... ...regulatory SME, provide support for compiling regulatory submissions, and ensuring data is effectively presented for the...Shift work$100.32k - $125.4k
...every story matters. Senior Specialist, International (China) Regulatory Affairs 164201 Senior Specialist, International (China) Regulatory... ...obtain and maintain regulatory approvals, preparing local submissions, supporting in-country Regulatory Affairs representatives,...Temporary workWork experience placementWork at officeLocal areaRemote workFlexible hours$110k - $150k
...office. Reports to the Chief Compliance Officer and focuses on regulatory filings, policy implementation, and day-to-day oversight of... ...Assist with SEC filings, licensing renewals, and other regulatory submissions. Monitor legal and regulatory developments and recommend...Contract workWork at office- Regulatory Affairs Specialist - Medical Devices Position: Regulatory Affairs Specialist - Medical Devices Location: California Employment... ...including 510(k)s, Technical Files, and other international submissions. Ensure compliance with FDA, EU MDR, ISO 13485, and other...Contract work
- Flourish Research in Northridge, CA is seeking a Regional Regulatory Specialist to support regulatory submissions, document management, and site readiness in a fast-paced clinical research environment. The role involves preparing regulatory documents, submitting updates...Monday to FridayShift work
- ...find your purpose here. Primary Function of Position The Sr. Regulatory Affairs Specialist’s primary responsibilities include developing... ...the impact of design/process changes, preparing regulatory submissions, maintaining regulatory filings and licenses. Essential Job...Local areaWorldwideFlexible hours
- Title: Regulatory Affairs Associate Location: Sylmar, CA Duration: 7 Months 100% Onsite Summary Responsible for filing necessary regulatory... ...updates, change assessments, and Notified Body submissions. Review/approval of engineering study protocols/reports and...Temporary workFlexible hours
$25 - $26 per hour
...endless growth opportunities. We are actively hiring a Regional Regulatory Specialist at the Flourish Research site in Northridge, CA!... ...documents Manage the full lifecycle of regulatory submissions to IRBs, sponsors, and regulatory agencies Submit study updates...Work at officeMonday to FridayFlexible hoursShift work$50 - $67 per hour
...Base pay range $50.00/hr - $67.00/hr Sr. Regulatory Specialist Fully remote in PST time... ...Position summary We’re hiring a Regulatory Affairs professional with a strong molecular... ...This role is a key contributor to FDA submissions (PMA/510(k)) and requires excellent scientific...Contract workRemote work$148.55k - $174.77k
## Senior Regulatory Affairs SpecialistApplylocations: California - Headquarterstime type: Full timeposted on: Posted 5 Days Agojob requisition... ...II and III devices and preparing and submitting regulatory submissions in the US, EU and outside of US (OUS) geographies.**What...$100k - $200k
Abbott Laboratories is seeking a Principal International Regulatory Operations Specialist to join its Diabetes Care Division. The role... ...changes, and leading cross-functional teams in managing submissions. Candidates should have a Bachelor’s degree in a scientific discipline...- ...experience in the field. Recent experience with Class III implantable medical devices; Proven successful track record of authoring/submission/approval of Class III implantable PMA supplements; knowledge of FDA PMA guidance documents and CFR regulations. Relies on...
$140k - $185k
...build on via Science Foundry. The Senior Regulatory Specialist will serve as the regulatory... ...within our Quality and Regulatory Affairs team, where each team member brings both... ...prepare, author, and coordinate regulatory submissions including IDEs, 510(k)s, PMAs,...Full timeLocal areaRemote workFlexible hours- Nutrien is seeking a Regulatory Affairs professional to manage state registrations for fertilizer/soil amendments and maintain compliance... ...with multi-state requirements. You will support renewals, new submissions, labeling updates, and data integrity in registration...
- ...to our organizational success. Department Website: dot.ca.gov Director’s EEO Policy: dot.ca.gov/programs/equal-employment-opportunity... ...electronically through CalCareers.ca.gov, or by mail for hard copy submissions. See the posting for the required documents and formats. If...Work experience placementWork at officeRemote workWeekend work
- ...human member of our team. Because we take the time to give each submission the attention it deserves, our review process may take a... ...departments and with the Compliance Division to meet necessary regulatory and compliance deliverables Reviews new regulatory requirements...Full timeTemporary workLive inWork at officeLocal areaRemote work
$97.5k - $136.5k
About The Role The Manager I, Regulatory Affairs Operations will report to the Director, Regulatory Affairs Operations, and will primarily assist in managing... ...Management System (Veeva Vault RIM) and regulatory submissions activities. The Manager I, Regulatory Affairs Operations...Work at officeLocal areaRemote work- Jobtailor is seeking a results-driven program coordinator to support scheduling, compliance, budgeting, and contract management across service operations in the United States. The role emphasizes safety, quality, and efficient resource allocation. The ideal candidate will...Contract workRelocation
Jobtailor
California, MO4 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Director — MedTech Submissions. Be the first to apply!
Related searches
- regulatory manager California, MO
- director global regulatory affairs California, MO
- manager regulatory affairs California, MO
- head compliance California, MO
- compliance manager California, MO
- compliance director California, MO
- senior director regulatory affairs California, MO
- quality regulatory manager California, MO
- regulatory affairs director California, MO
- corporate compliance manager California, MO