Regulatory Specialist
Saviance
Regulatory Specialist
Handles adverse event reports from scientific literature by collecting, reviewing, and entering global adverse events reports; routes applicable literature on adverse event cases to the appropriate clinical safety physician for review. Provides support to global personnel regarding global product safety policies, processes and procedures by updating SOPs, training tools/programs as necessary. Ensures regulatory compliance for expedited submission of case reports to regulatory authorities. Collaborates with internal and external customers to prepare quality periodic/annual safety summary reports; partners with global product safety physicians to maintain and communicate product safety profile analyses to appropriate persons and groups (e.g., regulatory agencies).
- ...healthcare, developing complete solutions which optimize the urine drainage process in the Acute Care Hospital setting. The Regulatory Affairs Specialist II is responsible for preparation of U.S and CE marking submissions/registration activities, along with supporting all...SuggestedFull timeWork at officeRemote work
- The Compliance Specialist reports to the Director Legal, Compliance, Privacy & Security (“Director”) and has a key role in supporting the... ...basis.Conduct research and develop written communication on regulatory requirements to ensure ongoing updates upon request. Manage compliance...SuggestedContract work
- ...Name: Atrium Medical CorporationJob Location: Merrimack, NH 03054 Employer will allow a hybrid work schedule.Job title: Regulatory Affairs Specialist IIEducation: Bachelor's degree in a scientific or engineering disciplineSOC Code: 13-1041.07SOC Occupation Title: Regulatory...SuggestedWorldwideFlexible hours
$117k - $120k
AMNEAL PHARMACEUTICALS Regulatory Affairs Specialist: With minimal supervision assists with the preparation of high-quality regulatory submissions to the Food and Drug Administration (FDA) as required, within company timelines and in accordance with regulatory guidelines...SuggestedFor contractorsLocal area- Job-ID31596302Reference25-04614 Job Description: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities...SuggestedWork at office
- Job Title: Regulatory Affairs SpecialistREMOTEContract: 1 Year and Possibility of ExtensionClient is seeking an experienced Regulatory Affairs contractor to support the preparation and submission of a US FDA 510k and the development of global regulatory documentation,...For contractors
- ...solutions, and safeguarding people, property, and profits. Position Summary The Compliance Associate supports RPM Living’s regulatory compliance program across property operations. This role assists with monitoring regulatory developments, maintaining compliance...Weekly payFull timeStart working todayWork at officeLocal area3 days per week
- ...processes, policies, and people delivering value. Learn More About ProSidian Consulting at DescriptionProSidian Seeks a Regulatory Compliance Specialist | Compliance / Risk / Regulatory: Risk, Compliance & Independent Certification Support [DOE0019019] for Program...Full timeContract workTemporary workFor contractorsWork at officeLocal areaRemote workFlexible hours
- Job-ID29247439Reference25-02134 Responsibilities: Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic submissions. Leader in the development of dossiers for registration of products in countries outside the US; including...Work at office
$120k - $160k
...members to perform at a higher level through a deep understanding of their bodies and daily lives.WHOOP is looking for a Regulatory Affairs Specialist II, Expansion to be a core member of the Digital Health team.As the Regulatory Affairs Specialist II, Expansion, you...Full timeWork at officeRelocation- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the...Immediate start
- ...Manufacturing, and/or Project Management within the IVD industry. Knowledge of FDA, and CE marking requirements for IVD products is preferred. Excellent verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.
- Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This role is responsible for ensuring compliance with...
- ...make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlaceYour role at Clorox:The Regulatory Affairs Specialist II provides regulatory leadership to support the compliance and safety of Clorox’s FDA-regulated Foods portfolio,...Full timeSummer workWork at officeRemote workFlexible hours3 days per week
- The 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...
- Job-ID31525652Reference25-04486 Responsibilities: The Regulatory Affairs Specialist is responsible for working with cross-functional teams to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality...
- .../financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual...Work at officeImmediate start
- ...approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.A Regulatory Affairs Specialist II position is available in the Diamond Research Laboratory. You will assist and support internal and external PIs, for...Work experience placement
- ...Ontario / Atlanta, GeorgiaClinical Services - Clinical Services - Regulatory Affairs - Regulatory Affairs /Full-time, Permanent /... ...leaders in a timely manner.Client Services As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance...Permanent employmentFull timeWork from home
- Overview This is a REMOTE position. The Regulatory Affairs Specialist 2 responsibilities are narrowly focused to a specific country and/or region in which the Specialist has proficient language skills (reading/writing/speaking). This position requires the ability to...H1bWork at officeLocal areaRemote workAfternoon shiftEarly shift
- The Regulatory Affairs Specialist 3 develops and executes regulatory strategy and integrates regulatory requirements throughout the product lifecycle. Relies on extensive experience and judgment to plan, create, develop and maintain materials needed for regulatory compliance...
- ...is working in the CMC area. Relevant experience is requiredExperience: 3 to 6 yearsExperience with drug/biologics licensurePrior regulatory experienceTechnical writing experience (CMC experience )Scientific background,Required Skills:CMC/ Regulatory writing experienceScientific...Work at officeImmediate start
- ...notifications.• Participate in team meetings as a representative of IA with both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical reports.• The candidate must be able to adhere to local and global...Work at officeLocal areaImmediate start
- ...will not offer sponsorship or take over sponsorship of an employment VISA for this position at this timeAbout the Role The Regulatory Affairs Specialist I supports product development, regulatory submissions, global registrations, and regulatory compliance activities...Hourly payInternshipWork at officeLocal areaShift work3 days per week
- ...United States and over 70 countries outside the United States. For more information, please visit GENERAL SUMMARY: The Regulatory Affairs Specialist will act as regulatory representative on cross functional New Product Development teams. Following the Phase Gate...Work at office
- ...Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help...For contractorsRemote work
- ...Worldwide Clinical Trials is seeking a Regulatory Affairs professional to plan, organize, and submit regulatory submissions across Germany and Switzerland, coordinating with SAR colleagues to ensure timely delivery. You will review and translate submission documents and...Local areaWorldwide
$120k - $150k
...Certificates, Waivers & COAs Partner closely with engineering and flight test teams to ensure compliance alignment early in design Regulatory Engagement Serve as primary Pivotal representative to: Aeronautical Authorities including FAA (and offices including AIR,...Work at officeLocal area- ...Our Client, an American Biotechnology company, is looking for a Regulatory Affairs Specialist 4 for their Sunnyvale, CA/Hybrid location. Responsibilities: Provide regulatory guidance to product teams, develop regulatory plans, and review and approve product...
$71.6k - $119.3k
...days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Meet the team: Regulatory Affairs is a team of more than 40 professionals located either at San Diego HQ or remotely around the globe. Our backgrounds...Work at officeRemote workWorldwideHome officeFlexible hours
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