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).
- 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...Suggested
- ...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...SuggestedWork at officeLocal areaImmediate start
$107.2k - $160.8k
...font-size: 30px; font-weight: bold; width: 883px; left: 5px; height: 72px; padding-left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality system and...SuggestedWork at officeLocal areaImmediate startFlexible hours- ...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...SuggestedWork experience placement
- ...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...SuggestedWork at officeImmediate start
- 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
- ...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
- 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...
- 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...
- 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...Contract work
- 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
- ...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-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...Work at office
- Job-ID29095910Reference26-23457Remote50% Remote Experience • 3-5 years of experience in regulatory compliance, information security, and/or data privacy • Demonstrated experience working within cross-functional teams including Legal, IT, Security Operations, and Governance...Remote work
- ...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
$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- Brecksville, OHDescriptionJob Title: Regulatory Affairs SpecialistDepartment: RegulatoryReports To: Director of Regulatory AffairsFLSA Status: ExemptSupervise the work of others: NoPosition Summary:This position is responsible for preparing submissions to various regulatory...Work experience placementWork at office
- ...Seeking a remote, 12-month contract Global Regulatory Affairs Specialist, the candidate will coordinate and support the maintenance of labeling intelligence, ensuring compliance and alignment with business needs while managing label tracking strategies throughout the product...Contract workLocal areaRemote work
- ...Regulatory Compliance Specialist Grand Canyon University! One of Arizona's leading institutions of higher learning. Located in the Valley of Sun in the heart of Phoenix, Arizona, GCU is an institutionally accredited, private, nondenominational Christian University....Local area
$110k - $125k
...you on your journey to better health, every step of the way. Role Overview Cymbiotika is seeking an experienced Regulatory Compliance Specialist to support product compliance and regulatory initiatives across dietary supplements, nutritional products, foods, and...Remote workWork from homeFlexible hours- ...To support regulatory compliance efforts, the contract Regulatory Affairs Specialist will manage regulatory submissions, provide guidance on global regulatory strategies, and represent the regulatory function within product development teams. Key Responsibilities Create...Contract workWork at officeRemote work
- ...Core States Group Permitting & Regulatory Compliance Specialist II At Core States Group, the work you do matters to the clients we serve, the communities we support, and the teams who rely on one another to deliver with excellence. Our Cause is powerful: to create...Work at officeImmediate startRemote workFlexible hours
$51.92k - $76.59k
...Under the direction of the Pharmacy Compliance Officer and/or Pharmacy Director, the Pharmacy Regulatory Compliance Specialist is responsible for assisting in the assessment and management of all legal, accreditation, and certification requirements to gain compliance...Work at office- ...Summary/Objective The Regulatory Compliance Specialist (RCS) supports Cardinal's product compliance, regulatory approvals, certification programs, risk management activities, and compliance testing efforts. The RSC works cross-functionally with Engineering, Quality...Full timeWork at officeWorldwideMonday to Friday
$86.5k - $98k
...organizations design and deliver compensation, benefits, pension, and health management programs that work. As our Regulatory Compliance Specialist, you'll translate complex federal and state requirements into actionable solutions that protect millions of plan members...Work at officeFlexible hours- ...TX 75050Atlanta, GA 30326The ESG & Sustainability Compliance Specialist is responsible for directly assisting the Assistant General Counsel... ...ESG data, prepares reports, and ensures compliance with regulatory requirements and industry standards.Collaborates with the internal...Work at office
- ...A critical role ensuring the safety, legality, and efficiency of the Mon EMS agency. Oversee non-clinical operations, including regulatory, privacy standards & compliance for organizational safety requirements, fleet, inventory & supply management and facilities maintenance...Work at officeLocal areaShift work
- GCL Technology Holdings Limited is seeking a capable finance professional to manage day-to-day accounting for its U.S. subsidiaries under US GAAP, oversee monthly close, and prepare financial statements. The role also coordinates with banks, tax agents, and external auditors...
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