Regulatory Affairs Specialist
Virtual Vocations Inc
Managing the promotional review process, the full-time Regulatory Affairs Specialist will coordinate the review and approval of promotional materials, serve as a liaison for internal and external stakeholders, and ensure compliance with regulatory standards in a remote work environment. Key responsibilities Coordinate the review and approval of advertising and promotional materials throughout the review lifecycle Serve as the primary liaison for submission requirements and review expectations, facilitating communication among cross-functional teams Maintain promotional review documentation and metrics to support process improvement and workload visibility Required qualifications Bachelor's degree in life sciences, pharmacy, communications, regulatory affairs, healthcare, business, or a related field 3+ years of experience in promotional review, regulatory affairs, or a related compliance function Strong understanding of promotional material review processes and document control practices Experience working in a regulated life sciences industry, such as medical devices or pharmaceuticals Regulatory Affairs Certification (RAC) or similar credential is preferred
$87.4k - $131.1k
...extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping,... ...Ingenyx.com Position Summary We are seeking a Regulatory Affairs Specialist to support global regulatory activities for medical devices,...SuggestedFull timeTemporary workFlexible hours- ...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...SuggestedImmediate start
- ...Description: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S... ...of international product registrations and related regulatory affairs activities, including execution of procedures and systems...SuggestedWork at office
- ...winning company that’s helping create meaningful and lasting change in the healthcare industry. Job Summary The Regulatory Affairs Specialist supports international regulatory compliance and market access activities for food supplements. The position evaluates...SuggestedFull timeLocal area
$80k - $90k
...-being of each individual on our team. Who We’re Looking For - Reporting to the Senior Manager, Regulatory , MANSCAPED® is seeking a Regulatory Affairs Specialist to support global regulatory compliance across current and future markets. This role will help ensure...SuggestedFull timeRemote workFlexible hours- 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-ID32758545Reference26-01317Remote50% Remote 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...Remote work
- ...provides flexibility to work 4 days on site and Friday remotely on a weekly basis in Covington, GA. *** Job DescriptionThe Regulatory Affairs Specialist II is responsible for implementation of regulatory strategies including domestic and international submissions and other...Full timeWork at officeRemote workDay shift
- 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
- ...healthcare, developing complete solutions which optimize the urine drainage process in the Acute Care Hospital setting. The Regulatory Affairs Specialist I is responsible for implementation of regulatory strategies including domestic and international submissions and other...Full timeWork at officeRemote workDay shift
- ...medical technology or similar. 5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the... ...verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.
- ...439Reference25-02134 Responsibilities: Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic... ...equivalent). A minimum of 3 years' experience in Regulatory Affairs Advanced experience in the areas that may include preparation...Work at office
- ...international medical device manufacturer has an exciting career opportunity for a highly talented and well-experienced Regulatory Affairs Specialist with FDA experience who will report directly into the Regulatory Affairs Manager. Essential Functions and Responsibilities...Work experience placementLocal area
- 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
$90k - $125k
Alameda, CAGeneral Administration - Regulatory Affairs /External /HybridIn this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to bring our life-saving technologies to patients worldwide...Temporary workWork at officeLocal areaWorldwide- 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
- ...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
- 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...
- ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical... ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or...Work at officeLocal areaImmediate start
- Job-ID31824874Reference26-00210 Responsibilities: 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...
- ...Job Description Job Description Regulatory Affairs Specialist Job Description Who We Are: Marketlab is a market leading healthcare solutions organization specializing in the design, manufacturing, and sourcing of private label products. It’s our mission...Temporary workWork at office
$38 - $56 per hour
...LHH Recruitment Solutions is seeking a Regulatory Affairs Specialist for a minimum 6-month remote contract opportunity. This position is open to candidates residing in California who have prior experience in the medical device industry. The ideal candidate will have a...Hourly payContract workLocal areaImmediate startRemote workMonday to Friday- ...Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site) A commercial-stage transplant technology company, part of a global medtech group, is changing how donor organs are preserved and assessed before transplant. Their...Permanent employmentFull time
$50 - $90 per hour
...Regulatory Affairs Specialist Actalent is seeking experienced Regulatory Affairs Specialist for medical device manufacturing client. Required Qualifications: ~5+ years experience in Regulatory Affairs and medical device regulations. ~ Strong understanding...Contract workTemporary workRemote workFlexible hours$80k - $100k
...Regulatory Affairs SpecialistAre you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology... ...an impact in the lives of others.The Regulatory Affairs Specialist is responsible for obtaining domestic and internal...Work experience placementWorldwide- ...making an impact in the lives of others. Learn about the Danaher Business System which makes everything possible. The _ Regulatory Affairs Specialist _ is responsible for obtaining and documenting our mission-critical, Indian regulatory clearances for Masimo’s amazing innovative...Work experience placementLocal areaRemote workWork from homeFlexible hours
- ...Regulatory Affairs Specialist (3-5) Location: Remote/Indianapolis, IN Duration: 19 Months Qualifications: ~3+ years of experience in a CMC/Chemistry Manufacturing and Controls position (regulatory document experience) OR 3+ years Module 3 experience (regulatory...Work at officeRemote work
- ...Regulatory Affairs Specialist IIILocation: Bridgewater, NJ Duration: 9 MonthsManager will consider candidates to be based in either Bridgewater, New Jersey or Cambridge, Massachusetts. Please specify on resume which location candidate is being submitted for.Preparing,...Worldwide
- ...Regulatory Affairs SpecialistRegulatory Affairs Specialist manages assigned projects of moderate complexity which include international regulatory activities; on-market compliance reports or assessment of design changes, manufacturing process and labeling changes for...
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