Search Results: 4,358 vacancies
...Responsibilities:
Provides administrative support for regulatory affairs manager
Provides RA support for change control projects... ...-registration for proposed device changes, prepares internal documentation for changes not requiring re-registration (FDA, EU, OUS)...
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Worldwide
...system will quickly have you in front of a live recruiter.
The Opportunity
Description
We're looking for a Regulatory Affairs Specialist III , working in Pharmaceuticals and Medical Products industry in Bridgewater, New Jersey, United States ....
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...companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ.
Role Overview
The Quality Assurance Document Control...
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Work experience placement
Flexible hours
Shift work
...Responsibilities:
Develop global regulatory strategies for medical device products to meet business objectives and collaborates... ..., timelines, and direction. Reviews and approves technical documentation.
Negotiate with regulatory authorities to resolve...
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...teams to deliver best in-class solutions for regulatory submissions. Assist in the creation of technical documentation (technical files and design dossiers) for Spine... .... The requirement is for 3 Regulatory Affairs Specialist.
Responsibilities:
Identify reference documents...
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Offshore
...Job title: CMC Regulatory Technical Writer II
Location: Bridgewater, NJ, Hybrid
Duration: 1 year
SHIFT SCHEDULE 1st shift... ...MS or PhD)
~ Must have experience with CTD (Common Technical Document) modules.
~ Will complete regulatory submissions, compliance...
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Contract work
Shift work
Day shift
...Description POSITION SUMMARY:
Responsible for all aspects of the documentation process including the label/supplement facts panel (SFP)... ...a specific SFP utilizing the correct SFP format according to regulatory guidelines.
Facilitate the interdepartmental and customer...
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Contract work
...healthcare and serve as a leader of positive change.
The Regulatory Specialist is responsible for promoting compliance with Federal... ...Organizes and maintains the regulatory binder; file essential documents, obtain signatures for delegation logs, training logs and other...
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Local area
...of the Regional Manager, the Clinical Documentation Quality Liaison is responsible for promoting... ...in the Clinical Documentation Specialist and Coder DRG and coaching of the CDMP... ...with Medicare Part B.
Knowledge of the regulatory environment.
Excellent knowledge of...
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...The Clinical Documentation Specialist RN facilitates improvement in the overall quality, completeness and accuracy of medical record documentation... ...A.
Familiar with Medicare Part B.
Knowledge of the regulatory environment.
Understand and support CDMP documentation...
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Full time
**Associate Director, Regulatory Affairs**
**Position Summary:**
Catalent is a global, high-growth, public company, and a leading partner... ...** will be interpreting and evaluating reports and other documents to be used in all typical regulatory submissions, reviewing new...
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...Responsibilities:
Bridging the gap between the Physician documentation and the Coding professional through compliance review of inpatient charts. Communicate in person, through query documents, via telephone with Physicians to improve or complete documentation necessary...
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Full time
About the job Assistant Document Control
Assistant Document Control needs 1 to 3 years of relevant experience in the pharmaceutical/biopharmaceutical industry
Assistant Document Control requires:
~ BA/BS degree or equivalent experience is preferred.
~1...
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...Please go through the below mentioned JD and let me know if you would be interested to explore the opportunity.
Job Title Regulatory Consultant
Location - New Jersey or Chicago, IL
Fulltime Hire
# Assertive,
# Situational Leadership,
# Process Mapping...
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Full time
...~10+ years' experience in Global Regulatory affairs, CMC submissions.
~ Knowledge on Insights and regulatory affairs.
~ Develop... ...status reporting for the duration of the project
~ Solicit and document requirements for the new Regulatory Analytics platform
~...
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...Summary
This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation... ...asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with...
Contract work
Summary:
The Revenue Cycle Specialist is responsible for billing and collecting payments... ...are billed appropriately and meets all regulatory and compliance requirements.
Role... ...from carriers by placing phone calls and documenting all communication in Athenahealth to...
Full time
...with the CEO of Gan & Lee Pharmaceuticals USA. The Sr. Manager, Document Management supports all Controlled Document Management at the... ...Participate in inspections performed by FDA and international regulatory agencies; also, audits performed by partners in own area of...
...Our Team:
The team is involved in developing and executing regulatory strategies for rabies vaccines in post marketing and in development... ....
- The RS contributes to content and reviews regulated documents (such as IB, PBRER, DSUR, RMP, etc.)
- The RS supports...
Worldwide
...around the world.
JOB SUMMARY:
The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and... ...changes to applications versus current available guidance documents and formulate filing strategies.
Interact with BPI partners...
Overseas
