CATEGORY: Regulatory Affairs JOBS

Clinical Quality Manager Richmond, VA

Category: Regulatory Affairs
We are currently seeking a highly qualified Clinical Quality Manager to join our Regulatory Affairs department in Richmond, VA. The successful candidate will be responsible for creating and enhancing clinical quality requirements and standards for our network of Contract Research Organizations (CROs) and will work with multiple business partners to prepare and assure FDA inspection readiness. In
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Manager Marketing Compliance Richmond, VA

Category: Regulatory Affairs
We are currently seeking a highly qualified candidate for the position of Manager, Marketing Compliance to join our Regulatory Compliance group within the Regulatory Intelligence and Engagement department at Altria Client Services in Richmond, Virginia. The Manager, Marketing Compliance reviews and provides guidance for designated operating company advertising, promotion and packaging materials
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Manager Regulatory Reporting & Submissions CMC Richmond, VA

Category: Regulatory Affairs
We are currently seeking a Manager Regulatory Reporting & Submissions in our Regulatory Affairs area. The position will use regulatory knowledge to oversee coordination, preparation, and timely submission of high quality documents for regulatory authorities and identify perceived gaps in product development plans that may pose regulatory issues with a focus on the product description/chemistry, m
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Manager, Quality Requirements Richmond, VA

Category: Regulatory Affairs
We are currently seeking a highly qualified Manager, Quality Requirements to join our Regulatory Quality Compliance department in Richmond, VA. The successful candidate will be responsible for creating and enhancing quality requirements and standards through independent research and interpretation of other FDA regulated industries and standards. This position will also work with multiple busines
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Medical Writer Richmond, VA

Category: Regulatory Affairs
We are currently seeking a Medical Writer in our Regulatory Affairs organization in Richmond, VA. The Medical Writer will communicate complex scientific information in clear and compliant written communications to ensure successful preparation of high quality documents for FDA product applications and submissions. Specific accountabilities include: * Coordinating with various subject matter ex
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Quality Compliance Auditor Richmond, VA

Category: Regulatory Affairs
We are currently seeking a highly qualified Quality Compliance Auditor to join our Regulatory Affairs department in Richmond, VA. The successful candidate will be responsible for conducting quality audits of internal, supplier, and/or clinical related operations to evaluate the level of conformance to company standards and/or regulations. In addition to direct auditing related activities, the in
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Regulatory Program Leader - Postmarket Surveillance and Advocacy Richmond, VA

Category: Regulatory Affairs
We are currently seeking Regulatory Program Leader – Postmarket Surveillance and Advocacy to join our Regulatory Affairs organization. The position will provide scientific expertise and strategic guidance to a broad spectrum of internal and external stakeholders charged with fulfilling our reduced-risk product strategies. Altria aspires to be the U.S. leader in authorized, non-combustible, reduc
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Regulatory Program Leaders - Science & Advocacy Richmond, VA

Category: Regulatory Affairs
Altria Client Services is currently seeking high-performing Regulatory Program Leaders – Science and Advocacy to join our Regulatory Affairs organization in Richmond, VA. Altria aspires to be the U.S. leader in authorized, non-combustible, reduced risk products. (Learn more at Altria.com) Our approach to regulatory advocacy relies on deep scientific expertise, understanding of consumers and effe
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SAS Programmer Richmond, VA

Category: Regulatory Affairs
We are currently seeking a highly qualified SAS Programmer to join our Clinical Operations department in Richmond, VA. The successful candidate will conduct SAS programming and analysis to support clinical studies of non-combustible tobacco products that have the potential to reduce harm. Specific accountabilities include: * Reviewing clinical study protocol, annotated case report forms and sta
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Senior Specialist Quality Compliance Richmond, VA

Category: Regulatory Affairs
We are currently seeking a Sr. Specialist Quality Compliance in our Product Quality Investigations group in Richmond, VA. The successful candidate will be responsible for providing guidance and technical support to Altria’s operating companies related to the investigation, documentation, and disposition of Product Quality Incidents (PQI’s). The incumbent will be expected to work collaboratively w
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