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KEY RESPONSIBILITIES

Regulatory:

Overall responsibility for compiling regulatory submissions to the Federal and State agencies, drafting submissions to include client Product Information, CareTria Facility Information, literature searches to support corporate submissions, client and/or government agency notification and other regulatory activities. Manages the renewal and maintenance of CareTria's federal and state distributor licenses for all CareTria's warehouse locations including the preparation of supporting documents for new and renewal licenses for submission to state licensing agencies Submits requests to Finance for payment for all licenses, permits and other required regulatory agency filings Maintains RA and QA departments expenditure documentation including reports to Finance Responds to requests and queries; serving as liaison with state regulatory officials in connection with licensing matters under the supervision of the Vice President of Regulatory Affairs and Compliance Stays abreast of regulatory updates and changes in license filings as they affect CareTria's warehouse facilities Manages surety bonding requirements to ensure CareTria maintains compliance with all applicable state licensing agencies Assists in the research and interpretation of state and regulatory regulations/rules related to wholesaler, third-party logistics provider and business licensing requirements Conducts regulatory research and assists the Compliance Manager and Compliance Analysts with updates to CareTria's mid-level prescriptive authority table Manages the updates to CareTria's wholesaler regulation database for CareTria warehouse facilities Assists with client audit questionnaires and compilation of responses to audit reports Assists with re-accreditation of CareTria by the National Association of Boards of Pharmacy for all warehouse locations, which includes annual compliance evaluations for all facilities When necessary, assists the Compliance Training Manager and/or QA with tracking, scheduling and coordinating internal PDMA and cGMP training When necessary, assists in the coordination of Client Compliance/CIA Training Prepares Knipper and client FDA, DEA and state submissions for Loss/Theft Reporting and other compliance violations Arranges all appointments and meetings for the Regulatory Affairs and Compliance department using own judgment; resolve telephone requests directly or through appropriate resource Maintains Regulatory Affairs and Compliance files Contacts state boards of pharmacy to facilitate manual adjudication for CareTria prescriber validation program Assists Vice President, Regulatory, Compliance and QA with projects and follow up as needed Document archiving as required The above duties are meant to be representative of the position and not all-inclusive.

MINIMUM JOB REQUIREMENTS

Education/Training:

Associate degree plus five years legal or compliance administrative work experience or comparable years of experience.

KNOWLEDGE, SKILLS & ABILITIES

: Knowledge of pharmaceutical industry, including drug storage and distribution Knowledge of inspection process for drug sample distribution Strong knowledge of PDMA and DSCSA Experience working on regulatory submissions Excellent communication skills, written and verbal Ability to understand and communicate legal risk Computer skills: Proficient in MS Office, Excel, and Word; basic understanding of data processing, ability to learn new business and warehouse management software/systems Excellent communication, organizational and data entry skills Detail oriented and has computer knowledge and good customer service awareness Notary Public Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The expected base pay range for this position is $90,000-$95,000 per year. 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Find & Apply For Regulatory Affairs Manager Jobs in Lakewood Township, New Jersey

Senior Manager, Regulatory Affairs (2026-8011)