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The job holder has responsibility and accountability for ensuring approved product dossiers are maintained in a state of compliance with respect to the manufacturing, testing, storage and distribution operations at GSK Rockville Biopharm facilities. Key Responsibilities: • Assist Biopharm site regulatory submission preparation & review of global submissions, variations/supplements for products produced by the Biopharm site. This includes both IND and approved commercial products. • Support Response to Questions (RTQ’s). Support Market Specific Requirements (MSR’s). Support renewals. • Support change notifications from Vendors by assessing regulatory impact. • Support changes to site specifications • Initiate change controls for new market submissions. • Support Annual Reports for commercial products. Support Periodic Product Review reports for commercial products. • Support change control assessments; provide advice and approval. Initiate RADARs and support Regulatory Implementation Strategy (RIS) meetings. • Support adherence to current regulatory requirements by supporting monthly Quality Regulatory Intelligence (QRI) meetings. Support Quality Alerts. • Attend monthly Regulatory Community of Practice (CoP) forums. • Support regulatory inspections from all health authorities. • Participate in self-inspections to ensure PAI readiness. • The incumbent is responsible for adhering and promoting GSK safety guidelines and procedures. A. Educational Background • BS/BA in Technical or Analytical discipline - Base level to ensure understanding of regulatory/ technical knowledge required to effectively ensure minimal compliance requirements are met • MS in Quality/Regulatory - Provides for greater depth and breadth in understanding and applying regulatory science to pharmaceutical manufacturing operations B. Job-Related Experience • Minimum 1-5 years industry experience in biopharmaceutical/biologics manufacturing environment. 0-3 years prior experience in regulatory functions. -- Highly regulated and complex environment, ability to effectively manage workload C. Other Job-Related Skills/Background • Good understanding and interpretation of Global regulations pertaining to the manufacture, holding, and distribution of biopharmaceuticals/biologics. • Extensive working knowledge of GSK marketed products (US & International) with emphasis on Chemistry, Manufacturing and Controls (CMC). • Good working knowledge of regulatory affairs, including submissions/supplements/variations and approved dossiers. • Demonstrated ability in conformance review of registered documentation and practices. • Comprehensive knowledge and application of the Quality Management system (QMS). • Excellent written and verbal communication skills. • Demonstrate Project Management and organizational skills. • Good working knowledge of applicable systems including electronic dossier submission systems
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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