Job Description :
Position Purpose
Functions as an Annual Report Strategist for Brands-NDA Annual Report (AR) team, working with CMC Global Regulatory Strategist - CMC (GRS-CMC) and Cross Functional Teams to prepare and submits the CMC contributions of US NDA/ANDA/BLA/PMA/IND Annual Reports as per defined timelines.
Position Purpose
Functions as an Annual Report Strategist for Brands-NDA Annual Report (AR) team, working with CMC Global Regulatory Strategist - CMC (GRS-CMC) and Cross Functional Teams to prepare and submits the CMC contributions of US NDA/ANDA/BLA/PMA/IND Annual Reports as per defined timelines.
Responsibilities
• Manages day-to-day regulatory activities associated with assigned Annual Reports within agreed upon timelines.
• Reviews changes made during the reporting period for completeness and accuracy. Develops initial Annual Report regulatory strategy while considering registered content and seeks endorsement by the CMC GRL.
• Authors and/or compiles CMC contributions based on changes made during the appropriate reporting period, i.e. Module 1 & 3 under the guidance from the CMC GRL as appropriate and within agreed timelines.
• Reviews all appropriate systems for post approval changes submitted and approved along with commitments made and fulfilled
• Reviews technical/supportive information for submission to support AR changes
• Manages and reviews stability contributions for accuracy and consistency with commitments
• Reviews and applies pertinent US regulatory guidelines to confirm Annual Reportable filing classifications.
• Develops technical justification of change for agency submission as needed
• Updates impacted dossier components as needed
• Coordinates M3.2.R Ancillary documents as needed
• Escalates delays in timelines and flags identified risks to the CMC GRL and/or appropriate leadership
• Coordinates internal document review and sign off.
• Utilizes Pfizer’s CMC systems, i.e. GDMS, PDM, SPA, etc., as appropriate.
• Ensures compliance to Pfizer internal procedures and training SOPs (Power 2 Learn).
• Manages day-to-day regulatory activities associated with assigned Annual Reports within agreed upon timelines.
• Reviews changes made during the reporting period for completeness and accuracy. Develops initial Annual Report regulatory strategy while considering registered content and seeks endorsement by the CMC GRL.
• Authors and/or compiles CMC contributions based on changes made during the appropriate reporting period, i.e. Module 1 & 3 under the guidance from the CMC GRL as appropriate and within agreed timelines.
• Reviews all appropriate systems for post approval changes submitted and approved along with commitments made and fulfilled
• Reviews technical/supportive information for submission to support AR changes
• Manages and reviews stability contributions for accuracy and consistency with commitments
• Reviews and applies pertinent US regulatory guidelines to confirm Annual Reportable filing classifications.
• Develops technical justification of change for agency submission as needed
• Updates impacted dossier components as needed
• Coordinates M3.2.R Ancillary documents as needed
• Escalates delays in timelines and flags identified risks to the CMC GRL and/or appropriate leadership
• Coordinates internal document review and sign off.
• Utilizes Pfizer’s CMC systems, i.e. GDMS, PDM, SPA, etc., as appropriate.
• Ensures compliance to Pfizer internal procedures and training SOPs (Power 2 Learn).
Candidate Profile
• Postgraduate in Pharmacy / Science
• Excellent oral and written English communication skills. Good conceptual and reasoning skills. Attention to details.
• Knowledge on Regulatory requirements of post approval changes for US Oral Solid Dosage form and sterile injectable manufacturing and regulatory data requirements for submission of ARs.
• Knowledge in retrieving information from company’s and regulatory agency databases.
• Basic level of knowledge on general standards, processes and policies of Pfizer/Pharmaceutical manufacturing Industry.
• Postgraduate in Pharmacy / Science
• Excellent oral and written English communication skills. Good conceptual and reasoning skills. Attention to details.
• Knowledge on Regulatory requirements of post approval changes for US Oral Solid Dosage form and sterile injectable manufacturing and regulatory data requirements for submission of ARs.
• Knowledge in retrieving information from company’s and regulatory agency databases.
• Basic level of knowledge on general standards, processes and policies of Pfizer/Pharmaceutical manufacturing Industry.
Additional Information
Qualification : M.Pharm, M.Sc
Location : Chennai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Global Regulatory Affairs
End Date : 15th December, 2018
Qualification : M.Pharm, M.Sc
Location : Chennai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Global Regulatory Affairs
End Date : 15th December, 2018
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