Work as Senior Manager – Regulatory @Glenmark Pharmaceuticals Ltd
Post : Senior Manager – Regulatory (Post approval Life cycle Management)
The objective of the role is to lead the team for strategic evaluation of post approval changes for US market as per regulatory guidelines. The incumbent would be responsible for all PLCM activities for US Market like Supplements – PAS, CBE-30, CBE-0, and Annual Reports. Would also be responding to Health authority deficiencies raised on post approval submissions.
• Strategically evaluate all change proposals (site transfer/alternate process API/alternate API vendors/excipients/container closure vendor/pre-launch changes or any other change to approved dossier) received from various stakeholders and provide guidance in terms of filing strategy.
• Planning, and ensuring timely submission of various supplements by providing guidance to team for submission of various supplement i.e. PAS, CBE-30 and CBE-0 and other general correspondence.
• Technical evaluation of the deficiency received from FDA and coordination with various responsible stakeholders to ensure quick turnaround time for replying to Complete response letters/Information requests received on supplements from USFDA. Also evaluation of response received from R&D/Plant to ensure that the responses submitted are technically responded to meet FDA’s requirements and in turn result in faster approval of proposed change.
• Monitoring of timely submission of Annual Reports (AR) to the agency within two months of anniversary date and also ensure that it meets internal timelines as captured in the AR database.
• Provide support to ensure patient/pharmacist queries received from the Pharmacovigilance team are responded in a timely manner.
• Ensure regulatory compliance at all levels of operations. Coordination for USP forum monograph submission.
• Provide support to devise best strategies for various cost benefit programmes (alternate process/alternate API/excipient/container closure vendor/site transfer/any other changes to approved dossiers) run across the organization for US market
• Maintenance of various regulatory database to capture the complete history of the product.
• Keep updated with various guidelines from Health authorities
• Bachelors Degree in Science – Preferably M.Pharm
• 11-15 years of relevant industry experience
• Sufficient knowledge and experience in post approval life cycle management of US.
• Planning and leading teams on PLCM activities like Supplements – PAS, CBE-30, CBE-0, and Annual Reports/Variations for emerging markets
• Sound knowledge in reviewing formulation and Analytical documents with respect to various dosage forms like oral solids/topical/respiratory and injectables dosage forms.
• Good written and oral communication skills. Command over written and oral English
• Should have team handling skills
Experience : 11-15 years
Qualification : B.Sc, M.Pharm
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory
End Date : 10th September, 2020
If the above job description matches with your profile then please email your CV at firstname.lastname@example.org
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube