Ankur Sharma

Seeking on entry in to the hollowed portal of pharmaceutical where my skill and ability are be utilized and enhanced that leading to my professional growth as well as organizational growth.

• Time Management
• Self Confidence
• Loyalty
• Hard Working

• Father's Name: Mr. Ramesh Sharma
• Date of birth: 11/21/1988
• Gender: Male
• Nationality: Indian
• Marital status: Married

• Zydus Lifesciences Ltd.-Sez-I, Ahmedabad:
• Lead IPQA
• Reviewed and updated Standard Operating Procedures SOPs to reflect changes in regulations and industry best practices.
• Oversaw the calibration and maintenance of laboratory equipment, guaranteeing accuracy in testing and analysis.
• Conducted thorough inspections of manufacturing processes to maintain product quality and compliance with regulatory standards.
• Collaborated with production teams to implement quality improvements and streamline operations for enhanced efficiency.
• Facilitated risk assessments for product quality and safety, implementing strategies to minimize potential issues.
• Prepared detailed reports on quality assurance activities, offering recommendations for improvements to senior management.
• Trained new staff in IPQA procedures, emphasizing the importance of quality assurance in pharmaceutical manufacturing.
• Monitored critical control points during production, taking immediate action to rectify any deviations detected.
• Led cross-functional teams in the execution of risk mitigation strategies.
• Mankind Pharmaceuticals Limited, Sikkim:
• Validation & Qualification team Member.
• Implemented continuous improvement initiatives to enhance validation methodologies and reduce time-to-market.
• Facilitated training sessions for team members on validation principles, techniques, and best practices.
• Reviewed and approved validation documents, ensuring accuracy, completeness, and compliance with internal and external standards.
• Led validation team in designing and executing comprehensive test strategies to confirm product quality and compliance.
• Oversaw the investigation and resolution of validation-related issues, mitigating risks and preventing product delays.
• Developed and maintained robust documentation for all validation processes, including protocols, reports, and standard operating procedures.
• Managed resource allocation effectively, ensuring optimal productivity and adherence to deadlines within the validation team.
• Coordinated with cross-functional teams to align validation activities with project timelines and business objectives.
• Utilized statistical tools and software for the design and analysis of validation studies.
• Prepare and execute equipment's and Utility Qualification protocols.
• Glenmark Pharmaceuticals Limited, Baddi, Himachal Pradesh:
• IPQA activity at shop floor. Overall responsible for the Process Validation & Cleaning Validation of drug products which includes Audit readiness, compliance of documents, concern raising and follow-up, status tracking, SOP gap assessment., Preparation and review of documents related to Equipment & Utility Qualification (HVAC & Compressed air. Review of Process Validation documents such as Risk Assessment, Change control, MFC, Batch Records, PPQ Protocol, PPQ reports. Execution of Temperature Mapping and Transport Validation, Issuance, retrieval and destruction of master and controlled documents like Batch records, SOPs, formats, log books.