Executive-AQA Reviewer

We are seeking a meticulous AQA - Data Reviewer to conduct quality reviews of key pharmaceutical documents and ensure compliance with regulatory standards, including 21 CFR. The ideal candidate will collaborate with cross-functional teams to maintain document integrity and support continuous quality improvement.Key Responsibilities:Conduct thorough quality...

Ensure Adherence and compliance to requirements of good manufacturing practices, GDP, EHS practices and company policies and procedures.Extending support to all the key functions to establish and effectively implement the quality system and procedures to maintain a state of compliance.review and approval of standard operating procedure, General testing...

Ensure Adherence and compliance to requirements of good manufacturing practices, GDP, EHS practices and company policies and procedures. Extending support to all the key functions to establish and effectively implement the quality system and procedures to maintain a state of compliance. review and approval of standard operating procedure, General testing...

Roles and ResponsibilitiesConduct quality reviews of documents, including CAPAs, change controls, and 21 CFR compliance.Ensure adherence to company policies and procedures through document review.Develop and maintain a thorough understanding of regulatory requirements for pharmaceuticals.Provide feedback on document quality and suggest improvements where...

Roles and Responsibilities Conduct quality reviews of documents, including CAPAs, change controls, and 21 CFR compliance. Ensure adherence to company policies and procedures through document review. Develop and maintain a thorough understanding of regulatory requirements for pharmaceuticals. Provide feedback on document quality and suggest improvements where...

Roles & ResponsibilitiesPerform activities as per safety precautions, cGMP, and adhere to Quality Policy.Perform and document activities as per good documentation practices (GDP) with data integrity.Verify laboratory ambience for a clean and safe workplace.Verify analytical instrument calibration.Ensure continuous training and development of team...

Roles & Responsibilities Perform activities as per safety precautions, cGMP, and adhere to Quality Policy. Perform and document activities as per good documentation practices (GDP) with data integrity. Verify laboratory ambience for a clean and safe workplace. Verify analytical instrument calibration. Ensure continuous training and development of team...

Role & responsibilitiesReview and approve Supplier qualification documents(NSQR,VQ Documents, etc.)Prepare and distribute corporate-approved supplier listsSupport regulatory and customer audits for vendor complianceManage vendor notifications and delist declarationsTrack and review vendor documents as per SOP timelinesAssess and introduce new suppliersEnsure...

Role & responsibilitiesPrepare and harmonize CQA SOPs, forms, and schedules.Manage document control: issuance, archival, retrieval, and destruction of GMP documents.Coordinate change controls, impact assessments, and approvals.Monitor SOP implementation and support sites during audits.Identify procedural gaps vs. global regulatory guidelines (ICH, WHO, 21...

Role & responsibilitiesKey Responsibilities:1. Process Development & Optimization:Design, implement, and optimize chemical synthesis and purification processes for APIs.Scale-up lab processes to pilot plant and commercial production.Improve yield, quality, and cost through continuous process improvements and parameter adjustments.2. Technology...