QA Manager

Role Summary:We are seeking a highly competent and detail-oriented Manufacturing QA Personnel with substantial experience in Sterile Injectable manufacturing, specifically focusing on Small Volume Parenterals (SVP) including Dry Powder, Liquid, and Lyophilized Injections. The selected candidate will ensure shop floor compliance and enforce GMP practices to...

Quality Oversight: Ensuring compliance with regulatory standards and internal quality procedures throughout the manufacturing process.Documentation Review: Manage and review quality-related documents, including SOPs, batch records, and quality manuals.Audit Preparation: Conducting internal audits and coordinate with QA Manager for external audits to ensure...

JOB TITLE : Sr. QA OfficerRequirements:B.Pharm/M.Pharm with 4–5 years QA experience in oral solid dosage form (tablet, capsule and Dry SyrupStrong documentation, audit preparedness, and regulatory understandingKey Responsibilities:1. Manage QMS:Deviation, Change Control, CAPA, Risk Assessment, Product Complaints, Recall2. Review & Maintain:BMR, BPR, MFR,...

Job descriptionResponsibilities:Lead and support the implementation, maintenance, and continuous improvement of Quality Management Systems (QMS).Review and approve Standard Operating Procedures (SOPs) relevant to the QA department.Develop and implement QA-related SOPs in alignment with regulatory and organizational standards.Oversee the review, approval,...

Role & responsibilitiesRequired QMS/QA Documentation and IPQA person with a minimum experience of five to eight years. The candidate should of Pharmaceutical Background.Preferred candidate profile

Knowledge and experience of Sheet Metal plant Validation Audit Process Job Types Full-time Permanent Schedule Day shift Work Location In person

Efficiently monitor all operations which affect the quality.Devise procedures for inspecting and reporting all the persisting quality issues.Assure the consistency and reliability of production with thorough checking procedures and final output.Supervise and guide inspectors, technicians, and all other staff.Report all malfunctions to production executives...

Following will be the responsibilities of the position holder: 1. To ensure cGMP compliance at site. 2. Responsible for Vendor Qualification and Management 3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status. 4. To review vendor documents for Vendor Qualification. 5. To perform the Vendor...

Following will be the responsibilities of the position holder:1. To ensure cGMP compliance at site.2. Responsible for Vendor Qualification and Management3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.4. To review vendor documents for Vendor Qualification.5. To perform the Vendor audit and...

Following will be the responsibilities of the position holder: 1. To ensure cGMP compliance at site. 2. Responsible for Vendor Qualification and Management 3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.4. To review vendor documents for Vendor Qualification. 5. To perform the Vendor audit...