33 Capa Management Jobs - Page 2

Detailed Job Role Oversee quality systems, conduct audits, approve batches, implement SOPs and CAPAs to maintain pharma quality standards. KRA (Key Responsibility Areas) Audits, batch reviews, SOP updates, CAPA management, GMP compliance KPI (Key Performance Indicators) Deviation closure rate, audit pass, CAPA closure time, complaint frequency Job Summary: We are seeking a diligent Quality Assurance Officer to oversee quality systems, conduct audits, approve batches, and ensure compliance with GMP standards. The ideal candidate will implement and maintain SOPs, manage CAPAs, and drive continuous improvement in pharmaceutical quality management. Key Responsibilities: Oversee and maintain the ...

Date: 21 Jun 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Job Title: Lead Manufacturing Operations -OSD Job Location: Biocon Park, Bengaluru Department: Drug Product Manufacturing About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in lett...

The Quality Lead position at ProPharma involves driving positive change and process improvement in the assigned region. This role serves as an independent and objective entity, supporting various operational teams and performing quality activities as per ProPharma Group's Quality Policy and procedures. The Quality Lead is responsible for Audit Management, Deviation and CAPA Management, Document Control, and other Quality Management System activities. Developing, managing, and executing quality management processes to ensure compliance with regulatory requirements is a key aspect of this role. Essential Functions: - Maintaining awareness of and ensuring adherence to applicable SOPs/controlled...

As a Senior Executive/ Assistant Manager in the Corporate Quality Assurance Pharmacovigilance department, located in Kandivali - West, Mumbai, your primary responsibility will be to ensure compliance with SOPs of the Corporate Pharmacovigilance cell and Corporate Quality Assurance. You will be expected to assist the Corporate pharmacovigilance cell in overseeing vendor compliance through periodic reviews and vendor audits. In this role, you will act as a liaison with internal and external auditors, taking responsibility for ensuring corrective actions are implemented according to their specifications. Your duties will also include persuading Corporate pharmacovigilance cell staff to adopt an...

The Manager-II in the MSTG department at Dadra is responsible for providing support in the execution and monitoring of trial, scale up, and exhibit process qualification batches. This includes preparing and reviewing new product documents such as material requirement sheets, master formula cards, bill of materials, risk assessment reports, sampling protocols, reports, exhibit batch manufacturing records, and exhibit protocols. Additionally, the role involves sharing process knowledge with cross-functional departments through presentations to facilitate smooth technology transfer. The Manager-II will also be involved in reviewing and evaluating product history and process parameters for techn...

As a Quality Operations Support at Sandoz, your major accountability is to adhere to the current GxP and compliance requirements while delivering quality operations to ensure product quality compliance and regulatory workflows. You will be responsible for ensuring compliance to Sandoz quality standards, relevant regulatory requirements, filed product quality standards, and service level agreements. Additionally, you will support the implementation of service quality and process improvement projects, as well as CAPA management within GQSI. It is crucial to comply with internal functional requirements, including KPI reporting, ticket management tools, and other internal procedures and processe...

We are looking for a meticulous and experienced Technology Transfer Manager to spearhead the efficient transfer of technology for solid dosage forms at Evertogen Life Sciences . This pivotal role involves overseeing the seamless transition of OSD products from R&D or third-party development to our manufacturing plant, ensuring successful scale-up, unwavering regulatory compliance, and adherence to the highest quality standards. The ideal candidate will champion the preparation and review of critical technical documents, including technology transfer protocols, BMR/BPR, and process validation reports, while actively coordinating with cross-functional teams such as QA, QC, RA, and Production. ...

Job Description Summary We are looking for a detail-oriented and compliance-focused QA and Compliance Executive to join our Commercials Department in Mumbai . This role is vital to ensuring that all pharmacovigilance (PV) processes, data documentation, and reporting meet global regulatory standards and internal quality benchmarks. You will play a central role in managing safety data, identifying adverse events, ensuring timely and accurate reporting, and supporting inspection readiness through audits and continuous process improvement. The ideal candidate will have strong knowledge of healthcare regulations such as EMA, FDA, HIPAA, and Good Pharmacovigilance Practices (GVP), along with hands...