Senior Executive - In Process Quality Assurance (IPQA) Pelltech Healthcare

5.0 - 9.0 years

0 Lacs

palghar, maharashtra

On-site

As a leading IPQA (In Process Quality Assurance) Team, your role will involve assigning tasks to IPQA chemists for day-to-day activities. You will participate in, review, and approve protocols and reports for various studies such as user requirement specifications, qualifications, validations, risk assessments, and other site-related activities. It is crucial to ensure that all commitments to regulatory authorities are fulfilled for the concerned batch and to actively contribute to the design, development, approval, and implementation of quality systems at the manufacturing site. Your responsibilities will include participating in external inspections of the manufacturing site, preparing CAP...

Posted 3 days ago

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Manager - Production -Tablets & Capsules Mfg Pelltech Healthcare

5.0 - 9.0 years

0 Lacs

palghar, maharashtra

On-site

As a Production Manager, you will be responsible for planning, organizing, coordinating, and controlling production activities according to the monthly production plan. Your role will involve monitoring and controlling the manufacturing department to ensure efficiency and quality standards are met. Your key responsibilities will include: - Investigating complaints, recording deviations and incidents, suggesting change control processes, handling non-conformance, returned goods, product recalls, vendor audits, and external testing laboratories audits. You will also be responsible for assessing their impacts, reviewing reports, and monitoring the implementation of Corrective and Preventive Act...

Posted 1 month ago

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QA-Assistant Manager/Dy.Manager Sterile/Injectable MJ Biopharm

10.0 - 18.0 years

12 - 17 Lacs

pune

Work from Office

Quality Management System: Oversight/Handling of Handling of Change Control, Incident / Deviation and CAPA. Following and tracking of Change Control, Incident /Deviation and CAPA. Involved in the investigation activity whenever required. Ensure that products are manufactured in compliance to Regulatory requirements and as per Good Manufacturing Practices. Ensure that production and manufacturing activities are undertaken in compliance to SOPs, systems, procedure and GMP/GLP requirements. Maintain GMP compliance in various departments to manage the production in line with the current GMP requirement. Handling of Change Control, Deviation, risk assessment and CAPA as per company procedure Veri...

Posted Date not available

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