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1.0 - 5.0 years

0 Lacs

gujarat

On-site

As a part of this role in the pharmaceutical industry, you will be responsible for handling CAPA (Corrective and Preventive Actions), OOS (Out of Specification) incidents, and deviations effectively. Your duties will also include the generation of Standard Operating Procedures (SOPs) to ensure smooth operations within the organization. Additionally, you will be involved in validation processes and maintaining compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). This is a full-time position with a day shift schedule. The ideal candidate should have a total work experience of 1 year in a similar role within the pharmaceutical sector. The work location for ...

Posted 1 month ago

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1.0 - 5.0 years

0 Lacs

gujarat

On-site

As a valuable member of our team in the pharmaceutical industry, you will be responsible for various key tasks including CAPA, OOS, Deviation management, SOP's generation, and ensuring Validation, GDP, GMP compliance. Your role will play a crucial part in maintaining high quality standards and regulatory requirements. This is a full-time position with a day shift schedule. The ideal candidate should have a total work experience of 1 year, preferably within the pharmaceutical sector. The work location for this role will be in person, providing you with the opportunity to actively engage with the team and processes.,

Posted 1 month ago

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