Executive

Job description

**Roles and Responsibilities** - Execute equipment & utility qualification, validation, and documentation activities according to OSD equipment requirements and cGMP guidelines. - Conduct IQ, OQ, PQ, URS, and other validation protocols as per SOPs. - Ensure compliance with regulatory requirements by maintaining accurate records of all validation activities. - Collaborate with cross-functional teams to resolve issues related to equipment performance and maintenance. - Develop and implement effective quality control procedures for pharmaceutical manufacturing processes. **Desired Candidate Profile** - 5-10 years of experience in Equipment Qualification & Validation (EQL) role in a pharmaceutical industry setting. - Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma). - Strong understanding of CGMP regulations and 21 CFR part 820 standards. - Proficiency in executing various types of validations such as IQ, OQ, PQ, URS etc.