Executive

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.