Specialist, Quality Assurance

Overview

Manage day-to-day quality and compliance activities at external manufacturing sites involved in the manufacturing and supply of P&G products. Ensure the sites follow the Quality Management System and that the Consumer Healthcare business meets customer expectations and regulatory and legal requirements.

What you'll do

• Support quality and compliance-related projects for Contract Manufacturing sites.
• Support supplier management-related activities.
• Support Quality Technical Agreement management as and when required.
• Manage Change Control activities.
• Manage NCR activities.
• Manage investigations and complaints.
• Manage CAPA activities via any other tool as and when implemented.
• Compile data and report scorecards.
• Support the review and approval of technical specifications.
• Review and approve validation and transfer documents.
• Support planning, supervising, and reporting of stability.
• Support self-inspection audits and CAPA compliance reports.
• Support GxP training activities.
• Support activities for technology transfer at sites.

What you'll need

• 3-5 years of desired experience.
• A degree in pharmaceutical sciences or equivalent.
• Previous experience in a technical department such as Operations, R&D, Quality Supervisor, or a similar management position.
• Strong working knowledge of the Quality Assurance department.
• Experience in the pharmaceutical industry and management.
• Proficiency in MS Office and electronic tools.
• Professional written and verbal communication skills.

Nice to have

• Management, FDA understanding, or a related field is preferred.

Details

• Location: Mumbai General Office.
• Employment type: Full time.
• This role reports to the Manager, Quality Assurance.