Asst. Manager
5 days ago
Roles and Responsibilities
- Ensure compliance with cGMP guidelines during batch manufacturing of eye drops, injectables, parenteral products, and injections.
- Monitor production processes to ensure quality standards are met.
- Conduct regular audits to identify areas for improvement and implement corrective actions.
- Collaborate with cross-functional teams to resolve issues related to formulation development and process optimization.
- Develop and maintain documentation for batch records, SOPs, and other relevant documents.
Desired Candidate Profile
- 8-12 years of experience in pharmaceutical industry with expertise in ophthalmic manufacturing.
- Bachelor's degree in Pharmacy (B.Pharma) or equivalent qualification from a recognized institution.
- Strong understanding of Batch Manufacturing, Injectables, Parenteral, Eye Drop & Injection processes.
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