Role Objective:-

We are looking for an experienced professional to lead and manage manufacturing documentation and compliance activities, ensuring adherence to cGMP standards and regulatory requirements while maintaining audit readiness.

Key Responsibilities:-

1.Ensure strict adherence to cGMP guidelines across manufacturing operations.

2.Review and approve SOPs, formats, batch records, and documentation

3.Handle deviations, CAPA, change controls, and risk assessments

4.Coordinate with QA, QC, Stores, Tech Transfer, and QMS teams

5.Monitor and track CAPA closure and ensure compliance

6.Approve validation protocols, cleaning validation, and qualification reports

7.Ensure timely completion of batch documentation

8.Conduct training on SOPs, deviations, and GMP practices

9.Maintain audit readiness and strong documentation practices

10.Optimize manpower and equipment utilization.

Qualifications & Experience:-

1.B.Pharm / M.Pharm

2.Minimum 12+ years of experience in production documentation

3.Experience in semi-solid dosage forms

4.Strong knowledge of cGMP, QMS, and regulatory compliance

5.Positive leadership and coordination skills

Apply Now: [email protected]

WhatsApp: (phone hidden)

📌 Manufacturing-Documentation Manager (North Goa)
🏢 Encube Ethicals
📍 North Goa