Ad-din Pharmaceuticals Ltd.

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Summary

Education

Experience

Additional Requirements

Having minimum 5-years working experience in any pharmaceuticals company in sterial area
Must be hard worker, self-motivated, honest, sincere & obedient
Must have experience in computer knowledge (Microsoft office, internet & email)

Lead the development, implementation, and maintenance of the Quality Management System (QMS) for the new sterile injectable and ophthalmic plant
Ensure compliance with Current Good Manufacturing Practices (cGMP), regulatory guidelines, and international standards during the establishment and operation of the plant
Oversee the validation and qualification of sterile production processes, equipment, and facilities
Coordinate and conduct internal audits, risk assessments, and root cause analyses to ensure continuous improvement in quality systems
Lead investigations of deviations, CAPAs & quality incidents & provide solutions to mitigate risks
Collaborate with regulatory bodies and internal teams to prepare for successful regulatory inspections and approvals
Ensure accurate and timely documentation of all activities related to the new sterile plant project
Identify and resolve technical and operational issues to ensure smooth project execution

Provident Fund, Gratuity, Festival Bonuses. Health Service benefits as per company policy.

Full Time

Jashore

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