UniMed & UniHealth

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Summary

Education

Experience

Additional Requirements

Having good communication skill both in English and Bangla
Good computer knowledge
At least 10 years experience in reputed pharmaceutical company (s) out of which 2-3 years in similar position will be preferred

Implement all quality functions of the Pharmaceutical Manufacturing Plant
Prepare and revise quality documents, this includes Site Master File, Quality Policy, Quality manual, Validation Policy & Documents, Validation Master Plan, Calibration master plan, Training manual, SOPs etc.
Provide guidance, interpretation, support, training, and input on the interpretation and implementation of regulatory guidelines, company procedures and policies
To monitor calibration process of monitoring and measuring equipment, calibration schedule and relevant documentation.
Coordination and execution BMR and BPR approval & issue of BMR and BPR for production
Coordinate and execute all the validation, qualification and technology transfer activities
To check and monitor that DQ, IQ, OQ & PQ of facilities, equipment and utilities are performed and documented as per regulatory requirements
To implement and maintain of ISO 9001 : 2015 QMS
Acts as a quality liaison with regulatory authorities, ISO 9001 : 2015 QMS inspectors, and external auditors during inspections
Oversee the nonconforming product, market complaint, product recall, change control, deviation procedure, release, rejection, annual product quality review (APQR) vendor qualification and corrective and preventive actions.
Co-ordination with other department to enhance and implement company’s Quality Management System.

We offer: Excellent work environment, attractive compensation package, medical assistance for employee and family members, provident fund, gratuity, festival bonus, profit share, group life insurance, faster career progression, requisite training

Full Time

Gazipur