Job Description

Experience:

2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements

JOB PURPOSE

Generic

Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with customers\xe2\x80\x99 requirements, living Group\xe2\x80\x99s Values and Code of Ethics.

Specific additions (if needed)

KEY ACCOUNTABILITIES

Quality Management/Continuous Improvement

Line Clearance and shop floor compliance

Assisting in Complaint Investigation system at site

Assisting in Qualification and validation system, change control system, deviations

Preparing & review the Annual Product Quality Review

Review of Batch Manufacturing & Packing Records

Coordination of cGMP Training activity.

Compliance

Ensure adherence to company Quality Standards, Local FDA MHRA regulations, by

Understanding the requirements Performing the Gap analysis to find out the gaps in existing system Preparing a compliance plan for closure of gaps Execution of compliance plans Review of completion for compliance activity Validations & Qualifications:

Ensure validated status of all equipment\xe2\x80\x99s, manufacturing processes, and cleaning processes

Review of protocols for qualification and validation of facility/ equipment / product / process

Review of validation reports after execution of validation of facility /equipment / product / process

Documentation Control:

Preparation and Review of SOPs

Controlled distribution and archival of documents & record

Control of master documents

Assuring quality of products by :

Ensuring SOP compliance

Review of Batch Manufacturing & Packing Records

Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints

Ensuring the effectiveness review of the implemented CAPA

cGMP Training:

To prepare training modules and organize training in GMP

Execute the training program in coordination with all concerned departments

Other:

Review of maintenance and calibration program

Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations

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