Piramal Pharma Hiring For Executive - Quality Assurance

Piramal Pharma Hiring For Executive - Quality Assurance

Piramal Pharma Hiring For Executive - Quality Assurance

Executive - Quality Assurance

Location:Mahad, Maharashtra

Full job description

• Preparation and updation of Validation Master Plan (VMP)

• Preparation of Process validation, Computer system validation protocol and report.

• Preparation of product matrix and Cleaning Validation/verification protocol and Report.

• Preparation of qualification and requalification protocol and report for processing equipment/instrument, utilities, and facility.

• Preparation of area validation protocol and reports.

• Preparation and review of quality risk assessments.

• Review of calibration certificate (External/internal).

• Preparation, issuance, review & archival of BMR/BPR.

• Batch Record storage, retrieval & destruction.

• Preparation of APQR.

• Line Clearance for Manufacturing, Packing & Dispensing activity.

• Sampling of Bulk and Finished goods.

• Review of production records and Finished Goods verification.

• Online observation of process deviation and effective implementation of CAPA.

• Management of Change Control / CAPA / Incidences.

• Handling of Change Control and follow-up for the implementation of Changes.

• To coordinate & maintain change control, deviation records.

• Complaint handling.

• Preparation and updation of Q.A departmental SOPs and loading it in DCS (Document Control System) ENSUR 4.2

• To give training as per the Training schedule.

• To coordinate training program of the company along with HR, including on Job Training.

• Documentation Management as per SOP.

• To provide necessary documents / data required by CQA and as per customer’s requirement.

• Conduct, monitor and review of compliance of Self Inspection Program.

• Audit compliance coordination, to compile CAPA and prepare response to Audit report in co-ordination with QA Head and technical team.

• Execution of requirements for food / Dietary supplements regulations for export market (US)-21 CFR Part 111

• Ensuring avoidance of breach of data integrity in area.

• Implementation of effective sanitation programme in area.

• Adherence to the requirements of EHS norms.

• Execution of various initiatives as are suggested by corporate functions.

• To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.

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