Sanofi  Pharma Ankleshwar Jobs For Fresher & Experienced - Officer QA

Sanofi  Pharma Ankleshwar Jobs For Fresher & Experienced - Officer QA

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’ requirements.

Education:

Graduate / Post Graduate in Pharmacy or Chemistry

Experience:

0 - 3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements

Job Location: Ankleshwar

Designation & Department: Officer QA

Technical skills & Competencies / Language

Knowledge of GMP and regulatory requirements

Good interpersonal skills and able to manage conflicts

Believes and lives in company values

Skilled in team work

Must be able to present complicated technical issues in an easy and understandable manner and obtain appropriate actions

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’s, 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 behaviours and promptly reporting other potentially hazardous situations

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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