Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.
Post : Officer - QA, Pharmacueticals
Job Description
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
Candidate profile
• Graduate / Post Graduate in Pharmacy or Chemistry
• 0 - 3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements
• 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
Additional Information
Experience : 0 - 3 years
Qualification : B.Sc, M.Sc, B.Pharma / M.Pharma
Location : Ankleshwar
Industry Type : Pharma
Functional Area : QA, Pharmacueticals
Job ID : R2537715
Last date : 20th June, 2020
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