Zentiva Hiring For Quality Assurance Department 

Zentiva Hiring For Quality Assurance Department 

About Zentiva

Zentiva is a producer of high-quality affordable medicines serving patients in Europe and beyond. With a dedicated team of more than 4 700 people and a network of production sites - including flagship sites in Prague, Bucharest, and Ankleshwar - Zentiva strives to be the champion of branded and generic medicines in Europe to better support people’s daily healthcare needs.

At Zentiva it is our aspiration that healthcare should be a right and not a privilege. More than ever, people need better access to high-quality affordable medicines and healthcare. We work in partnership with physicians, pharmacists, wholesalers, regulators, and governments to provide the everyday solutions that we all depend on.

Zentiva Job Vacancy details: 

Position: Officer - QA

Work Locations: India / Ankleshwar

Educational Qualification : 

B. Pharm / M. Pharm from reputed university

Experience:  

1 to 3 years similar experience in OSD manufacturing large unit.

Job Responsibilities: 

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

How To Apply For Zentiva Job 

Click Here For Apply