Senior Executive - QA

Posted Yesterday
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Ankleshwar, Bharūch, Gujarāt
Senior level
Pharmaceutical
The Role
The Senior Executive - QA is responsible for ensuring product quality through compliance with quality standards, local regulations, and effective training. This role involves performing in-process checks, managing documentation, executing validation protocols, and coordinating compliance activities while overseeing continuous improvement initiatives within the quality management system.
Summary Generated by Built In

Quality Management/Continuous Improvement 

Line Clearance and shop floor compliance 

Carry out in-process checks and calibration of IPQC instruments. 

Handle e tools i.e. SAP Hana, LIMS, eDMS, Track Wise system. 

Assisting in 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 

Experience: 7 to 10 years in QA

Top Skills

Sap Hana
The Company
HQ: Dolní Měcholupy
3,360 Employees
On-site Workplace
Year Founded: 1999

What We Do

Zentiva is a Pan-European Platform developing, manufacturing and providing high-quality and affordable medicines to more than 100 million people in Europe. Zentiva has 4 wholly owned manufacturing sites and a broad network of external manufacturing partners to ensure supply security. We offer solutions in key therapeutical areas like Cardiology & Circulation, Diabetes, Oncology, Respiratory, CNS and focus on expanding our portfolio in self-care. The company is Private Equity owned, delivering sustainable double-digit growth, with an ambitious 5-year plan for further strong (organic and inorganic) growth across Europe.

We are a team of almost 5,000 unique talents bonded together by our mission to deliver high-quality and affordable medicines to people who depend on them every day. We want Zentiva to be a great place to work, where everyone feels welcomed and appreciated and can be their true selves contributing to the best of their ability.

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