Zentiva hiring B Pharm & M Pharm Graduates | Pharma QC Job Role | Apply Now
Looking for a Pharma QC Job with a global pharmaceutical company? Zentiva is hiring a Quality Operations Specialist for its Ankleshwar, Gujarat location. This opportunity is ideal for Pharmacy professionals with experience in quality assurance, regulatory affairs, and pharmaceutical manufacturing. If you’re seeking a rewarding Quality Control Job in the pharmaceutical industry, this role offers excellent exposure to quality systems, compliance, and product quality reviews.
- Job Title: Quality Operations Specialist
- Department: Scientific Affairs
- Job ID: R2468955
- Location: Ankleshwar, Gujarat
About the Company
Zentiva is a leading pharmaceutical company focused on providing high-quality and affordable medicines to patients worldwide. The company operates across multiple markets and maintains strong quality and compliance standards throughout its manufacturing and commercial operations. This Pharma QC Job offers an opportunity to work in a quality-focused environment supporting global pharmaceutical operations.
Job Description
The Quality Operations Specialist will support quality assurance and compliance activities while ensuring adherence to corporate quality standards and regulatory requirements. The role primarily focuses on Product Quality Review (PQR) management, quality documentation, trend analysis, KPI monitoring, CAPA follow-up, stability data evaluation, compliance investigations, and quality operations support. This Quality Control Job provides valuable exposure to pharmaceutical quality systems, regulatory compliance, inspections, and continuous improvement initiatives.
Key Responsibilities
- Lead PQR reviews, documentation, and KPI tracking.
- Manage quality records, deviations, and compliance documentation.
- Analyze manufacturing, stability, and quality data.
- Follow up on CAPA actions and process improvements.
- Support audits, inspections, supplier reviews, and batch control activities.
Qualifications & Experience
- Education: B Pharm, M Pharm degree
- Experience
- Minimum 3–6 years of experience in Quality Assurance, Regulatory Affairs, Pharmaceutical Manufacturing
Required Skills
- Knowledge of cGxP, stability regulations, and PQR processes.
- Experience in pharmaceutical manufacturing and compliance.
- Proficiency in SAP, Quality Forward, Share/DrugTrack, and eDMS.
- Strong data interpretation and analytical review skills.
- Strong organization, communication, and decision-making abilities.
- Team-oriented, adaptable, and capable of managing priorities effectively.
Additional Responsibilities
- Ensure compliance with cGxP principles and Zentiva Quality Standards.
- Participate in mandatory quality training programs.
- Follow occupational health, safety, and environmental policies.
- Report adverse events and safety-related information as per internal procedures.
- Adhere to company policies, ethical standards, and governance requirements.
- Support ESG initiatives aligned with Zentiva’s sustainability strategy.
