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Executive Position in Quality Management System | Chemistry Job at Zentivia
Are you looking for a rewarding Executive Position in the pharmaceutical industry? Join our team as an Executive – Quality Management System (QMS) in Ankleshwar, India. This role is perfect for professionals seeking a Chemistry Job with hands-on experience in analytical assurance and compliance. You’ll be part of a dynamic QMS team ensuring accuracy, integrity, and adherence to industry standards. If you’re passionate about quality, data integrity, and analytical excellence, this opportunity is ideal for advancing your career in pharmaceutical jobs in India.
About Our Company
Our company is a trusted name in the pharmaceutical manufacturing industry, known for its commitment to innovation, compliance, and quality excellence. With advanced facilities and global regulatory approvals, we deliver safe and effective products that meet international standards. Our Quality Management System ensures consistency and reliability across all operations, from research to production. We offer diverse opportunities for professionals seeking an Executive Position or a rewarding Chemistry Job in analytical assurance and quality control. Join us to be part of a forward-thinking organization that values expertise, integrity, and continuous improvement in every aspect of pharmaceutical excellence.
Job Details
- Job Title: Executive/ Sr. Executive – QMS (Analytical Assurance)
- Department: Quality Management System
- Location: Ankleshwar
- Education: MSc in Chemistry or related field.
- Experience: Minimum 3–8 years of experience in Analytical Assurance within the pharmaceutical industry
Job Description
We are seeking a dedicated professional for an Executive Position in the QMS team. The role focuses on Analytical Assurance activities, ensuring that all quality control processes meet regulatory and internal standards. This Chemistry Job requires technical expertise in analytical testing and compliance to support product integrity in a leading pharmaceutical environment.
Key Responsibilities
- Lead Out-of-Specification (OOS) investigations and confirm root causes through analytical testing.
- Handle all Quality Management System documents, including incidents, deviations, and change control.
- Evaluate CAPA and ensure timely closure of quality actions.
- Review analytical documents such as worksheets, specifications, stability protocols, and logbooks.
- Approve stability protocols and ensure compliance with CGMP, FDA, MHRA, and ICH guidelines.
Why Join Us?
This is an excellent Executive Position for professionals passionate about Chemistry Jobs and quality excellence in the pharmaceutical sector. By joining our QMS team, you’ll work on impactful projects ensuring product reliability and global compliance, while advancing your career in a world-class manufacturing environment.
