Documentation Management Executive at Azurity Pharmaceuticals, Hyderabad – Apply Now!
Azurity Pharmaceuticals is hiring a Sr. Executive – Documentation Management in Hyderabad, offering an exciting opportunity for B.Pharm, Life Sciences, or Quality graduates to advance their career in a highly regulated pharmaceutical environment. This full-time role is ideal for professionals with 1–3 years of experience in documentation management, QMS, and regulatory compliance, with the chance to support GxP systems and contribute to continuous quality improvement.
About Azurity Pharmaceuticals
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company dedicated to providing innovative products that cater to the needs of underserved patients. As a leader in the industry, Azurity offers unique and high-quality medications across various therapeutic areas like cardiovascular, neurology, endocrinology, and more. With a focus on patient-centric care, Azurity continuously strives to expand its product portfolio and pipeline.
Job Details:
Job Title: Sr. Executive, Documentation Management
Location: Hyderabad
Azurity Pharmaceuticals is looking for a Senior Executive in Documentation Management to join our team in Hyderabad. Our inclusive workplace values diversity and is an Equal Opportunity Employer. We are seeking individuals who are dedicated and passionate about improving patient lives through innovative pharmaceutical solutions.
Team/Department Description:
The Associate of Documentation Management
will be responsible for maintaining a robust Quality Management System (QMS) in a regulated pharmaceutical environment. This role involves supporting compliance, integrity, and continuous improvement of controlled documentation and electronic quality systems.Principle Responsibilities:
- Maintain an inspection-ready Quality Management System (QMS) in line with industry regulations.
- Support validation and compliance of electronic quality systems.
- Manage the Documentation Management System for the accuracy of controlled documents.
- Ensure all documentation meets GxP and regulatory standards.
- Assist in continuous improvement initiatives for quality systems.
- Support Computer System Validation (CSV) program in alignment with regulations.
- Participate in audits and inspections.
Qualifications and Education Requirements:
- Bachelor’s degree in Life Sciences, Quality, or related field.
- 1–3 years of experience in documentation management, quality assurance, or regulatory compliance.
- Understanding of GxP principles, 21 CFR Part 11, EU Annex 11, and related regulations.
- Familiarity with electronic Document Management Systems and Computer System Validation practices.
- Strong attention to detail and organizational skills.
Keywords: Azurity Pharmaceuticals, Documentation Management, Quality Assurance, Pharmaceutical Industry, Regulatory Compliance, GxP, 21 CFR Part 11, EU Annex 11
