Quality Assurance Department

Roles & Responsibilities
• Assist in monitoring and maintaining quality standards across manufacturing operations
• Support implementation and adherence to GMP guidelines
• Review and maintain documentation including BMR, BPR, logbooks, and SOP records
• Assist in preparation, revision, and control of SOPs and quality documents
• Participate in in-process quality checks and line clearance activities
• Support investigation of deviations and help in documentation of findings
• Assist in CAPA tracking and follow-up activities
• Coordinate with Production and QC teams to ensure compliance with quality systems
• Support internal audits and regulatory inspection readiness
• Ensure proper archival and data integrity practices
• Monitor adherence to hygiene, safety, and compliance standards
• Maintain proper documentation practices as per regulatory requirements
• Perform other QA-related activities as assigned by the department head

Qualification
• B.Pharm (Bachelor of Pharmacy) or M.Pharm (Master of Pharmacy) (Freshers only)

Experience
• Entry-level opportunity
• Basic academic exposure to GMP and pharmaceutical quality systems preferred

Skills
• Strong understanding of pharmaceutical quality concepts
• Basic knowledge of GMP and regulatory compliance
• Good documentation and record-keeping skills
• Attention to detail and analytical mindset
• Good communication and interpersonal skills
• Ability to work in a team-oriented environment
• Willingness to learn and adapt in a fast-paced manufacturing setup
• Basic proficiency in MS Office

About the Organization
Stanex Drugs and Chemicals Pvt. Ltd. is a reputed pharmaceutical manufacturer based in Hyderabad, specializing in sterile injectables and life-saving formulations. The company operates with strong regulatory compliance standards and offers a structured platform for fresh graduates to begin and grow their careers in Quality Assurance.