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QA Validation Jobs For Life Sciences at VINS Bioproduct Ltd, Apply on Biotecnika
Job Description – QA Validation (Injectables)
Company: VINS Bioproduct Ltd
Role: QA – Validation
Location: Hyderabad
Note: This position is open to male candidates only
Job Description:
VINS Bioproduct Ltd is looking for a QA–Validation professional with injectable manufacturing experience to ensure validation activities comply with regulatory and quality standards. The role involves planning, execution, review, and approval of validation protocols and reports to maintain compliance with cGMP requirements.
Key Responsibilities:
· Review and approve validation protocols and reports for equipment, utilities, processes, and cleaning.
· Ensure compliance with cGMP, SOPs, and regulatory guidelines.
· Coordinate and support process validation, cleaning validation, and hold time studies.
· Participate in media fill validation and aseptic process validation.
· Ensure proper documentation for IQ, OQ, PQ activities.
· Review and manage change controls, deviations, and CAPA related to validation.
· Support regulatory audits and inspections (USFDA, WHO-GMP, EU-GMP).
· Ensure validation documents meet data integrity (ALCOA+) principles.
· Work closely with Production, Engineering, QC, and QA teams.
Requirements:
· Minimum 1 year of experience in QA Validation within injectable pharmaceutical manufacturing.
· Strong understanding of aseptic processing and sterile manufacturing.
· Knowledge of equipment, utility, and process validation.
· Familiarity with regulatory guidelines (USFDA, WHO-GMP, EU-GMP).
· Experience in validation documentation and compliance.
· Good analytical, communication, and coordination skills.
Qualification:
· BSc / MSc in any Life Sciences
· B.Pharm / M.Pharm
· BSc / MSc in Chemistry
Salary: Based on previous CTC and interview performance
CLICK HERE TO APPLY ONLINE
