Horizon Biolabs Pvt Ltd. is a NABL accredited GLP compliant Pharmaceutical Analytical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices Industries .
Seeking applications from candidates with science background (BSc/MSc/BPharm/Mpharm) in any discipline having 1-3 years of experience in Quality Assurance department in any Pharmaceutical testing laboratory /CRO or Pharmaceutical industry.
Roles and Responsibilities
ensures all GMP-related records, SOPs, and batch documentation comply with regulatory standards and Good Documentation Practices (GDP).
- Document Control & Management: Maintains, updates, and controls the versioning of SOPs, quality manuals, and forms, ensuring only current documents are in use.
- GMP Record Review: Reviews Raw data and records for accuracy, completeness, and adherence to established procedures (GDP) before COA release.
- Quality System Documentation: Manages documentation related to deviations, non-conformances, CAPA (Corrective and Preventive Actions), and change controls.
- Audit Support: Assists in organizing documentation for internal and external regulatory audits and customer audits
- Archiving & Retrieval: Maintains secured, organized, and easily retrievable archives for critical quality records.
- Training Coordination: Assists in training personnel on documentation standards and document management systems.
- Cross-functional Collaboration: Works with QC and other departments to update procedures and ensure compliance.
Freshers will be considered for trainee positions.
Good verbal and written communication skills desirable.
Job Types: Full-time, Permanent
Education:
Experience:
- total work: 1 year (Preferred)
Work Location: In person
