Location: Pydibimavaram, Andhra Pradesh
Job Type: Full-time
Qualification: M.Sc Chemistry
Experience: Relevant experience in Pharma QC preferred
About the Company
CTO SEZ is a leading pharmaceutical manufacturing unit specializing in high-quality drug formulations. With a strong focus on compliance and innovation, we ensure global standards in quality control and production. Join our dynamic team and contribute to excellence in pharmaceutical analysis and quality assurance.
Job Description: Quality Control Analyst
Key Responsibilities:
✔ Perform analytical testing using instruments like:
- HPLC, GC, UV, IR
- pH meter, Conductivity meter, KF Titrator
- Analytical/Microbalance, Autotitrator, Halogen Moisture Analyzer
- Hot Air Oven
✔ Ensure timely release of Raw Materials, Packaging Materials, In-Process, Intermediate, Bulk & Finished Products as per SLA.
✔ Handle SAP & Labware LIMS activities (Master preparation, review, approvals).
✔ Manage LIMS tickets, Audit Trail observations, and closure activities.
✔ Report OOS (Out of Specification), OOT (Out of Trend), and deviations as per SOP.
✔ Assist in root cause analysis (RCA) and investigations under QA guidance.
✔ Maintain compliance with cGMP, GLP, and regulatory standards.
Qualifications & Skills Required
- M.Sc in Chemistry (Analytical/Organic Chemistry preferred).
- Hands-on experience with HPLC, GC, Wet Lab instruments.
- Familiarity with SAP & LIMS (Labware LIMS preferred).
- Strong understanding of pharma QC guidelines (USP, IP, BP).
- Ability to work in a fast-paced GMP environment.