Ritsa Pharma is looking for professionals to join Quality Control team. Details are provided below 1. Position: Analyst / Senior Analyst 2. Department: Quality Control (OSD Oral Solid Dosage) 3. Experience Required: 0-8 years 4. Number of Positions: 10 5. Work Schedule: Monday to Saturday 6. Location: Genome Valley, Shamir pet, Hyderabad 7. Preference: Immediate joiners 8. Technical Expertise: -Hands-on experience with HPLC, UV, IR, GC instruments Strong understanding of GMP compliance -Knowledge and adherence to Data Integrity principles (ALCOA/ALCOA+) -Audits Faced: Involved in facing gregulatory regulatory and and Involved in facing regulatory and internal audits such as: USFDA / MHRA/WHO/GMP/ISO (mention whichever apply for the candidate) -Supported audit preparedness, documentation, and CAPA implementation 9. Roles & Responsibilities: -Performing routine and non-routine analysis of raw materials, in-process samples, finished products, and stability sampl...
Required Freshers and Experienced Analyst/Sr. Analyst - Quality Control (OSD Oral Solid Dosage)- 10 Positions
Ritsa Pharma is looking for professionals to join Quality Control team.
Details are provided below
1. Position: Analyst / Senior Analyst
2. Department: Quality Control (OSD Oral Solid Dosage)
3. Experience Required: 0-8 years
4. Number of Positions: 10
5. Work Schedule: Monday to
Saturday
6. Location: Genome Valley, Shamir pet, Hyderabad
7. Preference: Immediate joiners
8. Technical Expertise:
-Hands-on experience with HPLC, UV, IR, GC instruments
Strong understanding of GMP compliance
-Knowledge and adherence to Data Integrity principles (ALCOA/ALCOA+)
-Audits Faced:
Involved in facing gregulatory regulatory and and Involved in facing regulatory and internal audits such as: USFDA / MHRA/WHO/GMP/ISO (mention whichever apply for the candidate)
-Supported audit preparedness, documentation, and CAPA implementation
9. Roles & Responsibilities:
-Performing routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples. Operation, calibration, and troubleshooting of analytical instruments (HPLC, UV, IR, GC). Preparation and review of analytical documents, SOPs, COAs, and test reports.
-Ensuring compliance with GMP, GLP, and data integrity requirements.
-Maintaining lab documentation as per ALCOA+ principles.
-Handling OOS, OOT, deviations, and supporting investigations.
-Participating in internal and external audits; ensuring audit readiness.
-Maintaining good housekeeping, safety, and adherence to laboratory practices.
-Coordination with cross-functional teams to ensure timely release of batches and samples.
10. How to Apply:
Interested candidates can share their CVs at HR@ritsapharma.com
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