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SMS Pharmaceuticals Limited, a prominent pharmaceutical manufacturing company, has announced walk-in interviews for various positions across Quality Assurance, Quality Control, Production, Environmental Health & Safety, and HR & Administration departments at their Unit-II facility in Bachupally, Miyapur, Hyderabad.
Interview Details
Date: December 19-20, 2025
Time: 10:00 AM to 3:00 PM
Venue: SMS Pharmaceuticals Limited, Unit-II, S.V. Co-Operative Industrial Estate, Bachupally, Miyapur, Hyderabad-500090
Available Positions and Requirements
Quality Assurance (QA) – Stability
Qualification: B.Sc/M.Sc
Experience: 2-5 years
Key Responsibilities:
– Knowledge of Stability Schedule Preparation and Monitoring
– Stability Chamber Operations management
– Analytical Data and Audit trails review
Quality Control (QC)
HPLC Analyst
Qualification: B.Sc/M.Sc/B.Pharm
Experience: 2-5 years
Requirements:
– Hands-on experience in HPLC analysis of raw materials, intermediates, and finished products
– Knowledge of Empower software preferred
– Good documentation skills as per cGMP standards
– Exposure to regulatory environments (US-FDA, EU-GMP) desirable
QC Reviewer
Qualification: B.Sc/M.Sc/B.Pharm
Experience: 8-12 years
Key Responsibilities:
– Analytical Data Review including raw data, chromatograms, spectra, and calculations
– Documentation verification and validation
– Data Compilation and Certificate of Analysis (CoA) preparation
– Audit support and compliance management
Production – Chemist/Executive
Qualification: B.Sc/M.Sc/B.Pharm
Experience: 0-4 years
Requirements:
– Knowledge of Current Good Manufacturing Practices (cGMP)
– Handling of General Laboratory Reagents (GLR), Site Services Records (SSR)
– Experience with centrifuges, driers, and documentation activities
– Knowledge of Batch Manufacturing Records (BMR) and calibrations
EHS (Environment, Health & Safety) – Executive
Qualification: B.Sc/M.Sc/B.Tech
Experience: 5-8 years
Key Areas:
– Knowledge of MEE, ETP, STP, and RO systems
– Understanding of scrubbers and air pollution control equipment
– PCB guidelines and environmental laws
– Factory regulations and compliance
– Proficient in ISO 14001 and ISO 45001 standards
HR & Administration – Executive
Qualification: B.Com/MBA
Experience: 8-12 years
Responsibilities:
– Knowledge of recruitment processes and HR policies
– Provident Fund, ESI, and Factories Act compliance
– Shops & Establishment Act requirements
– General administration including security, housekeeping, transport, and canteen management
– Facilities management and pest control operations
Important Notes for Candidates
– Interested candidates should attend the walk-in interview with their pay slips, bank statements, and updated resume
– The recruitment is only for male candidates, with immediate joining preferred
– Candidates can scan the QR code provided in the official notification for location details
About SMS Pharmaceuticals Limited
SMS Pharmaceuticals Limited is a research-driven pharmaceutical company specializing in the manufacture of active pharmaceutical ingredients (APIs) and intermediates. The company maintains high standards of quality and regulatory compliance, serving both domestic and international markets.
FAQ:
1. What stability guidelines and regulatory requirements are followed in the QA–Stability role?
The QA–Stability function follows ICH guidelines (Q1A–Q1E) for stability studies. This includes preparation and execution of stability protocols, monitoring long-term, intermediate, and accelerated conditions, stability chamber qualification, data trending, OOS/OOT handling, and audit-ready documentation compliant with US-FDA and EU-GMP requirements.
2. What type of HPLC systems and software exposure is expected for QC HPLC Analysts?
Candidates should have hands-on experience with HPLC systems used for raw material, in-process, and finished product analysis. Familiarity with Empower software for data acquisition, integration, audit trail review, and compliance with 21 CFR Part 11 is preferred. Knowledge of method validation, system suitability, and troubleshooting is an added advantage.
3. What are the key responsibilities of a QC Reviewer during regulatory inspections?
A QC Reviewer is responsible for analytical data verification, chromatogram review, CoA preparation, and ensuring data integrity. During audits or inspections, the reviewer supports regulatory teams by presenting analytical records, addressing observations, ensuring ALCOA+ compliance, and coordinating CAPA implementation for analytical deviations.
4. What production equipment and GMP documentation should Production Chemists be familiar with?
Production Chemists should be experienced in operating centrifuges, dryers, reactors, and handling GLR and SSR documentation. Strong knowledge of BMR execution, yield reconciliation, deviation handling, calibration awareness, and adherence to cGMP guidelines is essential for batch manufacturing in API facilities.
5. What environmental compliance systems are critical for the EHS Executive role?
The EHS role requires in-depth knowledge of MEE, ETP, STP, RO systems, scrubbers, and air pollution control equipment. Candidates must ensure compliance with PCB regulations, Factory Acts, and environmental laws, along with implementation and maintenance of ISO 14001 and ISO 45001 management systems.
