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SMS Pharmaceuticals Limited Walk-In Interview for QA, QC, Warehouse, Production, Regulatory Affairs & Store Departments on 16th-17th May 2025

SMS Pharmaceuticals Ltd., a leading API manufacturer in India with cGMP and WHO-GMP compliant facilities, is hosting a walk-in interview for multiple roles at its Unit-II facility in Bachupally, Hyderabad. Established in 1990, SMS Pharma is a global player with a strong R&D and manufacturing team, exporting to 70+ countries and rated 3.9/5 for job security (AmbitionBox, 200+ reviews). The company specializes in APIs for oncology, anti-viral, and cardiovascular therapies, with USFDA and EDQM approvals.

Event Details

  • Interview Dates: 16th May 2025 (Friday) & 17th May 2025 (Saturday)
  • Time: 9:30 AM to 3:30 PM
  • Venue: SMS Pharmaceuticals Ltd., Unit-II, Plot No. 24, 24B, 36 & 37, S.V. Co-Operative Industrial Estate, Bachupally, Miyapur, Hyderabad – 500090, Telangana, India
  • Application Process: Attend the walk-in with required documents or scan the QR code (from official communication) to apply. Email CV to ehs@smspharma.com for pre-registration.
  • Note: Preferable for male candidates with API pharma experience (mandatory).
  • Contact: +91-40-25259999 for queries

Job Opportunities

1. Production

  • Experience: Fresher to 4 years
  • Qualification: B.Sc., M.Sc., B.Pharm, M.Pharm, B.Tech (Chemical)
  • Salary: ₹2.5–5.0 Lakhs/year (estimated, Hyderabad, industry standards)

Responsibilities:

  • Operate API production equipment (reactors, centrifuges, dryers) in cGMP environment.
  • Monitor processes, ensure batch compliance, and maintain BMR/BPR records.
  • Support scale-up and process optimization for API manufacturing.
  • Adhere to USFDA and WHO-GMP standards.

Preferences:

  • Knowledge of SSR/GLLegacy API manufacturing processes.
  • Exposure to QMS (deviations, CAPA) and data integrity.

2. Regulatory Affairs

  • Experience: 3–6 years
  • Qualification: M.Sc., B.Pharm, M.Pharm
  • Salary: ₹4.5–8.0 Lakhs/year (estimated)

Responsibilities:

  • Prepare and submit DMFs, CTDs, CEPs, and LOAs to regulatory bodies (USFDA, EDQM).
  • Ensure compliance with ICH Q7 and 21 CFR Part 11.
  • Coordinate with cross-functional teams for regulatory audits.
  • Maintain regulatory databases and documentation.
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Preferences:

  • Experience in API regulatory submissions for US/EU markets.
  • Familiarity with eCTD and query response management.

3. Quality Assurance (QMS)

  • Experience: 4–6 years
  • Qualification: B.Sc., M.Sc., B.Pharm, M.Pharm
  • Salary: ₹4.5–8.0 Lakhs/year (estimated)

Responsibilities:

  • Manage QMS elements (OOS, CAPA, deviations, change control) for API production.
  • Conduct IPQA, validation, and qualification per cGMP.
  • Review BMR/BPR and ensure USFDA audit readiness.
  • Maintain GDP and data integrity standards.

Preferences:

  • Experience in API plants with USFDA/EDQM approvals.
  • Proficiency in QMS software (e.g., Trackwise).

4. Quality Control – HPLC

  • Experience: 2–6 years
  • Qualification: B.Sc., M.Sc., B.Pharm, M.Pharm
  • Salary: ₹3.5–6.5 Lakhs/year (estimated)

Responsibilities:

  • Perform HPLC-based analysis for API testing (assay, impurities).
  • Validate analytical methods per ICH Q2.
  • Operate and maintain HPLC systems, ensuring 21 CFR Part 11 compliance.
  • Document results and support stability studies.

Preferences:

  • Hands-on experience with Agilent/Waters HPLC systems.
  • Knowledge of method development and troubleshooting.

5. Quality Control – Wet Lab

  • Experience: 2–4 years
  • Qualification: B.Sc., M.Sc., B.Pharm, M.Pharm
  • Salary: ₹3.0–5.5 Lakhs/year (estimated)

Responsibilities:

  • Conduct wet chemistry analysis (titration, LOD, sulfated ash).
  • Perform raw material, in-process, and finished product testing.
  • Maintain lab records per GLP and GDP.
  • Support QC documentation for USFDA audits.

Preferences:

  • Experience in API wet lab testing.
  • Familiarity with pharmacopoeial standards (USP, EP).

6. Stores

  • Experience: Fresher to 3 years
  • Qualification: B.Com, B.Sc., M.Com
  • Salary: ₹2.0–4.0 Lakhs/year (estimated)

Responsibilities:

  • Manage receipt, storage, and dispensing of RM, PM, and FG.
  • Maintain inventory records in SAP, ensuring FIFO/FEFO.
  • Prepare GRN, RGP/NRGP, and coordinate with QC/production.
  • Ensure GDP compliance in warehousing.

Preferences:

  • Experience in API warehouse operations.
  • Basic SAP/ERP proficiency.
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7. Mechanical Fitter

  • Experience: 4–6 years
  • Qualification: Diploma or ITI
  • Salary: ₹2.5–4.5 Lakhs/year (estimated)

Responsibilities:

  • Perform preventive maintenance and repairs on API equipment (pumps, reactors).
  • Troubleshoot mechanical issues in centrifuges, dryers, and gear boxes.
  • Maintain maintenance logs per cGMP standards.
  • Support USFDA audit readiness.

Preferences:

  • Experience in API plant maintenance.
  • Knowledge of predictive maintenance techniques.

8. Fabrication Fitter

  • Experience: 5–8 years
  • Qualification: Diploma or ITI
  • Salary: ₹3.0–5.0 Lakhs/year (estimated)

Responsibilities:

  • Fabricate and assemble API plant piping and structural components.
  • Perform welding, cutting, and fitting per engineering drawings.
  • Ensure compliance with cGMP and safety standards.
  • Support equipment installation and modification.

Preferences:

  • Experience in API facility fabrication.
  • Proficiency in TIG/MIG welding for SS/MS.

9. ETP-In Charge

  • Experience: 6–9 years
  • Qualification: Diploma, B.Sc., B.Tech
  • Salary: ₹4.0–7.0 Lakhs/year (estimated)

Responsibilities:

  • Manage Effluent Treatment Plant (ETP) operations for API facility.
  • Ensure compliance with CPCB/SPCB regulations.
  • Monitor treatment processes (primary, secondary, tertiary).
  • Maintain ETP documentation and support audits.

Preferences:

  • Experience in API plant ETP operations.
  • Knowledge of ZLD (Zero Liquid Discharge) systems.

Why Join SMS Pharmaceuticals?

  • Work in a USFDA/EDQM-approved API manufacturing facility in Hyderabad’s Genome Valley.
  • Contribute to a global portfolio of 100+ APIs for critical therapies.
  • Rated 4.0/5 for skill development, with training in cGMP and regulatory compliance (AmbitionBox).
  • Join a 1,000+ strong team with a ₹1,200 Cr+ turnover and 30+ years of legacy.
  • Career growth in a company exporting to 70+ countries with 6 manufacturing units.

How to Prepare and Attend

Documents to Carry:

  • Updated CV (highlighting API experience)
  • Academic mark sheets (B.Sc., M.Sc., B.Pharm, M.Pharm, B.Tech, Diploma, ITI, etc.)
  • Experience certificates
  • Last 3 months’ payslips and bank statement
  • Aadhaar, PAN copies
  • 2 passport-size photographs
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Preparation Tips:

  • Production: Study API manufacturing processes (SSR, GLR, centrifugation). Be ready for questions on BMR/BPR and cGMP.
  • Regulatory Affairs: Review DMF/CTD preparation and ICH Q7. Prepare for USFDA query handling scenarios.
  • QA-QMS: Focus on QMS tools (Trackwise), ICH Q7, and audit preparedness.
  • QC-HPLC/Wet Lab: Brush up on HPLC method validation and wet chemistry techniques. Know USP/EP standards.
  • Stores: Demonstrate SAP proficiency and GDP knowledge. Discuss FIFO/FEFO practices.
  • Mechanical/Fabrication Fitter: Highlight equipment maintenance or welding experience in API plants. Study cGMP compliance.
  • ETP-In Charge: Review CPCB/SPCB norms and ETP process flows. Discuss ZLD experience.
  • Interview Process: Expect technical questions, practical assessments (e.g., HPLC operation, QMS scenarios), and HR discussion. Telugu proficiency is a plus.
SMS Pharmaceuticals Limited Walk-In Interview for QA, QC, Warehouse, Production, Regulatory Affairs & Store Departments on 16th-17th May 2025

Important Notes

  • Eligibility: Candidates with API pharma experience are mandatory. Male candidates preferred due to shift-based roles.
  • Fraud Alert: SMS Pharma does not charge fees for recruitment. Verify communications via ehs@smspharma.com or hr@smspharma.com. Report suspicious activity to +91-40-25259999.
  • Previous Applicants: Candidates interviewed in the last 6 months at SMS Pharma should not reapply.

About SMS Pharmaceuticals

Founded in 1990, SMS Pharmaceuticals Ltd. is a Hyderabad-based global leader in API manufacturing, with 6 units across Telangana and Andhra Pradesh. With a ₹1,200 Cr+ turnover, 1,000+ employees, and approvals from USFDA, EDQM, and WHO-GMP, SMS serves 70+ countries. Its R&D center, recognized by DSIR, drives innovation in oncology, anti-viral, and cardiovascular APIs, making it a top choice for pharma professionals.

Join Our Mission

Join SMS Pharmaceuticals’ mission to deliver high-quality APIs that improve global healthcare! Attend the walk-in interview on 16th–17th May 2025 in Hyderabad and grow with a world-class API leader!

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