Maithri Drugs Pvt. Ltd., a USFDA-approved, fast-growing Active Pharmaceutical Ingredients (API) manufacturer based in Hyderabad, is hosting a Walk-In Interview for Quality Control (Method Validation) roles on May 10, 2025, at its Bonthapally facility in Sangareddy, Telangana. Founded in 2013, Maithri boasts 125+ global DMFs (50 US, 22 EU) and 22 CEPs, with a portfolio of 90+ products across CNS, anti-diabetic, and cardiovascular categories.
Rated 3.6/5 for job security on AmbitionBox (150+ reviews), it scores 3.3/5 for work-life balance due to shift demands. Roles offer ₹4–10 Lakhs per annum (Indeed). Apply on May 10, 2025, to join a leader in API excellence
Walk-In Interview Details
- Date: Saturday, May 10, 2025
- Time: 10:00 AM – 1:00 PM
- Venue: Maithri Drugs Pvt. Ltd., Sy. No. 205, 222 to 226, Bonthapally (V), Gummadidala (M), Sangareddy (D), Telangana, India 502313
- Landmark: Lane beside Bharat Petroleum Bunk, Bonthapally Kamaan
- Application Method: Attend walk-in with documents or email CV to careers@maithridrugs.com, subject: “QC Method Validation – Bonthapally.” Scan QR code for details at www.maithridrugs.com/careers.
- Contact: careers@maithridrugs.com, +91-8455-694101, +91-40-69076672
- Website: www.maithridrugs.com
Notes:
- Fraud Alert: Maithri does not charge fees. Verify via www.maithridrugs.com or info@maithridrugs.com.
Why Join Maithri Drugs?
Maithri’s Bonthapally facility, audited by USFDA, DCGI, WHO-GMP, and ISO 9001:2015, features advanced HPLC/GC systems for API testing. With ₹100–500 Crore revenue and 54.81% EBITDA growth (2023), it’s a key player in Hyderabad’s pharma hub. Rated 3.7/5 for learning, it offers robust training but faces feedback on slow promotions (3.4/5).
Benefits include free transport, subsidized canteen, health insurance, and group accident policy. Join India’s $24.4 billion pharma export market, growing at 10% CAGR (Invest India).
Job Position: Quality Control (Method Validation) – Junior Executive / Executive / Senior Executive
Seeking experienced professionals to ensure API quality through HPLC/GC method validation at Maithri’s Bonthapally facility.
Job Details
- Department: Quality Control (Method Validation)
- Qualification: B.Sc, M.Sc (Chemistry), B.Pharm, M.Pharm
- Experience: 4–9 years in HPLC/GC method validation for APIs
- Vacancies: ~5–10 expected (based on prior drives)
- Location: Bonthapally, Sangareddy, Telangana
- Work Mode: On-site, shift-based
- Employment: Full-time
Responsibilities
- Develop, validate, and optimize HPLC/GC analytical methods for APIs, ensuring accuracy, precision, and compliance with ICH guidelines.
- Review chromatograms, processing methods, and analytical data; sign off on results post-analysis.
- Prepare and review protocols, SOPs, raw data sheets, investigation reports, and excel validation sheets.
- Troubleshoot HPLC/GC instruments and handle performance verification.
- Support USFDA/EDQM audits by maintaining data integrity and audit-ready documentation.
- Conduct wet analysis (e.g., LOD, SOR, WC, TLC) as needed.
- Collaborate with QA/R&D for method transfer and regulatory submissions (e.g., DMF).
Required Skills and Qualifications
| Category | Details |
|---|---|
| Education | B.Sc, M.Sc (Chemistry), B.Pharm, M.Pharm |
| Experience | 4–9 years in HPLC/GC method validation for APIs; USFDA audit exposure |
| Technical Skills | HPLC, GC, Empower, LIMS; method validation (accuracy, precision, linearity) |
| Regulatory Knowledge | ICH Q2(R1), USP, USFDA, EDQM guidelines; cGMP, data integrity |
| Soft Skills | Analytical thinking, attention to detail, teamwork, time management |
| Preferred Expertise | SOP/protocol preparation, troubleshooting, wet analysis (LOD, SOR, TLC) |
Why This Role?
- Impactful Work: Ensure API quality for 40+ countries, with 85% of validations supporting DMF filings (Maithri data).
- Skill Development: Master HPLC/GC, ICH Q2, and USFDA compliance, rated 3.7/5 for learning (AmbitionBox).
- Stable Employer: Maithri’s 41 US DMFs, 13 CEPs, and 6.15% revenue growth (2023) ensure stability, though promotions lag (3.4/5).
- Benefits: Free transport, subsidized canteen, health insurance, accident policy, bonuses, and leaves (maternity, paternity, sick).
How to Prepare for the Walk-In
- Bring Documents: Updated CV, B.Sc/M.Sc/B.Pharm/M.Pharm certificates, payslips (last 3 months), bank statements (last 6 months), CTC structure, Aadhaar/PAN copies, photo.
- Dress Professionally: Wear formal attire (e.g., shirt, trousers).
- Research Maithri: Visit www.maithridrugs.com for API focus (e.g., Ipragliflozin L-Proline) and USFDA standards. Review ICH Q2(R1) for method validation.
- Prepare Questions: Expect queries on HPLC/GC troubleshooting, method validation parameters (e.g., specificity, robustness), or SOP preparation. Highlight USFDA audit experience. Sample question: “How do you handle a system suitability failure in HPLC?”
- Arrive Early: Reach by 9:45 AM; expect 1–2 hour wait (AmbitionBox). Free transport available from Balanagar X Roads/Kukatpally.
- Online Option: Email CV to careers@maithridrugs.com if unable to attend, specifying experience and role.
Verified by Trusted HRs
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Why Bonthapally, Telangana?
Bonthapally, part of Hyderabad’s pharma corridor, hosts Maithri’s USFDA-approved API facility, contributing to Telangana’s $10 billion pharma sector (12% CAGR, Invest India). Accessible via NH-44, it offers 150+ QC jobs (LinkedIn) but limited urban amenities (AmbitionBox). Ideal for API method validation careers.
Contact Information
- Email: careers@maithridrugs.com
- Phone: +91-8455-694101, +91-40-69076672
- Venue/Work Address: Maithri Drugs Pvt. Ltd., Sy. No. 205, 222 to 226, Bonthapally (V), Gummadidala (M), Sangareddy (D), Telangana, India 502313
- Corporate Office: Dwaraka Signature, Plot No. 14D/1, 2nd Floor, Sy. No. 74 & 75, Jaihind Enclave, Madhapur, Hyderabad, Telangana 500081
- Website: www.maithridrugs.com
- LinkedIn: Maithri Drugs Private Limited
Join Maithri Drugs on May 10, 2025, at Bonthapally to advance API quality through method validation. Apply now to redefine pharmaceutical excellence!