Maithri Drugs Private Limited, a fast-growing Hyderabad-based pharmaceutical company under the MSN Group, is hiring for Junior Manager and Senior Executive roles in Regulatory Affairs at its Technology Center in Gummadidala, Sangareddy, Telangana. With 51 US DMFs and 14 CEPs, Maithri Drugs is a leader in Active Pharmaceutical Ingredients (APIs), recognized for its R&D excellence and USFDA-compliant facilities.
Event Details
- Date: May 17, 2025 (Saturday)
- Time: 10:00 AM – 1:00 PM IST
- Venue & Work Location: Maithri Drugs Pvt. Ltd., Technology Center, Sy. No. 810/PART, 820/PART, 821/PART, Gummadidala (V) & (M), Narsapur Road, Sangareddy (D), Telangana, India – 502313
- Contact: +91-8455-694035 / +91-40-69076672
- Email: careers@maithridrugs.com
Job Opportunities
Junior Manager / Senior Executive – Regulatory Affairs
- Qualification: M.Sc. (Organic Chemistry) / M.Pharmacy
- Experience: 6–9 years in regulatory affairs (API focus preferred)
- Salary: ₹8.0–12.0 Lakhs/year (estimated for Hyderabad, based on industry standards and AmbitionBox data)
- Skills & Responsibilities:
- Prepare and review regulatory dossiers (DMF, CEP, eCTD) for USFDA, EDQM, and other global markets.
- Ensure compliance with ICH guidelines and cGMP.
- Coordinate with R&D, QC, and production for regulatory submissions and query responses.
- Conduct regulatory gap analysis and support USFDA audits.
- Manage submission timelines and maintain data integrity.
- Preferences:
- Experience in API regulatory affairs with US/EU filings (DMFs, CEPs).
- Strong knowledge of global regulatory requirements and QMS tools.
Benefits
- Free transportation (from Balanagar X Roads/Kukatpally)
- Subsidized canteen
- Group personal accident policy
- Health insurance
- Additional perks: Bonus, gratuity, LTA, leaves (maternity, paternity, casual, sick, earned), marriage gifts, salary advance
Why Join Maithri Drugs?
- Work in a USFDA-audited API manufacturing facility with 125+ global DMFs
- Join a company rated 3.9/5 for job security (AmbitionBox, 50+ reviews)
- Contribute to innovative APIs like Ipragliflozin L-Proline and Ketamine HCl
- Access a dynamic work culture (3.7/5 rating) with growth opportunities
- Be part of a ₹1,000 Cr+ MSN Group venture with 9 API plants
How to Apply
Attend the walk-in interview on May 17, 2025, at Maithri Drugs Technology Center, Gummadidala. Alternatively, email your resume to careers@maithridrugs.com with the subject “Regulatory Affairs – [Position]” by May 15, 2025. Scan the QR code (available in official Maithri Drugs communication) for more details and to apply. Bring:
- Updated resume
- Educational certificates (M.Sc., M.Pharmacy)
- Experience certificates
- Last 3 months’ payslips
- Last 6 months’ bank statements
- Latest increment letter
- Aadhaar and PAN card copies
- Recent passport-size photograph
Verified by Trusted HRs
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Preparation Tips
- Review ICH Q8–Q12 and DMF/CEP filing processes.
- Study USFDA and EDQM regulatory requirements for APIs.
- Prepare for questions on handling regulatory queries and audit compliance.
- Highlight experience in dossier preparation and QMS tools (e.g., CAPA, deviations).
Important Note
Maithri Drugs does not charge any fees for job applications. Beware of fraudulent invitations requesting payment. Verify communications via @maithridrugs.com emails or official channels. For queries, contact +91-8455-694035, +91-40-69076672, or visit www.maithridrugs.com. Follow Maithri Drugs on Facebook for updates.
About Maithri Drugs
Founded in 2013, Maithri Drugs Private Limited, part of the MSN Group, is a Hyderabad-based leader in API manufacturing, with a focus on R&D and regulatory excellence. With 51 US DMFs, 14 CEPs, and a USFDA-approved facility in Bonthapally, Maithri serves 35+ global markets, delivering high-quality APIs like Ipragliflozin L-Proline and Ketamine HCl.
Join Our Mission
Join Maithri Drugs’ mission to redefine quality and effectiveness in APIs! Attend the walk-in on May 17, 2025, in Gummadidala, Telangana!
