Shilpa Medicare Limited (SML) started its operations as API manufacturer way back in 1987 at Raichur, Karnataka- India. The commercial production in the SML was started in November 1989. Today Shilpa Medicare Limited is a global brand in manufacturing and supplying of affordable API and Formulation globally in different regulated markets.
WALK IN INTERVIEW
Analytical Services (QC Formulation) (Fresher can Attend)
Key Skills & responsibilities : Execute analytical method validation and monitor validation parameters in compliance with ICH and ANVISA guidelines; Preparation of method validation protocols & reports; Strong knowledge of formulation finished product analysis (oral and injectable) in line with regulatory requirements; Hands-on experience with analytical instruments such as HPLC, GC, UV-Visible spectrophotometer, and water content determination techniques (e.g., Karl Fischer).
Designation : Executive / Sr. Executive
Experience : 0 to 6 years (Fresher can Attend)
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc (Chemistry / Analytical Chemistry / Pharmaceutical Chemistry)
Quality Assurance (QMS)
Key Skills & responsibilities : Review QMS documents, SOPs, processes and records for compliance with GMP requirements; Support OOS, OOT, deviations, change controls, CAPA, risk assessments and investigations; Ensure compliance with ALCOA+ data integrity principles; Monitor QMS metrics and prepare quality trend reports; Support internal, customer and regulatory audits; Ensure QMS compliance and continuous quality improvement; Handle Computer System Validation (CSV) and qualification activities.
Designation : Executive
Experience : 4 to 8 years
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc (Chemistry / Analytical Chemistry / Pharmaceutical Chemistry)
Regulatory Affairs – ROW (Fresher can Attend)
Key Skills & responsibilities : Product registration for ROW markets – Africa, ANZ, Asia, LATAM, CIS & MENA; Preparation, compilation and review of CTD/country-specific dossiers; Coordination with cross-functional teams for dossier documents and submissions; Coordination with agents/partners for submissions and regulatory queries; Support regulatory audits and coordinate with auditors; Review of regulatory and quality documents for product registration; Handling renewals, variations, approvals and post-approval changes; Maintenance of regulatory dossiers and submission records.
Designation : Executive / Sr. Executive / Asst. Manager
Experience : 2 to 10 years (Fresher can Attend)
Qualification : B.Pharm, M.Pharm, M.Sc
Male candidate preferred
Walk in Interview
Date : 05th September 2026 (Saturday)
Time : 09:00 AM to 02:00 PM
Venue : Ujjwala Grand Gandi Maisamma, Domara Pochampally, Medak – Hyderabad Road,
Hyderabad, Telangana – 500043
Documents to Carry
1. Updated Resume
2. Latest Increment Letter / Offer Letter with CTC breakup
3. Last 3 months' payslips & 6 months' bank statement
4. Copies of all education certificates
5. Copy of Aadhaar & PAN Card
For Candidates Unable to Attend
Share your updated resume at : karthik.kumar@vbshilpa.com
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