About the Role:
Leeford Healthcare Limited is looking for experienced Senior Executives to join our Analytical R&D (AR&D) and Quality Control (QC) teams at our Formulation & Development unit. Candidates from pharma background are welcome to apply for the relevant function.
Key Responsibilities :
- Independently lead method development, validation, and troubleshooting
- Supervise routine and stability testing of raw materials and finished products
- Lead/review OOS, OOT investigations and CAPA
- Ensure audit-readiness and compliance with GMP/data integrity standards
- Guide and mentor junior QC staff
- Manage technology transfer of analytical methods from R&D to QC/manufacturing
- Prepare and review validation protocols and regulatory documentation
- Guide and mentor junior team members
Location: Baddi, HP
Job Type: Full-time
Requirements:
- M.Pharm / M.Sc (Chemistry) with 8–12 years of relevant pharma industry experience
- Strong hands-on expertise with HPLC, GC, UPLC, and related analytical instruments
- Audit exposure (USFDA/WHO-GMP/MHRA) preferred
- Team handling and mentoring experience
Pay: ₹40,000.00 - ₹51,000.00 per month
Benefits:
Work Location: In person
