[25+ Openings] Stallion Laboratories Walk-in Interview: QC Analyst & ADL Analyst Jobs

Stallion Laboratories Pvt. Ltd., a leading pharmaceutical formulation manufacturer with USFDA, UK MHRA, and WHO GMP approvals, announces a walk-in interview for experienced professionals in its OSD Formulation facility (Unit-II). The company seeks talented individuals for Quality Control (Analyst) and Analytical Development Laboratory (ADL Analyst) roles. With a strong emphasis on quality, innovation, and regulatory compliance, this opportunity suits those with 3-7 years in pharmaceutical analysis.

The walk-in interview occurs on Saturday, 10th January 2026, from 9:00 AM to 2:00 PM. Candidates with relevant experience in HPLC analysis, stability studies, or documentation should attend for immediate consideration.

Available Positions

Stallion Laboratories offers the following openings at its state-of-the-art Unit-II facility:

• Quality Control (Analyst) – Sr. Officer / Executive
  • Qualification: M.Pharm / B.Pharm / M.Sc
  • Skills Required: HPLC Analysis, Preparation of Specification, STP, TDS, and Pharmacopeial Updates
  • Vacancies: 20
  • Experience: 3 to 7 years
• ADL (Analyst) – Sr. Officer / Executive
  • Qualification: M.Pharm / B.Pharm / M.Sc
  • Skills Required: AMV/AMT (Analytical Method Validation/Transfer), Documentation
  • Vacancies: 7
  • Experience: 3 to 7 years

Roles & Responsibilities

Successful candidates handle key analytical and quality functions in a regulated environment:

• Perform routine and stability sample analysis using advanced instruments like HPLC.
• Prepare and update specifications, standard test procedures (STPs), and technical documents in line with current pharmacopeia.
• Conduct analytical method validation, method transfer, and related documentation for ADL roles.
• Ensure compliance with GMP, data integrity, and regulatory guidelines (USFDA, MHRA, etc.).
• Handle breakdown studies, investigations, and pharmacopeial updates.
• Maintain accurate records and support quality control processes for oral solid dosage forms.

Required Qualifications & Experience

• Educational Qualification: M.Pharm, B.Pharm, or M.Sc in relevant disciplines.
• Experience: Strictly 3 to 7 years in pharmaceutical QC or ADL, preferably in OSD formulations.
• Hands-on expertise in HPLC, analytical instrumentation, method validation, and documentation.
• Strong knowledge of regulatory requirements and good laboratory practices.

Salary, Benefits & How to Apply

• Salary: Competitive and commensurate with experience; expected range ₹4.5 – ₹8 Lakhs per annum for roles with 3-7 years experience (best-in-industry based on skills and performance).
• Benefits: Standard industry benefits including provident fund, gratuity, medical insurance, and opportunities for growth in a globally compliant organization.
• How to Apply: This is a walk-in interview. Interested candidates should attend in person with updated resume, recent photograph, and CTC break-up. No prior application needed, but sharing resume in advance to darshan.mistry@stallionlabs.com is appreciated.

Interview Date & Time: 10th January 2026 (Saturday), 9:00 AM to 2:00 PM

Venue: Stallion Laboratories Pvt. Ltd. Unit-II, Plot No. D-4,5,6,17,18,19, Gallops Industrial Park II, Vasna Chacharwadi, Dist. Ahmedabad-382 110, Gujarat, India.

For queries, contact: +91 9104744518

Don’t miss this chance to join a dynamic team at one of India’s respected pharmaceutical manufacturers!