Sipra Labs has announced a Walk-In Interview Drive for experienced professionals in the Analytical Lab, Accounts, and Quality Assurance (QA) departments. This recruitment drive offers excellent career opportunities for candidates with experience in pharmaceutical analysis, quality systems, and financial operations.

Walk-In Interview Details

• Company: Sipra Labs
• Interview Date: 19 September 2026 (Saturday)
• Time: 10:00 AM to 3:00 PM
• Industry: Pharmaceutical Manufacturing
• Mode: Walk-In Interview

Available Positions

1. Senior Analyst – HPLC

Department: Analytical Lab

Qualification:

• M.Sc
• M.Pharm
• B.Pharm

Experience: 4–6 Years

Key Responsibilities:

• HPLC and chromatographic analysis
• Method transfer and method validation
• Routine sample testing
• OOS/OOT investigation handling
• Data review and compliance activities
• Regulatory audit support (FDA, NABL, CDSCO)

2. Executive – Accounts

Department: Accounts

Qualification:

• B.Com
• M.Com
• MBA

Experience: 2–4 Years

Key Responsibilities:

• Accounts receivable management
• Client account reconciliation
• TDS reconciliation
• Bookkeeping and accounting activities
• MIS report preparation

3. Senior Executive – QA

Department: Quality Assurance

Qualification:

• M.Sc
• M.Pharm
• B.Pharm

Experience: 5–8 Years

Key Responsibilities:

• Quality Management System (QMS) compliance
• Deviation, CAPA and Change Control management
• OOS investigations
• Internal quality audits
• Data Integrity compliance under ALCOA+ principles

Documents Required

Candidates should carry:

• Updated Resume
• Last 3 Months Payslips
• Complete CTC Letter
• Educational Certificates (Photocopies)

Why Join Sipra Labs?

• Opportunity to work in a regulated pharmaceutical environment
• Exposure to FDA, CDSCO and NABL compliance systems
• Professional growth in analytical and quality functions
• Learning opportunities in advanced pharmaceutical operations

Technical FAQs

1. What is HPLC and why is it important in pharmaceutical analysis?

HPLC (High Performance Liquid Chromatography) is an analytical technique used to identify, quantify, and separate compounds in drug products. It ensures product quality, purity, and compliance with regulatory standards.

2. What is Method Validation in pharmaceutical laboratories?

Method Validation is the documented process of proving that an analytical method consistently produces accurate, precise, and reliable results according to regulatory requirements.

3. What does OOS mean in pharmaceutical quality systems?

OOS (Out of Specification) refers to test results that fall outside predefined acceptance criteria. OOS investigations help identify root causes and ensure product quality.

4. What is CAPA in Quality Assurance?

CAPA (Corrective and Preventive Action) is a quality management process used to eliminate existing issues and prevent future occurrences, ensuring continuous improvement and regulatory compliance.

5. What are ALCOA+ Data Integrity Principles?

ALCOA+ stands for:

• Attributable
• Legible
• Contemporaneous
• Original
• Accurate
• Complete
• Consistent
• Enduring
• Available

These principles ensure trustworthy and reliable pharmaceutical data.