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.
Sipra Labs Walk-In Interview– Analytical Lab, Accounts & Quality Assurance Jobs
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