Emcure Pharmaceuticals Ltd., one of India’s leading pharmaceutical companies, has announced a Walk-In Interview Drive for experienced Quality Control (QC) professionals at its Injectable Manufacturing Unit in Sanand, Ahmedabad, Gujarat. This recruitment drive offers an excellent opportunity for candidates with expertise in analytical testing, laboratory operations, and regulatory compliance within the pharmaceutical industry.

Overview of the Walk-In Drive

Particulars Details

Company Name

Emcure Pharmaceuticals Ltd.

Department

Quality Control (QC)

Profile

HPLC / GC / LIMS

Designation

Officer / Executive

Qualification

B.Pharm, M.Pharm, B.Sc, M.Sc

Experience

3 to 7 Years

Interview Date

26th June 2026 (Friday)

Time

10:00 AM to 4:00 PM

Location

Sanand, Ahmedabad, Gujarat

Manufacturing Facility

Injectable Unit

About the Opportunity

Emcure Pharmaceuticals is seeking talented professionals with hands-on experience in Quality Control operations for sterile injectable manufacturing. Selected candidates will contribute to analytical testing, method validation, regulatory compliance, and laboratory management activities while ensuring adherence to global quality standards.

The company is looking for candidates with practical exposure to analytical instruments such as HPLC, GC, UV Spectrophotometer, FTIR, and laboratory information systems (LIMS).

Key Responsibilities

The selected candidates will be responsible for:

Analysis of Raw Materials (RM), Packaging Materials (PM), in-process samples, finished products, and stability samples.

Operation and troubleshooting of HPLC, GC, UV, FTIR, and other analytical instruments.

Preparation and standardization of reagents and volumetric solutions.

Review and documentation of analytical data as per GMP and GLP guidelines.

Investigation and handling of OOS, OOT, deviations, and CAPA activities.

Environmental monitoring and water sample analysis.

Method validation, method verification, and stability study activities.

Calibration and preventive maintenance of laboratory equipment.

Ensuring compliance with Data Integrity requirements and international regulatory standards.

Coordination with Quality Assurance and Production departments for quality compliance activities.

Regulatory Exposure Required

Candidates should possess knowledge of:

USFDA Guidelines

EU GMP Requirements

WHO GMP Standards

Data Integrity Compliance

Good Laboratory Practices (GLP)

Good Manufacturing Practices (GMP)

Stability Guidelines

Analytical Method Validation

Eligibility Criteria

Educational Qualification

Candidates must possess any of the following qualifications:

B.Pharm

M.Pharm

B.Sc

M.Sc

Experience Required

Minimum: 3 Years

Maximum: 7 Years

Preferred Skills

HPLC Analysis

Gas Chromatography (GC)

Laboratory Information Management System (LIMS)

Stability Studies

Instrument Calibration

OOS/OOT Investigation

Method Validation

Documentation Practices

Documents to Carry

Candidates attending the walk-in interview should bring:

Updated Resume/CV

Educational Certificates

Current Salary Slip

CTC Proof

Experience Certificates

Government Photo ID

Recent Passport-Size Photographs

Interview Venue

Emcure Pharmaceuticals Ltd.

Plot No. SM-14-15-16/1, GIDC II,

Sanand, Ahmedabad, Gujarat

Why Join Emcure Pharmaceuticals?

Work with a globally recognized pharmaceutical organization.

Exposure to regulated markets including USFDA and EU GMP.

Opportunity to work in a modern injectable manufacturing facility.

Career growth in Quality Control and analytical sciences.

Collaborative and quality-driven work environment.

Technical FAQs

1. What is the significance of HPLC in pharmaceutical Quality Control?

HPLC (High-Performance Liquid Chromatography) is used for quantitative and qualitative analysis of pharmaceutical products. It helps determine assay, impurities, degradation products, and content uniformity while ensuring product quality and regulatory compliance.

2. What is OOS and how is it handled in a QC laboratory?

OOS (Out of Specification) refers to test results that fall outside predefined acceptance criteria. Handling involves laboratory investigation, root cause analysis, review of analytical procedures, and implementation of corrective and preventive actions (CAPA).

3. Why is method validation important in pharmaceutical analysis?

Method validation ensures analytical methods are accurate, precise, specific, robust, and reproducible. Regulatory agencies require validated methods to guarantee reliable testing results and product quality.

4. What role does LIMS play in Quality Control laboratories?

LIMS (Laboratory Information Management System) helps manage analytical data, sample tracking, instrument integration, audit trails, and documentation, ensuring data integrity and regulatory compliance.

5. What are the key data integrity principles in pharmaceutical QC?

Data integrity follows ALCOA+ principles:

Attributable

Legible

Contemporaneous

Original

Accurate

Additional principles include Complete, Consistent, Enduring, and Available records to meet regulatory expectations from USFDA, EU GMP, and WHO GMP.

Conclusion:

The Emcure Pharmaceuticals Walk-In Interview 2026 presents an excellent opportunity for experienced Quality Control professionals to join a leading injectable manufacturing facility. Candidates with expertise in HPLC, GC, LIMS, method validation, and regulatory compliance are encouraged to attend the interview with all required documents and take the next step in their pharmaceutical careers.