CORONA Remedies Limited, one of India’s rapidly growing pharmaceutical organizations headquartered in Ahmedabad, has announced a walk-in interview drive for experienced professionals in the Analytical Development Laboratory (ADL) and Quality Control (QC) departments. The company is seeking talented candidates with experience in pharmaceutical analysis, method development, quality testing, and microbiological operations.

This recruitment drive offers an excellent opportunity for candidates looking to build their careers in a dynamic pharmaceutical environment known for innovation, quality, and professional growth.

Walk-In Interview Details

Interview Date: 07 June 2026 (Sunday)

Time: 9:30 AM to 2:00 PM

Interview Venue:

CORONA Remedies Limited

Block S, Mondeal Business Park, Near Gurudwara,

S.G. Highway, Ahmedabad, Gujarat

Open Positions

1. Analytical Development Laboratory (ADL)

Designation: RA / SRA / RS / SRS

Qualification: B.Pharm / M.Sc

Experience: 2 to 8 Years

Key Responsibilities

Analytical method development and validation.

Method transfer activities for assays, related substances, dissolution, and solvent analysis.

Calibration and maintenance of analytical instruments.

Routine laboratory analysis and documentation.

Compliance with regulatory and GMP requirements.

Instruments Exposure

HPLC

GC/HS

IR Spectroscopy

UV Spectrophotometer

Dissolution Apparatus

2. Quality Control (QC)

Designation: Sr. Officer / Executive

Qualification: B.Pharm / M.Sc

Experience: 3 to 8 Years

Key Responsibilities

Analysis of raw materials, in-process samples, and finished products.

Stability testing and process validation support.

Investigation of OOS, OOT, laboratory incidents, and deviations.

Handling and troubleshooting analytical instruments.

Preparation and review of laboratory documentation.

Instruments Exposure

HPLC

Dissolution Apparatus

FTIR

UV Spectrophotometer

Weighing Balance

Friability Tester

Hardness Tester

3. Quality Control – Microbiology

Designation: Sr. Officer / Executive (Micro)

Qualification: M.Sc (Microbiology/Biotechnology)

Experience: 2 to 7 Years

Key Responsibilities

Microbiological testing of raw materials and finished products.

Water system analysis and environmental monitoring.

In-process sample testing.

Compliance with SOPs, GMP, and regulatory requirements.

Documentation and reporting of microbiological results.

Job Location

CORONA Remedies Limited

Near Super Gas Pump, Bavla-Bagodara Road, Vill-Bhayla, Taluka Bavla, District Ahmedabad, Gujarat.

Application Process

Candidates who are unable to attend the walk-in interview may share their updated CV through the official company email addresses mentioned in the recruitment notification.

Applicants should carry:

Updated Resume/CV

Educational Certificates

Experience Certificates

Latest Salary Documents

Passport Size Photographs

Government ID Proof

Why Join CORONA Remedies?

Growing pharmaceutical organization with a strong industry presence.

Exposure to advanced analytical and microbiological technologies.

Professional work culture focused on innovation.

Career advancement opportunities in regulated pharmaceutical operations.

Opportunity to work with experienced industry professionals.

Technical FAQs

1. What is the purpose of Analytical Method Validation in ADL?

Analytical Method Validation ensures that a testing method consistently produces accurate, precise, specific, and reproducible results suitable for its intended purpose according to ICH guidelines.

2. What is the difference between OOS and OOT results in Quality Control?

OOS (Out of Specification) refers to test results falling outside approved specifications, whereas OOT (Out of Trend) refers to results that are within specifications but show unusual variation compared to historical data.

3. Why is HPLC widely used in pharmaceutical laboratories?

HPLC provides high accuracy, sensitivity, and reproducibility for quantitative and qualitative analysis of APIs, impurities, degradation products, and finished pharmaceutical products.

4. What is Environmental Monitoring in Microbiology?

Environmental Monitoring involves routine assessment of cleanrooms, air quality, surfaces, and personnel to ensure microbial contamination remains within acceptable limits under GMP requirements.

5. What is Method Transfer in Pharmaceutical Analysis?

Method Transfer is the documented process of transferring an analytical method from one laboratory to another while demonstrating equivalent performance, accuracy, precision, and reliability.