India's DMPLOI - Jobs & Networking AppCorona Remedies Limited, one of India’s fastest-growing pharmaceutical companies, has announced a Walk-In Interview for experienced professionals in its R&D Centre (OSD Formulations). The company is hiring talented candidates for the Analytical Development Laboratory (ADL) team at its Ahmedabad, Gujarat facility.
This opportunity is ideal for candidates with experience in analytical method development, validation, HPLC, UV, Dissolution, and ICH guidelines who are looking to advance their careers in pharmaceutical research and development.
About Corona Remedies Limited
Corona Remedies Limited is a leading Indian pharmaceutical company headquartered in Ahmedabad, Gujarat. The organization is known for its innovation-driven culture, employee development, and quality-focused pharmaceutical products. With more than 5,000 employees, Corona Remedies continues to expand its R&D and manufacturing capabilities.
Walk-In Interview Details
Company: Corona Remedies Limited
Department: Analytical Development Laboratory (ADL)
Division: R&D Centre (OSD Formulations)
Designation: Research Associate to Senior Research Associate
Job Location: Corona Remedies Limited Plot No. 503, Village Bhayla, Near Super Gas, Bavla–Bagodara Highway, Bavla, Ahmedabad, Gujarat – 382220
Interview Venue: Corona House, S-Mondeal Business Park, Near Gurudwara, S.G. Highway, Ahmedabad, Gujarat
Walk-In Date: 19 July 2026
Interview Time: 10:00 AM to 03:00 PM
Educational Qualification
M.Sc. (Analytical Chemistry)
M.Pharm (Analytical Chemistry/Pharmaceutical Chemistry)
Experience Required
2–8 Years
Core Solid Oral Dosage (OSD) formulation experience is mandatory.
Job Responsibilities
Selected candidates will be responsible for:
Perform analytical method development for raw materials, in-process samples, and finished products.
Execute analytical method validation as per ICH Q2(R1) guidelines.
Develop, optimize, and validate analytical methods using HPLC, UV, GC, AAS, Karl Fischer (KF), and Dissolution instruments.
Prepare and review analytical validation protocols, reports, and technical documentation.
Troubleshoot analytical issues and provide technical support to cross-functional teams.
Ensure compliance with GLP, GMP, GDP, and regulatory requirements.
Maintain laboratory documentation, stability samples, and reference standards with complete data integrity.
Required Technical Skills
Strong knowledge of analytical method development and validation.
Hands-on experience with HPLC, UV, Dissolution, GC, AAS, and KF instruments.
Good understanding of ICH guidelines and pharmaceutical regulatory requirements.
Knowledge of GLP, GMP, GDP, and data integrity practices.
Excellent analytical, troubleshooting, documentation, and problem-solving skills.
Why Join Corona Remedies?
Opportunity to work in a growing pharmaceutical R&D organization.
Exposure to advanced analytical techniques.
Employee-focused work culture.
Career growth in Analytical Development and Formulation R&D.
Work alongside experienced pharmaceutical scientists.
How to Apply?
Eligible candidates can directly attend the walk-in interview with:
Updated Resume/CV
Educational Certificates
Experience Certificates
Latest Salary Slip
Passport-size Photographs
Government Photo ID Proof
Candidates who are unable to attend the interview can send their updated CV to:
karuendrak@coronaremedies.com
diteet@coronaremedies.com
Official Website: https://www.coronaremedies.com
Technical FAQs
1. What analytical instruments should candidates be proficient in?
Candidates should have practical experience with HPLC, UV-Visible Spectrophotometer, Gas Chromatography (GC), Atomic Absorption Spectroscopy (AAS), Karl Fischer (KF), and Dissolution Apparatus.
2. Why is ICH Q2(R1) important in Analytical Development?
ICH Q2(R1) provides internationally accepted guidelines for validating analytical methods by evaluating parameters such as accuracy, precision, specificity, linearity, robustness, detection limit, and quantitation limit.
3. What is meant by Core OSD formulation experience?
Core OSD (Oral Solid Dosage) experience refers to working with pharmaceutical products such as tablets and capsules, including analytical testing, method development, validation, stability studies, and regulatory documentation.
4. What is the role of GLP, GMP, and GDP in pharmaceutical laboratories?
GLP (Good Laboratory Practices): Ensures reliable laboratory testing.
GMP (Good Manufacturing Practices): Ensures products are consistently manufactured and controlled.
GDP (Good Documentation Practices): Ensains accurate, traceable, and compliant documentation.
5. What are the major responsibilities of an Analytical Development Laboratory (ADL) scientist?
ADL professionals develop and validate analytical methods, troubleshoot analytical problems, perform stability studies, support formulation development, ensure regulatory compliance, maintain data integrity, and prepare validation reports for pharmaceutical products.
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