Join Corona Remedies Private Limited, a fast-growing pharmaceutical company founded in 2004, headquartered in Ahmedabad, Gujarat. With a turnover of ₹600 Cr and operations in 20+ countries, Corona Remedies is known for its USFDA, EU-GMP, and ISO 9001:2015-certified facility producing oral solid dosages (OSD), ointments, and injectables.
We’re hosting a walk-in interview in Vapi on May 18, 2025, for Quality Assurance (QA), Quality Control (QC), Analytical Development Lab (ADL), Formulation Development & Technology Transfer (F&D), and Production roles to support our facility in Bhayla, Ahmedabad, targeting professionals with 2-7 years of experience in regulated markets like Europe and ROW.
Event Details: Walk-In Interview
This walk-in interview targets experienced professionals for QA, QC, ADL, F&D, and Production roles at our Bhayla facility, a key hub for OSD manufacturing. Candidates with exposure to Europe and Rest of World (ROW) markets are preferred.
Date and Time
- Date: Sunday, May 18, 2025
- Time: 9:00 AM – 5:00 PM IST
Interview Venue
Hotel Silver Leaf
Plot No. CM-14 & 15, Raghuvir Complex, Opp. Vapi Industries Association Ground, GIDC, Vapi, Gujarat – 396195
Job Location
- Corona Remedies Limited, Plot No. 503, Village Bhayla, Near Super Gas, Bavla-Bagodara Highway, Taluka Bavla, Ahmedabad, Gujarat – 382220
Job Opportunities at Corona Remedies
We’re hiring for QA, QC, ADL, F&D, and Production roles to drive quality and innovation at our Bhayla facility, compliant with cGMP standards. All positions require experience in USFDA/EU-GMP-regulated environments.
1. Quality Assurance (QA) – Officer / Sr. Officer / Executive
- Qualification: B.Pharm, M.Sc. (Chemistry), M.Pharm
- Experience: 3-7 years in QA for OSD/injectables
- Openings: Multiple (likely 3-5 based on QA needs)
- Salary: ₹4.0–8.0 Lakhs/year (estimated based on industry standards)
Key Responsibilities:
- Ensure compliance with cGMP, IPQA, and QMS processes
- Perform line clearances, in-process checks, and validation activities
- Manage documentation (SOPs, BMRs, BPRs) per 21CFR Part 11
- Conduct risk assessments, vendor qualifications, and OOS/OOT investigations
- Support regulatory audits (USFDA, MHRA) and market complaint resolutions
Key Skills:
- Expertise in QMS, IPQA, cleaning validation, and CSV
- Knowledge of regulatory requirements (Europe, ROW)
- Proficiency in handling OOS, OOT, and product recalls
- Strong audit preparation and documentation skills
2. Quality Control (QC) – Officer / Sr. Officer / Executive
- Qualification: B.Pharm, M.Sc. (Chemistry), M.Pharm
- Experience: 3-7 years in QC for OSD/injectables
- Openings: Multiple (likely 4-6 based on QC operations)
- Salary: ₹4.0–8.0 Lakhs/year (estimated based on industry standards)
Key Responsibilities:
- Perform sampling, testing, and analysis of raw materials, in-process, and finished products
- Operate and calibrate lab instruments like HPLC, UV, IR, and dissolution testers
- Conduct stability testing, process validation, and OOS/OOT investigations
- Document results in LIMS and ensure compliance with ICH Q2(R1)
Key Skills:
- Proficiency in HPLC, UV, IR, and dissolution testing
- Knowledge of cGMP, GLP, and regulatory standards (Europe, ROW)
- Experience with analytical deviations and lab incident reporting
- Strong analytical and troubleshooting skills
3. Analytical Development Lab (ADL) – Research Associate (RA) / Senior Research Associate (SRA) / Research Scientist (RS) / Senior Research Scientist (SRS)
- Qualification: M.Sc. (Analytical Chemistry), M.Pharm (Pharmaceutical Analysis)
- Experience: 2-7 years in ADL for OSD formulations
- Openings: Multiple (likely 3-5 based on ADL projects)
- Salary: ₹3.5–7.5 Lakhs/year (estimated based on industry standards)
Key Responsibilities:
- Develop and validate analytical methods for OSD as per ICH Q2(R1)
- Perform method transfer and routine analysis using HPLC, GC, UV, and IR
- Calibrate analytical instruments and document protocols
- Investigate OOS/OOT and review QC documents
Key Skills:
- Expertise in analytical method development and validation
- Proficiency in HPLC, GC, and dissolution testing
- Knowledge of regulatory guidelines (USFDA, EU-GMP)
- Strong documentation and data integrity skills
4. Formulation Development & Technology Transfer (F&D) – Research Associate (RA) / Senior Research Scientist (SRS)
- Qualification: M.Pharm (Pharmaceutics), Ph.D. (Pharmaceutical Sciences)
- Experience: 2-7 years in F&D for OSD, ointments, and injectables
- Salary: ₹4.0–8.5 Lakhs/year (estimated based on industry standards)
- Openings: Multiple (likely 2-4 based on F&D projects)
Key Responsibilities:
- Design, develop, and optimize formulations for OSD, ointments, and injectables
- Conduct pre-formulation studies and scale-up trials
- Support technology transfer from R&D to manufacturing
- Collaborate with ADL for method development and stability studies
Key Skills:
- Expertise in formulation development and process optimization
- Knowledge of QbD, scale-up, and technology transfer
- Familiarity with regulatory requirements (Europe, ROW)
- Strong project management and teamwork skills
5. Production – Officer / Sr. Officer / Executive
- Qualification: B.Pharm, M.Pharm, B.Sc. (Chemistry)
- Experience: 3-7 years in OSD/injectable production
- Salary: ₹4.0–8.0 Lakhs/year (estimated based on industry standards)
- Openings: Multiple (likely 4-6 based on production lines)
Key Responsibilities:
- Manage manufacturing operations (granulation, compression, coating, packing)
- Execute batch processes per BMR and ensure cGMP compliance
- Perform equipment cleaning, line clearances, and yield monitoring
- Document activities in BPRs and support process validation
Key Skills:
- Expertise in granulation, compression, coating, and packing
- Knowledge of cGMP and regulatory standards (Europe, ROW)
- Proficiency in BMR/BPR documentation and QMS
- Strong operational and troubleshooting skills
Why Join Corona Remedies?
Corona Remedies, with 1,200+ employees, is rated 3.7/5 on AmbitionBox for growth opportunities (3.9/5 at Bhayla). Our Bhayla facility supports generics for Europe and ROW, with a focus on quality and innovation. Employees praise USFDA/EU-GMP exposure (4.0/5) but note work-life balance challenges (3.6/5) due to shift work. Our “Care for Coronets” culture and Great Place to Work nomination reflect a supportive environment.
Key Benefits
- Work in a USFDA/EU-GMP-compliant facility
- Support generics for global markets (Europe, ROW)
- Gain expertise in HPLC, QMS, and formulation development
- Join a 21-year legacy with ₹600 Cr turnover
- Access career growth in Ahmedabad’s pharma hub
How to Apply
Attend the walk-in interview on May 18, 2025, from 9:00 AM to 5:00 PM at Hotel Silver Leaf, Vapi. Bring:
- Updated resume
- Educational certificates (B.Pharm, M.Sc., M.Pharm, Ph.D.)
- Experience letters and last 3 months’ payslips
- Aadhar and PAN cards
- Passport-size photographs (2)
- Preparation:
- QA: Review QMS, IPQA, and validation protocols
- QC/ADL: Study HPLC, ICH Q2(R1), and OOS investigations
- F&D: Prepare for QbD and technology transfer
- Production: Understand granulation, compression, and cGMP
- Be ready to discuss Europe/ROW regulatory exposure
- Note: Candidates unable to attend can email CVs to sagart@coronaremedies.com by May 16, 2025, with subject “Role Name – Bhayla”. Corona Remedies does not charge recruitment fees; verify communications via @coronaremedies.com emails.
About Corona Remedies
Corona Remedies operates a state-of-the-art facility in Bhayla, producing 200+ formulations for domestic and export markets. With 30+ trademarks and a focus on therapeutic segments like cardiology and diabetology, we drive innovation in pharmaceutical manufacturing. Our R&D center in Ahmedabad supports 50+ scientists, ensuring first-to-market products.
Our Mission
- Deliver high-quality healthcare solutions
- Uphold cGMP and global regulatory excellence
- Foster a dynamic, employee-centric culture
Attend the walk-in interview on May 18, 2025, in Vapi or email sagart@coronaremedies.com. Join Corona Remedies in Bhayla and advance pharmaceutical innovation