Corona Walk-In QC, QA, ADL and Production
Corona Remedies Hiring QC QA ADL Production Jobs
Corona Remedies hiring QC, QA, ADL and Production professionals. B.Pharm, M.Pharm, B.Sc, M.Sc candidates with 2–7 years experience can apply.
Corona Remedies Limited has announced a walk-in interview drive for experienced pharmaceutical professionals across Quality Control, Quality Assurance, Analytical Development Laboratory (ADL), and Production departments. The recruitment drive will be conducted in Vadodara for positions based at the company’s manufacturing facility near Ahmedabad, Gujarat.
This hiring initiative is an excellent opportunity for professionals with experience in pharmaceutical manufacturing, quality systems, analytical method development, laboratory operations, GMP compliance, and production operations. Candidates with qualifications including B.Pharm, M.Pharm, B.Sc, and M.Sc can apply for various openings depending on their expertise and experience.
As pharmaceutical manufacturing and regulated market operations continue to expand in India, skilled professionals with experience in analytical testing, quality management systems, formulation manufacturing, and regulatory-compliant operations remain highly sought after. This walk-in drive provides an opportunity to join one of India’s fastest-growing pharmaceutical organizations.
Primary Keyword: Pharmaceutical Quality Control Jobs
Company Overview
Corona Remedies Limited is one of India’s rapidly growing pharmaceutical companies with a strong presence across multiple therapeutic segments. Headquartered in Ahmedabad, the company has built a reputation for innovation, quality-driven manufacturing, and a people-centric work culture.
With a workforce of more than 4,000 employees, Corona Remedies continues to strengthen its position in the Indian pharmaceutical industry through investments in research, manufacturing excellence, product development, and regulatory compliance. The company’s “Care for Coronets” culture emphasizes employee growth, learning opportunities, and professional development.
Corona Remedies operates modern manufacturing facilities and focuses on delivering high-quality pharmaceutical products while adhering to stringent GMP, GLP, and regulatory requirements. The organization offers long-term career opportunities for professionals interested in pharmaceutical manufacturing, quality assurance, analytical development, and regulated market operations.
Job Role & Responsibilities
Quality Control (QC)
Designation: Quality Control Professional
Qualification: B.Sc, M.Sc, B.Pharm
Experience: 3–5 Years
Key Responsibilities
- Perform raw material analysis and testing.
- Conduct stability sample testing and evaluation.
- Operate analytical instruments as per approved procedures.
- Maintain laboratory records and analytical documentation.
- Ensure compliance with GMP and GLP requirements.
- Support routine testing of pharmaceutical products.
- Review analytical results and documentation.
- Follow quality control laboratory procedures and SOPs.
Required Technical Skills
- AMV / AMT Operations
- Raw Material Analysis
- Stability Studies
- Analytical Documentation
- GMP Compliance
- GLP Compliance
- Laboratory Testing
Quality Assurance (QA)
Designation: Quality Assurance Professional
Qualification: B.Pharm
Experience: 3–5 Years
Key Responsibilities
- Manage Quality Management System (QMS) activities.
- Handle Change Control, Deviations, and CAPA processes.
- Perform in-process quality checks.
- Conduct line clearance activities.
- Monitor GMP compliance across manufacturing operations.
- Review batch manufacturing and packaging records.
- Support laboratory quality assurance activities.
- Ensure adherence to regulatory requirements.
Required Technical Skills
- Change Control Management
- Deviation Handling
- CAPA Management
- QMS Operations
- Batch Record Review
- In-Process Quality Assurance
- GMP Monitoring
- Line Clearance
Analytical Development Laboratory (ADL)
Designation: Analytical Development Professional
Qualification: M.Sc, M.Pharm
Experience: 2–7 Years
Key Responsibilities
- Perform analytical method development activities.
- Conduct method validation and method transfer studies.
- Execute testing for assay, related substances, dissolution, and solvent analysis.
- Support analytical investigations and troubleshooting.
- Maintain laboratory records and documentation.
- Perform routine analytical testing.
- Ensure compliance with analytical procedures and regulatory guidelines.
Instrumentation Exposure Required
Candidates should have experience in calibration and operation of:
- HPLC
- GC
- HS-GC
- UV Spectrophotometer
- IR Spectrophotometer
- Dissolution Apparatus
Additional Requirements
- Exposure to regulated market products.
- Experience with OSD formulations.
- Experience with injectable products.
- Experience with semi-solid dosage forms.
Production Department
Areas: Granulation, Compression, Coating, Capsule Filling, Softgel Manufacturing
Qualification: B.Pharm
Experience: 3–5 Years
Key Responsibilities
- Operate pharmaceutical manufacturing equipment.
- Execute production activities as per approved procedures.
- Maintain batch manufacturing records.
- Ensure compliance with GMP requirements.
- Follow SOPs and production guidelines.
- Monitor manufacturing processes and product quality.
- Support production targets and operational efficiency.
- Maintain documentation and compliance records.
Required Technical Skills
- Granulation Operations
- Compression Operations
- Coating Processes
- Capsule Filling
- Softgel Manufacturing
- Production Documentation
- GMP Compliance
- Equipment Handling
Eligibility / Qualifications
Quality Control
- B.Sc
- M.Sc
- B.Pharm
Quality Assurance
- B.Pharm
Analytical Development Laboratory
- M.Sc
- M.Pharm
Production
- B.Pharm
Relevant Education Background
Bachelor of Pharmacy, Master of Pharmacy, Pharmaceutical Analysis, Pharmaceutical Chemistry, Pharmaceutics, Quality Assurance, Analytical Chemistry, Organic Chemistry, Industrial Pharmacy, Life Sciences, Formulation Development, Pharmaceutical Technology.
Experience Requirement
| Department | Experience |
|---|---|
| Quality Control | 3–5 Years |
| Quality Assurance | 3–5 Years |
| Analytical Development Laboratory | 2–7 Years |
| Production | 3–5 Years |
Why Join Corona Remedies?
Corona Remedies is recognized for its strong growth trajectory and employee-focused culture. The organization offers opportunities to work in regulated pharmaceutical environments while gaining exposure to modern manufacturing technologies, quality systems, analytical development projects, and compliance-driven operations.
Key Benefits
- Career Growth Opportunities
- Exposure to Regulated Markets
- Learning & Development Programs
- GMP-Compliant Manufacturing Environment
- Advanced Laboratory Infrastructure
- Employee-Centric Culture
- Long-Term Career Stability
- Opportunities Across Multiple Dosage Forms
Professionals seeking careers in pharmaceutical quality assurance, analytical development, regulatory-compliant manufacturing, and quality control laboratories can significantly benefit from these opportunities.
Location & Salary
Job Location: Bavla, Ahmedabad, Gujarat
Approximate Salary: ₹4.5 LPA – ₹10 LPA
(Salary may vary based on experience, department, technical expertise, and company policies.)
Application Process
Interested candidates can directly attend the walk-in interview.
Walk-In Interview Details
Date: 21 June 2026
Time: 9:30 AM to 2:00 PM
Interview Venue
Regenta Fairlark
Darshanam Capital
Canal Ring Road
Vasna-Bhayli Main Road
Opposite Essar Petrol Pump
Near Waves Club
Vadodara, Gujarat – 391410
Unable to Attend the Walk-In?
Candidates who cannot attend the interview may share their updated resumes through email.
Email IDs:
Candidates should carry updated resumes, educational certificates, experience documents, salary details, and government-issued identity proof during the interview.
Frequently Asked Questions (FAQs)
1. Which departments are hiring at Corona Remedies?
The company is hiring for Quality Control, Quality Assurance, Analytical Development Laboratory, and Production departments.
2. What qualifications are eligible?
B.Sc, M.Sc, B.Pharm, and M.Pharm candidates can apply depending on the position.
3. Is experience mandatory?
Yes. The openings require 2–7 years of relevant pharmaceutical industry experience.
4. What analytical instruments should ADL candidates know?
Candidates should have experience with HPLC, GC, HS-GC, UV, IR, and Dissolution instruments.
5. Where is the job location?
The selected candidates will work at Corona Remedies’ manufacturing facility in Bavla, Ahmedabad.
6. Can candidates apply through email?
Yes. Candidates unable to attend the walk-in interview can send their resumes to the official recruitment email addresses.
Summary
| Category | Details |
|---|---|
| Company | Corona Remedies Limited |
| Department Vacancies | Quality Control, Quality Assurance, Analytical Development Laboratory, Production |
| Qualification | B.Sc, M.Sc, B.Pharm, M.Pharm |
| Experience | 2–7 Years |
| Location | Bavla, Ahmedabad, Gujarat |
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