Corona Hiring CQA Officer/Executive

Corona Remedies CQA Jobs | MPharm QA | Gujarat

Corona Remedies hiring CQA Officer/Executive in Gujarat for B.Pharm, M.Pharm, M.Sc candidates with 3-7 years pharma QA experience.

Corona Remedies Limited has announced a new pharmaceutical hiring opportunity for experienced Quality Assurance professionals at its manufacturing facility in Gujarat. The company is currently recruiting Officer and Executive level candidates for its Corporate Quality Assurance (CQA) division.

Professionals searching for pharmaceutical quality assurance jobs, CQA executive vacancies, GMP compliance careers, regulatory affairs support roles, pharma manufacturing compliance jobs, and QA officer openings in Gujarat can explore this opportunity.

Candidates with 3 to 7 years of pharmaceutical manufacturing experience in Quality Assurance or Corporate Quality Assurance functions are eligible to apply.

The opening is suitable for candidates experienced in GMP compliance management, CAPA systems, deviation handling, internal audits, quality documentation review, vendor audit management, and regulatory inspection readiness.

Applicants with B.Pharm, M.Pharm, or M.Sc qualifications and strong exposure to pharmaceutical quality systems are encouraged to apply.

Company Overview

Corona Remedies Limited is one of India’s growing pharmaceutical companies known for its focus on innovation, healthcare quality, and patient-centric pharmaceutical solutions.

The company operates with a strong commitment toward regulatory compliance, pharmaceutical manufacturing quality, and healthcare innovation. Corona Remedies has built a reputation for maintaining high-quality standards across its manufacturing and operational processes.

Its pharmaceutical manufacturing operations follow stringent GMP and GDP practices to ensure product safety, quality consistency, and regulatory compliance.

The organization continues expanding its operations and strengthening its Corporate Quality Assurance systems to support pharmaceutical manufacturing excellence.

Working with Corona Remedies provides professionals exposure to:

• Pharmaceutical quality management systems
• GMP and GDP compliance frameworks
• Regulatory inspection preparedness
• Corporate Quality Assurance operations
• Internal and vendor audit systems
• CAPA and deviation management
• Pharmaceutical documentation control
• Compliance monitoring systems

Professionals looking to build long-term careers in pharmaceutical quality systems and compliance management can benefit from this opportunity.

Job Role & Responsibilities

Officer / Executive – Corporate Quality Assurance (CQA)

Candidates selected for the Corporate Quality Assurance department will be responsible for maintaining and strengthening pharmaceutical quality systems across manufacturing operations.

The role requires strong understanding of pharmaceutical compliance systems, documentation review processes, regulatory standards, audit handling, and cross-functional coordination.

Key Responsibilities

• Ensure implementation and compliance of GMP and GDP systems across manufacturing units
• Monitor pharmaceutical quality systems and regulatory compliance activities
• Review and approve quality documents including SOPs, BMRs, BPRs, protocols, and reports
• Handle deviation management and change control systems
• Support CAPA implementation and incident management processes
• Conduct internal audits and self-inspections
• Participate in vendor qualification and vendor audit activities
• Coordinate with QA and QC teams for regulatory audit preparedness
• Maintain documentation compliance according to pharmaceutical regulations
• Ensure quality system effectiveness across manufacturing operations

Documentation Responsibilities

Candidates should have exposure to reviewing and approving:

• SOPs
• BMR/BPR documents
• Validation protocols
• Investigation reports
• CAPA records
• Change control documents
• Quality management reports

Regulatory Compliance Exposure

The company is looking for candidates familiar with:

• GMP guidelines
• GDP compliance systems
• Pharmaceutical audit systems
• Regulatory inspection readiness
• Pharmaceutical documentation standards
• Pharmaceutical manufacturing compliance requirements

Skills Preferred

Candidates with the following expertise may receive preference during the selection process:

• Pharmaceutical Quality Assurance systems
• Corporate Quality Assurance operations
• GMP and GDP implementation
• Internal audit management
• Regulatory compliance handling
• CAPA system management
• Deviation investigation
• Vendor audit coordination
• Pharmaceutical documentation review
• Regulatory inspection support
• Pharmaceutical manufacturing compliance

Strong communication skills, documentation accuracy, analytical thinking, and coordination abilities are important for this role.

Eligibility / Qualifications

Candidates applying for this pharmaceutical quality assurance vacancy should possess one of the following qualifications:

• B.Pharm
• M.Pharm
• M.Sc

Relevant Courses

Pharmaceutical Quality Assurance, Industrial Pharmacy, Pharmaceutical Chemistry, Pharmaceutical Analysis, Regulatory Affairs, Quality Management Systems, Pharmaceutical Technology, Clinical Pharmacy, Organic Chemistry, Analytical Chemistry

Experience Required

• 3 to 7 years of pharmaceutical manufacturing experience
• Experience in Quality Assurance or Corporate Quality Assurance roles preferred
• Exposure to regulated pharmaceutical manufacturing environments is beneficial

Candidates currently working in pharmaceutical formulation plants, regulated manufacturing facilities, or corporate compliance teams may receive preference.

Why This Opportunity Stands Out

Corporate Quality Assurance roles are becoming increasingly important in the pharmaceutical industry due to rising global compliance requirements and regulatory expectations.

Professionals working in CQA departments gain exposure to company-wide quality systems and regulatory operations, making this one of the most valuable career paths in pharmaceutical manufacturing.

This opportunity at Corona Remedies provides candidates with:

• Exposure to advanced pharmaceutical quality systems
• Experience in regulatory audit coordination
• Hands-on work in GMP and GDP implementation
• Corporate-level compliance exposure
• Cross-functional pharmaceutical operations experience
• Career growth opportunities in pharmaceutical compliance management

The demand for experienced pharmaceutical quality professionals continues to grow due to increasing focus on global regulatory standards, manufacturing quality, and compliance-driven operations.

Work Environment & Career Growth

Corona Remedies focuses on innovation-driven pharmaceutical operations and quality-centric manufacturing systems.

Candidates joining the organization may receive opportunities to work on:

• Regulatory compliance projects
• Pharmaceutical quality system improvements
• Audit preparedness programs
• Documentation management systems
• Continuous improvement initiatives
• Cross-functional compliance coordination

Professionals with strong CQA experience can further grow into managerial, compliance leadership, and global regulatory support roles.

Location & Salary

Job Location

Bavla, Gujarat

Salary

Salary will be competitive and based on candidate experience, pharmaceutical industry exposure, compliance expertise, and interview performance.

Application Process

Interested candidates can apply by sharing their updated resume through email.

Email IDs

• sagart@coronaremedies.com
• anjaliv@coronaremedies.com

Company Location

Corona Remedies Limited (Plant) Plot No. 503, Near HP Petrol Pump Village: Bhayla, Bavla – 382220 Gujarat

Candidates should mention their current designation, total experience, current CTC, expected salary, and notice period while applying.

Important Note

Applicants should ensure that all qualification details, work experience, and compliance exposure mentioned in the resume are accurate and updated.

Candidates with strong pharmaceutical quality documentation and audit handling experience may have an advantage during shortlisting.

FAQs

1. What is the designation offered at Corona Remedies?

The company is hiring for Officer and Executive roles in Corporate Quality Assurance.

2. What qualifications are required for this CQA role?

Candidates with B.Pharm, M.Pharm, or M.Sc qualifications can apply.

3. How much experience is required?

Applicants should have 3 to 7 years of pharmaceutical Quality Assurance experience.

4. Is regulatory audit exposure important?

Yes. Candidates with audit coordination and regulatory compliance experience are preferred.

5. What quality systems knowledge is expected?

Candidates should have knowledge of GMP, GDP, CAPA, deviation management, and change control systems.

6. How can candidates apply?

Interested applicants can send their updated CV to the provided email IDs.

Summary Table

Company	Corona Remedies Limited
Department Vacancies	Corporate Quality Assurance (Officer / Executive)
Qualification	B.Pharm, M.Pharm, M.Sc
Experience	3 to 7 Years
Location	Bavla, Gujarat