Corona Hiring CQA Officer/Executive

BPharm MPharm CQA Officer Vacancy | Corona Remedies Gujarat

BPharm, MPharm, MSc candidates – CQA Officer/Executive vacancy at Corona Remedies Bavla Gujarat with 3–7 years QA experience.

Corona Remedies Limited is inviting experienced pharmaceutical quality professionals to join its Corporate Quality Assurance (CQA) team at the company’s manufacturing plant located in Bavla, Gujarat. The organization is hiring for the role of Officer / Executive – Corporate Quality Assurance, a critical position responsible for maintaining regulatory compliance and quality systems across pharmaceutical manufacturing operations.

Quality assurance plays a central role in pharmaceutical manufacturing. Every batch of medicine produced must follow strict regulatory standards established by global authorities such as the USFDA, WHO, and other regulatory agencies. Corporate Quality Assurance teams oversee these quality systems across manufacturing units and ensure that every department complies with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and other global pharmaceutical regulations.

This opportunity is suitable for professionals who have hands-on experience in pharmaceutical quality systems, regulatory documentation, deviation management, audit preparation, and compliance monitoring. Candidates who want to build long-term careers in pharmaceutical regulatory compliance and global quality systems will find this role particularly valuable.

Professionals selected for this role will contribute directly to maintaining product quality, regulatory readiness, and patient safety. Corporate QA professionals often work across multiple manufacturing functions including production, quality control laboratories, and regulatory affairs teams to maintain a strong pharmaceutical quality management system.

Company Overview

Corona Remedies Limited is a rapidly growing Indian pharmaceutical company focused on delivering high-quality healthcare products across multiple therapeutic areas. The organization operates with the vision of “Good Health for All” and places strong emphasis on innovation, patient safety, and regulatory compliance within pharmaceutical manufacturing.

The company manufactures a wide range of pharmaceutical formulations that serve domestic and international healthcare markets. With modern manufacturing facilities, advanced quality systems, and strong regulatory compliance frameworks, Corona Remedies continues to expand its footprint within the global pharmaceutical industry.

Pharmaceutical companies must maintain strict adherence to global regulatory standards to ensure medicines are safe, effective, and consistently manufactured. Corona Remedies has invested heavily in robust quality management systems, experienced regulatory teams, and well-structured quality assurance departments to ensure all pharmaceutical products meet international quality expectations.

Corporate Quality Assurance teams at Corona Remedies work closely with plant QA, quality control laboratories, production units, and regulatory affairs teams to ensure that every manufacturing process aligns with approved regulatory guidelines and pharmaceutical compliance frameworks.

Working with Corona Remedies provides professionals with exposure to regulated pharmaceutical manufacturing environments, global regulatory compliance systems, and modern pharmaceutical quality management practices.

Job Role & Responsibilities

The Officer / Executive – Corporate Quality Assurance (CQA) role focuses on ensuring consistent quality compliance across pharmaceutical manufacturing operations. Corporate QA professionals work at a strategic level to monitor quality systems, review documentation, and ensure readiness for regulatory inspections.

Implementation of GMP and Regulatory Compliance

Quality assurance teams ensure that manufacturing processes follow regulatory guidelines and global quality standards.

Key responsibilities include:

• Ensuring implementation of Good Manufacturing Practices (GMP) across manufacturing units
• Monitoring adherence to Good Documentation Practices (GDP)
• Supporting regulatory compliance programs within the organization
• Ensuring quality systems meet pharmaceutical regulatory expectations

These responsibilities help maintain consistency in pharmaceutical manufacturing processes and protect patient safety.

Review and Approval of Quality Documentation

Corporate QA professionals review critical pharmaceutical documents that support manufacturing operations.

Key responsibilities include:

• Reviewing and approving Standard Operating Procedures (SOPs)
• Reviewing Batch Manufacturing Records (BMR)
• Reviewing Batch Packaging Records (BPR)
• Reviewing protocols and validation reports
• Reviewing quality documentation generated by production and QC teams

Proper documentation ensures traceability, regulatory compliance, and data integrity within pharmaceutical manufacturing operations.

Deviation, Change Control and CAPA Management

Pharmaceutical quality systems require strong investigation and corrective action procedures.

Key responsibilities include:

• Monitoring deviation management systems
• Supporting change control processes
• Reviewing corrective and preventive actions (CAPA)
• Investigating incidents and quality events
• Ensuring corrective actions are implemented effectively

These systems help pharmaceutical companies identify risks, correct issues, and continuously improve manufacturing quality.

Audit and Inspection Readiness

Corporate QA teams ensure that manufacturing facilities remain prepared for regulatory inspections and internal audits.

Key responsibilities include:

• Conducting internal quality audits
• Performing self-inspections across manufacturing departments
• Supporting vendor audits for raw material suppliers
• Preparing manufacturing units for regulatory inspections
• Coordinating with plant QA and QC teams for audit readiness

Maintaining audit readiness ensures that pharmaceutical companies remain compliant with international regulatory authorities.

Cross-Functional Collaboration

Corporate QA professionals collaborate with multiple departments to ensure quality consistency.

Responsibilities include:

• Coordinating with plant QA and QC teams
• Supporting regulatory affairs during inspections
• Working with production teams to maintain compliance
• Supporting continuous improvement initiatives in quality systems

These collaborative activities ensure that quality systems operate efficiently throughout the organization.

Eligibility / Qualifications

Corona Remedies is seeking candidates with academic backgrounds in pharmaceutical sciences and relevant industry experience in quality assurance systems.

Required Educational Background

B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Microbiology, M.Sc Biotechnology, M.Sc Life Sciences

Candidates with strong knowledge of pharmaceutical regulatory systems and quality documentation practices will be preferred.

Experience Requirement

3 to 7 years of experience in pharmaceutical Quality Assurance or Corporate Quality Assurance roles.

Relevant experience may include:

• Pharmaceutical GMP compliance
• Documentation review and approval
• Deviation management and CAPA systems
• Audit and regulatory inspection preparation

Preferred Candidate Skills

The ideal candidate should demonstrate:

• Strong understanding of pharmaceutical quality systems
• Knowledge of GMP and GDP regulatory standards
• Experience reviewing BMR, BPR, and SOP documentation
• Familiarity with deviation and change control systems
• Experience conducting internal audits and vendor audits

Professionals who have worked in regulated pharmaceutical manufacturing environments will have an advantage.

Location & Salary

Job Location

Corona Remedies Limited (Manufacturing Plant)

Plot No. 503
Near HP Petrol Pump
Village Bhayla
Bavla – 382220
Gujarat, India

Bavla and Ahmedabad regions are among the most prominent pharmaceutical manufacturing clusters in India, hosting several large pharmaceutical companies and export-oriented manufacturing facilities.

Salary

Salary packages depend on candidate experience, quality system expertise, and regulatory exposure. Professionals with experience in corporate quality assurance and regulatory compliance often receive competitive compensation packages within the pharmaceutical industry.

Application Process

Interested candidates can apply by sending their updated resumes to the official recruitment email addresses provided by the company.

Send your CV to:

sagart@coronaremedies.com

anjaliv@coronaremedies.com

Applicants should mention the following details while applying:

• Current CTC
• Expected CTC
• Notice period

Candidates are encouraged to highlight their experience in pharmaceutical quality assurance, regulatory documentation, audit preparation, and compliance management within their resume.

Why Build a Career in Corporate Quality Assurance

Corporate Quality Assurance roles are among the most important positions within pharmaceutical organizations. Unlike plant-level QA, corporate QA teams oversee quality systems across multiple manufacturing units and ensure consistent regulatory compliance throughout the organization.

Professionals working in corporate QA gain deep expertise in regulatory compliance, pharmaceutical documentation systems, audit management, and global regulatory inspection readiness. These skills are highly valued across pharmaceutical companies, biotechnology firms, and regulatory consulting organizations.

Typical career progression includes:

• Corporate QA Executive
• Senior Quality Compliance Manager
• Regulatory Compliance Specialist
• Pharmaceutical Quality Systems Manager
• Global Quality Director

Because pharmaceutical products must meet strict international regulatory standards, professionals trained in corporate quality systems remain in high demand worldwide.

Frequently Asked Questions (FAQs)

Who can apply for the Corona Remedies CQA Officer role?

Candidates with BPharm, MPharm, or MSc qualifications and 3–7 years of pharmaceutical QA experience can apply.

What is Corporate Quality Assurance?

Corporate Quality Assurance oversees quality systems across manufacturing units and ensures regulatory compliance with GMP, GDP, and pharmaceutical regulatory guidelines.

What documentation is reviewed in this role?

CQA professionals review SOPs, BMR, BPR, protocols, reports, and other quality system documentation used in pharmaceutical manufacturing.

Where is the job location?

The position is based at the Corona Remedies manufacturing plant located in Bavla, Gujarat.

How can candidates apply?

Interested candidates can send their updated CV to the recruitment email addresses provided by the company.

Job Summary

Company	Corona Remedies Limited
Vacancies	CQA Officer, CQA Executive
Required Education	BPharm, MPharm, MSc Chemistry, MSc Microbiology, MSc Biotechnology
Experience	3–7 Years