Cadila Hiring QA and QC

Cadila Pharma QC QA Jobs | BPharm MPharm Gujarat

Cadila Pharmaceuticals hiring QA and QC professionals in Dholka. B.Pharm, M.Pharm, B.Sc, M.Sc candidates with 3–17 years experience can apply.

Cadila Pharmaceuticals has announced multiple job openings for experienced Quality Control and Quality Assurance professionals at its Dholka manufacturing facility in Gujarat. Candidates with formulation industry experience and qualifications such as B.Pharm, M.Pharm, B.Sc, and M.Sc Chemistry are invited to apply for various executive, assistant manager, deputy manager, manager, and senior manager positions.

This recruitment drive offers opportunities in Quality Management Systems (QMS), Computer System Validation (CSV), In-Process Quality Assurance (IPQA), Stability Studies, and Vendor Qualification functions. Professionals seeking pharmaceutical quality assurance jobs, quality control careers, GMP compliance roles, and regulatory manufacturing opportunities can explore these openings.

The pharmaceutical industry continues to invest heavily in quality systems, regulatory compliance, data integrity, and validation processes. As a result, experienced quality professionals remain among the most in-demand talent segments within the pharmaceutical manufacturing sector.

Company Overview

Cadila Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong presence in formulation development, manufacturing, research, and global healthcare markets. The company has established itself through its commitment to quality, innovation, regulatory compliance, and affordable healthcare solutions.

With advanced manufacturing facilities and a focus on current Good Manufacturing Practices (cGMP), Cadila Pharmaceuticals serves domestic and international markets through a diversified product portfolio. The organization regularly invests in quality systems, manufacturing excellence, validation programs, and compliance initiatives to meet global pharmaceutical standards.

For professionals looking to build a long-term career in pharmaceutical quality assurance, quality control, validation, and regulatory-compliant manufacturing, Cadila Pharmaceuticals offers a structured work environment and opportunities for career advancement.

Company Hiring Details

Cadila Pharmaceuticals is currently recruiting for the following positions at its Dholka Plant.

Quality Control – QMS Investigator

Position: Assistant Manager / Deputy Manager

Qualification: B.Sc Chemistry / M.Sc Chemistry

Experience: 6–10 Years

Key Responsibilities

• Conduct quality investigations and root cause analysis.
• Manage Quality Management System (QMS) activities.
• Review deviations, CAPA, and investigation reports.
• Support regulatory audits and compliance inspections.
• Ensure adherence to GMP and quality standards.
• Participate in continuous quality improvement programs.

Quality Assurance – CSV IT

Position: Assistant Manager

Qualification: B.Pharm / M.Pharm

Experience: 6–10 Years

Key Responsibilities

• Handle Computer System Validation (CSV) activities.
• Ensure data integrity compliance.
• Review validation protocols and reports.
• Support qualification and validation programs.
• Maintain compliance with regulatory requirements.
• Participate in audit readiness initiatives.

Quality Assurance – IPQA

Position: Executive

Qualification: B.Pharm / M.Pharm

Experience: 3–5 Years

Key Responsibilities

• Perform in-process quality assurance activities.
• Conduct line clearance verification.
• Monitor manufacturing operations for GMP compliance.
• Review batch records and documentation.
• Ensure adherence to approved procedures.
• Support deviation and investigation management.

Quality Assurance – Vendor Qualification

Position: Executive

Qualification: B.Pharm / M.Pharm

Experience: 3–5 Years

Key Responsibilities

• Perform supplier qualification activities.
• Review vendor documentation and quality records.
• Coordinate vendor audits and assessments.
• Monitor supplier quality performance.
• Support risk assessment and compliance activities.
• Maintain approved vendor databases.

Quality Control – Stability

Position: Manager / Senior Manager

Qualification: B.Sc Chemistry / M.Sc Chemistry

Experience: 14–17 Years

Key Responsibilities

• Manage stability studies and protocols.
• Review stability data and reports.
• Ensure compliance with ICH stability guidelines.
• Lead stability program execution.
• Support regulatory submissions and product lifecycle management.
• Coordinate cross-functional quality initiatives.

Job Role & Responsibilities

Selected candidates will work in highly regulated pharmaceutical manufacturing environments and contribute to quality assurance, quality control, validation, compliance, investigation, and stability management functions.

Common responsibilities may include:

• GMP compliance monitoring
• Quality documentation review
• Investigation and CAPA management
• Regulatory audit support
• Data integrity compliance
• Validation and qualification activities
• Stability program management
• Supplier quality management
• Risk assessment activities
• Continuous quality improvement initiatives

Professionals with experience in formulation manufacturing facilities, regulatory-approved plants, and pharmaceutical quality systems will have an advantage during the selection process.

Eligibility / Qualifications

Educational Qualifications

For Quality Control Positions

• B.Sc Chemistry
• M.Sc Chemistry

For Quality Assurance Positions

• B.Pharm
• M.Pharm

Relevant Courses

Bachelor of Pharmacy, Master of Pharmacy, Pharmaceutical Analysis, Pharmaceutical Quality Assurance, Pharmaceutical Chemistry, Industrial Pharmacy, Quality Management Systems, Analytical Chemistry, Organic Chemistry, Regulatory Affairs, Validation and Qualification, Pharmaceutical Technology.

Experience Requirements

• Executive Level: 3–5 Years
• Assistant Manager / Deputy Manager: 6–10 Years
• Manager / Senior Manager: 14–17 Years

Mandatory Requirement

Candidates must possess Formulation Manufacturing Experience.

Applicants from formulation pharmaceutical facilities with exposure to GMP, quality systems, validation, investigations, and regulatory compliance will be preferred.

Location & Salary

Location: Dholka, Gujarat

Approximate Salary: ₹5 LPA – ₹22 LPA

(Salary may vary depending on designation, experience, technical expertise, and internal compensation policies.)

Application Process

Interested candidates can share their updated resumes directly with the recruitment team.

Email Application

Email: jimit.sharma@cadilapharma.com

Contact Details

Mr. Jimit Sharma: 6355124377

Mr. Sanjay Makwana (HR)

Candidates are advised to mention their current designation, total experience, current CTC, expected CTC, notice period, and relevant department while applying.

Why Consider a Career at Cadila Pharmaceuticals?

Cadila Pharmaceuticals continues to be a preferred employer for professionals seeking careers in pharmaceutical quality assurance, pharmaceutical quality control, regulatory compliance, validation, and GMP-driven manufacturing operations.

Key benefits include:

• Exposure to regulated pharmaceutical environments
• Career growth opportunities
• Quality-focused work culture
• Advanced manufacturing infrastructure
• Validation and compliance-driven operations
• Learning opportunities in pharmaceutical quality systems
• Participation in regulatory audits and inspections

Frequently Asked Questions (FAQs)

1. Who can apply for these Cadila Pharmaceuticals jobs?

Candidates with B.Pharm, M.Pharm, B.Sc Chemistry, or M.Sc Chemistry qualifications and relevant formulation experience can apply.

2. Is formulation industry experience mandatory?

Yes. Cadila Pharmaceuticals has specifically mentioned that only candidates with formulation experience will be considered.

3. What departments are hiring?

The company is hiring for Quality Assurance and Quality Control departments.

4. Are managerial positions available?

Yes. Openings are available from Executive level up to Senior Manager level.

5. What is the experience requirement?

Depending on the role, candidates should have between 3 and 17 years of experience.

6. How can candidates apply?

Interested candidates can send their updated CV to jimit.sharma@cadilapharma.com.

Summary

Category	Details
Company	Cadila Pharmaceuticals
Department Vacancies	Quality Control (QMS Investigator, Stability), Quality Assurance (CSV IT, IPQA, Vendor Qualification)
Qualification	B.Sc Chemistry, M.Sc Chemistry, B.Pharm, M.Pharm
Experience	3–17 Years
Location	Dholka, Gujarat