Cadila Pharmaceuticals Hiring for Quality Assurance Positions | Virtual Drive for IPQA, Market Complaint, Process Validation & CSV-IT
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(Cadila Pharmaceuticals QA Virtual Drive 2026) |
Introduction
Cadila Pharmaceuticals Ltd. has announced a major virtual recruitment drive for experienced pharmaceutical professionals looking to build a successful career in Quality Assurance (QA). The company is hiring for multiple positions across IPQA, Market Complaint, TTD, Process Validation, and CSV-IT functions at its Dholka manufacturing facility near Ahmedabad, Gujarat.
This hiring drive offers excellent opportunities for candidates with formulation manufacturing experience who want to work with one of India's well-established pharmaceutical organizations. Professionals holding B.Pharm, M.Pharm, M.Sc, or MCA qualifications can apply based on the eligibility criteria specified for each position.
The interview process will be conducted virtually through Google Meet, making it convenient for candidates across India to participate.
About Cadila Pharmaceuticals
Cadila Pharmaceuticals Ltd. is one of India's oldest privately held pharmaceutical companies. Established in 1951, the company has built a strong reputation in pharmaceutical manufacturing, research, development, and healthcare innovation.
The company is headquartered in Ahmedabad, Gujarat, India, and operates across multiple therapeutic segments with a presence in both domestic and international pharmaceutical markets.
Cadila Pharmaceuticals employs thousands of professionals globally and continues to expand its operations in manufacturing, quality assurance, research and development, regulatory affairs, and healthcare services.
With a strong focus on quality, compliance, innovation, and patient safety, Cadila remains one of the preferred employers in the Indian pharmaceutical industry.
Job Overview Summary
Cadila Pharmaceuticals is conducting a virtual hiring drive for multiple Quality Assurance positions at its Dholka manufacturing facility. The company is looking for experienced formulation professionals who can contribute to pharmaceutical quality systems, compliance management, process validation, investigation handling, and computerized system validation activities.
The available positions span from Officer level to Manager level, offering opportunities for candidates with 1 to 12 years of pharmaceutical experience.
Candidates with expertise in formulation manufacturing, GMP compliance, validation activities, market complaints handling, and quality documentation are encouraged to participate.
Vacancy Details
| Position | Department | Qualification | Experience |
|---|
| Officer / Senior Officer / Executive | IPQA (OSD / Injectable) | B.Pharm / M.Pharm / M.Sc | 1–5 Years |
| Executive / Assistant Manager | Market Complaint | B.Pharm / M.Pharm / M.Sc | 4–12 Years |
| Executive | TTD | B.Pharm / M.Pharm / M.Sc / MCA | 2–5 Years |
| Senior Executive / Assistant Manager | Process Validation | B.Pharm / M.Pharm / M.Sc | 5–12 Years |
| Assistant Manager / Deputy Manager / Manager | CSV-IT | B.Pharm / M.Pharm / M.Sc / MCA | 5–10 Years |
Job Location
Dholka, Ahmedabad, Gujarat
Employment Type
Full-Time
Interview Mode
Virtual Interview (Google Meet)
Responsibilities Explanation
The selected candidates will be responsible for maintaining pharmaceutical quality standards and ensuring compliance with GMP and regulatory requirements.
IPQA Professionals
Candidates working in IPQA will monitor manufacturing activities, verify compliance during production, review batch documentation, and ensure adherence to approved procedures.
Market Complaint Team
Professionals in this department will investigate customer complaints, identify root causes, prepare investigation reports, recommend CAPA actions, and coordinate with various departments.
TTD Function
The TTD team will focus on quality-related documentation, deviation handling, compliance monitoring, and supporting quality management systems.
Process Validation Team
Candidates will execute process validation activities, prepare protocols, review validation reports, analyze validation results, and ensure process consistency.
CSV-IT Professionals
The CSV team will manage computer system validation activities, assess system compliance, prepare validation documentation, and support regulatory inspections involving computerized systems.
Overall, selected professionals will work closely with Production, QC, Engineering, Regulatory Affairs, and Quality departments.
Eligibility Criteria
Applicants should possess one of the following qualifications:
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B.Pharm
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M.Pharm
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M.Sc
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MCA (for applicable positions)
Experience Requirement
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Minimum: 1 Year
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Maximum: 12 Years
Important Requirement
Only candidates with formulation pharmaceutical experience are eligible to apply.
Candidates from API, chemical, or non-pharmaceutical industries may not fit the specified requirement.
Skills Required
Candidates with the following skills will have an advantage during the selection process:
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Good Manufacturing Practices (GMP)
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Quality Assurance Documentation
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In-Process Quality Assurance (IPQA)
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Process Validation
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Computer System Validation (CSV)
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Market Complaint Investigation
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Root Cause Analysis (RCA)
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CAPA Management
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Regulatory Compliance
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Data Integrity
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Pharmaceutical Quality Systems
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Validation Protocol Review
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SOP Preparation
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Change Control Management
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Audit Readiness
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Risk Assessment
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Cross-Functional Coordination
Strong communication and documentation skills are also highly desirable.
Salary Estimate
Cadila Pharmaceuticals has not officially disclosed the compensation package.
Based on current pharmaceutical industry trends:
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Officer Level: ₹3.5–6 LPA
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Senior Officer/Executive: ₹5–8 LPA
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Assistant Manager: ₹8–12 LPA
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Deputy Manager/Manager: ₹12–15+ LPA
Actual salary may vary depending on experience, skills, current compensation, and interview performance.
Interview Details
Interview Date
18 August 2026 (Tuesday)
Interview Time
2:30 PM to 5:00 PM
Mode
Google Meet (Virtual Interview)
HR Contact Person
Mr. Sanjay Makwana
Contact Number
8347434234
Email ID
sanjay.makwana@cadilapharma.com
Candidates should keep their resumes ready before attending the interview.
Required Documents
Applicants should prepare the following documents:
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Updated Resume
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Recent Passport Size Photograph
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Educational Certificates
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Experience Certificates
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Latest Increment Letter
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Last Three Months Salary Slips
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PAN Card
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Aadhaar Card
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Current CTC Details
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Notice Period Information
Having complete documentation may help speed up the selection process.
How to Apply
Interested candidates should send their updated resume to:
Email: sanjay.makwana@cadilapharma.com
Subject Line:
Application for QA Position – [Department Name]
Example:
Application for QA Position – Process Validation
Google Meet Link:
Frequently Asked Questions (FAQs)
Is this a work-from-home opportunity?
No. The positions are based at the Dholka manufacturing facility near Ahmedabad.
Can freshers apply?
No. The company is specifically looking for experienced professionals with formulation experience.
Which departments are hiring?
IPQA, Market Complaint, TTD, Process Validation, and CSV-IT.
Is formulation experience mandatory?
Yes. The recruitment notification specifically mentions formulation experience as mandatory.
What qualifications are accepted?
B.Pharm, M.Pharm, M.Sc, and MCA (for applicable positions).
What is the interview mode?
The interview will be conducted virtually through Google Meet.
What is the experience range required?
The company is hiring candidates with 1 to 12 years of experience depending on the role.
Final Conclusion
Cadila Pharmaceuticals' Quality Assurance Virtual Drive presents a valuable opportunity for experienced pharmaceutical professionals seeking career growth in QA, validation, compliance, market complaints, and computerized system validation functions.
With openings across multiple departments and experience levels, this recruitment drive allows candidates to explore career opportunities within a well-established pharmaceutical organization known for its quality standards and manufacturing excellence.
Professionals with formulation manufacturing experience, strong GMP knowledge, and pharmaceutical quality system expertise should consider applying at the earliest to maximize their chances of selection.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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