Cadila Pharmaceuticals Limited has announced a Walk-In Interview Drive for multiple positions at its Ankleshwar Plant. The company is inviting skilled pharmaceutical professionals to join its Production and QA/QC teams. This recruitment drive offers excellent career opportunities for candidates seeking growth in API manufacturing, quality systems, and laboratory operations.
Cadila Pharmaceuticals is recognized for its commitment to quality, innovation, and regulatory compliance, making it one of the most respected pharmaceutical companies in India.
About Cadila Pharmaceuticals
Cadila Pharmaceuticals Limited is a leading Indian pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality healthcare products. With advanced manufacturing facilities and a strong focus on research and development, the company serves both domestic and international markets.
The organization provides a dynamic work environment where employees can enhance their technical expertise while contributing to the production of quality medicines.
Job Openings
Department: Production
Designation: Junior Officer to Assistant Manager
Preferred Qualification:
Diploma in Chemical Engineering
B.E./B.Tech (Chemical)
B.Sc / M.Sc
Experience:
1 to 10 Years
Preferred Experience:
API Manufacturing Operations
Key Responsibilities
Executing production activities as per SOPs
Monitoring process parameters
Maintaining batch manufacturing records
Ensuring GMP compliance
Handling process equipment and troubleshooting
Department: QA/QC
Designation: Junior Officer to Assistant Manager
Qualification:
B.Sc / M.Sc (Chemistry)
Experience:
1 to 10 Years
Sections:
HPLC
GC
Reviewer
Microbiology
Key Responsibilities
Analytical testing of samples
Instrument operation and calibration
Laboratory documentation
Stability studies
Compliance with GMP and data integrity requirements
Review and approval of analytical data
Walk-In Interview Details
Interview Date
04 June 2026 (Thursday)
Interview Time
09:00 AM to 05:00 PM
Company
Cadila Pharmaceuticals Limited
Plant Location
Ankleshwar Plant
Interview Venue
Cadila Pharmaceuticals Limited – Unit II
Plot No. 3203, Ankleshwar GIDC,
Ankleshwar INA, Ankleshwar,
Gujarat – 393002
Contact Details
For any queries related to the walk-in interview, candidates may contact:
Mr. Shardulsinh Kathawadia
shardulsinh.k@cadilapharma.com
Mr. Nirmal Pandey
nirmal.pandey@cadilapharma.com
Candidates who are unable to attend the walk-in interview may also share their updated resumes through the above email IDs for consideration by the recruitment team.
Salary Package
The company has indicated the following annual CTC ranges:
Position
Annual CTC
Assistant Manager
₹7.50 LPA
Senior Executive
₹6.90 LPA
Executive
₹5.00 LPA
Junior Officer to Senior Officer
₹3.80 LPA
Final compensation may vary based on experience, skills, and interview performance.
Documents Required
Candidates should carry:
Updated Resume
Aadhaar Card
Last Three Months’ Salary Slips
Current Offer Letter (if applicable)
Educational Certificates
Experience Certificates
Passport Size Photographs
Why Join Cadila Pharmaceuticals?
Work with a reputed pharmaceutical company
Exposure to advanced API manufacturing processes
Opportunities in Production, QA, and QC functions
Competitive salary structure
Professional growth and learning opportunities
Strong quality and compliance culture
Technical FAQs
1. What is the role of HPLC in pharmaceutical quality control?
HPLC (High Performance Liquid Chromatography) is used to identify, quantify, and analyze active pharmaceutical ingredients, impurities, and degradation products. It is one of the most widely used analytical techniques in QC laboratories.
2. Why is API manufacturing experience valuable in production roles?
API manufacturing involves complex chemical reactions, process controls, solvent handling, and quality requirements. Candidates with API experience can effectively manage production operations while ensuring safety and compliance.
3. What is the difference between QA and QC in pharmaceuticals?
Quality Assurance (QA) focuses on systems, procedures, and compliance to prevent quality issues, while Quality Control (QC) focuses on laboratory testing and verification to ensure products meet quality specifications.
4. What is Data Integrity in pharmaceutical laboratories?
Data Integrity ensures that all records are complete, accurate, consistent, and reliable throughout their lifecycle. Regulatory agencies require compliance with ALCOA+ principles for maintaining trustworthy data.
5. What are GMP guidelines and why are they important?
Good Manufacturing Practices (GMP) are regulations that ensure pharmaceutical products are consistently produced and controlled according to quality standards. GMP helps prevent contamination, mix-ups, and product quality failures.
Conclusion
The Cadila Pharmaceuticals Walk-In Interview 2026 is an excellent opportunity for Production and QA/QC professionals seeking career advancement in the pharmaceutical industry. Candidates with experience in API manufacturing, analytical testing, quality systems, and GMP compliance are encouraged to attend the interview and explore exciting opportunities with one of India’s leading pharmaceutical organizations.
