Cadila Pharmaceuticals Limited has announced a Walk-In Interview Drive for experienced professionals at its Ankleshwar Plant, Gujarat. The company is inviting applications for multiple positions in Production, Quality Control (QC), and Quality Assurance (QA) departments. This opportunity is ideal for candidates with API manufacturing experience who are looking to advance their careers in a reputed pharmaceutical organization.

As a Great Place to Work® Certified company, Cadila Pharmaceuticals continues to expand its workforce by hiring talented professionals across key manufacturing and quality functions.

Job Details

Production Department

Designation: Junior Officer to Assistant Manager

Experience: 1–10 Years

Educational Qualification:

Diploma in Chemical Engineering

B.E./B.Tech (Chemical)

B.Sc / M.Sc

Preferred Experience:

API Manufacturing Experience

Quality Control (QC) / Quality Assurance (QA)

Designation: Junior Officer to Assistant Manager

Experience: 1–10 Years

Educational Qualification:

B.Sc / M.Sc (Chemistry)

Sections:

HPLC

Chemical Control (CC)

Reviewer

Microbiology

Salary Structure (Indicative CTC)

Position

Annual CTC

Assistant Manager

₹7.50 LPA

Senior Executive

₹6.90 LPA

Executive

₹5.00 LPA

Junior to Senior Officer

₹3.80 LPA

Salary may vary depending on experience, qualifications, and interview performance.

Walk-In Interview Details

Date: 13 June 2026 (Saturday)

Time: 09:00 AM to 05:00 PM

Venue

Cadila Pharmaceuticals Limited, Unit-II

Plot No. 3203, Ankleshwar GIDC,

Anklesvar INA, Ankleshwar,

Gujarat – 393002

Documents Required

Candidates are requested to carry:

Updated Resume/CV

Last 3 Months Salary Slips

Current Offer Letter (if applicable)

Aadhaar Card

Educational Certificates

Experience Documents

Contact Details

Mr. Shardulsinh Kathwadia

shardulsinh.k@cadilapharma.com

Mr. Nirmal Pandey

nirmal.pandey@cadilapharma.com

Why Join Cadila Pharmaceuticals?

Opportunity to work with a leading pharmaceutical manufacturer

Exposure to API manufacturing and quality systems

Career growth in Production, QC, and QA functions

Competitive compensation package

Great Place to Work® Certified organization

Candidates meeting the eligibility criteria are encouraged to attend the walk-in interview and explore rewarding career opportunities with Cadila Pharmaceuticals.

Technical FAQs

1. What is the role of HPLC in pharmaceutical Quality Control?

HPLC (High-Performance Liquid Chromatography) is used to identify, quantify, and verify the purity of raw materials, intermediates, and finished pharmaceutical products. It is a critical analytical technique for ensuring product quality and regulatory compliance.

2. What GMP practices should Production professionals follow in API manufacturing?

Production personnel must follow Good Manufacturing Practices (GMP), including proper documentation, line clearance, equipment cleaning verification, batch record maintenance, deviation reporting, and contamination control procedures.

3. What is the importance of microbiological testing in pharmaceutical manufacturing?

Microbiological testing helps monitor microbial contamination in raw materials, water systems, manufacturing environments, and finished products, ensuring product safety and compliance with pharmacopeial standards.

4. What are OOS and OOT results in Quality Control?

OOS (Out of Specification) refers to test results that fall outside approved specifications, while OOT (Out of Trend) refers to results that are within limits but significantly different from historical trends. Both require investigation and documentation.

5. Why is process validation important in API manufacturing?

Process validation demonstrates that a manufacturing process consistently produces products meeting predetermined quality attributes. It ensures product quality, process reliability, regulatory compliance, and patient safety.