Cadila Pharmaceuticals Recruitment– Deputy Manager, QC Biotechnology | Apply Now

Cadila Pharmaceuticals Ltd. has announced an excellent career opportunity for experienced biotechnology professionals. The company is hiring for the Deputy Manager – QC Biotechnology position at its Dholka, Gujarat manufacturing facility. Candidates with relevant experience in biotechnology quality control are encouraged to apply.

If you have expertise in analytical testing, microbiological techniques, molecular biology, and GMP-compliant laboratory operations, this is a great opportunity to join one of India’s leading pharmaceutical organizations.

Job Overview

Particular Details

Company Name

Cadila Pharmaceuticals Ltd.

Job Role

Deputy Manager

Department

QC Biotechnology

Job Location

Dholka, Gujarat

Experience Required

8–12 Years

Qualification

M.Sc. in Biotechnology / M.Tech in Biotechnology

CTC Offered

₹9.69 LPA

Job Type

Full-Time

Application Mode

Email

About Cadila Pharmaceuticals

Cadila Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong presence in domestic and international markets. The company is known for manufacturing high-quality formulations, APIs, biologics, and biotechnology products while maintaining global quality standards.

Key Responsibilities

Perform quality control testing for biotechnology products.

Ensure compliance with GMP, GLP, and regulatory guidelines.

Handle analytical instruments and biotechnology laboratory equipment.

Review laboratory data and maintain documentation.

Investigate laboratory deviations and OOS results.

Support method validation, method transfer, and stability studies.

Coordinate with QA, Production, and Regulatory Affairs teams.

Lead laboratory personnel and ensure smooth workflow.

Eligibility Criteria

Candidates should possess:

M.Sc. in Biotechnology or M.Tech in Biotechnology

8–12 years of relevant QC Biotechnology experience

Strong understanding of GMP, GLP, and pharmaceutical quality systems

Good analytical, documentation, and problem-solving skills

Salary

Annual CTC: ₹9.69 Lakhs Per Annum (LPA)

Job Location

Dholka, Gujarat, India

How to Apply

Interested and eligible candidates can send their updated CV to:

Email: ayushi.rana@cadilapharma.com

Ensure your resume highlights your biotechnology QC experience, technical skills, and current employment details.

Why Join Cadila Pharmaceuticals?

Reputed pharmaceutical organization

Competitive salary package

Career growth opportunities

Exposure to biotechnology quality systems

Professional work environment

Opportunity to work with advanced laboratory technologies

Technical FAQs

1. What analytical techniques are commonly used in QC Biotechnology?

QC Biotechnology laboratories frequently use ELISA, PCR, HPLC, UV-Visible Spectrophotometry, SDS-PAGE, Western Blotting, Endotoxin Testing, Cell-Based Assays, and Microbial Limit Testing depending on the product.

2. What is the importance of GMP in QC Biotechnology?

Good Manufacturing Practices (GMP) ensure biotechnology products are consistently tested, documented, and released according to quality standards, ensuring product safety, efficacy, and regulatory compliance.

3. What is an Out of Specification (OOS) result?

An OOS result occurs when a laboratory test falls outside the predefined acceptance criteria. It requires investigation to determine the root cause before batch disposition.

4. What is method validation in biotechnology laboratories?

Method validation confirms that an analytical procedure is accurate, precise, specific, linear, robust, and suitable for its intended purpose according to ICH and regulatory guidelines.

5. Which regulatory guidelines are important for QC Biotechnology professionals?

QC Biotechnology professionals should be familiar with ICH Guidelines, WHO GMP, US FDA, EU GMP, GLP, ALCOA+ data integrity principles, and applicable pharmacopeias (IP, USP, EP).