Cadila Pharmaceuticals Hiring QC & QA

B.Pharm/M.Pharm QC & QA Vacancies – Cadila Pharmaceuticals, Dholka

Cadila Pharmaceuticals hiring B.Pharm/M.Pharm professionals for QC & QA roles at Dholka, Gujarat. 2–10 years of experience. Apply now!

Cadila Pharmaceuticals, a globally recognized pharmaceutical company and a Great Place to Work Certified organization, is inviting skilled professionals to join its Quality Department at the Dholka manufacturing facility in Gujarat. This is a golden opportunity to be a part of one of India’s most trusted pharma brands with a strong legacy in research, innovation, and patient-centric solutions.

If you are an experienced professional in Quality Control (QC) or Quality Assurance (QA) with expertise in parenteral or OSD formulations, Cadila Pharmaceuticals offers you the platform to advance your career in a GMP-driven environment.

Company Overview

Cadila Pharmaceuticals Ltd. is one of India’s largest privately held pharmaceutical companies with a legacy spanning over six decades. Headquartered in Ahmedabad, Gujarat, Cadila is known for its commitment to innovation, quality, and global health improvement. The company operates across therapeutic areas including cardiology, oncology, neurology, gastroenterology, and anti-infectives, with products marketed in over 100 countries.

Recognized as a Great Place to Work (2024–2025), Cadila Pharmaceuticals fosters a culture of excellence, collaboration, and continuous learning.

Job Roles & Responsibilities

Open Positions at Dholka Plant:

Quality Control Department

• Designation: Officer / Executive / Sr. Executive
• Section: Microbiologist / QC Reviewer
• Qualification: B.Sc / M.Sc
• Experience: 2–7 years
• Requirement: Candidates with experience in Pharma Parenteral & OSD (Oral Solid Dosage) formulations preferred.

Key Responsibilities:

• Perform and review analytical tests for raw materials, intermediates, and finished products.
• Ensure laboratory compliance with cGMP, GLP, GDP, and ALCOA++ principles.
• Review analytical documentation and ensure timely approvals.
• Conduct microbiological testing, environmental monitoring, and sterility assessments.
• Support in method validation, calibration, and audit readiness.

Quality Assurance Department

• Designation: Officer / Sr. Executive / Assistant Manager / Manager
• Section: IPQA / Validation / Vendor Qualification
• Qualification: B.Pharm / M.Pharm
• Experience: 2–10 years
• Requirement: Minimum 2 years of experience in Pharma Parenteral & OSD manufacturing.

Key Responsibilities:

• Ensure compliance with GMP and regulatory requirements during manufacturing and packaging operations.
• Perform in-process quality checks and batch record review.
• Oversee process validation, cleaning validation, and vendor qualification.
• Manage quality documentation and coordinate with cross-functional teams.
• Support audit preparation and ensure CAPA implementation.

Eligibility / Qualifications

• Educational Background:
  • QC Department: B.Sc, M.Sc
  • QA Department: B.Pharm, M.Pharm
• Experience Range: 2 to 10 years depending on the position.
• Preferred Candidates: Professionals with hands-on exposure to Pharma Parenteral & OSD manufacturing.
• Relevant Courses: B.Sc (Microbiology, Chemistry), M.Sc (Analytical Chemistry, Pharmaceutical Chemistry), B.Pharm, M.Pharm (Quality Assurance, Pharmaceutics).

Location & Salary

Location: Dholka Plant, Gujarat, India
Company: Cadila Pharmaceuticals Pvt. Ltd.
Salary: Competitive, based on experience and current CTC.
Joining: Immediate joiners preferred.

Application Process

Interested candidates can apply by sending their updated CV to:

Email: jimit.sharma@cadilapharma.com
Email: sanjay.makwana@cadilapharma.com
Contact: Mr. Jimit Sharma – +91 63551 24377 (Available 9 AM to 5 PM)
Website: www.cadilapharma.com

Call to Action: Apply before October 20, 2025, to secure your interview slot and take the next step in your pharma career at Cadila Pharmaceuticals!

Why Join Cadila Pharmaceuticals?

• Work with a Great Place to Work Certified pharma leader.
• Exposure to global regulatory audits (USFDA, EU, WHO).
• State-of-the-art manufacturing and analytical facilities.
• Opportunity for career growth, training, and leadership development.
• Culture of quality, innovation, and patient safety.

FAQs

Q1: What are the open roles in Cadila Pharmaceuticals’ Quality Department?
Cadila is hiring for QC (Microbiologist/QC Reviewer) and QA (IPQA, Validation, Vendor Qualification) positions at its Dholka plant.

Q2: What qualifications are required?
B.Sc/M.Sc for QC and B.Pharm/M.Pharm for QA positions.

Q3: Is prior experience mandatory?
Yes. 2–10 years of experience in Pharma Parenteral or OSD manufacturing is required (except trainees if openings arise).

Q4: How can I apply?
Send your resume to jimit.sharma@cadilapharma.com or sanjay.makwana@cadilapharma.com.

Q5: What is the work location?
Cadila Pharmaceuticals, Dholka Plant, Gujarat, India.

Summary Table

Category	Details
Company	Cadila Pharmaceuticals Pvt. Ltd.
Vacancies	QC – Officer/Executive/Sr. Executive; QA – Officer to Manager
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm (Microbiology, Chemistry, QA, Pharmaceutics)
Experience	2 to 10 Years (Pharma Parenteral & OSD experience preferred)
Location	Dholka, Gujarat