Cadila Pharmaceuticals Hiring For QC QA Roles professionals in Dholka for formulation plant roles with 2–7 years experience.
About the Company
Cadila Pharmaceuticals is one of India’s leading pharmaceutical manufacturers with a strong presence in domestic and international markets. The company operates advanced manufacturing facilities compliant with global regulatory standards and is known for its commitment to quality, innovation, and patient safety.
With a focus on formulation development, regulated manufacturing, and quality-driven systems, Cadila Pharmaceuticals continues to expand its skilled workforce across various production and quality domains. Cadila Pharmaceuticals Hiring For QC QA Roles
Job Details
Company: Cadila Pharmaceuticals
Location: Dholka, Gujarat
Departments: Quality Control (QC) and Quality Assurance (QA)
Experience Required: 2–7 Years (Formulation Industry Mandatory)
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Salary (Estimated): ₹4.5 LPA – ₹8.5 LPA
Employment Type: Full-Time
Industry: Pharmaceutical Formulation Manufacturing
Job Description
Cadila Pharmaceuticals is inviting applications from experienced professionals for its Dholka formulation manufacturing facility. The company is seeking skilled candidates in analytical testing, microbiology, IPQA, and laboratory quality systems to ensure compliance with cGMP, GLP, and regulatory standards.
Quality Control (QC) – Officer to Executive
Sections:
- Microbiologist
- HPLC Analyst
- GC Analyst
- GLP (Good Laboratory Practices)
- Finished Product (FP) Testing
Qualification: B.Sc / M.Sc / B.Pharm
Experience: 2–7 years in formulation industry
Quality Assurance (QA) – Officer to Senior Executive
Sections:
- IPQA (In-Process Quality Assurance)
- Lab QA
Qualification: B.Pharm / M.Pharm
Experience: 2–7 years in formulation industry
Cadila Pharmaceuticals Hiring For QC QA Roles
Key Responsibilities
Quality Control Roles
- Perform analytical testing of raw materials, in-process samples, and finished products
- Operate and calibrate instruments such as HPLC and GC systems
- Conduct microbiological analysis and testing procedures
- Ensure compliance with GLP, cGMP, and regulatory standards
- Execute analytical methods and maintain documentation
- Record stability data and maintain laboratory logbooks
- Support investigations related to OOS and laboratory deviations
Quality Assurance Roles
- Conduct IPQA activities during manufacturing processes
- Review batch manufacturing records and documentation
- Monitor adherence to SOPs and quality systems
- Manage deviations, CAPA, and change control systems
- Support regulatory audits and internal inspections
- Ensure compliance with global regulatory guidelines
Cadila Pharmaceuticals Hiring For QC QA Roles
Skills/Qualifications
- B.Sc / M.Sc / B.Pharm / M.Pharm (as applicable to role)
- 2–7 years of experience in pharmaceutical formulation manufacturing
- Strong understanding of cGMP and GLP practices
- Hands-on experience with HPLC, GC, and analytical instruments
- Knowledge of IPQA processes and documentation review
- Familiarity with deviation management and CAPA handling
- Strong documentation and compliance skills
- Ability to work in regulated manufacturing environments
Cadila Pharmaceuticals Hiring For QC QA Roles
Benefits/Perks
- Competitive salary package based on experience
- Opportunity to work in a regulated formulation facility
- Exposure to global quality and compliance standards
- Career growth in QA and QC specialization domains
- Hands-on experience with advanced analytical technologies
- Stable and compliance-driven work environment
Cadila Pharmaceuticals Hiring For QC QA Roles
Why You Should Join
Joining Cadila Pharmaceuticals offers professionals an opportunity to work in a reputed pharmaceutical organization with strong regulatory exposure. Employees gain practical experience in advanced analytical systems, quality management frameworks, and global compliance standards.
The Dholka facility provides a structured, quality-focused work culture that supports career growth in analytical testing, IPQA monitoring, documentation control, and regulatory readiness. Cadila Pharmaceuticals Hiring For QC QA Roles
How to Apply
Interested and eligible candidates can share their updated CV via email to:
Ensure your resume clearly mentions your current role, total experience, formulation plant experience, and expertise in QC or QA functions. Cadila Pharmaceuticals Hiring For QC QA Roles
FAQs
1. What is the required experience for this job?
Candidates must have 2–7 years of experience in pharmaceutical formulation manufacturing.
2. Is formulation industry experience mandatory?
Yes, prior experience in formulation plants is mandatory for both QC and QA roles.
3. What qualifications are accepted?
B.Sc, M.Sc, B.Pharm, and M.Pharm qualifications are accepted depending on the department.
4. What is the job location?
The position is based in Dholka, Gujarat.
5. What is the salary range?
The estimated salary range is ₹4.5 LPA to ₹8.5 LPA depending on experience and role.
Cadila Pharmaceuticals Hiring For QC QA Roles
This is a valuable opportunity for experienced QA and QC professionals seeking career growth in a reputed pharmaceutical manufacturing organization.
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