Cipla Hiring Pharmacy Graduates | Quality Control Role – Apply Now
A rare chance has emerged for aspiring professionals in the quality control job sector at Cipla careers. Located in Rangpo, Sikkim, this position offers an opportunity to contribute to the pharmaceutical industry while ensuring compliance with regulatory standards. Candidates with a Pharma background in QC are encouraged to apply.
- Job Title: Team Member – QC
- Req ID: 105874
- Location: Rangpo, Sikkim
About The Company
Cipla is a renowned pharmaceutical company operating in the healthcare sector, known for its commitment to quality and innovation. With a strong presence in India and across the globe, Cipla focuses on providing affordable and accessible medicines. The organization is dedicated to maintaining high standards in quality control, ensuring that all products meet regulatory requirements and patient needs. This quality control job reflects Cipla’s ongoing efforts to enhance its operations and uphold its reputation in the industry.
Job Description
The quality control job at Cipla involves preparing and reviewing essential documentation to uphold the highest quality standards. The selected candidate will be responsible for ensuring compliance with current pharmacopoeial updates and regulatory requirements, thus playing a crucial role in maintaining Cipla’s commitment to quality.
Key Responsibilities
- Prepare documents like SOPs, specifications, and non-routine documentation to support timely analysis.
- Review applicable pharmacopoeia and guidelines, ensuring appropriate updates are made.
- Review instrument calibration data concerning operating documents.
- Evaluate and prepare documents for standardization across all units.
- Coordinate with cross-functional teams to simplify processes and ensure compliance.
- Maintain records of document issuance to ensure current versions are available.
- Identify and resolve queries during document reviews to avoid delays.
- Monitor implementation of pharmacopoeial updates to prevent non-conformances.
Eligibility Criteria
- Education: M.Sc / B.Pharm.
- Experience: 1–3 years of experience in the Quality Control department of a pharmaceutical organization, with knowledge of current regulatory standards and compliance requirements.
Required Skills
- Strong understanding of quality control processes and documentation.
- Ability to review and interpret pharmacopoeial guidelines.
- Excellent communication and coordination skills.
- Detail-oriented with a focus on compliance and quality.
- Proficient in preparing and revising SOPs and specifications.
- Ability to work collaboratively with cross-functional teams.
- Strong problem-solving skills to address document review challenges.
- Knowledge of cGMP requirements.
Why Join Cipla?
This Quality Control Job at Cipla Careers offers exposure to pharmaceutical QC documentation, pharmacopeial compliance, regulatory standards, and cross-functional quality processes. The role can help B. Pharm and M.Sc professionals strengthen their expertise in documentation-driven Quality Control operations.
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