Pharma Freshers Jobs at Cipla l BPharma Candidates Apply for Junior Team Member – QA Role
Looking to grow your career in quality assurance at a reputed pharmaceutical company? Cipla, a global leader in affordable healthcare solutions, is hiring a Junior Team Member – QA in Rangpo, Sikkim. This role focuses on maintaining regulatory compliance, supporting audit readiness, and ensuring product quality, aligning with Cipla’s commitment to excellence and patient care.
About Cipla
Cipla is a leading pharmaceutical company dedicated to providing high-quality, affordable healthcare solutions worldwide. With a focus on innovation and excellence, Cipla strives to make a positive impact on patients’ lives by offering a diverse range of pharmaceutical products.
Job Posting: Junior Team Member – QA
Posting Date: Jul 29, 2025
Country: India
State: Sikkim
Location: Rangpo
Req Id: 95138
Job Purpose
Review the compliance level of the site for deficiency response, prepare a master validation protocol, and report as per the company quality policy and applicable regulatory guidelines.
Key Accountabilities:
1. Collate, review, and provide required work plans on received deficiencies to HO to respond to regulatory authorities promptly.
2. Review the annual product quality review report at units for completeness and data correctness to ensure
compliance with cGMP requirements and audit readiness.3. Receive and distribute approval certificates, dossiers (TDP & RAP), and development reports at the unit for the execution of new products smoothly.
4. Collect, compile, and review raw data for timely submission of the MHRA, UK interim update document to corporate as per agency requirements.
5. Execute errorless submissions by reviewing product license, certificates, and other applications to adhere to legal requirements.
6. Support in CDSCO and state FDA inspection to be GMP compliant and getting product license, FDA stall approvals by ensuring cross-functional interaction.
Major Challenges:
A delay in receiving data for allotted work plans from units may impact the entire process of responding to deficiencies. Lack of detailed compliance with the appropriate root cause from the user department.
Key Interactions:
- SPOCs of process validation, APQR, and RA at the site, Unit QA heads, CQA, and A&C team.
- FDA officials.
Dimensions:
- Timely reviews, adherence to compliance, and audit support.
- Key decisions related to QA processes.
Education Qualification:
- B. Pharma/ M.Sc. with 3-4 years of experience in the quality assurance department.
- Licensing and registration experience (0-2 years).
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