Cipla- looking for QC Junior Team Member, B.Pharm, MSc Apply

Zydus Cadila Ltd; India; On-site; INR 350,000 - 520,000; Full time

Job summary

Cipla in India is seeking a QC Junior Team Member with M.Sc. or B.Pharma for 1-3 years of QC experience to work at our Rangpo site.

You will prepare, review and update specifications, SOPs and pharmacopoeia-aligned documents, support investigations, and ensure GMP compliance. The role involves coordination with QC/QA and maintaining CipDox records.

The position requires keeping up with regulatory changes and contributing to standardized processes at the site.

Qualifications

• M.Sc. or B.Pharma with 1–3 years in QC.
• Knowledge of latest regulatory standards and compliance norms.
• Experience in documentation and SOPs within pharma QC.
• Familiarity with pharmacopoeia, GMP practices, and record-keeping.

Responsibilities

• Prepare documents like SOPs, specifications, and non-routine paperwork and ensure site-wide availability.
• Review and update corporate QC documents in coordination with QC/QA.
• Check pharmacopoeia updates and ensure timely implementation.
• Maintain online documentation and records using CipDox.
• Coordinate with cross-functional teams to meet regulatory timelines.

Skills

Documentation control

SOP preparation

Regulatory compliance

GMP knowledge

Pharmacopoeia updates

Education

M.Sc.

B.Pharma

Tools

CipDox

Job description

Cipla- looking for QC Junior Team Member, B.Pharm, MSc Apply

Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms. To make healthcare more affordable globally, we are deepening our presence in the key markets of India, South Africa, the U.S. among other economies of the emerging world.

Job Description

Job Purpose

Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirements

Key Accountabilities (1/6)

• Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis
• Prepare / revise corporate documents like SOPs, general analytical methods etc. by coordinating with site QC/QA
• Review the applicable pharmacopoeia and guidelines and make appropriate updates
• Review instrument calibration data w.r.t operating documents

Key Accountabilities (2/6)

• Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body
• Review the new/revised monograph as per current pharmacopoeia
• Review the latest pharmacopeial updates and monitor its timely implementation to avoid any non-conformances
• Intimate the concerned stakeholders to initiate and complete activities before effective date of pharmacopoeia
• Escalate non-conformances timely to avoid any delays in operation

Key Accountabilities (3/6)

• Document all activities performed as per valid procedure online by using standard/approved formats or templates to ensure that all entries done are correct, accurate and authentic
• Maintain system integrity by updating documentations and deviations on CipDox while performing operations
• Maintain all the online documentation and timely entries and supporting documents
• Prepare new documents and update existing documents as per GMP requirement

Key Accountabilities (4/6)

• Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit
• Issue applicable bound books to units by maintaining the log of the same so the current format is available to record the relevant data entries
• Maintain correct and updated record of all the issuance of documents and bound books

Key Accountabilities (5/6)

• Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed
• Evaluate and prepare documents for standardization across all units at a site
• Coordinate with CFTs and check requirements as per existing procedures to simplify the process
• Provide suggestions and ideas by exploring new possibilities to achieve work simplification

Major Challenges

• Delay in verification of methods for pharmacopeial updates due to non-availability of data. Overcome by coordinating with QC and
• Inadequate time allotted for updating the documents due to late intimations and change in priorities. Overcome by understanding the requirements and proper planning and coordination with CFTs
• Delay in meeting final timelines of the activities due to delay in getting review comments for cross functional departments. Overcome by regular follow-ups and escalations

Candidate Profile

M.Sc. / B.Pharma1-3 years of experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms

Additional Information

• Experience : 1-3 years
• Qualification : M.Sc. / B.Pharma
• Location : Sikkim - Rangpo
• Industry Type : Pharma/ Healthcare/ Clinical research
• End Date : 30th September 2026