Cipla Recruitment 2025: Junior Team Member Opening in Quality Control

Cipla, a global pharmaceutical powerhouse with a presence in over 80 countries, is seeking a results-oriented Junior Team Member for its Quality Control (QC) department. The position is based at the company’s manufacturing facility in Rangpo, Sikkim.

Driven by the purpose of “Caring for Life,” Cipla is looking for individuals who can ensure that every product meets the highest standards of safety, efficacy, and compliance with global pharmacopeial requirements.

Job Purpose & Key Responsibilities

The primary focus of this role is to manage, update, and review technical documentation to ensure seamless QC operations and cGMP compliance.

Documentation & SOP Management: Prepare and revise Standard Operating Procedures (SOPs), specifications, and general analytical methods.
Pharmacopeial Compliance: Monitor the latest pharmacopeial updates (USP/BP/IP), supplements, and amendments. Ensure timely implementation of new monographs to prevent non-conformances.
Online Documentation: Maintain system integrity by performing real-time documentation of all activities using CipDox and approved templates.
Issuance & Control: Manage the issuance of bound books and controlled documents to various units, ensuring only the latest versions are in use.
Process Simplification: Collaborate with Cross-Functional Teams (CFTs) to harmonize and simplify documentation processes across the site.
Instrument Calibration: Review instrument calibration data against operating documents to maintain analytical accuracy.

Candidate Profile

Cipla is looking for candidates with a strong foundation in pharmaceutical quality standards and a meticulous approach to data integrity.

Criteria	Details
Education	B.Pharma or M.Sc
Experience	1 to 3 Years in a QC department
Key Knowledge	cGMP requirements, Regulatory standards, and Pharmacopeial guidelines
Location	Rangpo, Sikkim
Skills	Technical writing, coordination with CFTs, and time management

Major Challenges & Expectations

Candidates are expected to be proactive in overcoming operational hurdles, such as:

Coordinating with teams to ensure data availability for pharmacopeial updates.
Managing tight deadlines for document updates through proper planning.
Regular follow-ups with cross-functional departments to ensure timely review comments and final submissions.