Latest B Pharma Jobs at Cipla | Apply now for Junior Team Member Quality Control Position
Looking to build a career in pharmaceutical quality control? Cipla, a global healthcare leader, is hiring a Junior Team Member in Quality Control for its Rangpo, Sikkim facility. Suppose you have the right qualifications and experience. In that case, this permanent role offers an opportunity to work with one of the most trusted names in the pharma industry while ensuring compliance with top-tier quality standards.
About Cipla
Cipla is a global pharmaceutical leader dedicated to making healthcare more accessible and affordable. Founded in 1935, the company has built a strong legacy of innovation and quality across more than 80 countries. With a focus on respiratory, anti-retroviral, urology, cardiology, and oncology segments, Cipla is renowned for its commitment to patient-centric solutions and cutting-edge research. By adhering to the highest standards in quality control, regulatory compliance, and ethical practices, Cipla continues to improve lives through trusted, high-quality medicines. Cipla is a leading pharmaceutical company dedicated to providing high-quality healthcare products globally.
Job Details
Job Post – Junior Team Member in Quality Control
Country: India
State: Sikkim
Location: Rangpo
Req Id: 92005
Division & Department
Division: Quality
Department: Quality
Employment Details
Employment Type: Permanent
Job Purpose
Prepare, update, and review specifications, SOPs, policies, and operating documents for material analysis to ensure adherence to quality standards and regulatory requirements.
Qualifications
Education: M.Sc. / B. Pharma
Experience: 2 years in the QC department of a pharmaceutical organization
Skills and Competencies
- Collaboration
- Innovation
- Accountability
- Empathy
- Agility
- Domain Knowledge
- People Management
Accountabilities
- Prepare documents: SOPs, specifications, and non-routine documentation for timely availability and support during analysis.
- Review updates: Evaluate pharmacopeial updates to maintain compliance with standards.
- Review documents: Ensure compliance by referring to quality procedures.
- Issue documents: Maintain issuance records for document availability.
- Execute harmonization: Simplify processes and ensure standardized procedures.
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