About Cipla
Cipla is renowned for its commitment to healthcare and its mission to provide affordable medicines globally. The company operates in over 80 countries and has a strong presence in the pharmaceutical industry. Cipla's Sikkim facility is dedicated to maintaining high-quality standards and compliance with global regulatory requirements.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
Accountabilities
As a QC Junior Team Member, you will be responsible for:- Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis
- 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 assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements
- 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
- Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed
Qualifications
- Education: MSc in Chemistry or B Pharma.
- Experience: Minimum of 2 years of experience in the QC department of a pharmaceutical organization.
- Skills:
- Strong domain knowledge.
- Ability to collaborate and succeed.
- Innovation and excellence in performance.
- Accountability and empathy in leadership.
- Agility in actions.