Job Title: Team Member – Quality Control (QC)
Location: Rangpo, Sikkim, India
About Cipla:
Cipla, a leading global pharmaceutical company, is dedicated to providing high-quality, affordable medicines to patients worldwide. We uphold the highest standards of quality and compliance across all our operations. We are currently seeking a dedicated and meticulous Team Member for our Quality Control department in Rangpo, India.
The Opportunity:
Join our dynamic Quality Control team and play a vital role in ensuring the integrity and compliance of our pharmaceutical products. As a Team Member, you will be instrumental in managing critical documentation related to material analysis, ensuring strict adherence to predefined quality parameters, pharmacopeial standards, and cGMP (current Good Manufacturing Practices) requirements. This role offers an excellent opportunity to contribute directly to our commitment to regulatory excellence and continuous improvement.
Key Responsibilities:
- Documentation Management: Prepare, update, and review Standard Operating Procedures (SOPs), specifications, policies, and other operating documents for material analysis. Coordinate with site QC/QA for corporate document revisions, ensuring timely availability and accuracy.
- Regulatory Compliance: Actively monitor and evaluate the latest pharmacopoeial updates, supplements, and amendments. Assess the required document changes, ensure their timely implementation, and escalate any non-conformances to maintain full regulatory adherence.
- Quality Assurance: Scrutinize all assigned documents against predefined quality procedures and company policies, ensuring meticulous compliance with product quality aspects. Proactively identify and address any queries or issues encountered during document review to prevent operational delays.
- Record Keeping & Issuance: Manage the issuance of controlled documents and bound books to applicable units, maintaining accurate and up-to-date records to ensure that the most current versions are always accessible and utilized.
- Process Harmonization: Contribute significantly to the standardization and simplification of documentation processes across various units within the site. Collaborate effectively with cross-functional teams (CFTs) to identify opportunities for efficiency enhancement and procedural improvements.
Qualifications:
- Education: A Bachelor’s (B. Pharma.) or Master’s (M.Sc.) degree in a relevant scientific discipline.
- Experience: 1-3 years of proven work experience in a Quality Control department within a reputable pharmaceutical organization.
- Knowledge: Strong understanding of current regulatory standards, compliance norms, pharmacopoeial guidelines, and cGMP principles.
- Skills: Exceptional attention to detail, robust analytical and organizational skills, effective written and verbal communication, and a proactive, problem-solving approach to tasks.
Why Cipla?
At Cipla, you’ll be part of a purpose-driven organization that values innovation, quality, and a commitment to global health. Your expertise in quality control will directly support the delivery of safe and effective medicines to millions. We offer a dynamic work environment where your contributions are recognized, and professional growth is encouraged.
To Apply:
If you are passionate about quality control in the pharmaceutical industry and meet the qualifications outlined above, we encourage you to submit your application.
