“QC Junior Team Member Opportunity: Apply Now with B.Pharm/MSc at Cipla”

Post: Junior Team Member – QC

Job Description:

Job Purpose: Prepare, update, and review specifications, Standard Operating Procedures (SOPs), policies, and operating documents for material analysis. Ensure alignment with predefined quality parameters and compliance with relevant standards, pharmacopeia, and current Good Manufacturing Practice (cGMP) requirements.

Accountabilities:

I. Document Preparation:

• Prepare documents like SOPs, specifications, and non-routine documentation.
• Ensure timely availability across the site to provide support during the analysis.

II. Pharmacopeial Compliance:

• Review the latest pharmacopeial updates, supplements, and amendments.
• Evaluate updates required in the available document to ensure compliance with current pharmacopoeia through consent with regulatory bodies.

III. Quality Compliance:

• Review assigned documents by referring to the relevant backup and pre-defined quality procedures.
• Ensure compliance against quality requirements.

IV. Document Issuance:

• Issue documents to applicable units.
• Maintain a record in the issuance record (bound book) to ensure the current version of the common document is available at the unit.

V. Harmonization and Simplification:

• Execute harmonization and simplification processes of documents.
• Reduce complexities in processes and ensure standardized procedures are followed.

Candidate Profile:

• Educational Qualification: M.Sc. / B.Pharma
• Experience: 2 years in the QC department of a pharmaceutical organization

Competencies/Skills:

• Collaborate to Succeed
• Innovate to Excel
• Perform with Accountability
• Lead with Empathy
• Act with Agility
• Strong Domain Knowledge
• People Management

Additional Information:

• Experience: 2 years
• Qualification: M.Sc. / B.Pharma
• Location: Sikkim – Rangpo
• Industry Type: Pharma/ Healthcare/ Clinical Research
• End Date: 30th March 2024

This opportunity is ideal for candidates with a strong background in Quality Control, holding an M.Sc. or B.Pharma degree, and possessing 2 years of relevant experience. If you are a dynamic professional who thrives in a collaborative environment and has a passion for maintaining high-quality standards in pharmaceuticals, we invite you to apply. The position is based in Sikkim – Rangpo, and the application deadline is 30th March 2024. Join us in contributing to the healthcare and clinical research industry with innovation, accountability, and excellence.

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