About this Cipla Job
Here’s a quick overview of this job opportunity at Cipla Job Vacancy 2023 in Sikkim.
- Requisition ID: 79502
- Division: QC – Stability
- Department: Quality Control
- Employment Type: Permanent
- Location: Rangpo, Sikkim
Table of Contents
Job Purpose
The primary purpose of this role is to prepare, update, and review specifications, SOPs, policies, and operating documents for material analysis. The aim is to ensure alignment with predefined quality parameters and compliance with relevant standards, pharmacopeia, and cGMP requirements.
Accountabilities
- Document Preparation: Prepare documents such as SOPs, specifications, and non-routine documentation. Ensure their timely availability across the site to provide support during the analysis process. Review the applicable pharmacopoeia and guidelines and make necessary updates. Review instrument calibration data in relation to operating documents.
- Pharmacopeial Updates: Stay updated on the latest pharmacopeial updates, supplements, and amendments. Evaluate the updates required in existing documents to ensure compliance with the current pharmacopoeia through regulatory body consent. Review new/revised monographs and monitor timely implementation to avoid non-conformances. Intimate concerned stakeholders to initiate and complete activities and escalate non-conformances promptly to prevent delays.
- Document Review: Review assigned documents by referring to the relevant backup and predefined quality procedures. Ensure their compliance with quality requirements. Follow approved procedures and current Cipla policies for the review approach. Address and discuss queries or problems faced during document review to prevent further delays in document completion.
- Document Issuance: Issue documents to applicable units and maintain a record of the same in the issuance record (bound book) to ensure the current version of common documents is available at the unit. Issue applicable bound books to units, maintaining the log of the same to make the current format available for recording. Maintain correct and updated records of all document issuances and bound books.
- Harmonization and Simplification: Execute harmonization and simplification processes for documents to reduce complexities in processes and ensure standardized procedures are followed. Evaluate and prepare documents for standardization across all units at a site. Coordinate with CFTs and check requirements as per existing procedures to simplify the process. Provide suggestions and ideas for work simplification.
Education Qualification
Candidates should have an M.Sc. or B. Pharma degree.
Relevant Work Experience
1-3 years of experience in the QC department of a pharmaceutical organization.
Competencies/Skills
- Effective communication skills (clarity of thought, comprehension)
- Demonstrated potential for growth
- Job/Product/Technical Knowledge/Pharma domain knowledge
- Presentation and interpersonal skills (if applicable)
- Managerial or people management skills
- Safety awareness (if applicable)
- Relevance of previous experience
- Strong comprehension, analytical, and problem-solving abilities
- Emphasis on productivity and result orientation (if applicable)
- Positive attitude
- Qualification fitment
- Sales drive (if applicable)
- Desirable personality traits (individualistic/team player, outspoken, maturity, etc.)
Job Location
Rangpo, Sikkim
Shift Hours
As per company requirements
About Cipla
Cipla, a leading pharmaceutical company, is committed to providing high-quality healthcare solutions. They are dedicated to ensuring the highest standards of quality and safety in their products.
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Key Tags: Cipla Job Vacancy, QC – Stability, Pharma Jobs
