Table of Contents
About this Cipla Job Vacancy
- Division: Quality Control
- Department: Quality
- Employment Type: Permanent
- Location: Rangpo, Sikkim
Job Purpose
In this role, you will be responsible for preparing, updating, and reviewing various documents related to quality control processes. Your objective is to ensure that these documents align with predefined quality parameters and comply with relevant standards, pharmacopeia, and cGMP requirements.
Key Responsibilities
1. Document Preparation: Create documents such as Standard Operating Procedures (SOPs), specifications, and non-routine documentation. Ensure their timely availability across the site to support material analysis.
2. Pharmacopeial Compliance: Stay updated on the latest pharmacopeial updates, supplements, and amendments. Evaluate the need for updates in existing documents to ensure compliance with current pharmacopoeia standards through regulatory approvals.
3. Quality Review: Review assigned documents by referring to the relevant backup and predefined quality procedures. Confirm their compliance with quality requirements.
4. Document Distribution: Issue documents to applicable units while maintaining a record of issuances. This ensures that the most current version of documents is available at the unit.
5. Process Simplification: Participate in the harmonization and simplification of documents to reduce process complexities. Promote standardized procedures across the organization.
Educational Qualification
M.Sc. or B. Pharma
Relevant Work Experience
0 to 2 years of experience in the Quality Control (QC) department of a pharmaceutical organization.
Key Competencies/Skills
- Communication: Ability to communicate clearly and comprehend complex information.
- Growth Potential: Demonstrated potential for career growth and development.
- Technical Knowledge: Understanding of pharmaceutical products, processes, and quality control.
- Presentation and Interpersonal Skills: Effective communication and interaction with team members.
- Managerial Skills: Ability to manage people and tasks effectively (if applicable).
- Safety Awareness: Knowledge of safety protocols (if applicable).
- Analytical Skills: Ability to analyze and solve problems.
- Result Orientation: Focus on productivity and achieving desired outcomes (if applicable).
- Attitude: A positive and adaptable attitude.
- Qualification Fitment: Matching qualifications to job requirements.
- Personality Traits: Individualistic or team player, outspoken, and maturity level (etc.).
Job Location
Rangpoo
Shift Hours
To be determined.
This role offers an excellent opportunity for individuals with a background in quality control to contribute to maintaining high-quality standards within a pharmaceutical organization. If you meet the qualifications and are eager to grow in the field of quality control, we encourage you to apply.
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