C
Quality Control Assistant Analyst
Cosmos Pharm
Full-time
Healthcare
Mid Level
Salary: Open / Negotiable
Posted 1 hour ago
Deadline: Jun 13, 2026 3 days leftJob Description
Conduct laboratory analysis of raw materials, finished products, stability samples, and validation samples while ensuring compliance with cGMP, GDocP, and data integrity standards.
Key Responsibilities
- Analyze raw materials, finished products, stability, and validation samples according to approved procedures.
- Receive, handle, and store laboratory samples while maintaining sample integrity.
- Prepare and maintain test solutions, reagents, and volumetric solutions.
- Operate, calibrate, and perform maintenance on laboratory equipment.
- Prepare analytical reports and maintain laboratory records.
- Support review of raw material, finished product, and stability specifications.
- Update analysis status in manual and electronic systems.
- Report deviations, incidents, and unusual observations promptly.
- Ensure compliance with cGMP, GDocP, ALCOA principles, and data integrity requirements.
Requirements
- Degree in Chemistry, Pharmacy, Laboratory Technology, Microbiology, or related field.
- Minimum 3 years’ laboratory experience in pharmaceutical manufacturing.
- Strong understanding of GMP and GLP requirements.
- Experience with analytical QC methods and laboratory equipment.
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How to Apply
Job Details
- Industry
- Healthcare
- Type
- Full-time
- Experience
- Mid Level
- Salary
- Open
- Posted
- Jun 10, 2026
- Views
- 40
- Deadline
- Jun 13, 2026