QA Assistant – Process Validation Job Cosmos

Medical Jobs. Cosmos Jobs

Job Summary:

The QA Assistant – Process Validation will be responsible for supporting and executing validation activities across all
manufacturing processes to ensure compliance with regulatory and quality standards.

Key Responsibilities:

• Prepare process validation protocols outlining execution plans for validation activities.
• Collect and document samples at various manufacturing stages and submit them to QC for analysis.
• Conduct physical analysis of samples obtained during validation processes.
• Compile and prepare comprehensive validation reports upon completion of validation activities.
• Develop and execute hold time study protocols and generate corresponding reports.
• Ensure strict adherence to cGMP, GDocP, and ALCOA principles for data integrity and documentation.
• Report any non-compliance arising during validation protocol execution.
• Support quarterly updates of the Validation Master Plan.

Qualifications & Experience:

• Minimum Diploma in Pharmacy or a related field.
• At least 3 years of experience in a quality-related role, preferably within
• pharmaceutical manufacturing.

Key Competencies

• Strong analytical and problem-solving skills.
• Good understanding of GMP and regulatory requirements.
• Effective communication, numerical, and presentation skills.
• Basic knowledge of analytical techniques.
• Proficiency in MS Office (Word, Excel, PowerPoint, Access).
• Strong knowledge of quality documentation systems and data integrity standards.

Deadline; 10th May 2026, COB

How to Apply

Send application to recruitment@cosmos-pharm.com
Only shortlisted candidates will be contacted.