Job Description

Preffered male candidates only

Job Purpose

:

To ensure that all products manufactured by the facility meet internal and external quality standards through sampling, testing, and inspection. The QC officer plays a critical role in compliance with GMP (Good Manufacturing Practices), customer specifications, and regulatory requirements.

Key Responsibilities

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Product Testing

: Conduct in-process, finished product, and raw material testing as per standard procedures. Perform physical, chemical, and/or microbiological tests depending on product type. Ensure timely testing to meet production and shipping deadlines.

Documentation & Reporting

: Maintain accurate records of test results and observations. Prepare Certificates of Analysis (CoAs) and other QC documentation. Report deviations and non-conformities as per SOPs.

Sampling & Inspection

: Collect samples of raw materials, packaging materials, and finished goods. Conduct line clearance and in-process checks during production. Inspect incoming raw materials for quality compliance.

Compliance & Standards

: Ensure adherence to GMP, ISO, and customer-specific requirements. Participate in internal audits and regulatory inspections. Assist in validation and calibration of lab equipment.

Communication

: Collaborate with production, QA, and warehouse teams to resolve quality issues. Escalate quality concerns or OOS (Out of Specification) results promptly.

Continuous Improvement

: Contribute to root cause analysis and CAPA (Corrective and Preventive Action) processes. Suggest improvements to testing procedures and quality systems.

Qualifications & Experience

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Diploma or Master's degree in Chemistry, Microbiology, Pharmacy, or related field. 1-3 years of QC experience in a CMF or regulated manufacturing environment (pharma, cosmetics, food, etc.). Familiarity with GMP, GLP, and relevant regulatory standards.
Job Type: Full-time

Pay: ?20,000.00 - ?22,000.00 per month

Work Location: In person