TI
Job Description
Key Responsibilities:
- Coordinate and supervise the receipt, sampling, and storage of raw materials.
- Ensure proper documentation and labeling of all RM containers as per SOP.
- Maintain records of raw material specifications, COAs, MSDS, and vendor documents.
- Conduct or coordinate sampling of incoming raw materials in compliance with GMP and SOPs.
- Follow up with the Quality Control (QC) team for timely testing and approval/rejection of raw materials.
- Monitor inventory levels and notify procurement for reordering when required.
- Ensure proper segregation and identification of quarantined, approved, and rejected materials.
- Assist in supplier qualification and raw material risk assessments.
- Participate in internal and external audits, and support documentation requests.
- Ensure compliance with cGMP, GDP, and company safety and hygiene practices.
Qualifications:
- B.Sc. / M.Sc. in Chemistry, Microbiology, or related discipline
- OR
- B.Pharm / M.Pharm for pharmaceutical roles
- 1–4 years of experience in raw material handling in a pharmaceutical or manufacturing environment
Key Skills:
- Knowledge of GMP, GDP, and regulatory requirements for material handling (USFDA, WHO, etc.)
- Familiarity with raw material specifications, COAs, and MSDS
- Attention to detail and accurate record-keeping
- Good communication and coordination skills
- Basic knowledge of ERP systems or inventory software (e.g., SAP)