Details of the offer

Job Details
- Conduct analysis in compliance with GMP requirements and internal productions
- Maintain accurate record of analysis and perform documentation to company standards
- Prepare test solutions, volumetric solutions, and samples used in analysis
- Performs assigned sampling, physical, chemical tests and assay on RMs, active pharmaceutical ingredients, in-process, finished and stab products analysis in an FDA regulated lab environment
- Used variety of analytical instruments such as HPLC, KF, Titrator, UV Spectro, etc
- Perform analysis with a practical understanding of the test procedures and instrument operation
- Conducts laboratory investigation under the supervision of Laboratory Manager
- Complies with all regulatory, in-house requirements may include but not limited to safety, housekeeping, laboratory chemical waste, GMP, GLP, documentation
- Perform analysis with a practical understanding of the test procedure and instrument operation
- Organize work schedule to complete assigned tasks efficiently and on schedule
- Notify Manager immediately of nonconforming data or unexpected occurrences

**Qualifications**:

- Licensed Chemist (QC Supervisor position)
- Investigation writing skills
- Good communication skills and ability to supervise staffs
- Knowledge of FDA and GMP regulations is a plus but not required

Schedule:

- 8 hour shift


Nominal Salary: To be agreed

Source: Whatjobs_Ppc

Job Function:

Requirements

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