Job Description

• Completes documentation relating to material analysis and enters data into database/software systems
• Accountable for the accuracy and validity of all test results
• Other responsibilities include maintaining an audit ready lab, generation or revision of EM procedures, the support of other QC testing functions
• Maintain and perform daily operations of the QC on a daily basis in coordination with the QC Director/Supervisor to include testing of raw material/peptide samples and prioritizing projects
• Write and work with other QC Staff and other Department in the creation and approval of control documents such as specifications, SOPs, STMs
• Maintain and perform regular verification of the QC equipment for GMP compliance regularly in coordination with QC Director / Supervisor
• Maintain QC equipment maintenance program
• Implement and maintain GMP procedures such as following SOPs, Standard Testing Procedures (STPs), written procedure and maintaining proper documentation as necessary for Quality Control
• Perform all functions and duties of Associate Chemists and Technicians as needed
• Perform statistical analysis on processes

Job Types: Full-time, Permanent

Pay: ?15,000.00 - ?16,000.00 per month

Benefits:

• Provident Fund

Schedule:

• Day shift

Supplemental Pay:

• Performance bonus
• Yearly bonus

Education:

• Bachelor's (Preferred)

Experience:

• total work: 1 year (Preferred)
• Quality chemist: 1 year (Preferred)
• BSC: 1 year (Preferred)

Work Location: In person