THE ROLE
This individual will assist the QC Manager in managing Quality Checks for all raw materials and finished goods as well as maintaining all Quality documentation.
KEY RESPONSIBILITIES
- The incumbent works closely with the QC Manager on all aspects of Quality Control, in particular, on product reliability and compliance with all established product standards. Ensures that all aspects of quality within the organization are upheld.
- This position reports directly to the QC Manager.
- The incumbent maintains overall purviews for all aspects of quality within the organization and hence, is entrusted with developing checks to ensure that standards are maintained and/or exceeded.
- Inspects all incoming raw material for compliance according to current standards.
- Conducts periodic checks and analyses on all WIPs.
- Retains finished product samples from production to conduct checks and analysis.
- Prepare test solutions, compounds, or reagents for laboratory use.
- Assist QA with failure analyses, and corrective and preventive action response to customer’s complaint.
- Work with various departments on the maintenance of company quality manuals pertaining to operating procedures.
- Assist in GMP audits, validation, qualification, and change control.
- Assist in maintaining Product Quality and Technical File.
REQUIREMENTS
- Diploma in Chemical Process Technology, Pharm, Biotechnology / Degree in Chemistry, Quality Assurance
- Able to do 12-hour rotating shifts (4-day work week and night shift)
