Quality Control Supervisor
POSITION PURPOSE
- This individual will assist the QC Manager to manage Quality Checks for all raw material and finished goods as well as maintaining all Quality documentation, as well as supervising and guiding the lab technicians.
DIMENSIONS
- The incumbent works closely with the QC Manager on all aspects of Quality Control, in particular, on product reliability and compliance to all established product standards. Ensures that all aspects of quality within the organization is upheld.
NATURE AND SCOPE
A. Report Relationship – This position reports directly to QC Manager.
B. General Department Overview – Quality Control maintains overall purview for all aspects of quality within the organization and hence, is entrusted with developing checks to ensure that standards are maintained and/or exceeded.
C. Areas of Responsibility:
- Able to provide guidance and coach lab technicians.
- The incumbent inspects all incoming raw material for compliance according to current standards.
- The incumbent conducts periodic checks and analysis on all WIPs.
- The incumbent retains finished product samples from production to conduct checks and analysis.
- Assist QA on failure analyses, corrective and preventive action response to customer’s complaint.
- Assist in GMP audits, validation, qualification and change control.
- Assist in maintaining Product Quality and Technical File.
- Write technical papers or reports or prepare standards and specifications for processes, products, or tests.
D. Challenges of Position – Being a highly regulated industry, the incumbent is required to be aware of changes in regulatory requirements and effect those changes as required. Clear handing/taking over during shift changes to ensure work flow process continuity is essential.
E. Communication Network – The incumbent is expected to work closely with both internal and external parties and clearly communicate in non-technical terms. Must be able to handle multi-national staffs.
F. Measurement – The incumbent will be expected to ensure that all regulatory requirements such as ISO 13485 are adhered to. Work accuracies and documentation processes are to be upheld at all times. Exercise responsibility for proper functioning in compliance with good laboratory practice and cGMP.
G. Requirements – At least a Diploma in Chemical Process Technology, Pharm, Biotechnology / Degree in Chemistry, Quality Assurance.
POSITION PURPOSE
- This individual will assist the QC Manager to manage Quality Checks for all raw material and finished goods as well as maintaining all Quality documentation, as well as supervising and guiding the lab technicians.
DIMENSIONS
- The incumbent works closely with the QC Manager on all aspects of Quality Control, in particular, on product reliability and compliance to all established product standards. Ensures that all aspects of quality within the organization is upheld.
NATURE AND SCOPE
A. Report Relationship – This position reports directly to QC Manager.
B. General Department Overview – Quality Control maintains overall purview for all aspects of quality within the organization and hence, is entrusted with developing checks to ensure that standards are maintained and/or exceeded.
C. Areas of Responsibility:
- Able to provide guidance and coach lab technicians.
- The incumbent inspects all incoming raw material for compliance according to current standards.
- The incumbent conducts periodic checks and analysis on all WIPs.
- The incumbent retains finished product samples from production to conduct checks and analysis.
- Assist QA on failure analyses, corrective and preventive action response to customer’s complaint.
- Assist in GMP audits, validation, qualification and change control.
- Assist in maintaining Product Quality and Technical File.
- Write technical papers or reports or prepare standards and specifications for processes, products, or tests.
D. Challenges of Position – Being a highly regulated industry, the incumbent is required to be aware of changes in regulatory requirements and effect those changes as required. Clear handing/taking over during shift changes to ensure work flow process continuity is essential.
E. Communication Network – The incumbent is expected to work closely with both internal and external parties and clearly communicate in non-technical terms. Must be able to handle multi-national staffs.
F. Measurement – The incumbent will be expected to ensure that all regulatory requirements such as ISO 13485 are adhered to. Work accuracies and documentation processes are to be upheld at all times. Exercise responsibility for proper functioning in compliance with good laboratory practice and cGMP.
G. Requirements – At least a Diploma in Chemical Process Technology, Pharm, Biotechnology / Degree in Chemistry, Quality Assurance.