PRPS, GMP and GHP, Audit Plan, Tracking Status of Audits, tracking action plan. OSH Act, HACCP. The post
Responsible for preparing Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Responsible for writing Clinical Investigation Plans Provide clinical input into product development
Responsible for preparing Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Responsible for writing Clinical Investigation Plans Provide clinical input into product development
Awareness Incident Investigation Emergency Response Planning Reporting and Documentation Continuous Improvement
Awareness Incident Investigation Emergency Response Planning Reporting and Documentation Continuous Improvement
audit programme (Audit Plan, Tracking Status of Audits, tracking action plan). Coordinate external audits
audit programme (Audit Plan, Tracking Status of Audits, tracking action plan). ▪ Coordinate external
and responsibilities include but not limited to: Plan, develop and implement techniques, processes and
and responsibilities include but not limited to: Plan, develop and implement techniques, processes and
Demonstrate an understanding of APQP; PPAP; MSA; Control Plans; PFMEA (Core Tools) Continual Risk Management: Facilitate Continually measure, monitor and provide improvement plans for improving business systems efficiency and cost