Leads the project’s development and/or review of procedures, SOP’s and other documents related to Quality System.
Maintains Good Documentation practice (GDP) in quality system for new projects.
Ensures project compliance with all relevant GMP and Quality requirements.
Manages implementation of Quality system element pertaining to Change Control, Risk Mitigation and validation status as stated in Statement of Work (SOW).
Administration:
Ensures all project documentation follow company and regulatory requirements.
Completes all required reports and administrative tasks within designated timeframes. Knowledge and
Compliance:
Maintains current knowledge of topics relevant to role, the business and International standards through attendance at seminars, lectures, meetings and professional conferences.
Maintains knowledge of technological advancements in areas relevant to role.
Maintains up-to-date knowledge of industry trends, cutting-edge practices and techniques relevant to role and business.
Ensures all Company related activities comply with relevant Acts, legal demands and ethical standards at all times.
Extensive knowledge in Quality and Regulatory tools:
Quality Management System tools (PDCA Cycle, FMEA)
Root Cause analysis and/or Problem-solving approaches.
Proficient in statistical analysis.
Project Management Planning.
Excellent understanding of GxP principles: Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP); and Project Management principles
JOB QUALIFICATION
Relevant Qualifications:
Bachelor’s degree in Science preferably in Pharmacy/Chemistry/Microbiology and Biochemistry
Minimum of 5 years’ management experience and 5 years in Quality Assurance, Validation or Quality Control roles in the Pharmaceutical/Biotech/Medical device or Life Sciences industry.
Advanced degrees may compensate for the required experience stated above.
With sufficient knowledge of spoken and written English