Quality System Consultant (Experience from Life Science Industry)

Full-time Work Set Up:
Company selected to be on a Private Profile. | Industry: BPO / Call Centers

Quality System Consultant (Experience from Life Science Industry)

Full-time
Company selected to be on a Private Profile. | Industry: BPO / Call Centers

JOB DESCRIPTION

Quality Management (QM):

  • 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: 
  • Risk management (ICH Q9), Pharmaceutical Quality System (ICH Q10), Post-Marketing Changes (ICH Q12).
  • 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

OTHER JOB REQUIREMENTS

Education
Bachelor's/College Degree
Field of study
Engineering (Bioengineering/Biomedical)
Specialization
Quality Assurance

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