Job Description
What you will do:
Bring energy, knowledge, innovation and influence to carry out the following:
- Integrate a harmonized global risk management program into Site Quality Management System
- Be the primary contact between the Global Quality Risk Management Organization and our Biologics site.
- Co-ordinate execution of risk assessments, risk control and risk communication and review
- Ensure site risk register and inventory is maintained and communicated
- Provide risk management training on site as required
- Provide periodic update to Quality Council on site risk status
- Lead the Site Quality Risk Management Council governance process
- Represent organisation at Industry forums
- Manage and participate in the preparation and hosting of regulatory and customer audits
What skills you will need:
In order to excel in this role, you will more than likely have
- Minimum degree or post-graduate qualification (Science/ Pharmacy/ Engineering).
- 6-10 years’ working knowledge in Quality Assurance and Quality Risk Management Principles
- Understanding and practical application of GMP standards and regulations
- Working knowledge of Quality Risk Management regulations and best practises
- Seasoned in governance processes and management
- Proven record of influencing change
- Skilled supporting cross-functional investigations
- Analytical problem-solving skills
So, if you are ready to:
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.