Batch record review for AbbVie’s TPM’s
Batch record release of AbbVie product manufactured at TPM’s
Monitoring metrics and supporting initiatives to improve TPM performance
Assist in project team planning and preparation of quality documentation.
Coordination of documentation approval.
Participate in training and education programs for various aspects of quality assurance.
Partner and support activities related to TPM compliance and quality assurance goals.
Perform assessment to determine compliance processes, procedures and regulations to identify potential gaps and implement mitigating strategies.
Ensure metrics and KPI’s are being met.
Participate in investigations of quality events and determine potential corrective active to reduce re-occurrence.
Degree in Chemistry, Biology, Microbiology or other technical/scientific are is preferred (but not required)
Technical knowledge in as many of the following areas as possible: quality, regulatory, process sciences and or manufacturing
2+ years in quality assurance / quality control or relevant experience
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion.
It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
Whatsapp
