Solvita · 7 hours ago
BLA Quality & Regulatory Affairs Director
Solvita is a Biologics Manufacturing company, and they are seeking a Quality & Regulatory Affairs Director with extensive experience in quality and regulatory areas. The role involves leading BLA Pre Approval Inspections and developing GMP improvement plans to ensure compliance and mitigate risks during inspections.
Responsibilities
Proven Quality and Regulatory professional with 12+ years of experience in quality and regulatory area for a Biologics Manufacturing company, with proven track record of hosting and leading BLA Pre Approval Inspections
Able to assess, develop and lead execution of GMP improvement plans that mitigate risks of non conformances during inspections, while able to support BLA related clients
Experience supporting client sponsored BLA filings with focus on manufacturing PAI compliance is a must
Strong regulatory background with proven knowledge on process validation, test method validation, and leading Biologics manufacturing facilities through GMP improvement plans is required
Qualification
Required
Proven Quality and Regulatory professional with 12+ years of experience in quality and regulatory area for a Biologics Manufacturing company
Proven track record of hosting and leading BLA Pre Approval Inspections
Able to assess, develop and lead execution of GMP improvement plans that mitigate risks of non conformances during inspections
Able to support BLA related clients
Candidate must have a Bachelors or Master Degree in Engineering, Chemistry, Life Sciences, or related scientific disciplines
Experience supporting client sponsored BLA filings with focus on manufacturing PAI compliance
Strong regulatory background with proven knowledge on process validation, test method validation
Leading Biologics manufacturing facilities through GMP improvement plans