General Submission - Life Sciences Consultant

We are looking to connect with experienced consultants open to working now or on future assignments in cGMP pharmaceutical or biotech setting.

Requirements

• Compliance and Training
• CSV & CFR Part 11
• Data Integrity / Governance
• Commissioning and Qualification
• Quality System Implementation
• Compliance ~ cGxP Consulting
• Investigation and Deviation – CAPA
• FDA Remediation
• Audits and Assessments
• Mock FDA Inspections
• SOP / Policy Development
• M&A Due Diligence
• License Application Support