What are the responsibilities and job description for the General Submission - Life Sciences Consultant position at Medvacon Life Sciences?
We are looking to connect with experienced consultants open to working now or on future assignments in cGMP pharmaceutical or biotech setting on assignments involving:
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
While we are headquartered in Sparta, NJ, we continually have a high number of consulting and contracting assignments on 1099 across the US.
A member of our Talent team will be in touch to discuss your application in more detail. In the meantime, check out our website: Home — Medvacon Life Sciences LLC
Quality Grind Podcast: Quality Grind Podcast — Medvacon Life Sciences LLC
Blog Series: Blog — Medvacon Life Sciences LLC
Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.