General Submission - Life Sciences Consultant at Medvacon Life Sciences, LLC | Torre
General Submission - Life Sciences Consultant
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General Submission - Life Sciences Consultant

Medvacon Life Sciences, LLC
Emma
Emma
You'll elevate cGMP compliance and quality systems across diverse biotech and pharma assignments.
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Part-time

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Remote (for United States residents)
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Emma of Torre.ai
 2 months ago

Requirements and responsibilities

Job DescriptionWe 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 TrainingCSV & CFR Part 11Data Integrity / GovernanceCommissioning and QualificationQuality System ImplementationCompliance ~ cGxP ConsultingInvestigation and Deviation – CAPAFDA RemediationAudits and AssessmentsMock FDA InspectionsSOP / Policy DevelopmentM&A Due DiligenceLicense Application SupportWhile 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 LLCQuality Grind Podcast: Quality Grind Podcast — Medvacon Life Sciences LLCBlog Series: Blog — Medvacon Life Sciences LLCImportant Notice: Protecting Your InformationMedvacon 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.
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