maravailifesciences
Part-Time Document Control Associate I
At a Glance
- Location
- Jupiter, Florida, United States
- Work Regime
- onsite
- Experience
- 1–2 years
- Posted
- 2026-03-27T04:47:29-04:00
Key Requirements
Required Skills
Certifications
- ISO
Domain Knowledge
- Insurance
- Media
- Medical
Requirements
Experience with ISO 9001, ISO 13485, 21CFR820, 21CFR 211, or other regulated industry a plus.
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About the Company
:
Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.
At Maravai, we believe that diverse perspectives are the foundation of innovation.
Through an inclusive and
equitable
culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together,