Labeling Specialist
Jersey Cityonsitemid
Posted 106mo ago · via Smartrecruiters
About this role
Description: Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). Labeling documents include those prepared for FDA submissions, Annual Reports and PSURs in compliance with regulatory requirements and within company timelines. Candidate will be required to work with limited oversight and have a basic understanding of FDA labeling regulations and FDA guidance to the level of applying them effectively to all work output. Specific responsibilities include: •Assisting labeling managers with overall labeling process of brand prescription products •Proofreading of package insert as well as packaging components.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
We compare your skills against the role requirements.
2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Jersey City. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
More at Lance Soft Inc
- View →Post Market Regulatory Affairs SpecialistWest Chester, PA, United States
- View →Quality Assurance Specialist IIILexington, MA, United States
- View →Quality Assurance SpecialistMilford, MA, United States
- View →Clinical Program Manager IIILake Forest, IL, United States
- View →Software Test EngineerRaleigh, NC, United States
- View →Communication Specialist IIICollegeville, PA, United States