QCPD Specialist
Reykjavik Headquartersonsitemid
Posted 2w ago · via Workday
About this role
Alvotech is looking for a QA professional supporting combination product and devices R&D and Design Control activities, responsible for the review and approval of quality documentation throughout the product development lifecycle, ensuring compliance with 21 CFR Part 820 and ISO 13485 requirements. Partners closely with R&D teams to provide quality guidance, promote compliance, and support the effective execution of quality procedures. Contributes to the development and continuous improvement of the Quality Management System, authors and reviews quality procedures, leads cross-functional quality initiatives, supports regulatory inspections and health authority interactions, and independently manages quality improvement projects.…
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
For this role: r, teams
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 Reykjavik Headquarters. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
rteams
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