Core Diagnostics Regulatory Affairs Managers

Portugal - Portoonsite

Posted today · via Workday

About this role

JOB DESCRIPTION: Regulatory Affairs Manager Location: Porto/Portugal MAIN PURPOSE OF ROLE Serves as the primary Regulatory Affairs representative for the manufacturing site, providing strategic and operational regulatory support to ensure successful product commercialization and ongoing regulatory compliance. Responsible for developing and executing regulatory strategies for new product launches, product changes, manufacturing changes, and lifecycle management activities. Partners with cross-functional teams to assess regulatory impact, obtain required regulatory deliverables, maintain product and site compliance, and ensure alignment with evolving global regulatory requirements.…

Read the full description on 1000 Abbott Laboratories Inc(ALI)'s site →

What we'd score you on

reqspace match rubric

Five 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

We check your title trajectory against the seniority signal of the role.

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 Portugal - Porto. We weight your proximity and willingness to relocate.

Score yourself on this role.
Free · no card · written explanation included
See if I'm a fit →

Skills in this role

Pulled from the job description. These are the keywords we'll weight when scoring your fit.

rteams

More at 1000 Abbott Laboratories Inc(ALI)

See all open jobs at 1000 Abbott Laboratories Inc(ALI)