Senior Commissioning and Qualification Specialist

Reykjavik Headquartersonsitesenior

Posted today · via Workday

See if I'm a fit →Tailor my resume for this role →Apply on Workday ↗

About this role

Are you an experienced GMP professional with a passion for commissioning and qualification? Do you thrive in high‑impact projects that support cutting edge biopharmaceutical production? We are looking for a Specialist in Commissioning & Qualification (C&Q) to join our team and ensure that our facilities, systems, and equipment operate to the highest global standards. In this role, you will be responsible for the commissioning and qualification of GMP-critical systems, ensuring full compliance with EU and US regulatory expectations for parenteral biopharmaceutical manufacturing. You will lead and contribute to strategic projects, mentor colleagues, and collaborate across departments to drive quality and innovation.…

Read the full description on Alvotech'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.

Skills match

For this role: teams

Level fit

This role is senior-level. We check your trajectory against it.

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

Recency

A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.

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

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.

teams

More at Alvotech

See all open jobs at Alvotech →