GMP Project Manager 17343

Om jobbet

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.

Assignment Description

We are looking for a Sub-Project Manager

What You Will Work On

Lead and coordinate sub-project activities related to QC equipment

Manage supplier interactions and vendor coordination

Ensure compliance with GMP regulations and quality standards

Plan, track, and follow up on project progress and deliverables

Collaborate with internal teams and international stakeholders

Support implementation and lifecycle management of QC equipment

Handle documentation and reporting in line with regulatory requirements

Contribute to maintaining project timelines and quality objectives

What You Bring

Experience as a Project Manager within the pharmaceutical industry

Knowledge or experience working with QC equipment

Strong understanding of GMP requirements

Experience working with suppliers and vendor management

Ability to work in a fast-paced and international environment

Fluency in Swedish and English (written and spoken)

Availability to work onsite in Södertälje (~60%)