GMP Project Manager 17343
Veritaz AB
📍 Sverige
⏰ Heltid
📋 Vanlig anställning
🗓 Ansök senast 19 maj 2026
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Skapa ansökan – från 49 kr Gratis att söka · Ingen registrering · 49 kr/mån för obegränsatOm 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%)
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%)