Project Manager/Program Manager

Technical Project Manager – Pharmaceutical Manufacturing – 18379

Södertälje, Sweden
Onsite

Huy Tran

HR Administrator

cv@veritaz.se

Job Summary

  • Posted Date

    June 29, 2026

  • Work Type

    Onsite

  • Deadline

    2026-08-04

  • Schedule

    Full-time

  • Location

    Södertälje, Sweden

Job Description

Assignment Description

We are looking for an experienced Sub Project Manager

What You Will Work On

  • Lead auxiliary equipment workstreams across multiple pharmaceutical investment projects
  • Manage sub-project activities through procurement, execution, qualification, and project completion
  • Coordinate suppliers, contractors, engineering teams, and internal stakeholders
  • Drive technical discussions and resolve complex project challenges
  • Ensure successful delivery according to project scope, schedule, budget, and quality objectives
  • Develop and maintain project plans, resource plans, and timelines
  • Apply a structured risk-based approach to project management
  • Identify, assess, mitigate, and follow up on project risks
  • Monitor project progress and report status to project management and stakeholders
  • Ensure compliance with GMP standards and pharmaceutical project requirements
  • Support technical documentation, equipment qualification, and project decision-making
  • Collaborate closely with Engineering, Quality, Validation, Production, and Procurement teams
  • Drive proactive problem-solving and manage multiple parallel activities simultaneously
  • Ensure effective communication across all project stakeholders

What You Bring

  • Proven experience as a Project Manager or Sub Project Manager within the pharmaceutical industry
  • Experience leading at least one GMP-regulated investment project from initiation through completion (multiple projects are highly desirable)
  • Strong experience managing capital investment or engineering projects
  • Experience coordinating multiple parallel project activities
  • Strong knowledge of GMP regulations and pharmaceutical manufacturing environments
  • Experience applying risk-based project management methodologies
  • Strong project planning, budget management, resource planning, and scheduling skills
  • Experience working across different project phases, including procurement and qualification
  • Excellent stakeholder management and communication skills
  • Strong problem-solving ability with a proactive and delivery-focused mindset
  • Ability to manage multiple priorities in a fast-paced project environment
  • Fluent in Swedish and English, both written and spoken

 

If this sounds interesting, please send your CV to cv@veritaz.se

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