Project Manager Consulting assignment within Pharma &...
WeQuel
At WeQuel, we are now looking for a Project Manager in Uppsala, where you will play a key role in the client's Capital Portfolio Management function, focusing on driving several CAPEX projects from planning through execution to closure. You will own your projects end to end, working closely with the project team to make sure every project meets the client's standards and all applicable regulatory requirements for pharmaceutical and medical device products. Your projects may relate to facilities, manufacturing or Quality Control laboratories.
As a consultant with us, you will have the opportunity to work with one of our clients, leading companies within the pharmaceutical and medical device industries. There you will help bring new technology into operation, improve facilities and processes, and deliver sustainable, compliant solutions.
Your responsibilities:
End-to-end management of assigned CAPEX projects, from planning to closure
Evaluation of alternative execution solutions together with the project sponsor
Feasibility studies and preparation of Steering Committee material
Project execution in line with approved schedule, scope and budget
Risk assessments, budgeting and project planning, carried out independently
Continuous monitoring and follow-up of project progress
Primary authorship of User Requirement Specifications (URS), with support available
Procurement and purchasing activities, with support available
Chairing project meetings and taking part in pulse meetings
Monthly status reporting
Ensuring compliance with the client's standards and regulatory requirements
Handover of fully implemented, operational deliverables ready for use
You will take full ownership of your project flow and often work without a dedicated project team or with limited resources, while collaborating with a wide range of stakeholders across the organization.
Requirements:
Extensive project management experience, with a proven ability to deliver on time and within budget
Strong technical background (preferred)
Solid knowledge of pharmaceutical and medical device requirements: cGMP, 21 CFR Part 11, GAMP 5, MDR, ISO 13485 and ISO 14971
Strong sense of ownership
Confident running every aspect of a project independently
Assignment details:
Workload: 100%
Remote: 100% onsite
We offer
At WeQuel, you become part of a consultant team that values people first. We believe success is created through engagement, collaboration and development. We offer a flat organization with short decision paths, a strong sense of community and the opportunity to influence your own development.