Tasks & Responsibilities:
Define project charter and scope. In collaboration with Device Development Leader, clearly define deliverables of the project, ensuring project assumptions, constraints, and scope are shared and understood within the organization and the overall Technical Development Team.
Device Project deliverables: clearly plan project deliverables and forecast requirements, estimating team resources and budget.
Project integration: generate a comprehensive list of required documentation to ensure project information is readily accessible and allows seamless integration in collaboration with PMO for the overall projects portfolio.
Manage change management for project scope changes, integrating a change-management mentality within a fast-paced and complex organization to assure constant stakeholder alignment.
Schedule Management: Develop and maintain the project schedule, track progress.
Budget Management: Plan and manage the project budget, monitor expenditures in collaboration with other governing committees and the overall Technical Development Team.
Stakeholder Communication: Establish and maintain solid communication with internal and external stakeholders, provide updates and regular status reports, manage expectations in a faceted stakeholder environment.
Risk Management: Identify, monitor, and mitigate project risks and issues.
Resource Management: Allocate and manage resources in collaboration with the Device Development Leader, including personnel and materials.
Quality Management: Ensure project deliverables meet quality system requirements.
Must Haves:
BA/BS + a minimum of 15 years total work experience with at least 10 or more years of relevant business and/or technical experience in the medical device, pharmaceutical or biopharmaceutical industry, preferably from a multi-site global company.
Experience in drug-device combination products is considered an asset.
At least 10 years Project Management experience - Project Management Professional (PMP) certification or equivalent is preferred.
Proven experience in project management, including project planning, execution, and closure.
Strong leadership and team management skills.
Excellent communication and interpersonal skills.
Proficiency in project management software (e.g., MS Project, Smartsheet, Trello).
Solid understanding of project management methodologies (e.g., Agile, Waterfall).
Ability to manage multiple projects simultaneously and prioritize tasks effectively.
Strong foundation in engineering, biotechnology, or life sciences relevant to medical device development.
Understanding of clinical, regulatory, and manufacturing requirements to ensure smooth device development and industrialization.
Proven track record leading development projects and in-depth knowledge to apply project management methodologies and Design Control requirements.
Deep understanding of design controls, risk management, and quality systems (ISO 13485, FDA 21 CFR Part 820), with extensive knowledge of FDA regulations, ISO standards, and CE marking requirements to ensure strict compliance across all projects.
Adept at identifying project risks and implementing mitigation strategies to ensure project continuity and success.
Proven ability to cultivate, develop, and sustain high-performing teams that excel in collaboration, innovation, and efficiency.
Proven ability to communicate effectively with team members and stakeholders, fostering a collaborative environment.
CVs have to be uploaded in English / German.
Beginning of appointment: immediately
Job Area: Canton of Basel-City
Languages: We can only accept complete documents, see Your Candidature for further information.
Send the documents to the contact details below or use the form Online Candidature (see below).
Contact:
Personal Contact Basel AG
Elisabethenstrasse 4
4051 Basel
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