QA Engineer ensuring reliability across UK and Global web and mobile platforms for a B2B SaaS company. Leading manual quality assurance and influencing testing strategies.
About the role
- Senior Project Manager leading quality and regulatory projects for Stryker's Medical Division. Ensure on-time delivery of strategic initiatives for global market access and compliance.
Responsibilities
- Lead and execute multiple projects within the Divisional Quality Plan, especially those related to Environmentally Preferable Purchasing (EPP) and Product Environmental Compliance (PEC), driving results amid demanding timelines and evolving priorities.
- Build strong cross-functional relationships across global sites and effectively influence without direct authority.
- Communicate project updates, priorities, and performance to key stakeholders and leadership through clear, well‑structured presentations, requiring strong verbal communication, storytelling, and presentation skills to ensure alignment and engagement.
- Apply sound judgment to make informed decisions despite ambiguity, aligning goals with broader organizational objectives.
- Adapt quickly to changing environments and take on additional responsibilities as needed.
- Support Mergers and Acquisitions (M&A) activities, including integration planning, execution of pre/post‑close activities, and improving integration processes.
- Administer and enhance the Process Ownership Platform, including onboarding and training process owners and facilitating forums.
- Partner with internal teams (e.g., R&D, RA, Operations, Quality) to develop, deploy, and ensure compliance of divisional quality systems.
Requirements
- Bachelor’s in a Degree required; preferably in Engineering, Science or related focus.
- Minimum of 6+ years of professional experience with 1+ years of practical project management experience.
- Demonstrated ability to plan, track, facilitate, and close projects using applicable tools (Gantt, Burn downs, etc.) on time, within budget, and while controlling scope.
- Experience in FDA or Highly regulated environment.
- PMP certification or equivalent.
Benefits
- Bonus eligible
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