Minimum 3 years of project management experience, Associate or Bachelor's Degree in biology, science, or med tech.
Key responsabilities:
Directing cross-functional teams to complete project tasks
Interacting with internal and external stakeholders for timely project completion
Advising on project management strategies and supporting other project managers as needed
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Experienced supervisory professional that works under limited direction.
Applies subject matter knowledge in area of project management, with preferred secondary knowledge in regulatory affairs.
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
Primary Responsibilities:
Possesses well-developed skills in directing cross-functional teams to complete tasks necessary for project completion.
Skilled in drafting progress reports, presentations, strategy documents, Statements of Work, etc.
Interacts with internal and external stakeholders to ensure timely completion of timelines, projects, and submissions.
Participates in product planning, implementation of transitioning products, on-market changes, risk management, regulatory strategy, and creative problem solving.
Serves as the point of contact to internal and external stakeholders for the IVDR transition and other regulatory programs.
Advises on project management strategies, including expedited project planning where necessary.
Supports other project managers as required.
Education :
Associate or Bachelors Degree, preferably in biology, science, or med tech
Experience :
Minimum 3 years project management experience; 5 years experience preferred.
Language :
Proficient in English
Required profile
Experience
Level of experience:Senior (5-10 years)
Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
English
Check out the description to know which languages are mandatory.