Reporting to a Senior Manager within the Tissue Technology Program Management Organization, this position is responsible for leading cross-functional teams in the successful planning, direction and execution of one or more product lifecycle projects including new product introductions, strategic commercial programs, product pipeline programs, and process technology programs. This person will ensure clear communications with stakeholders and partners, as well as, participate in organizational issue resolution.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities are to:
- Act as an independent leader of projects working with cross-functional teams
- Establish project objectives and work plans including budgets and resource requirements. Delegate assignments to functional area team members and track key project activities to successful completion
- Ability to drive effective cross-functional team collaboration in an effort to optimize team strengths, while delivering commercialized products that are clear winners. Ensures that customer focused design requirements are at the center of Integra’s decision making process
- Demonstrated ability to proactively identify and resolve product and project risk
- Drives for program success while ensuring consistency and alignment across all functional projects by innovatively overcoming constraints, problems and issues
- Strong emphasis on exceeding customer expectations, while maximizing value to Integra and maintaining FDA/ISO compliance
DESIRED MINIMUM QUALIFICATIONS:
The requirements listed below are representative of the knowledge, skill and/or ability required for his position.
EDUCATION:
- BS Degree in Engineering, Physical or Life Sciences desired.
- PMP Certification preferred
EXPERIENCE:
- 5+ years of experience in product development and/or project management.
- Experience within matrix organizations.
- Experience with medical products preferred.
- Experienced with ISO and FDA quality systems regulations and medical design and development cycles.
