Sr Director, Quality Assurance - Software
Company: Disability Solutions
Location: Boston
Posted on: January 31, 2025
Job Description:
About the Job
The Sr Dir, Quality Assurance is responsible for the design,
development, implementation and maintenance of a compliant and
effective software design & development, risk management, change
management, and software lifecycle management system. This includes
partnering with the Technology and IT organizations to ensure
processes are compliance, dynamic and agile to meet the demands of
the business. The incumbent is responsible for identifying and
securing needed resources to ensure effectiveness.
Key Responsibilities
- Partner with FMI Senior Management to facilitate quality and
compliance activities related to software development and lifecycle
activities. Partner with cross functional team members to drive
quality improvement activities and lean principles within the
organization.--
- Ensure that software design and development practices
incorporate current global regulatory compliance expectations as
required by IEC 62304, ISO 13485, ISO 14971, and other applicable
regulations/standards.
- Responsible for directing the efforts associated with QA
functions related to software quality engineering, software change
management and the software development lifecycle.
- Lead software quality engineering and technical support for
product realization and market release and lifecycle
management.
- Oversite and leadership of quality events related to software
products.
- Responsible for the ownership, harmonization and ongoing
management of software development SOPs and Work Instructions
working with key stakeholders to ensure efficient and effective
procedures/processes.
- Ensure software development projects are resourced and
supported through the design and development process.
- Assist in establishing robust programs to ensure new software
products/solutions are designed and compliant to all applicable
regulations.
- Ensure software for FMI used in the medical device and
laboratory space are appropriately validated for their intended
use.
- Partner with appropriate Technology and IT partners to drive
CAPAs to closure in a timely manner.
- Manage the process for software risk management activities
throughout the software lifecycle.
- Function as the Subject Matter Expert on software design and
development and risk management matters.
- Lead software design transfer/deployment activities to ensure
success of new designs in manufacturing.
- Function as the quality champion for Technology/IT projects
impacting the quality assurance function and/or systems.
- Design, establish, implement and maintain a resource plan that
fully supports the needs of the business to support growth
initiatives.
- Other duties as assigned.
Qualifications
Basic Qualifications
- Bachelor's degree in science, engineering or related field and
12+ years of experience working in the medical device industry;
OR,
- Master's degree and 10+ years of experience working in the
medical device industry
- 5+ years of experience managing Software Quality Assurance in
the Medical Device Industry
Preferred Qualifications
- Master's or Advance Degree in science, engineering or related
field
- Experience with In Vitro Diagnostics
- Extensive knowledge of IEC 62304, ISO 13485, FDA CFR 820, IVDR,
ISO 14971 and emerging standards and regulations
- Continuous improvement experience preferred (6 Sigma, Lean,
GreenBelt/Black Belt)
- Excellent team building and leadership skills that motivate
team members to drive projects to a successful conclusion; must be
able to manage and lead without direct authority
- Excellent judgment skills in order to provide strong guidance
and counsel to the site and line staff
- Time management skills for oneself and of others on a team,
ability to drive projects to scheduled completion
- Strong data analysis skills
- Superior interpersonal, verbal and written communication
skills--
- Exceptional organizational, negotiation, and problem-solving
skills
- Demonstrated ability to work in a matrixed organizational
structure, developing strong relationships with all levels of
management
- Understanding of HIPAA and importance of patient data
privacy
- Commitment to reflect FMI's values: passion, patients,
innovation and collaboration.
#LI-Hybrid
Keywords: Disability Solutions, Newton , Sr Director, Quality Assurance - Software, Executive , Boston, Massachusetts
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