Job Title: Senior Quality Analyst/Engineer
Job Type: Contract
Job Location: Madison, WI
Summary
The Senior Quality Analyst/Engineer is responsible for assuring that activities, processes, and product related to managing the processes of CAPA, Change Management, investigations, deviations, Quality Management Review, Audit coordination, and metrics for the Madison facility This position will have a wide range of tasks which may include Quality System improvement initiatives, data maintenance, trending and reporting, deviation investigation, internal/external auditing, and direct involvement and collaboration with the Regulatory Affairs, Operations, Technical Operations, Engineering, and Materials Management groups to drive quality culture.
Principal Responsibilities
Develop and maintain quality system processes, including metrics reporting and tracking
Manage CAPA initiation, review, surveillance, and reporting
Facilitate the site Quality Management reviews
Facilitate and lead the site Change Management process
Support and lead root cause analyses through cross functional team involvement
Leading Good Documentation Practice training and Quality on the Floor coordination and performance
Interpret and properly apply all applicable regulatory requirements
Coordinate and provide direct support for facility audits by internal and external entities
Manage data collection and reporting when product recalls are required
Perform trending of Quality Systems to support FDA and Management reviews
Improve quality culture through site initiatives and improve existing procedures to better align with regulatory requirements
Review and approval of procedures, protocols, reports, etc., as required.
Department specific/Non-essential responsibilities:
Filing and management of documentation when required
Supporting other Quality System Functions
This role may be required to lead personnel (inside and outside) the Quality organization in support of the business need
Minimum Requirements
Experience / Skills:
Bachelor s, or higher, degree in science/technology program preferred
5+ years of Quality Assurance experience in a cGMP Quality Assurance/Compliant environment (medical devices preferred)
Effective communication, coaching/mentoring, and presenting skills
Ability to manage change
Self-motivated
Independent and sound decision making capabilities
Project management to deliver on time results
Leadership skills / Emotional Intelligence
Ability to utilize statistics at a moderate level for trending and interpretation of statistical data
Competencies:
Proficient with Microsoft Office tools, especially Excel, Word and Powerpoint
Technical writing
Statistical analysis - Minitab or other software equivalent, preferred.
Organizational Relationship/Scope:
The Senior Quality Analyst collaborates closely with Manufacturing, Quality Control, Engineering, Facilities, Materials Management, Regulatory Affairs, and Process Development. The individual must be able to perform in a fast-paced environment with strict adherence to timelines. The position is onsite during normal working hours M-F, but may be required to work extra hours or on weekends or holidays in order to support business needs.
Working Conditions:
The Senior Quality Analyst will mainly work in an office environment. Domestic and international travel will be required on a limited basis.
Never miss an opportunity! Create an alert based on the job you applied for.
