Lead Quality Systems Specialist

PURPOSE AND SCOPE:

Acts as a subject matter expert to support the organization with initial compliance and ongoing preparation, testing, and monitoring of conformance to established quality systems processes and standards for manufacturing and production.

A seasoned, experienced professional with full understanding of quality systems; resolves a wide range of issues in creative ways. Performs high level evaluation of internal controls, communications, risk assessments, and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Trains other staff members Responsible as back-up for manager when manager is not available Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them.

Facilitates internal training on quality assurance requirements, processes, and procedures. May perform audits and risk assessments. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. Normally receives little instruction on day-to-day work and general instructions on new assignments.

Acts as a back-up subject matter expert Provides assistance to lower-level staff with more complex tasks that require a higher level of understanding of functions. Escalates issues to supervisor/manager for resolution, as deemed necessary. Mentors other staff as applicable. Reviews and complies with the Code of Business Conduct and all applicable company policies and procedures, local, state, and federal laws and regulations.

Assists with various projects as assigned by a direct supervisor. Other duties as assigned. Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.

The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The individual will, for the most part, be seated and work at a computer and utilize telephone equipment. Travel may be required, as necessary.

None

Bachelor’s Degree required. Advanced Degree preferred or an equivalent combination of education and experience

6 – 8 years’ related experience or an equivalent combination of education and experience. Highly autonomous. Minimal supervision required. Self-starter with the ability to work well both independently and as part of a small team. Can prioritize tasks accordingly. Very detail-oriented, well organized, and driven to meet deadlines and program goals. Strong verbal and written communication skills. Good computer skills with knowledge of Microsoft Office including Access, email platforms, ERP software, and Microsoft Outlook Ability to work in a high stress environment given the nature and process.

Ability to generate moderately complex spreadsheets with graphs for trending data and presentations. Knowledge and application of metrics and charts for quality system processes. Excellent project prioritization, planning, and management. Corrections and Removals Ensures effective Recall Strategy (includes Customer and internal communications), Recall Tracking, and Recall Termination. Responsible for monthly recall status updates to FDA. Ensures timeliness of invoice payment submissions on outside vendor services.

Back-up keynote speaker to PQTF Monthly meetings on C&R Recalls. Product Safety Committee participant and back-up host. Responsible as back-up for manager when manager is not available Supports FADF, HHA, and Field Action Notification (Safety and Alert) creation activities. Back- up for witnessing, documenting, and coordinating recalled material destructions…