Regional Quality Systems Mgr

PURPOSE AND SCOPE:

The Regional Quality Systems Manager provides guidance for site development, deployment and maintenance of strategic quality requirements for Distribution Centers within the assigned region of the country.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

• A seasoned, experienced professional with a full understanding of Quality Systems; resolves a wide range of issues in creative ways.
• Assures compliance programs are implemented and maintained at the applicable sites within Distribution Centers.
• Maintains a physical presence at each Distribution Center (DC) within the assigned region a minimum of once per quarter.
• Works with business partners to mitigate compliance risk at responsible manufacturing sites and provide leadership to the Distribution Center organization.
• Proactively identifies risk management and compliance leveraging opportunities and interacts and influences both regulatory authorities and industry organizations in decision-making.
• 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. Makes decisions regarding the applicability of cGMP and ISO regulations to distribution center operations.
• Ensures there is a breadth of quality/compliance expertise in all product platforms or product types within FMCNA and provide compliance advice and coverage for all distribution sites.
• Responsible for the development and maintenance of an active audit program for the performance of required internal and external audits.
• Formulates and influences policy changes and ensures these changes are implemented across all DC sites.
• Provides innovative solutions to cross-functional compliance issues, assuring the solution falls within appropriate regulatory guidance's.
• May advise regulatory agencies or bodies regarding specific programs or processes, when applicable.
• Ensures key Distribution processes are defined, documented and process controls are in place.
• Recommendations continual process improvements and participate in the planning and implementing of process changes within the Distribution Centers.
• May provide assistance to junior level staff with more complex tasks that require a higher level of understanding of functions.
• May escalate issues to supervisor/manager for resolution, as deemed necessary.
• Mentor other staff as applicable.
• Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
• Assist 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.

PHYSICAL DEMANDS AND WORKING CONDITIONS:

• 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.
• May occasionally be required to lift and/or move up to 50 pounds.
• Travel up to 50%.

EDUCATION:

• Bachelor's Degree in Chemistry or related field required, engineering background a plus; Advanced Degree desirable

EXPERIENCE AND REQUIRED SKILLS:

• 5 - 8 years' experience in Quality Assurance, Regulatory Affairs and/or compliance; or a Master's degree with 3 years' experience; or a PhD without experience; or equivalent directly related work experience.
• Strong knowledge of FDA regulatory requirements and of standard quality assurance practices such as ISO 13485
• Professional quality discipline certifications (CQE, CQA, CQM or RAB) desired.
• Thorough technical knowledge of current Good Manufacturing Practices (cGMPs), Good Distribution Practices (GDPs_ and International regulatory requirements.
• Prior supervisor experience required.
• Strong oral and written communication skills.
• Hands-on experience interacting with regulatory authorities required. Experience as a health authority or regulator desirable.
• Detail and goal oriented; must be focused on teamwork and the customer.
• Strong project management skills with the ability to manage multiple projects. Strong prioritization skills.
• Strong technical, business and relations skills.
• Proficient with PCs and Microsoft Office applications.
• Prior knowledge of compliance training required.

Fresenius Medical Care maintains a drug-free workplace in accordance with applicable federal and state laws.

Fresenius Medical Care is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sexual orientation, gender identity, parental status, national origin, age, disability, military service, or other non-merit-based factors