Supervisor, Quality Control

Don’t just work somewhere, join Brasseler and be a valued team member of a world-class health care organization!

Our Culture:
Provides a safe and welcoming environment where team members can balance their lives and develop their careers. All people and experiences are valued and respected. Different perspectives are encouraged and lead to better results. This makes us who we are and enables us to be a world-class healthcare organization. All who join us are accountable to this charge.

Our Philosophy:

Quality products sold with integrity has been the hallmark of Brasseler USA from the beginning. Brasseler USA’s strong reputation of providing high quality, clinician endorsed and innovative dental and medical instrumentation nationally has spanned over 40 years. We have been offering a full-range of products made in the USA since 1976. Many of our products are manufactured at our headquarters in Savannah, GA.

Explore our career opportunities below to learn more.

This position is responsible for responsible for the coordination of activities for TSMs engaged in inspecting incoming materials, components, and finished products to ensure they are meeting the quality standards and customer specifications.  This position will lead the training of the Quality Control staff in the identification and correction of potential inspection non-conformances. 

KEY RESPONSIBILITIES: 

• Supervise daily activities of quality control staff
• Oversee and coordinate daily prioritization of QC testing, including scheduling of staff and equipment productivity assessments.
• Lead and direct activities and resources of the quality control department to meet company objective of producing highest quality product within established budget.
• Ensure product is manufactured in accordance with established practices, procedures, to meet customer/contractual obligations and in compliance with regulatory codes and standards.
• Continuous improvement to maximize product quality and minimize costs.
• Participate on teams as the Quality Control liaison as required.
• Provide feedback and evaluations as needed
• Review records and documents for completeness and compliance with Quality System Requirements and ISO requirements.
• Train staff in Quality Control principles.
• Support the Corrective Action program with hands on ownership for investigation and resolution of issues.
• Manage the Material Review Board for the assessment and disposition of non-conforming materials and closure of Non-conformance and Deviation Reports.
• Conduct process quality measurements/evaluations 
• Assist with monitoring, analyzing and reporting trends in key quality metrics.
• Ensure department timelines are met.

SPECIFIC KNOWLEDGE & SKILLS:

• Relevant experience in the medical device industry is required.
• Familiarity with FDA medical device regulations and ISO 13485 is required.
• Experience in QA support of automated medical device manufacturing.
• Experience with 3D Printing and Thermoforming a plus. 
• Experience in Process Validations (IQ, OQ, PQ) 
• Ability to read and interpret general technical/quality procedures and quality system regulations.
• Ability to create reports, business correspondence.
• Ability to effectively present information and respond to questions verbally, in writing, and in group presentations
• Must be skilled in Microsoft Word, Excel, Outlook, and Power Point 

GENERAL SKILLS & COMPETENCIES:

• Good management skills and ability to motivate teams
• Good verbal and written communication skills and ability to resolve disputes effectively
• Good presentation and public speaking skills
• Good decision making, analysis and problem-solving skills with ability to multi-task
• Ability to learn applicable computer systems and other business required competencies
• Understand financial information that impacts department
• Ability to plan and coordinate successful projects
• Communicate effectively with team(s)

MINIMUM WORK EXPERIENCE:

Typically 4 or more years of related support experience; 3 or more years of management experience.

PREFERRED EDUCATION:

Typically a Bachelor's Degree or global equivalent in related discipline.

TRAVEL / PHYSICAL DEMANDS:

Travel typically less than 10%. Office environment. No special physical demands required.

For more information about career opportunities at Henry Schein, please visit our website at: www.henryschein.com/careers

Benefits available include: Medical, Dental and Vision Coverage, 401K Plan with Company Match, Generous Time Off, Paid Parental Leave, Income Protection, Work Life Assistance Program, Flexible Spending Accounts, Educational Benefits, Worldwide Scholarship Program and Volunteer Opportunities.

*Benefits may vary by location or status.

Henry Schein is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.