Site Head of Quality at Trinity Biotech Site Head of Quality at Trinity Biotech in Jamestown, New York Posted in 1 day ago.

Type:

full-time

Job Title:

Site Head of Quality Location:

Jamestown, NY (on site)

Department:

Quality Reports To:

VP QARA Position Type:

Full-Time Job Summary:

The Site Head of Quality will be responsible for overseeing the development, implementation, and maintenance of our Quality Management System (QMS) to ensure compliance with industry standards and regulatory requirements. This role is critical in driving continuous improvement initiatives and ensuring the highest quality standards for our medical devices.

Key Responsibilities:

Acts as Management Representative and Person Responsible for Regulatory Compliance (PRRC) Develop, implement, and manage the Quality Management System (QMS) in accordance with

ISO 13485, FDA 21 CFR

Part 820, and other relevant regulations and standards. Lead and manage the Quality Assurance team, providing guidance, training, and performance evaluations. Effectively manage external suppliers and distributors. Establish quality objectives and key performance indicators (KPIs) to monitor and improve product and process quality. Oversee internal and external audit programs, ensuring compliance with regulatory requirements and driving corrective and preventive actions (CAPA). Collaborate with cross-functional teams, including R D, manufacturing, and regulatory affairs, to ensure quality considerations are integrated into all stages of product development and production. Drive continuous improvement initiatives using quality tools and methodologies such as Six Sigma, Lean, and root cause analysis. Manage customer complaints and feedback, ensuring timely and effective resolution of quality issues. Prepare and present quality reports to senior management, highlighting trends, risks, and opportunities for improvement. Ensure proper documentation and control of quality records in compliance with regulatory and company requirements. Stay current with industry trends, regulatory changes, and best practices to ensure ongoing compliance and improvement.

Qualifications:

Bachelor's degree in Quality Assurance, Engineering, Life Sciences, or a related field. 5+ years of experience in a quality management role, preferably within the medical device industry. In-depth knowledge of QMS standards and regulatory requirements, including ISO 13485 and

FDA 21 CFR

Part 820. Proven leadership and team management skills. Strong analytical and problem-solving abilities with experience in root cause analysis and CAPA. Proficiency in statistical analysis tools and software (e.g., Minitab) Excellent verbal and written communication skills. Strong organizational skills and attention to detail. Certification in quality management (e.g., ASQ Certified Quality Manager, Six Sigma) is a plus.