Quality Systems Specialist LaboratoryLocation: Greater Atlanta Area
About Our Client:
Our client is a highly respected organization within the manufacturing industry, recognized for delivering innovative, high-quality solutions to a global customer base. They are committed to operational excellence and continuous improvement, leveraging advanced technologies to remain competitive and forward-thinking. With a collaborative, performance-driven culture, the company empowers employees to take ownership of their work while supporting professional growth and long-term career development. This is an excellent opportunity to join a stable, reputable organization that values integrity, quality, and its people.
Key Responsibilities:- Coordinating and maintaining a robust, standardized, and effective laboratory Quality System aligned with regulatory requirements and Quality Agreements.
- Serving as the local Subject Matter Expert (SME) for Quality Systems, ensuring compliance and providing guidance across the organization.
- Ensuring laboratory processes, procedures, and organizational practices meet business needs and regulatory expectations.
- Promoting a culture of quality and compliance, increasing awareness and understanding of ISO, QSR, and related regulations.
- Leading the implementation and execution of Quality System processes to achieve performance and compliance objectives.
- Supporting and maintaining document control and record management processes.
- Leading the local implementation of annual Quality Objectives and Key Business Drivers for laboratory operations.
- Participating in and facilitating Quality Leadership meetings, ensuring actions are completed and quality initiatives progress effectively.
- Utilizing metrics and performance reporting to monitor effectiveness, identify improvement opportunities, and deliver business value.
- Driving continuous improvement initiatives through lessons learned, best practices, and proactive problem prevention strategies.
Qualifications: - Bachelors degree in Chemistry, Microbiology, or related laboratory sciences.
- At least 2 years of laboratory experience within a regulated industry.
- Strong knowledge of ISO 13485, ISO 17025, and 21 CFR Part 820 regulations.
- Proficiency with laboratory systems, document control, and metrics reporting.
- Excellent organizational, analytical, and process improvement skills.
- Effective communication and interpersonal abilities.
- Project leadership experience and a proactive approach to problem-solving.
- Experience in medical device or pharmaceutical industries.
- ASQ Certified Quality Engineer or Quality Auditor credential.
- NO C2C CANDIDATES
Interested Candidates please apply on our website at https://jobs.jblresources.com.
For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com.
JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.
**JBL is an Equal Opportunity Employer and E-Verify Company