Job summary
Job post source
This job is from a recruiting firm hiring for a separate company.
Job overview
The Quality Specialist role at GlobalMed Logistix involves maintaining the Quality Management System to ensure compliance with FDA and federal regulations in medical device distribution, directly impacting operational quality and regulatory adherence.
Responsibilities and impact
The Quality Specialist is responsible for investigating nonconformances, managing QMS documentation, verifying training completion, collaborating with managers to uphold compliance, and optimizing processes to support regulatory standards and business goals.
Experience and skills
Candidates should have a Bachelor's degree or equivalent experience, at least 1 year in Quality with knowledge of ISO 9001 and 13485, proficiency in Microsoft Office, strong communication skills, and experience in regulated industries is preferred.
Work environment and culture
The role requires adaptability, teamwork, integrity, and a quality-focused mindset within a fast-paced, collaborative environment adhering to strict compliance and continuous improvement.
Company information
GlobalMed Logistix is a leader in medical device distribution with a focus on compliance with FDA and federal regulations, supported by Consultora Partners & Solutions as the recruiting firm.
Job location and travel
The position is located on-site in Norcross, GA, requiring physical activity including lifting up to 50 pounds and navigating a warehouse environment.
Unique job features
The job emphasizes strict adherence to GMP, ISO standards, and involves detailed quality investigations and documentation in a regulated medical device distribution setting.
Company overview
Consultora Partners & Solutions is a company based in Charlotte, NC, specializing in logistics and procurement services. The firm appears to focus on roles such as Logistics Specialists and entry-level procurement positions, indicating its involvement in supply chain management and related corporate solutions. By offering expertise in these areas, the company likely generates revenue through consulting and operational support for businesses seeking to optimize their logistics and procurement processes. Further details about its history or broader scope of services are not provided in the available data.
How to land this job
Position your resume to highlight your familiarity with Quality Management Systems (QMS), nonconformance investigations, and compliance with FDA and GMP regulations, as these are core to the Quality Specialist role at Consultora Partners & Solutions.
Emphasize experience with ISO 9001 and 13485 standards, proficiency in Microsoft Office, and your ability to manage documentation, training logs, and cross-functional collaboration within regulated environments.
Apply through multiple channels including the Consultora Partners & Solutions corporate careers page, LinkedIn job postings, and relevant healthcare or medical device job boards to maximize your application visibility.
Connect with current employees in the Quality or Operations divisions at Consultora Partners & Solutions on LinkedIn, initiating conversations with ice breakers like commenting on recent company quality initiatives or asking about the integration of QMS in daily operations.
Optimize your resume for ATS by incorporating keywords such as 'Quality Management System,' 'nonconformance reports,' 'FDA compliance,' 'ISO 13485,' 'GMP,' and 'training verification' to ensure your resume passes initial automated screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application portals, and find LinkedIn contacts to network with, allowing you to focus your energy on preparing for interviews and skill enhancement.
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