Senior Production Manager

CorDx • Alpharetta, GA

99d

About The Position

CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health. With over 2000 employees across the world serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drug abuse, biomarkers and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare. We are seeking an experienced Senior Production Manager to oversee and optimize manufacturing operations in a regulated environment, ensuring compliance with ISO 13485 standards. The ideal candidate will have a strong background in production management within the medical device or healthcare manufacturing industry, driving efficiency, quality, and continuous improvement while maintaining compliance with regulatory and safety standards.

Requirements

• Minimum of 10 years of experience in production, manufacturing, or operations management.
• At least 5 years of leadership experience, with a proven track record of managing and developing teams.
• Experience overseeing teams of 5 or more direct reports in a manufacturing or production setting.
• Stable employment history, with an average job tenure of at least 30 months per role.
• Industry experience in life sciences, in vitro diagnostics (IVD), or related manufacturing is preferred.
• Relevant certifications in production, operations, or supply chain management (e.g., Six Sigma, PMP, CPIM) are highly desirable.
• Career stability—candidates should have worked at no more than seven companies.
• Proven experience in scaling production operations, improving efficiency, and implementing process improvements.

Responsibilities

• Manage daily manufacturing operations, ensuring production schedules are met while maintaining high-quality standards.
• Ensure manufacturing processes comply with ISO 13485 and regulatory requirements for medical device production.
• Work closely with Quality Assurance teams to implement and maintain Good Manufacturing Practices (GMP) and continuous improvement initiatives.
• Ensure documentation, production procedures, and risk management align with FDA and ISO 13485 guidelines.
• Supervise and mentor production staff, fostering a culture of safety, accountability, and professional growth.
• Utilize Lean, Six Sigma, and other process optimization techniques to enhance efficiency, reduce waste, and improve productivity.
• Oversee the maintenance and validation of production equipment to ensure compliance with quality and safety standards.
• Collaborate with procurement, logistics, and engineering teams to optimize material availability and minimize downtime.
• Investigate production issues, implement corrective/preventive actions (CAPAs), and ensure compliance with ISO 13485 risk management principles.

Benefits

• Highly competitive compensation package.
• Comprehensive medical, dental, and vision insurance.
• 401(k) plan with generous company contributions.
• Flexible paid time off (PTO) policy.
• Additional substantial benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Number of Employees: 1,001-5,000 employees