CorDx
About Us
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.
Job Title : Senior Production Manager
Location : Alpharetta, GA (On-site)
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. Responsibilities Production Oversight:
Manage daily manufacturing operations, ensuring production schedules are met while maintaining high-quality standards. •
ISO 13485 Compliance:
Ensure manufacturing processes comply with
ISO 13485
and regulatory requirements for medical device production. •
Quality & Process Improvement:
Work closely with Quality Assurance teams to implement and maintain
Good Manufacturing Practices (GMP)
and
continuous improvement initiatives . •
Regulatory Compliance:
Ensure documentation, production procedures, and risk management align with
FDA and ISO 13485
guidelines. •
Team Leadership:
Supervise and mentor production staff, fostering a culture of safety, accountability, and professional growth. •
Lean Manufacturing:
Utilize
Lean, Six Sigma, and other process optimization techniques
to enhance efficiency, reduce waste, and improve productivity. •
Equipment & Maintenance:
Oversee the maintenance and validation of production equipment to ensure compliance with quality and safety standards. •
Supply Chain Coordination:
Collaborate with procurement, logistics, and engineering teams to optimize material availability and minimize downtime. •
Root Cause Analysis:
Investigate production issues, implement corrective/preventive actions (CAPAs), and ensure compliance with
ISO 13485 risk management
principles. 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. 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. Equal Opportunity Statement:
We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.
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. Responsibilities Production Oversight:
Manage daily manufacturing operations, ensuring production schedules are met while maintaining high-quality standards. •
ISO 13485 Compliance:
Ensure manufacturing processes comply with
ISO 13485
and regulatory requirements for medical device production. •
Quality & Process Improvement:
Work closely with Quality Assurance teams to implement and maintain
Good Manufacturing Practices (GMP)
and
continuous improvement initiatives . •
Regulatory Compliance:
Ensure documentation, production procedures, and risk management align with
FDA and ISO 13485
guidelines. •
Team Leadership:
Supervise and mentor production staff, fostering a culture of safety, accountability, and professional growth. •
Lean Manufacturing:
Utilize
Lean, Six Sigma, and other process optimization techniques
to enhance efficiency, reduce waste, and improve productivity. •
Equipment & Maintenance:
Oversee the maintenance and validation of production equipment to ensure compliance with quality and safety standards. •
Supply Chain Coordination:
Collaborate with procurement, logistics, and engineering teams to optimize material availability and minimize downtime. •
Root Cause Analysis:
Investigate production issues, implement corrective/preventive actions (CAPAs), and ensure compliance with
ISO 13485 risk management
principles. 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. 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. Equal Opportunity Statement:
We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.