Senior Production Manager

CorDx

• $110K — $130K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Minimum of 10 years in production, manufacturing, or operations management.
  • At least 5 years of leadership experience, effectively managing and developing teams.
  • Experience managing teams of 5 or more in a production setting.
  • Stable employment history with an average tenure of at least 30 months per role.
  • Preferred experience in life sciences or in vitro diagnostics (IVD) manufacturing.
  • Relevant certifications in production or operations management (e.g., Six Sigma, PMP, CPIM) are highly desirable.
  • Demonstrated experience in scaling operations and implementing process improvements.

Responsibilities

  • Manage daily manufacturing operations, ensuring production schedules meet high-quality standards.
  • Ensure compliance with ISO 13485 and regulatory requirements for medical device production.
  • Collaborate with Quality Assurance to implement Good Manufacturing Practices and continuous improvement initiatives.
  • Align documentation and production procedures with FDA and ISO 13485 guidelines.
  • Supervise and mentor production staff, promoting safety, accountability, and professional development.
  • Utilize Lean and Six Sigma techniques to enhance efficiency and reduce waste.
  • Oversee maintenance and validation of equipment, ensuring compliance with quality and safety standards.
  • Coordinate with procurement and logistics teams to optimize material availability and minimize downtime.

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.
Full Job Description
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.

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