Senior Production Manager

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.

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.
• 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.
• Candidates should have worked at no more than seven companies.
• Proven experience in scaling production operations, improving efficiency, and implementing process improvements.

Qualifications

• Stable employment history.

Skills

• Strong leadership and team management skills.
• Experience with Lean, Six Sigma, and other process optimization techniques.
• Knowledge of ISO 13485 and regulatory requirements for medical device production.
• Ability to work in a regulated environment.

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.

Pay

Competitive compensation package.

Schedule

On-site position in Alpharetta, GA.