Production Manager

Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease. We are currently developing a new class of TAVR designed to mimic the performance of a healthy aortic valve. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team.

We are seeking an experienced Production Manager to lead manufacturing operations supporting the production of our biomimetic DurAVR® transcatheter heart valve and related cardiovascular technologies. This role is responsible for overseeing daily production operations, developing high-performing manufacturing teams, and ensuring products are manufactured safely, efficiently, and in full compliance with regulatory and quality requirements. The Production Manager will partner closely with Quality, Engineering, Supply Chain, and other cross-functional teams to drive operational excellence while supporting scale-up as the organization prepares for commercial readiness.

At Anteris Technologies, you’ll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies — and help build the organizational foundation supporting that impact.

Primary Duties and Responsibilities

• Lead day-to-day manufacturing operations, ensuring production targets, quality standards, and delivery commitments are met.


• Build, coach, and develop a high-performing production team, fostering a culture of accountability, safety, collaboration, and continuous improvement.


• Ensure manufacturing activities comply with applicable regulatory requirements, including FDA Quality System Regulation (QSR), ISO standards, and internal quality systems.


• Partner with Quality Assurance to maintain compliance, support investigations, and ensure adherence to standard operating procedures and documentation practices.


• Drive continuous improvement initiatives to enhance efficiency, yield, and product quality using Lean, Six Sigma, or similar operational excellence methodologies.


• Coordinate production schedules and resource planning to support demand forecasts, inventory targets, and operational priorities.


• Oversee the effective use of labor, equipment, and materials to optimize productivity and minimize waste.


• Monitor key production metrics and operational performance indicators, preparing reports and implementing actions to improve outcomes.


• Collaborate with Engineering, Supply Chain, Quality, and R&D teams to support process transfers, manufacturing scale-up, and product lifecycle management.


• Ensure production staff are trained and qualified on applicable procedures, work instructions, and regulatory requirements.


• Promote a safe working environment by ensuring compliance with all safety policies, procedures, and regulatory guidelines.

Skills, Knowledge, Experience & Qualifications

Required Qualifications:

• High school diploma or GED required; additional technical training, certifications, degrees, or equivalent manufacturing leadership experience strongly valued.


• 7+ years of experience in a regulated manufacturing environment, preferably in medical device, biotechnology, or another highly regulated industry.


• 3+ years of leadership experience supervising or managing production teams.


• Strong understanding of manufacturing processes, quality systems, and regulatory requirements.


• Demonstrated ability to lead teams, manage priorities, and drive operational performance in a fast-paced environment.


• Strong problem-solving, analytical, and decision-making skills.


• Excellent communication and collaboration skills with the ability to work cross-functionally.


• Proficiency with standard business systems and manufacturing tools, including ERP or manufacturing execution systems.

Preferred Qualifications:

• Experience supporting cardiovascular or implantable medical device manufacturing.


• Experience in cleanroom or highly controlled manufacturing environments.


• Lean Manufacturing, Six Sigma, or other operational excellence certifications.


• Experience supporting manufacturing scale-up or commercialization readiness.

Compensation

Target base salary range: $100,000 - $125,000, plus annual incentive opportunity and equity eligibility.  Final compensation will be based on experience and alignment with role requirements.  Unfortunately, we are unable to sponsor work visas (OPT, H1B, etc.) at this time.

What We Offer:

• Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.


• Inclusive Team Environment – a collaborative and dynamic work environment with a culture of innovation and excellence.


• Competitive compensation package, including salary, performance-based bonuses, and stock options.


• Career development opportunities and a chance to be part of a growing company that values its employees.

Health and Wellness Offerings:

• Medical, Dental, and Vision Plans


• Flexible Spending Account (FSA)


• 401k + Company Match


• Life, AD&D, Short Term and Long-Term Disability Insurance


• Bonus Plan Eligibility


• Employee Equity Program


• Paid Holidays & Vacation


• Employee Assistance Program

Note: We may require proof of COVID-19 vaccination to comply with the state, local municipality, and/or travel regulations.

Anteris Technologies recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.