Production Manager

The Opportunity

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic.

Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.

The Role

As we continue to grow as QuidelOrtho we are seeking a Production Manager to work in our manufacturing facility in Pompano Beach Florida. The Production Manager is responsible for overseeing the end-to-end production processes to ensure compliance with regulatory standards, operational efficiency, and product quality. This role demands strategic leadership, cross-functional coordination, and continuous improvement across manufacturing operations.

This position will be located onsite in Pompano Beach, FL.

The Responsibilities

• Production Oversight: Direct all site-based activities across manufacturing and support functions to meet customer expectations and business goals.
• Regulatory Compliance: Ensure operations comply with QSR/GMP,FDA CBER, ISO standards, and other relevant medical device regulations.
• Strategic Planning: Develop and execute plans for new product introductions (NPI), technology transfers, and capital expenditures.
• Quality & Safety: Maintain inspection-ready conditions, lead emergency management actions, and uphold Health, Safety, and Environmental standards.
• Team Leadership: Build and manage high-performing teams, conduct performance reviews, and lead succession planning efforts.
• Perform other work-related duties as assigned.

The Individual

Required:

• Minimum Associate Degree or equivalent in a relevant subject.
• Minimum 5 years of experience in a manufacturing environment, with at least 2 years in a supervisory or lead role, preferably in medical device production.
• Strong understanding of production processes, regulatory requirements, and quality systems.
• Effective communication and interpersonal skills for team direction and stakeholder engagement.
• Ability to manage routine operational challenges, prioritize tasks, and maintain productivity.
• Commitment to upholding health, safety, and environmental standards.

Preferred:

• Experience with SAP or similar ERP systems
• Data analysis and basic process optimization
• Basic project management skills
• Continuous improvement mindset

The Key Working Relationships

Internal Partners: Production Manager, Quality, HSE, Planning, Raw Materials

External Partners: Suppliers, Auditors, and regulatory Inspectors

The Work Environment

Work is primarily conducted in office and manufacturing settings, with regular movement between production areas. The role may involve exposure to controlled chemicals and requires adherence to safety protocols. Flexible working hours may be necessary to meet production demands; occasional overtime may be required.

Physical Demands

Mainly office-based with frequent movement to and from production areas. May involve standing for extended periods and occasional lifting of materials in compliance with safety guidelines.

Equal Employment Opportunity

QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com