Production Manager

QuidelOrtho•Pompano Beach, FL

12d•Onsite

About The Position

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. 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.

Requirements

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.

Nice To Haves

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

Responsibilities

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