QuidelOrtho
Site Director, Operations
QuidelOrtho, Pompano Beach, Florida, us, 33072
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 Site Director, Operations. The Site Director, Operations will be Fully responsible for the business operations of Pompano Manufacturing Site to ensure that product production continues to comply with business strategies and meet the requirements of medical device regulations and customer needs.This is an onsite position in Pompano Beach, FL.The Responsibilities
Direct all site-based activities across all direct and support functions at Pompano Manufacturing site for all lines of business to achieve or exceed customer expectations in line with the annual operating plan
Establish the vision and direction for Manufacturing Operations and associated departments in line with the overall company and site strategic goals.
Deliver all project justifications and action implementation plans for NPI, Tech Transfer and Capital Expenditure activities as outlined and agreed in the annual operating plan
Ensure that all Manufacturing Operations under span of responsibility are carried out in compliance with the Quality Management System and all regulations and laws governing business and quality operations (QSR/GMP, ISO, etc.).
Champion the QuidelOrtho Improvement Culture (QIC) and execute the annual QIC roadmap laid out to promote the QIC principles and drive site improvement.
Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Ensure Health, Safety, Environment, and GMP programs are maintained. Ensure the facility is operated at inspection ready condition at all times to include leading emergency management actions and involvement and drive for Business Continuity
Develop talent through personal example and employee development strategies while operating robust succession planning processes to develop next generation leaders and capabilities.
The Individual
Required:Familiar with the requirements of medical device production laws and regulations.
At least 7 years working experience in senior management positions of Class II/III medical device production, preferably in IVD industry.
Ability of strategic planning of medical device production.
Excellent leadership and team management skills.
Good public relations, interpersonal communication and language skills.
Strong ability to resist pressure and promote coordination
The Key Working Relationships
Internal:Global Operation, Quality, Finance, etc.External:SuppliersThe Work Environment
The work environment characteristics are representative of an office, laboratory and manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines.Salary Transparency
The salary range for this position takes into account a wide range of factors including: education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, its is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on that facts and circumstances of each case. A salary range for this position is $128,000 - $218,000 .QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time) and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.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.#LI-HF1
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 Site Director, Operations. The Site Director, Operations will be Fully responsible for the business operations of Pompano Manufacturing Site to ensure that product production continues to comply with business strategies and meet the requirements of medical device regulations and customer needs.This is an onsite position in Pompano Beach, FL.The Responsibilities
Direct all site-based activities across all direct and support functions at Pompano Manufacturing site for all lines of business to achieve or exceed customer expectations in line with the annual operating plan
Establish the vision and direction for Manufacturing Operations and associated departments in line with the overall company and site strategic goals.
Deliver all project justifications and action implementation plans for NPI, Tech Transfer and Capital Expenditure activities as outlined and agreed in the annual operating plan
Ensure that all Manufacturing Operations under span of responsibility are carried out in compliance with the Quality Management System and all regulations and laws governing business and quality operations (QSR/GMP, ISO, etc.).
Champion the QuidelOrtho Improvement Culture (QIC) and execute the annual QIC roadmap laid out to promote the QIC principles and drive site improvement.
Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Ensure Health, Safety, Environment, and GMP programs are maintained. Ensure the facility is operated at inspection ready condition at all times to include leading emergency management actions and involvement and drive for Business Continuity
Develop talent through personal example and employee development strategies while operating robust succession planning processes to develop next generation leaders and capabilities.
The Individual
Required:Familiar with the requirements of medical device production laws and regulations.
At least 7 years working experience in senior management positions of Class II/III medical device production, preferably in IVD industry.
Ability of strategic planning of medical device production.
Excellent leadership and team management skills.
Good public relations, interpersonal communication and language skills.
Strong ability to resist pressure and promote coordination
The Key Working Relationships
Internal:Global Operation, Quality, Finance, etc.External:SuppliersThe Work Environment
The work environment characteristics are representative of an office, laboratory and manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines.Salary Transparency
The salary range for this position takes into account a wide range of factors including: education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, its is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on that facts and circumstances of each case. A salary range for this position is $128,000 - $218,000 .QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time) and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.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.#LI-HF1