Site Quality Director
Job Posting for Site Quality Director at Kindeva Drug Delivery Careers
Kindeva Drug Delivery
Kindeva Drug Delivery is a global pharmaceutical contract developer and manufacturer (CDMO) business. This position is for the Site Quality Director for our Northridge operations. Our Northridge site manufactures and packages pharmaceutical products.
Kindeva is navigating a period of dynamic change and growth as a result of business opportunities in its pipeline and ongoing commercial product manufacture. It partners with global pharmaceutical companies to commercialize products, primarily through inhalation and transdermal delivery technologies. We are looking for a talented Site Quality Director to join our team. The person would lead our Quality team at our Northridge site focused on leading the Site Quality Operations.
Summary of Position:
This role is responsible for the Quality Organization at the Northridge site. This person will play an important role in leading the execution of quality processes in support of the development and manufacture of medicinal drug products.
Primary Job Responsibilities:
This role must maintain strong working relationships cross-functionally with leaders, employees, and external partners across the global enterprise. This position reports to the VP of Quality.
Skills & Experience:
California residents should review our Notice for California Employees and Applicants before applying.
Covid-19:
Safety for our employees and our communities is a key priority for Kindeva Drug Delivery. Kindeva encourages everyone who can get vaccinated to get vaccinated.
Our Covid-19 task force monitors the external environment and will continue to evaluate our policies and procedures.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Kindeva Drug Delivery is a global pharmaceutical contract developer and manufacturer (CDMO) business. This position is for the Site Quality Director for our Northridge operations. Our Northridge site manufactures and packages pharmaceutical products.
Kindeva is navigating a period of dynamic change and growth as a result of business opportunities in its pipeline and ongoing commercial product manufacture. It partners with global pharmaceutical companies to commercialize products, primarily through inhalation and transdermal delivery technologies. We are looking for a talented Site Quality Director to join our team. The person would lead our Quality team at our Northridge site focused on leading the Site Quality Operations.
Summary of Position:
This role is responsible for the Quality Organization at the Northridge site. This person will play an important role in leading the execution of quality processes in support of the development and manufacture of medicinal drug products.
Primary Job Responsibilities:
- Lead the Quality Organization at the Northridge manufacturing site.
- Work closely with customers and internal teams in support of delivering drug products to the market per customer expectations.
- Lead GMP compliance for the site which includes leading both customer and health agency inspections at the site.
- Establish and execute quality practices that are in alignment with global processes to meet both customer and internal requirements that support the required regulatory compliance requirements of our products.
- Responsible for driving continuous improvement and resolving critical & complex incidents that may occur at the sites. These activities should be carried out with cross functional teams, data driven mindset and sustainable improvement methods.
- Member of the Global Quality Leadership team focused on implementing the Kindeva Quality Policy.
- Member of the Northridge Site Leadership focused on executing site operational plans.
This role must maintain strong working relationships cross-functionally with leaders, employees, and external partners across the global enterprise. This position reports to the VP of Quality.
Skills & Experience:
- Bachelor’s degree
- 5 years’ work experience working in a regulated business.
- Excellent interpersonal and organizational skills to interface with internal customers, management, and outside suppliers.
- Works effectively in a cross functional team environment.
- Continuous Improvement mindset.
- Preferred Skills & Experience:
- Bachelor’s or higher degree with a technical background
- Strong quality background that includes management of Health Agency inspections
- Team Leader or direct supervision of a group of professionals
- Strong written and oral communication skills
California residents should review our Notice for California Employees and Applicants before applying.
Covid-19:
Safety for our employees and our communities is a key priority for Kindeva Drug Delivery. Kindeva encourages everyone who can get vaccinated to get vaccinated.
Our Covid-19 task force monitors the external environment and will continue to evaluate our policies and procedures.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Salary.com Estimation for Site Quality Director in Los Angeles, CA
$234,009 to $316,455
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