We are currently looking to fill an Associate Director, Material and Supplier Quality position. This position leads a department responsible for material and supplier quality operations and oversight globally for Regeneron. Responsible for providing professional expertise and leadership within the supplier and material quality function. Proactively identify and implement industry standard methodologies for GMP across this area, as well as, work with Supply Chain, Procurement and Quality Control to ensure compliance in this area. Represents MSQ function in FDA and other regulatory inspections.
The work location is onsite at Regeneron's Rensselaer, NY facility - not a remote based opportunity.
In this role, a typical day might include the following:
Defines and implements quality standards, systems, and metrics for clinical and commercial operations.
Organizes departmental resources to meet goals and timings, coordinates prioritization of activities with area management.
Performs compliance monitoring of area operations, including trending of failures and evaluating efficiency of corrective actions.
Reviews customer and partner requirements and implements required processes, as needed, to meet expectations regarding Quality.
Participates in preparation for and execution of regulatory and customer audits, ensures observations are addressed and completed on schedule.
Responsible for all aspects of material and supplier quality including review and approval of the following types of documents.
Interviews, hires, orients, and trains incoming personnel.
Develops and leads departmental budget, contracts, and schedules.
Ensures safety and operational standards are maintained.
This role may be for you if you:
Are knowledgeable in industry practices and regulations
Have detailed knowledge of Material and Supplier quality
Excel in a quality driven organization
Have an understanding of biologics manufacturing operations
To be considered for this role you must hold a Bachelor’s degree in life sciences or related field and the following amount of experience in a pharmaceutical/biologics manufacturing environment for each level:
5+ years of experience in a managerial position is preferred. May substitute proven experience for education requirement.
Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.
Salary Range (annually)
$119,000.00 - $227,200.00