Sr. Manager QA Drug Product (Filling)
$126.3k - $206.1kRegeneron Pharmaceuticals, Inc
Regeneron is currently seeking a Sr Manager Quality Assurance to join our internal QA Drug Product Manufacturing team. This role is responsible for quality floor oversight of the filling (i.e. equipment prep, formulation, and filling) operations for SA12. As a Sr. Manager QA, a typical day might include the following: Provide leadership to multiple teams under your supervision, including being responsible for Quality oversight of all equipment prep, formulation, and filling (multiple lines) Responsible for programs that support the department, for example: area walkthroughs Support development and growth of team, including your people leaders Leadership point of contact for escalation of events, process updates, etc. This role might be for you if you have: Proven leadership in cGMP environments, including experience speaking and preparing for regulatory inspections and audits. Strong collaboration and communication cross-functionally Ability to think critically, and continuously improve processes Ability to lead a department through a fast-paced and dynamic environment Gowning and Environment Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire Salary Range (annually): $126,300.00 - $206,100.00. 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. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. #J-18808-Ljbffr Regeneron Pharmaceuticals, Inc
- Regeneron is seeking a Sr Manager Quality Assurance to oversee QA operations for drug product manufacturing in East Greenbush, NY. This role involves leading teams and maintaining quality standards across all filling operations. Candidates should have at least 8 years in...Senior
$126.3k - $206.1k
Regeneron is currently seeking a Sr Manager Quality Assurance to join our internal QA Drug Product Manufacturing team. This role is responsible for quality floor oversight of the filling, equipment prep, formulation, and filling operations for SA12. Typical day and responsibilities...SeniorMonday to Friday$126.3k - $206.1k
Regeneron is currently seeking a Sr Manager Quality Assurance to join our internal QA Drug Product Manufacturing team. This role is responsible for quality floor oversight of the filling (i.e. equipment prep, formulation, and filling) operations for SA12. Responsibilities...SeniorMonday to Friday- Regeneron is seeking a Sr Manager Quality Assurance to lead the QA Drug Product Manufacturing team during filling, formulation, and related equipment prep. This role drives quality oversight and ensures compliance across multiple lines. You will mentor and develop a high...Senior
$126.3k - $206.1k
Regeneron Pharmaceuticals, Inc is seeking a Sr Manager Quality Assurance in East Greenbush, NY, responsible for quality oversight in filling operations. You will lead multiple teams, ensuring compliance with cGMP regulations while supporting team development. Ideal candidates...Senior- Regeneron is seeking a Principal Quality Assurance (QA) Specialist/Reviewer to support our Fill Finish facility in Rensselaer, New York. In this role,... ...relevant experience, and a strong background in sterile drug product manufacturing. Join us to make a difference by...Senior
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$92.2k - $206.1k
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Regeneron in the Town of East Greenbush seeks a Principal QA Validation Specialist to lead its Quality Assurance department. The role involves managing the utilities and EMPQ team for the fill-finish facility, ensuring compliance with regulatory standards and leading qualifications...- ...Senior Manager, Medical Device Quality Assurance (QA) Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our... ...oversight across two critical functions: Combination Products Sustaining Engineering and Compliance. The position will...SeniorContract workMonday to Friday
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...Principal Quality Assurance (QA) Specialist/Reviewer to support our Fill Finish facility. In this... ...with multiple levels of management Reviews primary data... ...matter Monitors production processes and quality systems... ...Experience with sterile drug product manufacturing, fill...Monday to Friday- Regeneron in Rensselaer, New York, is looking for a Senior Drug Product Manufacturing Sciences and Technology Specialist to support process validation and technology transfer in biopharmaceutical production. This role involves ensuring operational consistency, troubleshooting...Senior
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- Regeneron Pharmaceuticals, Inc is hiring a Principal QA Material Supplier Specialist to manage supplier-initiated changes to GMP materials in East Greenbush... ...Supplier Change Notifications, ensuring compliance and product quality. Candidates should possess a Bachelor’s degree...
- ...years of experience and a degree in Life Sciences or Engineering, you will work closely with teams to uphold high quality assurance standards in the drug manufacturing process. This position emphasizes collaboration and commitment to quality. #J-18808-Ljbffr Regeneron
- Regeneron seeks a Senior Drug Product MSAT Specialist to join the Process Science Drug Product Engineering team, supporting equipment qualification, process validation, tech transfer, and cGMP start-up for internal or external manufacturing sites. The role provides on-...Senior
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