Supervisor - CCS Quality Control

Supervisor - CCS Quality Control

Job Locations

US-NY-Rye

Job ID

2025-7655

Category

Technician

Minimum Rate

USD $125,000.00 / Yr.

Maximum Rate

USD $135,000.00 / Yr.

Work Location Type

Physical

Overview

Founded in 1964, New York Blood Center (NYBC) has served the tri-state area for more than 60 years, delivering 500,000 lifesaving blood products annually to 150+ hospitals, EMS and healthcare partners. NYBC is part of New York Blood Center Enterprises (NYBCe), which spans 17+ states and delivers one million blood products to 400+ U.S. hospitals annually. NYBCe additionally delivers cellular therapies, specialty pharmacy, and medical services to 200+ research, academic and biopharmaceutical organizations. NYBCe's Lindsley F. Kimball Research Institute is a leader in hematology and transfusion medicine research, dedicated to the study, prevention, treatment and cure of bloodborne and blood-related diseases. NYBC serves as a vital community lifeline dedicated to helping patients and advancing global public health. To learn more, visit nybc.org. Connect with us on Facebook, X, Instagram, and LinkedIn.

Responsibilities

The Quality Control Supervisor is responsible for coordinating and supervising the daily product QC and environmental testing activities related to cell therapy manufacturing in a GMP and GTP compliant facility. The primary responsibilities of this role are focused on the analytical and / or microbial testing in place to support the manufacturing of aseptically processed cell therapy products. Secondary responsibilities of this role will include providing technical leadership, daily oversight, and subject matter expertise in GXP based testing.

Supervision Exercised :

This position supervises quality control staff in the laboratories and associated cleanrooms as applicable.

This position does not perform or supervise CLIA or NYS CLEP regulated testing.

Provides the analytical and / or microbiological expertise, leadership, and guidance to ensure operations and staff implement appropriate microbial controls to meet regulatory requirements.

Provides expertise to support product dispositions, investigations, risk analyses, and mitigations related to aseptic processing and testing.

Leads investigations for out-of-specification test results, corrective actions, and verification of effectiveness.

Leads collaboration to develop and implement process improvement strategies.

Train, supervise, and mentor personnel to develop a strong team of highly skilled professionals responsible for conducting analytical and / or microbial testing.

Coordinate and maintain proficiency testing in conjunction with the Medical Lab Director for relevant QC testing.

Ensures regulatory and accreditation compliance in conjunction with the lab management including FDA, NYSDOH, AABB, and FACT as applicable.

Oversee the technical transfer, qualification, and validation of QC Analytical test methods.

Support product stability programs including generation of stability protocols, execution of stability testing, and generation of stability reports.

Reviews / audits documentation to ensure processes are performed and documented as directed by standard operating procedures.

Develops, reviews, and / or approves procedures, forms, protocols, and reports in support of manufacturing and testing activities.

Reviews and maintains an adequate supply inventory.

Establish positive working relationships with internal and cross-functional teams.

Participate in Continuing Education activities. Completes hours required by governmental agencies and / or accreditation organizations.

Responsible for appropriate use of laboratory reagents, laboratory equipment and other resources.

Assist in evaluating new technologies, assays, and clinical research protocols.

Assist in conducting data analysis and preparing reports.

Responsible for keeping individual and staff training requirements up to date.

Any related duties as assigned.

Qualifications

Education :

• Bachelor's or higher degree from a program with a major in biology, chemistry, clinical laboratory technology, or the physical sciences.
• Master's degree with 3 years of cGMP experience.

Experience :

Knowledge :

Skills :

Abilities :

Any combination of education, training and experience equivalent to the requirements above that has supplied the necessary knowledge, skills, and experience to perform the essential functions of the job.

For applicants who will perform this position in New York City or Westchester County, the proposed annual salary is $125,000.00p / yr. to $135,000.00p / yr. For applicants who will perform this position outside of New York City or Westchester County, salary will reflect local market rates and be commensurate with the applicant's skills, job-related knowledge, and experience.