GMP Quality Control Scientist ; 2nd Shift

Andelyn Biosciences is a biopharmaceutical Contract Development and Manufacturing Organization (CDMO) that specializes in advancing novel gene therapies from concept to commercialization.

Located in
Columbus, OH
, the company operates out of the Andelyn Corporate Center (ACC) for clinical and commercial cGMP manufacturing of viral vectors and plasmids and the Andelyn Development Center (ADC) for preclinical non-cGMP activities.

The name“Andelyn”is a hybrid of two gene therapy
patients
who participated in pivotal Phase I clinical trials at Nationwide Children’s Hospital. Andrew received the first U.S. investigational gene therapy for Duchenne muscular dystrophy in 2006. Evelyn received experimental gene therapy for spinal muscular atrophy in 2015. “Andelyn” combines their names to represent all the families who have courageously participated in the research that makes today’s gene therapies possible.

Through this journey, we have been able to acceleratethedevelopment and manufacturing of innovative therapies to bring more treatments to more patients. We are Turning Hope Into Reality™ through our
ACCTS
ions.

A
CCOUNTABLE in our actions.

C
OMPASSIVE in our thinking.

T
RUST WORTHY in our communications.

S
UPPORTIVE of one another.

Employees are expected to perform the following essential functions under the framework of our ACCTS
ions.

The GMP Quality Control (QC) Scientist I will perform assigned tasks to support the daily operations of the GMP QC laboratory. The primary objective is to ensure that all activities within the GMP QC laboratory facility comply with the requisite regulations (21 CFR Part 211 Subpart I, 21 CFR Part 11, et. al.). Working in close collaboration with QC Management, and senior QC staff the Scientist I will aid all day-to-day lab operations, including project and timeline management, materials management, assisting with laboratory investigations, SOP generation and revision, and assay performance.

The Scientist I will aid QC Management in ensuring that their assigned tasks are performed by following appropriate regulatory practices, analytical methods, and Standard Operating Procedures (SOPs) for GMP.

• Operate within the Quality Management System applicable to the manufacture of phase-appropriate material in the CMF
• Maintain compliance with applicable regulatory requirements for cellular and gene therapy products
• Works in close collaboration with the QC Management and senior QC staff to cultivate and enact strategic direction of the GMP area including determination of schedule and project timelines/capabilities.
• Provides QC Management with all laboratory data generated from QC laboratory tasks, including in-process, release, and stability testing. Manages and reviews the compilation of all data and ensures its correctness
• Assists in shipment and communications with all external QC laboratory activities in coordination with QC Supervisor
• Assists QC Management with the management of laboratory investigations, the QC portion of deviation investigations, OOS results, process change controls, and required process SOP revision and remediation
• Works in close collaboration with the QC Management and senior QC staff to ensure continuous improvement objectives are identified and met using metrics and other statistical means
• Works in close collaboration with the QC Management and senior QC staff to ensure new projects and technologies are sought for incorporation into the GMP area
• Respond to, and take action from, alarm notifications from the applicable monitoring system(s) for laboratory temperature-controlled storage units that occur at any point throughout the assigned period of responsibility .
• Exercise discretion, judgment, and…