Sr. Specialist, Quality Control

CELULARITY LLC; Florham Park (NJ); On-site; USD 110,000 - 150,000; Full time

Job summary

Celularity Inc. in Florham Park, NJ, is seeking a Sr. Specialist, Quality Control, to support routine product testing for clinical and commercial products, including microbiological activities and assay management.

The role requires interfacing with multiple groups, performing tasks independently, interpreting results, and serving as QC SME during audits when needed. Candidates should have a Bachelor's degree in a scientific discipline and at least 5 years of quality control experience in a cGMP

Qualifications

• Bachelor’s degree in a scientific discipline is required.
• Minimum of 5+ years of quality control and/or analytical experience in a cGMP-regulated environment.
• Understanding and application of good laboratory practices.
• Strong organizational and time management skills.
• Ability to work well in a team and communicate effectively.
• Independent, self-starting, and adaptable.
• Excellent attention to detail and PPE as required.

Responsibilities

• Perform routine testing of cellular, tissue, in-process and final product samples.
• Record results in controlled documents and electronic systems.
• Assist with assay troubleshooting, calibration, and maintenance.
• Support disposition activities and product release readiness.
• Generate Certificates of Analysis and coordinate testing with QA.
• Participate in internal audits and regulatory inspections.

Skills

Quality control

Analytical testing

cGMP compliance

Documentation & record-keeping

Team collaboration

Time management

Communication skills

Independent work

Adaptability

PPE compliance

Education

Bachelor's degree in a scientific discipline

Job description

Description

About Celularity

Celularity Inc. (Nasdaq: CELU) is a longevity-focused regenerative and cellular medicine company developing and manufacturing allogeneic and autologous cell therapies derived from the postpartum placenta. Celularity leverages the placenta’s unique biology, immunologic properties and scalable availability to develop therapeutic solutions targeting fundamental mechanisms of aging and age-related disease.

Purpose

The Sr. Specialist, Quality Control, is responsible for supporting routine product testing for clinical and commercial products, product visual inspection, retain/sample oversight, microbiological activities and assay management. This role must interface with multiple groups, independently perform tasks, interpret results, and troubleshoot. Additionally, when needed, this position will serve as QC SME during audits.

Role & Responsibilities

• Perform routine testing of company’s cellular, tissue, in-process and final product samples according to approved methods, specifications and procedures.
• Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment.
• Accurately record testing activities and results in controlled documents and/or electronic systems.
• Assist with assay and equipment troubleshooting, cleaning and maintenance.
• Support clinical and commercial disposition activities by ensuring required testing and activities are complete within established timelines.
• Generate product Certificates of Analysis and ensure completeness and accuracy. Work with Quality team to facilitate readiness for product release.
• Initiate or support investigations associated with deviations and OOS/OOT results.
• Support equipment calibration and qualification activities.
• Support execution of analytical method transfers. Ensure proper training, qualification and implementation of transferred methods.
• Coordinate and execute testing and inspection of incoming raw materials, components or supplies used in cGMP manufacturing.
• Collect and prepare samples in accordance with approved sampling plans.
• Manage retain, stability, in-process, raw material and finished product samples as needed.
• Prepare samples for testing and shipment to external laboratories. Review incoming test reports. Maintain receipt and timely filing of testing results.
• Perform routine and timely visual inspection of cellular, tissue and finished product evaluating compliance to defined quality attributes.
• Execute routine environmental monitoring activities in support of cGMP manufacturing and quality control operations, as applicable.
• Participate in internal audits, regulatory inspections and 3rd party audits.

Requirements

Minimum Qualifications (Must have)

• Bachelor’s degree in a scientific discipline required.
• Minimum of 5+ years of quality control and/or analytical experience in a cGMP-regulated environment.
• Ability to understand, follow, interpret and apply good laboratory practices.
• Strong organizational and time management skills
• Ability to work well in a team environment
• Dynamic individual with the ability to communicate and engage others
• Independent and self-starting.
• Eager and adaptable
• Excellent verbal and written communication skills as well as strong focus and attention to detail.
• Ability to don personal protective equipment (PPE) during various role responsibilities

Celularity Inc. is an equal opportunity employer

***THIS ROLE DOES NOT PROVIDE RELOCATION