New · posted Oct 15
Celularity · Biotechnology
Sr. Specialist, Quality Control
- Florham Park, NJ
- On-site
- Full-time
- Senior & Principal
Open until filled
The role
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.
Description
What you need
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
What you'll do
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.
Pay
$80,000 – $95,000 a year
Employer providedWhere you'll work
Florham Park, NJOn-siteOpen in Maps (opens in a new tab)
More jobs in Florham Park, NJFrom the posting
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.
Equal opportunity, accessibility and legal noticesCelularity's statements, word for word
Celularity Inc. is an equal opportunity employer
***THIS ROLE DOES NOT PROVIDE RELOCATION
***NO AGENCIES PLEASE
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 8% below the US median for Quality Control roles at this level.
This roleEmployer provided
Senior & Principal roles in New Jersey8 roles publishing pay
Senior & Principal roles in the US49 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $80,000 | — | $95,000 |
| New Jersey (middle half) | $86,250 | $97,500 | $102,125 |
| All US (middle half) | $78,500 | $95,000 | $108,500 |
This role: Celularity's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 275 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Celularity's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods13
- GMP and compliance7
- Collaboration and leadership5
- Documentation and SOPs3
- Validation and qualification2
- Investigations and CAPA1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- FDA21 CFR Part 58 (GLP)(official source, opens in a new tab)Good laboratory practice for nonclinical laboratory studies
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
Company hiring pulse
Celularity on Regulatory Jobs
- 3
- Open roles
- 3
- Distinct roles
- 1
- Locations
By discipline
- Quality3 100%
By level
- Senior & Principal2 67%
- Director1 33%
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Sr. Specialist, Quality Control at Celularity
Open until filled. $80K–$95K a year, employer provided.