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Job Title: Quality SupervisorJob Description

We are seeking a dedicated Quality Supervisor to join our dynamic team within the pharmaceutical industry. This role focuses on ensuring high-quality standards in analytical methods and quality control, particularly within the cell and gene therapy sectors.

Responsibilities

+ Oversee and perform assays including Endotoxin, Flow Cytometry, and PCR analytical methods.

+ Ensure compliance with GMP regulations and quality control standards.

+ Support lab investigations, deviations, CAPAs, and change controls.

+ Manage and lead a team, providing guidance and support to achieve operational goals.

+ Interact effectively with clients and health authorities, maintaining excellent communication.

+ Stay adaptable to evolving demands and manage multiple priorities in a dynamic environment.

+ Travel between facilities as needed and work flexible hours, including evenings and weekends.

Essential Skills

+ Master's Degree with 3+ years of experience in the pharmaceutical industry or GMP environment, or Bachelor's Degree with 2+ years of relevant experience.

+ In-depth knowledge of analytical assays such as Flow Cytometry, PCR, and ELISAs.

+ Extensive experience in Quality Control with a solid understanding of compendial methods and regulatory guidance.

+ Strong communication skills and ability to work with minimal supervision.

Additional Skills & Qualifications

+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation.

+ Familiarity with FDA, EMEA, ICH, USP, and cGMP regulations.

+ Knowledge of Gene/Cell therapy products, particularly in clinical production.

Work Environment

This role is based in a growing CDMO focused on Cell and Gene Therapy at a brand new site. The environment is dynamic, requiring adaptability and a collaborative spirit. The work involves flexible hours and may require travel between facilities.

Job Type & Location

This is a Permanent position based out of NA, New Jersey.

Pay and Benefits

The pay range for this position is $100000.00 - $110000.00/yr.

401 medical dental vision

Workplace Type

This is a fully onsite position in Princeton,NJ.

Application Deadline

This position is anticipated to close on Oct 10, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.