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Urgent! Quality Operations Supervisor Job Opening In Princeton – Now Hiring Actalent
Job Title: Quality Operations Supervisor
Job Description
The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily Quality Operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites.
This position involves operational quality oversight, direct engagement in batch record review, deviation management, and on-the-floor support, while managing staff.
The role serves as the primary interface between site operations and Quality Operations leadership, providing proactive support to Manufacturing, Warehousing, and QC operations, and ensuring product quality and compliance objectives are consistently met.
Responsibilities
+ Ensure site-wide GMP compliance and product quality.
+ Apply advanced knowledge of GMP, quality, and risk management to identify and mitigate potential risks or process gaps.
+ Serve as the Quality primary point of contact between site operations and QO leadership.
+ Provide hands-on, on-the-floor QO support in manufacturing cleanrooms, warehouse operations, and QC laboratories.
+ Review and approve deviations, CAPAs, and Change Controls.
+ Oversee critical quality activities including apheresis material receipt, production document issuance, batch record review, and final product shipment.
+ Review and approve GMP documentation to ensure compliance and accuracy.
+ Supervise, mentor, and develop QO staff.
+ Promote a strong culture of quality, compliance, teamwork, and accountability within the QO team.
+ Coordinate with cross-functional teams to allocate resources and resolve operational challenges.
+ Contribute to continuous improvement of QO processes.
+ Support audit and inspection readiness, and serve as SME during client and regulatory interactions.
+ Lead continuous improvement initiatives to enhance compliance, efficiency, and operational excellence.
Essential Skills
+ 5+ years of experience in Cell/Gene Therapy OR MS/PhD in a relevant field.
+ 3+ years of people management experience.
+ Experience with QMS - CAPA investigations and deviations oversight.
+ Strong knowledge of GMP, quality systems, and risk management principles.
+ Hands-on experience providing QO support in GMP environments.
+ Excellent organizational, communication, and problem-solving skills.
+ Flexibility to work shift-based schedules and travel between sites as needed.
Additional Skills & Qualifications
+ Bachelor’s degree in a scientific discipline (Biology, Chemistry, Microbiology, or related) with 5–7 years of experience in GMP/Quality Operations.
+ Master’s degree with 3–5 years relevant experience preferred.
+ In-depth knowledge of GMPs and ability to apply them in compliance with U.S., EU, and global regulatory standards.
+ Experience with cell and gene therapy manufacturing in clinical or commercial settings.
+ Expertise in aseptic manufacturing processes.
Work Environment
The work environment is a growing Contract Development and Manufacturing Organization (CDMO) specializing in Cell/Gene Therapy at a brand-new site.
The role involves working in manufacturing cleanrooms, warehouse operations, and QC laboratories.
Flexibility to work varying hours, including evenings, weekends, and shifts, is required.
Job Type & Location
This is a Permanent position based out of New Jersey.
Pay and Benefits
The pay range for this position is $100000.00 - $110000.00/yr.
401k medical dental vision
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Nov 6, 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
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Unlock Your Quality Operations Potential: Insight & Career Growth Guide
Real-time Quality Operations Jobs Trends in Princeton, United States (Graphical Representation)
Explore profound insights with Expertini's real-time, in-depth analysis, showcased through the graph below. This graph displays the job market trends for Quality Operations in Princeton, United States using a bar chart to represent the number of jobs available and a trend line to illustrate the trend over time. Specifically, the graph shows 97510 jobs in United States and 139 jobs in Princeton. This comprehensive analysis highlights market share and opportunities for professionals in Quality Operations roles. These dynamic trends provide a better understanding of the job market landscape in these regions.
Great news! Actalent is currently hiring and seeking a Quality Operations Supervisor to join their team. Feel free to download the job details.
Wait no longer! Are you also interested in exploring similar jobs? Search now: Quality Operations Supervisor Jobs Princeton.
An organization's rules and standards set how people should be treated in the office and how different situations should be handled. The work culture at Actalent adheres to the cultural norms as outlined by Expertini.
The fundamental ethical values are:The average salary range for a Quality Operations Supervisor Jobs United States varies, but the pay scale is rated "Standard" in Princeton. Salary levels may vary depending on your industry, experience, and skills. It's essential to research and negotiate effectively. We advise reading the full job specification before proceeding with the application to understand the salary package.
Key qualifications for Quality Operations Supervisor typically include Other General and a list of qualifications and expertise as mentioned in the job specification. Be sure to check the specific job listing for detailed requirements and qualifications.
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Before the Interview:To prepare for your Quality Operations Supervisor interview at Actalent, research the company, understand the job requirements, and practice common interview questions.
Highlight your leadership skills, achievements, and strategic thinking abilities. Be prepared to discuss your experience with HR, including your approach to meeting targets as a team player. Additionally, review the Actalent's products or services and be prepared to discuss how you can contribute to their success.
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