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Mass Biologics Quality Control Jobs (NOW HIRING)

Cellares

Manager, Quality Control

Bridgewater, NJ

$90K - $210K/yr

Strong background in cell biology, immunology, and molecular biology and associated analytical ... mass manufacturing the living drugs of the 21st century. The company is both developing and ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

Strong background in cell biology, immunology, and molecular biology and associated analytical ... mass manufacturing the living drugs of the 21st century. The company is both developing and ...

ATCC

Senior Director, Quality

Manassas, VA · On-site

Demonstrated experience overseeing QC laboratory operations, method validation, and release testing for biological materials. * Strong capability in CAPA, deviation management, change control, risk ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

Biomarker & Biologics Location: Exton, PA ( Onsite) Position Summary The QC Manager is responsible for oversight of the Quality Control function supporting compliant biologics and biomarker testing ...

VIVEX BIOLOGICS INC

Quality Control Microbiologist

Miami, FL · On-site

$24.50 - $32/hr

Job purpose The Quality Control Microbiologist (QCM) is responsible for performing and managing ... An equivalent combination of education and experience in a regulated environment (e.g., Biologics ...

VIVEX BIOLOGICS INC

Quality Control Microbiologist

Miami, FL · On-site

$24.50 - $32/hr

Must perform applicable QC testing and related functions in accordance with standard operating ... An equivalent combination of education and experience in a regulated environment (e.g., Biologics ...

VIVEX Biologics, Inc.

Quality Control Analyst

Miami, FL · On-site

$23 - $30.75/hr

Job purpose The Quality Control Analyst is responsible for performing and managing results of ... An equivalent combination of education and experience in a regulated environment (e.g., Biologics ...

VIVEX BIOLOGICS INC

Quality Control Analyst

Miami, FL · On-site

$23 - $30.75/hr

Job purpose The Quality Control Analyst is responsible for performing and managing results of ... An equivalent combination of education and experience in a regulated environment (e.g., Biologics ...

WuXi Biologics

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Job Title - Scientist I, QC Work Location - Cranbury, NJ Job Summary: We are seeking a self ... Qualifications: * Full-time undergraduate degree or above, majoring in biology, chemical ...

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Mass Biologics Quality Control information

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How much do mass biologics quality control jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for mass biologics quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What are some common challenges faced in Mass Biologics Quality Control and how are they addressed?

In a Mass Biologics Quality Control role, professionals often encounter challenges such as maintaining strict adherence to regulatory guidelines, managing large volumes of documentation, and ensuring consistent accuracy in analytical testing. Addressing these challenges involves rigorous training, utilizing robust laboratory information management systems (LIMS), and fostering strong communication within cross-functional teams. Continuous professional development and regular internal audits also help maintain high standards and adapt to evolving regulatory requirements.

What are the key skills and qualifications needed to thrive in Mass Biologics Quality Control?

To thrive in Mass Biologics Quality Control, you need a solid background in biology, chemistry, or a related field, typically supported by a relevant degree and laboratory experience. Familiarity with analytical techniques (such as HPLC, ELISA), laboratory information management systems (LIMS), and GMP/GLP regulations is essential. Attention to detail, critical thinking, and effective teamwork are crucial soft skills for ensuring accuracy and compliance. These competencies are vital to maintain product quality, regulatory adherence, and patient safety in biologics manufacturing.

What is Mass Biologics Quality Control?

Mass Biologics Quality Control refers to the processes and procedures used at MassBiologics to ensure that biological products, such as vaccines and therapeutics, meet rigorous safety, purity, and potency standards. Quality control professionals perform laboratory tests, analyze samples, and review data to confirm compliance with regulatory requirements. This work is essential for protecting public health and ensuring that only high-quality products are released for distribution.
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What are the most commonly searched types of Mass Biologics Quality Control jobs? The most popular types of Mass Biologics Quality Control jobs are:
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Infographic showing various Mass Biologics Quality Control job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Manager, Quality Control

Cellares

Bridgewater, NJ

$90K - $210K/yr

Full-time

Re-posted 19 days ago

Job description

We are seeking an innovative and highly motivated individual to join our team as the Manager of Quality Control at our GMP manufacturing facility located in Bridgewater, NJ. This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products.

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products.  They will interface across different parts of the company to support novel products used in cell and gene therapy. This role will report to the Senior Director of Quality Control.

Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. 

Responsibilities
  • Schedule/Manage routine and non-routine analysis of in-process, finished goods, or stability samples
  • Ensure the quality control lab is held to GxP standards and safety standards
  • Create/Review and approve Certificate of Analysis
  • Conduct investigation regarding out of specifications (OOS) results and address and manage deviations related to analytical procedures
  • Review and approve data to ensure accuracy and regulatory compliance
  • Create/Review and approve new and revision of analytical test methods
  • Create/Review and approve method validation protocols/reports and other documentation such as analytical reports
  • Create/Review and approve stability protocols and reports
  • Create/Review and approve quality control operation procedures
  • Manage the validation of analytical methods used in QC as well as the transfer and validation of methods to contract testing laboratories
  • Manage training of other analysts to perform laboratory procedures and assays
  • Participate in internal assessments and audits as required
  • Manage stability program
  • Serve as Quality Control representative during cross-functional/project meetings
  • Serve as subject matter expert between Quality Control and other departments, vendors, or contractors
  • Support Quality Systems such as Change Control, Deviation, CAPA, Audits, Quality Metrics
  • Manage and grow a phase appropriate team of Quality Control personnel
  • Establish user requirements for purchase of new Cellares GMP lab equipment
  • Manage equipment validation, calibration, maintenance, and troubleshooting
  • Assemble and report contract laboratory testing data
  • Assist in the preparation of dossiers and data packages in support of Cellares products for regulatory agencies
  • Other duties as assigned
Requirements
  • BA or B.S. degree in a science discipline required, or comparable experience; M.S. in a scientific discipline is preferred
  • Minimum of 7 years experience in a cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment
  • At least 2 years in a managerial role
  • Prior experience related to method development/validation preferred
  • Strong background in cell biology, immunology, and molecular biology and associated analytical assays
  • Strong working knowledge of quality systems and regulatory requirements including 21 CFR Part 11/210/211
  • Must have working knowledge of controlled documentation, data systems, cGMPs, SOPs, analytical testing, and auditing
  • Identifying, authoring, and supporting OOS, DRs, and CAPAs
  • Equipment IQ/OQ/PQ experience
  • Proficient in MS Office products including, Word, Excel, Outlook, and Power Point
  • Excellent interpersonal, verbal, written communication and organization skills
  • Self-awareness, integrity, authenticity, and a growth/entrepreneurial mindset
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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