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Quality Assurance Cdmo Jobs (NOW HIRING)

Catalent, Inc.

Supervisor, Quality Assurance

Kansas City, MO · On-site

  • Medical

  • Life

  • Retirement

  • PTO

... CDMO) whose mission is to develop, manufacture, and supply products that help people live better ... The Quality Assurance Supervisor will manage the day-to-day activities and employees within their ...

Forma Life Sciences

Quality Assurance Specialist

Irvine, CA · On-site

$71K - $85K/yr

  • Medical

  • PTO

What We Do Forma is a next-generation Contract Development and Manufacturing Organization (CDMO ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...

Forma Life Sciences

Quality Assurance Specialist

Irvine, CA · On-site

$71K - $85K/yr

  • Medical

  • PTO

What We Do Forma is a next-generation Contract Development and Manufacturing Organization (CDMO ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...

Abzena Inc.

QA Specialist

San Diego, CA · On-site

$90K - $125K/yr

More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The QA Operations Specialist will support the Abzena operations teams to drive ...

Cambrex

Quality Assurance Engineer

Charles City, IA · On-site

  • Medical

  • Life

  • Retirement

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Key Quality Assurance customer support person to answer, address and/or compile relevant data to ...

SpectronRx

QA Administrative Assistant

Indianapolis, IN

$27 - $28/hr

Quality Assurance Administrative Assistant COMPANY OVERVIEW SpectronRx is a growing Contract Development and Manufacturing Organization (CDMO) based in Indianapolis, Indiana, and production locations ...

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Quality Assurance Cdmo information

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How much do quality assurance cdmo jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for quality assurance cdmo in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality assurance CDMO?

To thrive as a Quality Assurance CDMO (Contract Development and Manufacturing Organization), you need a solid background in quality management systems, regulatory compliance (such as cGMP and ISO), and a degree in life sciences or a related field. Familiarity with tools like LIMS, CAPA systems, and experience with FDA or EMA audit processes is typically required. Strong attention to detail, problem-solving abilities, and effective communication are essential soft skills for this role. These competencies ensure that products meet stringent quality standards and regulatory requirements, safeguarding patient safety and organizational reputation.

What are some common challenges faced by quality assurance professionals in a CDMO environment, and how can they be addressed?

Quality Assurance professionals in a Contract Development and Manufacturing Organization (CDMO) often encounter challenges such as adapting to diverse client requirements, ensuring compliance with varying regulatory standards, and managing multiple projects simultaneously. To address these challenges, professionals must be adept at communicating with cross-functional teams, stay updated on evolving regulations, and develop strong project management skills. Emphasizing collaboration, continuous training, and proactive risk management can help QA professionals excel in this dynamic and fast-paced environment.

What is a quality assurance CDMO?

A Quality Assurance CDMO refers to the quality assurance function within a Contract Development and Manufacturing Organization (CDMO). CDMOs are companies that provide services to pharmaceutical and biotechnology firms to develop and manufacture drugs. The Quality Assurance (QA) team ensures that all products and processes meet regulatory standards and client requirements. Their role includes overseeing compliance, conducting audits, reviewing documentation, and ensuring that manufacturing practices align with Good Manufacturing Practice (GMP) guidelines. This helps ensure the safety, efficacy, and quality of the pharmaceutical products produced.

What is the difference between Quality Assurance Cdmo vs Quality Control Specialist?

AspectQuality Assurance CdmoQuality Control Specialist
CertificationsGMP, ISO, QA certificationsGMP, ISO, QC certifications
Work EnvironmentRegulatory compliance, process validation, documentationProduct testing, inspection, sample analysis
Industry UsagePharmaceutical, biotech, CDMO companiesManufacturing, production facilities

Quality Assurance Cdmo professionals focus on establishing and maintaining quality systems, ensuring compliance, and validating processes within CDMO settings. In contrast, Quality Control Specialists primarily perform product testing and inspection to verify quality. Both roles are essential in the pharmaceutical industry but differ in scope and responsibilities.

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Quality Assurance Cdmo jobs near you
Infographic showing various Quality Assurance Cdmo job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $93,338 per year, or $44.9 per hour.

Supervisor, Quality Assurance

Catalent, Inc.

Kansas City, MO • On-site

Full-time

Medical, Life, Retirement, PTO

Re-posted 27 days ago

Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

59th of 86 rated pharmaceutical

Job description

Supervisor, Quality Assurance
Position Summary
  • Shift: Monday - Friday 8:00am - 4:30pm
  • 100% on-site

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The Quality Assurance Supervisor will manage the day-to-day activities and employees within their Quality Group. This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs). This individual will constantly evaluate the internal processes and procedures and work to create an efficient quality area while maintaining the highest possible quality standards. The Supervisor follows established protocols and work plans. Comply with divisional and site Environmental Health and Safety requirements
The role:
  • Oversee daily workflow of QA activities on the packaging and distribution floor, including but not limited to: in-process audits, line clearance, cleaning verification, and labeling approval
  • Train and mentor associates as needed
  • Resolve problems/issues with internal clients
  • Identify continuous improvement opportunities within QA
  • Independently lead improvement and/or other projects within QA
  • Independently author SOPs and forms
  • Effectively utilize problem solving tools (i.e., fishbone, five whys) to lead investigations
  • Communicate effectively with both internal and external customers, peers and management to facilitate the smooth and timely completion of projects
  • Conduct packaging audits (on-the-floor)
  • Identify and report cGMP or SOP compliance issues as necessary

The candidate:
  • Bachelor's degree in physical science preferred; may substitute relevant experience for education.
  • Minimum 3 years of experience in a Quality Assurance role in a GxP facility
  • Strong knowledge of cGMPs and ability to ensure compliance with SOPs and regulatory requirements
  • Experience supporting QA activities on a manufacturing/packaging floor (e.g., audits, line clearance, in-process checks)
  • Experience leading or supporting deviations, investigations, and root cause analysis (e.g., fishbone, five whys)
  • Ability to work cross-functionally and resolve issues with internal stakeholders
  • Strong communication skills with internal and external customers
  • Ability to manage multiple priorities and work effectively under pressure to meet deadlines
  • Strong organizational skills and ability to handle multiple activities simultaneously

Why you should join Catalent:
  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.

What Catalent employees say

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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