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Quality Assurance Cdmo Jobs (NOW HIRING)

mriglobal

Senior QA Specialist

North Kansas City, MO · On-site

$80K - $110K/yr

Direct experience in a CRO, CDMO, commercial pharmaceutical, medical device, or other relevant GxP quality assurance role. * Ability to manage diverse responsibilities in a fast-paced, highly complex ...

Siegfried Ltd

QA Supervisor

Indiana, PA · On-site

$70 - $90/hr

## QA SupervisorApplylocations: Evionnaztime type: Full timeposted on: Posted Yesterdayjob requisition ... En tant que CDMO entièrement intégrée, Siegfried est l'une des rares organisations capables ...

INCOG

Senior QA Specialist, Supplier Quality

Fishers, IN

$77K - $106K/yr

Join our dynamic Quality Assurance team as a QA Senior Specialist - Supplier Quality, where you'll ... At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture ...

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

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 ...

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Quality Assurance Cdmo information

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How much do quality assurance cdmo jobs pay per hour?

As of Sep 5, 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 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 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 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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What cities are hiring for Quality Assurance Cdmo jobs?

Cities with the most Quality Assurance Cdmo job openings:

What states have the most Quality Assurance Cdmo jobs?

States with the most job openings for Quality Assurance Cdmo jobs include:

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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 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.

Senior QA Specialist

mriglobal

North Kansas City, MO • On-site

$80K - $110K/yr

Full-time

Posted 10 days ago

Job description

Basic Function/Nature and Scope

The Senior Quality Assurance Specialist provides quality input and oversight for GMP, GLP, and ISO 9001:2015 programs and projects under the direction of senior QA staff or management. The position audits programs, facilities, and documentation to verify compliance with applicable regulatory and MRIGlobal requirements; maintains required quality documentation; supports Principal Specialists, QA management, and other areas of the QA program; assists with client audits; and provides technical expertise to resolve compliance issues. The specialist may also support other MRIGlobal facilities, conduct follow-up or subcontractor audits, and assess readiness to meet client requirements. Responsibilities are performed independently and require knowledge of applicable regulations and internal processes and procedures.

Essential Functions

  • Manages and follows up on deviations, CAPAs, and other quality events.
  • Performs quality audits of laboratory facilities, operations, documentation, and processes; documents findings; and reports results to management.
  • Reviews and audits study reports to verify that they are complete, accurate, supported by the raw data in the study file, and compliant with applicable regulatory requirements.
  • Evaluates responses to inspection and client audit reports and performs follow-up with respondents, management, or others, as needed, through resolution.
  • Inspects/audits equipment SOPs, maintenance, and calibration records.
  • Establishes and maintains QA files and records in compliance with applicable regulatory and MRIGlobal requirements
  • Writes, reviews, and revises quality related policies, protocols, and procedures.
  • May conduct training sessions for staff on quality and/or regulatory topics
  • Performs other tasks and duties as assigned.

 Success Factors

  • Promotes a mindset of quality and continual process improvement.
  • Knowledge of a broad range of technical disciplines
  • Applies knowledge across multiple interdisciplinary fields.
  • Organizes and prioritizes work effectively while maintaining close attention to detail.
  • Ability to work independently and in a team environment across organizational lines
  • Ability to wear personal protective equipment during audits if necessary
  • Proficient in Microsoft business applications and able to learn new software.
  • Communicates complex concepts clearly in writing and orally and represents MRIGlobal professionally in interactions with staff, clients, and regulatory agency personnel.

 Minimum Qualifications

  • Bachelor's degree (B.S./B.A.) in Chemistry, Biology, Engineering, or related science from a four-year university or college.
  • At least three years of experience in science, GxP quality assurance, and/or training roles, or an equivalent combination of education and experience.
  • Excellent computer skills including familiarity with Microsoft business applications.
  • U. S. Citizenship is required.

 Preferred Qualifications

  1. Direct experience in a CRO, CDMO, commercial pharmaceutical, medical device, or other relevant GxP quality assurance role.
  2. Ability to manage diverse responsibilities in a fast-paced, highly complex organization.

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