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Quality Assurance Cdmo Jobs (NOW HIRING)

Quality Assurance Specialist II

Albany, NY · On-site

$67K - $83K/yr

  • Retirement

  • PTO

Quality Assurance Specialist II - Albany, NY Build your future at Curia, where our work has the ... Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ...

Quality Assurance (QA) Customer Quality Lead Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with ...

Quality Assurance Specialist II - Albany, NY Build your future at Curia, where our work has the ... Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ...

Quality Assurance (QA) Customer Quality Lead Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with ...

QA Technician Assistant II - 1st Shift

Irvine, CA · On-site

$27 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Join our Quality Assurance team and play a critical role in ensuring products are manufactured ... Gain hands-on experience in a pharmaceutical CDMO environment * Work closely with Manufacturing, QC ...

New

The Quality Assurance Specialist III serves as an embedded quality partner to manufacturing ... Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ...

Showing results 41-60

Quality Assurance Cdmo information

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$15

$44

$64

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 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.

More about Quality Assurance Cdmo jobs

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:

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.

Quality Assurance Specialist II

Curia, Inc.

Albany, NY • On-site

$67K - $83K/yr

Full-time

Retirement, PTO

Posted 9 days ago


Curia rating

7.6

Company rating: 7.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz


Job description


Quality Assurance Specialist II - Albany, NY
Build your future at Curia, where our work has the power to save lives.
The Quality Assurance (QA) Specialist II is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight to operations. This role includes identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action. The QA Specialist II primarily works in the cGMP areas to manage adherence to the quality system and assist in and/or initiate the resolution of deviations.
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.
We proudly offer
• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform
• And more!
Responsibilities
• Represent Curia Quality Assurance when managing issues that require immediate corrective action. Ensure such action taken is appropriate and correctly documented
• Review quality control testing for compliance with internal SOPs and specifications
• Report back to appropriate management as to personnel performance, highlighting those areas and individuals in need of improvement as well as those exceeding expectations
• Author, review, and/or approve Quality Management System documents, including, but not limited to, change controls, SOPs, deviations, CAPAs, etc.
• Perform and/or participate in internal audits, external audits, investigations, and/or inspections
• With supervision, may respond or manage responses to clients regarding manufacturing, testing and/or documentation issues
• May develop and/or maintain Quality System metrics for management review
• Provide on the floor support to operations, including coordinating and performing day to day activities as needed
• May assist in developing and conducting training of personnel to execute production in full accordance with cGMP's and Curia's quality system to ensure real-time compliance
• May perform QA visual inspection activities when required
• Participate in regulatory and client audits
• Other duties as assigned
Required
• BA/BS Degree in Chemistry or a relevant field and 3 years of related work experience in pharmaceutical, biotechnology, medical device, and/or cGMP FDA-regulated industry
OR
• MA/MS Degree in Chemistry or a relevant field and 1 year of related work experience in pharmaceutical, biotechnology, medical device, and/or cGMP FDA-regulated industry
Pay range: $67,000 - $83,200
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

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