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Qc Associate Scientist Jobs (NOW HIRING)

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

$75K - $80K/yr

Our client, a leading contract manufacturer and research organization of API's, is looking for a skilled QC Associate Scientist to join their team in Lake County, OH! Location: Lake County, OH Salary ...

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

We're hiring an Associate Scientist with analytical experience to join a global leader in the ... Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory ...

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

Pay Rate Low: 75000 | Pay Rate High: 90000 We're hiring an Associate Scientist with analytical ... Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory ...

Viatris

QC Associate Scientist

San Antonio, TX

Every day, we rise to the challenge to make a difference and here's how the Associate Scientist, QC role will make an impact: Key responsibilities for this role include: * Testing of chemical ...

New

Olon USA LLC

Associate Scientist, QC

Painesville, OH · On-site

Associate Scientist, QC Essential Responsibilities * Perform HPLC, GC, FTIR, KF, DSC, TGA, NMR, etc. * Inspect and perform complex chemical analyses on raw materials, in-process samples, and finished ...

Olon USA LLC

Associate Scientist, QC

Painesville, OH · On-site

Associate Scientist, QC Essential Responsibilities * Perform HPLC, GC, FTIR, KF, DSC, TGA, NMR, etc. * Inspect and perform complex chemical analyses on raw materials, in-process samples, and finished ...

Symple Lending LLC

Quality Control Associate

Irvine, CA · On-site

$21 - $25/hr

We are seeking a meticulous and detail-oriented Quality Control Associate to join our team. The ... Bachelor's degree in a relevant field, such as Quality Assurance, Engineering, or Science ...

Integrated Resources INC

NC · On-site

IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I ... Quality Control Associate Location: Research Triangle Park, NC Duration: 12+ months (possibility of ...

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Qc Associate Scientist information

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How much do qc associate scientist jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for qc associate scientist in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $40.87 per hour, depending on experience, location, and employer.

What is the difference between Qc Associate Scientist vs Qc Analyst?

AspectQc Associate ScientistQc Analyst
Required CredentialsBachelor's degree in Life Sciences, Chemistry, or related field; often some laboratory experienceBachelor's degree in Science; entry-level to mid-level laboratory experience
Work EnvironmentLaboratories within pharmaceutical, biotech, or manufacturing companiesQuality control labs in similar industries, focusing on testing and analysis
Employer & Industry UsageCommonly used in biotech and pharmaceutical industries for product testing and validationWidely used in manufacturing and quality assurance departments across industries

The Qc Associate Scientist and Qc Analyst roles share similar educational backgrounds and work environments, primarily focusing on laboratory testing within the pharmaceutical and biotech sectors. The Associate Scientist often involves more scientific analysis and method development, while the Qc Analyst emphasizes routine testing and data recording. Both roles are essential for maintaining product quality and compliance.

How does a QC Associate Scientist typically collaborate with other teams within a laboratory setting?

As a QC Associate Scientist, you will often work closely with cross-functional teams such as manufacturing, quality assurance, and research and development. Collaboration involves communicating test results, resolving discrepancies, and ensuring that all products meet regulatory and internal quality standards. Regular meetings and data sharing are common, and you may also participate in investigations or troubleshooting efforts when deviations occur. These interactions are key to maintaining workflow efficiency and upholding product integrity.

What are QC Associate Scientists?

QC Associate Scientists are professionals who work in quality control laboratories, primarily within the pharmaceutical, biotechnology, or related industries. They are responsible for conducting tests and analyses on raw materials, in-process materials, and finished products to ensure they meet established quality standards and regulatory requirements. Their duties often include preparing samples, operating laboratory equipment, documenting results, and assisting in method development and validation. QC Associate Scientists play a crucial role in maintaining product safety and integrity by identifying deviations and supporting investigations. They usually work under the supervision of senior scientists or QC managers.

What are the key skills and qualifications needed to thrive as a QC Associate Scientist, and why are they important?

To thrive as a QC Associate Scientist, you need a strong background in chemistry, biology, or a related field, typically with a bachelor's or master's degree, and experience in laboratory testing and data analysis. Familiarity with analytical instruments (such as HPLC, GC, and PCR), laboratory information management systems (LIMS), and GMP/GLP regulations is essential. Attention to detail, problem-solving abilities, and effective communication skills help ensure accuracy and collaboration within quality control teams. These competencies are vital for maintaining product quality, regulatory compliance, and the integrity of scientific results.
More about Qc Associate Scientist jobs
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Qc Associate Scientist jobs near you
QC Associate Scientist

QC Associate Scientist

Astrix Inc

Concord, OH • On-site

$75K - $80K/yr

Full-time

Posted 11 days ago

Job description

Our client, a leading contract manufacturer and research organization of API's, is looking for a skilled QC Associate Scientist to join their team in Lake County, OH!
Location: Lake County, OH
Salary: $75,000 - $80,000 per year
Employment Type: Full-time
Position Summary
The QC Associate Scientist will support a GMP-regulated API analytical laboratory by performing routine and non-routine analytical testing, method transfers, and investigations. This role requires strong expertise in HPLC and GC analysis, experience working within cGMP environments, and the ability to collaborate cross-functionally to support project timelines and quality objectives.
Responsibilities
  • Perform routine HPLC and GC analyses in a GMP API analytical laboratory.
  • Execute and support GMP analytical method transfers, including preparation of transfer protocols and final reports.
  • Conduct additional analytical techniques as needed, including but not limited to: FTIR, IC, Karl Fischer (KF), XRD, NMR, DSC, TGA, particle size analysis, Titrations, UV-Vis spectroscopy, and optical rotation.
  • Coordinate release testing for raw materials, intermediates, and active pharmaceutical ingredients (APIs).
  • Perform out-of-specification (OOS) investigations and support root cause analysis.
  • Ensure timely and compliant generation of analytical data to meet project and regulatory timelines.
  • Review analytical data for technical accuracy and adherence to good documentation practices.
  • Maintain compliance with cGMP, GLP, and laboratory safety requirements.
  • Collaborate effectively with Quality Assurance, Production, and Technical teams.
  • Perform other duties as assigned.

Qualifications
  • Bachelor's degree (B.S.) in Chemistry or related scientific discipline required.
  • Minimum of 5 years of experience in a pharmaceutical analytical laboratory or equivalent combination of Strong hands-on experience with HPLC and GC instrumentation.
  • Proficient with standard laboratory equipment (balances, pipettes, pH meters, etc.).
  • Solid understanding of analytical chemistry principles and laboratory safety practices.
  • education and experience.
  • Demonstrated experience working in cGMP/GLP environments, including QC or stability testing.
  • Experience interacting with Quality Assurance and regulatory documentation.

*This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! *
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