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Quality Control Associate Scientist Jobs (NOW HIRING)

Quality Control Associate

Exton, PA · On-site

$45K - $55K/yr

Quality Control Associate Salary Range: $45,000 - $55,000 Location: Exton, PA (On-site) About ... Quality control, editing, and formatting of scientific reports and data. * Writing technical ...

Quality Control Associate Salary Range: $45,000 - $55,000 Location: Exton, PA (On-site) About ... Quality control, editing, and formatting of scientific reports and data. * Writing technical ...

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Quality Control Associate Shift: 1stShift Hours: Monday - Thursday, 5:30 am TO 3:30 pm , Monday through Thursday with the occasional Friday Location: Reserve Plant - 573 W. 10th Street, Reserve, LA ...

Job title: QC Associate Duration: 12 months Location: Tucson, AZ The Quality Control Associate ... Scientists, Design Transfer Operations, project teams, etc). ● Adheres to 95% or above internal ...

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Quality Control Associate Scientist information

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How much do quality control associate scientist jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for quality control associate scientist in the United States is $34.52, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $39.66 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Associate Scientist vs Quality Control Analyst?

AspectQuality Control Associate ScientistQuality Control Analyst
CredentialsBachelor's degree in life sciences or related field; sometimes requires GMP or GLP trainingBachelor's degree in sciences; often requires similar certifications
Work EnvironmentLaboratories in biotech, pharmaceutical, or manufacturing settingsLaboratories focused on testing and quality assurance in similar industries
Job ResponsibilitiesAssisting in method development, data analysis, and supporting quality control processesPerforming routine testing, data recording, and ensuring product compliance
Industry UsageCommonly used in biotech, pharma, and manufacturing sectors

The main difference between a Quality Control Associate Scientist and a Quality Control Analyst lies in their scope of responsibilities. Associate Scientists often engage in method development and data analysis, while Analysts focus on routine testing and data recording. Both roles require similar educational backgrounds and work in laboratory environments within the biotech and pharmaceutical industries.

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

To thrive as a Quality Control Associate Scientist, you need a solid background in chemistry, biology, or a related field, often supported by a bachelor's degree and laboratory experience. Familiarity with analytical techniques such as HPLC, GC, PCR, as well as proficiency with laboratory information management systems (LIMS) and GMP/GLP regulations, is typically required. Attention to detail, problem-solving, and effective communication are crucial soft skills for accurate data analysis and cross-functional collaboration. These competencies ensure that products meet stringent quality standards and comply with regulatory requirements, which is essential for safety and efficacy in the life sciences industry.

What are Quality Control Associate Scientists?

Quality Control Associate Scientists are professionals responsible for testing and analyzing products, materials, or processes to ensure they meet predefined quality standards. They typically work in industries like pharmaceuticals, biotechnology, food production, or manufacturing. Their duties include conducting laboratory experiments, documenting results, troubleshooting issues, and maintaining compliance with regulatory guidelines. Their work helps ensure product safety, consistency, and effectiveness before products reach consumers.

What are some common challenges faced by Quality Control Associate Scientists, and how can they be addressed?

Quality Control Associate Scientists often encounter challenges such as managing tight deadlines, troubleshooting unexpected test results, and ensuring compliance with rigorous regulatory standards. Effective time management and strong attention to detail are critical for handling high sample volumes and maintaining data integrity. Collaboration with cross-functional teams, such as manufacturing and quality assurance, helps resolve issues more efficiently. Continuous training and staying updated with the latest industry regulations can also mitigate many common challenges in this role.
More about Quality Control Associate Scientist jobs
What job categories do people searching Quality Control Associate Scientist jobs look for? The top searched job categories for Quality Control Associate Scientist jobs are:
Infographic showing various Quality Control Associate Scientist job openings in the United States as of June 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $71,807 per year, or $34.5 per hour.

Quality Control Associate

Advanced Regenerative Manufacturing Institute Inc

Manchester, NH • On-site

Full-time

Posted 24 days ago


Job description

Overview

The Advanced Regenerative Manufacturing Institute (ARMl)IBioFabUSA is a Member-based non-profit organization founded to build the biofabrication industry and transform the future of healthcare. ARMI provides wrap-around commercialization services to companies seeking to bring life-saving regenerative technologies to patients, as well as to innovators seeking to commercialize enabling technologies that will grow the industry's impact.

The Impact That You Will Make

Quality Control (QC) Associates are instrumental to supporting PD-through-GMP operations. Taking a phase-appropriate approach, QC Technicians at ARMI help to maintain the facility, materials, and processes within a state of continuous control.

The QC Associate reports to the Sr. QC Manager, and works closely with Quality Assurance, Process Development, Operations Support, and Program Management. This is an excellent opportunity for a technical professional to make an impact while learning about the cutting-edge fields of tissue engineering and automation.

Your Role

  • Perform microbial and particulate sampling of ISO 7-9 cleanrooms
  • Assist with the identification and trending of microbial recoveries
  • Maintain ownership of QC equipment, ensuring units remain clean, calibrated, and validated, as necessary
  • Support routine lab cleaning and material inventory
  • Create and revise QC SOPs, test methods, and data forms
  • Review data and executed forms generated by other QC team members
  • Identify and communicate potential continuous improvements to the Quality System
  • Support site readiness for audits and regulatory inspections
  • Document all operations according to GDP

Your Skills and Experiences

  • Associate's or Bachelor's degree in a biological science discipline; or, 1+ year of GMP bio-/pharmaceutical manufacturing industry experience
  • Experience with environmental monitoring equipment (e.g., air samplers, media plates)
  • Aseptic gowning experience within a controlled cleanroom environment
  • Familiarity with GDP, GLP, and GMP principles
  • Experience with electronic Quality Management Systems
  • Knowledge of FDA GMP regulations, especially 21 CFR Part 210, 211, 610
  • Strong verbal and written technical communication skills
  • Competency with MS Office suite, especially MS Word and Excel
  • Collaborative attitude, sense of curiosity, and eagerness to manifest positive change
  • Exceptional interpersonal, written and verbal communication skills
  • Experience working in a fast-paced, dynamic, collaborative team environment
  • High energy, commitment, initiative, and perseverance

Work Environment

  • Cleanroom laboratory environment with exposure to biologics, chemical reagents, and analytical instruments
  • Occasional weekend coverage may be required
  • Occasional overtime may be required to meet project deadlines

By applying, I understand that any offer of employment is contingent upon the successful completion of a background check, in accordance with applicable laws.