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Qc Scientist Jobs (NOW HIRING)

Adecco Healthcare & Life Sciences is hiring a second shift QC Scientist I for our Medical Supply partner in Cincinnati, OH. The anticipated hourly wage for this position is $25. Hourly wage may ...

Adecco Healthcare & Life Sciences is hiring a second shift QC Scientist I for our Medical Supply partner in Cincinnati, OH. The anticipated hourly wage for this position is $25. Hourly wage may ...

Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...

Job Title: QC Scientist I (Bioassay) The QC Scientist I (Bioassay) supports Good Manufacturing Practice (GMP) manufacturing by performing analytical testing for commercial products and stability ...

Job Title: QC Scientist I (Bioassay) The QC Scientist I (Bioassay) supports Good Manufacturing Practice (GMP) manufacturing by performing analytical testing for commercial products and stability ...

Job Title: QC Scientist I (Bioassay) The QC Scientist I (Bioassay) supports Good Manufacturing Practice (GMP) manufacturing by performing analytical testing for commercial products and stability ...

Job Title: QC Scientist I (Bioassay) The QC Scientist I (Bioassay) supports Good Manufacturing Practice (GMP) manufacturing by performing analytical testing for commercial products and stability ...

Job Title: QC Compendial Scientist I The QC Compendial Scientist I supports Good Manufacturing Practice (GMP) manufacturing by performing compendial and analytical testing for commercial product ...

Job Title: QC Scientist I Join a dynamic laboratory team to perform routine chemical analysis on samples using established methods. Utilize analytical instrumentation such as HPLC, mass spectrometry ...

Monday - Friday 8:00am - 5:00pm Purpose and Scope The Quality Control Scientist I - NMR is a technical leader within the QC functional area with a primary role in scientific development, testing and ...

Monday - Friday 8:00am - 5:00pm Purpose and Scope The Quality Control Scientist I - NMR is a technical leader within the QC functional area with a primary role in scientific development, testing and ...

Job Title: QC Scientist I Join a dynamic laboratory team to perform routine chemical analysis on samples using established methods. Utilize analytical instrumentation such as HPLC, mass spectrometry ...

Jeans and T-shirt acceptable Apply today to join a growing scientific team dedicated to quality, innovation, and operational excellence. Pay Details: $25.00 per hour Benefit offerings available for ...

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Qc Scientist information

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$34

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How much do qc scientist jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for qc 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 Qc Scientist vs Quality Control Technician?

AspectQc ScientistQuality Control Technician
CredentialsBachelor's or higher in life sciences, chemistry, or related fields; often with certificationsHigh school diploma or associate degree; technical training
Work EnvironmentLaboratories, research facilities, quality assurance departmentsManufacturing plants, laboratories, production lines
Job ResponsibilitiesDesign experiments, analyze data, develop testing methods, interpret resultsPerform routine tests, document results, monitor quality standards
Industry UsagePharmaceutical, biotech, food, and beverage industriesManufacturing, production, and quality assurance sectors

While both roles focus on quality, Qc Scientists are involved in method development and data analysis, whereas Quality Control Technicians perform routine testing and monitoring to ensure product standards are met.

What are QC Scientists?

QC Scientists, or Quality Control Scientists, are professionals who ensure that products, materials, or processes meet established quality standards and regulatory requirements. They typically work in industries like pharmaceuticals, biotechnology, food production, and manufacturing. Their duties may include conducting laboratory tests, analyzing data, maintaining documentation, and troubleshooting quality issues. QC Scientists play a crucial role in preventing defects and ensuring the safety and efficacy of products before they reach consumers.

What typical challenges might a QC Scientist encounter when working with cross-functional teams in a pharmaceutical setting?

QC Scientists often collaborate closely with R&D, production, and regulatory teams to ensure products meet quality standards. One common challenge is aligning differing priorities—while QC focuses on rigorous testing and compliance, production may prioritize timelines. Effective communication and adaptability are key for resolving discrepancies in data interpretation and ensuring timely delivery of results. Building strong relationships across departments helps QC Scientists advocate for quality while supporting overall project goals.

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

To thrive as a QC Scientist, you need a solid background in chemistry, biology, or related sciences, often supported by a relevant degree and experience in laboratory environments. Familiarity with analytical instruments like HPLC, GC, and spectrophotometry, as well as knowledge of GMP regulations and laboratory information management systems (LIMS), is typically required. Attention to detail, problem-solving abilities, and strong communication skills set outstanding QC Scientists apart. These competencies ensure accurate testing, regulatory compliance, and effective collaboration in maintaining product quality and safety.
More about Qc Scientist jobs
What cities are hiring for Qc Scientist jobs? Cities with the most Qc Scientist job openings:
What states have the most Qc Scientist jobs? States with the most job openings for Qc Scientist jobs include:
Quality Control Scientist, Controls

Quality Control Scientist, Controls

Capricor Therapeutics

San Diego, CA • On-site

Full-time

Posted 5 days ago


Job description

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.

The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, designing and executing analytical studies, and troubleshooting and optimizing analytical methods used in QC testing. 
 
This position plays a critical role in ensuring assay reliability, reproducibility, and regulatory compliance within the QC laboratory. The individual will provide scientific leadership for assay control strategies, oversee analytical lifecycle activities for control materials, and collaborate with Quality Control, Analytical Development, Process Development, Manufacturing, and Quality teams to ensure robust analytical readiness across Capricor’s therapeutic programs. 
Responsibilities
  • Lead the development, qualification, and maintenance of positive and negative control materials used in QC analytical assays.
  • Establish and oversee assay control strategies to ensure reliable assay performance and consistency across QC testing programs.
  • Serve as the scientific owner for control materials within the analytical lifecycle framework, including control generation, qualification, monitoring, and lifecycle management.
  • Design and execute analytical studies to evaluate assay performance, control suitability, assay robustness, and method reliability.
  • Provide scientific leadership for assay troubleshooting and optimization activities to improve assay robustness and reproducibility.
  • Evaluate assay performance trends and control performance data to identify opportunities for improving assay reliability.
  • Analyze experimental data, interpret results, and generate scientific reports, study summaries, and technical documentation.
  • Document experimental work and study outcomes in accordance with GMP and data integrity requirements.
  • Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, control qualification records, and analytical lifecycle documentation.
  • Support regulatory inspection readiness by ensuring analytical control strategies, documentation, and study records meet regulatory expectations. 
  • Provide scientific support for investigations including deviations, OOS/OOT events, and assay performance issues.
  • Collaborate with Analytical Development, Process Development, Manufacturing, and Quality teams to support assay lifecycle management and continuous improvement initiatives.
  • Manage multiple scientific projects and timelines to support QC laboratory priorities.
  • Perform additional QC duties as assigned. 
Required Qualifications (Must‑Haves)
  • Ph.D. in Biological Sciences, Biochemistry, Molecular Biology, Bioengineering, or a related discipline.
  • Strong background in primary cell culture and analytical assay development, troubleshooting, and experimental design.
  • Hands-on experience with analytical techniques such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell-based assays.
  • Experience designing and executing analytical studies and interpreting experimental data.
  • Strong understanding of assay controls, assay performance monitoring, and analytical method lifecycle management.
  • Strong written and verbal communication skills with the ability to clearly summarize complex scientific findings.
  • Ability to work independently and manage multiple scientific projects in a fast-paced environment. 
Preferred Qualifications (Nice‑to‑Haves)
  • Experience working in GMP or regulated laboratory environments.
  • Experience supporting analytical method qualification, validation, or lifecycle management.
  • Experience working with cell-based assays or mammalian cell culture systems.
  • Experience supporting deviations, assay investigations, or technical reports in regulated environments.
  • Experience with cell therapy, biologics, or exosome-based products. 
Work Environment & Physical Requirements
  • Laboratory-based role requiring routine bench work.
  • Work involves analytical instrumentation, laboratory documentation, and computer-based data analysis.
  • Ability to lift up to 20 pounds.
  • Occasional participation in cross-functional meetings and technical discussions. 
Why Capricor?
Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.

Come Work With Us!
At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.

Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.



Notice to Recruiting Agencies
Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.