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Qc Associate Jobs

6 Job Offers

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Sr. QC Chemistry Associate I
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Autograph Operations Sticker QC Associate
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Join our team as an Autograph Operations Sticker QC Associate in Sunnyvale, CA. Requires 2+ years of QC and inventory experience, strong attention to detail, and data entry accuracy.
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QC Sample Management Associate Scientist
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Join Alvotech in Reykjavik as a QC Sample Management Associate Scientist. Requires a bachelor's degree, 1-3 years of pharma experience, and strong English skills. Grow in a global, innovative culture.
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Iceland, Reykjavík
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Production Associate 2 - Glass Intercept QC 2nd shift
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United States, North Brunswick Township
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HTP Analytical QC Associate Scientist
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Qc Microbiology Associate
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Join a leading pharmaceutical company as an IT/Application Development & Management Junior to modernize finance automation. This fully remote role in Europe focuses on configuring Redwood platforms and integrating SAP S/4 HANA and SAP ECC systems. You’ll develop automation logic, design front-end...
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About the Qc Associate role

Explore a world of opportunity in QC Associate jobs, a critical and dynamic profession within the biotechnology, pharmaceutical, and manufacturing industries. Quality Control Associates are the guardians of product integrity, ensuring that every item, from life-saving medications to complex medical devices, meets stringent standards of safety, identity, strength, purity, and quality before reaching the consumer. This role sits at the heart of compliance and excellence, making it a foundational and rewarding career path for detail-oriented science professionals.

Professionals in these jobs typically work in laboratory settings, performing a wide array of analytical tests on raw materials, in-process samples, and finished products. Common responsibilities include executing standardized test methods such as HPLC, GC, ELISA, pH, conductivity, and various microbiological assays like sterility and endotoxin testing. Beyond bench work, QC Associates are responsible for the meticulous documentation of all procedures and results in accordance with Good Manufacturing Practices (GMP) and other regulatory guidelines. They analyze data, interpret results against specifications, and report findings, often using sophisticated laboratory information management systems (LIMS). A significant part of the role involves troubleshooting assay discrepancies, participating in laboratory investigations for out-of-specification (OOS) results, and supporting corrective and preventive actions (CAPA). Furthermore, they contribute to maintaining laboratory efficiency by calibrating instruments, managing reagent and supply inventory, and ensuring a clean and safe work environment.

The typical profile for QC Associate jobs includes a bachelor’s degree in chemistry, biology, microbiology, pharmaceutical sciences, or a related life science field. Hands-on laboratory experience, often gained through academic projects or prior roles, is highly valued. Employers seek candidates with a strong understanding of GMP/GLP principles, exceptional attention to detail, and robust analytical and problem-solving skills. Proficiency in technical writing for drafting and reviewing standard operating procedures (SOPs) and test reports is essential. Successful associates are organized, able to manage multiple priorities in a fast-paced setting, and possess clear communication skills to collaborate effectively with quality assurance and production teams. For those with a passion for science and quality, pursuing QC Associate jobs offers a stable and impactful career with a clear pathway to advancement into senior analyst, supervisory, or specialized technical roles, playing an indispensable part in delivering safe and effective products to market.