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QC Scientist Raw Materials (Compendial Testing Focus)
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Eurofins
Gaithersburg, MD (In Person)
$73,840 Salary, Full-Time
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Job Description
Company DescriptionThe work we do at Eurofins Professional Scientific Services matters — and so do our employees. At Eurofins PSS, we are committed to your professional growth, providing opportunities to build and expand your expertise within the biopharmaceutical industry. Whether you are strengthening your foundation in cGMP environments or deepening your knowledge of compendial and regulatory-driven testing, we offer the tools, training, and support to help you succeed.
Our teams are collaborative, quality-focused, and committed to maintaining the highest scientific and data integrity standards. We provide a structured yet supportive environment where employees can develop technical expertise while maintaining a healthy work-life balance and accessing a competitive benefits package.
Eurofins Scientific is a global leader in life sciences, offering a broad range of analytical testing services that support safer, healthier, and more sustainable products. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins partners with leading organizations worldwide to ensure compliance with stringent quality and regulatory standards. Our work spans pharmaceutical, environmental, food, and clinical testing, with deep expertise in areas such as pharmacopeial (USP/NF, Ph. Eur., JP) testing, analytical chemistry, and GMP laboratory services.
If you're seeking a rewarding career within a scientifically rigorous, compliance-driven environment, we invite you to apply and grow with us.
Job DescriptionMake an Impact Where Compendial Expertise MattersEurofins PSS is seeking a QC Scientist with strong compendial assay experience to support the launch of a new raw materials testing laboratory. This is a hands-on role ideal for candidates experienced in USP/NF, Ph. Eur., and JP monograph testing, looking to apply their expertise in a growing GMP environment.
You'll play a key role in ensuring raw materials meet quality and regulatory standards through compendial and wet chemistry testing, while contributing to the buildout of a new lab.
What You'll DoPerform compendial raw materials testing in accordance with USP/NF, Ph. Eur., and JP monographsExecute physicochemical assays including appearance, pH, titrations, and wet chemistry methodsRun and interpret HPLC/UPLC, GC, and FTIR analyses in support of monograph requirementsReview and evaluate results against specifications; identify OOS/OOT trendsAuthor and revise SOPs related to compendial methods and raw materials testingSupport deviations, investigations, CAPAs, and change controlsTroubleshoot analytical methods and instrumentationMaintain cGMP-compliant documentation aligned with ALCOA principlesContribute to lab startup activities, method implementation, and continuous improvementQualificationsRequiredBS in Chemistry, Biochemistry, or related field3+ years pharmaceutical QC experience with a strong focus on compendial testingHands-on experience performing USP/NF, Ph. Eur., or JP monograph assaysExperience with raw materials testing and physicochemical methodsProficiency in HPLC/UPLC, GC, and FTIRStrong understanding of cGMP documentation and data integrityPreferredExperience supporting compendial method transfers, verifications, or troubleshootingFamiliarity with OOS/OOT investigations tied to compendial assaysLean/6 Sigma exposureAbility to thrive in a startup or build-phase lab environmentAdditional InformationPosition is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Gaithersburg, MD, are encouraged to applyExcellent full-time benefits include:
Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidayYearly goal-based bonus & eligibility for merit-based increases
Our teams are collaborative, quality-focused, and committed to maintaining the highest scientific and data integrity standards. We provide a structured yet supportive environment where employees can develop technical expertise while maintaining a healthy work-life balance and accessing a competitive benefits package.
Eurofins Scientific is a global leader in life sciences, offering a broad range of analytical testing services that support safer, healthier, and more sustainable products. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins partners with leading organizations worldwide to ensure compliance with stringent quality and regulatory standards. Our work spans pharmaceutical, environmental, food, and clinical testing, with deep expertise in areas such as pharmacopeial (USP/NF, Ph. Eur., JP) testing, analytical chemistry, and GMP laboratory services.
If you're seeking a rewarding career within a scientifically rigorous, compliance-driven environment, we invite you to apply and grow with us.
Job DescriptionMake an Impact Where Compendial Expertise MattersEurofins PSS is seeking a QC Scientist with strong compendial assay experience to support the launch of a new raw materials testing laboratory. This is a hands-on role ideal for candidates experienced in USP/NF, Ph. Eur., and JP monograph testing, looking to apply their expertise in a growing GMP environment.
You'll play a key role in ensuring raw materials meet quality and regulatory standards through compendial and wet chemistry testing, while contributing to the buildout of a new lab.
What You'll DoPerform compendial raw materials testing in accordance with USP/NF, Ph. Eur., and JP monographsExecute physicochemical assays including appearance, pH, titrations, and wet chemistry methodsRun and interpret HPLC/UPLC, GC, and FTIR analyses in support of monograph requirementsReview and evaluate results against specifications; identify OOS/OOT trendsAuthor and revise SOPs related to compendial methods and raw materials testingSupport deviations, investigations, CAPAs, and change controlsTroubleshoot analytical methods and instrumentationMaintain cGMP-compliant documentation aligned with ALCOA principlesContribute to lab startup activities, method implementation, and continuous improvementQualificationsRequiredBS in Chemistry, Biochemistry, or related field3+ years pharmaceutical QC experience with a strong focus on compendial testingHands-on experience performing USP/NF, Ph. Eur., or JP monograph assaysExperience with raw materials testing and physicochemical methodsProficiency in HPLC/UPLC, GC, and FTIRStrong understanding of cGMP documentation and data integrityPreferredExperience supporting compendial method transfers, verifications, or troubleshootingFamiliarity with OOS/OOT investigations tied to compendial assaysLean/6 Sigma exposureAbility to thrive in a startup or build-phase lab environmentAdditional InformationPosition is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Gaithersburg, MD, are encouraged to applyExcellent full-time benefits include:
Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidayYearly goal-based bonus & eligibility for merit-based increases