Eurofins
At Eurofins Professional Scientific Services (PSS), we believe the work we do matters, and so do our employees. As part of Eurofins Scientific, a global leader in analytical testing, we support the biopharmaceutical industry by providing top-tier scientific talent and services. Our team members benefit from career development opportunities, work-life balance, and a competitive benefits package, all within a mission-driven organization focused on safety, health, and sustainability.
Job Description
We are seeking a GMP Flow Cytometry Scientist to join our Quality Control team in Exton, PA. This role is responsible for executing flow cytometry-based assays and supporting analytical testing in a GMP-regulated environment. The ideal candidate will have hands-on experience with flow cytometry, mammalian cell culture, and a strong understanding of cGMP and GDP principles. Key Responsibilities Perform flow cytometry testing to support assays such as percent transduction efficiency and CD90. Execute analytical methods for in-process, bulk intermediate, final drug product, and raw material testing. Cross-train in cell culture and other analytical techniques (e.g., ELISA, qPCR). Review and analyze QC data for accuracy, completeness, and compliance with SOPs. Investigate and document nonconforming results, including OOS investigations and CAPA execution. Maintain data integrity and adhere to ALCOA++ and Good Documentation Practices. Support equipment qualification, standardization, and maintenance. Author and revise SOPs, protocols, technical reports, and change controls. Participate in internal audits and GEMBA walk-throughs to ensure compliance. Collaborate with Manufacturing, QA, and Facilities to meet operational goals. Qualifications
Bachelor’s degree in Biochemistry, Chemistry, or a related scientific discipline and at least 2 years of relevant experienceORMaster’s degree in a related field with 1-2 years of relevant experience At least 2 years of mammalian cell culture experience Demonstrated experience working in a GMP setting, with a strong understanding of Good Documentation Practices (GDP) and data integrity principles (ALCOA++). Familiarity with analytical instruments such as flow cytometers, UV absorbance plate readers, microscopes, and pH meters. Strong written and verbal communication skills. Willingness to work occasional evenings and weekends as needed. Must be authorized to work in the United States indefinitely without sponsorship. Additional Information
The position is full-time, First Shift, Monday through Friday. some evening and weekend work may be required as needed. Candidates currently living within a commutable distance of Exton, PA, are encouraged to apply. Excellent full-time benefits include: Medical Coverage: Comprehensive medical insurance options Dental & Vision: Full dental and vision coverage available Life & Disability Insurance: Employer-sponsored plans Retirement: 401(k) plan with company match Paid Time Off: Vacation days, paid holidays, and additional PTO options If you're passionate about analytical science, thrive in a GMP-regulated environment, and want to contribute to life-changing therapies, we want to hear from you! Apply today to join Eurofins PSS as a GMP Flow Cytometry Scientist
and take the next step in your scientific career! Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
#J-18808-Ljbffr
We are seeking a GMP Flow Cytometry Scientist to join our Quality Control team in Exton, PA. This role is responsible for executing flow cytometry-based assays and supporting analytical testing in a GMP-regulated environment. The ideal candidate will have hands-on experience with flow cytometry, mammalian cell culture, and a strong understanding of cGMP and GDP principles. Key Responsibilities Perform flow cytometry testing to support assays such as percent transduction efficiency and CD90. Execute analytical methods for in-process, bulk intermediate, final drug product, and raw material testing. Cross-train in cell culture and other analytical techniques (e.g., ELISA, qPCR). Review and analyze QC data for accuracy, completeness, and compliance with SOPs. Investigate and document nonconforming results, including OOS investigations and CAPA execution. Maintain data integrity and adhere to ALCOA++ and Good Documentation Practices. Support equipment qualification, standardization, and maintenance. Author and revise SOPs, protocols, technical reports, and change controls. Participate in internal audits and GEMBA walk-throughs to ensure compliance. Collaborate with Manufacturing, QA, and Facilities to meet operational goals. Qualifications
Bachelor’s degree in Biochemistry, Chemistry, or a related scientific discipline and at least 2 years of relevant experienceORMaster’s degree in a related field with 1-2 years of relevant experience At least 2 years of mammalian cell culture experience Demonstrated experience working in a GMP setting, with a strong understanding of Good Documentation Practices (GDP) and data integrity principles (ALCOA++). Familiarity with analytical instruments such as flow cytometers, UV absorbance plate readers, microscopes, and pH meters. Strong written and verbal communication skills. Willingness to work occasional evenings and weekends as needed. Must be authorized to work in the United States indefinitely without sponsorship. Additional Information
The position is full-time, First Shift, Monday through Friday. some evening and weekend work may be required as needed. Candidates currently living within a commutable distance of Exton, PA, are encouraged to apply. Excellent full-time benefits include: Medical Coverage: Comprehensive medical insurance options Dental & Vision: Full dental and vision coverage available Life & Disability Insurance: Employer-sponsored plans Retirement: 401(k) plan with company match Paid Time Off: Vacation days, paid holidays, and additional PTO options If you're passionate about analytical science, thrive in a GMP-regulated environment, and want to contribute to life-changing therapies, we want to hear from you! Apply today to join Eurofins PSS as a GMP Flow Cytometry Scientist
and take the next step in your scientific career! Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
#J-18808-Ljbffr