Catalent
Scientist, QC Analytical
Catalent, Hanover, Maryland, United States, 21098
The
Scientist, QC Analytical
is responsible for supporting analytical testing in order to support GMP manufacturing for both clinical and commercial clients. The Scientist, QC must demonstrate technical knowledge, be familiar with basic scientific/regulatory principles, possess initiative, and maintain a strong commitment to scientific excellence. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. Shift:
Monday - Friday 2pm-11pm The role: Perform assays such as ELISA, DNA/RNA extraction and gel electrophoresis, qPCR, ddPCR, HPLC, Capillary Electrophoresis, Appearance, Osmo, and pH Document testing per GMP/GDP procedures Generate internal and external documents such as assay protocols, summary reports, and SOPs Provide analytical support to QC method services for method verification of platform test methods Support release and stability testing for raw materials, components, standards, intermediate/finished products Review laboratory work and approve data packages as designated by the Supervisor Provide instrumentation care, maintenance, troubleshooting, and data interpretation Responsible for document writing (laboratory investigations, out of specifications, deviations, CAPAs), data interpretation/presentation, statistical analysis, and trending The candidate: Masters’ in a Life Sciences discipline with 0 – 2 years of experience working in a cGMP QC laboratory. Experience with any of the following techniques is preferred: ELISA, qPCR, ddPCR, HPLC, CE Knowledge/expertise relevant to QC analytical methods used for protein chemistry and molecular biology Experience within the biologic, pharmaceutical, or medical device industry performing direct hands-on work in QC function with a strong familiarity of general GMP practices Experience in writing SOPs The anticipated salary range for this position in Maryland is $74,080 - $101,860 plus an annual bonus target. The final salary offered to a successful candidate may vary, depending on several factors including type and length of experience within the job, type and length of experience within the industry, skillset, education, and business needs. Why you should join Catalent: Competitive medical benefits and 401K 152 hours PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career!
Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Visit
Catalent Careers
to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to
DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability.
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Scientist, QC Analytical
is responsible for supporting analytical testing in order to support GMP manufacturing for both clinical and commercial clients. The Scientist, QC must demonstrate technical knowledge, be familiar with basic scientific/regulatory principles, possess initiative, and maintain a strong commitment to scientific excellence. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. Shift:
Monday - Friday 2pm-11pm The role: Perform assays such as ELISA, DNA/RNA extraction and gel electrophoresis, qPCR, ddPCR, HPLC, Capillary Electrophoresis, Appearance, Osmo, and pH Document testing per GMP/GDP procedures Generate internal and external documents such as assay protocols, summary reports, and SOPs Provide analytical support to QC method services for method verification of platform test methods Support release and stability testing for raw materials, components, standards, intermediate/finished products Review laboratory work and approve data packages as designated by the Supervisor Provide instrumentation care, maintenance, troubleshooting, and data interpretation Responsible for document writing (laboratory investigations, out of specifications, deviations, CAPAs), data interpretation/presentation, statistical analysis, and trending The candidate: Masters’ in a Life Sciences discipline with 0 – 2 years of experience working in a cGMP QC laboratory. Experience with any of the following techniques is preferred: ELISA, qPCR, ddPCR, HPLC, CE Knowledge/expertise relevant to QC analytical methods used for protein chemistry and molecular biology Experience within the biologic, pharmaceutical, or medical device industry performing direct hands-on work in QC function with a strong familiarity of general GMP practices Experience in writing SOPs The anticipated salary range for this position in Maryland is $74,080 - $101,860 plus an annual bonus target. The final salary offered to a successful candidate may vary, depending on several factors including type and length of experience within the job, type and length of experience within the industry, skillset, education, and business needs. Why you should join Catalent: Competitive medical benefits and 401K 152 hours PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career!
Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Visit
Catalent Careers
to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to
DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability.
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