Catalent Pharma Solutions
Scientist, QC Analytical
Catalent Pharma Solutions, Harmans, Maryland, United States, 21077
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 8am-5pm 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 Analytical support to QC method services of method verification of platform test methods Supports release and stability testing for raw materials, components, standards, intermediate/finished products Reviews laboratory work and approves 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, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. 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 is an Equal Opportunity Employer, including disability and veterans.
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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 8am-5pm 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 Analytical support to QC method services of method verification of platform test methods Supports release and stability testing for raw materials, components, standards, intermediate/finished products Reviews laboratory work and approves 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, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. 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 is an Equal Opportunity Employer, including disability and veterans.
#J-18808-Ljbffr