TALENT Software Services
Scientist - II (Associate) - PA/NJ Only Scientist - II (Associate) - PA/NJ Only
TALENT Software Services, Rahway, New Jersey, us, 07065
Scientist - II (Associate) - PA/NJ Only
Seeking a motivated individual to work as a senior bioanalytical bench scientist within our Good Laboratory Practices (GLP) bioanalytical laboratory. This senior scientist position is part of Global Preclinical Development and is based in Rahway, New Jersey.
Main responsibilities include:
Independently developing, optimizing, and troubleshooting ligand binding assay (LBA) methods to support projects with a focus on method quality and efficiency.
Writing bioanalytical methods and assuming project responsibility for delegated bioanalytical tasks.
Implementing LBA for analysis of biological samples in a GLP environment, including sample preparation, instrument setup, data processing, and interpretation.
Establishing LBA capability within the team, including equipment purchasing, lab setup, and workflow development.
Ensuring documentation is accurate, real‑time, and compliant with GLP and departmental guidelines.
Preparing independent reports on sample analysis and validation, assembling documents for regulatory submissions, and maintaining required training for SOPs, safety guidance, and other applicable guidelines.
Adhering to short‑term goals, objectives, and timelines agreed upon with management while working independently.
Interacting with partners in other functional lines such as Drug Safety, Metabolism, Quality Assurance, and program management.
Completing any additional bioanalytical assignments directed by management.
Possessing strong multitasking skills and acting as a team player.
Qualifications:
Minimum educational requirement:
Ph.D. in chemistry, biochemistry, or related scientific discipline with 3 years of industrial experience, or an M.S. with at least 7 years of industrial experience, preferably in a bioanalytical laboratory.
Required experience and skills:
Experience in developing, validating, and implementing ligand binding assays under GLP; excellent written and verbal communication skills; experience with LIMS systems such as Watson; proficiency with Microsoft Office products.
Preferred experience and skills:
Highly motivated individual aspiring to learn and develop; experience in LC‑MS/MS assay.
Must be able to travel between the Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required.
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Main responsibilities include:
Independently developing, optimizing, and troubleshooting ligand binding assay (LBA) methods to support projects with a focus on method quality and efficiency.
Writing bioanalytical methods and assuming project responsibility for delegated bioanalytical tasks.
Implementing LBA for analysis of biological samples in a GLP environment, including sample preparation, instrument setup, data processing, and interpretation.
Establishing LBA capability within the team, including equipment purchasing, lab setup, and workflow development.
Ensuring documentation is accurate, real‑time, and compliant with GLP and departmental guidelines.
Preparing independent reports on sample analysis and validation, assembling documents for regulatory submissions, and maintaining required training for SOPs, safety guidance, and other applicable guidelines.
Adhering to short‑term goals, objectives, and timelines agreed upon with management while working independently.
Interacting with partners in other functional lines such as Drug Safety, Metabolism, Quality Assurance, and program management.
Completing any additional bioanalytical assignments directed by management.
Possessing strong multitasking skills and acting as a team player.
Qualifications:
Minimum educational requirement:
Ph.D. in chemistry, biochemistry, or related scientific discipline with 3 years of industrial experience, or an M.S. with at least 7 years of industrial experience, preferably in a bioanalytical laboratory.
Required experience and skills:
Experience in developing, validating, and implementing ligand binding assays under GLP; excellent written and verbal communication skills; experience with LIMS systems such as Watson; proficiency with Microsoft Office products.
Preferred experience and skills:
Highly motivated individual aspiring to learn and develop; experience in LC‑MS/MS assay.
Must be able to travel between the Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required.
#J-18808-Ljbffr