Scientist - II
Employer
Careers Integrated Resources Inc
Location
Rahway, New Jersey, US
Salary
Competitive
Closing date
Aug 7, 2025
Apply on website
Job Title: Scientist - II
Location: Rahway, NJ
Duration: 12 Months+
Pay Range: $50.00 - $53.45/Hour. on W2
Job Summary:
Seeking a motivated individual to work as a senior bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a bioanalytical senior scientist position with primary duties in performing laboratory work, preparing reports, and interacting with internal and external partners.
This position is a part of the Bioanalytical group, Global Preclinical Development, based in Rahway, New Jersey.
NOTES: Must be able to travel between Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required.
Main Responsibilities Include:
Independently developing, optimizing, and troubleshooting ligand binding assay (LBA) methods to support projects with method quality and efficiency in mind; writing bioanalytical methods and assuming project responsibility in delegated bioanalytical aspects.
Proficiently and independently implementing LBAs for the analysis of biological samples in a GLP environment. Duties include, but are not limited to, sample preparation, instrument setup, data processing, and interpretation; independently resolving issues encountered during method implementation.
Establishing LBA capabilities within the team, including equipment procurement, laboratory setup, and workflow design.
Ensuring all documentation is completed in real time, accurately, and in compliance with current GLP and departmental guidelines.
Preparing sample analysis and validation reports independently; assembling documents for regulatory submissions; ensuring compliance with training requirements for company and departmental SOPs, safety-related guidelines, and other applicable standards.
Achieving short-term goals, objectives, and timelines independently, with minimal management oversight.
Collaborating with cross-functional partners in areas such as Drug Safety and Metabolism, Quality Assurance, and Program Management.
Completing other relevant and applicable bioanalytical assignments as directed by management.
Demonstrating the ability to multi-task effectively and work collaboratively in a team environment.
Qualifications:
Minimum Educational Requirement:
Ph.D. in chemistry, biochemistry, or a related scientific discipline with at least 3 years of industrial experience
OR
M.S. in chemistry, biochemistry, or a related scientific discipline with at least 7 years of industrial experience, preferably in a bioanalytical laboratory
Employer
Careers Integrated Resources Inc
Location
Rahway, New Jersey, US
Salary
Competitive
Closing date
Aug 7, 2025
Apply on website
Job Title: Scientist - II
Location: Rahway, NJ
Duration: 12 Months+
Pay Range: $50.00 - $53.45/Hour. on W2
Job Summary:
Seeking a motivated individual to work as a senior bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a bioanalytical senior scientist position with primary duties in performing laboratory work, preparing reports, and interacting with internal and external partners.
This position is a part of the Bioanalytical group, Global Preclinical Development, based in Rahway, New Jersey.
NOTES: Must be able to travel between Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required.
Main Responsibilities Include:
Independently developing, optimizing, and troubleshooting ligand binding assay (LBA) methods to support projects with method quality and efficiency in mind; writing bioanalytical methods and assuming project responsibility in delegated bioanalytical aspects.
Proficiently and independently implementing LBAs for the analysis of biological samples in a GLP environment. Duties include, but are not limited to, sample preparation, instrument setup, data processing, and interpretation; independently resolving issues encountered during method implementation.
Establishing LBA capabilities within the team, including equipment procurement, laboratory setup, and workflow design.
Ensuring all documentation is completed in real time, accurately, and in compliance with current GLP and departmental guidelines.
Preparing sample analysis and validation reports independently; assembling documents for regulatory submissions; ensuring compliance with training requirements for company and departmental SOPs, safety-related guidelines, and other applicable standards.
Achieving short-term goals, objectives, and timelines independently, with minimal management oversight.
Collaborating with cross-functional partners in areas such as Drug Safety and Metabolism, Quality Assurance, and Program Management.
Completing other relevant and applicable bioanalytical assignments as directed by management.
Demonstrating the ability to multi-task effectively and work collaboratively in a team environment.
Qualifications:
Minimum Educational Requirement:
Ph.D. in chemistry, biochemistry, or a related scientific discipline with at least 3 years of industrial experience
OR
M.S. in chemistry, biochemistry, or a related scientific discipline with at least 7 years of industrial experience, preferably in a bioanalytical laboratory
Job ID: 488171130
Originally Posted on: 8/5/2025
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