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Job Requirements of Radiology Technologist:
-
Employment Type:
Contractor
-
Location:
Neptune City, NJ (Onsite)
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Radiology Technologist
Careers Integrated Resources Inc
Neptune City, NJ (Onsite)
Contractor
Job Title: Radiology Technologist
Location: Neptune, NJ 07754
Duration: 3 Months+
Pay Range: $55 - $60/Hour. on W2
Job Summary:
Main Responsibilities Include:
Qualifications:
Minimum Educational Requirement:
Required Experience and Skills:
Preferred Experience and Skills:
Location: Neptune, NJ 07754
Duration: 3 Months+
Pay Range: $55 - $60/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
Required Experience and Skills:
- Experience in developing, validating, and implementing ligand binding assays under GLP.
- Excellent written and verbal communication skills.
- Experience with Watson LIMS or other Laboratory Information Management Systems.
- Proficiency in Microsoft Office applications.
Preferred Experience and Skills:
- Highly motivated with a strong desire for continuous learning and development.
- Experience with LC-MS/MS assays.
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