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Bioanalytical Senior Scientist
Bioanalytical Senior ScientistNet2Source (N2S) • Rahway, NJ, US
Bioanalytical Senior Scientist

Bioanalytical Senior Scientist

Net2Source (N2S) • Rahway, NJ, US
30+ days ago
Job type
  • Full-time
Job description

Title : Bioanalytical Senior Scientist

Location : Rahway, NJ

Duration : 12+ months(Extendable)

Pay Range : $45 -$53 per hour on W2.

NOTES : Must be able to travel between Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required.

Qualifications :

Minimum Educational Requirement :

  • Ph.D. degree in chemistry, biochemistry or related scientific discipline with 3 years of industrial experience, or Master of Science degree in chemistry, biochemistry or 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.
  • Possess excellent written and verbal communication skills.
  • Experience in Watson or other LIMS systems.
  • Proficiency with Microsoft Office products.
  • Preferred Experience and Skills :

  • Highly motivated individual with the aspiration to learn and develop himself / herself.
  • Experience in LC-MS / MS assay.
  • Responsibilities :

    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. Main responsibilities include :

  • Independently developing, optimizing and troubleshooting LBA methods to support projects with method quality and efficiency in mind; writing bioanalytical methods; assumption of project responsibility in delegated bioanalytical aspects.
  • Proficiently and independently implementing ligand binding assays (LBA) for the analysis of biological samples in a GLP environment, with duties inclusive of, but not limited to, sample preparation, setting up instruments, processing, and interpreting data; solving issues encountered during method implementation independently.
  • Establishing LBA capability within the team including equipment purchasing, setting up lab and LBA workflow.
  • Ensuring that all documentations are in real time, accurate and compliant with current GLP and departmental guidelines.
  • Preparing reports (sample analysis and validation) independently; Assembling all documents for regulatory submissions; Compliance with and maintenance of required training for company and departmental SOPs, safety-related guidance and other guidelines as relevant / applicable.
  • Adherence to short term goals, objectives and timelines agreed upon with management, via working independently (e.g., with little to no management oversite in this regard).
  • Interaction with partners in other functional lines, such as Drug Safety and Metabolism, Quality Assurance, and program management.
  • Any relevant / applicable additional BA assignments as directed by management.
  • Ability to multi-task and be a team player.
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    Senior Scientist • Rahway, NJ, US

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