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Contract Duration: 12+ Months 100% Onsite job About the Role We are seeking a highly motivated
Senior Bioanalytical Scientist
to join a GLP bioanalytical laboratory, based in
Rahway, New Jersey . This role is ideal for a scientist who thrives in a collaborative, fast-paced environment and is excited to apply their expertise in
ligand binding assays (LBA)
to support regulatory projects. The position requires both hands-on bench science and cross-functional collaboration with internal and external partners. Responsibilities
Independently develop, optimize, and troubleshoot
LBA methods
with a focus on efficiency and regulatory compliance. Implement LBAs for biological sample analysis in a
GLP environment , including sample prep, instrument setup, data processing, and troubleshooting. Establish and expand LBA capabilities, including lab setup, workflow design, and equipment procurement. Prepare and review
bioanalytical methods, validation reports, and sample analysis reports
in compliance with GLP and departmental SOPs. Assemble documents for
regulatory submissions
and ensure all documentation is accurate and timely. Maintain required training and compliance with
GLP, SOPs, and safety guidelines . Manage multiple projects, meet short-term objectives, and deliver on timelines with minimal oversight. Collaborate with cross-functional partners, including
Drug Safety and Metabolism, Quality Assurance, and Program Management . Perform additional bioanalytical assignments as directed by management. Qualifications
Minimum Educational Requirement Ph.D. in Chemistry, Biochemistry, or related field
with 3+ years of industrial experience OR Master’s degree in Chemistry, Biochemistry, or related field
with 7+ years of industrial experience , preferably in a bioanalytical laboratory. Required Experience & Skills Proven experience in
developing, validating, and implementing LBAs
under GLP. Strong written and verbal communication skills. Experience with
Watson LIMS or other LIMS systems . Proficiency with
Microsoft Office Suite . Experience & Skills Self-motivated with a strong desire to learn and grow. Experience with
LC-MS/MS assays . Additional Information
Must be able to travel between
Rahway, NJ
and
West Point, PA
sites as needed. Travel may be required
up to 50% .
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Contract Duration: 12+ Months 100% Onsite job About the Role We are seeking a highly motivated
Senior Bioanalytical Scientist
to join a GLP bioanalytical laboratory, based in
Rahway, New Jersey . This role is ideal for a scientist who thrives in a collaborative, fast-paced environment and is excited to apply their expertise in
ligand binding assays (LBA)
to support regulatory projects. The position requires both hands-on bench science and cross-functional collaboration with internal and external partners. Responsibilities
Independently develop, optimize, and troubleshoot
LBA methods
with a focus on efficiency and regulatory compliance. Implement LBAs for biological sample analysis in a
GLP environment , including sample prep, instrument setup, data processing, and troubleshooting. Establish and expand LBA capabilities, including lab setup, workflow design, and equipment procurement. Prepare and review
bioanalytical methods, validation reports, and sample analysis reports
in compliance with GLP and departmental SOPs. Assemble documents for
regulatory submissions
and ensure all documentation is accurate and timely. Maintain required training and compliance with
GLP, SOPs, and safety guidelines . Manage multiple projects, meet short-term objectives, and deliver on timelines with minimal oversight. Collaborate with cross-functional partners, including
Drug Safety and Metabolism, Quality Assurance, and Program Management . Perform additional bioanalytical assignments as directed by management. Qualifications
Minimum Educational Requirement Ph.D. in Chemistry, Biochemistry, or related field
with 3+ years of industrial experience OR Master’s degree in Chemistry, Biochemistry, or related field
with 7+ years of industrial experience , preferably in a bioanalytical laboratory. Required Experience & Skills Proven experience in
developing, validating, and implementing LBAs
under GLP. Strong written and verbal communication skills. Experience with
Watson LIMS or other LIMS systems . Proficiency with
Microsoft Office Suite . Experience & Skills Self-motivated with a strong desire to learn and grow. Experience with
LC-MS/MS assays . Additional Information
Must be able to travel between
Rahway, NJ
and
West Point, PA
sites as needed. Travel may be required
up to 50% .
#J-18808-Ljbffr