AbbVie
Overview
Senior Scientist I role at AbbVie. This position involves leading analytical development activities for biologics within the Operations – Product Development Science and Technology – Biologics division, supporting GMP release and stability, specification setting, and process development across the drug development lifecycle. Base pay range
$94,000.00/yr - $178,500.00/yr Responsibilities
Lead method development, troubleshooting and analytical testing to support AbbVie pipeline programs using separation-based methods (e.g., HPLC: SEC, IEX, RPLC; capillary electrophoresis such as CE and icIEF) and other analytical approaches. Advance scientific excellence by implementing novel analytical techniques to enhance method robustness and capability across lifecycle support for early and late-stage programs. Collaborate with Analytical Development, quality control, bioprocess development, and R&D to provide analytical support for pipeline programs (ELISA, bioassays, mass spectrometry, biophysical methods, spectrophotometric and compendial methods). Participate in cross-functional, multi-site meetings/projects and coordinate analytical activities within the Analytical Development team. Contribute to the preparation and review of internal technical documents to ensure compliance; author regulatory submissions and respond to agency deficiency letters. Mentor or supervise junior team members. Preferred Qualifications
PhD in chemistry, biochemistry, biological sciences, chemical engineering or related scientific disciplines with 0–2 years of relevant experience. Experience in analytical method development, validation, and transfer for biological products; methods may include HPLC/UPLC, capillary electrophoresis, spectrophotometry, mass spectrometry, biophysical methods, ELISA and bioassays. Strong troubleshooting, critical thinking, and problem-solving abilities. Ability to lead and manage projects of significant scope and complexity, meeting deliverables and timelines. Effective communication with stakeholders and collaboration with cross-team partners. Qualifications
Bachelor’s Degree or equivalent with typically 10 years of experience, Master’s Degree or equivalent with typically 8 years of experience, PhD with no experience required. Solid theoretical and practical understanding of the relevant scientific discipline. Additional Information
The compensation range described below is the range of possible base pay compensation at posting; actual pay depends on factors including geographic location and may be modified in the future. We offer a comprehensive benefits package including paid time off, medical/dental/vision insurance and 401(k) for eligible employees. This job is eligible to participate in short-term and long-term incentive programs. Note: No amount of pay is considered wages or compensation until earned, vested, and determinable. Compensation remains at the Company’s discretion and may be modified, in compliance with applicable law. AbbVie is an equal opportunity employer. US & Puerto Rico only - learn more about equal employment opportunity and reasonable accommodations at the provided links. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more.
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Senior Scientist I role at AbbVie. This position involves leading analytical development activities for biologics within the Operations – Product Development Science and Technology – Biologics division, supporting GMP release and stability, specification setting, and process development across the drug development lifecycle. Base pay range
$94,000.00/yr - $178,500.00/yr Responsibilities
Lead method development, troubleshooting and analytical testing to support AbbVie pipeline programs using separation-based methods (e.g., HPLC: SEC, IEX, RPLC; capillary electrophoresis such as CE and icIEF) and other analytical approaches. Advance scientific excellence by implementing novel analytical techniques to enhance method robustness and capability across lifecycle support for early and late-stage programs. Collaborate with Analytical Development, quality control, bioprocess development, and R&D to provide analytical support for pipeline programs (ELISA, bioassays, mass spectrometry, biophysical methods, spectrophotometric and compendial methods). Participate in cross-functional, multi-site meetings/projects and coordinate analytical activities within the Analytical Development team. Contribute to the preparation and review of internal technical documents to ensure compliance; author regulatory submissions and respond to agency deficiency letters. Mentor or supervise junior team members. Preferred Qualifications
PhD in chemistry, biochemistry, biological sciences, chemical engineering or related scientific disciplines with 0–2 years of relevant experience. Experience in analytical method development, validation, and transfer for biological products; methods may include HPLC/UPLC, capillary electrophoresis, spectrophotometry, mass spectrometry, biophysical methods, ELISA and bioassays. Strong troubleshooting, critical thinking, and problem-solving abilities. Ability to lead and manage projects of significant scope and complexity, meeting deliverables and timelines. Effective communication with stakeholders and collaboration with cross-team partners. Qualifications
Bachelor’s Degree or equivalent with typically 10 years of experience, Master’s Degree or equivalent with typically 8 years of experience, PhD with no experience required. Solid theoretical and practical understanding of the relevant scientific discipline. Additional Information
The compensation range described below is the range of possible base pay compensation at posting; actual pay depends on factors including geographic location and may be modified in the future. We offer a comprehensive benefits package including paid time off, medical/dental/vision insurance and 401(k) for eligible employees. This job is eligible to participate in short-term and long-term incentive programs. Note: No amount of pay is considered wages or compensation until earned, vested, and determinable. Compensation remains at the Company’s discretion and may be modified, in compliance with applicable law. AbbVie is an equal opportunity employer. US & Puerto Rico only - learn more about equal employment opportunity and reasonable accommodations at the provided links. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more.
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