Bachelor's, Master's or Ph.D. in Biochemistry or related field, 8 years industry experience with Bachelor's, 6 years with Master's, or 4 years with Ph.D..
Key responsabilities:
Support analytical activities for biologics candidates
Coordinate with CROs/CDMOs for testing and method transfers
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Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of experience, we help our clients achieve better outcomes by conducting candid conversations and anticipating potential issues through our customized solutions. Visit our website to learn more: www.advancedclinical.com.
Scientist Consultant III - Biologics Analytical Development
Location: Remote
Position Type: Full-Time, Contract
Department: Quality Control / Analytical Services
Position Overview
We are seeking a highly skilled Scientist Consultant (QC/AS) III to join our team in support of late-stage biologics candidates. This is an exciting opportunity to contribute to cutting-edge work in biologics analytical development. The ideal candidate will have a strong background in analytical chemistry and biologics, with experience in working with CROs/CDMOs to coordinate analytical testing and support method transfers. The role will also involve authoring/reviewing analytical methods and protocols, evaluating method validations, and supporting regulatory submissions.
Key Responsibilities
Support analytical activities for late-stage biologics candidates.
Coordinate with CROs/CDMOs for analytical testing and provide support as needed.
Author and review analytical methods, protocols, and standard operating procedures (SOPs).
Facilitate method transfers to CROs/CDMOs and ensure alignment with regulatory requirements.
Evaluate analytical method validations and contribute to the optimization of methods.
Interface with regulatory teams to support the authoring/reviewing of analytical sections for Biologics License Applications (BLAs).
Effectively communicate core principles of common biologics analytical methods to non-expert stakeholders.
Basic Qualifications
Bachelor’s Degree in Biochemistry, Molecular Biology, or a related scientific field with at least 8 years of industry experience.
Master’s Degree in Biochemistry, Molecular Biology, or a related scientific field with at least 6 years of industry experience.
Ph.D. in Biochemistry, Molecular Biology, or a related scientific field with at least 4 years of industry experience.
Preferred Qualifications
Expertise in common analytical methods for biologics, such as Size Exclusion Chromatography (SEC), Capillary Electrophoresis (CE), IsoElectric Focusing (IEF), Enzyme-Linked Immunosorbent Assays (ELISA), and cell-based assays.
Strong understanding of regulatory requirements for biologics and experience working with regulatory teams.
Excellent written and verbal communication skills with the ability to explain complex scientific concepts to non-experts.
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Required profile
Experience
Level of experience:Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.