What are the responsibilities and job description for the Principal Scientist/Sr. Principal Scientist, Analytical Development position at Neurocrine Biosciences?
At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs, but few options.
What We Do:Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visitneurocrine.com, and follow the company on LinkedIn, X (Formerly Twitter) and Facebook. (*in collaboration with AbbVie)
About the Role:
This position will serve as the SME for potency method development and analytical development lead for multiple projects, with a focus on antibodies and bio-conjugates. Guide analytical activities related to drug substance and drug product development from preclinical through commercial phase. Develop, establish, and validate/qualify potency methods used to control in process intermediates, drug substance, and drug products. Contribute to the development and implementation of control strategies. Responsible for keeping work in compliance with cGMP, safety, and regulatory requirements. Participates in analysis and evaluation of material and products at all stages of development process. Monitors and evaluates completion of tasks and projects._
Your Contributions (include, but are not limited to):Lead potency analytical method development and validation/qualification activities for the characterization of antibodies and/or bio-conjugates utilizing cell-based bioassays, ELISA, and relevant techniques within cGMP compliance in support of preclinical through commercialization
Represent Analytical development on cross-functional teams. Maintain accountability for analytical deliverables and progress on CMC and manufacturing plans for all development projects
Direct laboratory work and/or lab personnel within the company and at external vendors
Ensure laboratory safety practices
Support off-site analytical method transfers, manufacturing support, and interaction with external vendors
Provide input into CMC regulatory documentation and supporting work
Leverage literature, ICH/Regulatory guidance, and practical experience to perform this work and influence CMC strategies
Contribute to development of policies and department strategies
Build and enhance internal and external professional relationships
Support career development and technical growth of team members
Present finding at varying levels across the company
Other duties as assigned
BS/BA in Analytical Chemistry/Cell & Molecular Biology or related discipline and 15 years of experience in the analytical/pharmaceutical development field. Experience in method transfer in Analytical Chemistry OR
MS/MA in Analytical Chemistry or related discipline and 13 years of experience OR
PhD in Analytical Chemistry or related discipline and 7 years of relevant experience; may include postdoc experience
Expert knowledge and understanding of analytical chemistry, bioanalysis, and a thorough understanding of bioprocess as well as formulation development
Extensive experience and expertise with antibody and bio-conjugate modalities compounds, focusing on analytical development and potency method development
Excellent interpersonal skills with strong oral and written communication abilities
Excellent laboratory and productivity skills
Proficient in characterization of antibody and bio-conjugate modalities using various modern technologies. They may include but not limited to cell-based potency bioassays, ELISA, LC (RP, SEC, IEX, HILIC), capillary electrophoresis, gel electrophoresis, mass spectrometry, and molecular analysis
Method development, validation, qualification, and transfer experience in Analytical Development
Comprehensive understanding of cGMP requirements in drug substance and drug product
Expert knowledge of cross-functional understanding related to drug development
Knowledge of FDA, EMA, WHO, and ICH regulatory requirements
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Neurocrine Biosciences is an EEO/AA/Disability/Vets employer.
We are committed to building a diverse, equitable, and inclusive workplace, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
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The annual base salary we reasonably expect to pay is $153,800.00-$222,850.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.
Salary : $153,800 - $222,850
