Who We Are:
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 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, endocrine and psychiatric disorders. The company\xe2\x80\x99s diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson\xe2\x80\x99s disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. *in collaboration with AbbVie
About the Role: Responsible for scientific support of research and development, tech transfer and commercialization of drug substance processes, batch manufacturing and regulatory document contribution through individual input. Provides project management support for CMC programs or Chemical Development projects, may lead work streams or projects within Chemical Development . May train lower level scientists and/or team members.
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Your Contributions (include, but are not limited to):
Supports project planning efforts. Participates on cross-functional teams and may represent Chemical Development. Maintains accountability for assigned deliverables for R&D and manufacturing plans for Chemical Development projects
Independently plans and executes activities towards the goals of one or more project work streams to support Chemical Development Programs
Ensures laboratory work is done productively and practices safe laboratory skills
Performs process R&D and optimizes synthetic routes
Recommends alternatives, researches new methods and techniques to solve problems
Assists with managing off-site synthesis, manufacturing activities and may interact with contractors
May provide input for portion(s) of CMC regulatory documentation and supporting work
May train lower level scientists and/or team members
Builds and enhances internal and external professional relationships
Other duties as assigned
Requirements:
BS/BA degree in Chemistry and 5+ years of experience in experience in pharmaceutical/process development field, including API manufacturing experience, OR
MS/MA degree in Chemistry and 3+ years of similar experience above, OR
PhD in Chemistry and some relevant industry experience; may include postdoc experience
Strong understanding of organic chemistry and a well-developed understanding of process chemistry as well as current literature
Strong laboratory and productivity skills
API Manufacturing experience
Good understanding of cGMP requirements in API
Demonstration of cross-functional understanding related to drug development
Demonstrates solid level of understanding project / group goals and methods
Consistently recognizes anomalous and inconsistent results and interprets experimental outcomes
Able to explain the process behind the data and implications of the results
Strong knowledge of one or more scientific disciplines, becoming expert in one discipline
Strong knowledge of scientific principles, methods and techniques
Strong knowledge and demonstrated ability working with a variety of laboratory equipment/tools
Ability to work as part of a team; may train lower levels
Excellent computer skills
Strong communications, problem-solving, analytical thinking skills
Detail oriented yet can see broader picture of scientific impact on team
Ability to meet multiple deadlines, with a high degree of accuracy and efficiency
Strong project management skills
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\xe2\x80\x99t line up to exactly what we have outlined in the job description.
_ The annual base salary we reasonably expect to pay is $103,200.00-$165,200.00. 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 20% 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.
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