Principal Research Scientist I -Chemistry (onsite North Chicago, IL)
Principal Research Scientist I -Chemistry (onsite North Chicago, IL)
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1 Vacancy
Job Description
AbbVie (NYSE:ABBV) is a global researchbased biopharmaceutical company formed in 2013 following separation from Abbott. AbbVie combines the focus and passion of a leadingedge biotech with the expertise and capabilities of a longestablished pharmaceutical leader to develop and market advanced therapies that address some of the worlds most complex and serious diseases. AbbVie employs approximately 50000 people worldwide and markets medicines in more than 170 countries. AbbVie Product Development Science & Technology (PDS&T) is seeking a Principal Research Scientist Peptide Chemistry to conduct latestage development and commercialization of Peptides from registration through commercialization and the product lifecycle. We are seeking a highly motivated candidate with a proven track record of accomplishment in the field of peptide manufacturing development to work in a multifunctional team environment at our North Chicago IL location.
Key Responsibilities:
The candidate will contribute to and/or lead crossfunctional project teams associated with manufacturing process development process characterization/justification transfer of technology to manufacturing sites and support manufacturing activities for peptides and potentially other modalities:
o Provide leadership in a matrixed team setting while acting as an SME for peptide processes interacting with various crossfunctional groups and stakeholders and contributing to AbbVies peptide manufacturing strategies.
o Set project strategies define project responsibilities and timelines
o Author and review key regulatory documents laboratory data technical memos and reports.
The position involves multidisciplinary interactions with organic chemists analytical chemists engineers and solidstate scientists.
The position also entails interfacing with many groups external to PDS&T for example: Manufacturing Operations Regulatory Affairs Quality Assurance etc.
Responsibilities:
Effectively functions as a principal investigator generating original technical ideas and demonstrating creative out of the box thinking to solve difficult problems and champion new technologies to achieve project goals. Make significant contributions to project team through labbased activities. Independently responsible for project science within his/her area of expertise on one or more project teams.
Authors and/or reviews technical reports manufacturing batch records and regulatory documents concerning Chemistry Manufacturing and Control (CMC) subjects. Primary author of publications presentations and/or primary inventor of patents.
Potential to mentor/supervise a team of one or more individuals evaluate the performance of those individuals and be accountable for the effective performance of those individuals.
Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances or competitive threats and respond with appropriate new strategies.
Qualifications :
Bachelors Degree or equivalent education and typically 14 years of experience; masters degree or equivalent education and typically 12 years of experience; PhD and typically 6 years of experience in organic chemistry with a focus on peptide synthesis. Candidates with less experience may be considered for other opportunities.
Experience in peptide process development and commercialization.
A broad range of functional expertise in modern organic chemistry mechanistic understanding compound purification control strategy development and standard analytical methodology (e.g. HPLC UPLC LCMS NMR).
Demonstrated scientific communication and presentation skills. Experienced and demonstrated success as author of publications presentations and/or primary inventor of patents.
Strong interpersonal and communication skills for facilitating collaborations and a demonstrated ability to lead crossfunctional process development teams.
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our shortterm incentive programs.
This job is eligible to participate in our longterm incentive programs
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
