About this role
Seeking a highly motivated individual, knowledgeable in biologics drug substance manufacturing process and digital transformation, to join the PDS&T Biologics MSAT team. This individual would lead global MSAT initiatives related to digital transformation for our MSAT data processes. The candidate should be a discipline expert who represents scientists’ needs, defines strategies, influences, and executes digital transformation strategy.
Responsibilities:
Lead digital transformation initiatives within PDS&T Biologics MSATServe as a point of contact for PDS&T Biologics MSAT in partnering with local MSAT, BTS, and other enterprise teams to develop key data and digital systems capabilities; Represent scientists' needs and advocate for the work processes and culture needed for digital transformation.Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.Proactively seek out new information, internally and externally, and incorporate this into individual project(s) as well as the overall program to ensure an industry-leading data and digital strategy for biologics process and analytics development.Partner with scientists to develop and implement data analytics and modeling tools that support data visualization and predictive modeling and seize opportunities to pursue project relevant leads that are in line with the group’s strategy.Inform and execute a digital transformation strategy for capturing, retrieving, and connecting critical data related to PDS&T Biologics MSAT workflows, promoting reusability and advanced analytics.Collaborate with AI and digital science teams to revolutionize daily operations through transformative programs.Define KPIs/dashboards and communicate progress on initiatives to stakeholders.Support the influence of leadership and cross-functional stakeholders for digital transformation with PDS&T Biologics MSAT business priorities. Bachelor’s Degree or equivalent education and typically 12 years of experience, Master’s Degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience.Possess thorough theoretical and practical understanding of own scientific discipline.Effective writer and communicator of research or other regulatory materials. 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 long-term 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 Company's sole and absolute discretion unless and until paid and may be modified at the Company’s 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.
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