Job Title: Senior Process Data Scientist
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This role requires a highly skilled professional to provide data and analytical support to establish, organize and maintain effective data coordination and data evaluation services pertaining to process monitoring and modeling of biological drugs.
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The successful candidate will be responsible for utilizing scientific principles to gather requirements from users, evaluate existing systems, and provide guidance on the utilization of potential new data architecture, infrastructure, systems, and tools.
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Key responsibilities include interfacing and collaborating with various departments across the business, analyzing data sources, data infrastructure and architecture, collating data, and preparing documentation in support of testing and validation activities.
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The ideal candidate will have strong communication and interpersonal skills, possess logical troubleshooting and problem-solving skills, and have a proven track record to communicate effectively with multiple partners.
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Required qualifications include a BS/BA or equivalent experience in mathematics/statistics, or related field with 5+ years' experience; or equivalent combination of education and experience. Experience in a biopharmaceutical cGMP manufacturing setting is an advantage.
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Responsibilities:
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* Gathering requirements from users, evaluating existing systems, and providing guidance on the utilization of potential new data architecture, infrastructure, systems, and tools.
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* Interfacing and collaborating with various departments across the business.
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* Analyzing data sources, data infrastructure and architecture, collating data, and preparing documentation in support of testing and validation activities.
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* Running quality system events pertaining to data integrity and data management.
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* Troubleshooting computer systems and developing solutions to technical issues using critical thinking skills and process analysis.
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* Presenting on project status and team metrics during cross-functional meetings and to upper management.
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* Generating design, requirements, and testing documentation in support of validation activities.
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* Automating routine tasks and data solutions to continuously improve processes.
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* Providing audit and regulatory submission support where applicable.
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* Providing coaching and mentoring to junior members of the team.
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Requirements:
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• Strong communication and interpersonal skills.
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• Logical troubleshooting and problem-solving skills.
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• Proven track record to communicate effectively with multiple partners.
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• BS/BA or equivalent experience in mathematics/statics, or related field with 5+ years' experience.
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• Equivalent combination of education and experience.
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• Biopharmaceutical cGMP manufacturing experience (advantage).
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