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, and proficiency in at least one language. Direct knowledge and experience in automation qualification or verification within a biopharmaceutical or pharmaceutical cGMP environment is desired. Experience
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internally and externally-facing medical channels, including scientific communication platforms (SCPs), publications, plain language summaries (PLS), congress narratives/content, advisory board content
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internally and externally-facing medical channels, including scientific communication platforms (SCPs), publications, plain language summaries (PLS), congress narratives/content, advisory board content
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equipment. Strong knowledge of Computerized Systems, Compliance regulations and standards. Understanding of programming, and proficiency in at least one language. Teamwork spirit, good communication skills
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correlational rules between heterogenous data sources for effective analytics and reporting • Successfully bridge engineering and business with ability to speak the common language of both • Provide coverage
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studies, insights, the Clinical Development Plan and regulatory strategy to ensure teams use accurate, consistent language and referencing aligned with the overarching MST strategy. Ensure the product-level
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interpersonal effectiveness and communication skills (written and oral) Nice-to-Have Relevant pharmaceutical or medical device experience Understanding of programming, and proficiency in at least one language
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the MST) with evolving evidence from clinical studies, the Clinical Development Plan and regulatory strategy to ensure teams use accurate, consistent language and referencing aligned with the overarching