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degree with 0+ years of experience. Familiar with process controls equipment. Understanding of programming, and proficiency in at least one language. Knowledge of Computerized Systems. Teamwork spirit
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or equivalent with 7+ years of clinical research experience and/or quality management experience. Skills in more than one language are an advantage in this role. English is required. Experience with drug
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regulations Understanding of Network/Server/Virtualization best practices Understanding of software/document repositories/versioning Understanding of programming, and proficiency in at least one language
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antibody API materials for clinical (including late stage clinical) and cGMP commercial phases. Understanding of programming, and proficiency in at least one language. PHYSICAL/MENTAL REQUIREMENTS Physical
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. Oral presentation skills: Strong oral presentation skills, including ability to present, explain and defend data analyses before internal and external (including Regulatory Authority) audiences. Language
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analyses before internal and external (including Regulatory Authority) audiences. Language skills: High fluency in written English and strong functional fluency in spoken English. Personal skills: Strong
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deal with a large volume of requests / deliverables on a regular basis. Ability to quickly/effectively prioritize and balance competing tasks in real-time. Demonstrated ability to flex language and style
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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 on ad
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and training abilities. Nice to Have DeltaV and/or PLC experience. Understanding of programming, and proficiency in at least one language. Direct knowledge and experience in automation qualification
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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