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data science models to solve problems in a business environment setting. Experience with supporting commercial strategies and tactics, experience in pharmaceutical or healthcare industry is preferred
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Automation Engineering or Validation in a GMP Manufacturing environment. Experience with test plans, user requirements, and system lifecycle documents. Comfortable working in a manufacturing environment
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/Historian knowledge (SQL, AVEVA PI). MES experience - Rockwell PharmaSuite. Vmware and virtualization knowledge. Basic networking knowledge. PHYSICAL/MENTAL REQUIREMENTS Office and plant environment
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PHYSICAL/MENTAL REQUIREMENTS Office and plant environment. Keyboarding, lifting, standing, bending, walking. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Weekend and off hours work required
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regulations and standards Proactive approach and strong critical thinking skills Flexible to work in a team environment within own team and interdepartmental teams Excellent communication and interpersonal
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analytical abilities and problem-solving skills. Ability to provide leadership, set priorities and be accountable to timeline . Training in a GCLP/GLP/GMP environment and other international regulatory
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achievement of operational targets. Ensure a safe working environment for the laboratory. Lead initiatives to improve safety performance and colleague engagement. Support continuous process performance
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Engineering, or equivalent science related or engineering discipline. 4+ years of demonstrated experience in Automation Engineering or Validation in a GMP Manufacturing environment. Experience with test plans
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the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines
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within the local clinical development environment with a goal to enhance Pfizer reputation in scientific leadership. Responsible for proactively providing local intelligence Provide country/regional level