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, and 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. What You
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changing needs of the regulatory environment Works with RQA colleagues on cross GxP audit plans as required Coaches colleagues - leads training for routine and non-routine site and process audits Advises
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and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate
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, serum), detect the presence of anti-drug antibody and neutralizing anti-product antibody activity utilizing various platform in a regulated (GLP, GCP) environment against challenging timelines. Timely
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Laboratory experience in a relevant field of science Strong attention to detail and ability to collaborate and work in team environment Good Computer skills including word processing, Excel, PowerPoint and
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PHYSICAL/MENTAL REQUIREMENTS Frequent sitting, standing, walking required. Ability to perform mathematical calculation and perform complex data analysis required. The work environment ranges from office, to
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and investigators/medical professionals Is a team player, works well in a team environment both as a leader and a key contributor Has a global perspective and mindset, with the ability to work
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. High attention to detail. Ability to consolidate comments from multiple sources (e.g., emails, meeting minutes). NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Ability to flex working
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and create business impact." PHYSICAL/MENTAL REQUIREMENTS Standard business office conditions; sitting, standing as appropriate NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Infrequent