Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
PHYSICAL/MENTAL REQUIREMENTS Ability to work in a laboratory environment performing experiments in a laboratory fume hood. Ability to perform complex data analysis. NON-STANDARD WORK SCHEDULE, TRAVEL
-
. Perform review of environmental conditions for controlled areas. Act with ownership and make quality decisions. Obtain certification as a controlled drug agent (CDA). Identify and initiate deviation process
-
awareness of changing external regulatory environment to ensure this thinking is reflected in the science performed within the function. Represent CRD to ensure good collaboration, proactive engagement, and
-
applications including Word Processing, Excel, and PowerPoint Ability to work in a team setting. PHYSICAL/MENTAL REQUIREMENTS Work in a lab environment for the majority of the workday. Work with various types
-
an environment of inclusion and collaboration. It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Contribute
-
advancing innovative ideas into tangible assets. This individual will thrive in a matrixed environment with ample opportunities for personal growth and development. How You Will Achieve It Design, execute
-
Exceptionalinterpersonalskillsandmasteryofworkingandinfluencingatalllevelsinamatrix environment. Excellentcommunicationskills;canarticulatecomplexconceptstoadiverse audience. RolemodelforthePFEValues(Courage,Excellence,Equityand Joy
-
cross functional teams in a dynamic, results-driven environment to drive innovation Mastery of complex business, engineering, and analytic issues with proven ability to provide in-depth evaluations
-
SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Other Job Details: Last Date to Apply for Job: May 26th, 2024 Work Location Assignment: On Premise On Premise colleagues work in a Pfizer site because it's needed
-
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