Senior Master Data Analyst
hace 1 mes
Pfizer Senior Master Data Analyst in Bothell, United StatesWhy Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer-oriented. Whether you are involved in development, maintenance, compliance, or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve The Senior Master Data Analyst position creates, reviews, and verifies the modifications of Master Data specific to the Bothell site for LIMS and Quality SAP tables. This role leads department projects and provides customer support and training.
In your role, you will be joining a team that is accountable for assuring the compliant validation of information technology systems. Your work will involve creating formal validation documentation (including standard operating procedures) as per governmental regulations and coordinating activities with clients, programmers/developers, and operating personnel, in-country or global, as appropriate.
As a Senior Master Data Analyst, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.
It is your dedication and hard work that will make it possible for customers and patients to receive the medicines they need, when they need them.
How You Will Achieve It Creates new Master Data objects of varying technical complexity.Reviews and verifies Master Data Analyst updates to existing Master Data objects.Processes Master Data updates for Change Controls, document updates, and Core release functionality upgrades.Reviews Sample Management with end users.Provides troubleshooting expertise and support for all Laboratory System activities and end users including instrument interfaces in conjunction with Digital and Laboratory (EM, AQ, IQ, CQ, BQ) Departments.Aids in interfacing with site personnel on integration of sample management and electronic system processes to ensure optimal business processes.Aids in updating Master Data and corresponding departmental SOP and training materials as needed in accordance with global procedures and processes, as requested.Participates in all Laboratory System Release, User Council, Master Data Network, and Lab of the Future Meetings.Certified Site Trainer and Certified Core System Trainer: required to deliver end-user training and train Master Data Analysts.Assists with verification testing for Core Releases.Contributes to the completion of moderately complex projects.Manages own time to meet agreed targets.Develops plans for short-term work activities on own projects (timelines, work plans, deliverables) within a Work Team.Qualifications Must-Have High School Diploma (or Equivalent) and 8 years of relevant experience OR an associate's degree with 6 years of experience OR a bachelor's with at least 3 years of experience OR a Master's with more than 1 year of experience.LIMS/EMPOWER/SAP or ALM experience.Knowledge of Laboratory/Sample Management processes and Laboratory Methods.Excellent knowledge of Microsoft Office.Able to effectively work independently or within a team environment on multiple projects.Demonstrate attention to detail and organizational skills.Strong oral, written, communication, presentation, and interpersonal skills.Capable of interfacing with multiple levels of individuals within the organization.Nice-to-Have Relevant pharmaceutical experience.Experience with system development and system administration requirements inclusive of Database Management Systems (DBMS), Application implementation, Network Infrastructure (network devices, servers, operating systems), IT security, and Web Technologies.Experience with laboratory systems, automated manufacturing systems (SCAD, PLC, HMI), Network Qualification.Experience in Validation principles and validation documentation.PHYSICAL/MENTAL REQUIREMENTS N/A
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS This role will require 24-hour support, if needed.
The annual base salary for this position ranges from $78,000 to $130,000. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental, and vision coverage.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address, and the type of payments or other value received, generally for public disclosure. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability, or veteran status. Pfizer also complies with all applicable national, state, and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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