Why 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 trainings.

In your role, you will be joining a teamthatis accountable for assuring the compliant validation of information technology systems. Your work will involvecreatingformal validation documentation (including standard operating procedures)asper governmental regulationsandcoordinating activities with clients, programmers/developersand 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.

• Process Master Data updates for Change Controls, document updates and Core release functionality upgrades.

• Lead/manage department projects.

• Reviews Sample Management with end users.

• Provide 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.

• Aid in interfacing with site personnel on integration of sample management and electronic system processes to ensure optimal business processes.

• Aid in updating Master Data and corresponding departmental SOP and training materials as needed accordance with global procedures and processes, as requested.

• Participate 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 training Master Data Analyst.

• Assist with verification testing for Core Releases.

• Contribute to the completion of moderately complex projects.

• Manage own time to meet agreed targets.

• Develop 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 associates degree with 6 years of experience OR a bachelors with at least 3 years of experience OR Masters 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.

Work Location Assignment:On Premise

The annual base salary for this position ranges from $78000,00 to $130000,00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10,0% 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. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Quality Assurance and Control