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Associate Business Analyst, Laboratory Management Systems

Employer
Pfizer
Location
Pearl River, New York
Salary
Competitive
Closing date
Dec 16, 2021

View more

Discipline
Other, Other
Position Type
Full Time
Organization Type
Pharma
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Why Patients Need You

Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve

As an Associate Business Analyst, you will be at the center of our operations and you'll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of developing written end-user requirements for data systems used in various laboratory processes. These various processes are used to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer's vaccine programs according to Standard Operating Procedures. You will perform user testing of data systems and execute test scripts, as needed, prior to validation and deployment in the Production environment. In addition, you will be part of a dynamic team and should possess a strong work ethic and collaborative spirit.

Your significant experience of applying knowledge of principles, concepts, and practices of the discipline will make you a critical member of the team. You are proactive in contributing to all team discussions and creating an environment of 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

  • Perform job responsibilities in compliance with current Good Manufacturing Practices/ Good Laboratory Practice (cGMP/GLP) and all other regulatory agency requirements.
  • Assist in the development and writing of end-user requirements for data system builds requested by functional assay leads as well as for functional enhancements to existing builds
  • Assist and perform end-user testing of various data system builds against end-user requirements to ensure that these systems function as intended by the end user
  • Collaborate with laboratory assay SMEs and Pfizer RI/IT organizations on data system projects according to VRD priorities
  • Attend regular meetings with functional assay leads to review and monitor various data system projects
  • Review and approve various standard operating procedures (SOPs), as assigned
  • Maintain compliance with SOP periodic review process
  • Monitor the SOP review and approval workflows for authored SOPs
  • Author, review and approve technical reports, as assigned
  • Maintain strict compliance with departmental and site safety regulations
  • Stay current on all departmental and corporate training.


Qualifications

Must-Have

  • Bachelor's Degree in a science-related discipline such as computer science, mathematics, or biological science
  • Minimum 2 years of assay development experience in a GLP Laboratory environment
  • Minimum of 1 year direct, hands-on experience with LabWare LIMS
  • Must have strong verbal and written communication skills
  • Strong attention to detail and ability to collaborate and work in team environment
  • Proficient in Microsoft Office 365 applications


Nice-to-Have

  • Hands-on industry experience with the development and testing of electronic data systems
  • The ability to understand and effectively describe complex laboratory and data-handling processes both verbally and in writing
  • Experience with SAS
  • Experience with creating flow charts and testable, line-item requirements
  • Experience executing test scripts


NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Occasional evening and weekend work to meet critical deliverables

OTHER JOB DETAILS

Eligible for Relocation Package

Eligible for Employee Referral Bonus

#LI-PFE

Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.

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. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

EEO & Employment Eligibility

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.

Research and Development

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