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

As a member of our Quality, Informatics and Data Operations (QIDO) team, you will assist with data integrity (DI) initiatives and provide quality guidance and oversight to Vaccines Research and Development colleagues that aligns with CFR and EMA guidelines for bioanalytical laboratories and Pfizer quality standards. You will primarily be responsible for the testing and validation associated with implementation of DI solutions and assisting with Quality Assurance oversight activities of the Vaccine R&D laboratories. Efforts should be made to seek and embrace continuous improvement opportunities within VRD with an emphasis on quality and data integrity.

How You Will Achieve It

• Partner with Informatics operations analysts, architects, developers/engineering leads and equipment asset owners to ensure VRD information system landscape meets short-term and long-term needs.
• Ensure compliant processes exist, and follow those processes, for data collection on instruments and that validated processes exist for non-standard systems.
• Ensure compliance related projects are properly established and deadlines communicated.
• Review and approve SOPs, Test Methods, validation documentation and reports for compliance with CFR, EMA and VRD SOP requirements as a DI or Quality reviewer.
• Review and participate in Data Integrity and compliance assessments of laboratory instruments and software.
• Identify performance gaps in information systems and investigate new areas for improvements.
• Escalate Data Integrity concerns or potential Quality Events to VRD management in a timely manner.
• Participate and lead where appropriate in the validation of computer systems, instrument qualifications, or hardware processes.
• Write departmental SOPs; maintain technical paperwork and migrate such data to archive repository.
• Provide support across various Quality management processes, including the VRD change control programs.
• Maintain strong connections and communications with line SMEs, leading efforts to map the sequential movement of information and data that feed into digital products to ensure data integrity.
• Lead efforts acrossBioProcess R&Dgrouplines toidentifygaps and define solution requirements for Digital Products by understanding end user requirements.
• Maintain and continuously develop knowledge of global GxP regulations and guidelines as they apply to VRD. This knowledge should be used to make quality decisions in all job responsibilities.
• Completes all cGMP/cGLP/cGCP/GCLP, corporate and safety training in conformance with Departmental requirements.

QUALIFICATIONS

Must Have

• BS in a relevant scientific field and 0-2 years of cGMP or GLP/GCLP experience OR
• Strong communication and collaboration skills
• Laboratory or manufacturing experience in a GxP regulated industry preferred
• Experience with information systems preferred
• Experience with Microsoft Office and data base applications

PHYSICAL/MENTAL REQUIREMENTS

• Ability to perform work while standing/sitting.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• This position may require weekend or evening work to meet critical business timelines.
• This position may require travel to scientific meetings, between Pfizer sites, to external laboratories, and other business-related travel.

Other Job Details:

• Last Date to Apply for Job: 02 OCTOBER 2024
• Eligible for Employee Referral Bonus

Work Location Assignment:Flexible

The annual base salary for this position ranges from $64,600.00 to $107,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% 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.

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