Scientist, QC Portfolio Management
Job Description
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
The resource will work on-site at the Pfizer, Sanford, North Carolina facility and will be a member of Pfizer’s Quality Control Portfolio Management team to support multiple quality programs. The resource will analyze chemical, or biological or microbiological qualities of products. The resource will perform the analytical or chemical or microbial testing in the GMP laboratory setting and collaborate with the external teams. Additionally, the resource will document all the data to in accordance with cGMP and data integrity principles. The resource will also write, review or approve protocols.
How You Will Achieve It
Independently plan and execute laboratory experiments.
Collaborate with trainers, colleagues and subject matter experts to perform the assays in the laboratories, including the use of computational predictive tools, modeling software, and data visualization tools as necessary.
Assisting teams in completing the assays required for the validation and transfer of methods.
Engage with the method development team and participate in both in-process and final product sample analyses.
Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes.
Prepare technical reports, critically review data as second analyst for the validations, and evaluate new instrumentation and analytical techniques as required.
Independently analyze experimental data and provide conclusive insights.
Mentor junior analysts and offer technical guidance when required.
Qualifications
Must-Have
Bachelor’sDegree(BA/BS)and 6+ years of experience.
Master’sdegree(MA/MS)and 4+ years of relevant experience.
Proficiency with word processing, spreadsheets, PowerPoint,and relevant scientific software.
Strong knowledge of data analysis tools, experience in presenting scientific data and results in both written and oral formats.
Extensive hands-on experience and strong background in either Chemistry, Microbiology or molecular biology assays.
Demonstrated experience with assay qualification, validation and when required sample analysis.
Experience with troubleshooting assays and improving method performance.
Nice-to-Have
Experience with method validation and method transfer skills to manufacturing site.
Experience with bio-process downstream development.
Work Location Assignment:On Premise
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. 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. This position requires permanent work authorization in the United States.
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.
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