Scientist, Pre-Clinical Assay Group
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
Worldwide Research and Development (WRD) at Pfizer combines research and technology units that have deep disease area expertise and cutting-edge science and platforms to discover and develop innovative therapeutic programs in small molecules and biotherapeutics, including vaccines. In your role, you will work closely with other biochemists, medicinal chemists and biologists and apply your background/skills to understanding the underlying biochemical pathways and characterizing the molecular interactions between chemical compounds and target protein(s).
As a Scientist, 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 be recognized as a technical expert and a scientific contributor. With your deep knowledge of the discipline, you will be an active team member who influences at the project team level. You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience and consulting others. Your ability to plan will help in preparing short-term work activities on projects. Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide your team members.
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Apply technical skills and functional knowledge to projects/ assignments within own work group/ project team independently and proactively.
Act as a technical resource within own work group/project team.
Act as scientific expert for development, optimization,and transfer of analytical methods for characterization of vaccines/therapies.
Design, plan, and execute assay development, qualification,and transfer studies with guidance to support the release, stability,and characterization testing of early vaccine/therapy candidates.
Prepare and review technical documents including study protocols and reports, risk assessments and provide input for regulatory and GMP (Good Manufacturing Practices) relevant documents.
Present scientific data at internal meetings in global interdisciplinary teams.
Manage daily, weekly,and monthly laboratory activities, such as monitoring of equipment, completion and review of equipment logbooks, periodic laboratory cleaning and managing the laboratory waste, checking PMO status of labequipmentand resolving discrepancies.
Manage storage of reagents and test solutions in accordance with departmental procedures.
Participate in continuous improvement of scientific and regulatory processes via update/creation of SOP’s, design and implementation of laboratory and study based processes and development of best practices for bioanalytical data generation.
Contribute to the development of new technologies, coordinate internal and external collaborations.and drive the implementation into routine processes.
Be responsible for QC and peer review of raw data,results, and final reports from other colleagues within the regulated group, participate in internal and external audits providing required information to auditors, as needed.
Bachelor’sDegree(BA/BS)and 6+ years of 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.
Good understanding of immunology and cellular biology.
Demonstrated experience with assay qualification, validation and when required sample analysis.
Master’sdegree(MA/MS)and 4+ years of relevant experience.
Proficiency and ability to utilize techniques such as LC/MS to develop methods.
Experience with Documentum Document Management Systems, Watson Lims, Ariba Purchasing software
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
potential travel up to 10-20%
Work Location Assignment:Flexible
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.
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