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 associate scientist is responsible for the preparation of samples for preclinical and clinical serology studies to support vaccine development & clinical studies. This work will be performed within the Robotics and Automation area of the Clinical Immunology and High-throughput Operations (CIHO) group within Pfizer Vaccine Research & Development (VRD). The responsibilities include, but are not limited to, performing robotic sample preparation, instrument qualification, and data organization. In addition, the associate scientist may train other analysts. All work is to be performed in a compliant manner, according to applicable SOPs and cGxP guidelines, as required.
How You Will Achieve It
- Performs sample preparation for preclinical and clinical serology assays to support vaccine development and clinical studies. This includes manual and robotic sample preparation, use and maintenance of appropriate equipment, and preparation of relevant reagents. With the guidance of the supervisor, the incumbent performs moderately complex experiments and calculations, and discusses conclusions.
- Completes required documentation for all laboratory work. This includes the use of laboratory information management systems and/or paper forms.
- May train other analysts on established, basic technologies that he/she has become proficient.
- May participate in the qualification of new instruments and robotic methods following established protocols or scripts.
- Satisfactorily completes all required laboratory, cGxP and safety training, in conformance with departmental requirements.
- Where applicable, performs job responsibilities in compliance with cGxP and all other regulatory agency requirements.
Qualifications
Must-Have
- Bachelor's Degree with 0-2 years of laboratory experience in a relevant field of science including but not limited to microbiological techniques acquired in academic/industrial setting.
- Strong communication and computer/technical skills.
Nice-to-Have
- Knowledge of Laboratory Information Management Systems
- Experience with robotic liquid handling
PHYSICAL/MENTAL REQUIREMENTS
- Work is primarily performed at the laboratory bench or at an office desk using a computer. The job involves lifting loads, generally not more than 20 pounds.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- This position involves a non-standard work schedule, working Sunday through Thursday. A scheduled workday would consist of a total of 8 hours, between 10:00 a.m. and 9:00 p.m., according to business need. This schedule will be evaluated on a monthly basis.
Other Job Details:
- Last Date to Apply for Job: June 6th, 2024
- Work Location Assignment: On Premise
On Premise colleagues work in a Pfizer site because it's needed to get their job done. They may have flexibility to work remotely from time to time, but they are primarily on-site.
The annual base salary for this position ranges from $54,700.00 to $91,100.00. 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.
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.
Research and Development
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