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Sr. Associate Scientist
4 months ago
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 a Senior Associate 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 responsible for supporting the clinical testing of on the market or pre-market vaccines. You will perform various assays to monitor the efficacy of vaccine candidates. Your skills and expertise will ensure that all work is to be done in a compliant manner according to relevant Standard Operating Procedure (SOP) guidelines and Good Lab Practices cGLP and/or (Current) Good Manufacturing Practices (part of GxP) cGMP guidelines.
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
Contribute to achievement of immediate work group goals and collaborate with other team members.
Satisfactorily completes all GLP (Good Laboratory Practices) and safety training in conformance with requirements.
Perform sample preparation for clinical molecular assays to support vaccine development and clinical studies.
Complete required documentation for laboratory work involving assays.
Execute qualifications/validations of new instruments and custom methods.
Organize assigned work according to established departmental priorities.
Interact with external vendors to obtain quotes, and purchase reagents for clinical testing where applicable.
Identify and report any experimental problems, proactively troubleshoot causative factors, and implement necessary corrections following discussion with supervisor.
Manage manual and robotic sample preparation, use and maintenance of appropriate equipment, and preparation of relevant reagents.
Train other analysts on established technologies and supervise junior staff.
Qualifications
Must-Have
General
Bachelor's Degree with 3+ years of experience working in a BSL-2 laboratory with molecular assays
Effective verbal and written communication skills
Good record of following SOPs and performing clinical laboratory work compliantly
Laboratory Skills
Experience with working in a high-throughput clinical testing environment
Experience with aseptic techniques
Experience in developing and troubleshooting molecular assays
Basic laboratory skills in the area of solution making, molecular biology, biochemical assays and sample processing
Knowledge
Ability to use appropriate software to perform data analysis
Experience with being a subject matter expert (SME) for an assay
Experience with experimental design and the interpretation of results
Proficiency with personal computers, including word processing, Excel, PowerPoint and relevant scientific software
Experience with overseeing skills assessments (OJTs)
Nice-to-Have
General
Experience programming in Excel VBA or R-Shiny
Effectively communicate and cooperate with colleagues within and across teams
Resource Management
Collaborate with team members to perform assigned tasks for the purpose of achieving team goals
Experience with assisting in team resource allocation/scheduling
Knowledge Skills
Experience with genetic sequencing
Has had experience with contributing to problem solving such as troubleshooting assay anomalies, within the constraint of SOPs
Experience with performing quality data review
Has contributed ideas for process improvement
Understands the scientific principles behind assays they have been involved in, and present scientific data at team meetings
Author and update documents
Decision Making
Ability to analyze, trend, and troubleshoot quality controls/long-term panel data
Has successful experience with providing scientific input on assays
Demonstrate scientific judgment and decision-making skills
Leadership
Responsible for laboratory operations, examples are:
Communicate with vendors for technical questions, repairs, and quotes
Order and manage inventory
Manage reagent bridging workflow
Generate and resolve tickets with Informatics & Data Operations team
PHYSICAL/MENTAL REQUIREMENTS
- This position requires the typical physical demands of a general scientific laboratory environment during set up and operation of pharmaceutical laboratory equipment.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- This position may require occasional weekend work hours, as necessary. Individuals will be required to adhere to safe work practices including the proper use of personal protective equipment (PPE).
Other Job Details:
Last Date to Apply for Job: June 17, 2024
Work Location Assignment: On PremiseOn 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 $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.
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
