Senior Associate Scientist - NonRegulated ADC Bioanalytics
Pfizer Inc.
Washington – Bothell, NY
Job posting number: #7288033 (Ref:pf-4922608)
Posted: October 27, 2024
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
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 assist with development and qualification of bioanalytical methods in support of characterization, toxicology and stability studies for bioprocess and formulation development of early phase vaccines.
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 innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe
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 to complete assigned work within own work group/project team.
Conduct scientific studies to support quantitative bioanalsyis and provide solutions to technical problems.
Be a collaborative member of your team by collaborating with other colleagues to support bioanalytical sample analysis consistent with drug development timelines.
Work closely with scientists, analysts, and other colleagues to meet study objectives
Support the authorship of development reports, and regulatory submission documents.
Support initiatives to develop best practices, test methods, and work processes to drive efficiencies.
Effectively communicate experimental observations and results.
Follow instructions to complete timesensitive assignments and contribute to the completion of project experiments and milestones.
Record experimental details and data into an electronic (digital) laboratory notebook.
Review the laboratory experiments and other written records of fellow scientists.
Ensure safe working practices are followed and maintained both intheir ownand others’ work.
Qualifications
Must-Have
Bachelor's Degree(BA/BS) with 3+ years of experience OR Master's Degree with 0+ years of experience.
Excellent organizational and communication (oral and written) skills.
Comfort in using computational models.
Knowledge and hands-on experience developing ligand-binding assays, utilizing various platforms and demonstrated analytical problem solving skills
Broad understanding and skill in areas of bioanalytical laboratory techniques for biotherapeutics
Ability to use appropriate software to perform analysis of data
Experience with experimental design and the interpretation of results
Effective verbal and written communication skills
Proficiency with personal computers, including word processing, Excel, PowerPoint and relevant scientific software
Nice-to-Have
Strong foundational understanding of basic principles of physical, organic and analytical chemistry.
Experience conducting and optimizing routine laboratory experiments.
Industry experience with a focus in biotherapeutics
Good understanding or experience in the Quality Control review of work conducted in a regulated laboratory
Skills in other areas, such as RT-PCR, digital PCR, cell-based assays and/or reagent characterization
PHYSICAL/MENTAL REQUIREMENTS
Standard laboratory activity lifting and working at a lab bench and data analysis.
Other Job Details:
Last Date to Apply for Job: October 30th, 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.
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.
