À propos de ce poste Senior Scientist- Analytical Research and Development chez Pfizer
What You Will Achieve
As a Senior 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 whose decisions impact the projects. You will perform qualitative and quantitative analyses of organic and inorganic compounds to determine chemical and physical properties during chemical syntheses, or drug product development process.
You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience. You will be forecasting and planning resource requirements for your project team. Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide team members.
It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
This colleague will be responsible for developing analytical strategies in support of pharmaceutical drug substance and/or drug products during all development phases, including supporting manufacturing process development, developing, validating and transferring analytical methods, designing stability studies for shelf life assignments, and developing impurity control strategies.
Collaborates with colleagues and subject matter experts to assess the most appropriate analytical approach to support project activities, including use of computational predictive tools, modelling software and data visualization tools where appropriate.
Perform lab work and delegate responsibilities and review peer lab work as appropriate,
Through effective communication and collaboration with multidisciplinary team members, this colleague will have the opportunity to present data at team meetings and be actively involved in solving technical challenges that arise during development.
The candidate must be able to collaborate with and mentor peers as well as effectively interact with colleagues at all levels of the organization.
Author relevant sections of global regulatory submissions in support of new drug approvals. They will also prepare technical reports, critically review data, and may evaluate new instrumentation and analytical techniques/approaches.
Proficient with a wide variety of software and information systems and the curiosity to continue learning new techniques to solve complex analytical problems.
Proficient with a breadth of relevant methodologies such as, chromatography, dissolution, IR spectroscopy, mass spectrometry, particle size analysis and NMR, with expertise in one or more of these techniques.
Qualifications
Must-Have
Ph.D. in Analytical Chemistry or related field, with 0 to 3 years of relevant industrial experience or MS in Analytical Chemistry or related field with 7 to 8 of years of experience.
Demonstrated ability to meet timelines with minimal supervision and experience leading multi-disciplinary teams.
Demonstrated ability to learn new techniques and solve complex analytical problems.
Demonstrated oral and written communication skills, including visualization of data and drafting reports.
Attention to detail, strong organizational skills, the ability to multitask, and effective interpersonal and communication skills.
Proficient with a breadth of relevant methodologies such as, chromatography, dissolution, IR/Raman spectroscopy, mass spectrometry, particle size analysis, and NMR, with expertise in one or more of these techniques.
Nice-to-Have
Experience in the pharmaceutical industry.
Prior experience with analysis of peptide therapeutics.
Experience with trace level impurity analysis
Understanding and prior experience in global regulatory submission processes.
Familiarity about separation technology including liquid chromatography, gas chromatography, SFC, etc.
Experience with a wide variety of software and information systems utilized in the pharmaceutical industry (eg LIMS, Chromatographic Software, Veeva, electronic notebooks).
The ability to use computational predictive tools, modelling software or data visualization tools.
PHYSICAL/MENTAL REQUIREMENTS
Ability to perform calculations and data analysis is required.
This role requires the use of laboratory equipment and working in laboratories. Some lifting may be required.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Some travel may be required.
Relocation support available
Work Location Assignment: On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
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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.
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Research and Development