A Scientist position is available in the Downstream process development group within Bioprocess R&D. The successful applicant will have experience in laboratory research, and a desire to continue in a laboratory-focused role. This position will join a larger team of scientists across multiple sites focused on
developing and optimizing recovery and purification processes for recombinant proteins and biological macromolecules for early- and late-phase clinical trials. The Scientist will be responsible for working with fellow scientists to develop robust, efficient, scalable strategies for improving process performance.ROLE RESPONSIBILITIES
The job function requires judgment and innovation to achieve a solution within standard practices and procedures. Responsibilities will include conducting experiments, tests, analyses as part of a variety of research and development activities, e.g., small-scale studies, pilot plant and manufacturing downstream
purification studies. The Scientist will be expected to summarize, evaluate the study results, develop and test new hypotheses to improve the fundamental understanding of recovery and purification processes. This position will support process validation, quality by design, regulatory approaches, and innovative research. This position will be expected to prepare internally reviewed technical reports and make oral presentations to scientists and management. The successful candidate must be able to endorse change to business infrastructure to ensure pipeline, legacy and technology success.BASIC QUALIFICATIONS
- Bachelor's degree with 6+ years of experience or Master's degree with 4+ years of experience in a biological or engineering discipline (Biotechnology, Chemistry/Biochemistry, Chemical/Biochemical Engineering, or equivalent).
- Experience in laboratory research required, preferably in recombinant protein/biomolecule purification process development, technology transfer and/or bioprocess manufacturing.
- A good understanding of protein/biomolecule chemistry, analytics, and bioprocess technology is required.
- Demonstrated ability to drive for results and generate innovative solutions with minimum supervision.
Applicants should be self-motivated, organized, capable of working independently, and in a collaborative environment.
- The successful candidate will possess strong oral and written communication skills.
- Experience in transferring Biotherapeutic processes to pilot plants or manufacturing organizations, and knowledge of data acquisition and controls systems in these environments is a plus.
- Strong analytical and computer skills are desirable.Sound understanding of statistical experimental design and analysis is a benefit.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- This position will require standing for long periods of time in a laboratory setting.
- Occasional lifting of equipment may be required.
Other Job Details:
- Occasional travel to vendor, Pfizer or contract manufacturing/research sites may be required
- Eligible for Employee Referral Bonus: YES
- Locations Available in both Chesterfield MO or Andover MA
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Research and Development