Qualified candidates will deliver results in a fast-paced matrix-oriented setting, be a contributor to key process purification steps and hold responsibility for various downstream process development activities. This advertised role is in support of products and process development for biotherapeutics and vaccines, including antibodies, antibody-drug conjugates, therapeutic proteins, and polysaccharides in commercial operations and late-stage clinical development.
The candidate will work across downstream purification functions, projects, and global sites.ROLE RESPONSIBILITIES
- The MSAT downstream purification group is responsible for providing support to the upstream team, as well as downstream development purification/optimisation activities and providing support to routine manufacturing operations.
- Candidate should have in-depth scientific knowledge and experience in a wide array of techniques such as UF/DF, Flow through Column Chromatography as well as Bind and Elute Chromatography and ideally familiar with standard downstream equipment, e.g. AKTAs.
- Development and qualification of purification techniques
- Ensure the proper and timely execution in all aspects of purification processing to support group activities.
- Perform scale-down purifications of biologics using precipitation, depth filtration, ultrafiltration and chromatography with the assistance of lab supervisor/designee.
- Qualified candidates will serve as a purification and biochemistry resource for the department and project teams, while proactively keeping historical product knowledge and experience.
- B.A./B.S with 4.5+ years or MS with 3+ years of experience developing purification strategies and methods in support of product and process development and assessing the quality and characteristics of biotherapeutics.
- Demonstrated technical writing skills and effective communication are strongly desired.
- Experience with technologies focused on purification of biomolecules and polysaccharides such as AKTA, UF/DF, Column Chromatography
Other Job Details:
- Knowledge and experience in Critical Quality Attributes (CQA) principles and practices and product specifications and specification setting.
- Demonstrated technical skills and scientific expertise in purification process development and troubleshooting
- Experience with Microsoft Office, Excel, Word, etc.
- Change agile, functional in a fast-paced team environment where multi-tasking required.
- Enthusiastic about communicating to a broad range of stakeholders (from novices to experts) and seeking agreement in complex situations.
- Curiosity about seeking and applying current relevant scientific literature.
Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.Sunshine Act
- Eligible for Employee Referral Bonus: Yes
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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.
Research and Development