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Associate Scientist, Downstream Process Development
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Associate Scientist, Downstream Process Development - Contract - Gaithersburg, MD
Proclinical is seeking a dedicated and innovative Associate Scientist to join our Downstream Process Development Department. This is a contract position based in Gaithersburg, MD.
Primary Responsibilities:
The successful candidate will play a pivotal role in the development, scale-up, and technical support of cGMP manufacturing for protein-based vaccines. This role involves designing scientifically sound and scalable purification processes, generating materials for developmental studies, and providing technical support. The ideal candidate will be self-motivated, well-organized, and highly productive.
Skills & Requirements:
- MS in a relevant scientific discipline or BS with relevant experience.
- Hands-on Downstream purification experience.
- Knowledge in purification of vaccines/biologics; Experience in various chromatography methods, filtration, and TFF unit operations at bench scale and/or pilot scale is a plus.
- Capable of performing multiple functions in a fast-paced environment.
- Strong technical protocol/report writing, and good organization skills.
- Excellent record keeping abilities to adequately record, analyze and document data generated in support of regulatory requirements.
- Demonstrated verbal and written skills in communicating scientific and technical information.
- Proficient in Window based software including Excel, PowerPoint and Word.
The Downstream Process Development Associate Scientist will:
- Support the development of purification processes by reviewing and compiling relevant literature data.
- Perform scale-up of processes to deliver materials for pre-clinical and clinical studies.
- Execute optimization experiments to ensure the process is robust, high in purity, yield, and scalable for clinical stage manufacturing.
- Design experimental work under the supervision of senior scientists.
- Process complex data and clearly communicate the implications of the results.
- Generate, manage, evaluate, and maintain critical data in a highly organized manner and provide assessment reports.
- Provide reagents and other supplies for various projects and departments.
- Support process characterization studies, process validation, and tech transfer process as needed.
- Maintain inventory of lab supplies and order lab consumables as needed.
- Prepare buffers and column packing at different scales.
- Perform testing of in-process samples.
- Operate the glass washing instruments and autoclaves as needed.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCQA
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