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发帖数: 593 | 1 Scientist (Last Date to Apply for Job: August 16, 2017)
Please apply from the Pfizer Website
https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/USA---NC---
Sanford/Scientist_1609311-2
The qualified candidate will join the Manufacturing Science and Technology (
MSAT) organization as a Scientist supporting biological therapeutics and
vaccines. Within MSAT, the candidate will work in the Purification Group,
which develops processes for isolation and purification of recombinant
proteins, polysaccharides, bioconjugates, and other biologics.
Projects may include execution of processes at lab and pilot scales, process
development and characterization, scale-up and tech transfer to commercial
manufacturing, process simulation and modeling, process troubleshooting, new
technology development and implementation.
The incumbent will run various recovery and purification unit operations,
including preparative chromatography, Tangential Flow Filtration (TFF), and
Normal Flow Filtration (NFF) at lab and pilot scales, as well as providing
support for commercial scale operations as needed.
The scope of the project work may include tasks in any or all of the
following stages: scope definition, feasibility studies, cost/benefit
analyses, design, specification development, project planning,
implementation, and post-implementation monitoring and follow-up.
The incumbent must be capable of contributing to cross-functional projects
and may lead some activities with involvement and coaching from their
supervisor.
Utilizing a high level of technical expertise, the incumbent is responsible
for moderately complex projects related to the development, scale-up and/or
characterization of processes, equipment, and control strategies, process
optimization, qualification of alternate raw materials and components, and/
or technology transfer to GMP commercial manufacturing facilities.
The candidate must be able to execute, analyze, document, and communicate
results from experimental studies conducted at lab, pilot or commercial
scales. The candidate must be able to interpret data and make
recommendations to optimize processes, improve yields, and enhance the
smooth transition from development through to successful implementation.
The incumbent will be responsible for troubleshooting and resolving process
issues, diagnosing technical problems, and determining short and long term
solutions. The incumbent will be required to work both independently and in
team environments and be able to coordinate multiple technical projects
simultaneously in a well-organized fashion.
The incumbent will be expected to prepare technical reports, provide oral
presentations to scientists and management, and assist in the preparation of
regulatory filing documents, as required.
Occasionally, some work on shifts, weekends and/or holidays may be required
to meet business or customer needs. Occasional domestic and/or international
travel may also be required.
Degree in Chemical/Biochemical Engineering, Biochemistry, or other related
biotechnology discipline: Ph.D. degree; M.S. degree with a minimum of 2
years of relevant experience; B.S. degree with a minimum of 4 years of
relevant experience.
Technical knowledge and skills in purification of biologics achieved through
industrial or academic experience in research and development, technical
operations, manufacturing, etc.
Experience with operating, monitoring and/or control of purification
processes including Chromatography, Tangential Flow Filtration (TFF), and
Normal Flow Filtration (NFF). |
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