Scientist I - Analytical Development
Location: College Station
Posted on: June 23, 2025
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Job Description:
The work we do at FUJIFILM Diosynth Biotechnologies Texas has
never been more important—and we are looking for passionate,
mission-driven people like you who want to make a real difference
in people’s lives. From developing the next vaccine to advancing
cell and gene therapies, we collaborate with industry leaders to
tackle complex challenges and deliver meaningful solutions. If
you’re ready to help transform the future of medicine, join
FUJIFILM Diosynth Biotechnologies. We offer a flexible work
environment and we’re proud to cultivate a culture that will fuel
your passion, energy, and drive—what we call Genki. Our
state-of-the-art biomanufacturing facility is located in in College
Station, Texas, which combines a small-town feel with vibrant
culture, top-notch schools, and close proximity to big city life.
Nestled between major hubs, it’s a dynamic location that blends
convenience with innovation. Essential Functions: • Participates in
the development of new analytical methods, processes or
technologies • Ability to work with team members and client to
troubleshoot and solve complex problems to keep the client
satisfied and happy with end results. • Clearly articulate in
presentations to senior management and/or internal customers
regarding problems, updates, and/or results. • Participate in the
transfer of analytical methods from other collaborators/clients. •
Maintain a laboratory notebook according to company guidelines. •
Summarize results and generate reports. • Understands and applies
required techniques in support of projects and studies according to
pre-defined plans and protocols. • Maintain analytical
instrumentation as needed and interface with external vendors for
instrument installation and operation qualifications. • May train
or provide guidance to lower level scientists • May direct
technical work encompassing one aspect of a project under the
oversight of more senior staff. • Stay abreast of new technologies
in the field. • Expand expertise to other types of assays. • Ensure
lab is maintained (organized, clean, properly supplied). • As
appropriate, writes SOPs/procedures/instructions • As appropriate,
may participate in assay qualification process • As appropriate,
writes and reviews analytical plans, protocols or summary reports •
As appropriate, may write SME content of technical reports (memos,
development reports etc.) • All other duties as may be assigned.
Required Skills & Abilities: • Advanced knowledge of basic, viral
vector, chemical and/or biochemical analysis and associated
techniques. • Independent use and application of more complex
instrumentation, computer systems and software for data acquisition
and analysis. • Experience with analytical instrumentation such as
analytical chromatography/ELISA, DLS, Nanosight or CE. • Experience
in assay development. • Ability to work with minimal supervision. •
Able to monitor on going experiments and identify and resolves or
suggests alternates or solutions to complex occurrences. • Ability
to understand basis of experimental design. • Work professionally
as part of a team and independently. • Ability to work on multiple
projects. • Some knowledge of cGMP (current Good Manufacturing
Practices). • Some knowledge of statistics for analytical
chemistry. • Demonstrated knowledge of analytical techniques
demonstrated through industry or academic performance. • Ability to
work on multiple problems of higher complexity. • Implementation of
new methods and processes. • Adequately assembles reports and
presentations describing scientific information. • Familiarity with
available new technologies and vendor offerings. • Ability to
clearly communicate in writing and verbally to senior management
and/or internal clients. • Ability to write and perform detailed
analytical procedures. Working Conditions & Physical Requirements:
The physical demands described here are representative of those
that must be met by an employee to successfully perform the
essential functions of this job. Reasonable accommodations may be
made to enable individuals with disabilities to perform the
essential functions. While performing the duties of this job, the
employee is regularly required to: • Experience prolonged standing,
along with some bending, stooping, and stretching. • Use hand-eye
coordination and manual dexterity sufficient to operate a keyboard,
photocopier, telephone, calculator, and other office equipment. •
Potential for exposure to hazardous chemicals, gases, fumes, odors,
mists, and dusts, and other hazardous materials. • Ability to lift
50 pounds on occasion and 25 pounds regularly. • Ability to wear
PPE. • Attendance is mandatory. Minimum Qualifications (in addition
to the required skills and abilities): • Master’s Degree in a
science related field; OR • Bachelor’s Degree in a science related
field, with four (4) years of relevant experience; OR • Associate’s
Degree in a science related field, with six (6) years of relevant
experience. Preferred Qualifications • Experience working in a GMP
environment
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