Overview:

The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy, and drive - what FDB call Genki. 

College Station, Texas may be a small, university town, but the lively cultural scene and local amenities make it a great place for families as well as those who want the ease of small-town life and the convenience of living close to the vibrant pulse of big cities. Eighty-seven percent of Texas' population lives within a 180-mile radius, so we are in the center of it all in Texas. And our site is nestled in the hub of innovation, representing a source of pride for the area.

Summary: 

The Downstream Process Development Scientist II functions to design, execute, and interpret complex laboratory experiments and activities necessary for gene therapy, vaccine, and recombinant protein purification process development with priorities set by supervisor/project lead to achieve project goals.  The individual will typically lead customer process transfer projects.  The individual should display good technical knowledge and scientific understanding of downstream purification of viruses, proteins, and plasmid DNA as well as having knowledge of process development at both small and large process scales.

External US:

Essential Functions: 

Leads the technical transfer of viral and protein purification programs into Manufacturing with limited supervision

Collaborates with cross-functional teams to deliver program milestones

Manages project priorities with input from supervisor and/or department head

Functionally supervise work of junior scientists across multiple process transfer projects with oversight from the supervisor

Presents data both internally and externally in routine scientific meetings and may present outside of department to clients/customers/leadership.

Authors and reviews protocols, scientific reports, and data presentations

Works closely with process sciences and manufacturing group to assist and support process transfer into manufacturing

Represents Downstream Process Development group during internal meetings and participates in customer-facing communications

Cross-train in Upstream PD, Virology and Analytical Development groups to gain knowledge and functional capability in these areas

Assists in and contributes to Process Development programs at the direction of more senior scientists

Perform all other duties as assigned

Required Technical Knowledge and Experience

Individual will have broad knowledge/expertise relevant to downstream processing of protein, virus, and plasmid DNA based products expressed in mammalian, bacterial, insect and yeast cells. Knowledge/expertise should be practical and focused on lab-related activities:

Experience with general BSL-2 level laboratory techniques and maintenance

Demonstrated proficiency in the operation of downstream processing equipment; chromatography (including the AKTA line of chromatography systems), UFDF, depth filtration, etc.

Advanced understanding of liquid chromatography (IEX, HIC, Affinity, SEC, etc.), direct and tangential filtration, and centrifugation

Thorough understanding  viral and/or protein purification strategies

Expert understanding of laboratory and chemical safety

Excellent understanding of protein analytical techniques

Good understanding of protein and viral biochemistry

Experience with drug substance formulation and characterization

Demonstrated experience with complex problem solving and/or prevention analysis affecting both PD and GMP activities

Experience in a GMP setting and good understanding of cGMP regulations/procedures

Required Skills & Abilities:

Excellent written and oral communication skills

Ability to work closely with other members of a project group and receive constructive feedback

Ability to work independently and reliably across multiple projects

Ability to oversee junior scientists' work and provide positive guidance

Takes initiative in finding opportunities to improve group functions and tasks, as well as continuously developing own technical skills and knowledge

Proficient in the use of Excel, Word, PowerPoint, and familiar with Microsoft Visio.

Produces consistent, excellent-quality work

Consistently meets deadlines and communicates issues affecting program delivery in a timely manner

Can solve complex problems arising during transfer and GMP activities

Takes initiative in setting and achieving personal and professional goals

Excellent organizational and stress-management skills

The ability to work in team oriented environment is essential, as this person will work closely with other members of the Process Development Group and participate on multidisciplinary project teams.

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 required skills & abilities):

PhD in a science related field; OR

Master’s Degree in a science related field with four (4) years’ of relevant experience; OR

Bachelor’s Degree in a science related field with six (6) years’ of relevant experience; OR

Associates Degree in a science related field with eight (8) years’ of relevant experience.

Preferred Qualifications:

Experience working in a GMP environment.

Join us!  FDB is advancing tomorrow’s medicine, impassioning employees to chase the impossible and continually expand their potential.  We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community, and the world at large.

We are an equal opportunity and affirmative action employer.  All qualified applicants will receive consideration without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, disability, protected veteran status or any other characteristic protected by applicable federal, state, or local law. If an accommodation to the application process is needed, please email (url removed) or call (phone number removed).

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.