Process Development Downstream Associate Scientist
Posted on Sep 21, 2024 by Fujifilm
College Station, TX
Research
Immediate Start
Annual Salary
Full-Time
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 Associate Scientist functions to assist in the planning and execution of 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 typically provides technical support for GMP activities and represents the Downstream Process Development group during process transfer and manufacturing support. This individual will have familiarity with a range of purification technologies including centrifugation, filtration technologies (TFF and depth), chromatographic separations and basic laboratory analytical techniques (SDS-PAGE, spectroscopy, pH/conductivity meters, etc.)
External US:
Essential Functions:
Prepare, execute, and monitor viral and protein purification processes at the direction of project leads, appropriately observing and recording data
Independently prepares, executes, and maintains liquid chromatography systems
Independently prepares, executes, and maintains direct and tangential flow filtration systems
Prepares buffers, samples, and records data
Maintains the process development lab and its equipment
Technically and physically support GMP activities during preparation and execution
Communicate effectively, both within the PD group and cross-functionally
Author and edit standard operating procedures and work instructions
Maintain detailed laboratory notebooks following FDBT procedures
Perform all other duties as assigned
Required Technical Knowledge and Experience:
Experience with general laboratory setting and techniques (pipetting, dilutions, aseptic technique, etc.)
Good understanding of relevant sciences (physics, chemistry, biochemistry)
Good understanding viral and/or protein purification strategies
Excellent understanding of laboratory and chemical safety
Experience with protein analytical techniques
Experience with routine equipment troubleshooting
Familiar with cGMP concepts
Understanding and application of the scientific method in problem solving
Required Skills & Abilities:
Excellent written and oral communication skills
Ability to work well with other members of a group in a team-based environment
Ability to work independently and reliably at the direction of project leads and/or senior scientists
Ability to learn in a fast-paced, high-integrity, scientific group setting
Ability to effectively provide guidance to others on processing equipment and general lab procedures
Takes initiative in improving own work and responsibilities outside on normal job functions
Proficiency with Microsoft Office applications
Good self-discipline and attention to detail.
Must have good planning, organizational, and time 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):
Bachelor’s Degree in a science related field and one (1) years of relevant experience; OR
Associate’s Degree in a science related field and four (4) years of relevant experience.
Preferred Qualifications:
GMP experience.
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.
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 Associate Scientist functions to assist in the planning and execution of 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 typically provides technical support for GMP activities and represents the Downstream Process Development group during process transfer and manufacturing support. This individual will have familiarity with a range of purification technologies including centrifugation, filtration technologies (TFF and depth), chromatographic separations and basic laboratory analytical techniques (SDS-PAGE, spectroscopy, pH/conductivity meters, etc.)
External US:
Essential Functions:
Prepare, execute, and monitor viral and protein purification processes at the direction of project leads, appropriately observing and recording data
Independently prepares, executes, and maintains liquid chromatography systems
Independently prepares, executes, and maintains direct and tangential flow filtration systems
Prepares buffers, samples, and records data
Maintains the process development lab and its equipment
Technically and physically support GMP activities during preparation and execution
Communicate effectively, both within the PD group and cross-functionally
Author and edit standard operating procedures and work instructions
Maintain detailed laboratory notebooks following FDBT procedures
Perform all other duties as assigned
Required Technical Knowledge and Experience:
Experience with general laboratory setting and techniques (pipetting, dilutions, aseptic technique, etc.)
Good understanding of relevant sciences (physics, chemistry, biochemistry)
Good understanding viral and/or protein purification strategies
Excellent understanding of laboratory and chemical safety
Experience with protein analytical techniques
Experience with routine equipment troubleshooting
Familiar with cGMP concepts
Understanding and application of the scientific method in problem solving
Required Skills & Abilities:
Excellent written and oral communication skills
Ability to work well with other members of a group in a team-based environment
Ability to work independently and reliably at the direction of project leads and/or senior scientists
Ability to learn in a fast-paced, high-integrity, scientific group setting
Ability to effectively provide guidance to others on processing equipment and general lab procedures
Takes initiative in improving own work and responsibilities outside on normal job functions
Proficiency with Microsoft Office applications
Good self-discipline and attention to detail.
Must have good planning, organizational, and time 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):
Bachelor’s Degree in a science related field and one (1) years of relevant experience; OR
Associate’s Degree in a science related field and four (4) years of relevant experience.
Preferred Qualifications:
GMP experience.
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.
Reference: 202125646
https://jobs.careeraddict.com/post/95498836
Process Development Downstream Associate Scientist
Posted on Sep 21, 2024 by Fujifilm
College Station, TX
Research
Immediate Start
Annual Salary
Full-Time
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 Associate Scientist functions to assist in the planning and execution of 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 typically provides technical support for GMP activities and represents the Downstream Process Development group during process transfer and manufacturing support. This individual will have familiarity with a range of purification technologies including centrifugation, filtration technologies (TFF and depth), chromatographic separations and basic laboratory analytical techniques (SDS-PAGE, spectroscopy, pH/conductivity meters, etc.)
External US:
Essential Functions:
Prepare, execute, and monitor viral and protein purification processes at the direction of project leads, appropriately observing and recording data
Independently prepares, executes, and maintains liquid chromatography systems
Independently prepares, executes, and maintains direct and tangential flow filtration systems
Prepares buffers, samples, and records data
Maintains the process development lab and its equipment
Technically and physically support GMP activities during preparation and execution
Communicate effectively, both within the PD group and cross-functionally
Author and edit standard operating procedures and work instructions
Maintain detailed laboratory notebooks following FDBT procedures
Perform all other duties as assigned
Required Technical Knowledge and Experience:
Experience with general laboratory setting and techniques (pipetting, dilutions, aseptic technique, etc.)
Good understanding of relevant sciences (physics, chemistry, biochemistry)
Good understanding viral and/or protein purification strategies
Excellent understanding of laboratory and chemical safety
Experience with protein analytical techniques
Experience with routine equipment troubleshooting
Familiar with cGMP concepts
Understanding and application of the scientific method in problem solving
Required Skills & Abilities:
Excellent written and oral communication skills
Ability to work well with other members of a group in a team-based environment
Ability to work independently and reliably at the direction of project leads and/or senior scientists
Ability to learn in a fast-paced, high-integrity, scientific group setting
Ability to effectively provide guidance to others on processing equipment and general lab procedures
Takes initiative in improving own work and responsibilities outside on normal job functions
Proficiency with Microsoft Office applications
Good self-discipline and attention to detail.
Must have good planning, organizational, and time 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):
Bachelor’s Degree in a science related field and one (1) years of relevant experience; OR
Associate’s Degree in a science related field and four (4) years of relevant experience.
Preferred Qualifications:
GMP experience.
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.
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 Associate Scientist functions to assist in the planning and execution of 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 typically provides technical support for GMP activities and represents the Downstream Process Development group during process transfer and manufacturing support. This individual will have familiarity with a range of purification technologies including centrifugation, filtration technologies (TFF and depth), chromatographic separations and basic laboratory analytical techniques (SDS-PAGE, spectroscopy, pH/conductivity meters, etc.)
External US:
Essential Functions:
Prepare, execute, and monitor viral and protein purification processes at the direction of project leads, appropriately observing and recording data
Independently prepares, executes, and maintains liquid chromatography systems
Independently prepares, executes, and maintains direct and tangential flow filtration systems
Prepares buffers, samples, and records data
Maintains the process development lab and its equipment
Technically and physically support GMP activities during preparation and execution
Communicate effectively, both within the PD group and cross-functionally
Author and edit standard operating procedures and work instructions
Maintain detailed laboratory notebooks following FDBT procedures
Perform all other duties as assigned
Required Technical Knowledge and Experience:
Experience with general laboratory setting and techniques (pipetting, dilutions, aseptic technique, etc.)
Good understanding of relevant sciences (physics, chemistry, biochemistry)
Good understanding viral and/or protein purification strategies
Excellent understanding of laboratory and chemical safety
Experience with protein analytical techniques
Experience with routine equipment troubleshooting
Familiar with cGMP concepts
Understanding and application of the scientific method in problem solving
Required Skills & Abilities:
Excellent written and oral communication skills
Ability to work well with other members of a group in a team-based environment
Ability to work independently and reliably at the direction of project leads and/or senior scientists
Ability to learn in a fast-paced, high-integrity, scientific group setting
Ability to effectively provide guidance to others on processing equipment and general lab procedures
Takes initiative in improving own work and responsibilities outside on normal job functions
Proficiency with Microsoft Office applications
Good self-discipline and attention to detail.
Must have good planning, organizational, and time 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):
Bachelor’s Degree in a science related field and one (1) years of relevant experience; OR
Associate’s Degree in a science related field and four (4) years of relevant experience.
Preferred Qualifications:
GMP experience.
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.
Reference: 202125646
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