Kincell is a technology-forward contract development and manufacturing organization (CDMO) that streamlines analytical development, process development, CMC consulting and early-stage GMP cell therapy manufacturing.
Our focus is on developing and manufacturing immune cell therapies, including autologous and allogeneic CAR-T, CAR-NK, and CAR-M programs.
For more information, please visit our website at www.kincellbio.com.
The Scientist II will lead process development runs and be a process development expert. Staying current with best practices and advancements is anticipated and should result in creative and inspiring suggestions for alternative methodologies and processes. He/She will lead in solving complex problems by applying current best technical practices and be able to connect cross-functionally to leverage methodologies used in other fields as well as his/her own. The Scientist II will demonstrate a sense of urgency while maintaining respect for best practices and an understanding of the importance and applicability of quality and controls in development activities.
Problem-solving, data analysis, and interpretation will be focused and data-driven and result in thorough documentation and pointed technical reports suitable for area management. The Scientist II will be well versed in internal and external best practices, lead internal and external runs and operations, and be an SME in interactions with company colleagues. It is expected that he/she will continuously improve operational effectiveness and participate in recruiting technical staff to maintain an effective level of technical ability for all business requirements.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
- Leads process development operations and runs
- Creates data presentations suitable for cross functional and client meetings
- Proactively prepares for initial and follow up conversations with internal scientists and clients and prepares responses to likely questions/discussion topics
- Independently designs experiments to facilitate the development of cell therapy production processes and process improvements
- Assists with process transfer into facility and to destination unit
- Leads internal process improvement initiatives
- Ability to identify and breakdown complex problems
- Other duties as assigned
Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
- S. degree and 5+ years, or a M.S. degree and 3+ years in Bioprocess or Bioscience industry experience, or a Ph.D. degree in life sciences with 1+ years of relevant industry experience.
- Experience with eukaryotic cell culture, aseptic technique, and experience with general laboratory equipment (e.g centrifuge, scales, pumps, welders/sealers) required
- Experience with chromatography, cGMP manufacture, and technology transfer is a plus.
- Experience with the development of CGT and other bioprocesses is highly desired.
- The ability to independently design experiments, analyze data, and interpret and present experimental results is required.
- Excellent verbal and written communication skills are required.
- Ability to multitask, strategically and tactically.
- Strong organizational skills; able to prioritize and manage complex processes/projects.
- An equivalent combination of education and experience may be considered.
Physical Demands
- Adjusting or moving objects weighing up to 25lbs
Travel Requirements
- N/A
Location
- This is a site-based position located in Gainesville, FL, and it will require some non-standard working hours, including early morning or late evening.
#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.
What We Do
Kincell is a technology-forward contract development and manufacturing organization (CDMO) that streamlines analytical development, process development, CMC consulting and early-stage GMP cell therapy manufacturing.
Our focus is on developing and manufacturing immune cell therapies, including autologous and allogeneic CAR-T, CAR-NK, and CAR-M programs.
For more information, please visit our website at www.kincellbio.com