SPECTRAFORCE
Overview
Position Title:
Scientist, BioPharma Manufacturing MSAT
Work Location:
Westborough, MA 01581
Assignment Duration:
12 months
Company:
SPECTRAFORCE
Purpose:
The candidate will be involved in planning, direction, and execution of projects related with stem cell culture and differentiation. Activities will focus on maintaining and developing robust stem-cell based production and differentiation processes from small (6-well plate) to large (multi-layer Cellstacks or suspension) scales with the appropriate level of compliance and documentation suitable for cGMP manufacture. The candidate will work closely within the team and across functional groups. The candidate should be a highly motivated self-starter who is comfortable working in a hands-on environment.
Responsibilities
Responsible for experimental study and development plans, preparing required protocols, executing studies, conducting data analysis and preparation of final reports.
Conducts studies to confirm optimized processes to demonstrate process robust and reproducibility at the appropriate scale required.
Able to effectively troubleshoot technical issues or process deviations to ensure production proceeds as scheduled.
Support commercial readiness tasks including process scale-up, process and raw material qualification that meet compliance requirements.
Duties, responsibilities and activities may change at any time with or without notice
Qualifications Required:
BS or MS degree in biology, biochemistry, chemical engineering, bioengineering, or related scientific field with relevant experience of 8+ years for BS or 3+ years for MS.
Extensive cell culture experience with solid knowledge of cell biology principles.
Must be highly self-motivated, with solid communication skills, and demonstrate the ability to work in a team environment and lead other professionals and peers.
Detail oriented with good organizational skills and documentation practices.
Ability to work effectively, independently, as well as part of a team.
Knowledgeable in process and analytical development, phase appropriate technology transfer, process comparability and qualification, process monitoring and GMPs, ICH, ISPE, and BPE guidelines.
Ability to work in a fast-paced team environment with fluctuating priorities and collaborate effectively with others.
This position requires on-site work.
Preferred:
Deep knowledge and experience with various human cell culture platforms, especially in human pluripotent stem cell culture and differentiation processes towards products for regenerative medicine
Experience in cell/gene therapy GMP manufacturing, scale-up/scale-down, and tech transfer
Proficiency in using Microsoft Office software (Excel, PowerPoint, Word), common lab &
Direct experience on process characterization, development of process control strategy, process qualification and validation
Understanding of industry expectations with respect to phase appropriate requirements while advancing products from clinical to commercial state
Seniority level
Associate
Employment type
Contract
Job function
Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Scientist, BioPharma Manufacturing MSAT
Work Location:
Westborough, MA 01581
Assignment Duration:
12 months
Company:
SPECTRAFORCE
Purpose:
The candidate will be involved in planning, direction, and execution of projects related with stem cell culture and differentiation. Activities will focus on maintaining and developing robust stem-cell based production and differentiation processes from small (6-well plate) to large (multi-layer Cellstacks or suspension) scales with the appropriate level of compliance and documentation suitable for cGMP manufacture. The candidate will work closely within the team and across functional groups. The candidate should be a highly motivated self-starter who is comfortable working in a hands-on environment.
Responsibilities
Responsible for experimental study and development plans, preparing required protocols, executing studies, conducting data analysis and preparation of final reports.
Conducts studies to confirm optimized processes to demonstrate process robust and reproducibility at the appropriate scale required.
Able to effectively troubleshoot technical issues or process deviations to ensure production proceeds as scheduled.
Support commercial readiness tasks including process scale-up, process and raw material qualification that meet compliance requirements.
Duties, responsibilities and activities may change at any time with or without notice
Qualifications Required:
BS or MS degree in biology, biochemistry, chemical engineering, bioengineering, or related scientific field with relevant experience of 8+ years for BS or 3+ years for MS.
Extensive cell culture experience with solid knowledge of cell biology principles.
Must be highly self-motivated, with solid communication skills, and demonstrate the ability to work in a team environment and lead other professionals and peers.
Detail oriented with good organizational skills and documentation practices.
Ability to work effectively, independently, as well as part of a team.
Knowledgeable in process and analytical development, phase appropriate technology transfer, process comparability and qualification, process monitoring and GMPs, ICH, ISPE, and BPE guidelines.
Ability to work in a fast-paced team environment with fluctuating priorities and collaborate effectively with others.
This position requires on-site work.
Preferred:
Deep knowledge and experience with various human cell culture platforms, especially in human pluripotent stem cell culture and differentiation processes towards products for regenerative medicine
Experience in cell/gene therapy GMP manufacturing, scale-up/scale-down, and tech transfer
Proficiency in using Microsoft Office software (Excel, PowerPoint, Word), common lab &
Direct experience on process characterization, development of process control strategy, process qualification and validation
Understanding of industry expectations with respect to phase appropriate requirements while advancing products from clinical to commercial state
Seniority level
Associate
Employment type
Contract
Job function
Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr