As a Scientist - Purification Process Development you are required to perform leadership both inside and outside the laboratory and will rely on industry expertise and the exploration of novel technologies in order to build robust and efficient purification processes. We are looking for a candidate with experience in biologics or gene therapy purification development and bioprocess analytics.
Responsibilities:
Lead and conduct viral/non-viral vector purification process development and process analytics
Develop and optimize robust viral/non-viral vector purification process using advanced knowledge of column chromatography filtration and other downstream purification technology
Develop conduct maintain analytical assays such as ELISA DLS Octet QPCR/ddPCR HPLC and CE-SDS etc. for in-process sample testing to support process development
Provide scientific and technical expertise for in-process sample testing activities including product quality and process impurity methodologies
Perform troubleshooting experiments and communicate findings with appropriate working groups
Maintain industry knowledge and keep abreast of new and relevant technologies
Perform data analysis contribute to technical reports external publications patent applications and internal/external presentations
Lead scale-up activities to implement a manufacturing process based on DSP development knowledge
Communicate effectively with internal and external teams e.g. CDMOs for tech transfer activities
Mentor and support junior staff and build a culture of support and collaboration
Required Skills Experiences Education and Competencies:
PhD in Biotechnology Biochemistry Chemical Engineering or related discipline or masters degree with a minimum of 4 years of relevant experience or a bachelors degree with a minimum of 6 years of relevant experience
Technical experience in modern analytical techniques such as spectrophotometry ELISA DLS Octet QPCR/ddPCR HPLC and CE-SDS
Significant experience knowledge and understanding of purification technologies and operations such as:
Filtration unit operations at various scales including depth filtration tangential flow filtration etc.
Protein purification chromatography
Virus clearance and inactivation
Familiarity with advanced purification technologies and process analytical technologies
Familiarity with analytical method transfer analytical method bridging across organizations
Experience with process technology transfers and performing gap analyses and risk assessments
Understanding of critical quality attributes and the principles of Quality by Design and ability to apply DOE to downstream development
Expertise in technical report writing
Preferred Qualifications:
Experience in AAV and/or non-viral purification development
Experience in writing CMC components of regulatory dossiers
Knowledge of product comparability target product profile and quality risk assessment activities
Viral clearance study design and execution
Late-stage purification experience such as design space mapping and process robustness studies
Ability to work in Biosafety Level 2 follow safe lab procedures and maintain good laboratory practices (GLPs)
Ability to work under minimal supervision and function within a collaborative team-oriented environment
Excellent organization and communication skills
Innovative critical and creative thinker unafraid of proposing aggressive solutions to complex problems
Experience with biophysical characterization
Experience in continuous manufacturing and process analytical technology
Experience in mentoring junior staff
Ability to build and nurture cross-functional relationships
Ability to communicate and represent group in diverse multi-functional meetings
The hourly range for roles of this nature are $40.00 to $60.00/hr. Rates are heavily dependent on skills experience location and industry.
cyberThink is an Equal Opportunity Employer.
Job Title: Scientist Duration (Contract): 12 Months Client Location: Waltham MA 02451 Location Preference: Onsite Job Description: As a Scientist - Purification Process Development you are required to perform leadership both inside and outside the laboratory and will rely on industry expertise an...
Job Title: Scientist
Duration (Contract): 12 Months
Client Location: Waltham MA 02451
Location Preference: Onsite
Job Description:
As a Scientist - Purification Process Development you are required to perform leadership both inside and outside the laboratory and will rely on industry expertise and the exploration of novel technologies in order to build robust and efficient purification processes. We are looking for a candidate with experience in biologics or gene therapy purification development and bioprocess analytics.
Responsibilities:
Lead and conduct viral/non-viral vector purification process development and process analytics
Develop and optimize robust viral/non-viral vector purification process using advanced knowledge of column chromatography filtration and other downstream purification technology
Develop conduct maintain analytical assays such as ELISA DLS Octet QPCR/ddPCR HPLC and CE-SDS etc. for in-process sample testing to support process development
Provide scientific and technical expertise for in-process sample testing activities including product quality and process impurity methodologies
Perform troubleshooting experiments and communicate findings with appropriate working groups
Maintain industry knowledge and keep abreast of new and relevant technologies
Perform data analysis contribute to technical reports external publications patent applications and internal/external presentations
Lead scale-up activities to implement a manufacturing process based on DSP development knowledge
Communicate effectively with internal and external teams e.g. CDMOs for tech transfer activities
Mentor and support junior staff and build a culture of support and collaboration
Required Skills Experiences Education and Competencies:
PhD in Biotechnology Biochemistry Chemical Engineering or related discipline or masters degree with a minimum of 4 years of relevant experience or a bachelors degree with a minimum of 6 years of relevant experience
Technical experience in modern analytical techniques such as spectrophotometry ELISA DLS Octet QPCR/ddPCR HPLC and CE-SDS
Significant experience knowledge and understanding of purification technologies and operations such as:
Filtration unit operations at various scales including depth filtration tangential flow filtration etc.
Protein purification chromatography
Virus clearance and inactivation
Familiarity with advanced purification technologies and process analytical technologies
Familiarity with analytical method transfer analytical method bridging across organizations
Experience with process technology transfers and performing gap analyses and risk assessments
Understanding of critical quality attributes and the principles of Quality by Design and ability to apply DOE to downstream development
Expertise in technical report writing
Preferred Qualifications:
Experience in AAV and/or non-viral purification development
Experience in writing CMC components of regulatory dossiers
Knowledge of product comparability target product profile and quality risk assessment activities
Viral clearance study design and execution
Late-stage purification experience such as design space mapping and process robustness studies
Ability to work in Biosafety Level 2 follow safe lab procedures and maintain good laboratory practices (GLPs)
Ability to work under minimal supervision and function within a collaborative team-oriented environment
Excellent organization and communication skills
Innovative critical and creative thinker unafraid of proposing aggressive solutions to complex problems
Experience with biophysical characterization
Experience in continuous manufacturing and process analytical technology
Experience in mentoring junior staff
Ability to build and nurture cross-functional relationships
Ability to communicate and represent group in diverse multi-functional meetings
The hourly range for roles of this nature are $40.00 to $60.00/hr. Rates are heavily dependent on skills experience location and industry.