Job type full-time
Qualifications
Us work authorization (required)
Process engineering: 1 year (preferred)
Benefits pulled from the full job description
Dental insurance flexible schedule health insurance paid time off vision insurance
Not provided by employer
Full job description
Ivexsol, incIs a burgeoning vector manufacturing company founded on a truly transformative, next-generation technology that enables the creation of stable lentiviral vector producer cell lines for virtually any therapeutic geneThis technology will revolutionize the way gene therapy vectors are manufactured, sold, and employed by therapy providers, and in doing so, enable us to make a significant contribution to the elimination of suffering due to human diseaseWe are actively recruiting for creative and ethical teammates with the vision and courage to innovate beyond today’s perception of what is possible to transform vector production so that no patient is left waiting for a cure.
Ivexsol’s viral vector process development and production (vpp) team is seeking a process scientist or engineer to answer key scientific questions and develop downstream processes for lentiviral vector production to advance ivexsol’s missionThe successful candidate will be expected to provide hands-on expertise in process development using serum-free suspension culture as the production platform while thriving in a fluid work environment that is rapidly evolving from a small biotech to a global manufacturer of gene-delivery vehicles.
Responsibilities:
Action on downstream development of lentiviral vector production in alignment with the company goals and objectives
Develop an understanding of lentiviral vector physical and chemical properties to improve downstream purification process
Support the establishment of the pd lab, including installation of equipment, implementation of workflow, process records, and sops.
Deliver high-quality data using state-of-the-art production platforms for both transient systems and stable cell lines.
Execute, and analyze scientific data in collaboration with upstream and analytical development groups.
Support cross-functional projects with scientists, process engineers, and internal teams.
Collect and keep detailed, accurate records of data.
Report results at regular laboratory meetings.
Participate in internal and external collaborations to evaluate and implement new process technologies
Make use of problem solving, critical thinking, and effective written and oral presentation skills in a matrixed team environment
To always act in an ethical manner: treating the team, the public, and the planet, in the way you would want others to treat you
Requirements:
Candidate must be authorized to work in the united states.
Bs/ms in cell biology, biochemistry, bio- or chemical engineering, or a related discipline, with 0-2+ years of hands-on experience in gene therapy industry
Knowledgeable of viral vector process development and manufacturing
Proficient at small to medium scale downstream process development using bioreactors (1l – 20l) with relevant knowledge of purification, formulation & analytical development.
Able to develop, revise, and review sops, protocols, batch records, process development and technical reports
Experience with cgmp manufacturing, process automation, and technology transfer
Commitment to the highest-quality research with outstanding technical skills and scientific rigor
Be creative, innovative, communicative, collaborative, courageous, courteous, caring, careful, and consistently ready to do your best work
Outstanding decision making, organizational, and analytical skills.
Be able to work both independently and as a team member
Experienced in data analysis and interpretation including relevant software-based scientific tools.
During this time of a global pandemic, it is especially important that prospective applicants be familiar with sars-cov2 regulation and mitigation strategies as while we will encourage remote work when possible, as a lab scientist, there will be on-site work for which you will be required to wear appropriate ppe when working in the same physical location with other members of the scientific team, and be comfortable with rapidly changing rules and expectations with regard to this challenge.
Job type: full-time
Benefits:
Dental insurance
Flexible schedule
Health insurance
Paid time off
Vision insurance
Schedule:
Monday to friday
Covid-19 considerations:
Ivexsol requires every employee to be fully vaccinated prior to being allowed to work onsite at an ivexsol facility.
Ability to commute/relocate:
Boston, ma: reliably commute or planning to relocate before starting work (preferred)
Application question(s):
How many years have you worked in the biotech or pharma industry?
Experience:
Process engineering: 1 year (preferred)
Upstream process development: 1 year (preferred)
Work location: one location
Hiring insights
Hiring 1 candidate for this role
Job activity
Posted 19 days ago
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