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1 job found for ups order processor forklift in california

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    • arcadia, california
    • permanent
    • $170,000 - $200,000 per year
    job summary: This role will be responsible for preclinical development, IND enabling studies, and technology transfer to manufacturing and MSAT, including management of Cell Process Development, Vector Process Development, and Analytical/Bioassay Development. This candidate will also be responsible for clinical process development including process optimization by DOE, QbD, and other statistical based methodologies.   location: Arcadia, California job type: Permanent salary: $170,000 - 200,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Process Science including, Process Development, Analytical/Bioassay Development and CMC leadership for all pre-clinical and clinical Theragent cell therapy programsOversee all process sciences personnel and activities, including allogeneic/autologous cells, viral vectors, and technology developmentDevelops manufacturing platforms to enable current and new product formats, increased product control, lower cost, and lower operational complexity. - Works strategically to accelerate the development and implementation of novel technologies for integration into new and existing drug product platform processes.Play a key role in project team meetings and decisions working closely with other functions such as Research, Regulatory Affairs, Manufacturing, Quality, Clinical, Finance, Program Management, Business Development, and othersPrepare and present to leadership and external clients and stakeholders on process development strategy, latest data and conclusions, plans and roadmap to meet client and Theragent development goalsExecutes on IND development timelines against operational planBuilds a strong scientific and technical team, provides necessary training and ongoing coaching, discipline, and recognition of direct staff, including performing annual performance reviewsSupports technology transfer of products and processes into the cGMP facility, and serves as a key SME with external manufacturing organizations and key clients as well as material/component and equipment vendorsInvestigates and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior managementInteracts with outside vendors and senior managementParticipates in multi-functional project teams, as necessaryTakes corrective action to bring about required changes using change control procedures  qualifications: Bachelor's degree in immunology, biology, bioengineering, or related field (or equivalent experience required), advanced degree preferredAt least 10 years of experience managing a technical team in the cell therapy biotechnology industryDirect experience with cell and gene therapy process development, IND filing, and supporting clinical products is expectations requiredAt least 5 years managing an analytical science or multi-functional bioanalytical laboratory technical teamMinimum of 5 years' experience in FDA-regulated industry. with 5 years' experience in managing warehouse materials and/or cold chain distribution.  skills: CMC, Cell Biology, IND, GMP (Good Manufacturing Practice), Process Engineering Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: This role will be responsible for preclinical development, IND enabling studies, and technology transfer to manufacturing and MSAT, including management of Cell Process Development, Vector Process Development, and Analytical/Bioassay Development. This candidate will also be responsible for clinical process development including process optimization by DOE, QbD, and other statistical based methodologies.   location: Arcadia, California job type: Permanent salary: $170,000 - 200,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Process Science including, Process Development, Analytical/Bioassay Development and CMC leadership for all pre-clinical and clinical Theragent cell therapy programsOversee all process sciences personnel and activities, including allogeneic/autologous cells, viral vectors, and technology developmentDevelops manufacturing platforms to enable current and new product formats, increased product control, lower cost, and lower operational complexity. - Works strategically to accelerate the development and implementation of novel technologies for integration into new and existing drug product platform processes.Play a key role in project team meetings and decisions working closely with other functions such as Research, Regulatory Affairs, Manufacturing, Quality, Clinical, Finance, Program Management, Business Development, and othersPrepare and present to leadership and external clients and stakeholders on process development strategy, latest data and conclusions, plans and roadmap to meet client and Theragent development goalsExecutes on IND development timelines against operational planBuilds a strong scientific and technical team, provides necessary training and ongoing coaching, discipline, and recognition of direct staff, including performing annual performance reviewsSupports technology transfer of products and processes into the cGMP facility, and serves as a key SME with external manufacturing organizations and key clients as well as material/component and equipment vendorsInvestigates and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior managementInteracts with outside vendors and senior managementParticipates in multi-functional project teams, as necessaryTakes corrective action to bring about required changes using change control procedures  qualifications: Bachelor's degree in immunology, biology, bioengineering, or related field (or equivalent experience required), advanced degree preferredAt least 10 years of experience managing a technical team in the cell therapy biotechnology industryDirect experience with cell and gene therapy process development, IND filing, and supporting clinical products is expectations requiredAt least 5 years managing an analytical science or multi-functional bioanalytical laboratory technical teamMinimum of 5 years' experience in FDA-regulated industry. with 5 years' experience in managing warehouse materials and/or cold chain distribution.  skills: CMC, Cell Biology, IND, GMP (Good Manufacturing Practice), Process Engineering Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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