safety specialist.

job summary: This role will independently design and execute experiments, mentor technical staff, collaborate with other cross functional teams to support research projects under the supervision of R & D director. Passion for excellence and innovation are critical. This role will work closely with our internal colleagues and external collaborators to efficiently progress early-stage cell therapy products through to IND filing.   location: Arcadia, California job type: Permanent salary: $100,000 - 130,000 per year work hours: 9 to 5 education: Doctorate   responsibilities: Lead planning, design, and execution of experiments related of development and characterization of cellular immunotherapy products in coordination with R & D Director.Analyze, and report complex data to cross functional teams in a clear and concise mannerMentor and train scientific staff on technical skills required to effectively perform experiments and to facilitate progression of projectsManage multiple research projects simultaneously with the R & D team and collaborate with other departments (Process Science, Analytical Science, Quality, Manufacture) as necessary.Contribute to various preclinical projects within R& D and those required by clients through in-depth scientific knowledge and demonstrated experience in analytical methods used in cellular immunotherapy fieldCollaborate with Process science team to scale up lentiviral and CAR-T productsPerforms a wide range of non-routine exploratory experiments as requiredMaintain precise laboratory notebooks, electronic records following high standards of data quality and integrity.Prepare scientific/technical reports, summaries, protocols, etc, and present them to internal and external stakeholders.Constantly improvise research strategies and adopt technologies to stay upfront in the field of immunotherapy  qualifications: Ph. D in the field of Immunology, Cell biology, Virology or Cancer biology or related life science discipline with 3+ years (Scientist) or 5+ years (Senior Scientist) or Master's degree with 7 + years relevant research experience in Immunology/Cancer biology.In depth scientific and technical understanding of cellular immunotherapy and tumor immunology.2+ years of managing research laboratory research team/associates in immunotherapy or cancer biology or relevant research projects is required for senior scientist level.Prior research experience in antibody therapies, bispecific antibodies, and cellular therapies preferredDemonstrated ability to independently design, plan and troubleshoot experiments, interpret results, and present to the R&D team and external clients.Self-motivated and creative, able to work within a team and collaborate with external teams as needed to accomplish project objectives and deliverables.Possess ability to identify problems early, technically trouble shoot and resolve challenges in early development and preclinical validation of CAR-T productsUnderstands the importance of data integrity to enable a smooth transition of discovery research to manufacture and clinical trials.Familiarity with FDA regulation of biologics and cell therapy products, IND-filing, GLP/GMP process is a plus.Ability to stay organized, prioritize tasks, manage time efficiently, and provide creative solutions to meet program needsExcellent interpersonal, verbal, and written communication skillsComfortable working in a fast-paced startup environment and flexible to adjust workload based upon changing prioritiesA strong academic research experience evidenced by high caliber publications in peer-reviewed journals is preferredIntellectually curios candidates with passion for innovation and discovery research are welcome  skills: Biology, Chemistry, GLP (Good Laboratory Practice), ICH Regulations, GMP (Good Manufacturing Practice) 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.EOEDisclaime 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.EOEDisclaime 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: Fortune 500 Manufacturer is seeking a direct-hire Environmental Engineer. This position is located near Wilmington, California. The Environmental Engineer will manage the site's environmental permits as well as oversee various environmental and sustainability projects. The salary is commensurate with experience ranging up to $100K, plus an opportunity for a bonus, relocation assistance, and other great benefits! All candidates must be legally authorized to work in the United States of America.  location: Wilmington, California job type: Permanent salary: $80,000 - 100,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Manage the site's environmental permits as well as assigned environmental and sustainability projectsDevelop and implement policies and procedures to continually improve the facilities environmental programLead the site efforts toward achieving company Energy and Emissions Objectives (2030 Goals)Develop capital cost, design and installation plans for new equipment specifically environmental equipment #LI-ZR1   qualifications: Experience level: ExperiencedMinimum 2 years of experienceEducation: Bachelors  skills: EHSEnvironmentalManufacturingProductionSustainabilitySafety 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. 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.