Cell Tester Job Description Sample
Cell Processing Specialist Car-T Cell Therapy - Morris Plains, NJ
Cell Processing Specialist CAR-T Cell Therapy - Morris Plains, NJ
Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. Novartis recently received the first ever FDA approval for a CAR-T cell therapy for children and young adults with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or has relapsed at least twice; a novel immunocellular therapy, a one-time treatment that uses a patient's own T cells to fight cancer, and is the first therapy based on gene transfer approved by the FDA. Therapy will be manufactured for individual patients using their own cells at the Novartis Morris Plains, New Jersey facility where Novartis continues to advance its CAR-T manufacturing expertise. The Morris Plains site plans to hire over 300 Quality, Production, Supply Chain and Bioanalytics associates in the next 10-12 months.
Due to the nature of the starting materials (patient cells) the Cell processing Specialist role requires the highest level of proficiency and ownership. The Specialist will be responsible for end to end processing and verification of patient derived clinical and commercial cellular immunotherapy products.
Specific responsibilities will include:
End to end ownership for the processing of the assigned patient starting material in the clean room environment.
Maintain and prepare equipment/environment for use.
Document all steps in the assigned Batch record in line with GMP requirements.
Conduct all necessary processing/verification steps for the assigned lot with the highest skill level of aseptic technique.
Assist on Deviation Investigations, Change Controls, Safety Inspections and CAPAs.
Perform execution of assigned qualification/ validation activities.
Be responsible for successful on time completion of a required training curriculum composed of Global Operating Procedures (GOPs), Standard Operating Procedures (SOPs), Aseptic Techniques, Gowning Qualifications and other relevant training, including HSE for the specific role.
Perform other duties as assigned. Examples might be: successful completion of assigned PU project initiatives and/or work stream tasks, such as process improvements, efficiencies, Innovation Quality Productivity (IQP).
Maintain an "audit ready" module.
Selected associates must:
Be able to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) area for extended periods of time.
Be able to work with automated cell processing equipment such as Elutra, CS5, or Sepax.
Be knowledgeable in the use of production related IT systems such as SAP and MES.
Possess sound cell biological decision making.
Internship / Drive Tester / Tester /Atp Tester
Internship / Drive Tester / E911 Tester /ATP TESTER
(Part Time /on call job )
This position is an entry level job for Fresher / collage Graduate/Drive Tester / RF engineer/ ATP Tester where the tester will learn different aspects and concepts Cellular Network Telecommunication, also the tester will be interacting and working closely with senior engineers. This is a field position where the tester will have go the cell site and conduct a test by using Mobile Testing App, the tester will be responsible of collecting the required data, upload the collected data to specific folder in the server then one senior RF Engineer will check and validate the data.
The tester will have to use his own car, we will provide GAS.
Good communication skills, and execute all the work orders provided by senior engineers
Ability to manipulate smart phone, like install APP, close App.
Fast learner by showing good internist and enthusiasm.
Good at navigation by using GPS to find site location.
Ability to drive long distance, some sites you may have to drive up 2 hours to get them.
Good driving record.
Cell Processing Associate Car-T Cell Therapy Morris Plains, NJ
Cell Processing Associate CAR-T Cell Therapy
The Cell Processing Associate is responsible for intermediate processing of patient derived clinical and commercial cellular immunotherapy products. Due to the nature of the starting material (patient cells) this role requires basic proficiency and ownership of the process.
Intermediate ownership for the processing of the assigned Patient starting material in the clean room environment.
Ability to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) areas for extended periods of time.
Maintains and prepares equipment/environment for use.
Ability to work with automated cell processing equipment such as the wave bioreactor.
Ability to perform in process operations such as: bioreactor sampling, static sampling and in process environmental monitoring.
Knowledgeable in the use of production related IT systems such as SAP and MES.
Documents all steps in the assigned Batch record in line with GMP requirements.
Conduct all necessary processing steps for the assigned lot with highest skill level of aseptic technique.
Assist with deviation investigations and inspections.
Participation in assigned qualification/ validation activities, as necessary.
Responsible for successful on time completion of required training curriculum comprising of the necessary Global Operating Procedures (GOPs), Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including HSE for the specific role.
Maintains an "audit ready" module.
Perform other duties as assigned; ie. batch record review, process streamline improvements, safety walk-thrus.
Scientist I Single Cell Transcriptomic Approaches To Cell Types In The Mouse Nervous System
The Allen Institute for Brain Science, located in Seattle, Washington, is committed to understanding how the brain works and helping to unlock the mysteries of neurological diseases and disorders affecting millions worldwide.
The Allen Institute is seeking an exceptional candidate who will be part of a Seattle-based multidisciplinary team within the Cell Types Program. The successful candidate will participate in high-throughput single cell transcriptome data generation and analysis to support the effort funded by the newly awarded BRAIN grant from the NIH, which aims to define all cell types in the adult mouse brain. The candidate will be a Ph.D. graduate in life sciences or computational biology and will possess strong experimental and computational skills. She/he will collaborate with several other departments on the identification and classification of cell types in the mouse nervous system.
Work within the Molecular Genetics team on experimental design, execution, and research associate training in order to generate large-scale single cell transcriptome datasets.
Work with Modeling, Analysis and Theory team to timely and iteratively analyze single cell data from the internal single cell transcriptomics pipeline and facilitate generation of cell type taxonomy.
Design and execute validation and follow-up experiments to place the transcriptomics results in the neurobiological context.
Write and publish manuscripts, grant progress reports and grant applications.
Present work internally and externally at conferences.
Evaluate new single cell RNA-seq platforms and techniques.
Work with Electrophysiology and Neuroanatomy teams to facilitate data organization and integration in an effort to create multimodal neuronal taxonomy.
Ph.D. in life sciences or computational biology (e.g., Neuroscience, Genomics, Genetics, or related field).
Knowledgeable in genomic data generation from primary tissues (rodent handling, dissection, single cell collection, molecular biology, and next generation sequencing).
Knowledgeable about developmental neurobiology and systems neurobiology
Knowledgeable about RNA-seq, ATAC-seq and/or ChIP-seq data
Proficiency in R and Linux shell scripting.
2+ years of experimental experience in genomic data generation from primary tissues (rodent handling, dissection, single cell collection, molecular biology, and next generation sequencing).
2+ years of experience working in a rodent model system studying a neurobiological problem in vivo (e.g., developmental neurobiology, systems neurobiology).
2+ years of computational experience working with RNA-seq, ATAC-seq and/or ChIP-seq data, preferably at the single cell level.
Ability to develop, test, implement, and share new experimental and computational tools quickly, in an iterative manner, after feedback from experimental, data production, and analysis teams.
Experience with additional programming languages (Perl, Python, Matlab) preferred.
Exceptional oral and written communication skills.
Ability to work independently as well as part of a team to meet aggressive timelines in a collaborative environment.
It is the policy of the Allen Institute to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, the Allen Institute will provide reasonable accommodations for qualified individuals with disabilities.
Senior Mechanical Engineer – Cell Qualification And Cell R&D
This person's primary role will be ensuring current and future battery cell mechanical designs meet the requirements of Tesla's current and future battery modules, and vice versa. This person will work closely with Tesla's cell characterization and qualification team as well as battery module teams to design and execute mechanical methods that directly impact Tesla's product lifetimes and reliability. This role also involves working with module production teams to ensure cell requirements are met in actuality, not only by design. This person will work to qualify and iterate upon cell mechanical designs based on Tesla's needs and the capabilities of Tesla's cell suppliers. This person must exhibit the knowledge, leadership, and drive needed to not only challenge the status quo, but also define and execute the optimal path forward.
Design, develop, prototype, and execute mechanical test and characterization methods for battery cells and cell components
From first principles and experimental data, determine cell mechanical requirements such as maximum loads, limits of plastic deformation
Manage cell and cell-module interface requirements and work with validation teams
Be familiar with finite element methods (FEA) for mechanical modeling; work with FEA/modeling engineers to validate models and extract material parameters from mechanical tests that you have designed and performed
Produce meaningful and compelling analyses and data visualizations beyond Excel
Author technical presentations and summarize high-impact technical findings
Work in a laboratory and/or production environment, not just at a desk
Collaborate with and proactively build professional relationships with engineers, scientists, and technicians across different groups
Degree in Mechanical Engineering or similar
MS or PhD with 2+ years professional experience
BS with 4+ years professional experience
CAD; drafting; GD&T; tool / fixture / jig design
Design and execution of mechanical characterization experiments
Mechanical load frame operation, e.g. Instron, MTS, stress, strain, and creep measurements
Working with machine shops, rapid prototyping, and additive manufacturing
Building test fixtures using extruded aluminum framing and electromechanical parts e.g. pneumatic or solenoid actuators
Data acquisition systems; analog and digital signals
Extensive working knowledge of precision dimensional inspection tools
Working knowledge & relevant coursework in finite element analysis (FEA) methods
Ability to break down complex technical topics and deliver visual technical presentations (e.g. PowerPoint) to groups of engineers, scientists, and technicians
MATLAB, Python, LabVIEW, R
Mechanical testing of composite materials
Other materials test laboratory equipment
Ability to demonstrate a strong interest or passion for lithium-ion battery technology
Experience with mechanical testing of batteries
Knowledge of safety hazards of working with and mechanical testing of lithium and lithium-ion batteries
Please send most current resume and cover letter to PEControls@tesla.com
Director, Cell Line And Cell Culture Bioprocess Development
Five Prime Therapeutics, Inc. (NASDAQ: FPRX) is a publicly traded, clinical-stage biotechnology company focused on discovering and developing innovative immuno-oncology protein therapeutics to improve the lives of patients with serious diseases. We have an industry-leading and differentiated drug discovery platform. Our comprehensive proprietary libraries of the extracellular proteome, differentiated screening capabilities and protein therapeutic generation and engineering capabilities comprise a unique and powerful IND engine that will continue to generate important development programs. This uniquely positions us to discover novel pathways and targets in immuno-oncology. Our success with our drug discovery platform has led to a pipeline that is on track to more than double to five development programs in clinical trials across multiple indications in 2018. We also have several undisclosed research programs at different points of the target validation and molecule generation phases that have the potential to yield our next wave of development-stage therapeutic biologics. And we continue to fuel this process at the earliest stages with new screens planned this year.
Five Prime is committed to innovation and outstanding science to develop effective new drugs for the treatment of severe diseases. We value our culture of openness, collaboration and productivity. The company is in a strong financial position and has an effective executive team and Board of Directors. Discover more about FivePrime at www.fiveprime.com.
Reporting to the VP Manufacturing Sciences, this position will be responsible for providing strategic input relates to CMC decisions and will contribute significantly to the development and success of the Manufacturing Sciences team. Partner with other functional leaders from Analytical, Formulation, Supply Chain, CMO management and Quality in support of the project teams and of the organization.
This position will lead the Cell line and Cell Culture Bioprocess team for clinical and commercial manufacture of mAbs, fusion proteins and other novel biologics. The responsibilities include development of cell line and cell culture process, production of preclinical supplies at in-house bioprocess pilot plant, oversight of technology transfer to Contract Manufacturing Organizations (CMOs) and support of regulatory submissions. In addition, this individual will be accountable for overall management of the function such as resource planning, employee engagement and workflow enhancement.
Essential Functions and Duties
Key member of the Manufacturing Sciences leadership team to assess and support CMC strategy
Oversee cell line development for the selection of production cell line for master cell bank manufacturing.
Lead cell culture process development, optimization, characterization/validation, scale up and technology transfer to CMO's.
Manage process development experimental design, execution and writing process development plans/reports.
Introduce new technology to enhance workflow and capabilities.
Manage bioprocess suite, trouble-shooting of processes, instrumentation, and equipment to ensure timely in-house manufacturing to support preclinical animal studies.
Provide supervision for technology transfer and oversee CMO activities. Review, or approve batch records and SOPs; address production issues at CMO's in collaboration with quality and regulatory teams.
Acts as a mentor for the junior staff, provide coaching and emphasize best practices.
Partner with QA and Regulatory to support batch releases and regulatory submissions.
PhD in biochemistry, chemical/biochemical engineering or related disciplines
12+ years of in-depth technical experience in cell culture bioprocess development for protein drugs.
Solid knowledge and experiences in mammalian cell culture process engineering and process scale-up/scale-down design is essential.
Leadership experience with proven capability as a successful leader in a strategic multifunctional environment, highly skilled in leading change and people agility
Strong business acumen and critical thinking
Proven experience in process characterization and validation.
Hands on experiences with technology transfer of manufacturing process.
Must be scientifically knowledgeable, team-orientated, and passionate in biopharmaceutical development.
Knowledge of cGMP's, regulatory guidelines, validation practices, and other relevant regulatory requirements.
Excellent interpersonal communication and presentation skills.
At FivePrime, we believe a diverse workforce drives our success as a company. We are always working to create an environment where different backgrounds and viewpoints are valued and celebrated.
FivePrime is an equal opportunity employer. FivePrime makes employment decisions, including in recruitment and selection, without consideration of race, color, national origin, religion, sex, gender, gender identity or expression, sexual orientation, age, veteran status or disability.Please call or reply with any comments.
All your information will be kept confidential according to EEO guidelines.
Cell Production Operator
Panasonic Corporation is working to manufacture photovoltaic (PV) modules and cells for solar panels at Tesla's factory in Buffalo, New York.
Panasonic's role is to manufacture and supply our SHJ (Silicon Heterojunction) PV cells and modules that feature industry-leading module conversion efficiency and outstanding temperature coefficient characteristics, which result in more power than similarly rated solar panels.
This collaboration makes optimum use of both companies' strengths to enhance the competitiveness of their products, generating a synergy effect between Panasonic's technological and manufacturing expertise in the photovoltaic business and Tesla's strong sales channels, rich creativity and market-leading, cutting-edge innovation.
As a valued partner and strong customer of Panasonic, Tesla is making a long-term purchase commitment for products manufactured at the Riverbend factory.
This is an opportunity that's made to order for a career-minded individual who wants to make a difference and contribute to a more sustainable future based on renewable energy. Join this creative technology collaboration and grow with it as operations continue to expand.
The most successful employees at PESSNY are results driven and able to continuously adapt to an ever-changing startup environment. They report to work on time and never settle for anything less than the best. They work well in a team environment but also have the drive to succeed when they are on their own. A strong focus on fairness and honesty with a humble attitude are what defines our top performers. Is that you?
Currently, PESSNY has an immediate opening available for a Cell Production Operator.
What You'll Get to Do:
Key tasks with respect to the Cell Production Department:
Meet department KPI's:
Production plan achievement rate (On-time delivery)
Productivity (Output per head)
Production loss (Failure cost)
Production cost (Direct/Indirect labor, Depreciation, Indirect material, Power, Maintenance & Repair...)
Inventory amount and Inventory difference
Support production material movement and processes based on work standards, work instructions, process inspection standards
Support PC Technicians and Engineer in: Production planning progress control, Raw materials, WIP and FG control/stock reduction, IDM manage & cost reduction, SAP updating & MES management, new technology installation
Report progress and issues to PC Tech and QC
What You'll Bring:
Education & Experience
Education: High school degree and above
Experience in manufacturing facility
Problem solving power
Sense of responsibility
Ability to collaborate with relevant departments
Equipment maintenance skills
High awareness about safety
Basic PC work
Employee lifting up to 25 pounds, transporting work
Handles general chemicals and gas used in solar cell manufacturing.
Mainly in the clean room.
The noise level of working environment is usually moderate.
Irregular shift (Saturdays, Sundays and public holidays)
In-house inspector registration required
Candidates must be willing to work in a clean room environment, wearing coveralls, hoods, booties, safety glasses and gloves.
No cosmetics shall be worn in the cleanrooms. This includes: lipstick, eye shadow, eyebrow pencil, mascara, eye liner, false eye lashes, fingernail polish, hair spray, mousse, or the heavy use of aerosols, after shaves and perfumes.
This position will require exposure to strong magnets that will interfere with pacemaker/defibrillator function. For safety reasons, candidates with a pacemaker/defibrillator cannot be considered for this position.
In addition to an environment that's as innovative as our products, we offer competitive salaries and benefits.
What We Offer:
Family like environment with an entrepreneurial spirit
Collaborative culture that thrives on innovation and new ideas
Rewards and recognition for great achievements
Growth opportunities for career development
Flexible work arrangements to help balance life and work
Competitive benefits and compensation package
Panasonic is proud to be an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity, sex, sexual orientation, national origin, disability status, protected veteran status, and any other characteristic protected by law or company policy. All qualified individuals are required to perform the essential functions of the job with or without reasonable accommodation.
Pre-employment drug testing is required for safety sensitive positions or as may otherwise be required by contract or law. Due to the high volume of responses, we will only be able to respond to candidates of interest. All candidates must have valid authorization to work in the U.S. Thank you for your interest in Panasonic Corporation of North America.
Location/Division:Buffalo, NY, USAJob Requisition:HF7015
(Usa-Ca-South San Francisco) Research Associate, Facs And Cell Sorting, Verily Life Sciences
Apply to this job on the Verily Life Sciences career site at Verily Careers.
For more information about this role please see the Verily Life Sciences career site above.
At Google, we don’t just accept difference - we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products and our community. Google is proud to be an equal opportunity workplace and is an affirmative action employer.
We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. If you have a disability or special need that requires accommodation, please let us know.
To all recruitment agencies: Google does not accept agency resumes.
Please do not forward resumes to our jobs alias, Google employees or any other company location. Google is not responsible for any fees related to unsolicited resumes.
Global Medical (Or Scientific) Director, Cell & Gene Therapies Unit
Under the leadership of the Global Head Medical Affairs, CGTU, and working collaboratively with other members of the global team, provides strategic direction to the region and country medical teams and ensures execution of the medical strategy and tactical plan in regards to cell and gene therapies. The role requires broad scientific and therapeutic area expertise, clear business understanding, excellent communication skills, and a proven ability to interact successfully with thought leaders, in order to identify and address the relevant medical needs of patients, HCPs and other stakeholders.
Participates in IDMT to gain strategic and planning alignment across regions and functions. May attend GPT on an agenda-driven basis.
Contributes to establishing and implementing appropriate policies and standards for global and local clinical studies as well as other activities defined in the Medical Plan for the therapeutic area (e.g., publication, registries, Medical Expert management).
Encourages and fosters collaboration, and optimizes resources across CGTU medical teams.
Manages all operational aspects and drives execution of Global Medical Affairs clinical trials in partnership with global line functions, assigned clinical operations team members, and regional/country medical associates.
Works collaboratively across functions to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information.
Provides Medical leadership to CTT's for Novartis sponsored GMA trials.
Develops medical launch strategy and supports medical training and medical education to internal and external audiences
Provides medical support for educational events (e.g. stand-alone meetings, scientific symposia) and scientific congresses within legal and compliance regulations.
Provides medical review and approval of key scientific communications, medical information documents and commercial documents within P3 legal and compliance regulations.
Provides medical input on overall publication strategy and is a key member of publication planning team providing GMA medical input on individual publication plans.
Provides medical leadership in interactions with key external stakeholders e.g., may lead advisory boards.
Ensures that planning of medical activities and budgets are aligned with global medical affairs processes/standards. Accountable to efficiently manage budgets and resources, including budget planning for future activities.
Responsible for developing clinical components of key documents – regulatory & safety – from GMA studies supporting submissions and post-marketing commitments to health authorities, when applicable.
Key Performance Indicators
Successful execution of Novartis-sponsored clinical trials and of investigator-initiated trial programs to high quality.
Development of high quality scientific communications and medical information.
Effective use of budget and resources in delivering high-quality Medical Affairs program.
Delivery and maintenance of strategically aligned Medical Plans across global/region/countries
Comprehensive data generation/dissemination plan for each therapeutic area
Execution of all activities within budget
Associate Scientist/Scientist - Cell And Tissue Engineering
The Job Details are as follows:
Develop, implement, and execute analytical strategies to assess the biology of epithelial, endothelial, mesenchymal, and other cell types and to optimize their utility in lung tissue engineering applications.
Key Accountabilities /
Prepare human and non-human organs, tissues, scaffolds, and cells for experimentation using appropriate surgical handling techniques, dissection, cannulation and suturing; utilize sterile technique when indicated
Design and perform experiments to evaluate cell behavior, health, morphology, differentiation, etc. in tissue engineered lung constructs using a combination of 2D and 3D cell culture and recellularization systems
Design and perform experiments to test the cellular effects of mechanical stimuli, such as vascular fluid flow and mechanical ventilation, on endothelial, epithelial and other cell types in tissue engineered lung constructs
Develop strategies to optimize cellular morphology and phenotype in engineered lung constructs to best facilitate pulmonary airway and vascular function
Operate and maintain all equipment necessary for lung construct assessment including bioreactor systems, mechanical ventilators, and computer control systems
Record all laboratory data in the in-house data management system(s)
Regularly present and discuss data with laboratory staff and program leaders
Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues
PhD in life sciences or medical field with focus on pulmonary biology, molecular medicine, and/or endothelial or epithelial molecular mechanisms
1-4 years of post-doctoral training in pulmonary biology, molecular medicine, and/or endothelial or epithelial molecular mechanisms
Experience interrogating cellular or molecular phenotype or function
Facility with appropriate word processing, spreadsheet, presentation and related standard software
Experience with laboratory instrumentation and data software
Preferred Knowledge, Skills, and Abilities:
Facility with appropriate word processing, spreadsheet, presentation and related standard software
Experience with laboratory instrumentation and data software
Good team member skills; must work well with others
Good written and oral communication skills
Ability to initiate and manage day-to-day tasks effectively
Ability to organize and present data
Ability to independently follow experimental methods and protocols
United Therapeutics Corporation is an Equal Opportunity/Affirmative Action Employer - EOE Minorities / Females / Protected Veterans / Individuals with Disabilities
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