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Cell Manufacturing Quality Specialist Jobs

Associate Manufacturing Quality Specialist
By Diebold Nixdorf At , North Canton
Remote - Work from HomeNo
Develops working knowledge of established process control systems and when changes or deviations may be required.
Generally, less than 2 years’ experience in area of responsibility.
Gain understanding of and capability in Manufacturing Quality methods, processes and practices.
Assisting with routine inspections for assigned products / components,
Assisting with product and process audits to help verify the quality of production processes,
Production Engineer, Cell Materials & Manufacturing
By Tesla At Fremont, CA, United States
Experience with process monitoring, statistical process control, process dashboards and their use in improving the precision and rigor of chemical processing
Experience with some or all of the following industries and production environments:
Family-building, fertility, adoption and surrogacy benefits
401(k) with employer match, Employee Stock Purchase Plans, and other financial benefits
Voluntary benefits to include: critical illness, hospital indemnity, accident insurance, theft & legal services, and pet insurance
Provide technical support to production teams on processing activities in a novel chemical plant
Manufacturing Quality Process Specialist
By The Clorox Company At United States
Previous manufacturing experience considered a benefit
Proactively look for areas of improvement in both process and personnel capabilities. Create process to close gaps
Collaborates with the Business Quality Manager to determine prioritization of work and inputs to the overall quality strategy
5+ years of Quality specific experience
Interpersonal skills to effectively lead and influence across a broad network
Excellent oral/written communication and people skills
Document Controller, Cell Manufacturing
By Tesla At , Austin
Bachelor's Degree (Construction management preferred) or equivalent of relevant experience and evidence of exceptional ability.
Ability to effectively prioritize with strong time management skills in a fast-paced environment.
Support the document management team by operating as a contact for document control issues, support, and ongoing management of the system.
Provide document management support to Cell Engineering teams, ensuring that final and working documents are readily accessible to team members.
3-5 years of experience in an administrative capacity preferably with an architecture, design or construction firm.
Flexibility and proven ability to handle and manage frequent changes effectively and efficiently.
Production Engineer, Cell Manufacturing
By Tesla At , Austin
Experience with process monitoring, statistical process control, process dashboards and their use in improving the precision and rigor of chemical processing
Experience with some or all of the following industries and production environments:
Provide technical support to production teams on processing activities in a novel chemical plant
Develop operating procedures, safety protocols, and maintenance plans for large scale chemical process equipment.
Planning and coordinating operations of various unit operations, ensuring consistent flow while minimizing quality variability
Create sustainable data acquisition systems and monitor to present relevant high quality data visualization for team to accelerate development
Training Supervisor, Cell Manufacturing
By Tesla At , Austin
Experienced using a Learning Management System (LMS) preferred.
Work with Production and Quality Management, Leads and Workstation Trainers on implementing training related initiatives.
Work with management to determine training needs and determines subsequent training and development priorities.
4 years of supervisory experience or demonstrated proficiency performing similar duties/responsibilities preferred.
Lead internal training audits to ensure that training requirements are followed.
Partners with the Training Instructors to implement and train cross-functional teams on the certification system.
Associate, Cell Therapy Manufacturing (Contract)
By Allogene Therapeutics At , Newark, 94560, Ca $34 - $37 an hour
Timely completion of training assignments to ensure the necessary technical skills and knowledge are applied compliantly during GMP operations
Perform tasks in a manner consistent with safety policies, quality systems, and cGMP requirements
Update and revise manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements·
Must maintain and apply knowledge regarding donor information, screening and testing, labeling and product acceptability and release criteria
Bachelors or Associates in relevant science or engineering discipline with 0-2 years of experience in cGMP biologics or cell therapy manufacturing
Cell culture processing experience in handling and propagation of human primary cells is strongly preferred
Specialist, Quality Assurance Incoming Material Disposition, Cell Therapy
By Bristol Myers Squibb At , Devens, 01434, Ma
Works in electronic systems such as SAP, Learning Management, and Document management
Any combination of education, experience, and military service in line with recommendations above will be considered.
Experience in a laboratory, manufacturing, quality, or warehouse environment desired.
Previous work/academic experience where attention to detail and personal accountability were critical to success.
Strong communication skills and the ability to follow written and verbal instructions.
0-2 years of directly relevant experience in a regulated cGMP environment.
Senior Specialist, Quality Assurance Investigations, Cell Therapy
By Bristol Myers Squibb At , Devens, 01434, Ma
Must have knowledge and experience with cGMP manufacturing, quality, and compliance as well as US and global cGMP requirements.
Excellent verbal and written communication skills with ability to prepare written communications and communicate problems to management with clarity and accuracy.
REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities
Able to recognize conflict and escalate to management.
Demonstrates a high degree of attention to detail, with strong documentation expertise. Able to effectively multi-task and demonstrate strong organizational skills.
Working knowledge of applicable business systems including SAP, LIMS/Celabs, Maximo and/or Veeva Vault.
Research Specialist, Cell Culture
By Howard Hughes Medical Institute At , Ashburn, 20147, Va $64,460 a year
A competitive compensation package, with comprehensive health and welfare benefits.
Manage projects, update progress, and perform other duties as assigned.
Master of Science degree in Cell Biology, Molecular Biology, Biotechnology, or Life Science with two years of working experience.
Experience with fluorescence microscopy and cell imaging technology to evaluate cell health and gene modifications.
Experience reviewing scientific literature, following technology development in iPSC, gene editing and related fields, and applying new technologies to enhance productivity.
Communication skills to interact with team members and users, and to update researchers on the status of work in progress.
Manager, Quality Control, Microbiology, Cell Therapies
By Laguna Source At Philadelphia, PA, United States
* Collaborate on site qualification, validation, and commissioning activities as required.
* 6+ years of BioPharma, BioPharmaceutical, Pharmaceutical or Biotechnology industry experience.
* Experience leading Microbiology Supervisors and staff.
* Expertise leading microbiology related investigations with successful experience resolving related deviations.
* Experience ensuring GMP compliance, providing GMP documentation and regulatory inspection readiness.
* Expertise leading microbiology related methods development, methods qualification, and methods validation activities.
Senior Scientist, Stem Cell Manufacturing
By InVitro Cell Research, LLC At New York City Metropolitan Area, United States
Ensure manufacturing and QC SOPs are followed and work closely with ICR's QC Manager
A MS or PhD and at least 3 years of experience in cell manufacturing under GMP conditions; industry experience preferred
Position title and compensation are commensurate with experience.
Optimize cell and stem cell production protocols, including advising on scale-up process development
Troubleshoot issues with manufacturing pipelines and conduct failure analyses when needed
Contribute original research to ICR's regenerative medicine goals
Global Head Of Cell And Gene Manufacturing
By Sanofi At Waltham, MA, United States
Strong Communication and stake-holder management skills
Prior experience as biologics manufacturing site leader, facility design, supply chain management, operational excellence
Extensive prior experience (>10 years) managing manufacturing teams delivering clinical supplies complying with US/EU and other global requirements under cGMP conditions
Prior experience with Cell and Gene Therapy, vaccine, or biologics manufacturing
Prior experience in cell and gene therapy manufacturing operations
Responsible for managing manufacturing operations relating to the global internal and external clinical manufacturing
Production Engineer, Cell Manufacturing
By Tesla At Austin, TX, United States
Experience with process monitoring, statistical process control, process dashboards and their use in improving the precision and rigor of chemical processing
Experience with some or all of the following industries and production environments:
Family-building, fertility, adoption and surrogacy benefits
401(k) with employer match, Employee Stock Purchase Plans, and other financial benefits
Voluntary benefits to include: critical illness, hospital indemnity, accident insurance, theft & legal services, and pet insurance
Provide technical support to production teams on processing activities in a novel chemical plant
Manufacturing Associate, Cell Therapy
By Bristol Myers Squibb At , Summit, 07901, Nj
Motivated, team consciousness individuals are needed to fulfill job requirements.
Or Operations experience or High School diploma/GED and 4 years of Manufacturing or Operations experience.
or Operations experience or High School diploma/GED and 4 years of Manufacturing or Operations experience.
Production of blood component lots through selection, activation, transduction, cell culture, harvest, and cryopreservation.
Aseptic technique is required for most activities: tube welding, connections, and transfers, at minimum.
Weighs and measures in-process materials to ensure proper quantities are added/removed.
Production Supervisor, Cell Manufacturing (Mrc), Gftx
By Tesla At , Austin, Tx

What to Expect As a Production Supervisor you will have the critical task of managing the priorities, equipment, and people associated with the production line. Your experience in fast-paced ...

Associate Director (Cell Therapy Manufacturing Logistics)
By AstraZeneca At , Gaithersburg, 20878, Md
Experience leading supply planning for a biotech manufacturing facility
Experience building and leading a team of direct reports
Experience working in a cGMP environment
Excellent collaboration and communication skills
Experience establishing and leading supply planning for cell therapy manufacturing (autologous and allogeneic)
Experience supporting supply of clinical cell therapy products to multiple regions of the world
Cell Quality Engineer, Cell Engineering
By Tesla At , Fremont, Ca
M.S. in Mechanical Engineering, Chemical Engineering, Material Science with 1-2+ years of industry experience.
Quality control experience in test/manufacturing environment
Implement quality control for cell processes/test models to ensure proper detection and outlier rejection criteria at Fremont production.
Provide support to cell quality lab on field return cases and necessary reliability tests for validation.
Support manufacturing introductions of new in-house manufacturing lines and mass production cell models.
Produce cogent and intelligible data visualizations, author technical presentations and summarize high-impact technical findings.
Product Specialist - Capital Equipment/Cell Analysis
By Agilent Technologies Inc. At , New York, 10022, Ny $108,000 - $180,000 a year
Knowledge or experience with Seahorse and Real-time Cell Analysis Solutions or similar is a plus.
2+ more years of experience in industry in a research, application, or sales role
Strong practical and theoretical knowledge of Cell Analysis Solutions or Capital Equipment
Candidates with technical or research experience within oncology, toxicology and immunology expertise is a plus.
Strategic selling competence and/or challenger sales experience plus.
Great written, verbal and presentation skills
Cell Manufacturing Quality Specialist
By Dana-Farber Cancer Institute At , Boston, 02215, Ma

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED: