3 Cell Therapy Jobs

As a highly skilled professional with a Ph.D. specializing in Immunology or Immuno-oncology and possessing 5-6 years of experience in academia and/or industry, you will be responsible for developing new cell therapy products. This includes conducting Process Development and validations to advance the product to the next stage. Your role will involve analyzing existing processes to identify areas for improvement, designing and developing new processes, and implementing them to enhance efficiency and productivity. Additionally, you will be tasked with scaling up the production process for seamless tech transfer to the GMP scientists. Your extensive experience in developing process documentation and training materials will be crucial, as you will be monitoring and tracking process performance to ensure compliance with regulatory and legal requirements. Your expertise will also be utilized in planning, implementing, and supervising process trials, as well as advising on equipment modifications for Process Improvement. A strong background in working with various immune cells and a deep understanding of both innate and adaptive immune systems are essential for this role. Preference will be given to candidates with previous experience in gene and/or cell therapy drug development teams. Proficiency in designing and delivering genes using viral or non-viral transfer techniques, as well as constructing viral vectors using advanced molecular synthesis and cloning techniques, is required. Familiarity with gene-editing tools such as CRISPR/Cas9 or TALEN is also necessary. Your expertise in molecular biology techniques like cloning, sub-cloning, real-time and quantitative PCR will be invaluable. You should be able to multitask and contribute to multiple projects under tight timelines while upholding integrity, accuracy, safety, and quality standards. Strong verbal, written, and presentation skills are essential, and previous experience in writing grants and research articles will be advantageous. The ideal candidate will have experience in team management or working in a cross-functional group and collaborating with clients. Leadership skills are a must to drive a team towards excellence, providing technical and scientific recommendations, troubleshooting effectively, and demonstrating innovative capabilities on a daily basis. Effective communication and collaboration within a highly matrixed team environment are vital to advance the company's cell therapy pipeline. Understanding sterile practices, work ethics, safety, health, and environmental regulations is crucial. You will be involved in compliance monitoring inspections, regulatory agency interactions, and the preparation and review of protocols, reports, and regulatory documents as per program requirements. Key competencies required for this role include expertise in cell therapy design and development, preparing and implementing quality compliant documentation, exceptional presentation and communication skills, effective team management, strong interpersonal skills, adept stakeholder management, and efficient vendor management.,

As a Quality Control Testing Technician in a Cell Therapy Lab, your primary responsibility is to ensure the quality and safety of cell therapy products through rigorous testing and analysis. You will work in a highly regulated environment, adhering to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to support the development and production of cell-based therapies. This role requires a strong attention to detail, analytical skills, and the ability to work collaboratively with cross-functional teams. You will execute a variety of tests to assess the quality, purity, and potency of cell therapy products, including but not limited to viability assays, sterility testing, endotoxin testing, and identity testing. Operate and maintain specialized laboratory equipment and instruments used in cell therapy testing, such as flow cytometers, PCR machines, and automated cell counters. Maintain accurate and detailed records of all testing activities, ensuring compliance with regulatory requirements. Document deviations, investigations, and corrective actions as necessary. You are expected to stay current with industry regulations and standards related to cell therapy and ensure all testing activities align with applicable GMP, GLP, and other regulatory requirements. Participate in the validation and optimization of testing methods, ensuring that methods are robust, accurate, and reproducible. Work closely with Research and Development teams to transfer validated methods into routine quality control testing and collaborate with Production teams to troubleshoot and resolve any issues related to product quality. Conduct environmental monitoring to ensure the cleanliness and sterility of the laboratory environment. Analyze test results and prepare detailed reports for review by senior management. Communicate any deviations or trends that may impact product quality. Participate in continuous improvement initiatives to enhance laboratory processes and procedures, providing input on improving efficiency and reducing testing turnaround times. Train and mentor junior staff members on laboratory techniques, safety protocols, and quality control procedures. Qualifications required for this role include a postgraduate or masters degree in Life Sciences/Biochemistry/Microbiology. Previous experience in a quality control or analytical testing role within the biopharmaceutical or cell therapy industry will be of added value but not compulsory. A strong understanding of GMP, GLP, and other regulatory requirements, excellent communication and teamwork skills, attention to detail, and a commitment to quality are essential for this position. This job description is a general outline of the responsibilities and qualifications typically associated with the position of a Quality Control Testing Technician in a Cell Therapy Lab. Specific duties and qualifications may vary depending on the organization and the stage of development and production of cell therapy products.,

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Cytiva, one of 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the which makes everything possible. The Field Applications Specialist is responsible for supporting the Customer, Account Manager, Workflow Specialist, and core commercial team. Provides deep scientific knowledge in the customer context, including tests and demos to prove competitive advantage. This position reports to the Senior Manager of the Gen Med FAS Team in APAC and is part of the Gen Med Commercial APAC Team located in India and will be working remotely to cover India as well as APAC. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Collaborates with Account Managers, and Sales Specialists within their territorybased on customer demand for scientific application. Responsible for providing pre and post-sale support, product demonstrations, seminars, training and supporting territory sales objectives. Applies highest level of scientific and technical product knowledge in modality, including solution impact, capabilities and functions within context of Cytiva customers. Supports customers with in-depth technical support, remotely, in person or in the lab. Conducting demos or experiments for or with the customer. Following up on samples with technical advice and/or experimental support. Responsible for regional customer training, developing application driven training courses and demonstrations, at customer sites and high-level scientific meetings. Build and strengthen strong technical relationships with customer. Identify potential opportunities of scalability of an application, identify products and services that will provide significant cost savings and productivity gains for the customer, and persuasively educates and articulates thebenefits to the customer. Who you are: Cross selling, upselling, value positions and funnel management. Understanding of customers key business drivers. Insight with networks and contacts. Comprehensive Cell Therapy, Viral Vector or nucleic acid process (upstream/downstream) expertise. Bachelor's Degree in biotechnology, life sciences or relevant field. Preferably in cell biology, biochemistry, and immunology 5 years of applications experience must be from Biotechnology industry. Travel: Ability to travel - 50-75 % travel, overnight, within territory or locations It would be a plus if you also possess previous experience in: QlikSense or Sales Force Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit .