Staff Technical Product Manager at Cellares
South San Francisco, CA 94080
About the Job
South San Francisco, CAProduct Management – Product Management /Full Time /On-sitePosition SummaryWe are seeking an innovative and highly motivated Staff Technical Product Manager who will contribute significantly to the development of our advanced cell therapy manufacturing platform. The primary focus of this position will be to understand user needs and workflows for instruments used for cell therapy manufacturing
This individual will interact with customers, partners, and internal subject matter experts to understand and document their cell therapy manufacturing processes and develop actionable requirements for the engineering, analytical and process development teams
This person will work closely with the technical teams overseeing complex projects and should have a structured methodology for gathering, managing and communicating customer feedback.This is a multidisciplinary role and this individual will interface across many parts of the company (with scientists, researchers, process development, and engineers) to develop the best solutions possible
The successful candidate will be a resident expert in representing the voice of the customer and translating them to tangible engineering requirements.Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.ResponsibilitiesDefine and communicate product vision and strategy, outlining the product's direction and ensuring alignment with strategic objectivesSynthesize a coherent product roadmap based on customer input, industry trends, business goals, and engineering competencies, ensuring that it drives the prioritization of the product backlog and software developmentServe as the internal customer and partner advocate with cross-functional teamsWork with our partners and customers, capture their critical needs, then gather and prioritize system requirementsWork closely with cross-functional teams, including software developers, quality assurance professionals, UI/UX designers, and other stakeholders, to implement changes that improve product quality, usability, and user satisfactionWrite clear and concise system requirements that detail what needs to be built and whyIdentify and prioritize key features and functions based on feedback from internal stakeholders and external customersDrive differentiated solutions to the market through customer focus, data-driven decision making, and clear, frequent, and open cross-functional communicationStay up-to-date on industry trends, competitors, and best practices, and share this knowledge with the team and leadershipRequirementsBachelor degree or higher in Engineering or Biological Sciences12+ years of extensive, hands-on Product Management experience in the biotechnology or medical device industries, especially experience bringing a product to marketExperience with large scale automation and benchtop instrumentation in pharma/biotech is highly desirableDomain expertise in cell therapies is highly desirableFamiliarity with human cell biology, immunology, cell isolation, cell culture, characterization, and gene editingKnowledge of regulatory requirements and quality standards, such as FDA, ISO, and GMP, applicable to the cell therapy marketExcellent verbal, written, presentation and interpersonal skillsStrong analytical and problem-solving skillsProactive, creative, self-motivated, flexible to work in a small company environment and assume a wide variety of tasksDesire to be part of a rapidly evolving organization, with a compelling technology, and taking products and processes to the next levelSelf-awareness, integrity, authenticity, and a growth mindset$90,000 - $210,000 a yearCellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options
All displayed pay ranges are approximate, negotiable, and location dependent.This is CellaresCellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century
The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies
The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation
Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale
Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey
The company is backed by world-class investors and has raised over $355 million in financing.Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
This individual will interact with customers, partners, and internal subject matter experts to understand and document their cell therapy manufacturing processes and develop actionable requirements for the engineering, analytical and process development teams
This person will work closely with the technical teams overseeing complex projects and should have a structured methodology for gathering, managing and communicating customer feedback.This is a multidisciplinary role and this individual will interface across many parts of the company (with scientists, researchers, process development, and engineers) to develop the best solutions possible
The successful candidate will be a resident expert in representing the voice of the customer and translating them to tangible engineering requirements.Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.ResponsibilitiesDefine and communicate product vision and strategy, outlining the product's direction and ensuring alignment with strategic objectivesSynthesize a coherent product roadmap based on customer input, industry trends, business goals, and engineering competencies, ensuring that it drives the prioritization of the product backlog and software developmentServe as the internal customer and partner advocate with cross-functional teamsWork with our partners and customers, capture their critical needs, then gather and prioritize system requirementsWork closely with cross-functional teams, including software developers, quality assurance professionals, UI/UX designers, and other stakeholders, to implement changes that improve product quality, usability, and user satisfactionWrite clear and concise system requirements that detail what needs to be built and whyIdentify and prioritize key features and functions based on feedback from internal stakeholders and external customersDrive differentiated solutions to the market through customer focus, data-driven decision making, and clear, frequent, and open cross-functional communicationStay up-to-date on industry trends, competitors, and best practices, and share this knowledge with the team and leadershipRequirementsBachelor degree or higher in Engineering or Biological Sciences12+ years of extensive, hands-on Product Management experience in the biotechnology or medical device industries, especially experience bringing a product to marketExperience with large scale automation and benchtop instrumentation in pharma/biotech is highly desirableDomain expertise in cell therapies is highly desirableFamiliarity with human cell biology, immunology, cell isolation, cell culture, characterization, and gene editingKnowledge of regulatory requirements and quality standards, such as FDA, ISO, and GMP, applicable to the cell therapy marketExcellent verbal, written, presentation and interpersonal skillsStrong analytical and problem-solving skillsProactive, creative, self-motivated, flexible to work in a small company environment and assume a wide variety of tasksDesire to be part of a rapidly evolving organization, with a compelling technology, and taking products and processes to the next levelSelf-awareness, integrity, authenticity, and a growth mindset$90,000 - $210,000 a yearCellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options
All displayed pay ranges are approximate, negotiable, and location dependent.This is CellaresCellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century
The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies
The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation
Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale
Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey
The company is backed by world-class investors and has raised over $355 million in financing.Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
