senior scientist

Genentech

<div><h3 class="jobSectionHeader">The Position</h3><h1 class="jobSectionHeader">
Technical Development Senior Scientist</h1>
The Pharma Technical Development (PTD) organization is responsible for translating scientific concepts into manufacturable products and ensuring a reliable supply of quality therapeutics to patients. PTD operates through collaboration and continuous process improvement to achieve its mission.
The Global Analytical Development and Quality Control (ADQC) function provides integrated analytical control strategies for the biologics pipeline. This includes developing, validating, and executing physico-chemical, immunochemical, and biological methods. ADQC's work directly supports CMC development, process development, product characterization, and drug delivery for biologics, spanning from early research (molecular assessment) through post-launch activities.
This position is based in South San Francisco, on site. 
The Opportunity
A Technical Development Senior Scientist position is available in Bioassay US within Genentech&rsquo;s PTD - ADQC. This is a critical hands-on position designed for an individual eager to develop deep expertise in cell engineering and molecular biology to advance our biotherapeutic pipeline.
You will be directly involved in the creation of next-generation cellular tools, enabling the generation mechanism-of-action (MOA) and characterization assays. This role provides an exceptional opportunity to work under the mentorship of a Technical Development Senior Principal Scientist, implementing cutting-edge technologies to drive the design and progression of novel assays.
If you are passionate about precision cell line engineering and thrive in a fast-paced, inclusive team environment, we encourage you to apply. 
Key Responsibilities
The successful candidate will be a core contributor to our cell engineering pipeline, focusing on the following areas:<ul><li>
You provide hands-on support for generating and maintaining mammalian cell lines required for functional assays and cell binding.</li><li>
Executing specialized molecular biology techniques, including vector design/cloning and production of viral vectors (i.e., lentiviral) to create reporter cell lines and stable expression cassettes.</li><li>
Applying CRISPR gene editing and other advanced cellular modification techniques to create precise cellular models for studying drug MOA.</li><li>
You perform quantitative analysis of engineered cell lines using techniques like FACS and PCR.</li><li>
Driving continuous improvement by incorporating current scientific and innovation trends, and collaborate cross-functionally to acquire necessary data to enable portfolio deliverables.</li><li>
You maintain meticulous laboratory records, contribute data to technical reports, present findings at internal group meetings, and represent our work at major external scientific conferences.</li></ul>
Who You Are (Required)<ul><li>
Ph.D. in a relevant field (e.g., Cell Biology, Molecular Biology, Bioengineering).</li><li>
Demonstrated proficiency in aseptic technique and maintaining cultures of a variety of mammalian cell types.</li><li>
Strong fundamental skills in molecular cloning, nucleic acid purification, and design principles for gene expression cassettes, reporters, and knockout strategies.</li><li>
Practical experience with nucleic acid delivery methods such as lipofection, nucleofection, and/or viral transduction (e.g., lentivirus).</li><li>
Experience with FACS-based methods for analyzing cell surface expression and/or functional reporters.</li><li>
Detail-oriented, highly organized, and demonstrated ability to manage and prioritize tasks for multiple projects concurrently.</li><li>
Strong oral and written communication skills suitable for documenting work and presenting data to the immediate team.</li></ul>
Relocation benefits are not available for this job posting.
The expected salary range for this position based on the primary location of California is 104,700.00 - 170,000.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.</div>

Technical Development Senior Scientist

U.S. Pharmacopeia

<div>Description
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
Brief Job Overview
This is a professional, highly technical, non-supervisory position that supports the food ingredients program unit team (PUT) within USP&rsquo;s Global Science and Standards Division (GSSD). The incumbent reports to a local management position at the India site as well as functionally reporting to a management position in the Foods PUT in the US. The incumbent will support the development and technical stewardship of Food Chemicals Codex (FCC) standards, other scientific products, outreach and awareness (in India, US, and internationally), and internal strategic initiatives. These activities require the ability to identify and critically evaluate published information on chemical analysis of food ingredients, regulatory and safety reviews of foods, and data and supplier documents to support development of standards and guidance documents. The successful candidate may develop proposals, coordinate, and lead specific technical studies related to food analysis. The incumbent may present technical talks to academics, the food industry, and regulators to advocate for the work of the program, to solicit feedback, and to support program goals related to awareness and capacity building. The incumbent will work collaboratively with industry stakeholders, the Food Ingredients Expert Committee, the PUT, and other USP program units and departments.
How will YOU create impact here at USP?
The Sr. Scientist I/II has the following responsibilities:
<ul><li>Provide scientific expertise to USP&rsquo;s Foods PUT with a focus on identifying, developing, and supporting food standards and other fit-for-purpose solutions.</li>
<li>Perform critical evaluation of technical data related to food quality and purity including working closely with internal and external laboratories on analytical method development, validation, and data analysis.</li>
<li>Works with USP staff, the USP Food Ingredient Expert Committee (FI EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Food Ingredient monograph and RS development.</li>
<li>Supports in the preparation of data packages and briefing materials to present to the FI EC and other expert bodies; manages projects appropriately and ensures impeccable work-product delivery.</li>
<li>Foster collaboration and communication with other USP program units and departments,</li>
<li>Keep abreast of global trends and developments in related scientific fields and share learnings with managers and colleagues.</li>
<li>Communicate effectively with stakeholders from industry, academia, scientific organizations, and regulatory agencies.</li>
<li>Assist and guide Expert Committees and related expert bodies to support the development of FCC standards and other program products.</li>
<li>Performs other related duties in support of the Foods Program Unit as assigned.</li>
</ul>Who is USP Looking For?
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
<ul><li>Senior Scientist I: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 7-10 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 11-13 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted.</li>
<li>Senior Scientist II: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 10-13 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 13-15 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted</li>
<li>Candidates must have experience related to food safety, food quality, or analytical chemistry as well as outstanding written and verbal communication skills in English.</li>
<li>Ability to review, analyze, and interpret and report on data from various analytical tests such as from HPLC, GC, LC/MS, GC/MS, IR, Raman, UV-Vis, NMR, ICP-MS, AA, etc.</li>
<li>Experience in developing, validating, using, or evaluating food analytical methods</li>
<li>Ability to communicate effectively and diplomatically with technical and non-technical stakeholders</li>
<li>Experience in working directly in or with the food industry, such as experience with food quality systems, regulatory affairs, and supply chain management</li>
</ul>Additional Desired Preferences
<ul><li>Ability to manage and prioritize multiple concurrent, complex projects with minimal direction and a history of successful timely project management</li>
<li>Experience applying food regulations from local or international regulatory bodies, and collaborating with scientific standards organizations is a plus</li>
<li>Ability to rapidly and expertly assess complex technical issues in a fast-paced environment</li>
<li>Ability to embrace change. Adaptable, willing to learn, strong interpersonal and technical presentation skills; strong knowledge of MS Office and related products.</li>
<li>Ability to operate independently where appropriate, yet understands when to escalate issues and how to establish effective working relationships</li>
<li>Ability to work well with diverse employees and customers in a cooperative and friendly manner</li>
<li>Able work flexible hours when needed</li>
</ul>Supervisory Responsibilities
None, this is an individual contributor role.
Benefits
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Job Category Chemistry &amp; Scientific Standards
Job Type Full-Time</div>

Senior Scientist I /Senior Scientist II, Documentary Standards ( Foods)

US Pharmacopeia

<div>
 
 Description
 
 
 
 At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
 
 
 USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
 
 
 
 Brief Job Overview
 
 
 
 This is a professional, highly technical, non-supervisory position that supports the food ingredients program unit team (PUT) within USP&rsquo;s Global Science and Standards Division (GSSD). The incumbent reports to a local management position at the India site as well as functionally reporting to a management position in the Foods PUT in the US. The incumbent will support the development and technical stewardship of Food Chemicals Codex (FCC) standards, other scientific products, outreach and awareness (in India, US, and internationally), and internal strategic initiatives. These activities require the ability to identify and critically evaluate published information on chemical analysis of food ingredients, regulatory and safety reviews of foods, and data and supplier documents to support development of standards and guidance documents. The successful candidate may develop proposals, coordinate, and lead specific technical studies related to food analysis. The incumbent may present technical talks to academics, the food industry, and regulators to advocate for the work of the program, to solicit feedback, and to support program goals related to awareness and capacity building. The incumbent will work collaboratively with industry stakeholders, the Food Ingredients Expert Committee, the PUT, and other USP program units and departments.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 
 The Sr. Scientist I/II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Provide scientific expertise to USP&rsquo;s Foods PUT with a focus on identifying, developing, and supporting food standards and other fit-for-purpose solutions.
 </li>
 <li>
 Perform critical evaluation of technical data related to food quality and purity including working closely with internal and external laboratories on analytical method development, validation, and data analysis.
 </li>
 <li>
 Works with USP staff, the USP Food Ingredient Expert Committee (FI EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Food Ingredient monograph and RS development.
 </li>
 <li>
 Supports in the preparation of data packages and briefing materials to present to the FI EC and other expert bodies; manages projects appropriately and ensures impeccable work-product delivery.
 </li>
 <li>
 Foster collaboration and communication with other USP program units and departments,
 </li>
 <li>
 Keep abreast of global trends and developments in related scientific fields and share learnings with managers and colleagues.
 </li>
 <li>
 Communicate effectively with stakeholders from industry, academia, scientific organizations, and regulatory agencies.
 </li>
 <li>
 Assist and guide Expert Committees and related expert bodies to support the development of FCC standards and other program products.
 </li>
 <li>
 Performs other related duties in support of the Foods Program Unit as assigned.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 
 
 <ul>
 <li>
 Senior Scientist I: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 7-10 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 11-13 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted.
 </li>
 <li>
 Senior Scientist II: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 10-13 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 13-15 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted
 </li>
 <li>
 Candidates must have experience related to food safety, food quality, or analytical chemistry as well as outstanding written and verbal communication skills in English.
 </li>
 <li>
 Ability to review, analyze, and interpret and report on data from various analytical tests such as from HPLC, GC, LC/MS, GC/MS, IR, Raman, UV-Vis, NMR, ICP-MS, AA, etc.
 </li>
 <li>
 Experience in developing, validating, using, or evaluating food analytical methods
 </li>
 <li>
 Ability to communicate effectively and diplomatically with technical and non-technical stakeholders
 </li>
 <li>
 Experience in working directly in or with the food industry, such as experience with food quality systems, regulatory affairs, and supply chain management
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Ability to manage and prioritize multiple concurrent, complex projects with minimal direction and a history of successful timely project management
 </li>
 <li>
 Experience applying food regulations from local or international regulatory bodies, and collaborating with scientific standards organizations is a plus
 </li>
 <li>
 Ability to rapidly and expertly assess complex technical issues in a fast-paced environment
 </li>
 <li>
 Ability to embrace change. Adaptable, willing to learn, strong interpersonal and technical presentation skills; strong knowledge of MS Office and related products.
 </li>
 <li>
 Ability to operate independently where appropriate, yet understands when to escalate issues and how to establish effective working relationships
 </li>
 <li>
 Ability to work well with diverse employees and customers in a cooperative and friendly manner
 </li>
 <li>
 Able work flexible hours when needed
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 Benefits
 
 
 
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

<div>
 At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we&rsquo;ll give you what you need to make it happen. It won&rsquo;t always be easy, growing takes grit. But at ABB, you&rsquo;ll never run alone. Run what runs the world.
 
 
 This Position reports to:
 
 
 R&amp;D Department Lead
 
 
 
 
 
 
 Your role and responsibilities:
 
 
 
 You will be a member of the ABB India Corporate Research Center (INCRC), at the ABB Innovation Center (AIC) located in Bangalore, India. INCRC researchers perform high-end research on diverse topics to develop cutting-edge technologies for ABB&rsquo;s global businesses to propel the organization towards a productive and sustainable future. We collaborate with other ABB corporate research centers, R&amp;D units, and academic institutes. The position offers the opportunity to work in a dynamic, global, and creative environment, collaborating with a wide range of experience and expertise. You will work in applied research projects, developing innovative Control and Artificial Intelligence technologies toward building intelligent autonomous systems for the Industry, Transport, and Infrastructure sectors.
 
 
 The work model for the role is Onsite
 
 
 You will be mainly accountable for:
 
 
 <ul>
 <li>
 Requirements gathering and identification of use cases to aim towards fully autonomous process plants, and minimizing expert interventions in designing, deploying, and maintaining advanced control applications
 </li>
 <li>
 Evaluation of the state-of-the-art Control and Artificial Intelligence approaches and/ or development of a new approach for identified use cases.
 </li>
 <li>
 Development of a proof of concept, prototypes, and support in pilot evaluation and productization of solutions.
 </li>
 <li>
 Contribute to building and managing the laboratory setup for experimental research
 </li>
 <li>
 Communication of project results to Technical experts and Management.
 </li>
 <li>
 Creation of Intellectual property (invention disclosures) and publications in scientific journals and conferences.
 </li>
 <li>
 Travel to customer sites and ABB locations on a need basis.
 
 
 
 </li>
 </ul>
 
 Qualifications For The Role (Mandatory)
 
 
 
 <ul>
 <li>
 Ph.D. in Chemical/ Control/ Electrical/ Instrumentation/ Mechanical engineering with a strong publication and patent record, with a minimum of 7 years of experience; industrial research experience is preferred.
 </li>
 <li>
 Experience in the development of model-based or model-free controllers, such as Model Predictive Control, Approximate Dynamic Programming, and Reinforcement Learning
 </li>
 <li>
 Knowledge of operation and control in the process industry e.g., Oil and Gas, Pulp and Paper, Metals, etc, is preferred.
 </li>
 <li>
 Good knowledge of Deep Learning, Reinforcement Learning, Supervised and unsupervised learning, Multivariate statistics, Time-series analysis, Signal Processing, and related areas.
 </li>
 <li>
 Experience in the usage of Machine learning for the development of predictive maintenance, diagnosis, and monitoring solutions.
 </li>
 <li>
 Proficiency in Matlab and Python programming languages.
 </li>
 <li>
 Ability to communicate effectively in English with internal and external partners, including the academic community.
 
 
 </li>
 </ul>
 We value people from different backgrounds. Could this be your story? Apply today or visit www.abb.com to read more about us and learn about the impact of our solutions across the globe.
 
 
 
 Fraud Warning:
 
 Any genuine offer from ABB will always be preceded by a formal application and interview process.
 
 
 We never ask for money from job applicants.
 
 
 For current open positions you can visit our career website https://global.abb/group/en/careers and apply.
 
 
 Please refer to detailed recruitment fraud caution notice using the link https://global.abb/group/en/careers/how-to-apply/fraud-warning.
</div>

Senior Scientist

Q-CTRL

About the team Q-CTRL's Quantum Sensing Research team performs basic and applied research in quantum sensing and quantum-enabled navigation. It is a highly dynamic team comprising approximately 30 specialists in theoretical and experimental atomic physics, cold-atom interferometry, navigation modelling, and modern Bayesian estimation and signal processing techniques. The Quantum Sensing Research and Quantum Sensing Engineering teams work closely together, translating novel quantum sensing research into a useful capability and product. We are focussed on pushing the boundary of what is possible in quantum sensing and ensuring our R&D has real-world impact. About the role We are seeking a new Senior Scientist to help improve the calibration, noise measurement, signal extraction, and validation procedures of Q-CTRL's quantum inertial sensors for the use in GPS-denied or contested environments. You will work closely with experts in quantum sensing to deliver novel navigation capabilities that solve pressing challenges in maritime and aeronautical positioning and navigation. A key focus of the role will be developing and implementing methods for the extraction of useful real world outputs and performance metrics of our sensors while in the field, as well as the calibration and noise characterisation of these sensors. You will be operating in the crossover of ultra precise next generation quantum sensors and classical inertial navigation systems, pushing these to their limit to extract signals of value from real world systems. The test and validation procedures, performance metrics and signal processing algorithms you develop will inform the continued improvement of our quantum sensors and their deployment for a given navigation end-user or application. What you'll be doing: <ul> <li>Perform essential research and development into novel quantum control solutions and sensor fusion algorithms to enhance the performance of real world quantum sensors (including atom interferometers and magnetometers).</li> <li>Analyse sensor performance in realistic environments, and measure, characterise and calibrate noise metrics for performance enhancement.</li> <li>Work closely with our quantum control engineers, experimental physicists, and sensor hardware specialists to deploy your developed test and validation procedures on real quantum sensor hardware.</li> <li>Collaborate with your colleagues in the Quantum Sensing (Inertial) Team, the Quantum Sensing Division, and the company more broadly.</li> <li>Share your insights into sensor test, characterization, calibration and validation with the broader Quantum Sensing Division, company, external stakeholders and customers through verbal presentations and written outlets (e.g., academic publications, technical reports, blog posts).</li> <li>Other duties within the Employee's skills and experience, or with reasonable training.</li> </ul> Ideally you'll have: <ul> <li>A PhD in Physics, Engineering or a closely related discipline.</li> <li>Experience in the theory, calibration, optimisation, testing and validation of inertial sensors and inertial navigation systems.</li> <li>Experience with atom interferometry, Cold and/or ultracold atomic systems, Quantum sensing in warm atomic vapours, Pulse-level optimisation and quantum control techniques.</li> <li>Experience developing error budget, noise characterisation and sensor metrology.</li> <li>Demonstrated ability to account for real world effects of sensor misalignment using coordinate systems transformations, scale factor and transfer function inversion and co-location limitations.</li> <li>Finally, you will have a strong desire to work with a world leading team and a company that is fundamentally building the future of the quantum technology industry.</li> </ul> It would be fantastic if you have these skills but not essential: <ul> <li>Expertise with Python and Rust programming language for scientific computing.</li> <li>Experience designing, operating and testing inertial navigation system hardware and working closely with both theoretical and experimental teams.</li> <li>Demonstrated experience in improving sensor performance through careful calibration and noise/error measurements.</li> </ul> About Q-CTRL Q-CTRL is the global leader in AI powered quantum control infrastructure software. We build the tools that make quantum technology useful, solving the hardest challenges in quantum computing and quantum sensing to deliver real world impact. Founded in 2017, we operate globally with offices in Sydney, Los Angeles, San Francisco, Berlin, and Oxford. Our teams bring together technical and multi disciplinary expertise across the product lifecycle, and we're hiring talent to help scale every part of the business. We work quickly to turn cutting edge science into deployable technology. In 2024 we raised US$113 million in Series B funding, the largest aggregate investment for a quantum software company. Six months later we delivered the first commercial quantum advantage with Ironstone Opal, our field validated quantum navigation solution for defense and industry. At Q-CTRL, we prioritize outcomes over hours. We offer flexibility, equity potential, and competitive benefits that reflect our high performance culture. If you're ready to help shape the future of quantum, we'd love to hear from you! To recruitment agencies, we do not accept unsolicited branded profiles and are not responsible for any fees related to unsolicited resumes.

Senior Scientist, Inertial

<div>At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we&rsquo;ll give you what you need to make it happen. It won&rsquo;t always be easy, growing takes grit. But at ABB, you&rsquo;ll never run alone. Run what runs the world.
This Position reports to:
R&amp;D Department Lead<div> 
Your role and responsibilities:
You will be a member of the ABB India Corporate Research Center (INCRC), at the ABB Innovation Center (AIC) located in Bangalore, India. INCRC researchers perform high-end research on diverse topics to develop cutting-edge technologies for ABB&rsquo;s global businesses to propel the organization towards a productive and sustainable future. We collaborate with other ABB corporate research centers, R&amp;D units, and academic institutes. The position offers the opportunity to work in a dynamic, global, and creative environment, collaborating with a wide range of experience and expertise. You will work in applied research projects, developing innovative Control and Artificial Intelligence technologies toward building intelligent autonomous systems for the Industry, Transport, and Infrastructure sectors. 
The work model for the role is Onsite 
You will be mainly accountable for:<ul><li>
Requirements gathering and identification of use cases to aim towards fully autonomous process plants, and minimizing expert interventions in designing, deploying, and maintaining advanced control applications
</li><li>Evaluation of the state-of-the-art Control and Artificial Intelligence approaches and/ or development of a new approach for identified use cases.</li><li>
Development of a proof of concept, prototypes, and support in pilot evaluation and productization of solutions.</li><li>
Contribute to building and managing the laboratory setup for experimental research</li><li>
Communication of project results to Technical experts and Management.</li><li>
Creation of Intellectual property (invention disclosures) and publications in scientific journals and conferences.</li><li>
Travel to customer sites and ABB locations on a need basis.</li></ul></div><div> 
Qualifications for the role (Mandatory)<ul><li>
Ph.D. in Chemical/ Control/ Electrical/ Instrumentation/ Mechanical engineering with a strong publication and patent record, with a minimum of 7 years of experience; industrial research experience is preferred.</li><li>
Experience in the development of model-based or model-free controllers, such as Model Predictive Control, Approximate Dynamic Programming, and Reinforcement Learning</li><li>
Knowledge of operation and control in the process industry e.g., Oil and Gas, Pulp and Paper, Metals, etc, is preferred.</li><li>
Good knowledge of Deep Learning, Reinforcement Learning, Supervised and unsupervised learning, Multivariate statistics, Time-series analysis, Signal Processing, and related areas.</li><li>
Experience in the usage of Machine learning for the development of predictive maintenance, diagnosis, and monitoring solutions.</li><li>
Proficiency in Matlab and Python programming languages.</li><li>
Ability to communicate effectively in English with internal and external partners, including the academic community.</li></ul></div><div></div> 
We value people from different backgrounds. Could this be your story? Apply today or visit www.abb.com to read more about us and learn about the impact of our solutions across the globe.
Fraud Warning: Any genuine offer from ABB will always be preceded by a formal application and interview process. 
We never ask for money from job applicants.
For current open positions you can visit our career website https://global.abb/group/en/careers and apply.
Please refer to detailed recruitment fraud caution notice using the link https://global.abb/group/en/careers/how-to-apply/fraud-warning.</div>

GC Therapeutics

<div>
 
 
 Scientist / Senior Scientist &ndash; Cell Line Development
 
 
 
 
 
 
 
 Company Overview
 
 
 
 GC Therapeutics is the first genome-wide cell landscape exploration company using an integrated synthetic biology and AI-driven platform for cell programming. Its patent-pending and proprietary pluripotent stem cell di&fflig;erentiation technology platform TFome&trade; was developed in Professor George Church&rsquo;s lab, a pioneerin synthetic biology,and allows for the development of unique cell therapies with significantly streamlined manufacturing, improved cell quality, efficiency, and speed. GC Therapeutics is basedin Cambridge, MA. For additional information, please visitwww.gc-tx.com.
 
 
 
 
 
 
 Job Purpose
 
 
 
 GC Therapeutics is seeking a highly motivated Scientist or Senior Scientist to join our Cell Line Development (CLD) team. This role focuses on iPSC scale-up and differentiation from benchtop to production-scale bioreactors. The ideal candidate will engineer novel cell therapy products derived from human induced pluripotent stem cells (iPSCs) for regenerative and cell-based therapies and will contribute to the development of cell line candidates for early-phase clinical trials as part of a team developing iPSC derived cellular products and related quality control assays.
 
 
 
 
 
 
 Duties and Responsibilities
 
 
 <ul>
 <li>
 Culture iPSC lines including maintenance and analysis (e.g. cell culture, preparation of media, passaging, cryopreservation)
 </li>
 <li>
 Perform cell engineering on iPSCs to generate products for cell therapies.
 </li>
 <li>
 Design and execute experiments to optimize cell engineering processes for iPSCs and iPSC-derived cells .
 </li>
 <li>
 Perform, analyze and interpret experimental data, ensuring comprehensive documentation of methodologies and outcomes.
 </li>
 <li>
 Maintain a detailed laboratory journal, summarize results, and create presentations for meetings
 </li>
 <li>
 Troubleshoot iPSC cell line engineering challenges, improving process robustness for GMP readiness.
 </li>
 <li>
 Implement process changes for GMP compliance and support technology transfer to process development team.
 </li>
 <li>
 Contribute to the development of product characterization assays (e.g., identity, purity, potency, mechanism of action and functional assays).
 </li>
 <li>
 Draft and review batch records, SOPs and regulatory support documents for cell line engineering processes.
 </li>
 <li>
 Maintain accurate and complete records, ensuring compliance with documentation management systems.
 </li>
 <li>
 Collaborate with a multidisciplinary team including Analytical Development, Quality Assurance, Manufacturing, Operations, R&amp;D, etc.
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 
 
 
 Essential Qualifications:
 
 
 
 <ul>
 <li>
 Advanced degree in cell biology, biochemical or biomedical engineering, cell therapy, or a related field with 2+ years of industry experience.
 </li>
 <li>
 Strong expertise in iPSC culture and maintenance, cell engineering, characterization of engineered cells, and cloning
 </li>
 <li>
 Hands-on experience with various cell type differentiation, characterization and experimental in-process and endpoint analysis including flow cytometry, ELISA and microscopy
 </li>
 <li>
 Significant experience with molecular biology tools for integration site and off-target analysis.
 </li>
 <li>
 Analyze differentiated cell products and establish QC metrics.
 </li>
 <li>
 Optimize, refine and scale differentiation protocols for candidate cell therapeutic products.
 </li>
 <li>
 Experience with documentation management systems
 </li>
 <li>
 Experience with working in the Controlled Non-classified Space.
 </li>
 <li>
 Knowledge of iPSC 2D and 3D cultures.
 </li>
 <li>
 Proficiency in quality management system and data analysis tools.
 </li>
 <li>
 Strong problem-solving, analytical, and documentation skills.
 </li>
 <li>
 Ability to work independently and collaboratively in a cross-functional team.
 </li>
 <li>
 Willingness to work outside normal hours including weekends to support lab activities as needed.
 </li>
 </ul>
 
 
 
 
 
 Additional Preferred Qualifications:
 
 
 <ul>
 <li>
 Experience with operations in GMP facilities and GMP guidelines.
 </li>
 <li>
 Experience in scale-up, process development using 3D culture, organoids and bioreactor systems.
 </li>
 <li>
 Proven track record and strong publications in stem cell or developmental biology.
 </li>
 <li>
 Knowledge of FlowJo, next generation sequencing (NGS), bioinformatics (R, Python).
 </li>
 <li>
 Expertise in genome integrity assessment and off-target characterization.
 </li>
 <li>
 Familiarity with automation, high throughput (HTP) imaging and cell cloning.
 </li>
 <li>
 Familiarity with relevant guidelines from the FDA, EMA and ICH.
 </li>
 </ul>
 
 
 
 
 
 Experimental Techniques:
 
 
 
 
 Cellular Biology:
 
 
 <ul>
 <li>
 Design and execute synthetic biology-based differentiation of iPSCs.
 </li>
 <li>
 Optimize, and scale iPSC derived differentiation for therapeutic cell products.
 </li>
 <li>
 Perform assays including Flow Cytometry, ELISA, ICC, cell-based assays and microscopy.
 </li>
 <li>
 Conduct DOE studies to optimize parameters affecting engineered iPSC growth and differentiation.
 </li>
 </ul>
 
 
 Molecular Biology:
 
 
 <ul>
 <li>
 Perform PCR, qPCR and ddPCR for cell characterization.
 </li>
 <li>
 Characterize target cells using next-generation sequencing (e.g., library preparation for bulk and single cell RNA-seq)
 </li>
 <li>
 Conduct genome integrity assessment and off-target characterization
 </li>
 </ul>
 
 
 General Laboratory:
 
 
 <ul>
 <li>
 Lead experimental design, data analysis, and presentation of results to team members.
 </li>
 <li>
 Maintain detailed and well-organized records of all experimental activities.
 </li>
 <li>
 Provide scientific and technical guidance to junior staff or contract manufacturing organizations (CMOs).
 </li>
 <li>
 Ensure compliance with GDP, GMP, safety regulations, and company policies.
 </li>
 <li>
 Stay current on scientific advancements and contribute to innovative research.
 </li>
 </ul>
 
 
 
 
 
 Pay Range
 
 
 
 $120,000 - $145,000
 
 
 (This range reflects the base salary only and does not include additional compensation such as annual bonus and equity awards, which are part of the total compensation package.)
 
 
 
 
 
 Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
 
 
 
 
 
 At GC Therapeutics, our generous competitive benefits package also include generous PTO, paid holidays, Medical, Dental, Vision, 401(k), Life and Disability Insurance and transportation subsidy.
 
 
 
 
 
 
 Equal Opportunity Workplace:
 
 GC Therapeutics is an equal opportunity employer. We provide equal employment opportunities to all applicants for employment and existing employees without regard to ancestry, national origin, place of birth, race, color, gender, sexual orientation, marital status, pregnancy, religion, age, disability, gender identity, results of genetic testing, service in the military or otherwise to the full extent of all federal, state and local laws. GC Therapeutics&rsquo; equal employment opportunity policy applies to all terms and conditions of recruiting, hiring, placement, training, compensation, transfer, leave of absence, employment, promotion, layoff and termination of employment.
 
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