the chance to make a significant impact on the future of agriculture while working alongside world-renowned scientists. About the Role: As a Plant Transformation Research Associate, you will play a crucial role in our mission to enhance crop yields and sustainability.
You will work closely with senior scientists to conduct experiments, maintain plant cultures, and generate valuable data that will drive our discovery and production goals. This position offers hands-on experience in cutting-edge plant biotechnology and the opportunity to contribute to groundbreaking research. Responsibilities: Collaborate with senior scientists to perform all aspects of plant cell culture and transformation
Employ exceptional sterile techniques and proficiency in working within a laminar flow hood Maintain impeccable laboratory practices and database tracking for all projects Effectively communicate research progress and results to team members Qualifications: Bachelor's or Master's degree in Biology or equivalent Hands-on experience in plant cell culture and transformation, preferably with soybean or related species Proven ability to plan, organize, and execute project tasks independently Excellent verbal and written communication skills Authorization to work in the United States Location: Plastomics is headquartered in St.
Louis, Missouri, a hub for agricultural biotechnology innovation.
We offer a competitive salary, comprehensive benefits package, and the chance to work in a dynamic and collaborative environment.
Join Our Team: If you are a highly motivated individual with a passion for plant science and a desire to make a real difference in the world, we encourage you to apply. Become part of a team that is revolutionizing agriculture and shaping the future of sustainable food production. To Apply: Please submit your resume and a cover letter highlighting your relevant experience and skills
quickly and broadly, managing deadlines and deliverables while applying the latest theories to develop new and improved products, processes, or technologies. From creating experiments and prototyping implementations to designing new architectures, our research scientists work on real-world problems that span the breadth of computer science, such as machine (and deep) learning, data mining, natural language processing, hardware and software performance analysis, improving compilers for mobile platforms, as well as core search and much more.
As a Research Scientist, you'll also actively contribute to the wider research community by sharing and publishing your findings, with ideas inspired
by internal projects as well as from collaborations with research programs at partner universities and technical institutes all over the world. Google Research is building the next generation of intelligent systems for all Google products.
To achieve this, we're working on projects that utilize the latest computer science techniques developed by skilled software engineers and research scientists. Google Research teams collaborate closely with other teams across Google, maintaining the flexibility and versatility required to adapt new projects and foci that meet the demands of the world's fast-paced business needs. The US base salary range for this full-time position is $133,000-$194,000
bonus equity benefits. Our salary ranges are determined by role, level, and location.
The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits. Learn more about benefits at Google.
Minimum qualifications: Ph D degree in Computer Science, a related field, or equivalent practical experience. One or more scientific publication submission(s) for conferences, journals, or public repositories. Preferred qualifications: 2 years of coding experience. 1 year of experience owning and initiating research agendas. - Author research papers to share and generate impact of research results across the team and in the research community. - Help in growing research business across teams by sharing research trends and best practices within the community. - Define the data structure, framework, design, and evaluation metrics for research solution development and implementation under minimal guidance.
Identify timelines and obtain resources needed. - Identify new and upcoming research areas by interacting with potential external and internal collaborators. Help in developing long-term research strategy and plans to expand the impact of Google research with some guidance. - Contribute to conducting experiments based on the research question. Develop research prototypes or conduct simulations to further evaluate the impact of research, finalize hypotheses, and refine the research methodology under minimal guidance.
Requisition #: 103061454791287494pca3lyuhf
release and characterization testing of different cell therapy candidates. The group supports c GMP-compliant in-process Quality Control (QC) support of c GMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround c GMP testing of in-process materials.
In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. Responsibilities Execute
test methods following established procedures, compliant with c GMPs and in some cases turning data around in a rapid manner Manage test deliverables and training activities to defined test schedules Collaborate with colleagues to align on test requests Maintain compliance of a c GMP environment ranging from instruments, to reagents, data packs, etc.
Manage analytical databases and perform data analysis to support assay performance and control Contribute to assay investigations for out of expectation results or test failures Lead or support internal assay transfers from analytical development teams Write simple technical reports & SOPs, including clear and concise technical data presentation
and discussion. Generate of materials for internal/external presentations as needed Participate in interdepartmental meetings and project specific sub-team meetings Train on new approaches needed for incoming programs and act periodically as the lead to train colleagues.
Plan, prioritize and execute simple and complex experiments with the relevant controls with little guidance from their supervisor. Acquire, compile, analyze, and interpret data with minimal supervision. Work within a broader team to support the development and implementation of new ways of working and methodologies. Basic Qualifications Master's degree in Biology/Biochemistry or related discipline or Bachelor's degree with a minimum of two years of relevant experience in the Biotechnology/medical industry.
Experience with molecular biology techniques, cell culture and cellular based assay development Preferred Qualifications Experience using and developing molecular techniques such as residual, identity, and strength assays (including platforms ranging from flow cytometry, ELISAs, and cell counting). A minimum of 1 year experience in a c GMP environment. Experience validation and transfer analytical methods. Experience using Quality by Design (Qb D) principles and have used Design of Experiment (DOE) approaches for method development/optimization.
Sanofi Inc. and its U. S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; interaction, gender, gender identity or expression; affectional or interactionual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA#LI-SAAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
Position Overview/Department Description This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi's CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports c GMP-compliant in-process Quality Control (QC) support of c GMP Manufacturing cutting edge methods such as flow cytometry.
The selected candidate will execute rapid turnaround c GMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. Responsibilities Execute test methods following established procedures, compliant with c GMPs and in some cases turning data around in a rapid manner Manage test deliverables and training activities to defined test schedules Collaborate with colleagues to align on test requests Maintain compliance of a c GMP environment ranging from instruments, to reagents, data packs, etc.
Manage analytical databases and perform data analysis to support assay performance and control Contribute to assay investigations for out of expectation results or test failures Lead or support internal assay transfers from analytical development teams Write simple technical reports & SOPs, including clear and concise technical data presentation and discussion.
Generate of materials for internal/external presentations as needed Participate in interdepartmental meetings and project specific sub-team meetings Train on new approaches needed for incoming programs and act periodically as the lead to train colleagues. Plan, prioritize and execute simple and complex experiments with the relevant controls with little guidance from their supervisor. Acquire, compile, analyze, and interpret data with minimal supervision. Work within a broader team to support the development and implementation of new ways of working and methodologies. Basic Qualifications Master's degree in Biology/Biochemistry or related discipline or Bachelor's degree with a minimum of two years of relevant experience in the Biotechnology/medical industry.
Experience with molecular biology techniques, cell culture and cellular based assay development Preferred Qualifications Experience using and developing molecular techniques such as residual, identity, and strength assays (including platforms ranging from flow cytometry, ELISAs, and cell counting). A minimum of 1 year experience in a c GMP environment. Experience validation and transfer analytical methods. Experience using Quality by Design (Qb D) principles and have used Design of Experiment (DOE) approaches for method development/optimization.
Sanofi Inc. and its U. S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; interaction, gender, gender identity or expression; affectional or interactionual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA#LI-SAAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
PDN-99ea6241-64e8-49d7-83a2-0ae3476a4e6c
subjects4. Screening and scheduling subjects5. Getting voluntary subject consent6. Teaching subjects about protocol expectations for them7. Performing study/protocol procedures in a detailed, accurate manner8. Maintaining study files9. Tracking subjects, avoiding lost-to-follow-up10.
Documenting an adverse event11. Processing and shipping lab work12. Maintaining communication and correspondence (by telephone, email, fax, etc. ) with subjects, sponsor, monitor and other site study personnel13. Completing case report forms (CRF's) for PI review and approval14. Helping study monitors with CRA corrections15. Maintaining study-specific supplies16. Preparing for study closure and archiving Knowledge of Spanish and / or Phlebotomy Training will be an added advantage.
