Life Insurance Jobs in Peninsula
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Looking for Life Insurance jobs in Peninsula? Browse our curated listings with transparent salary information to find the perfect Life Insurance position in the Peninsula area.
SAP Data Specialist (Contract)
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. (E.g., Material Master, BOMs, Recipes, Production Versions, Business Partner, etc. As an equal opportunity employer, Allogene is committed to a diverse workforce. Proven change management and project management competency. Develop LSMW scripts for data mass maintenance. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. Perform Change Control steps related to Master Data Change Actions. )Drive MRP implementation by collaborating with planning team, setting up test data and conducting training workshops.Facilitate Weekly Governance forum meeting & steward the SAP ECM Data Creation Workflow process.Maintain data creation forms, data dictionary and training documents. Responsibilities include, but are not limited to:Create and maintain Master Data elements in SAP Production, Quality and Development environments.
Region Manager, North East
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 10, 2023
Corcept Therapeutics, a company dedicated to cortisol modulation, has been pioneering this field for 25 years. They have developed over 1000 proprietary selective cortisol modulators, including Korlym, the first treatment for Cushing's syndrome. Their team of over 300 professionals, including medical practitioners, scientists, and industry experts, strive to advance cortisol modulation science for treating serious diseases. They aim to revolutionize treatment for severe endocrine, oncology, metabolism, and neurology disorders. The Role of the Regional Manager (RM) involves leading a team of Clinical Specialists, formulating sales strategies, and engaging with key customers to drive business growth. The RM must have proven success in leading sales teams, strong clinical acumen, and the ability to collaborate cross-functionally. The pay range for this position is $190,000 - $215,000, with potential for bonuses and equity grants.
Customer Engineer
Company: SambaNova Systems
Location: Peninsula
Posted Sep 11, 2023
SambaNova Systems is hiring a post-sales Customer Engineer to provide technical leadership and support for their AI solutions. The ideal candidate should have extensive experience in system engineering, software, and managing technical customer relationships. They will be responsible for product adoption, implementation, support, and becoming a trusted advisor for identified customers. The role involves working with strategic customers in the region, collaborating with internal teams, and addressing multiple stakeholders. The individual will also be required to travel to customer sites and trade shows, and provide off-hours support during significant events. The base salary for this position ranges from $150,000.00/year up to $200,000.00/year.
Director, Global Event Management
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Corcept Therapeutics, a company dedicated to cortisol modulation, is seeking a Director of Global Event Management. The role involves leading corporate event and scientific congress planning, managing exhibit agencies, and overseeing meeting logistics. The ideal candidate should have 10+ years of congress and meeting planning experience, strong interpersonal skills, and a deep understanding of the pharma industry. The pay range is $218,500 - $257,000, with potential for bonuses and equity grants.
Director of Risk Management
Company: BitGo
Location: Peninsula
Posted Sep 09, 2023
BitGo, a leading digital asset financial services provider, is seeking a Director of Risk Management. Founded in 2013, BitGo offers liquidity, custody, and security solutions, processing 20% of global Bitcoin transactions. The company supports over 600 coins and tokens, serving more than 1500 institutional clients in 50 countries. The Director of Risk Management will assist in managing and expanding the enterprise-wide risk management program, ensuring alignment with industry standards and regulatory obligations. The role requires knowledge of risk management frameworks, information security, and privacy standards, along with strong staff management and interpersonal skills.
Associate Director, Process and Product Development
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. Responsibilities include, but are not limited to:Manage, lead and mentor a high performing team of scientists and provide oversight and technical leadership for the development of formulation, aseptic filling, cryopreservation, drug product container, storage, and post thaw processes and proceduresDevelop robust processes for formulation, fill/finish, and cryopreservation for chimeric antigen receptor T-cell (CAR-T) products utilizing QbD DOE principlesEstablish and qualify representative fill/finish scale-down models to identify CPPs that impact Drug Product CQAsCollaborate with CMC and clinical teams to evaluate dosage form options to enable dosing requirements for in-use dosing and administration stability studies and other TPP objectivesUse risk assessment/management tools and apply QbD principles for successful technology and knowledge transfer to internal and external Drug Product manufacturing sitesLead and facilitate cross-functional activities in support of pipeline priorities by working collaboratively across CAR-T Process Sciences, Analytical Development, Internal/External Manufacturing, Quality, and Regulatory groupsDrive and coordinate studies while managing timelines to meet corporate goalsImplement process advancements for scaling-up and introduction into a GMP manufacturing environmentAct as internal expert and maintain state-of-the-art knowledge in the field of cellular cryopreservation and cryobiologyOther duties as assigned Position Requirements & Experience:Ph.D. in Chemical Engineering, Biochemistry, Molecular & Cell Biology, Immunology or the related field with at least 8 years of relevant experience required 10+ years (or at least 10 years 12+ years with a Master’s degree M.S.) This individual will lead the development, characterization and implementation of state-of-the-art formulation, aseptic filling, and cryopreservation drug product processing technologies to deliver scalable and robust clinical and commercial manufacturing processes. of relevant experience requiredA demonstrated foundational understanding of mammalian or primary cell culture, biochemistry, molecular & cell biology and immunology (required for enhanced product & process understanding)Strong knowledge and hands-on experience with cell therapy process development and cryopreservationFormulation science experience, especially with cryoprotectant additivesStrong scientific understanding of cell biology and cryopreservation Experience working in or supporting a cGMP-regulated environmentExperience in cell therapy manufacturing processesAbility to work in a fast-paced, startup environmentStrong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneouslyExcellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelinesExperienced leader of scientific teamsExperienced project management/leadership skillsStrong interpersonal skills including verbal and written communication are essential in this collaborative work environmentCandidates must be authorized to work in the U.S. We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. All approved Allogene Therapeutics positions are accessible via the Allogene Careers page at www.allogene.com/careers.LI-AW1 We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.Please be aware that the FBI recently issued a warning about an increased number of fake job postings for remote work employment that target applicants' personally identifiable information. For more information, please visit www.allogene.com, and follow @AllogeneTx on Twitter and LinkedIn. About the role:Allogene is seeking an Associate Director, Process and Product Development to lead the Drug Product Team for Allogene’s CAR-T cell therapies.
Associate Director, Process and Product Development
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 09, 2023
Allogene Therapeutics is hiring an Associate Director, Process and Product Development to lead the Drug Product Team for their CAR-T cell therapies. The role involves managing a team of scientists, developing robust processes for formulation, aseptic filling, and cryopreservation, and collaborating with CMC and clinical teams. The ideal candidate should have a Ph.D. in a relevant field with at least 8 years of experience, strong knowledge in cell therapy process development and cryopreservation, and experience in a cGMP-regulated environment.
Manager, Analytical Development
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Corcept Therapeutics is a company that believes in the potential of cortisol modulation to improve health. They have been working on this for 25 years and have developed over 1000 proprietary selective cortisol modulators. They are committed to building a culture that values diverse perspectives and are working to deliver better outcomes for people affected by serious diseases.
Associate Director, Process and Product Development
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. This individual will lead the development, characterization and implementation of state-of-the-art formulation, aseptic filling, and cryopreservation drug product processing technologies to deliver scalable and robust clinical and commercial manufacturing processes. Responsibilities include, but are not limited to:Manage, lead and mentor a high performing team of scientists and provide oversight and technical leadership for the development of formulation, aseptic filling, cryopreservation, drug product container, storage, and post thaw processes and proceduresDevelop robust processes for formulation, fill/finish, and cryopreservation for chimeric antigen receptor T-cell (CAR-T) products utilizing QbD DOE principlesEstablish and qualify representative fill/finish scale-down models to identify CPPs that impact Drug Product CQAsCollaborate with CMC and clinical teams to evaluate dosage form options to enable dosing requirements for in-use dosing and administration stability studies and other TPP objectivesUse risk assessment/management tools and apply QbD principles for successful technology and knowledge transfer to internal and external Drug Product manufacturing sitesLead and facilitate cross-functional activities in support of pipeline priorities by working collaboratively across CAR-T Process Sciences, Analytical Development, Internal/External Manufacturing, Quality, and Regulatory groupsDrive and coordinate studies while managing timelines to meet corporate goalsImplement process advancements for scaling-up and introduction into a GMP manufacturing environmentAct as internal expert and maintain state-of-the-art knowledge in the field of cellular cryopreservation and cryobiologyOther duties as assigned Position Requirements & Experience:Ph.D. in Chemical Engineering, Biochemistry, Molecular & Cell Biology, Immunology or the related field or equivalent experience Relevant experience in the pharmaceutical/biotech industryA demonstrated foundational understanding of mammalian or primary cell culture, biochemistry, molecular & cell biology and immunology (required for enhanced product & process understanding)Strong knowledge and hands-on experience with cell therapy process development and cryopreservationFormulation science experience, especially with cryoprotectant additivesStrong scientific understanding of cell biology and cryopreservation Experience working in or supporting a cGMP-regulated environmentExperience in cell therapy manufacturing processesAbility to work in a fast-paced, startup environmentStrong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneouslyExcellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelinesExperienced leader of scientific teamsExperienced project management/leadership skillsStrong interpersonal skills including verbal and written communication are essential in this collaborative work environmentCandidates must be authorized to work in the U.S. We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. All approved Allogene Therapeutics positions are accessible via the Allogene Careers page at www.allogene.com/careers.LI-AW1 We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.Please be aware that the FBI recently issued a warning about an increased number of fake job postings for remote work employment that target applicants' personally identifiable information. For more information, please visit www.allogene.com, and follow @AllogeneTx on Twitter and LinkedIn. About the role:Allogene is seeking an Associate Director, Process and Product Development to lead the Drug Product Team for Allogene’s CAR-T cell therapies. Led by world-class management with significant experience in cell therapy, our fully integrated, in-house team of researchers is dedicated to discovery and translational research, development, and cell manufacturing.At Allogene, we are developing a pipeline of off-the-shelf CAR T cell candidates, with the goal of delivering readily available cell therapy faster, more reliably, and at greater scale to more patients.
Manager, Statistical Programming: Job ID - 1185
Company: Ascendis Pharma
Location: Peninsula
Posted Sep 11, 2023
The job posting is for a Statistical Programmer position in the pharmaceutical or bio-pharmaceutical industry. The incumbent will provide programming support to the study team, develop and maintain standard programs, and lead the programming aspect of a project. The position requires a comprehensive knowledge of CDISC standards, clinical trial study design, and electronic data submission requirements.
Analog Mixed-Signal Chip Lead Engineer
Company: Lightmatter
Location: Peninsula
Posted Sep 10, 2023
Lightmatter is seeking a collaborative engineer or scientist with deep expertise in mixed-signal and analog design, as well as breadth across other engineering disciplines. The ideal candidate will be a key member of the analog team, architecting the world's first photonic computers. Responsibilities include supporting micro-architecture development, collaborating with design engineering teams, and overseeing the layout and verification of designs. Requirements include a MS with 12+ years or Ph.D. with 8+ years of experience in the semiconductor industry, deep understanding of analog and mixed-signal circuit design, and experience leading the design of multiple analog/mixed-signal chips. Benefits include comprehensive health care, 401k matching, life insurance, generous time off, and a flexible, hybrid workplace model. The base compensation range is $220,000 to $280,000.
Analog Mixed-Signal Chip Lead Engineer
Company: Lightmatter
Location: Peninsula
Posted Sep 10, 2023
Lightmatter recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. Actual pay will be based on several factors including work experience, location and education. In accordance with the Colorado, California and New York law, the range provided is Lightmatter's reasonable estimate of the compensation for this role. Responsibilities Support micro-architecture development with chip architects by conducting feasibility studies Collaborate with members of our design engineering teams (packaging, digital, analog, photonics) to define chip partitions Responsible for the top-level design including schematic/layout hierarchy and floor planning Work cross-functionally with analog, digital, and photonics block designers to integrate circuit IPs Plan for Power Delivery Network (PDN) and support its design implementation Plan for ESD strategy and support its design implementation Plan for Test strategy and support its design implementation Oversee the layout and verify the design to ensure a successful tape-out Work with Program Managers to meet the deliverable timelines at various stages in the product development Define production and bench-level test plans Validate performances of the circuits in the lab Requirements MS with 12+ years of relevant experience, OR Ph.D. with 8+ years of experience Semiconductor industry experience in Analog/Mixed-signal IC design Deep understanding of analog and mixed signal circuit design including CMOS device characteristics, noise, mismatch, linearity, and design trade-offs Experience leading the design of multiple analog/mixed-signal chips and their tape-outs Experience with mixed-signal mode verification methodologies Experience with integration flows and their challenges Familiarity with packaging effects, supply isolations, ESD structures, and high-frequency circuit layout for optimum performance Experience designing chips with 2.5/3D packaging is a plus Working knowledge of RTL, PnR, Modeling, and Design verification flows is a plus Experience with Cadence Design Environment Experience testing analog circuits in a lab environment Strong ability to work collaboratively with people across multiple functional areas Benefits Comprehensive Health Care Plan (Medical, Dental & Vision) 401k matching Life Insurance (Basic, Voluntary & AD&D) Generous Time Off (Vacation, Sick & Public Holidays) Paid Family Leave Short Term & Long Term Disability Training & Development Flexible, hybrid workplace model Stock Option Plan Base Compensation Range: $220,000 to $280,000. You will need both deep expertise in mixed-signal and analog design and breadth across other engineering disciplines, such as photonics and digital electronics, semiconductor device physics, thermal/packaging, and machine learning. *We are open to hiring a candidate in the Boston, MA or Mountain View, CA areas for this role. This is fundamentally an interdisciplinary team, and outside-the-box thinking is the daily norm. In this role, you will be a key member of the analog team architecting the world's first photonic computers. If you're a collaborative engineer or scientist who has a passion for innovation, solving challenging technical problems, and doing impactful workwork like building the world's first optical computers, consider joining the team at Lightmatter! The successful candidate will demonstrate an eagerness to refresh and grow their competency in these areas.