Life Insurance Jobs in IN Mumbai

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Looking for Life Insurance jobs in IN Mumbai? Browse our curated listings with transparent salary information to find the perfect Life Insurance position in the IN Mumbai area.

Sr. Director, Product Development

Company: Masco Corporation

Location: Indianapolis, IN

Posted Oct 09, 2023

It is the Company's policy to prohibit discrimination in any employment opportunity (including but not limited to recruitment, employment, promotion, salary increases, benefits, termination and all other terms and conditions of employment) based on race, color, sex, sexual orientation, gender, gender identity, gender expression, genetic information, pregnancy, religious creed, national origin, ancestry, age, physical/mental disability, medical condition, marital/domestic partner status, military and veteran status, height, weight or any other such characteristic protected by federal, state or local law. Company: Delta Faucet Company Full time Hiring Range: $130,300.00 - $204,820.00 Actual compensation may vary based on various factors including experience, education, geographic location, and/or skills. E-Verify Participation Poster: English & Spanish E-verify Right to Work Poster: English, Spanish LI-Remote We know that in a diverse, inclusive company, ideas flow freely, all voices are heard and all perspectives are valued. For us, inclusion means welcoming differing opinions, collaborating, allowing people to come to work as who they are and recognizing everyone's contributions. Delta Faucet Company is an E-Verify employer. At Delta Faucet Company, we view diversity as a mosaic of thoughts and perspectives that come from people's varied cultural backgrounds, experiences, education, career paths and other influences that make each of us unique. Product Development and Execution: Be responsible for the end-to-end product development lifecycle, from conceptualization to launch and ongoing optimization.Collaborate closely with cross-functional teams, including sales, marketing, growth & analytics, program management, and operations, to ensure successful product delivery.Use data-driven insights, user feedback, and market research to inform product decisions and iterate on features and experiences. The Company makes employment decisions only based on merit. Beyond the competitive benefits and compensation, Kraus proudly offers an exciting and fun environment, steeped in creativity and commitment to our employees and communities.

Director of Business Development (Remote)

Company: Genezen Laboratories

Location: Indianapolis, IN

Posted Oct 09, 2023

This role requires a comprehensive understanding of the gene and cell therapy market space, viral vector process development and manufacturing technologies, and the drug development regulatory environment, as well as a demonstrated ability to influence positive outcomes without direct reporting authority.ESSENTIAL JOB FUNCTIONS Understand the overarching business development strategy, sales processes, structure, and desired customer experienceIdentify and engage with new prospective clients using sources such as databases, publications, market analysis, trade shows, and contactsGenerate new leads, contact decision-makers, and screen and qualify potential new business opportunitiesLead and work closely with the commercial and technical teams to progress potential customers through the sales process (technical calls, RFP, proposals, visits, contracting, etc. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live. )Lead customer meetings/business due diligence evaluationsAdvise on proposal generation for assigned opportunities and accounts, including detailed RFP responses and proposal development, including inputs from scientific and operations teamsWork with commercial leadership to drive negotiation of agreements and achieve sales objectivesDocument pipeline effectively in CRM, maintain prospect databases, and provide forecasting dataContribute to the implementation of marketing initiatives, including providing market information, distributing materials, and attending trade showsMonitor and evaluate industry trends and customer drivers as well as internal capabilities and technologiesMeet regularly with management and stakeholders to discuss updates and potential impact to strategyDemonstrate exemplary skills in leadership, communication, and account/relationship management while maintaining extremely high quality and efficiency standardsSPECIAL JOB REQUIREMENTSAdaptability required as work schedule may change based on business needs, including flexibility for different time zonesCriminal background check requiredOther duties as assignedKNOWLEDGE, SKILLS AND EXPERIENCEEDUCATION / CERTIFICATIONS / LICENSESEssential/DesiredBS in Biology, Biochemistry, or ChemistryEssentialAdvanced Degree in the life sciences and/or businessDesiredON-THE-JOB EXPERIENCE 5+ years of sales/technical experience or client relationship experience, ideally in a bio-manufacturing or CDMO environmentEssentialExperience with CRM SoftwareEssentialBiologics experience specifically with gene and cell therapiesDesiredExperience within a regulated environment and ability to interact effectively with process development and quality assurance/quality control professionalsDesiredExperience with negotiating long-term commercial contracts; strong negotiation skillsDesiredSKILLS / ABILITIES Strong influencing skills and attention to detail with the ability to manage multiple competing priorities and projects across functionsEssentialTact and diplomacyEssentialHigh levels of initiative, self-motivation, and energy with an ability to work well within a commercial teamEssentialHighly organized with an ability to manage complex information and work effectively to deadlinesEssentialAmbitious, performance-oriented, and able to work independentlyEssentialPHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands:Work EnvironmentSit for long periods of timeMovementRepeated hand movements, typing, use of keyboard and mouseFrequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and armsOccasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawlLiftingFrequently lift and/or move up to 10 poundsOccasionally lift and/or move up to 25 poundsVisionFrequently utilize close vision and the ability to adjust focusCommunicationFrequently required to communicate by talking, hearing, using telephone and e-mailGENEZEN'S VALUE-BASED COMPETENCIESGrowth MindsetBelieve that skill is developed through dedication and hard work.Intelligence & talent are just the starting point.Mistakes are valuable lessons, not shameful indictments.FlexibilityAdapt rapidly to a quickly changing, CDMO environment.Respond by constructively creating & impacting opportunity through active participation.Team FocusWork together; succeed together; fail together.IntegrityDo the right thing, on time, every time.Speak up when needed.Exercise respect.Inclusion Embrace the unique viewpoint of each individual.Join the ongoing journey to a more inclusive workplace and community where we all help each other get better.GENEZEN'S BENEFITSPaid vacation days, amount based on tenurePaid sick time9 observed holidays + 1 floating holiday + 1 volunteer day401(k) plan with company match up to 6% of salary, vested immediatelyShare Appreciation RightsChoice of several healthcare plansFSA and HSA programsDental & vision careEmployer-paid basic term life/personal accident insuranceVoluntary disability, universal life/personal accident insuranceAccidental Death & Dismemberment (AD&D) InsuranceADDITIONAL DETAILSNothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.This position is located in Fishers, Indiana.This position requires a criminal background check.Genezen is an Equal Opportunity Employer.Genezen participates in EVerify.Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.Genezen is located in Fishers, Indiana, a suburb of Indianapolis. Every employee contributes to the success of the company and you can be part of that team.JOB SUMMARYWork closely with the Commercial team to implement Genezen’s overall business development strategy.  That includes identifying and engaging new prospective CDMO clients, coordinating client visits and proposals, negotiating agreements, maintaining a relationship with current clients, and achieving sales objectives. Fishers was named the 1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Genezen is different. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZENMany people have worked in environments where you feel like just another nameless part of an enormous machine. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work.

Tea and Flavor Systems Technologist

Company: FFP

Location: Indianapolis, IN

Posted Oct 01, 2023

Maintain laboratory equipment. Collaborative. Maintain knowledge of beverage client's strategies, brands, and products. Multitasks. Teamwork- Work well with the varied teams within FFP. Ability to lift up to 25 lbs Benefits Medical, Dental, Vision, and Prescription Drug Insurance on Day 1 Health and Wellness Incentives 10 Days of PTO 10 Paid Company Holidays 5 Personal Days 401(k) Health Savings Account (H.S.A.) Ability to stand for prolonged periods of time while working in the lab Ability to work in a production environment. Gathering product or ingredient-related information from vendors Maintain a safe and clean work environment by complying with procedures, rules, and regulations and Good Manufacturing Practices Develop beverage systems which showcase FFP flavors, ingredients, and technologies as integrated solution systems. Requirements MINIMUM REQUIREMENTS: 5 years of experience with bachelor's degree in Food Science or related science. Maintain laboratory and sample inventory of ingredients and supplies.

Account Executive (AE) Inbound - US

Company: Hubstaff

Location: Indianapolis, IN

Posted Oct 09, 2023

For this particular position, we are looking for someone living in the US, giving preference to someone living in one of the following states: Illinois, Indiana, Minnesota, Washington, Oregon, New Mexico, Florida, Nevada, Arizona,Texas, Utah, Georgia, or Maryland. So while 2020 had us virtually meeting because of the pandemic, we met in Portugal (in 2019), Mexico (in 2018), and we had our first in-person retreat after Covid-19 in the Dominican Republic (Feb 2022). In addition, you can read more about us on our website and learn more about our history and work philosophy on our blog. We are giving preference for a professional located in one of the following states: Illinois, Indiana, Minnesota, Washington, Oregon, New Mexico, Florida, Nevada, Arizona,Texas, Utah, Georgia, or Maryland. Main benefits offered to our employees in the US: 25 PTO days/year + health insurance + generous maternity and paternity leave + equipment and self-growth annual bonuses + 100% remote work + working hours flexibility + 401k, among other benefits. Annual Salary: USD $120,000 OTE (USD 40/Hour ($84,000 Base) + $36,000 Commissions) Commissions are uncapped, so you can earn well above the $120K mark. You can find more about Hubstaff and what it's like working with us here. Our current average AE quota attainment year-over-year is 126%. We are scaling our sales team, so you'll be successful if you are able to onboard yourself quickly and have a go-getter, hands-on attitude The drive and energy to manage a large pipeline We're looking for an empathetic salesperson who is a good listener and can adapt well to change and has a strong work ethic Proficient in using Linkedin, Hubspot, Aircall, Pandadocs A self-starter with a track record of successful, credible achievements Benefits Hubstaff is a fast-growing time-tracking and project management startup that fully embraces remote work. This is an employment position and a non-exempt role.

Sr. Software Developer - Hybrid

Company: Federal Home Loan Bank of Indianapolis

Location: Indianapolis, IN

Posted Sep 29, 2023

FHLBank Indianapolis is a cooperative bank dedicated to strengthening communities in Indiana and Michigan. They offer a flexible hybrid workforce model, competitive pay, tuition reimbursement, student loan repayment assistance, and an awesome benefits package. The company values diversity, equity, and inclusion, and promotes learning and development. They are seeking a Software Development Lead with expert object-oriented programming skills, extensive experience with MS.NET development environment, and knowledge of relational databases. The role involves leading a team of software developers, designing system architecture, and providing technical leadership.

Senior IT Business Analyst

Company: Allegion

Location: Indianapolis, IN

Posted Oct 10, 2023

Whatever your background, experience, race, color, national origin, religion, age, gender, gender identity, disability status, sexual orientation, protected veteran status, or any other characteristic protected by law, we will make sure that you have every opportunity to impress us in your application and the opportunity to give your best at work, not because we're required to, but because it's the right thing to do. © Allegion plc, 2020 | Block D, Iveagh Court, Harcourt Road, Dublin 2, Co. Dublin, Ireland REGISTERED IN IRELAND WITH LIMITED LIABILITY REGISTERED NUMBER 527370 Allegion is an equal opportunity and affirmative action employer Privacy Policy At Allegion, we are dedicated to building a diverse, inclusive, and authentic workplace. Together, we embrace all differences and similarities among colleagues, as well as the differences and similarities within the relationships that we foster with customers, suppliers and the communities where we live and work. So, if you're excited about this role but your past experience doesn't align perfectly with every item in the job description, we encourage you to apply anyway. As our values state, "this is your business, run with it". If for any reason you cannot apply through our career site and require an accommodation or assistance, please contact our Talent Acquisition Team. As we grow, we want you to grow with us. Allegion is committed to building and maintaining a diverse and inclusive workplace. Promote partnerships, collaboration, and communication across different functional and business teams for the delivery of solution Responsibilities: Analyze Business Requirements: Collaborate with stakeholders, including field service managers, technicians, and customers, to understand business processes and requirements related to field service operations.

Quality Assurance Director

Company: Genezen Laboratories

Location: Indianapolis, IN

Posted Oct 04, 2023

Responsible for raw material inspection and release, Quality on the floor, disposition of drug product/drug substance, QA review of quality control data, root cause analysis, risk management, technical writing, deviation, change and CAPA management, document/records management, quality metrics reporting, data integrity, training management, QA review of method qualification/validation, process qualification/validation, and equipment/utilities/ facilities qualification and continuous improvement.  Responsible for ensuring internal audits, client audits, supplier quality management, managing regulatory inspections, and quality systems are implemented effectively, efficiently, and compliantly at the site. Help build scalable, phase appropriate Quality systems as the organization continues to grow.ESSENTIAL JOB FUNCTIONS / DUTIESAct as a leader in the Quality organization, helping define and drive the Quality vision, mindset, and culture of the entire company in close collaboration with the Vice President of QA and RegulatoryDevelop overall program, implementation, and continuous improvement of the Quality Systems, which encompass but not limited to: QMS (Deviation, Change Control, CAPA), Documentation, Training, Supplier Management, Internal/Customer Audits and Customer Complaints.Ensure that Quality Systems are designed and operating in a way to provide appropriate support in all GxP areas of the company and are in compliance with current ISO and GMP standards (cGMP) both US FDA and EU applicable to gene therapy as appropriate for early phase clinical trialsDevelop, implement, and maintain corporate policy and procedures for the Quality Management System in accordance with ICH Q10 modelTake lead role in evaluating continuous improvement options for the Quality Systems post initial implementationResponsible for supporting all client projects as the quality lead and attending all meeting for current and prospective clients.Develop user requirements and contribute to the configuration, validation, implementation, and lifecycle management of the electronic Quality Management System (eQMS - Veeva)Develop, implement, and oversee a Quality Supplier Management Program that serves all GxP areas including introduction and qualification of suppliers and materials, supplier material changes, supplier complaintsEnsure that all products manufactured at the site are produced, tested, and released in compliance with SOPs, cGMP’s, US FDA, and EU requirements.Establish and continuously improve the Incoming Quality Assurance (IQA), Quality Oversight, and Batch Release programsResponsible for all raw material and final product release from the facilityEstablish department / individual goals and key performance indicators in alignment with company and operational goalsMaintain and report applicable department and delivery metricsEstablish the Quality Management Review Program, including facilitating creation of the presentation materials to include the Key Performance indicators, the meeting agenda, and attendance, and to orchestrate the material presentationManage internal quality improvement initiatives: evaluate internal processes, suggest/design/implement improvements, create/revise relevant SOPs/PoliciesAct as subject matter expert and provide training on all Quality Management Systems, including but not limited to change control, quality events, investigation, and implementation of effective CAPAsOwn and oversee the compilation of the Site Master File (SMF)Coach, train, and develop the Quality teamDevelop budget for department and ensure adherence to the budgetDrive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountabilityStay current with regulatory guidance as it applies to the Gene Therapy and early phase clinical trialsAct as a member of the site leadership team and engage in business decision-making from a Quality perspectiveEnsure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the QA departmentSPECIAL JOB REQUIREMENTSAdaptability required as work schedule may change based on business needsCriminal background check and drug screen requiredOther duties as assignedKNOWLEDGE, SKILLS & EXPERIENCEEDUCATION / CERTIFICATIONS / LICENSESEssential/DesiredBS degree in science or related fieldEssentialIn depth Knowledge in industries regulated in-part by, 21 CFR Part 11, 21 CFR 210, 21 CFR 211, 21 CFR 600, 21 CFR 610, Eudralex Volume 4, ICH Quality Guidelines, and Guidance to Industry dockets, as applicable for early phase clinical trialsEssentialCertified AuditorDesiredON-THE-JOB EXPERIENCE 10+ years of experience Quality Professional in Pharmaceutical and/ or Biological ManufacturingEssential7+ years of experience Quality SystemsEssential5+ years of experience Quality ManagementEssentialExperience conducting Supplier Audits, including for APIDesiredExperience with Phase I/II IND clinical trialsDesiredSKILLS / ABILITIES Manage multiple projects, set priorities, and work in fast-paced environmentEssentialCommunicate confidently and effectively with management, peers, and key stakeholdersEssentialDemonstrate effectiveness in task completion, decision-making, empowerment of others, deviation/nonconformance management, training, and problem solvingEssentialDemonstrated ability to develop quality systems and a quality management planEssentialPHYSICAL DEMANDSWhile performing the duties of this job, the employee is required to meet the following physical demands:Work EnvironmentOccasionally exposed to loud noise levelsPosition can be combination of remote and on-siteRegularly sit for long periods of timeMovementFrequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and armsOccasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawlLiftingFrequently lift and/or move up to 10 poundsOccasionally lift and/or move up to 25 poundsVisionFrequently utilize close vision and the ability to adjust focusCommunicationFrequently required to communicate by talking, hearing, using telephone and e-mailGENEZEN'S VALUE-BASED COMPETENCIESGrowth MindsetBelieve that skill is developed through dedication and hard work.Intelligence & talent are just the starting point.Mistakes are valuable lessons, not shameful indictments.FlexibilityAdapt rapidly to a quickly changing, CDMO environment.Respond by constructively creating & impacting opportunity through active participation.Team FocusWork together; succeed together; fail together.IntegrityDo the right thing, on time, every time.Speak up when needed.Exercise respect.Inclusion Embrace the unique viewpoint of each individual.Join the ongoing journey to a more inclusive workplace and community where we all help each other get better.GENEZEN'S BENEFITSPaid vacation days, amount based on tenurePaid sick time9 observed holidays + 1 floating holiday + 1 volunteer day401(k) plan with company match up to 6% of salary, vested immediatelyShare Appreciation RightsChoice of several healthcare plansFSA and HSA programsDental & vision careEmployer-paid basic term life/personal accident insuranceVoluntary disability, universal life/personal accident insuranceAccidental Death & Dismemberment (AD&D) InsuranceADDITIONAL DETAILSNothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.This position is located in Fishers, Indiana.This position requires a criminal background check.Genezen is an Equal Opportunity Employer.Genezen participates in EVerify.Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.Genezen is located in Fishers, Indiana, a suburb of Indianapolis. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live. Fishers was named the 1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Every employee contributes to the success of the company and you can be part of that team.PURPOSELeads the Quality Assurance team, including Quality Systems and Quality Operations. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZENMany people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work.

Downstream Process Development - Subject Matter Expert

Company: Genezen Laboratories

Location: Indianapolis, IN

Posted Oct 04, 2023

Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live. The individual will provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders.ESSENTIAL JOB FUNCTIONSBe accountable for establishing the downstream platform from small scale through intermediate scale (50L) lentiviral and retroviral vector processes.Responsible for monitoring and reporting on process performance, identifying opportunities, and implementing changes to improve process, product safety, and product quality.Develop and support process optimization efforts to increase process robustness, reduce costs, and improve viral yield and purity.Design and execute experiments independently: accurately record, analyze, and communicate data to senior management and team members.Maintain open communication via one-on-one and team meetings.Stay current with relevant technologies and needs to be adept at identifying new approaches.Perform and lead single-use system design manifold, selection, implementation, configurations in between Upstream bioreactor and downstream unit operations and control strategies.Develop SOP and batch records for downstream processesResponsible for the process transfer from or to clients and to in-house manufacturing plant.Maintain external technical relationships and collaborate with equipment and material suppliers.Serve as process SME for regulatory and client audits.Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the assigned functional area.SPECIAL JOB REQUIREMENTSAdaptability required as work schedule may change based on business needsCriminal background check requiredOther duties as assignedKNOWLEDGE, SKILLS AND EXPERIENCEEDUCATION / CERTIFICATIONS / LICENSESEssential/DesiredBS, MS, or PhD in biological engineeringDesiredON-THE-JOB EXPERIENCE 5-8 years of relevant industry experienceDesiredSolid foundation in the fundamentals of biochemical engineering, virology and cell biologyEssentialEntrepreneurial experience dealing with customers in product developmentDesiredPharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing OrganizationsDesiredExperience with cell culture technologies, molecular biology, upstream processing, and aseptic processingDesiredSKILLS / ABILITIES Solid knowledge of principles of chromatography with AKTA system and Unicorn software and TFFSolid knowledge of principles of aseptic techniqueWorking knowledge of cGMPs related to the production of viral therapeuticsDesiredAbility to interface successfully with multi-disciplined teamsDesiredExtremely detail-oriented with strong technical skills & mechanically inclined/knowledge of hand toolsDesiredPHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands:Work EnvironmentFrequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowningRegularly required to work around large machinery and typical utilities seen in pharmaceutical facilitiesOccasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shockOccasionally exposed to extremely loud noise levelsSpending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is requiredMovement Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and armsOccasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawlLiftingFrequently lift and/or move up to 10 poundsOccasionally lift and/or move up to 25 poundsVisionFrequently utilize close vision and the ability to adjust focusCommunicationFrequently required to communicate by talking, hearing, using telephone and e-mailGENEZEN'S VALUE-BASED COMPETENCIESGrowth MindsetBelieve that skill is developed through dedication and hard work.Intelligence & talent are just the starting point.Mistakes are valuable lessons, not shameful indictments.FlexibilityAdapt rapidly to a quickly changing, CDMO environment.Respond by constructively creating & impacting opportunity through active participation.Team FocusWork together; succeed together; fail together.IntegrityDo the right thing, on time, every time.Speak up when needed.Exercise respect.Inclusion Embrace the unique viewpoint of each individual.Join the ongoing journey to a more inclusive workplace and community where we all help each other get better.GENEZEN'S BENEFITSPaid vacation days, amount based on tenurePaid sick time9 observed holidays + 1 floating holiday + 1 volunteer day401(k) plan with company match up to 6% of salary, vested immediatelyShare Appreciation RightsChoice of several healthcare plansFSA and HSA programsDental & vision careEmployer-paid basic term life/personal accident insuranceVoluntary disability, universal life/personal accident insuranceAccidental Death & Dismemberment (AD&D) InsuranceADDITIONAL DETAILSNothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.This position is located in Fishers, Indiana.This position requires a criminal background check.Genezen is an Equal Opportunity Employer.Genezen participates in EVerify.Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.Genezen is located in Fishers, Indiana, a suburb of Indianapolis. Fishers was named the 1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Every employee contributes to the success of the company and you can be part of that team.JOB SUMMARYDirect the development and establishment of processes in Process Development.  This individual is accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Genezen is different. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZENMany people have worked in environments where you feel like just another nameless part of an enormous machine. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients.

Software Developer

Company: IBM

Location: IN Bangalore

Posted Oct 13, 2023

The job posting is for a software engineer to work on IBM App Connect, a SaaS integration solution. The role involves developing high-quality applications, improving user experience, and collaborating with stakeholders.

Cloud Engineer - OpenShift Container Platform

Company: IBM

Location: IN Bangalore

Posted Oct 11, 2023

To collaborate. If so lets talk. To invent. Required Technical and Professional Expertise Relevant industry experience of 5 – 9 years’ experience Software engineering or equivalent work experience 4+ years of proven experience with Linux operating system at least as a power user 3+ years of experience in a Linux environment with one or more language like Golang Hands-on experience with Git/Github/Gitlab/Opensource/Public Cloud Experience with writing test cases (unit/functional/integration etc) Good understanding and hands on with Kubernetes development and Containers; OpenShift Container Platform experience is a plus Good written and verbal communication skills in English Problem-solving and troubleshooting skills including performing root cause analysis Ability to work under minimal supervision on complex issues to deliver great results on schedule Ability to work equally well as both an individual contributor and a team member Any experience with public cloud service – IBM Cloud Amazon Web Services (AWS) Microsoft Azure or Google Cloud Platform (GCP) Ability to quickly learn new technologies frameworks and techniques; ability to facilitate technical conversations within your team and with external stakeholders Keen interest contributing to and building communities in open source Ability to self-learn Preferred Technical and Professional Expertise Open-source development experience Development experience with Kubernetes To make markets. Your Role and Responsibilities Play an active role in OpenShift and RHACM development on the Power Architecture Collaborate with Worlwide IBM and Red Hat teams to design and implement innovative solutions for product development and life cycle automation Coordinate with team leads architects and other engineers on the design and architecture of our offerings Be responsible for the quality of our offerings participate in peer code reviews and continuous integration (CI) and respond to security threats Lead technical design and architecture discussions with peers from within and outside of the team Work with Open-Source communities to influence changes to keep Power Architecture current Work with the Quality Engineering (QE) team to ensure that projects are tested correctly Publicize the work of the team through blogs web postings or conference talks Learn new technologies and languages as needed to ensure the product keeps current with the latest trends in the industry. To consult. To code. Not just to do something better but to attempt things you’ve never thought possible. To design.

Infrastructure Specialist: Google DevOps

Company: IBM

Location: IN Hyderabad

Posted Oct 13, 2023

The role involves providing support for operations and production incidents, requiring deep understanding of AWS platform's technology, configuration, access controls, and capabilities. The position demands at least 5+ years of experience in Infra DevOps, App DevOps, and creating container platform clusters. Knowledge of Google Component services, Kubernetes, Docker, and CRIO is essential. The role also involves identifying tools for integrating into CI/CD pipeline and defining quality gates. Preferred skills include understanding SLA management, services health management, and key metrics monitoring, along with any cloud certifications.

Application Database Administrator

Company: Finish Line

Location: Indianapolis, IN

Posted Oct 10, 2023

The Finish Line, Inc. prohibits discrimination against employees and applicants for employment based on the individual's race or color, religion or creed, national origin, alienage or citizenship status, marital status, sex, pregnancy status, age, military status, disability, or any other protected characteristic or class protected by law. The Finish Line, Inc. provides reasonable accommodation for disabilities in accordance with applicable laws. EEOC Statement: The Finish Line, Inc. is an Equal Opportunity Employer and is committed to complying with all federal, state, and local EEO laws. (This email address and phone number is only for individuals seeking accommodation when applying for a job.) Employees may be asked to perform additional duties outside of normal job scope on a temporary basis per company policy. Applicants who require accessibility assistance to submit an employment application can either call Finish Line at (317) 613-6890 or email us at [email protected]. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. A member of our Talent Acquisition team will respond as soon as reasonably possible. The company reserves the right to modify this job description with or without notice. Physical Demands - The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Frequently Asked Questions

What are typical salary ranges for Life Insurance roles by seniority?
Entry‑level Underwriters earn $55k–$70k, mid‑level $70k–$90k, senior Underwriters $100k–$130k. Claims Adjusters range $50k–$75k at entry, $75k–$95k mid, and $110k–$140k senior. Actuaries start $80k–$95k, mid $95k–$120k, senior $120k–$160k.
Which skills and certifications are essential for a career in Life Insurance?
Core skills include risk analysis, financial modeling, and proficiency with policy admin systems (Guidewire, Salesforce). Certifications such as CPCU, ASOP, FSA, or Actuarial Society exams (E, F, P) plus data tools (SAS, Tableau) are highly valued.
Is remote work available in Life Insurance positions?
Yes, many underwriting, claims, and data‑analytics roles support full or hybrid remote work. Companies use cloud‑based policy platforms (Guidewire Cloud, Salesforce Lightning) and VPN‑secure analytics tools to enable distributed teams.
What career progression paths exist within the Life Insurance industry?
Typical paths move from Analyst/Associate to Senior Analyst, then to Manager, Director, and VP levels. Actuaries can progress to Lead Actuary or Chief Actuary, while Underwriters may advance to Lead Underwriter or Risk Management Director.
What are the current industry trends shaping Life Insurance careers?
Digital transformation, AI‑driven underwriting, and personalized policy pricing are reshaping roles. ESG considerations, regulatory updates (e.g., Solvency II, IFRS 17), and the rise of fintech partnerships are driving demand for tech‑savvy, data‑driven professionals.

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