2347 Life Sciences Jobs - Page 20

Job Overview Provide leadership for Lifecycle Safety, Service Operations (SO), developing cross-functional integrated delivery plans for safety operations throughout all stages of the Lifecycle Safety opportunity chain. Provide leadership for a combination of designated Lifecycle safety operations service lines and direction for specified accounts. Participate actively in local and global initiatives, as needed. Provide line management for assigned staff who are deployed in Service Operations. Primary point of contact for assigned customers or account Essential Functions Accountable to monitor and track project financials/ budget to ensure agreed margins are maintained Independently engage assigned customers on escalation, scope expansion and look for additional business opportunities Lead a high quality and efficient Service Operations team. Develop and review the team reporting structure for IQVIA while adhering to governing standard operating procedures (SOPs), work instructions and applicable regulatory guidelines and regulations. Accountable to meet all project specific SLA and KPI s Direct and support operational decisions in collaboration with senior management. Ensures financial project performance through oversight of key performance metrics. (revenue, direct costs, time-sheet costs, utilization and realization). Act as mentor and coach to less experienced managers, as appropriate. Lead and support ongoing overarching operational, strategic and tactical initiatives as assigned/ agreed, ensuring timely and complete delivery. Direct project resource assignments including staff hiring, and training in collaborations with senior management. Direct and/or participate in cross-functional teams and other process improvement initiatives. Lead and anticipate actively in local and global initiatives, as needed. Support in designing functional strategy Demonstrate and cascade the organizational vision and mission, core values Ability to independently participate in Request for proposal (RFP) and bid defense Ability to represent IQVIA in various industry forums and conference as required Qualifications Bachelors Degree Scientific or healthcare discipline or allied life sciences Bachelor s degree in health science or related area, and 15 years experience in Contract Research Organization or Pharmaceutical company or life science services company, including 10 years of experience in managing a workforce of up to 400+ employees, operating with senior/executive management teams or equivalent combination of education, training and experience. Ability to clearly articulate to large group and build consensus. Ability to address large audience during townhalls and other external forums. Excellent interpersonal skills, effective communication. Engagement with global delivery hubs. In-depth knowledge of Safety service lines. willingness to increase knowledge across Safety service lines and develop new skills. Proven Staff management skills, strong leadership, motivational and influencing skills. Ability to work on multiple projects and manage competing priorities. Effective mentoring and developed coaching skills. Excellent presentation, report writing skills and customer focus skills. Ability to achieve results through communication and facilitation in a matrix service delivery environment with shared accountabilities. Sound judgment, decision-making and problem solving skills. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Ability to support in drafting SOP, Operation, Technical Project documents. Ability to understand and analyze performance Metrix and numbers to support operations. End to End Project management exposure. Excellent team leadership and customer services skills. strategic customer focus. Strategic understanding of business processes across opportunity chain and all phases of product lifecycle. Strong analytical, judgment and decision-making skills. Strong innovation/solution skills. Strong communication (written and verbal) and presentation skills. Strong problem-solving, influencing, negotiation, conflict management and collaboration skills. Highly effective time management and delegation skills, ability to manage multiple competing priorities, meet multiple demanding timelines and work creatively in fast-paced environment. Strong ability to deliver results to the appropriate productivity, budgetary and quality metrics. Demonstrated flexibility, initiative, proactivity, ownership and accountability. In depth knowledge of and ability to apply GCP/ICH/Good Pharmacovigilance Practice and applicable regulatory guidelines. Strong ability to establish and maintain effective working relationships with coworkers, managers and customers. - Extensive use of keyboard requiring repetitive motion of fingers. Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Regular sitting for extended periods of time. May require occasional travel. Flexibility to operate in shifts. Flexibility to support in global time zones as required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide Let s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.

Th ne, India| Bengaluru, India| India| Remote Save this job Job Description Job Overview Receive, analyze and extract snapshots from the holter recording received from trial sites according to study specific trial protocol. Perform quality control on extracted snapshots. Essential Functions Analyze Holter Flashcards/Tapes, in accordance with Holter standard operating procedures. Advise investigator site appropriately if the Holter flashcards/Tapes being received shows relevant abnormalities or study protocol Alert criteria. Be aware of and work to specific trial protocol. Understand and comply with core operating procedures and work instructions of Cardiac Safety Services. Coordinate between the different teams so as to report the holters within established turnaround times(TAT). Extract snapshots Perform quality control on the extracted snapshots. Operationally responsible for their respective protocols as Operations Leader. Serve as mentor for junior Holter staff. Qualifications Other Any of the following medical qualification - M.B.B.S., B.H.M.S., B.A.M.S., and at least 1 year of relevant experience or equivalent combination of education, training, and experience Ability to use Microsoft office (Excel,Word.Powerpoint etc) Ability to establish and maintain effective working relationships with coworkers, managers, and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Save this job LEARN ABOUT HOW WE WORK Join our Global Talent Network Let s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.

As the Engineering Manager, you will lead a talented, cross-functional team of engineers and data scientists to design and develop transformative solutions for our Personalization Science products. Your role will focus on the application of advanced AI technologies, specifically LLMs and NLP, to enhance existing product capabilities and develop new capabilities for our clients. You will be instrumental in setting technical direction, fostering team collaboration, and ensuring project alignment with strategic business goals. Responsibilities: - Team Leadership: Recruit, mentor, and manage a team of software engineers and data scientists, fostering a collaborative and high-performance culture. - Technical Guidance: Provide expertise in LLMs, NLP, and machine learning (ML) technologies to guide the team in developing and implementing innovative solutions. - Project Management: Oversee the end-to-end delivery of product features, from ideation and prototyping through development, deployment, and optimization. - Collaboration: Work closely with Product, and other cross-functional teams to align technical initiatives with business objectives and ensure seamless integration with our other solutions. - Strategy Development: Define and implement technical strategies for NLP and LLM applications, staying abreast of industry advancements and evolving best practices. - Quality Assurance: Ensure high standards for code quality, testing, and reliability, balancing innovation with the need for robust, scalable production systems. - Continuous Improvement: Drive an agile development process with continuous improvement, focusing on both individual and team development, system refinements, and process optimization. Qualifications: - Education: Bachelor s degree in computer science, engineering, or equivalent work experience - Experience: 8+ years in software engineering or data science, with 3+ years in a leadership or management role - Technical Expertise: Strong background in LLMs, NLP, and machine learning frameworks (e.g., TensorFlow, PyTorch, Hugging Face), with experience in deploying production-level solutions. - Project Management Skills: Proven experience managing cross-functional teams with agile methodologies (i.e. SCRUM) - Communication Skills: Excellent interpersonal and communication skills with a track record of working effectively across functions. - Problem-Solving Skills: Analytical mindset with a strong ability to tackle complex, abstract problems and drive impactful solutions. - Preferred Skills: Familiarity with cloud platforms (e.g., AWS, GCP), MLOps best practices, and deployment of scalable AI models in production environments. . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Job Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for surveillance activities for selected products. Essential Functions Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported Perform medical safety review of the protocol, Investigative Brochure, and/or Case Report Forms (CRFs) for appropriate safety content and data capture, as applicable Provide aggregate reviews of safety information, including but not limited to clinical data, postmarketing, literature review and observational studies to maintain oversight of a product s safety profile (e.g: DSUR, RMP, PBRER, ad hoc regulatory reports etc) Ensure service delivery from productivity, compliance and quality perspective within regulatory /contracted timelines. Lead and participate in the initiatives taken for the same from team delivery perspective Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing other safety team members in single case assessment. Ensure update of watch list, list of expectednsess, labeling list/RSIs etc for the assigned products and develop such additional capabilities within the team Lead, drive and participate in training activities, product transitions, audit preparation and knowledge exchange initiatives Review and sign off on the Project Safety Plan and Medical Monitoring Plan per medical safety scope agreed in contract, as applicable Attend project meetings, medical safety team meetings, and represent safety and clinical data review findings during client meetings, as applicable Act as Lead Safety Physician, or additional team support, and/or back up on assigned projects as applicable Provide medical escalation support for medical information and EU Qualified Persons for Pharmacovigilance projects, as applicable 24 hour medical support as required on assigned projects Maintain awareness of medical safety-regulatory industry developments Provide support and participate in signal detection efforts, e.g. strategy meetings etc. as applicable Qualifications Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Req Three (3 years) experience practicing clinical medicine after award of medical degree. Graduate, and/or Residency training can qualify for clinical practice experience Req Two (2) years of pharma experience Pref Sound knowledge of Medicine In-depth knowledge of applicable global, regional and local clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Knowledge of Pharmacovigilance- ICSR and Aggregate reports In-depth knowledge of departmental standard operating procedures (SOPs) Skill in use of multiple safety databases Adequate Computer skills, especially Microsoft word, excel & PowerPoint Good communication skills- verbal and written Ability to establish and maintain effective working relationships with managers, co-workers, investigative site staff, clients and regulatory agency representatives Ability to establish and maintain effective working relationships with coworkers, managers and clients A valid medical license, or equivalent, from the country or region in which he/she resides and works Pref . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Role Purpose: Act as a trusted Finance Partner to the IQVIA India business teams. Providing financial analysis support, insights and business partnering to business leaders. Providing control, co-ordination, and management of data flow for strategic planning, management reporting, budgeting, forecasting, and support of ad-hoc analysis to meet operational requirements. Providing accurate and timely business performance input to local/regional stakeholders. Excellent presentation and communication skills. Proficiency in PowerPoint Presentation (PPT) and Excel tools. Analysis of balance sheet and profit & loss items and reporting. Principal Accountabilities: Analyze monthly actual financial results and prepare variance analysis versus Plan and Forecast Lead the monthly management accounts closing and forecast process which includes loading the nos. in the financial systems Monitor and report areas of operational risk and/or opportunity. Business partnering with other regional/country finance leaders to manage regional financial matters. Provide direction and guidance on cost optimization and efficiencies to business. Manage and present budget and forecast analysis to senior management at business reviews. Research and report ad hoc information and reporting requests. Review and suggest actions on an ongoing basis to automate/improve existing financial processes and implement new processes if opportunity exists. Lead/participate in the implementation of new financial systems, wherever applicable. Manage and review books of accounts on the core accounting system compliant with India GAAP and in compliance with all local and IQVIA Corporate accounting requirements. Perform financial close process covering monthly and YTD activities. Effectively resolve and escalate issues, demonstrate a consistent timely track record of deliverables. Ensure robust audit trail and documentation of all financial transactions. Minimum Education, Experience & Specialized Knowledge Required: GRE 150: Chartered Accountant or Cost Management Accountant degree with 6 - 8 years relevant experience Excellent presentation and communication skills. Proficiency in PowerPoint Presentation (PPT) and Excel tools. Industry preference - Healthcare / IT / IT S sector and in a multinational company environment. Familiarity with corporate finance, proven track record of success Prior working in SAP/People Soft/Oracle will be an added advantage . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

The primary duties and responsibilities of the "Full Stack Software Engineer" include, but are not limited to: -Designing, coding, and debugging software. -Improving the performance of existing software. -Maintaining and upgrading existing software. -Recommending new technologies that can help increase productivity. -Investigating software-related complaints and making necessary adjustments to ensure optimal software performance. Required Skills: -6+ years of experience -Proven expertise and hands-on experience using front-end frameworks such as React, JavaScript / Typescript, and backend development with JavaScript / Typescript using NodeJs -Using cross-platform frameworks such as React-Native would-be a plus. -Strong analytical skills -Good communication skills -Excellent organizational skills -Proven experience applying DevOps principles and developing CI/CD using automation tools such as TerraForm -Proven experience in software development methodologies. -Proven experience building complex web systems. -Ability to multi-task. -Experience with AWS / Azure (not only Virtual Machines usage, but other managed services) specifically AWS Rekognition and AWS Audio Transcriber . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Job Overview Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions. Assists in the development of detailed documentation and specifications. Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions. Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience. Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities. Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications Bachelors Degree Req 1-3 years of related experience Req Works willingly and effectively with others in and across the organization to accomplish team goals. Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline. Knowledge of consulting methods, tools and techniques, related to one s functional area. Knowledge of current events and developments within an industry and major competitors. Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies. Effective time management skills. . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Join global organization with 82000+ employees around the world, as a Automation Tester based in IQVIA Bangalore . You will be part of IQVIA s world class technology team and will be involved in design, development, enhanced software programs or cloud applications or proprietary products. Job Description: Authors and executes automation test cases for larger computer systems within the scope of a broader defined testing strategy. Ensures creation of test data to support test case execution and supports creation and maintenance of libraries of reusable test data sets. Work as part of sprint test team to gain necessary input and execute appropriate revisions to ensure accurate and complete software testing activities. Leverages quality engineering tools for test planning and management, test case authoring, test case execution and issue/defect tracking Performs review of deliverables produced by other members of the IT department throughout the Systems Development Life Cycle, for completeness and detail ensuring the specifications are of a high quality and can be used to write test scripts. May participate in technical meetings with Business Analysts and Developers Reviews requirements specifications for testability and verifying/ensuring traceability of testing to requirements and vice versa Possess a detailed understanding of the requirements elicitation, analysis, and specification process including user requirement specifications and functional specifications for larger, complex applications. Reports status, progress and concerns in a proactive, consistent and accurate manner to the QA Lead. Perform different types of testing like unit, functional, non-functional, security and data validations SKILLS 2+ years of experience in Automation Testing Technologies like Selenium Programming Language: Java, C#, Scripting Languages Experience with Product based testing and different testing methodology Ability to deconstruct problems/systems into smaller components; organize components as part of larger system Demonstrate and articulate the application of logical, analytical thought to a testing issues Excellent oral/written interpersonal skills; user focused; work well with team members. Very strong knowledge/skills around test case creation and test execution; ability to create and execute test cases as part of broader testing strategy. Test case creation and execution would be for discreet portions or multiple portions of larger sized systems that are complex and may interface with other products Ability to author and execute test cases as well as to assist in authoring test plans and strategies and coordinate testing and testing assignments. Requires minimal technical instructions and guidance with complex tasks Solid understanding of relational database theory, multi-tiered application architecture and cloud technologies Involved in the Designing, Preparing, Execution and Maintenance of the test cases. Hands on experience in writing SQL Queries and back end database validation . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

CorroHealth Hiring Fresher's Eligibility Criteria: - -Work Location - Chennai -Graduation - Paramedics (B. pharm, M. pharm) , Non-Paramedics " (BSC biotech, B.sc microbiology, BE - Bio medical engineering) "Note - No Nursing / No BPT" -Graduation Percentage - Minimum 60% and above -Medical Coding Certificate - Not Mandatory -Work Mode - Work from Office -Preferably looking for IN & Around Tamil Nadu Interested Can Connect to below mentioned Contact number & Email Contact - 9043979492 Email - sushil.chandrasekar@corrohealth.com

CorroHealth Hiring Fresher's 2024 (Batch) Eligibility Criteria:- -Work Location - Chennai -Graduation - Paramedics (B. pharm, M.pharm), Non Paramedics (BSC biotech, B.sc microbiology, BE - Bio medical engineering)"Note - No Nursing / No BPT" -Graduation Percentage - Minimum 60% and above -Medical Coding Certificate - Non Mandatory -Work Mode - Work From Office -Preferably looking for IN & Around Tamil Nadu Interested Can Connect to below mentioned Contact number & Email Contact - 9176418460 (Whatsapp) Email - Madhumitha.mohan@corrohealth.com

Job Details Strong skills in Core Java, J2EE, , JavaScript, JSP, and DHTML/Web Page development. Experience in Labvantage LIMS development Strong relational database knowledge and experience using either Oracle and/or SQL Server.

Job description Huge Openings For Medical Coding Fresher Location : Chennai Role & responsibilities Must be a graduate in life science (Life Science Graduates like Pharmacy, biotechnology, microbiology, biochemistry, zoology, anatomy) No Nursing / No BPT Graduation Percentage: Minimum 60% and above Medical Coding Certificate:Not Mandatory -Work Mode:Work From Office Must have good communication skills. Candidates should not have any Backlogs. Only Life Science Graduates. Age Criteria: Less than 28 years. Perks and benefits sponsorship CRC Certification - AAPC Attractive Incentives Interested Candidates Call Reshma HR - 9361279443

Roles and Responsibilities Teach students preparing for IIT JEE, NEET, courses in Physics, Chemistry, Mathematics, and Biology. - Subjects - Physics, Chemistry, Mathematics, Biology. Location Pakyong & Namchi Near gangtok You can also whatsapp your CV on - 9625004154 Develop and deliver engaging lesson plans to ensure effective learning outcomes. Conduct regular assessments and provide feedback to students on their progress. Collaborate with colleagues to develop curriculum materials and teaching methods. Participate in faculty meetings and contribute to school development initiatives.

A Medical Coder reviews patient records and assigns standardized codes (ICD-10, CPT, HCPCS) for diagnoses, procedures, and treatments. 17 Years of Expertise Trainer. Comprehensive curriculum aligned with industry standards.

Job description Huge Openings For Medical Coding Fresher Location : Chennai Role & responsibilities Must be a graduate in life science (Life Science Graduates like Pharmacy, biotechnology, microbiology, biochemistry, zoology, anatomy) No Nursing / No BPT Graduation Percentage: Minimum 60% and above Medical Coding Certificate:Not Mandatory -Work Mode:Work From Office Must have good communication skills. Candidates should not have any Backlogs. Only Life Science Graduates. Age Criteria: Less than 28 years. Perks and benefits sponsorship CRC Certification - AAPC Attractive Incentives Interested Candidates Call Damy HR - 8778691270 Email ID - damaris.davisjayakumar@corrohealth.com

The Senior Consultant position at ZoomRx offers a unique opportunity to work in a rapidly-growing market research and consulting company that focuses on the intersection of data, healthcare, and technology. As a Senior Consultant, you will play a crucial role in developing strategic narratives for senior management teams of blockbuster drugs by leading custom market research studies, analyzing complex datasets, and providing data-driven insights to support clients in various aspects of their business lifecycle. In this role, you will have the chance to build lasting relationships with top pharmaceutical and biotechnology companies, lead multiple projects, and collaborate with cross-functional teams to deliver high-quality, impactful results. You will be responsible for managing client relationships, driving project success, mentoring junior team members, and contributing to internal initiatives aimed at organizational learning and growth. Successful candidates for the Senior Consultant position at ZoomRx possess 5+ years of experience in primary market research, with a focus on quantitative research methodologies in the Life Sciences and Healthcare domain. They should demonstrate proficiency in leading consulting projects, managing client relationships, and delivering data-driven strategic insights. Proficiency in MS Office tools, a background in life sciences or a quantitative field, and experience in healthcare market intelligence functions are preferred qualifications for this role. Working at ZoomRx offers a collaborative environment where everyone is encouraged to take risks, learn from mistakes, and grow towards achieving their career goals. As a Senior Consultant, you will have the opportunity to exercise creative control, develop deep expertise in various life sciences topics, and work alongside smart, grounded peers who thrive on high-performance teamwork. Additionally, you will be part of a vertically integrated organization that empowers you to provide clients with tailored solutions efficiently and effectively. If you are a proactive, analytically-driven professional with a passion for delivering high-quality work and making a meaningful impact in the healthcare industry, the Senior Consultant role at ZoomRx is an ideal opportunity for you to excel and grow in your career.,

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Rubini 9600405840 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

As an Industry & Functional AI Decision Science Consultant within the Accenture Strategy & Consulting Global Network - Data & AI practice, you will have the opportunity to work on high-visibility projects with esteemed Pharma clients worldwide. You will collaborate with leaders in strategy, industry experts, and business intelligence professionals to shape innovative solutions leveraging emerging technologies. Your role will involve supporting the delivery of consulting projects, developing assets and methodologies, and working on a variety of projects such as Data Modeling, Data Engineering, Data Visualization, and Data Science. Additionally, you will be expected to acquire new skills that are applicable across different industry groups, support strategies and operating models, and make presentations to clients when necessary. We are seeking individuals with a Bachelor's or Master's degree in Statistics, Data Science, Applied Mathematics, Business Analytics, Computer Science, Information Systems, or a related quantitative field. The ideal candidate will have proven experience working on Life Sciences, Pharma, or Healthcare projects, with a solid understanding of Pharma datasets including commercial, clinical, Real World Evidence (RWE), and Electronic Medical Records (EMR). Proficiency in Statistical Models, Machine Learning, hypothesis testing, multivariate statistical analysis, and optimization is essential, along with hands-on experience in handling datasets like Komodo, RAVE, IQVIA, Truven, and Optum. Strong programming skills in languages such as R, Python, SQL, and Spark are required, as well as experience with cloud platforms like AWS, Azure, or Google Cloud for deploying language models. Familiarity with Data Visualization tools like Tableau, Power BI, Qlikview, or Spotfire is advantageous. In this role, you must possess excellent analytical and problem-solving skills, a data-driven mindset, proficiency in Excel, MS Word, PowerPoint, and strong communication, interpersonal, and presentation skills. Your ability to solve complex business problems, deliver client satisfaction, and build points of view on industry trends will be crucial to your success in this position. Join us in a culture committed to accelerating equality for all and engage in boundaryless collaboration across the organization.,

You are a highly experienced and motivated Subject Matter Expert (SME) for Veeva Vault QMS, responsible for leading the deployment and optimization of Quality Management System processes. Your deep domain expertise in QMS processes within the life sciences or pharmaceutical industry will be crucial in driving compliance, efficiency, and user adoption through effective system design and implementation. Your key responsibilities include serving as the SME for Veeva Vault QMS, leading deployment, configuration, and optimization efforts. You will analyze existing QMS processes and workflows, identify gaps, inefficiencies, and areas for improvement, and work closely with stakeholders, business users, and functional SMEs to gather requirements. Your role involves designing, implementing, and refining user-friendly QMS processes and workflows aligned with global regulatory requirements such as 21 CFR Part 11, GxP, and ISO standards. You will also support validation and testing of QMS functionalities, ensuring documentation compliance, provide training and ongoing support, and collaborate cross-functionally with various teams. To excel in this role, you should have a minimum of 8 years of experience in the QMS domain within pharma/biotech/life sciences, with proven expertise in leading or acting as an SME for Veeva Vault QMS deployment. Your deep understanding of Quality Management processes like CAPA, Change Control, Audit Management, and Deviations is essential, along with strong knowledge of industry regulations and compliance frameworks such as GxP, 21 CFR Part 11, and ISO standards. Excellent communication, stakeholder engagement, problem-solving skills, and experience in driving process design and change management initiatives are key requirements. Preferred qualifications include Veeva Vault QMS certification, a background in Quality Assurance or Regulatory Operations, and experience in global delivery models involving onsite-offshore collaboration. Your role as a liaison between business and technical teams will ensure seamless integration and solution delivery, making you a vital asset in the optimization of QMS processes.,

You will be responsible for driving international sales growth for Single Use Bioprocessing solutions. Your role will involve providing sales support and coordination for global sales teams, conducting market research, and tracking industry trends. Developing and maintaining strong client relationships in key international markets will be crucial, along with identifying and qualifying international sales leads. You will also assist in pricing strategies, proposals, and RFP responses, while maintaining accurate CRM records and managing the sales pipeline. Collaboration with regional sales teams to align market strategies and preparing reports on sales performance, market trends, and customer feedback will be part of your responsibilities. Additionally, you will support participation in international trade shows, events, and conferences. To qualify for this position, you should possess a Bachelors/Masters degree in Business, Biotechnology, or Life Sciences, along with 2-5 years of experience in international sales and business development. An understanding of Single Use Bioprocessing solutions is essential, as well as strong negotiation and communication skills. You should also be willing to travel internationally. If you meet the qualifications and are interested in this opportunity, please send your resume to hr@cellbios.com.,

Role & responsibilities US Staffing US IT OR Non IT Recruiter Location: Hyderabad Work Model: Hybrid(4+1) Work Hours: EST Time Zone Type: Full-Time Key Responsibilities: Sourcing, identifying, and engaging IT candidates through various channels including job boards, social media, networking events, and internal databases. Screening resumes, conducting phone interviews, and assessing candidates' technical skills and cultural fit for specific roles. Working closely with hiring managers to understand job requirements and team culture to effectively match candidates. Maintain regular communication with candidates throughout the recruitment process. Coordinate salary expectations, negotiations, benefits, and interviews. Knowledge, Skills & Attributes: Bachelor's degree in Business, Human Resources, or a related field. Experience recruiting for both permanent and contract positions. Excellent communication skills(verbal & written). Ability to work independently with minimum supervision in a fast-paced agency network. A strong will to learn and stay up to date with new technologies. Goal-oriented and ambitious. Professional, adaptable, and resilient - ability to withstand setbacks, yet apply 100% efforts throughout the work day. Advanced computer skills, especially in MS Excel, MS Outlook, and MS Powerpoint. Must have demonstrated ability to work within tight deadlines. Willing to work from office in the EST shift. Preferred Qualifications: Bachelors degree in any field Kindly share only relevant profiles at astha.vajpai@spectraforce.com

Responsible for study design, edit specifications and system configurations. The Clinical database designer is accountable for associated quality and timely delivery of assigned study design components in collaboration with other project stakeholders. Essential Functions Interprets the study protocol. Design and update the eCRF. Create and update Edit Specification Document. Generate specifications for EDC build components (eg, Rights and Roles, System Settings and Home Page) Complete the Study Authorization Form and Trial Capacity Request Form (InForm) Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document. Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates. Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan. Escalate potential quality issues. Ensure the completion and documentation of all project-specific training, as we'll as staying current with required Standard Operating Procedures. Reviews build timelines and provide input as applicable. All responsibilities are essential job functions unless noted as nonessential (N). Qualifications Bachelors Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req 0-2 years of relevant core Technical designer experience and total exp being 5+ yrs. Req

Design, implement, and maintain CI/CD pipelines to facilitate automated build, test, and deployment processes. Collaborate with development teams to understand application requirements and architect infrastructure solutions that support scalability, reliability, and performance. Configure and manage cloud-based infrastructure (AWS, Azure, Google Cloud, etc) using Infrastructure-as-Code (IaC) tools like Terraform or CloudFormation. Monitor system performance, identify bottlenecks, and take proactive actions to optimize infrastructure and application performance. Implement and manage containerization platforms (Docker, Kubernetes) to facilitate application deployment and scaling. Maintain and improve configuration management systems (Ansible, Puppet, Chef) for efficient management of infrastructure. Implement and manage monitoring and logging solutions to ensure the availability and reliability of systems. Collaborate with security teams to implement best practices for infrastructure and application security. Automate repetitive tasks to increase efficiency and reduce manual intervention. Participate in on-call rotations and incident response to handle system emergencies and ensure high availability. Qualifications and skills: Bachelors Degree Req 1-5 years of related experience Req Collaboration; Continuous Deployment; Continuous Integrations; Script Programming; Teamwork AWS CloudFormation; Build Automation; Infrastructure As Code (IaC); Red Hat Ansible; Terraform 24*7 shift

The EAM Data Steward is responsible for supporting the integrity and accuracy of data within Illumina s SAP Enterprise Asset Management (EAM) system. This entry-level role assists in the daily maintenance of master data and supports operational processes across various functions including Facilities, Manufacturing Equipment Engineering, and Calibration. The role offers hands-on exposure to EAM operations, data management practices, and cross-functional collaboration in a dynamic, technology-driven environment. Key Responsibilities: Assist with the execution of EAM data entry and updates based on provided standards and guidelines. Support the maintenance of Med Tech master data in SAP. Follow documented work instructions, job aids, and procedures to ensure data accuracy. Perform data checks and validation under the supervision of senior team members. Help prepare reports and basic metrics related to EAM activities and performance. Participate in User Acceptance Testing (UAT) and document observations or discrepancies. Collaborate with team members to support data alignment and system functionality. Contribute ideas for process improvements and efficiency gains. Provide basic support for audits and data quality reviews. Support the setup of remote sites under the guidance of senior staff. Required Qualifications: Bachelor s degree in engineering, life sciences, IT, or a related field. 0-2 years of experience working in SAP or enterprise software systems. Basic knowledge or exposure to EAM, CMMS, or maintenance processes is a plus. Strong attention to detail and organizational skills. Effective written and verbal communication. Proficiency in Microsoft Excel, Word, and Outlook. Ability to work in a team environment and follow instructions with minimal oversight. Eagerness to learn, grow, and take on new responsibilities over time.

Responsible for study design, edit specifications and system configurations. The Clinical database designer is accountable for associated quality and timely delivery of assigned study design components in collaboration with other project stakeholders. Essential Functions Interprets the study protocol. Design and update the eCRF. Create and update Edit Specification Document. Generate specifications for EDC build components (eg, Rights and Roles, System Settings and Home Page) Complete the Study Authorization Form and Trial Capacity Request Form (InForm) Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document. Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates. Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan. Escalate potential quality issues. Ensure the completion and documentation of all project-specific training, as we'll as staying current with required Standard Operating Procedures. Reviews build timelines and provide input as applicable. All responsibilities are essential job functions unless noted as nonessential (N). Qualifications Bachelors Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req 0-2 years of relevant core Technical designer experience and total exp being 5+ yrs. Req . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com