2350 Life Sciences Jobs - Page 48

In This Role, Your Responsibilities Will Be: Job Responsibilities include: Align and offer value proposition to existing overall architecture for the shared IntegrityManager framework Update framework as underlying geospatial library (ESRI ArcGIS SDK) changes Provide software estimation and work breakdown plans, and track progress to milestones Perform software development and maintenance of our core pipeline integrity products: High Consequence Area Analysis, Risk Modeling, Assessment Management, Alignment Sheet Generation, and Reporting Providing technical support to, and solving specific geospatial/integrity data management problems posed by, project managers and clients Lead the technical design and development for new products, new features, and any significant changes to the core framework Design, develop, optimize, modify, and debug software using C# and SQL (SQL, T-SQL, and PL-SQL) Troubleshoot performance issues in both SQL Server and Oracle environments Convert concepts into deliverable solutions Communicate with clients and the rest of the team (oral, written & visual) Work closely with product managers to ensure products meet client needs Lead and mentor junior developers Design and develop new tools directly or indirectly related to IntegrityManager Who You Are: You quickly and decisively act in constantly evolving, unexpected situations. You adjust communication content and style to meet the needs of diverse partners. You always keep the end in sight; puts in extra effort to meet deadlines. You analyze multiple and diverse sources of information to define problems accurately before moving to solutions. You observe situational and group dynamics and select best-fit approach. For This Role, You Will Need: A BSc. or higher in Computer Science, Engineering, Mathematics or related field 7+ years of experience preferred MUST HAVE experience with object-oriented languages C# MUST HAVE experience with SQL, preferably SQL and T-SQL including a strong background in DDL and creating and maintaining stored procedures MUST HAVE demonstrable experience with geospatial application development, preferably using ESRI ArcObjects or ESRI ArcPro SDK. MUST HAVE experience as a product architect - designing and managing core frameworks and engines using patterns Demonstrated problem solving and troubleshooting skills Preferred Qualifications That Set You Apart: Experience in the pipeline or utility industry Experience as a Technical Lead on projects Good working knowledge of the . NET Framework Our Culture & Commitment to You: . Emersons compensation and benefits programs are designed to be competitive within the industry and local labor markets . We also offer a comprehensive medical and insurance coverage to meet the needs of our employees. We are committed to creating a global workplace that supports diversity, equity and embraces inclusion . We welcome foreign nationals to join us through our Work Authorization Sponsorship . We attract, develop, and retain exceptional people in an inclusive environment, where all employees can reach their greatest potential . We are dedicated to the ongoing development of our employees because we know that it is critical to our success as a global company. . Safety is paramount to us, and we are relentless in our pursuit to provide a Safe Working Environment across our global network and facilities. Through our benefits, development opportunities, and an inclusive and safe work environment, we aim to create an organization our people are proud to represent. Our Commitment to Diversity, Equity & Inclusion This philosophy is fundamental to living our company s values and our responsibility to leave the world in a better place. Learn more about our Culture & Values and about Diversity, Equity & Inclusion at Emerson . If you have a disability and are having difficulty accessing or using this website to apply for a position, please contact: . WHY EMERSON Our Commitment to Our People . We have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world s most complex problems for our customers, our communities, and the planet. You ll contribute to this vital work while further developing your skills through our award-winning employee development programs. We are a proud corporate citizen in every city where we operate and are committed to our people, our communities, and the world at large. We take this responsibility seriously and strive to make a positive impact through every endeavor. . Emerson is a global leader in automation technology and software. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability. With global operations and a comprehensive portfolio of software and technology, we are helping companies implement digital transformation to measurably improve their operations, conserve valuable resources and enhance their safety. We offer equitable opportunities, celebrate diversity, and embrace challenges with confidence that, together, we can make an impact across a broad spectrum of countries and industries. Whether you re an established professional looking for a career change, an undergraduate student exploring possibilities, or a recent graduate with an advanced degree, you ll find your chance to make a difference with Emerson. Join our team - let s go!

Plaksha is looking for Project Scientist to join our dynamic team and embark on a rewarding career journeyDesign and conduct experiments to explore scientific theories, develop new products, or solve complex problems in areas such as biology, chemistry, physics, or environmental science. Collect and analyze data using advanced techniques and instruments, ensuring accuracy and reproducibility. Document findings in detailed reports and publish results in peer-reviewed journals. Collaborate with cross-functional teams, including engineers and researchers, to apply scientific insights to real-world challenges. Ensure compliance with safety and ethical standards in all research activities. Continuously update knowledge through literature review and participation in conferences or workshops.

Job Overview Support the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department, primarily in one geography. With guidance, conduct recruiting activity for management teams as assigned. Essential Functions Work with management in assigned service areas, business units or departments to source, select and hire qualified candidates to fill vacant positions using cost-effective techniques and in accordance with company policies, procedures and processes. Write job postings to post and advertise positions. Review applications and conduct interviews to obtain information regarding applicants work history, education, training, job skills, and salary requirements. Create and coordinate job advertising in various media. Attend job fairs and develop and maintain contacts with colleges, universities, alumni groups, and other organizations to identify potential applicants. Work with external recruiters and employment agencies to identify and recruit candidates. Utilize Internet online recruiting sources to identify and recruit candidates. Meet with functional business leaders and executive management, as required, to discuss and establish staffing objectives and ensure they are achieved. Assist with training line management on recruiting, interviewing, and the selection process as required. Support a diverse workforce and comply with local and regional hiring guidelines and procedures, particularly for applicant tracking. Keep abreast of market trends and demands impacting the company s ability to attract competitive candidates; coordinate with the compensation team on salary offer considerations and equity concerns. Ensure the provision of timely employee-related information to management teams as necessary. May be responsible for meeting established financial targets and assisting with business development activities depending on business line. Qualifications Bachelors Degree Req 1 year experience within a staffing function as a recruiter or combination of recruiter and specialist experience Req Or Equivalent combination of education, training and experience Req Sound knowledge of legislation in the recruiting process Strong computer skills including Microsoft Office applications and HRIS applications Strong verbal and written communication skills Strong attention to detail Good problem-solving, judgment and decision-making skills Good understanding and awareness of the commercial environment and market trends Good customer service skills Very high degree discretion and confidentiality Ability to multi-task, prioritize and plan routine activities Ability to establish and maintain effective working relationships with coworkers, managers and clients . 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

In This Role, Your Responsibilities Will Be: Lead a multi-functional engineering team of 50+ members teams to develop and support Emerson s Flow Controls products Oversee the design, development, and testing of embedded systems for new products. Collaborate with cross-functional teams including hardware, software, and firmware engineers. Ensure compliance with industry standards and regulations. Manage project timelines, budgets, and resources. Drive innovation and continuous improvement in product development processes. Provide Architectural & System engineering direction to Embedded team members Lead and/or assist new product development activities such as create architecture design, new circuit designs, leverage existing designs, identify and use proven technologies and Provide guidance/support for debugging to the team Build an inclusive and encouraging environment for employees within the organization. Attract, develop, appraise, and retain qualified and skilled staff Ensure that the necessary resources (people, technology, budget) are allocated efficiently to meet the needs of the group s development and growth. Develop and manage budget to fund yearly operations and infrastructure development Support global business development team to Showcase Emersons comprehensive capabilities and diverse product portfolio to our customers to unlock new business growth opportunities Ensure projects/programs are well defined, prioritized, tracked, and communicated in a consistent and effective manner through PI and sprint planning. Closely collaborate with global team to define the solutions roadmap, prioritize and deliver productized solutions Propose customized architecture and solutions that surpass customer needs, giving long-term value by addressing customers difficulties. Share regular updates with senior management and other key partners regarding the performance, challenges, and success of the productized solution Who You Are: You facilitate an open dialogue with a wide variety of contributors and stakeholders and model collaboration across the organization and deliver messages in a clear, compelling, and concise manner. You focus on the highest priorities and sets aside less critical tasks and set aggressive goals and has high standards. You consistently use multiple methods to develop others. For This Role, You Will Need: Bachelor s degree in Electronics Engineering or related field. Total 20+Years of experience with 15+ years of experience in electronics design. Minimum 5 years of leadership experience - Engineering, Solutions/ Programs, Research & Development or Product Management Knowledgeable in microcontroller-based board level design, Precision Analog design, High Speed Design, Precision Analog Design & Power supply & well-versed global Hardware development cycle Strong knowledge of embedded systems and electronics design. Proven track record of successful product development and launch. Excellent leadership and team management skills. Strong problem-solving and decision-making abilities. Effective communication and interpersonal skills. Preferred Qualifications That Set You Apart: Masters Degree Experience working with Global teams Familiarity with industrial digital communication protocols (e.g. 4-20mA, HART, Modbus) Understanding of Secure Life Cycle Development, Cyber Security Requirements (CRA, IEC62443 etc.,) Experience with international safety and hazardous location design, including intrinsic safety & SIL standards design Experience in the Process Industry. Knowledge of industry standards and regulations. Experience with project management tools and methodologies WHY EMERSON Our Culture & Commitment to You: . . . Equal Opportunity Employer Emerson is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment. ABOUT EMERSON Emerson is a global leader in automation technology and software. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability. With global operations and a comprehensive portfolio of software and technology, we are helping companies implement digital transformation to measurably improve their operations, conserve valuable resources and enhance their safety. We offer equitable opportunities, celebrate diversity, and embrace challenges with confidence that, together, we can make an impact across a broad spectrum of countries and industries. Whether you re an established professional looking for a career change, an undergraduate student exploring possibilities, or a recent graduate with an advanced degree, you ll find your chance to make a difference with Emerson. Join our team - let s go!

Job description We are seeking for Experienced and Talented HR professionals from pharmaceuticals or life sciences background to Join our sister concern Company "Plus Plus Life Sciences" Roles and Responsibilities Designing and updating job descriptions Crafting emails for attracting passive candidates Sourcing potential candidates using various online platforms (e.g. professional forums like Naukri, LinkedIn etc.) Screening incoming resumes as well as application forms Interviewing candidates via various mediums (e.g. in-person, phone, video) Preparing and distributing assignments as well as language, logical reasoning, and numerical tests Advertising jobs on careers pages, job boards, and social media Providing contacts of qualified applicants to the company's Hiring Managers Sending job offer and recruiting emails, and also answering queries related to compensation and benefits Monitoring HR metrics (e.g. source of hire, time-to-hire, and time-to-fill, etc.) Hosting recruitment events and participating in job fairs Collaborating with management for identifying future staffing needs Providing guidance and consultancy to new recruits and also helping them onboard Desired Candidate Profile At least an MBA/PGDM in Human Resources Management or a relevant field Prior experience as an HR Recruiter in Pharmaceutical or Life sciences field. Sound knowledge of all HR processes (e.g. recruitment, onboarding, training, talent management etc.) Sound knowledge of all labor regulations Experience with resume databases, Naukri Portal, and referral programs Sound knowledge of full-cycle recruiting Strong verbal as well as non-verbal communication skills Exceptional time-management and organizational skills Website - https://pluspluslifesciences.com

Position Summary: We are seeking a seasoned Data Analytics Manager with 15+ years of expertise to lead our analytics and software teams based in Bangalore. In this role, you will oversee the delivery of analytics, advanced analytics, AI/automation, and digital/software initiatives, supporting global business services India, global supply chain, quality and manufacturing functions. You will also collaborate closely with data engineering teams to ensure scalable architecture, and seamless integration across platforms. We re seeking a strategic leader who can build and manage large teams, foster cross-functional collaboration, and cultivate a culture of continuous improvement and innovation in a global context. Position Responsibilities: Lead and manage a reporting/AI/digital/data analysts team and collaborating closely with Data Enginneering team to build up robust apps. Collaborate closely with cross-functional teams, including business analysts, operations, IT, and business stakeholders, to understand opportunities around applying digital, data, automation technologies to drive a significant business impact Define project scope, goals, and deliverables in collaboration with stakeholders, ensuring alignment with business goals and objectives. Develop and implement project plans, schedules, and budgets, tracking progress and managing resources to ensure successful project delivery. Develop and implement advanced analytics/insights strategies, frameworks, best practices to support business goals. Oversee the design, development, and deployment of solutions, ensuring that they meet the highest standards for performance, scalability, and security. Utilize machine learning techniques to build predictive models and improve processes. Provide leadership and guidance to analytics teams, fostering a culture of collaboration, innovation, and continuous improvement. Manage relationships with external vendors, partners, and service providers, ensuring timely delivery of contracted services and solutions. Monitor project risks, issues, and dependencies, proactively identifying and mitigating risks to minimize project disruptions and delays. Lead continuous enhancement of project delivery processes, tools, and methodologies by leveraging industry best practices, incorporating lessons learned, and proactively introducing innovative approaches to strengthen team capabilities. Provide senior leadership with regular project status updates, reports, and metrics, highlighting key achievements, milestones, and areas for improvement. The listed responsibilities are an essential but not exhaustive list of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. Preferred Experience/Education/Skills: Bachelors degree in Computer Science, Engineering, or related field. Advanced degree (e.g., MBA) preferred. 15+ years of experience in leading analytics teams supporting a global organizations supply chain, quality or manufacturing functions. Excellent leadership, communication, and interpersonal skills, with the ability to influence senior executives and guide teams through complex challenges. Strong domain expertise in building insights, dashboards, reports, scorecards, and reporting applications, with a deep understanding of industry-specific challenges, processes, and technologies. Strong domain expertise in life sciences, with a deep understanding of industry-specific challenges, processes, and technologies. Proven track record of delivering complex projects on time and within budget, particularly those supporting global operations (e.g., manufacturing, supply chain). Deep understanding of data, analytics, AI, and Automation architecture principles, design patterns, and best practices, with experience developing end-to-end business solutions. Experience with advanced analytics and automation tools like Tableau, PowerBI, UIPath, Thoughtspot, R/Python, CortexAI, etc. Experience with big data processing frameworks like Apache Spark and cloud-based data platforms like Snowflake. Experienced in project management tools such as JIRA, Azure DevOps, Confluence and Certifications such as PMP, Agile, or equivalent is highly desired. Experience with cloud platforms such as AWS, Azure, or Google Cloud Platform is a plus. Reporting Applications, Reports & Dashboards, Automation Architecture Specialist, Design Patterns, Analytics, Data & Ai

Position Summary: The Senior Manager, Global Asset Solutions and Facilities India leads a Center of Excellence (COE) function that provides global program management, systems, process excellence, solutioning and reporting strategy in support of Global Facilities and Asset Lifecycle Management Global Business Process (ALM GBP) teams. The Global Asset Solutions Sr. Manager drives key strategic and global solutions and dashboard reporting of key performance metrics to the broader Global Facilities and GO organization for all of ALM GBP and facilities operations. Key measures of success include but are not limited to; delivering to service levels (primarily to the internal customers they support and enable), impact and effectiveness of Global Planning and Engineering programs, EAM solutions and management, BAS monitoring and solution, and overall staff performance in the support of Company s functional businesses (i.e. total cost of operations, asset life optimization, $/SF of tenant improvements initially and over time in response to business churn, speed/responsiveness. Responsibilities: Global roadmap of all Asset Lifecycle Management and Facilities technology and future strategy. This roadmap and strategy should facilitate and enable regional and functional teams to benefit from enterprise level insight and strategy while also allowing for necessary regionalization to execute at specific sites. Global/central governance and administration of the Enterprise Asset Management (EAM) tool. Striving to optimize both the global and local value of this system and its use by regional teams in the management of their assets. EAM global policy for GO is set by this team. Global/central management and implementation of Company s Archibus and AutoCAD drawings and related record tools and program. This includes setting global process, tool governance, and related record standards and procedures as well as active management of Archibus and associated drawings. This function also sets and administers the system roadmap for the AutoCAD. BMS Facilities environmental control (EMS) and Building Automation (BAS) technology strategy, policy, data standards, monitoring and metrics. EAM, system admin/ownership, architecture, projects and enhancements, data standards, monitoring, metrics, and documentation. PM/CM technology strategy to support and improve business processes driving global standardization. Operational strategy, metrics, SNOW data standards, policy, roadmap. Global operations alarm strategy Responsible for ensuring strict adherence to Company guidelines for document management strategies and document control. Collaborates with Quality, Life Cycle Management and other functions as needed. Engages Facilities Operations, Project and Engineering team to provide technology solutions to fulfill all required Compliance programs are being followed. Facilitates global engineering and compliance discussions for innovation and process improvements. Partnership across GO to drive programs and processes. Ensure that all company procedures and policies are complied with and carried out accordingly. In depth knowledge in Biotech s practice and standards especially related to MDSAP regulations, ISO 13485:2016 and 21 CFR Part 11 and Part 820 and how these standards apply to facilities and/or utility systems. May need to travel to support programs and perform other duties as assigned. All listed requirements and experience are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities. Requirements and Experience: High level of business acumen and experience in highly diverse corporate environment. Experience developing and driving technology roadmaps and strategies Partner and collaborate with global peers and counterparts in Facilities, Real Estate, Security, EHS, and GO across all sites. Closely work with IT, HR, Finance/accounting and Procurement business partners. Experience building and sustaining high performing matrixed teams. Collaborative, able to integrate and bring together individuals under common goals and accountabilities. Possess technical, business and financial acumen. Excellent verbal and written communication skills with requisite interpersonal skills to partner, collaborate and build relationships with business partners, suppliers, and regional teams and develop presentations at all levels. Comfortable with dealing with ambiguity and continuing change in a fast paced and growing hi-tech company Strategic thinker; anticipates and develops business opportunities and priorities for future action while also executing on concrete business objectives Customer focused, very responsive, and action oriented to meet business needs while maintaining a positive, professional outlook. Ability to travel up to 20% of the time; both domestic and international. Proficient in use of Microsoft Office (Project, Word, Excel, Outlook, Access). Proficient in AutoCAD, BMS systems, and SAP EAM. Ability to deal effectively with pressure, multiple tasks, deadlines, and rapidly changing priorities. Aptitude to multi-task and lead projects / negotiations. Ability to negotiate the best deal for ILMN and influence upward. Preferred Educational Background: BS Degree in Engineering, Business or related 12+ years of experience in (combined) facilities management and operations, administration, preferably in a biotechnology, life sciences or pharmaceutical related industry and Asset Management solutions. Bms System, Sap Eam, Microsoft Office, Autocad, Lead Project

Role & responsibilities Looking for candidate who focus specifically on the pharma and healthcare sector, such as those specializing in pharmaceutical domain terminologies & functions. Min 3 years experience is required. 2-8 years in pharmaceutical or healthcare recruitment This is a permanent work from home. Interested candidates can send their CV on alka.p@peoplesource.in Immediate joiners will be preferred. Alka Pathak Tiwari Senior Recruitment Consultant (M) - +91 8720862919 Email: alka.p@peoplesource.in

Applications are invited for the post of Junior Research Fellow (JRF) for the ANRF (SERB), Govt. of India, Funded Project in School of Biosciences and Technology, VIT, Vellore. Title of the Project : Phosphorylation dependent regulation of Arginine and Glutamine rich protein-1 (ARGLU1) by P21 activated kinase-1 (PAK1) – a regulatable molecular switch with therapeutic potential in breast cancer File : CRG/2022/000911 Qualification : M.Sc in Biochemistry/Genetics/ Molecular Biology Desirable (if any) : Prior experience in Animal Studies & Cell line analysis and training in abroad university Stipend : 31,000 Sponsoring Agency : ANRF (SERB), Govt. of India No. of Positions : 1 Duration : 3 Years Principal Investigator Dr. Ganesh Venkatraman Professor, Department of Biomedical Sciences School of Bio Sciences and Technology (SBST) VIT, Vellore 632 014, Tamil Nadu. E.Mail: ganesh.v@vit.ac.in Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo, etc. on or before (25/06/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. The selected candidate will be expected to join at the earliest.

Responsibilities: * Deliver engaging biology lessons using science teaching methods * Collaborate with department on curriculum development & assessment * Prepare students for board exams through practice tests & feedback Provident fund Health insurance Food allowance

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Priya 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

Job Description: Data Scientist with Pharma Background Role Overview: The Data Scientist will leverage expertise in pharmaceutical manufacturing data, particularly Electronic Batch Records (EBR), to develop predictive models, ensure data integrity, and drive analytics initiatives that enhance manufacturing compliance and efficiency. This role requires collaboration with cross-functional teams including manufacturing, quality assurance, regulatory, and IT to transform raw EBR data into actionable insights aligned with Good Manufacturing Practices (GMP) and Pharma 4.0 initiatives. Core Responsibilities Analyze and interpret large-scale EBR and manufacturing datasets to identify trends, anomalies, and opportunities for process improvement and risk mitigation. Develop and deploy advanced statistical models and machine learning algorithms to predict batch quality outcomes, detect deviations, and optimize production workflows. Ensure data integrity and compliance by working closely with quality and regulatory teams to maintain audit trails, electronic signatures, and documentation standards as per cGMP requirements. Integrate EBR data with other enterprise systems such as MES, LIMS, and ERP to create unified data models supporting end-to-end manufacturing analytics. Collaborate with IT and software developers to implement data pipelines, dashboards, and visualization tools that provide real-time insights to manufacturing and quality stakeholders. Lead efforts in digital transformation projects aligned with Pharma 4.0, including automation, real-time monitoring, and advanced analytics. Communicate complex analytical findings effectively to both technical and non-technical stakeholders to drive data-driven decision-making. Participate in validation and qualification activities for analytics solutions to ensure compliance with regulatory standards. Provide training and support to manufacturing teams to facilitate adoption of analytics tools and foster a data-driven culture. Required Skills and Experience Strong statistical and mathematical background with expertise in data mining, predictive modeling, and causal analysis. Hands-on experience with pharmaceutical manufacturing data, especially Electronic Batch Records (EBR), and understanding of batch production processes. Knowledge of regulatory compliance requirements related to data integrity, cGMP, and audit readiness in pharma manufacturing. Proficiency in programming languages such as Python and/or R for data analysis, modeling, and automation. Experience with cloud platforms (e.g., AWS) and big data technologies for scalable analytics solutions. Familiarity with integrating and analyzing structured and unstructured data from MES, LIMS, ERP, and EBR systems. Ability to manage complex data integration challenges and maintain secure, compliant data environments. Excellent problem-solving skills and ability to work collaboratively across geographies and functions. Prior experience in pharma or biotech industry analytics roles, preferably involving Medical Affairs or manufacturing data analytics. Knowledge of natural language processing (NLP) and advanced visual analytics is a plus. Preferred Qualifications 4+ years of advanced analytics experience, including machine learning and statistical modeling. 7+ years of experience with a strong focus on pharmaceutical data science. Experience in causal inference, AI/ML applications, and predictive modeling in pharma contexts. Familiarity with electronic signature systems, digital audit trails, and EBR software platforms. Strong communication skills to translate analytics into business insights and influence decision-making.

Master s in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences or Pharmacy; Bachelor s degree in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences, or Pharmacy with an MBA/PGDBM Skill Set: Very good communication skills; good academic record; Medium to Expert level Excel (very good knowledge of Excel functions, hands-on application with Excel data analysis, text analysis, standardizations, etc.) and PowerPoint capabilities Responsibilities Assisting senior analysts and consultants on projects related to business analytics in the pharmaceutical and biotech domains Work on various aspects of analytics, including epidemiology, competitor analysis, disease treatment patterns, pipeline analysis, forecasting, etc Assist in making PowerPoint presentations and Excel models addressing client-specific business issues Work actively with cross-functional teams of domain experts and statisticians Exposure to business analysis procedures and practices related to top global pharmaceutical and biotech companies

Master s in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences or Pharmacy; Bachelor s degree in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences, or Pharmacy with an MBA/PGDBM Very good communication skills; good academic record Responsibilities Assisting senior analysts and consultants on projects related to business analytics in the pharmaceutical and biotech domains Work on various aspects of analytics, including epidemiology, competitor analysis, disease treatment patterns, pipeline analysis, forecasting, etc Assist in making PowerPoint reports and Excel models addressing client-specific business issues Work actively with cross-functional teams of domain experts and statisticians Exposure to business analysis procedures and practices related to top global pharmaceutical and biotech companies

Description Sr Medical Writer (Redaction) Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, Job Responsibilities Authoring andQuality Assurance of Project Activities Executes project specific activities with high quality and in defined timelines according to standard processes and operating procedures Marking /QC/Review and/or editing of pertinent documents such as: o Clinical study documents or any other documents for regulatory submission i-e , clinical study reports, patient narratives, clinical summaries etc for different regulations (EMA policy 0070, Health Canada PRCI, EUCTR regulation, final rule-NIH) o Protocol and results summaries to support clinical trial disclosure commitments Systematically perform quality control checks of documents prepared by colleagues against pre-specified checklist generated in the project or SOP Perform detailed analyses on a planned and ad hoc basis, relating to processes and their outputs Ensure to abide with Client process 2 Additional Activities Completion of Internal and Client specific training Assist in mentoring and training of team members depending upon project requirement(s) Qualifications We are looking for 4-8 yearsexperience medical writer who will be involved in redactions/anonymization of clinical documents as part of preparation for different regulations (EMA policy 0070, Health Canada PRCI, EUCTR regulation, final rule-NIH) Candidate should be well versed with all the related regulations, perform quality review, client communication and management, Experience in preparing disclosure documents (such as Protocol Registration Form and Result Registration Form) for clinicaltrials gov and for various other clinical registries will be added advantage Resource should understand & comprehend protocol and clinical study report from disclosure perspective Good understanding of Clinical Trial Disclosure fundamentals is expected Qualification Requirement Educational qualifications: A minimum of a scientific graduate degree in life sciences, Good knowledge of regulatory requirements or guidance pertinent to the service line, Good understanding of clinical development processes including principles of clinical study operations and ICH-GCP guidelines Clear written and verbal communication skills Good knowledge of basic computer applications, e-g MS Word/ PowerPoint/ Excel, will be required, Person should understand & comprehend protocol and clinical study report from disclosure perspective, Good understanding of clinical trial disclosure fundamental Core competencies for this role include ability to demonstrate: o Analytical capabilities with scientific and clinical data o Professional working environment o Ownership of the work allocated o Commitment to highest quality outputs, including high attention to detail o Enthusiasm and pro-activity o Effective team working Ability to build rapport/ relationships with project-specific client colleague Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job,

We are seeking a highly motivated and experienced scientist to join our team. The candidate will be responsible for converting business requirements into explanations and scenarios that are comprehensible to subject matter experts and can be later translated into user stories by business analysts. Collaborating with a team of subject matter experts to offer a researcher?s perspective, aiding in anticipating and identifying end-user requirements for software product development. Key Responsibilities Supporting R&D Activities: Supporting the software development team in executing proof of concept studies and contributing to the development process to create the final solution or software product. Participate in cross-functional brainstorming and contribute to product vision and roadmap. Reviewing and Signing off User Stories: Collaborating with subject matter experts and the development team to review user stories, ensuring alignment with desired business outcomes. Signing off on requirements based on the anticipated business benefits that the execution of those stories and epics will deliver. Showcasing Product Releases: Presenting product releases to stakeholders. Supporting Marketing/Business Development: Offering product and innovation expertise to support marketing and business development efforts. Participating in Prioritization and Planning Meetings: ?Actively participating in stakeholder meetings to triage and offer insights that assist in prioritizing and preparing the product roadmap for projects. Bridging Business Development and Product Development: Serving as a liaison between these two teams. Product Testing: Engaging in testing activities, including either direct testing or providing support to SMEs, QAs, and developers in testing the product before the final release. Offering domain expertise to assist QAs in writing effective test cases. Design and validate models or algorithms related to NLP, AI, machine learning, or data mining as applicable. Required Skills and Qualifications Ph.D. in a relevant?field (e.g., Life science, Engineering etc.). Proven experience in designing and conducting research projects. Proficiency in data mining and statistical software/tools. Strong analytical and problem-solving skills. Excellent written and verbal communication skills. Ability to work independently and collaboratively in a team environment. Ability to convert theoretical concepts into practical, scalable software solutions. Demonstrated publication record in reputable scientific journals is preferred. Role? Research Scientist Product Development

With support from Senior Project Manager, ensure all project work is completed to the sponsors satisfaction, on time and within budget and in accordance with policies and procedures. Essential Functions Under supervision, plan, initiate, execute, control, and deliver projects in accordance with the Scope of Work agreed with the customer. Lead the Connected Devices cross-functional teams to ensure successful delivery of assigned projects. Ensure that consistent and appropriate project specific guidelines are documented and circulated to all project team members and that the team is we'll-trained on these guidelines. Track project progress, identify and evaluate project risks and take advice from superiors on corrective action as appropriate. Prepare and present project information at internal and external meetings. With guidance, manage the project financials accurately and appropriately ensuring project goals are achieved according to customer s expectations and within the scope of the project. Ensure revenue recognition and forecasts are calculated accurately and change orders executed where appropriate. Conduct an End of Project review meeting to ensure that all project activities have been completed in full. Keep Connected Devices leadership fully informed of any project issues that may impact quality, budget, and timeliness of project delivery to the customer s satisfaction. Request support and advice for timely issue resolution as required. Provide input to line managers on their project team members performance relative to project tasks to aid career development. Qualifications Bachelors Degree Life science or health care related discipline Pref Three years industry experience Pref Or Equivalent combination of education, training and experience Pref Good leadership skills Good ability to prioritize, schedule and organize Good interpersonal and communication skills Good problem solving skills Excellent customer service skills Good Microsoft Office skills Ability to establish and maintain effective working relationships with coworkers, managers and clients

1. Lead business analysis efforts for pharmaceutical IT projects, gathering and documenting detailed business requirements from stakeholders across various departments. 2. Collaborate closely with stakeholders, including business users, IT teams, and external vendors, to translate business needs into functional and technical specifications. 3. Drive process analysis and optimization, identifying opportunities for automation, system improvements, and business efficiency in operations. 4. Lead requirements workshops and meetings, ensuring alignment on project scope, objectives, and timelines with key business and IT stakeholders. 5. Ensure thorough documentation of business requirements, use cases, user stories, and process flows in alignment with company standards and best practices. 6. Act as the liaison between business stakeholders and development teams, ensuring that business needs are effectively communicated and addressed in the IT solution design. 7. Support the development and testing process, ensuring that solutions meet the defined business requirements and deliver the expected outcomes. 8. Manage stakeholder expectations by providing regular project updates, risk assessments, and issue resolution, ensuring smooth communication and delivery. 9. Facilitate change management activities, ensuring proper training, documentation, and support for end-users during system transitions and implementations. 10. Drive continuous improvement initiatives in business analysis practices, staying current with industry trends and new technologies to enhance business processes and solution delivery. Must Have 1. bachelors or masters degree in Business Administration, Information Technology, Life Sciences, or a related field. 2. 8+ years of experience in business analysis, with at least 3 years in a leadership role within pharmaceutical, biotech, or healthcare IT environments. 3. Proven expertise in business process analysis and mapping, with strong experience in optimizing processes and identifying system solutions that enhance business performance. 4. Solid understanding of business functions and how IT systems support these processes. 5. Experience with pharmaceutical IT systems, such as LIMS, CTMS, EDC, ERP, or CRM systems, and understanding how they integrate with business processes. 6. Strong leadership and team management skills, with experience guiding a team of business analysts or cross-functional teams through complex projects. 7. Excellent communication and stakeholder management skills, with the ability to effectively engage business, technical, and executive stakeholders. 8. Proficiency in requirements gathering techniques, including workshops, interviews, surveys, and use case analysis, as we'll as documentation best practices. 9. Experience with Agile and Waterfall methodologies, with a strong understanding of project life cycles and IT solution delivery. 10. Ability to identify and manage project risks and ensure timely resolution of issues, balancing stakeholder needs and project constraints.

SBO Manager (HEVA) will be functionally aligned to Global HEVA business partners (BPs)/Global HEVA Evidence Synthesis lead and will support execution of multiple activities Manage assigned Evidence Synthesis projects in the assigned portfolio to plan and generate robust health economics and value based evidence to maximize the value propositions from both a global and US perspective working within the Market Access tripod by working with Global HEVA BPs/Global HEVA Evidence Synthesis lead Work with Global HEVA BPs/Global HEVA Evidence Synthesis lead to manage and execution of quality research projects, economic models, trial design recommendations and other activities in support of programs/products as required Support HEVA BPs/Global HEVA Evidence Synthesis lead in the planning, design, implementation, and completion of innovative evidence-based research programs that are consistent with program/product strategies. The research programs developed by Global HEVA BPs will provide appropriate evidence and/or tools to be used for internal decision making and for external audiences at product launch and over product life cycle Collaborate with Global HEVA BPs/Global HEVA Evidence Synthesis lead to seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access Create complex and specialized strategic content without supervision Develop and maintain TA expertise Develop and review content created by HEVA associates Coach HEVA associates People: (1) Develop and maintain effective relationships with key internal stakeholders including Medical Affairs, Clinical Development, Commercial and Market Access (2) Constantly assist and provide effective feedback to HEVA associates (senior or junior) in developing knowledge and sharing expertise (3) Work effectively with global HEVA teams across various time zones Performance: (1) Manage the HEVA evidence generation projects in collaboration with Global HEVA BPs: Develop research plan to support pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide strategic support with individuals and institutions, which may serve as resources for evidence generation purpose, etc; Work closely with the HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes; Lead development of core value dossier (CVD) and AMCP dossiers under the strategic direction of Global HEVA BPs Process: (1) Develop complex HEVA strategic evidence material (2) Build expertise in the field of HEVA for the assigned Therapeutic area (3) Manage core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (4) Accountable for adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes at SBO (5) Leverage advanced training delivery tools & techniques thereby enhancing the effectiveness of training delivery (6) Design an overall plan of action basis end-customers feedback & improve course content and delivery Stakeholder: (1) Work closely with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Liaise with these teams to prepare relevant & customized deliverables and ensure milestones and timelines are on track for assigned the projects About you Experience : 8+ years of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia. Soft skills : Demonstrate effective communication, organizational and interpersonal skills; Able to work effectively as part of a multidisciplinary global teams; Able to work independently, but in concert with the direction provided by their management, in accordance with defined functional policies and precedents, budgetary guidelines, company values, ethics and applicable law; Ability to handle multiple projects across different therapeutic areas; Ability to work we'll in a cross-functional team; Understanding of the disease environment and the evolution of the market access landscape and implications for the business; Proven track record working successfully in a project/matrix-oriented environment; Excellent communication skills and ability to understand and present complex information in digestible ways for internal (eg senior management) and external audiences; Strong team spirit, sense of transversality, multicultural awareness and ability to drive matrix teams Technical skills : Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies; Understands reimbursement decisions to determine value drivers and how evidence is used in decision making and how it impacts various payers (eg, providers, patients, health systems); Knowledge of methods and principles of health economics, health technology assessment (HTA) reviews Education : Advanced degree in life sciences/pharmacy/similar discipline or medical degree Languages : Excellent knowledge of English language (spoken and written)

Master s in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences or Pharmacy; Bachelor s degree in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences, or Pharmacy with an MBA/PGDBM Experience: 3-4 years Skill Set: Strong in quantitative analytics and domain knowledge; should be able to deliver small to medium-sized projects and support consultants/project managers on large projects; should be able to handle quick turnaround projects Responsibilities: It is well documented under the Skill Set and Project Experience sections Project Experience: Market assessment (independent delivery of a complete market assessment report) Competitive Intelligence track pipeline/product news create market event write-ups to be sent to clients (e.g. new trial start, trial design change, approvals, breakthrough designations, release of positive clinical data) Forecasting (should have been a major contributor with experience creating epidemiology-based forecasts with a medium level of complexity independently) Analyze sales/Rx/transaction data (experience analyzing transaction data needed) Secondary Research: Extremely proficient in secondary research to dig up hard-to-find details Excel: Expert level (programming not needed, added advantage if knows some VBA) PowerPoint: Expert Level (should be able to create a final report that is professional and neatly formatted) Language & Executive Presentation: Proficient in editing presentations and use of business language, very high attention to detail, should be able to cut the clutter and get the point across as crisply and graphically as possible

Business Consultant (Junior to Senior Level) Master s in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences or Pharmacy; Bachelor s degree in Microbiology, Biotechnology, Biochemistry, Public Health, Life Sciences, or Pharmacy with an MBA/PGDBM Skill Set: Strong in quantitative analytics and domain knowledge; should be able to execute/manage large projects and allocate/monitor work among team members/ work actively with cross-functional teams of domain experts and statisticians; proposal writing; should be able to handle quick turnaround projects; present the study findings to clients (through online/ face to face if needed) Responsibilities: It is well documented under the Skill Set and Project Experience sections Project Experience (Also indicates the Project types to be managed): Market assessments (independently creating a complete market assessment report, experience guiding the analysts to create the market assessment, review/edit, ensure accuracy, and should be responsible for delivery) Identify & screen BD&L opportunities (responsibilities same as above) Forecasting (develop forecast models from scratch based on epidemiology, current and future treatment evolution, deduce assumptions and inputs, incorporate persistency modeling, survival analysis), trend-projection/time series analysis, data analytics (running univariate analysis/multiple regressions, solve pricing/targeting problems using large internal datasets, optimization), create and evaluate product P&Ls/NPV/eNPV analysis. Should be able to develop approach/methodology for specific analytical problems and initial project brief. (Independent delivery experience a must) Others (not a must): Competitive Intelligence (Secondary-based), experience in preparing for and covering conferences (ASCO/ASH) with the ability to create brief reports (usually by the end of the day) and comprehensive reports highlighting implications of specific abstracts for client s products PowerPoint: Expert Level (Should be able to create a final report that is professional and neatly formatted) Language & Executive Presentation: Proficient in editing presentations and use of business language, very high attention to detail, should be able to cut the clutter and get the point across as crisply and graphically as possible

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Leader of information technology system project/program, directing all phases from inception through completion. Role and responsibilities: Lead, manage, and drive the execution of global IT Data Center and Real Estate Facility projects from initiation through to completion. Ensure projects are delivered on-time, within scope, and on budget. Develop detailed project plans, timelines, and milestones. Establish realistic deadlines and ensure resources are aligned to meet project objectives. Define and manage project scope in collaboration with stakeholders. Continuously assess scope changes and communicate any adjustments to timelines, budgets, or deliverables. Act as the central point of contact for all teams involved in the project. This includes cross-functional collaboration with IT, Real Estate, Facilities Management, Procurement, Legal, and Finance teams. Regularly engage with senior leadership and stakeholders to provide updates on project progress, key decisions, risks, and other critical factors. Tailor communication to different stakeholder needs, from technical teams to senior executives. Coordinate with external vendors, contractors, and consultants for the delivery of equipment, services, and support. Manage third-party relationships to ensure contractual obligations are met and project quality standards are maintained. Budget Control and Cost Management: Develop detailed budgets for each project phase. Track project expenses against forecasts, ensuring that any deviations are identified and addressed early. Appropriately allocate resources and manage them efficiently. Work closely with resource managers to ensure the right skills are available and utilized for successful project delivery. Proactively identify potential risks or bottlenecks in project delivery. Develop risk management plans, ensuring that preventive measures are in place and contingency plans are prepared. Quickly identify project issues and work collaboratively with the project team to develop effective solutions to maintain project timelines and outcomes. Maintain comprehensive documentation for all projects, including project charters, status reports, meeting notes, and post-project reviews. Ensure all documentation is clear, accurate, and readily available to stakeholders. Provide regular and ad hoc project status reports to senior leadership, highlighting key achievements, challenges, and resource needs. Prepare detailed project updates and executive summaries. Ensure all projects comply with Boston Scientific s internal policies, including regulatory requirements and industry best practices. This includes IT security, data governance, and sustainability standards for Real Estate facilities. Contribute to the continuous improvement of project management processes and methodologies. Implement best practices that align with organizational goals and improve overall project efficiency. Work effectively across different time zones, cultures, and markets within the APAC region. Understand regional challenges and adapt project management strategies accordingly. Support and coordinate with global teams, ensuring alignment of project goals and consistent execution across regions. Experience: 8-12 years of proven experience in managing IT infrastructure projects, including IT Data Centers and Real Estate Facility projects. Experience in managing complex global projects across different geographic locations, particularly in the APAC region. Hands-on experience in managing large-scale projects involving cross-functional teams. Experience in the MedTech, healthcare, or life sciences industry is a significant advantage. Certifications: Project Management Professional (PMP), PRINCE2, or similar project management certification preferred. Technical Skills: Strong understanding of IT infrastructure, data center operations, and real estate facility management. Familiarity with data center design and construction is highly desirable. Proficiency in project management tools Like MS Project, Jira, and GoPMO) is a plus. Educational Background: Bachelor s degree in Engineering or Information Technology, A Master s degree in Business Administration (MBA), or a related field, is a plus. Requisition ID: 601339 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Leader of information technology system project/program, directing all phases from inception through completion. Role and responsibilities: Lead, manage, and drive the execution of global IT Data Center and Real Estate Facility projects from initiation through to completion. Ensure projects are delivered on-time, within scope, and on budget. Develop detailed project plans, timelines, and milestones. Establish realistic deadlines and ensure resources are aligned to meet project objectives. Define and manage project scope in collaboration with stakeholders. Continuously assess scope changes and communicate any adjustments to timelines, budgets, or deliverables. Act as the central point of contact for all teams involved in the project. This includes cross-functional collaboration with IT, Real Estate, Facilities Management, Procurement, Legal, and Finance teams. Regularly engage with senior leadership and stakeholders to provide updates on project progress, key decisions, risks, and other critical factors. Tailor communication to different stakeholder needs, from technical teams to senior executives. Coordinate with external vendors, contractors, and consultants for the delivery of equipment, services, and support. Manage third-party relationships to ensure contractual obligations are met and project quality standards are maintained. Budget Control and Cost Management: Develop detailed budgets for each project phase. Track project expenses against forecasts, ensuring that any deviations are identified and addressed early. Appropriately allocate resources and manage them efficiently. Work closely with resource managers to ensure the right skills are available and utilized for successful project delivery. Proactively identify potential risks or bottlenecks in project delivery. Develop risk management plans, ensuring that preventive measures are in place and contingency plans are prepared. Quickly identify project issues and work collaboratively with the project team to develop effective solutions to maintain project timelines and outcomes. Maintain comprehensive documentation for all projects, including project charters, status reports, meeting notes, and post-project reviews. Ensure all documentation is clear, accurate, and readily available to stakeholders. Provide regular and ad hoc project status reports to senior leadership, highlighting key achievements, challenges, and resource needs. Prepare detailed project updates and executive summaries. Ensure all projects comply with Boston Scientific s internal policies, including regulatory requirements and industry best practices. This includes IT security, data governance, and sustainability standards for Real Estate facilities. Contribute to the continuous improvement of project management processes and methodologies. Implement best practices that align with organizational goals and improve overall project efficiency. Work effectively across different time zones, cultures, and markets within the APAC region. Understand regional challenges and adapt project management strategies accordingly. Support and coordinate with global teams, ensuring alignment of project goals and consistent execution across regions. Experience: 8-12 years of proven experience in managing IT infrastructure projects, including IT Data Centers and Real Estate Facility projects. Experience in managing complex global projects across different geographic locations, particularly in the APAC region. Hands-on experience in managing large-scale projects involving cross-functional teams. Experience in the MedTech, healthcare, or life sciences industry is a significant advantage. Certifications: Project Management Professional (PMP), PRINCE2, or similar project management certification preferred. Technical Skills: Strong understanding of IT infrastructure, data center operations, and real estate facility management. Familiarity with data center design and construction is highly desirable. Proficiency in project management tools Like MS Project, Jira, and GoPMO) is a plus. Educational Background: Bachelor s degree in Engineering or Information Technology, A Master s degree in Business Administration (MBA), or a related field, is a plus. Requisition ID: 601339 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Job Title: Validation Analyst Location: Bangalore Function: Validation Services ESSENTIAL DUTIES AND RESPONSIBILITIES Plan, execute, and document software validation activities for both off-the-shelf and custom integrations in an FDA-regulated environment. Conduct comprehensive end-to-end validation of software integrations using tools such as Postman and SOAP UI to verify data accuracy, compliance, and system interoperability. Perform validation of AI-driven software integrations to ensure functionality, integrity, and regulatory alignment. Develop and execute validation test plans, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols, as well as test scripts and traceability matrices. Collaborate with cross-functional teams including Software Development, Quality Assurance, Regulatory Affairs, and IT to align validation activities with internal standards and external regulatory requirements. Utilize Azure DevOps for managing requirements, tracking test execution, and maintaining validation documentation. Validate software in cloud-hosted environments, ensuring compliance with security, performance, and data integrity standards. Participate in system risk assessments and contribute to the development of risk mitigation strategies. Ensure strict adherence to FDA 21 CFR Part 11, GxP, and other applicable regulatory guidelines throughout all validation processes. Document all validation efforts thoroughly and produce detailed reports to support internal reviews and external audits. Provide guidance and mentorship to junior validation analysts, promoting best practices and continuous improvement. EDUCATION AND EXPERIENCE REQUIRED: Education: Bachelor s degree in computer science, Engineering, or a related technical field. Minimum of 2-3 years of experience in API testing, Integration testing, and AI-driven solutions and workflows, preferably in a regulated industry. Experience: 2-3 years of hands-on experience in API testing, integration testing, and AI software validation, preferably within a regulated industry (e.g., life sciences, healthcare, or pharmaceuticals). Proficient in using Postman and SOAP UI for API and web service validation. Experience validating AI-driven solutions and workflows. Demonstrated expertise with Azure DevOps for test case management, execution tracking, and reporting. Solid understanding of cloud deployment models (IaaS, PaaS, SaaS) and best practices for validating applications in cloud environments. Familiarity with FDA regulations, including 21 CFR Part 11 and GxP, as well as risk-based validation methodologies. Strong knowledge of software development life cycles (SDLC) and validation life cycle processes, including Agile, Scrum, and SAFe frameworks. Excellent verbal and written communication skills, with the ability to collaborate effectively across cross-functional teams. Preferred Skills: Familiarity with continuous integration/continuous deployment (CI/CD) pipelines. Experience with database validation and data migration projects. Experience with API testing. COMPENSATION & BENEFITS: Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits. EMPLOYMENT TYPE: Full Time, Permanent COMMITMENTS: Standard Hours 40 hours per week, one hour lunch, Monday - Friday. Additional hours as needed. Willing to work in shifts as and when needed.

JOB DESCRIPTION Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The EHS Specialist position reports to the and is part of the Custom Engineering team located in Pune and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: EHS Responsibilities: To adhere to the Company EHS policy, organization and arrangements in consultation with various stake holders. To implement EHS Procedures and develop local work procedures to comply with legal obligations. To review and develop the Health & Safety Management Plan and communicate the plan at all level. Sustain EHS Compliance, identify, prevent and resolve potential EHS issues and to mitigate EHS liabilities associated with current operations. Support for Department: To advise and support the Site Environment, Health & Safety Committee making sure that the committee takes ownership of the Site Environment, Health & Safety Plan. To advise Site Leader in ensuring that their Plant has key staff mobilized to carry out the Environment, Health& safety activities e.g. Risk/Impact assessors, First aiders, Fire wardens etc. Accident investigation and prevention: To receive and investigate reports of accidents, dangerous occurrences and fire damage, determine their causes and make recommendations for improving recurrence prevention and controls. To monitor that all EHS related accidents/incidents are properly investigated by department managers and lessons learnt are shared appropriately. To maintain a system for recording, reporting and investigating injuries, accidents and dangerous occurrences& Environmental Incidents. Environment Health & Safety (EHS)Training: To identify the training needs for associates & contractors and develop training matrix. Liaise with managers to nominate associates & contractors for training courses. Design, develop, upgrade content on EHS training and impart trainings as required. To monitor training and report progress on training against annual targets to the Site EHS Committee.Prepare a PPE matrix covering the entire premises on the basis of risk assessment of the respective area/activity. Who you are: Education requirement BE/B Tech/B.Sc. with a Diploma in Industrial Safety from a recognized institute Desirable Qualification: NEBOSH IGC/IOSH certification. 2-4 years practical experience with Health and Safety standards and procedures in Corporate or Manufacturing Industry. Exposure to OHSAS 18001 & ISO 14001 management systems preferable Able to implement Global EHS policies and accommodate local cultural and regulatory requirements Join our winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.