2347 Life Sciences Jobs - Page 18

Management Level: Ind&Func AI Decision Science Consultant Job Location: Bangalore / Gurgaon Must-have Skills: Excellent understanding of Pharma data sets commercial, clinical, Leverage ones hands on experience of working across one or more of these areas such as real-world evidence data, Statistical Models/Machine Learning including Segmentation & predictive modeling, hypothesis testing, multivariate statistical analysis, time series techniques, and optimization. Good-to-have Skills: Programming languages such as R, Python, SQL, Spark, AWS, Azure, or Google Cloud for deploying and scaling language models, Data Visualization tools like Tableau, Power BI. Job Summary This role involves driving strategic initiatives, managing business transformations, and leveraging industry expertise to create value-driven solutions. Provide strategic advisory services, conduct market research, and develop data-driven recommendations to enhance business performance. Key Responsibilities An opportunity to work on high-visibility projects with top Pharma clients around the globe. Personalized training modules to develop your strategy & consulting acumen to grow your skills, industry knowledge, and capabilities. Provide Subject matter expertise in various sub-segments of the LS industry. Support delivery of small to medium-sized teams to deliver consulting projects for global clients. Responsibilities may include strategy, implementation, process design, and change management for specific modules. Work with the team or as an Individual contributor on the project assigned which includes a variety of skills to be utilized from Data Engineering to Data Science Develop assets and methodologies, point-of-view, research, or white papers for use by the team and the larger community. Acquire new skills that have utility across industry groups. Support strategies and operating models focused on some business units and assess likely competitive responses. Also, assess implementation readiness and points of greatest impact. Additional Information Proficient in Excel, MS Word, PowerPoint, etc. Ability to solve complex business problems and deliver client delight. Strong writing skills to build points of view on current industry trends. Good communication, interpersonal, and presentation skills About Our Company | Accenture (do not remove the hyperlink) Qualification Experience: Proven experience (4+ years) in working on Life Sciences/Pharma/Healthcare projects and delivering successful outcomes. Educational Qualification: Bachelors or Masters degree in Statistics, Data Science, Applied Mathematics, Business Analytics, Computer Science, Information Systems, or other Quantitative field.

Job Description Role: Business analyst Experience : 4- 8 years Location : Chennai Employment Type : Full-Time Key Skills : Healthcare & Life Sciences Domain, Any Certification (Good to have) Essential skills • Experienced in the application of the organisations information technology principles, architecture, and strategy. • Strong knowledge and application of business analysis principles. • Excellent communication skills, both written and verbal. Strong business analysis skills used to document user requirements. • Effective time management skills. • Ability to stay up to date on complex new applications, processes, and procedures. • Strong ability to prioritise and manage projects/tasks simultaneously. Key Responsibilities : Gather and document business and functional requirements across healthcare and life sciences projects Work closely with cross-functional teams for product design, process optimization, and regulatory compliance Analyze data related to clinical trials, patient records, or claims Drive gap analysis and impact assessment for new systems or features Ensure alignment with HIPAA, GxP, or other regulatory frameworks

Role & responsibilities Responsible to manage the Air Freight Operations for South India and satellite offices for Healthcare vertical. Effectively managing and overall accountable for the performance of the Air Freight department with the team of eleven staff members. Form sales & marketing strategies for Branch & Corporate Sales force to accomplish the budget and given growth targets. Responsible for appropriate staffing in the department and to drive future-oriented workforce planning, in line with productivity targets. Administrative & functional responsibility of Airfreight team by monitoring the carrier performance, better negotiations, customer retention / relationships. Successfully maintained strong business relationship with Airlines, custodian / ground handling agencies and performed better procurement. Rate Procurement and negotiation with Carrier, overseas & Customers • Vendor Management • Maintaining Carrier relationship & Capacity management • Business development • Carrier Claim Management. Ensure performance for critical business (Pharma ) Preferred candidate profile Candidates having strong knowledge in Air Freight Operations would be considered.

As a Histopathology Technician at our company, you will be responsible for preparing high-quality tissue blocks and slides using standard histology techniques. This includes tasks such as fixation, embedding, sectioning, and staining. Additionally, you will operate and validate Morphles proprietary devices to ensure quality assurance and provide feedback. Collaboration with engineering and product teams to enhance sample preparation protocols and automation workflows will be a key part of your role. In this position, you will also play a crucial role in real-world customer scenarios by troubleshooting sample-related issues, providing demo support, and training lab personnel on best practices. It will be essential to maintain lab equipment and documentation in compliance with GLP and NABL/ISO standards. Furthermore, you will have the opportunity to contribute to R&D validation studies and workflow optimization for digital pathology. The ideal candidate for this role holds a Bachelors or Masters degree in Histopathology, Life Sciences, or a related field and has 2-5 years of hands-on experience in a histopathology lab. Proficiency in tissue processing, microtomy, staining (H&E and special stains), and slide preparation is required. Experience with microtomes, slide scanners, or digital pathology tools would be advantageous. Familiarity with quality standards and documentation (NABL/ISO/GLP) is preferred. Strong attention to detail, excellent communication skills, and a collaborative mindset are qualities we value in potential candidates. Joining our team means being part of a young, focused, and goal-oriented group within a fast-growing deep-tech company that is redefining cancer diagnostics. You will enjoy the benefits of having an in-house chef providing hot food and a continuous flow of tea/coffee on the house. Your contributions will directly impact life-saving innovations deployed globally, and you will experience an open, collaborative, and ownership-driven work culture.,

As an experienced SAP CO (Controlling) Consultant at Level L4, you will be responsible for leading greenfield S/4HANA implementation projects within the life sciences and pharmaceutical industries. Your expertise in SAP CO will be crucial in designing and configuring the module to meet specific business requirements and regulatory standards. You will play a key role in overseeing system integration, testing, validation, and data migration activities to ensure successful project execution and regulatory compliance. Client interaction is a fundamental aspect of this role, as you will conduct meetings to gather requirements, present solutions, and provide project updates. Facilitating workshops to engage clients, understand their operational challenges, and deliver tailored solutions will be part of your responsibilities. Building and maintaining strong client relationships throughout the project lifecycle will be essential. In the realm of consulting and advisory, you will provide expert advice on SAP CO best practices, S/4HANA capabilities, and industry-specific standards, with a focus on the life sciences and pharmaceutical sectors. Developing innovative solutions to meet client needs while ensuring compliance with industry regulations such as GMP (Good Manufacturing Practices) will be a key aspect of your role. Additionally, you will conduct system assessments and audits, offering recommendations for process improvements and compliance. Project management will be a significant part of your responsibilities, including developing and managing project plans, coordinating with cross-functional teams, and monitoring project milestones to ensure timely completion of deliverables. You will also be involved in providing training sessions for end-users and key stakeholders, as well as creating and maintaining comprehensive documentation to support project activities. This role offers the opportunity to work with NTT DATA Business Solutions, a fast-growing international IT company and one of the world's leading SAP partners. If you are ready to transform SAP solutions into value and contribute to impactful projects within the life sciences and pharmaceutical industries, we invite you to join our team and make a difference. For any further queries related to this job description, please feel free to reach out to our Recruiter, Ramakrishna Kodi, at Ramakrishna.kodi@bs.nttdata.com.,

Job Description At PwC, as part of the risk and compliance team, you focus on ensuring regulatory compliance and managing risks for our clients by providing advice and solutions. Your role involves guiding organizations through complex regulatory landscapes and strengthening their internal controls to effectively mitigate risks. Specifically in regulatory risk compliance at PwC, your main responsibilities include confirming adherence to regulatory requirements and helping clients mitigate risks. You will offer guidance on compliance strategies and assist clients in navigating intricate regulatory environments. Motivated by curiosity, you are a dependable team player. In our dynamic work environment, you are expected to adapt to collaborating with various clients and team members, each bringing unique challenges and perspectives. Every experience presents an opportunity for learning and personal growth. Your role entails taking ownership and consistently delivering high-quality work that adds value for our clients and contributes to the team's success. As you progress within the Firm, you will establish a strong professional reputation, creating more avenues for growth and development. The skills, knowledge, and experiences crucial for excelling in this role include: - Embracing a growth mindset and taking responsibility for your own development. - Valuing diverse perspectives, needs, and emotions of others. - Cultivating habits that sustain high performance and foster personal growth. - Actively listening, asking clarifying questions, and articulating ideas effectively. - Seeking, reflecting on, acting upon, and providing feedback. - Analyzing facts and identifying patterns by gathering information from various sources. - Committing to understanding the business operations and developing commercial awareness. - Adhering to professional and technical standards, such as specific PwC tax and audit guidelines, upholding the Firm's code of conduct, and independence requirements. Job Description Title: HIA Spend Transparency Reporting Analyst Location: Bangalore At PwC, we bring together individuals with diverse backgrounds and expertise to collaboratively solve significant challenges and lead with purpose for our clients, communities, and the global society. With 429 of the Fortune 500 global companies engaging with PwC, our impact is widespread and substantial. The PwC Advisory Acceleration Center in Bangalore is a part of our Advisory business in the US, focused on developing a comprehensive portfolio of solutions for Risk Consulting, Management Consulting, Technology Consulting, Strategy Consulting, Forensics, and vertical-specific solutions. Driven by a high-performance culture that prioritizes excellence, diversity, and inclusion, we offer a supportive network and access to global leadership development frameworks and cutting-edge digital technologies to facilitate your career growth and success. Central to our firm's ethos is a genuine care for our people. Ranked as the 3rd most attractive employer globally by Universum, PwC's commitment to Responsible Business Leadership, Diversity & Inclusion, work-life balance, career coaching, and continuous learning and development makes it an exceptional place to work, learn, and excel. Join us at PwC if you believe in making a meaningful impact now and in the future! Job Overview: HIA Spend Transparency Reporting Associate Preferred Title: HIA Spend Transparency Reporting Analyst Roles and Responsibilities: As an HIA Spend Transparency Reporting Analyst, you will be responsible for collecting all internal and external HCP and HCO program documentation, including invoices, proof of service documents, and contracts. Your tasks will involve reconciling and reviewing invoices for reportability as per CMS guidelines, reporting transparency data into the system of record, correcting identified errors, flagging anomalies, and meeting strict SLA timelines and reporting deadlines at local, national, and international levels. Additional Responsibilities may include: - Collecting and reconciling invoices for stand-alone activities in the system of record. - Reviewing and categorizing invoice items by spend type and HCP/HCO participation. - Completing transparency reporting templates with itemized spend and transfer of value data. - Managing invoice/contract requests and updating Smartsheet tracker. - Requesting recipient and Client IDs for OUS and US HCPs/HCOs using outreach systems. - Creating compliance checklists for each HCP/HCO activity. - Collaborating with clients, compliance, legal, and business teams to ensure project delivery. - Standardizing processes, maintaining playbooks/SOPs as part of change management. - Ensuring timely delivery of deliverables and reporting any issues or risks proactively. - Acting as the point of contact for regular reports and follow-up activities with clients. - Fulfilling any other responsibilities integral to the role. Skills Required: - Minimum of 2 years of experience, preferably in the pharmaceutical or life sciences domain with regulatory reporting knowledge. - Ability to evaluate HCP, HCO, and Patient engagement logically and critically while following process steps. - Proficiency in synthesizing data from multiple sources and identifying anomalies or inconsistencies. - Strong financial acumen for reconciling invoices and expenses. - Attention to detail and comfort with data entry. - Proficient in MS Office Word, Excel, and PowerPoint applications. - Excellent English language reading comprehension and writing skills. - Capacity to thrive in a fast-paced environment with a focus on quality and accuracy. - Strong team player capable of working with minimal guidance. - Previous experience with transparency background check is a plus. Desired Skills: - Familiarity with Analytical tools like Alteryx, Power BI, and other Data Analytics/Automation tools. - Basic European language reading comprehension and writing skills, particularly in French, German, Spanish, Italian, or Russian.,

You will be joining Dr. Reddy's Laboratories, a global pharmaceutical company with a legacy dating back to 1984 and headquartered in Hyderabad, India. The company is dedicated to making affordable and innovative medicines accessible to all. Dr. Reddy's product portfolio includes APIs, generics, branded generics, biosimilars, and OTC products, with key markets in the USA, India, Russia & CIS countries, China, Brazil, and Europe. As part of our commitment to sustainability and ESG actions, we focus on environmental stewardship, patient access, diversity, and governance. In your role as a Territory Business Manager based in Surat, you will be responsible for driving sales and increasing market share in your assigned territory. This full-time, on-site position entails developing and nurturing strong relationships with healthcare professionals, ensuring product availability, implementing marketing strategies, and achieving sales targets. Your responsibilities will also include analyzing market trends, competitive activities, and customer requirements to maximize sales opportunities. To excel in this role, you should have a proven track record in sales within the pharmaceutical or healthcare industry. You must possess the ability to establish and maintain strong professional relationships with healthcare providers in the Gastroenterology segment. Strong analytical and problem-solving skills are essential, along with excellent communication and interpersonal abilities. A good understanding of market trends and the competitive landscape is crucial. You should be comfortable working both independently and as part of a team, and be willing to travel extensively within your designated territory. While not mandatory, a Bachelor's degree in Life Sciences, Pharmacy, or a related field would be advantageous for this position.,

At EY, youll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And were counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. Managing the global workforce in todays fast-changing and highly disrupted environment is becoming increasingly complex. As a member of our People Consulting (PC) practice, you will be part of a team that supports clients in aligning their HR function with the organizational plans while keeping employee experience as one of the core considerations. When you join us, you will gain cross-functional, multi-industry, and a truly global work experience to take your career in the right direction. We are looking for Managers with expertise in Change Management to join the PC team. This is a fantastic opportunity to be part of a leading global professional services organization while being instrumental in the growth of the PC team. Your Key Responsibilities - Enable delivery and execution of change management strategy for global large transformation programs in partnership with global EY offices. - Establish change management expertise within the practice, grow and lead a team of change and learning design specialists. - Provide advice and guidance as a subject matter expert and work effectively as part of a large, distributed program team. - Ensure high-quality deliverables are produced for the project by exhaustive internal reviews and obtain excellent feedback from the client and global project counterparts. - Manage engagement risk, project economics, manage escalations, and ensure effective planning and budgeting. - Lead development of thought leadership, collateral, tools, techniques, methodologies to enhance change management and broader capability offering within the practice. - Support leadership in developing the practice through collaboration with EY global offices and demand generation for change management projects. - Perform the role of a counselor and coach, define and set goals, conduct performance reviews, and ensure ongoing learning and development of the team. - Collaborate with subject matter experts across the HR service areas (learning and development, staffing, talent management, diversity, compliance) to provide insights on overall strategic and operational performance. Skills And Attributes For Success - High integrity and commitment to work in a new and challenging environment. - Ability to manage ambiguity and be proactive. - Strong communication and presentation skills. - Cross-cultural awareness and sensitivity. - High energy levels, agility, and adaptability. - Open to travel for client projects that are approved as per EY and country-specific travel advisory guidelines. To qualify for the role, you must have - Postgraduate degree or equivalent with a specialization in Human Resources (India or abroad). - 7 -10+ years of relevant experience. - Experience leading change management efforts on global client projects. - A track record of designing and implementing medium-large scale change programs including HR Transformation, Human-Centered Design, Digital Strategy, and ERP Transformation. - Experience in advising and guiding clients on complex transformation programs with key domain expertise in business readiness, business adoption, change strategy, visioning, execution, stakeholder management, benefits management, and communication. - Experience in managing a delivery team of at least 5+ individuals, providing advice and guidance on career development, L&D, and performance management. - Experience in learning design and content development using techniques of instructional design and application of it to enable a change program. - Experience in selling and delivering work that spans across the full project lifecycle. - Must have a JLPT Certification (N1-N2 Level). Ideally, you will also have - APMG, PROSCI, or equivalent certification. - Experience in creating project budget and resource estimates for several domains within HR and technology transformations. - Experience facilitating solution workshops and design sessions across multiple industry verticals and geographies. - Experience in identifying and deploying leading-edge communication and stakeholder engagement tools and techniques. - Experience in leading and supporting a network of Change practitioners to work in a cross-functional and client-facing environment. - Expertise in recommending and leveraging new age/digital solutions to enable change such as automation, gamification, advanced analytics/visualization, day-in-life-of workshops. - Experience in identifying and leveraging data-driven change management techniques to drive the transformation. - Knowledge of one or more HCM cloud - Oracle, SAP, Service Now, Blue Yonder, or other out-of-box HR technologies. - Domain understanding of Cyber and Supply Chain is a plus. - Experience in Pharma, Healthcare, Life Sciences, Energy, Public sector, Manufacturing, and TMT (Technology, Media, and Telecom) sectors is preferred. - Working knowledge of Project management. What We Look For Technical experts with commercial acumen, relevant experience, and a high degree of enthusiasm to adapt and learn in a fast-moving environment. Knowledge and experience of working in a cross-cultural setup. What Working At EY Offers At EY, we are dedicated to helping our clients, from startups to Fortune 500 companies, and the work we do with them is as varied as they are. You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees, and you will be able to control your development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer: - Support, coaching, and feedback from some of the most engaging colleagues around. - Opportunities to develop new skills and progress your career. - The freedom and flexibility to manage your role in a way that's right for you. EY | Building a better working world EY exists to build a better working world, helping to create long-term value for clients, people, and society and build trust in the capital markets. Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform, and operate. Working across assurance, consulting, law, strategy, tax, and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.,

You should possess over 6 years of experience in SAP PLM, with a successful track record in implementation projects. Your expertise should lie in Specification Management, Recipe Development, PLM Labeling, and Workflow Management. It is essential to have experience in Change Management processes within SAP PLM and integrating SAP PLM with third-party systems. You should be adept at PLM data modeling and data migration activities and ideally be familiar with S/4HANA upgrades and migrations. A strong background in FMCG and/or life sciences industries would be advantageous. As a candidate, you must be capable of managing PLM master data creation and configuration processes. Proficiency in system setup, release management, and incident handling for SAP PLM is required. If you meet these qualifications and are interested in this opportunity, please forward your updated resume to Venkatesan.Selvam@gyansys.com. Thank you for considering this role.,

NanoMicro is a technology startup globally recognized for its leadership in producing spherical, monodisperse particles through proprietary manufacturing processes. These innovative methods enable high-yield, cost-effective production across various industries and applications. Meeting purification needs from laboratory to manufacturing scale in small molecule pharmaceuticals and biopharmaceuticals requires continuous integration of advancements in chromatography and resin technology, along with adept management of evolving business and scientific challenges. We provide comprehensive purification solutions for small molecule and biopharmaceutical sectors, including small molecule therapeutics, antibody and protein therapeutics, peptide therapeutics, oligonucleotide therapeutics, vaccine discovery and development, and plasma proteins, among others. NanoMicro has become an OEM supplier for chromatography vendors worldwide, supporting pharmaceutical and biopharmaceutical purification under various brands. The company has also introduced its own brand internationally, with a strategic focus on India, successfully expanding operations within major accounts. This is an opportune time to build a larger team aimed at increasing market share in all areas of biopharmaceutical purification. Opportunities at NanoMicro are open to candidates from various disciplines, such as sales, business development, and scientific research, with a primary focus on application support and scaling up in the biopharmaceutical space. We encourage employees to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners. Our workplace fosters cooperation, mutual respect, diversity, and inclusivity. NanoMicro prioritizes employee growth by supporting professional development and skill enhancement, providing opportunities throughout the organization. Position: India Sales Leader Key Responsibilities: - Develop and execute business plans to grow the Biopharmaceutical market. - Identify and manage new business opportunities. - Maintain strong relationships with customers and team members. - Work with cross-functional teams to align and implement strategies. - Monitor market trends and competitors for growth opportunities. - Represent the company at industry events to promote products. - Present business development updates and analysis to senior management for decision-making. Qualifications: - A Master's degree in Life Sciences is required; a PhD is preferred. - Demonstrated success in business development within the biopharmaceutical sector. - In-depth knowledge of both upstream and downstream workflow processes. - Exceptional communication, negotiation, and interpersonal abilities. - Capacity to work autonomously as well as collaboratively within a fast-paced and evolving environment. - Flexibility and willingness to travel as necessary to achieve business goals. Experience: - 10+ years of experience with a minimum of 4 years driving pan India sales team. - Candidates with 5-6 years of experience can be considered for the Business Manager role. To Apply: Please send your resume to srinivas@nanomicrotech.com,

You will play a crucial role in the transformation of Patient Safety and Pharmacovigilance (PS&PV) into a future-driven organization and an enterprise-level enabler of the overall Development and Novartis strategy. Your primary responsibility will be to provide project management expertise to key PS&PV projects, ensuring the successful execution of project activities. Your major accountabilities will include contributing to the development of the long-term PS&PV technology roadmap, being curious and leveraging internal and external technologies to foster innovation within PS&PV, identifying regulatory, market, and digitalization trends, evaluating innovative vendors and technologies, and executing or contributing to innovation projects in alignment with the roadmap. Additionally, you will lead or contribute to major projects as an Innovation lead, identify appropriate technologies and partners, introduce new technologies to the organization, and drive change management and innovation culture within PS&PV. Furthermore, you will work towards building trust within the organization, being the preferred innovation partner for the business, and enhancing PS&PV operational excellence through process improvements. You will collaborate with internal and external stakeholders to ensure visibility of PS&PV innovation activities and provide project leadership and management support to key projects while promoting best practices in projects and initiatives. Your performance will be measured based on the satisfaction of business and technology stakeholders, contribution to key enterprise projects with safety relevance, timely and high-quality delivery of projects within budget, and broad involvement in innovation activities within PS&PV. To be considered for this role, you should have 4-5 years of Pharmacovigilance experience in Life Sciences or Information Technology, fluency in spoken and written English, knowledge of systems and regulations, experience in technology innovation, project management, and modern system and data architecture principles. Additionally, you should have a passion for challenging the status quo and possess strong interpersonal and leadership skills. At Novartis, we believe in helping people with diseases and their families through innovative science and a community of smart, passionate individuals like you. By collaborating, supporting, and inspiring each other, we aim to achieve breakthroughs that positively impact patients" lives. If you are ready to contribute to creating a brighter future together, we invite you to join our Novartis Network to explore suitable career opportunities and benefit from our comprehensive handbook outlining personal and professional growth opportunities.,

The position of OECD GLP QA Auditor at Ribosome Research Centre in Kim is a full-time on-site role. As the GLP QA Auditor, your primary responsibility will be to conduct quality audits, ensure compliance with GLP regulations and guidelines, prepare audit reports, and recommend corrective actions. Your day-to-day tasks will involve reviewing study protocols, performing study-based inspections, facility-based inspections, and carrying out quality assurance activities. Additionally, you will collaborate with research staff to enhance quality management practices. To excel in this role, you must have prior experience in an OECD GLP environment. Proficiency in quality auditing, auditing skills, and quality management practices is essential. Strong written and verbal communication skills are also crucial for effective performance. A Master's degree in any life sciences field (e.g., Biotechnology, Pharmacology) is a mandatory qualification. Furthermore, your ability to work efficiently in a team-oriented environment will be key to succeeding in this position.,

The Data Warehouse Engineer will be responsible for managing and optimizing data processes in an Azure environment using Snowflake. The ideal candidate should have solid SQL skills and a basic understanding of data modeling. Experience with CI/CD processes and Azure ADF is preferred. Additionally, expertise in ETL/ELT frameworks and ER/Studio would be a plus. As a Senior Data Warehouse Engineer, in addition to the core requirements, you will oversee other engineers while also being actively involved in data modeling and Snowflake SQL optimization. You will be responsible for conducting design reviews, code reviews, and deployment reviews with the engineering team. Familiarity with medallion architecture and experience in Healthcare or life sciences industry will be highly advantageous. At Myridius, we are committed to transforming the way businesses operate by offering tailored solutions in AI, data analytics, digital engineering, and cloud innovation. With over 50 years of expertise, we aim to drive organizations through the rapidly evolving landscapes of technology and business. Our integration of cutting-edge technology with deep domain knowledge enables businesses to seize new opportunities, drive significant growth, and maintain a competitive edge in the global market. We go beyond typical service delivery to craft transformative outcomes that help businesses not just adapt, but thrive in a world of continuous change. Discover how Myridius can elevate your business to new heights of innovation by visiting us at www.myridius.com and start leading the change.,

As a Sales & Application Expert for Personal Care Ingredients with a focus on dsm-firmenich at S KUSHALCHAND INTERNATIONAL PVT. LTD. (SKIL), your role will be crucial in driving growth within the Personal Care Ingredients division. You will be responsible for promoting and supporting dsm-firmenich's premium skin, sun, and hair care actives throughout India. Engaging directly with formulators, R&D experts, brand owners, and CMOs, you will play a vital role in product development, innovation, and representing a highly respected portfolio. Your key responsibilities will include providing technical application support to personal care and cosmetic formulators, cultivating and managing relationships with key clients such as brands, R&D heads, and CMOs, monitoring market trends, competition, and customer feedback, conducting product demos and trainings, as well as representing SKIL at exhibitions and trade fairs. Additionally, you will collaborate closely with the global team at dsm-firmenich on pipeline management, pricing strategies, and sample coordination. To excel in this role, you should ideally have 7 to 15 years of experience in B2B Sales/Application of Personal Care Ingredients, possess hands-on knowledge of actives from dsm-firmenich, BASF, Croda, Givaudan, etc., hold a degree in Cosmetic Technology, Chemistry, or Life Sciences, demonstrate a strong understanding of formulation science coupled with commercial acumen, exhibit excellent communication, presentation, and client engagement skills, and be willing to travel as required. Whether you are based in Mumbai or open to relocation, the salary offered will be based on your experience and current market standards. If you are excited about this opportunity and meet the desired profile, we encourage you to reach out by sending your updated CV to Ashwin Gokarn at ashwingokarn@skushalchand.com. Let's start the conversation and explore how you can contribute to our team and drive success in the personal care ingredients sector.,

Job Description Identify missing records and information that are necessary in the completion of the medical review assessment. Adhere to Department of Labor, state and company timeframe requirements. Coordinates physician reviewer referral as needed and follows up timely to obtain and deliver those results. Track status of all utilization management reviews in progress and follow up on all pending cases. Work closely with management team in the ongoing development and implementation of utilization management programs. Respond to inbound telephone calls pertaining to medical reviews in a timely manner, following client a established protocols. Process customer calls consistent with program specified strategies and customer satisfaction measurements to include but not limited to proper answering procedure, eg opening and closing remarks. Learn new methods and services as the job requires. Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Reach Us: HR Shanmugapriya - 8072891550

In this role you will be responsible for: The coder reads the documentation to understand the patient's diagnoses assigned - Transforming of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes - Creating uniform vocabulary for describing the causes of injury, illness & death is the role of medical coders - Medical coding allows for Uniform documentation between medical facilities - The main task of a medical coders is to review clinical statements and assign standard codes. Requirements of the role include: - 2025 PASSED OUTS ARE NOT ELIGIBILE TO APPLY FOR THIS ROLE 0 -1 Year of experience in any Healthcare BPO - University degree or equivalent that required 3+ years of formal studies in Life science/BPT/Pharm/Nursing - Good knowledge in human Anatomy/Physiology - 1+ year(s) of experience using a computer with Windows PC applications that required you to use a keyboard, navigate screens, and learn new software tools - Ability to work scheduled shifts from Monday-Friday 7:30 AM to 5:30 PM IST and the shift timings can be changed as per client requirements. - Flexibility to accommodate overtime and work on weekends basis business requirement. - Ability to communicate (oral/written) effectively in English to exchange information with our client. Must be a CPC-A Certified and working from office mandatory Interested please share resumes to pushpa.shanmugam@nttdata.com

Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager. Essential Functions Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that dont require extensive programming expertise) with guidance. May serve in the role of back-up to a DOC or DTL. May conduct data review. May write and resolve data clarifications. May lead database audit team. May develop and test databases and edit specifications. May perform testing of programming. May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." Qualifications Bachelors Degree Clinical, biological or mathematical sciences, or related field Req Equivalent combination of education, training and experience in lieu of degree. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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.

ql-editor "> Job Summary: The Contract & Proposal (C&P) professional will be responsible for managing the end-to-end process of drafting, negotiating, and finalizing proposals and contracts related to bioanalytical services. This role bridges scientific understanding with commercial acumen, ensuring timely, compliant, and competitive proposals are delivered to clients and sponsors in alignment with business objectives. Key Responsibilities: Collaborate with Business Development, Project Management, and Scientific teams to understand client requirements and scope of work. Prepare detailed technical and commercial proposals for bioanalytical services (e.g. PK/PD studies, method development & validation, sample analysis). Coordinate internal costing exercises and build accurate pricing models based on resource and timeline inputs. Draft, negotiate, and finalize various contract types (e.g., MSA, CDA, SOW, Work Orders) with clients. Review RFPs and RFIs, and prepare responses ensuring compliance with client guidelines and internal standards. Maintain a database of approved proposal templates, standard pricing modules, and contract clauses. Track proposal status, feedback, negotiations, and closure timelines in coordination with BD. Support audit and compliance documentation related to contracts and pricing. Ensure alignment with regulatory requirements (GLP/GCP), industry standards, and corporate policies in all documentation. Build strong relationships with external sponsors and internal cross-functional teams. Required Qualifications: Bachelor s or Master s degree in Life Sciences, Pharmacy, Chemistry, or related field. 2-7 years of experience in C&P or Proposal Development roles in a Bioanalytical or Clinical CRO. Strong understanding of bioanalytical lab services, GLP/GCP compliance, and clinical study structures. Proficiency in MS Excel, Word, and PowerPoint; experience with CRM tools is a plus. Excellent communication, negotiation, and writing skills. Detail-oriented with strong analytical and time management skills. Preferred Attributes: Experience dealing with international clients (US/EU/APAC) in a regulated environment. Ability to manage multiple proposals simultaneously with tight deadlines. Familiarity with regulatory frameworks (USFDA, EMA, DCGI) relevant to bioanalytical studies.

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

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 Senior Marketing Manager APAC Customer Strategy and Initiatives is responsible for managing the operations for $160M marketing funnel additions across all the OpCos in APAC. Additionally, some of the frequent asks from the commercial teams in the region and APAC leadership include market insights and sizing studies. With a focus on CX, this role will combine customer insights obtained through VoC with market insights obtained through sizing studies to form a view of the market. This helps the marketing and commercial teams to manage customer needs effectively by refining the communication objectives, deploy the right channels and providing critical feedback to commercial teams. This position reports to the Director Regional Marketing, APAC and is part of the Demand Generation Marketing located in Bengaluru and will be working remotely to cover APAC region . At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Create methods for customer data collection through Voice of Customer surveys, Behavioral Segmentation data, internal data sets, market sizing reports and by use of other CX tools. Work closely with sub-regional marketing teams to develop content and channels strategy based on customer needs and insights. Support execution of the campaigns based on content and channels strategy inclusive of sub-regional marketing plans using tools such as Kapost and through internal stakeholder meetings. Provide feedback to commercial teams from customer insights and create a process to close feedback loop to customers or plug the gaps in service/ engagement. Work with the regional marketing leads to develop sales tools and value proposition documents based on commercial inputs and customer insights. Continuously validate with customers the communication plans across customer buying journey. Who you are: Preferably a graduate in Life Sciences, though not a must. Long standing experience in designing cross-channel B2B CX strategy, with an exposure to Bioprocessing industry. Experience in customer engagement through prior experience in commercial or field marketing, marketing insights or execution functions. Experience of managing content marketing software. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel up to 20% of the time within APAC region; globally as and when required It would be a plus if you also possess previous experience in: Having created content and channels strategy and delivering consistent customer interactions across channels. Customer data collection using various tools and analyzing them for creating action plans. Managing customer buying journey process for delivering end-to-end experience. Using Predictive Analytics for designing customer experiences. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info . At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide. 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.

Job title : Project Specialist Learning Location: Hyderabad Job type: Permanent and Full time About the job Our Team: Sanofi Global Hub (SGH) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions . Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed below: He/She The selected person will support the Authorized Requester process and analytics for the iLearn Learning Management System. He/She will apply proven analytical and problem-solving skills to maximize full transparency of the upskilling initiatives lead by the designated functions supported by this position Manages daily enquiries and communicating out standard responses. Researches and resolves issues that may arise during iLearn requests. People: Performs independently while being a good team player Collects key information from stakeholders and transposes data to forms and iLearn Authorized Requester Portal. Process: Adapts easily and accepts new challenges; Contributes with creative ideas to enhance work processes. Coordinating translation of documents, managing communications on a weekly/bi-weekly basis out to global colleagues: Certificate completion, gamification, post webinar attendance. Creating eLearning modules through authoring tools Stakeholder: Process iLearn requests according to procedures in a timely manner. Preparing reports for executive leadership that effectively communicate trends, patterns, and predictions using relevant data. Experience and ability to build effective working relationship and collaborate with different stakeholders About you Experience : 5-7 years of Experience in relevant industry Soft skills : Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills : Learning Management Systems, Instructional designing, Project Management experience Education : Undergraduate degree in management, computer, science or life sciences Languages : Excellent knowledge of English language (spoken and written)

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 Security Operations Analyst is responsible for monitoring, analyzing, and responding to security incidents to protect the organization s digital assets and infrastructure. By proactively identifying threats and vulnerabilities, they play a critical role in minimizing risk and ensuring business continuity. This position reports to the Senior Manager, Security Operations and is part of the Information Security Team which operates globally. This will be an on-site role, based at our office in Bangalore working as part of a global team. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Perform advanced security incident analysis and digital forensics to identify threats and mitigate risks. Lead complex security investigations, including malware analysis, network traffic analysis, and endpoint detection. Provide guidance to L1 and L2 SOC analysts, improving the quality of information coming into the Security Operations team. Investigate and respond to escalated security incidents in a timely manner. Collaborate with our engineering teams to optimize and fine-tune SIEM (e.g., Splunk, Microsoft Sentinel, Elastic Security) and other security tools. Conduct proactive threat hunting to uncover hidden threats and vulnerabilities within the organization. Partner with other IT and security teams to improve the organizations security posture. Produce detailed reports and recommendations for remediation and security improvements, including hosting post incident reviews with wider technical teams. Who you are: Minimum 5+ years of experience in a corporate IT environment, with at least 2 years in an L3 or senior analyst role. Deep knowledge of security frameworks such as MITRE ATT&CK, NIST, CIS Controls, and ISO 27001. Experience with SIEM platforms (e.g., Splunk, Sentinel, QRadar, ArcSight) and EDR/XDR solutions. Vendor certifications are a plus. Hands-on experience with incident response, threat hunting, and forensic investigations. Familiarity with cloud security (AWS, Azure, Google Cloud) and modern attack techniques. Certifications such as OSCP, CEH are a plus. It would be a plus if you also possess previous experience in: Scripting and automation (Python, PowerShell, Bash) to improve SOC processes SME in EDR, SIEM, UBA, DLP or Data Security Operation Technology (OT) environments Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info . 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.

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

Whats this role about? Heres how youll contribute: Must have experience migrating data to Veeva Vault from other QMS (Caliber, Trackwise and Home grown), DMS (Biovia, Trackwise, Omnidocs) and LMS systems Expertise in leading & preparing the data migration strategy. Manages and oversees the process of data migration from one system to another and Data Migration Lead ensures the quality and integrity of migrated data before and after the migration. Job Responsibilities: Clearly determine the expectations for the format of the data with the business stakeholders Assess data type, data volume, pick lists, and metadata Design the Extract, Transform, Load process Determine the plan for delta loading / how to handle new data that is created during migration Nice to Have Experience in the pharmaceutical and life sciences industry Experience with Clinical, Regulatory, Quality, or Safety business processes Project Management experience for enterprise software implementations Experience with GxP and software validation regulations Experience with the migration verification process How we d like you to lead: Advantage Zensar We are a technology consulting and services company with 11, 800+ associates in 33 global locations. More than 130 leading enterprises depend on our expertise to be more disruptive, agile and competitive. We focus on conceptualizing, designing, engineering, marketing, and managing digital products and experiences for high-growth companies looking to disrupt through innovation and velocity. Zensar Technologies is an Equal Employment Opportunity (EEO) and Affirmative Action Employer, encouraging diversity in the workplace. Please be assured that we will consider all qualified applicants fairly, regardless of race, creed, color, ancestry, religion, sex, national origin, citizen status, age, sexual orientation, gender identity, disability, marital status, family medical leave status, or protected veterans status. Zensar is a place where you are free to express yourself in an environment that values individuality, nurtures development and is mindful of wellbeing. We put our people and customers at the center of everything that we do. Our core values include: Putting people first Client-centricity Collaboration Grow. Own. Achieve. Learn. with Zensar