2347 Life Sciences Jobs - Page 28

Job title: Safety Data Sheets Manager Location: Hyderabad About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams in the area of regulatory compliance, maintenance of product licenses and technical writing of CMC documents. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support global quality activities with a focus on technical writing. Main responsibilities: Management of a team experts with purpose to improve the performance of management of Safety Data Sheets and specifications within SAP-EHS. As a manager, you are responsible for the process of managing Safety Data Sheets in due time to prevent occupational / environmental/ Process safety events which may lead to business interruption Provision of strategic advice to the businesses regarding regulatory compliance linked to substances (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations Act with efficiency with the Global Product Stewardship team. Edit and maintain Safety Data Sheets using our IT tools. Independent evaluation and validation of substance data for classification and labelling according to international/local regulations e.g., GHS/CLP, Seveso, and transport regulations. Document all product stewardship information including references, reports to track and to justify evolutions in the versioning (SDSs, Hazard Classification Sheets & data), that support SDS decision. Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases. Communicating effectively in a written and oral ways results & conclusions with contacts of sites and Business Units. About you: Experience: 10+ years of industry experience including 5+ years experience in Product Stewardship. 2 years of experience to lead a group in the EHS field. Soft skills: Professional experience in the field of product safety/product stewardship, chemical laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets. Ability to rank relative compliance risks, high sense of responsibility and compliance and prioritize resulting actions. Ability to keep abreast of compliance changes. Strong proficiency in common chemical regulations. Ability to provide clear concise explanations. Have critical thinking, problem solving & planning skills. Technical skills : Knowledge in national regulatory aspects according ECHA Guidance for the editing of SDSs. Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed. Proven experience of SERC - SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus (e.g. tool from Opesus). Experience on Extended SDS. Knowledge on Biocides would be a plus. Knowledge in biological agents / biosafety would be a plus. Education: Master s degree in science or Technical discipline at minimum. Languages : Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas.

Job title: Safety Data Sheets expert Location: Hyderabad About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting M&S teams in the area of regulatory compliance, maintenance of product licenses and technical writing of CMC documents. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support quality activities with a focus on technical writing. Main responsibilities: Provision of strategic advice to the businesses with regards to regulatory compliance linked to substances (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations. Act with efficiency with the Global Product Stewardship team. Edit and maintain Safety Data Sheets using our IT tools. Independent evaluation and validation of substance data for classification and labelling according to international regulations e.g., GHS/CLP, Seveso, and transport regulations. Documents all product stewardship information including references, reports to track and to justify any modification in the versioning of the documents used by Product Stewardship (SDSs, Hazard Classification Sheets & data). Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases. Communicating effectively in a written and oral ways results & conclusions with contacts of sites and Business Units. About you: Experience : 5+ years of industry experience including 2+ years experience in Product Stewardship. Soft skills: Be able to work effectively in a team and on your own initiative. Self-starter with the ability to perform under rapidly evolving contexts. Data-based decision maker and methodical in the analysis. Good coordination and communication skills. Ability to provide clear concise explanations. Have critical thinking, problem solving & planning skills. Able to work independently, team player and networker. Important sense for transversal impact. Ability to communicate effectively, orally and in writing. Technical skills : SDS-Writing - Certified competent person according to 18 (4) Hazard Substance Ordinance (Germany) Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed. Proven experience of SERC - SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus (e.g. tool from Opesus). Experience on Extended SDS would be a plus. Knowledge on Biocides and in biological agents would be a plus. Professional experience in the field of product safety/product stewardship, chemical laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets . Education : Bachelor s degree in science or Technical discipline at minimum. Languages : Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas.

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.

Supervisor, Image Operations _ Office Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Supervisor, Image Operations to join our diverse and dynamic team. As a Supervisor, Image Operations at ICON, you will oversee the management and processing of imaging data for clinical trials, ensuring high-quality standards and timely delivery of results. Your leadership will be essential in optimizing imaging workflows, maintaining compliance with regulatory requirements, and fostering a culture of excellence within the image operations team. What You Will Be Doing: Supervising and managing the image operations team, ensuring efficient processing, analysis, and reporting of imaging data in accordance with study protocols. Collaborating with cross-functional teams, including clinical operations, data management, and imaging vendors, to support the integration of imaging data into clinical trial processes. Implementing and monitoring standard operating procedures (SOPs) to ensure compliance with regulatory guidelines and internal quality standards. Providing training and mentorship to team members, promoting professional development and a culture of continuous improvement in imaging operations. Tracking and analyzing key performance indicators (KPIs) related to image operations to identify trends and areas for enhancement. Your Profile: Bachelor s degree in a relevant scientific discipline such as radiology, biomedical engineering, or life sciences; advanced degree is a plus. Significant experience in imaging operations, data analysis, or related roles within the clinical research or pharmaceutical industry. Strong leadership skills, with experience managing teams and driving collaboration in a fast-paced environment. Excellent organizational and problem-solving skills, with a focus on attention to detail and compliance. Effective communication skills, with the ability to build relationships and collaborate with internal and external stakeholders. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Supervisor, Image Operations _ Office Based We are currently seeking a Supervisor, Image Operations to join our diverse and dynamic team. As a Supervisor, Image Operations at ICON, you will oversee the management and processing of imaging data for clinical trials, ensuring high-quality standards and timely delivery of results. Your leadership will be essential in optimizing imaging workflows, maintaining compliance with regulatory requirements, and fostering a culture of excellence within the image operations team. What You Will Be Doing: Supervising and managing the image operations team, ensuring efficient processing, analysis, and reporting of imaging data in accordance with study protocols. Collaborating with cross-functional teams, including clinical operations, data management, and imaging vendors, to support the integration of imaging data into clinical trial processes. Implementing and monitoring standard operating procedures (SOPs) to ensure compliance with regulatory guidelines and internal quality standards. Providing training and mentorship to team members, promoting professional development and a culture of continuous improvement in imaging operations. Tracking and analyzing key performance indicators (KPIs) related to image operations to identify trends and areas for enhancement. Your Profile: Bachelor s degree in a relevant scientific discipline such as radiology, biomedical engineering, or life sciences; advanced degree is a plus. Significant experience in imaging operations, data analysis, or related roles within the clinical research or pharmaceutical industry. Strong leadership skills, with experience managing teams and driving collaboration in a fast-paced environment. Excellent organizational and problem-solving skills, with a focus on attention to detail and compliance. Effective communication skills, with the ability to build relationships and collaborate with internal and external stakeholders. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Oversee the execution of a health & safety strategy tailored to the services provided by IPS. Align with organizational objectives and regulatory requirements. Ensure IPS remains at the forefront of new concepts in safety technology for construction management, process safety, and wellness. Articulate and implement new concepts and initiatives. Interact with clients to ensure best class programs are implemented as part of the overall IPS offerings. Provide guidance and leadership to regional health & safety teams, ensuring consistency and adherence to global standards. Manage current IPS health & safety staff members. Promote a comprehensive program that prioritizes wellness across all key initiatives. Provide guidance to management in order to minimize risk associated with existing or new health & safety services. Periodic review and update policies to reflect emerging risks, regulatory changes, and industry best practices. Design and implement a comprehensive health and safety risk assessment program across project sites, identifying potential non-compliance actions, hazards and implementing effective control measures to mitigate risks. Effectively leverage protocols for incident reporting, investigation, and corrective action, promoting a proactive approach to health and safety risk management. Training and Education: Develop and deliver industry specific training programs for project personnel at all levels. Promote a culture of continuous learning and improvement, encouraging employees to actively participate in safety initiatives that contribute to a safe work environment. Analyze and utilize metrics to track the effectiveness of health & safety initiatives, benchmarking performance against industry standards and internal targets. Develop and deliver reports to leadership, highlighting trends, accomplishments, and areas for improvement. Establish and maintain relationships within internal stakeholders, project teams, clients and contractors to foster collaboration and promote a shared commitment to safety excellence. Oversee the execution of a health & safety strategy tailored to the services provided by IPS. Align with organizational objectives and regulatory requirements. Ensure IPS remains at the forefront of new concepts in safety technology for construction management, process safety, and wellness. Articulate and implement new concepts and initiatives. Interact with clients to ensure best class programs are implemented as part of the overall IPS offerings. Provide guidance and leadership to regional health & safety teams, ensuring consistency and adherence to global standards. Manage current IPS health & safety staff members. Promote a comprehensive program that prioritizes wellness across all key initiatives. Provide guidance to management in order to minimize risk associated with existing or new health & safety services. Periodic review and update policies to reflect emerging risks, regulatory changes, and industry best practices. Design and implement a comprehensive health and safety risk assessment program across project sites, identifying potential non-compliance actions, hazards and implementing effective control measures to mitigate risks. Effectively leverage protocols for incident reporting, investigation, and corrective action, promoting a proactive approach to health and safety risk management. Training and Education: Develop and deliver industry specific training programs for project personnel at all levels. Promote a culture of continuous learning and improvement, encouraging employees to actively participate in safety initiatives that contribute to a safe work environment. Analyze and utilize metrics to track the effectiveness of health & safety initiatives, benchmarking performance against industry standards and internal targets. Develop and deliver reports to leadership, highlighting trends, accomplishments, and areas for improvement. Establish and maintain relationships within internal stakeholders, project teams, clients and contractors to foster collaboration and promote a shared commitment to safety excellence. 10+ years of global industrial Environmental, Health, and Safety experience. Experience in the Life Sciences industries is strongly preferred. Degree in Occupational Health & Safety, Engineering, or related field; advanced degree preferred. Previous management experience leading teams is a must. Professional certification in health & safety (e.g., CSP, CIH CSCS, NEBOSH) highly desirable. Strong leadership skills with the ability to inspire, motivate, and influence teams at all levels of the organization. Excellent communication, negotiation, and interpersonal skills, with the ability to effectively engage diverse stakeholders and drive consensus. Analytical mindset with keen attention to detail and the ability to leverage data and metrics to drive informed decision-making. Demonstrated experience in crisis management, incident investigation, and emergency response planning. Ability to travel and work effectively with diverse groups. Job Description Oversee the execution of a health & safety strategy tailored to the services provided by IPS. Align with organizational objectives and regulatory requirements. Ensure IPS remains at the forefront of new concepts in safety technology for construction management, process safety, and wellness. Articulate and implement new concepts and initiatives. Interact with clients to ensure best class programs are implemented as part of the overall IPS offerings. Provide guidance and leadership to regional health & safety teams, ensuring consistency and adherence to global standards. Manage current IPS health & safety staff members. Promote a comprehensive program that prioritizes wellness across all key initiatives. Provide guidance to management in order to minimize risk associated with existing or new health & safety services. Periodic review and update policies to reflect emerging risks, regulatory changes, and industry best practices. Design and implement a comprehensive health and safety risk assessment program across project sites, identifying potential non-compliance actions, hazards and implementing effective control measures to mitigate risks. Effectively leverage protocols for incident reporting, investigation, and corrective action, promoting a proactive approach to health and safety risk management. Training and Education: Develop and deliver industry specific training programs for project personnel at all levels. Promote a culture of continuous learning and improvement, encouraging employees to actively participate in safety initiatives that contribute to a safe work environment. Analyze and utilize metrics to track the effectiveness of health & safety initiatives, benchmarking performance against industry standards and internal targets. Develop and deliver reports to leadership, highlighting trends, accomplishments, and areas for improvement. Establish and maintain relationships within internal stakeholders, project teams, clients and contractors to foster collaboration and promote a shared commitment to safety excellence. Qualifications & Requirements 10+ years of global industrial Environmental, Health, and Safety experience. Experience in the Life Sciences industries is strongly preferred. Degree in Occupational Health & Safety, Engineering, or related field; advanced degree preferred. Previous management experience leading teams is a must. Professional certification in health & safety (e.g., CSP, CIH CSCS, NEBOSH) highly desirable. Strong leadership skills with the ability to inspire, motivate, and influence teams at all levels of the organization. Excellent communication, negotiation, and interpersonal skills, with the ability to effectively engage diverse stakeholders and drive consensus. Analytical mindset with keen attention to detail and the ability to leverage data and metrics to drive informed decision-making. Demonstrated experience in crisis management, incident investigation, and emergency response planning. Ability to travel and work effectively with diverse groups.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Radiometer, 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. At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. We re a team that celebrates diverse ideas and continuous improvement. Here, you ll find a place to grow and make a real impact, with your unique perspective driving us forward in improving patient care. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. Learn about the Danaher Business System which makes everything possible. Clinical Application Specialist, West Zone will be pivotal in developing our scientific arm and will play a major role in scaling up the scientific dialogue on our products and enhancing engagement with key customers in the region This position is part of the Sales function located in Mumbai , reporting to the Zonal Sales Manager, West and will be working in a remote set-up. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. If you thrive in a multifunctional & fast paced role and want to work to build a world-class organization read on. In this role, you will have the opportunity to: Leader for product demonstrations across the region, ensure compliance to the demo standard process guidelines, organize demo feedback sessions with end user, solve queries, provide clarifications. Joint sales visits for Strategic Accounts with Sales Representatives. Work strategically with the Zonal Sales Manager to position our solutions in new/adjacent markets and finding new applications of our solutions to cater to that market. Drive win-against competition program. Drive client engagement for the region and work with Key accounts Address the clinical queries of end users within the defined turn-around time. This might need reaching out to experts in other zones in India or other countries Work collaboratively with the Marketing Function to develop a network of Key Users Build scientific capacity for the products and its applications for the zonal sales and service team. The essential requirements of the job include: Educational qualification - Bachelor/master s in science or MBA equivalent with a functional background that has experience of the Healthcare & Diagnostics landscape in the Indian market 5+ years of experience in clinical and application roles with a Medical Devices, Diagnostic company Post-Graduate in Science (specialization: Biochemistry, Biotechnology, Biomedical, Ph.D preferred, Fresh medical doctors can apply It would be a plus if you also possess previous experience in: Experience of having managed a sales function in the past Radiometer, 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 Radiometer, 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 Radiometer 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.

Description 15+ years of experience in the field of clinical domain and must have at least 5+ years of experience in the field of SAS programing in generating SDTM, ADM, TLF and complete submission package preparation. Must have a solid understanding of end to end clinical domain from Drug discovery to Regulatory approval process. Must have worked as an Business Analyst or Product Manager on Clinical Systems development. Having experience in Statistical Computing environments will be of great advantage. Proficiency in solution design within the clinical business, conduct demos to internal and external stakeholders. Very good in collaboration with Customers and internal technical stake holders. Ability to ideate and write requirement specifications and thorough hands on with the latest SDLC process and tools used in the application development. Ability to manage and guide the BAs, Testers and developers in all the functional aspects and provide Test data support. Ability to perform user acceptance testing as per the business use cases and report the issues. An excellent team player and people management skills to manage the teams as needed. Must be flexible working in the global work environments. Must be abreast of latest news and innovations in the Clinical / Life Sciences industry Understanding of application of Gen AI on clinical use cases, problem solving ability using Gen AI will be of great advantage

About Godrej Agrovet: Godrej Agrovet Limited (GAVL) is a diversified, Research & Development focused agri-business Company dedicated to improving the productivity of Indian farmers by innovating products and services that sustainably increase crop and livestock yields. GAVL holds leading market positions in the different businesses it operates - Animal Feed, Crop Protection, Oil Palm, Dairy, Poultry and Processed Foods. GAVL has a pan India presence with sales of over a million tons annually of high-quality animal feed and cutting- edge nutrition products for cattle, poultry, aqua feed and specialty feed. Our teams have worked closely with Indian farmers to develop large Oil Palm Plantations which is helping in bridging the demand and supply gap of edible oil in India. In the crop protection segment, the company meets the niche requirement of farmers through innovative agrochemical offerings. GAVL through its subsidiary Astec Life Sciences Limited, is also a business-to-business (B2B) focused bulk manufacturer of fungicides & herbicides. In Dairy and Poultry and Processed Foods, the company operates through its subsidiaries Creamline Dairy Products Limited and Godrej Tyson Foods Limited. Apart from this, GAVL also has a joint venture with the ACI group of Bangladesh for animal feed business in Bangladesh. For more information on the Company, please log on to www.godrejagrovet.com . Designation Location Job Purpose Roles & Responsibilities: Educational Qualification: Experience: Skills: An inclusive Godrej Before you go, there is something important we want to highlight. There is no place for discrimination at Godrej. Diversity is the philosophy of who we are as a company. And has been for over a century. It s not just in our DNA and nice to do. Being more diverse - especially having our team members reflect the diversity of our businesses and communities - helps us innovate better and grow faster. We hope this resonates with you. We take pride in being an equal opportunities employer. We recognize merit and encourage diversity. We do not tolerate any form of discrimination on the basis of nationality, race, color, religion, caste, gender identity or expression, sexual orientation, disability, age, or marital status and ensure equal opportunities for all our team members. If this sounds like a role for you, apply now! We look forward to meeting you. Powered by Froala Editor

Engage with patients at clinics for health assessments, input data via mobile app, explain nutrition plans, and support clinic ops. Requires strong communication, patient care focus, and experience in healthcare or wellness fields. Perks and benefits Insurance—Mediclaim, Annual Leaves

Job Description Digital Buildings - Global Engineering Centre (GEC) BMS Software Manager Our mission in Schneider Electric is to be the digital partner for Sustainability and Efficiency. We drive digital transformation by integrating world-leading process and energy technologies, end-point to cloud connecting products, controls, software and services, across the entire lifecycle, enabling integrated company management, for homes, buildings, data centres, infrastructure and industries. We are the most local of global companies . We are advocates of open standards and partnership ecosystems that are passionate about our shared Meaningful Purpose, Inclusive and Empowered values. The mission in the GEC is to drive the strategic transformation of the engineering function within the Digital Buildings systems & project business to increase our competitiveness & improve our margins through establishing a collaborative working relationship between the Country and our Global Engineering Centre for BMS in India. What is the role? Individual Contributor role based in Bangalore and reporting to the Deputy General Manager - Engineering. An exciting and challenging role for BMS Software Engineer to join our team . Key responsibilities for this role include, but are not limited to Knowledge of DDC programming in proprietary programming platforms, PLC programming in FBD and / or Script or Ladder diagram Knowledge of building management system protocols like BACnet, LonWorks, Modbus, OPC and others Command on communication to interact single-handedly with global customers, understand requirements and translate them to deliverables Minimum 3-10 years of experience as a BMS Software Engineer Ability to plan and implement work utilizing engineering standards and technology principles and established company processes and procedures Familiarity with standard progress reporting tools and processes will be an added advantage Exposure to HVAC domain systems and applications like Air Handling Units, Chiller/Boiler Systems, Variable Air Volume Boxes etc. and ability to engineer a turnkey solution around them Working knowledge and understanding of electrical engineering concepts Ability to troubleshoot different HVAC Software Control loops Ability to perform functionality checks as per requirements and specifications Ability to understand and interpret sequences of operation, plant schematics and system architecture in order to design a working solution as per specifications Knowledge of the theoretical / practical aspects of building automation regulations and codes relating to air conditioning and management of air, water plants etc. across different geographies Ability to ensure quality, defect free deliverables, on time deliveries with customer satisfaction Ability to perform offline programming, testing and FAT implementation and documentation to ensure robust, high-quality deliverables Collaborate with Design and Graphics teams for effective and timely deliveries Work experience in global projects and/or in global engineering centers will be considered as an advantage What are we looking for? We at Global Engineering Center - an engineering excellence point of contact that provide turnkey BMS engineering solutions to SE branches across the world - are looking for someone who gets excited by innovation. We need someone who is tech-savvy and is happy to discover as well as learn new systems, is self-driven and confident to work for a value-based organization whose solutions are cutting edge. We need an engineer who is focused, collaborative and passionate about sustainability outcomes. We do not want to narrow the field; however, we do believe that instrumental to your success in this role will be the following skills Bachelor s degree in Instrumentation/Engineering/ Electrical Engineering/ Electronics & Telecommunication Engineering/ Mechanical Engineering Proven experience in BMS software DDC, with know-how of software programming in field of healthcare, life sciences and data center Good programming, logic development and troubleshooting skills Ability to work in remote (offshore) teams situated across time zones Product Lines: Building Management System (BMS / SCADA / DDC) Location: Bangalore Qualifications B.E Mechanical (HVAC)/ Electronics & Communication, Instrumentation Schedule: Full-time Req: 009HLL

Engage with patients at clinics for health assessments, input data via mobile app, explain nutrition plans, and support clinic ops. Requires strong communication, patient care focus, and experience in healthcare or wellness fields. Perks and benefits Insurance—Mediclaim, Annual Leaves

Engage with patients at clinics for health assessments, input data via mobile app, explain nutrition plans, and support clinic ops. Requires strong communication, patient care focus, and experience in healthcare or wellness fields. Perks and benefits Insurance—Mediclaim, Annual Leaves

VSM Software (P) Ltd is an ISO certified company catering to the global needs of Pharma and Banking industries. In both these verticals, we offer solutions and services in specific areas. VSM has Strong founding team based in India and the US A great leadership team who come with high levels of educational qualifications and relevant industry experience Skilled and trained IT and Subject Matter professionals We have a local presence in 5 countries and are further expanding our delivery reach. About the team At VSM, our sales team is a dynamic and diverse group of professionals dedicated to driving growth and building strong relationships with our clients. We pride ourselves on our collaborative spirit and commitment to excel. Our team consists of individuals with extensive experience across various industries, bringing a wealth of knowledge and insights to the table. We consistently meet our sales targets through innovative strategies and a customer-centric approach. We aim in building lasting relationships with clients and ensuring to understand and meet their unique needs. Responsibilities You shall be the first point of contact for our prospects. Prospect new leads alongside your inside sales representative, via tailored and relevant outreach campaigns (social, email and cold calling) Ability to connect with Senior leaders of a Pharma and life sciences organisation. Build, develop and manage your sales pipeline Determine the exact needs and resolve issues or objections presented by the prospects Schedule appropriate next steps for the leads Lead and communicate effectively with customers Travel to customer locations and marketing events as needed Achieve or exceed monthly quotas of qualified opportunities

The Opportunity: ArisGlobal is seeking a Associate Director - Product Management - Agentic AI to both create and grow a strategic revenue-generating product line within our Agentic AI solutions platform. In this role, you will translate high-priority opportunity areas into products, iterating quickly toward validated outcomes. You ll combine practical product leadership with commercial thinking, leveraging your understanding of emerging AI opportunities to inform our broader platform trajectory. This is a customer-facing, zero-to-one build role, ideally suited to someone with a background in data-driven decision support and insight generation, combined with experience of developing Agentic AI propositions. Key Responsibilities: Product Creation, Management & Growth: Drive the zero-to-one product build, leveraging entrepreneurial DNA and experience with lean startup, design thinking, service design, and other relevant methodologies. Translate strategic priorities into roadmaps, MVP definitions, user stories, and delivery plans. Operate with autonomy and pace, taking new products from concept through early validation to scale. Identify opportunities to increase revenue, lower operational costs, and improve customer retention by analyzing product performance and customer feedback. Customer Development: Engage with key stakeholders in life sciences to validate need, value, and usability. Run lean product discovery cycles across hypothesis-driven themes. Serve as a key external representative of the product trusted, credible, and customer-aware. Cross-Functional Collaboration: Work collaboratively across internal teams including Engineering, Sales, Services, and Marketing to ensure alignment on product priorities, effective go-to-market execution, and customer adoption. Work, as needed, with key external partnerships, as required to build out and commercialise new propositions. Clearly communicate product vision and benefits to internal stakeholders, enabling effective product launches and adoption strategies. Why Join Us?: You ll help build one of the most strategic products within a bold new wave of Agentic AI capabilities. This is a rare chance to take full product ownership, drive innovation with real customer impact, and work within a supportive team that s moving fast to shape the future of AI-powered development in life sciences. Skill Requirements: Required: 12+ years of experience in Product Management in B2B2C, B2B, or B2C space. 3+ years in AI-focused product management in B2B2C, B2B, or B2C space. Good experience in Agentic AI Experience working closely and driving product requirements for Data Engineering, ML Engineering, and Data Science teams. Proven track record of launching AI-driven enterprise SaaS solutions at scale. Deep curiosity and awareness of emerging AI technologies and trends, along with an ability to conceptualize how they can drive practical business value. Analytical mindset, skilled at using metrics to drive product decisions and continuously improve user experience. Strong communication skills, comfortable translating complex ideas into clear business value for diverse stakeholders. Proven ability to prioritize and execute effectively in dynamic environments. Entrepreneurial DNA, with experience in zero-to-one product builds and methodologies such as lean startup, design thinking, and service design. Preferred: Prior experience building AI products or platforms designed to automate or augment enterprise workflows. Understanding of modern platform architectures, scalability, and performance considerations for AI-driven products. Formal degree in a technical field such as Machine Learning, Statistics, or Computer Science. Familiarity with core AI platform elements and knowledge of AI tooling stack across one/many public cloud and data vendors. Experience managing large, technically complex product programs spanning multiple teams. A high degree of independent drive. Experience in contextual intelligence, information design, and insight generation.

Educational Bachelor of Engineering,Bachelor Of Technology,Bachelor Of Comp. Applications,Bachelor of Pharmacy,Master of Pharmacy,Master Of Technology,Master Of Comp. Applications Service Line Application Development and Maintenance Responsibilities a.Essential Skills: 2-10 years of total IT industry experience, with at least 3 years in Clinical or Regulatory solutions for Life Sciences clients. Should be well familiar with Life Sciences Domain - Clinical Trials, Drug Safety, Pharmacovigilance Familiarity with the complete working of CSV tool Exposure to US Life Sciences market Experience of leading development team, working with client teams/SMEs and leading them through the project life cycle. Additional Responsibilities: Ability to develop value-creating strategies and models that enable clients to innovate, drive growth and increase their business profitability Good knowledge on software configuration management systems Awareness of latest technologies and Industry trends Logical thinking and problem solving skills along with an ability to collaborate Understanding of the financial processes for various types of projects and the various pricing models available Ability to assess the current processes, identify improvement areas and suggest the technology solutions One or two industry domain knowledge Client Interfacing skills Project and Team management Preferred Skills: Domain-LifeSciences-Clinical Trials Compliance & Safety Technology-Regulatory Compliance-Regulatory Compliance System

Job Summary: We are seeking a motivated and detail-oriented fresher to join our healthcare team as a Medical Coder. The role involves reviewing patient medical records and accurately assigning Hierarchical Condition Category (HCC) codes to ensure compliance with risk adjustment and insurance requirements. This is an excellent opportunity for individuals looking to build a career in medical coding within the healthcare industry. Key Responsibilities: Review and analyze medical records to assign accurate codes. Ensure compliance with ICD-10-CM coding guidelines and risk adjustment models. Validate diagnosis codes based on physician documentation and medical necessity. Assist in improving documentation accuracy by collaborating with healthcare providers. Maintain strict confidentiality of patient health information (PHI). Keep up to date with changes in coding guidelines and insurance policies. Qualifications & Skills: Bachelors or Masters degree in Life Sciences, Healthcare, or a related field. Basic understanding of ICD-10-CM coding and risk adjustment principles. Knowledge in Anatomy and Physiology Strong analytical and attention-to-detail skills. Good communication and computer skills. Benefits: Comprehensive training on Medical coding. Certification assistance and career growth opportunities. 100% Placement with competitive Salary. Interested candidates share your resume to hr@touchstoneind.com or Call KAVI HR @ 89259 55900

BA - Primary Skills (Must Have) Understanding and experience of working in an environment which has adopted Agile Philosophy and SCRUM Framework Requirement Elicitation Preparing Business Requirements Document (BRD), Process Definition Document (PDD), Functional Requirements Document (FRD), System Requirements Document (SRD) and Requirement Traceability Matrix Document (RTM) Scope finalization and Approval Management Preparing Wireframes, Process Flow Diagrams & Flow Charts using any recognized Tool like Lucid Charts, Balsamiq, Visio etc Requirement Prioritization Product Backlog Management and Refinement i.e. Framing user stories in Jira from the detailed functional requirements document using JIRA or Azure DevOps Driving Grooming Sessions for the Scrum Team - During Sprint Planning Performing Functional testing of requirements and extending testing support to UAT users by, logging defects, retesting defects Proficient in delivering the project demos to the stakeholders & conducting Training for the end user s Experienced in drafting user guide/manual, process flowcharts, and training materials (If necessary) Skilled in handling multiple projects in parallel and preparing the requirements Strong oral and written communication Client relationship management BA - Secondary Skills (Good To Have/Could Have) Experience of working in Health Care Domain/Industry Understanding of Automation and Tools like Automation Anywhere (AA), UiPath, Blue Prism etc Knowledge of Robotic Process Automation (RPA) Process development effort estimation and helping management team for cost estimation for clients. Involved in RFP, POC demo for multiple clients Knowledge of Database and SQL Queries Understanding of API s and its implementation Overall understanding of System Integration aspects Understanding on Testing approaches

ABOUT THE ROLE Centre for Wildlife Studies (CWS) is recruiting a GIS/ RS Fellow to work on a range of ongoing and upcoming research and conservation research projects with national and international collaborators. KEY RESPONSIBILITIES 1. Satellite Data & Algorithm Identification: Identify various satellite datasets and algorithms for detecting forest fires. 2. Model Development for Wildfire Prediction: Prepare the AI/ML models to predict wildfires. 3. Field Assessment of Model Performance: Travel to field sites and assess the performance of AI/ML models 4. API Development & Training: Develop API to host models through Power BI and train forest department staff to use it. 5. Manuscript & Report Preparation: Assist in writing manuscripts, articles, and reports. 6. Outreach & Communication Materials: Create outreach and communication materials as required. 7. Administrative Support: Coordinate team meetings, maintain accounts, handle grant reporting, and supervise field assistants. REQUIRED SKILLS 1. Educational Background: Postgraduate degree in life sciences, engineering, or related fields (e.g., environmental sciences, geography, geoinformatics) with strong AI/ML expertise. 2. GIS/RS Project Experience: Significant experience in conducting GIS/RS projects. 3. Modeling Skills: Expertise in model development, model selection, variable identification, testing/training, and accuracy measurement. 4. Account & Grant Management: Experience with handling accounts and grant reports. 5. Language Proficiency: Proficiency in spoken and written Telugu and English. 6. Team Collaboration: Ability to work independently and collaboratively within a team.

We are looking for a proactive and detail-oriented Junior React Developer to join our established frontend team. You will help build and maintain dynamic, user-friendly web applications using React. This is a fantastic opportunity for someone early in their development career to work alongside experienced developers and contribute to real-world projects from day one. Responsibilities Develop and maintain web applications using React and related technologies. Collaborate with designers, backend developers, and product managers to deliver high-quality user interfaces. Write clean, maintainable, and efficient code following best practices. Participate in code reviews and actively contribute to improving development processes. Assist in debugging and troubleshooting issues across browsers and devices. Contribute to the improvement of our accessibility and performance standards. Requirements 2-5 years of professional experience with JavaScript, including React. Basic understanding of HTML5, CSS3, and responsive design principles. Familiarity with Git and version control workflows. Eagerness to learn and grow in a fast-paced development environment. Strong communication and collaboration skills. Ability to take direction and also work independently when needed. Desirable (Nice to Have) Experience or knowledge of web accessibility standards (e.g., WCAG, ARIA). Familiarity with testing tools such as Jest, React Testing Library, or Cypress. Experience working with REST APIs. Exposure to CSS-in-JS libraries (e.g., styled-components, Emotion). Knowledge of modern frontend tooling (Vite, ESLint ).

Review Site Visit Reports (SVRs) to ensure they meet or exceed quality standards and support goals of quality, subject safety, data integrity and regulatory compliance. Use tools and techniques to ensure the efficient and effective review of Site Visit Reports and their associated attachments, in compliance with IQVIA SOP, ICH/ GCP guidelines, and protocol requirements. Essential Functions Oversee a caseload of SVRs for assigned studies, ensuring compliance to the protocol, processes, timelines, IQVIA/applicable SOPs, and GCP guidelines. Review SVRs to ensure findings requiring corrective and /or preventative action plans are documented and followed up to resolution, to ensure high quality reports. Participate on the project team for all SVR review activities and identifies and escalate CRA and /or site issues, relevant trends, and related risk factors to the project team and appropriate parties in a timely manner to optimize quality of project delivery. Provide guidance to Clinical Project Managers (CPMs) at project start-up and throughout the study and partner with the project team members to decrease the level of corrections/additions needed on reports by providing insight and training of the SVR annotations. Identify and track the project team compliance to SOPs for submission and approval of the SVRs through communication with the CRAs and line managers. Participate in meetings with project team to discuss any SVR review issues illustrative of quality/performance deficiencies across PIs/sites and CRAs. Assist with identification of the trends emerging from the Issue Escalation Log. Provide coaching to CRAs to decrease the level of corrections/additions needed on reports. Provide quality improvement support such as quality checks, data trending, providing back up support and mentoring and coaching of junior staff members. May take on special project assignments related to function/corporate initiatives.

At Tenthpin we are seeking talented, client-facing, and collaborative SAP Developer (ABAP, CAPM) to join our rapidly growing team. The successful applicant will have exceptional technical expertise in ABAP programming and S/4 HANA implementations, with a passion for delivering innovative solutions that add substantial value to our clients, contributing to our reputation as one of the recent success stories within the Management Consulting Industry. The Opportunity As an SAP Developer, you will be responsible for designing, developing, and maintaining ABAP programs and enhancements to support our clients needs. You will also be expected to demonstrate strong technical proficiency in S/4 HANA implementations, contributing as part of an exceptional team to deliver high-quality solutions. Traditionally this has been classic ABAP but now we work with clients moving to ABAP Eclipse and RAP as part of a Clean Core approach. Some of our developers have also built some CAPM (Cloud Application Programming) skills to be able to support extensions to developments that have been made in nodeJS or Java. Key Responsibilities The role will include but not be limited to: Development: Design, develop, and maintain ABAP programs and enhancements, ensuring optimal performance and adherence to best practices. S/4 HANA Expertise: Take responsibility for ABAP development within the S/4 HANA environment, providing technical expertise and solutions that align with the client s business objectives and maximise a clean core approach. Consulting/Professional Services: Collaborate with clients to understand business requirements, provide technical guidance, and deliver effective ABAP solutions that meet project goals. Your Experience First and foremost, you are a genuine Management Consultant with exceptional communication skills, the ability to see the bigger picture, and a collaborative approach to creating exceptional solutions. You will also have relevant SAP skills, including: ABAP and S/4 HANA Expertise: You have proven experience as an ABAP Consultant with a focus on S/4 HANA implementations. Highly desirable to have experience in Eclipse, ABAP in the Cloud , and RAP or have initial learning of these skills through SAP certification Advantage to have experience or training in CAPM Cloud Application Management for SAP Build using nodeJS or Java: whilst not a core skill it is useful to supplement ABAP skills and provide flexibility for interesting new developments.. Experience Level: You have 6-10 years of experience in large-scale SAP implementation projects and have been part of at least 2 full project lifecycles. Technical Knowledge: In-depth understanding of ABAP programming language and SAP technologies is essential. Consulting Expertise: Experience in a consulting or professional services environment is required, with the ability to work closely with clients to understand their needs. Communication Skills: Strong interpersonal and communication skills to work collaboratively with cross-functional teams and clients. Problem-Solving: You possess strong problem-solving skills, with the ability to analyze complex business requirements and develop effective technical solutions. Certifications: C_ABAPD SAP Certified Associate Backend Developer - ABAP Cloud is expected; either you have this certification or are keen to achieve it The following additional certifications demonstrate broader skills and are an advantage: o C_CPE SAP Certified Associate Backend Developer - SAP Cloud Application Programming Model o C_LCNC SAP Certified Associate Low-Code/No-Code Developer - SAP Build o C_AIG SAP Certified Associate SAP Generative AI Developer o C_FIORD SAP Certified Associate SAP Fiori Application Developer Why Tenthpin Tenthpin is a Global Consulting and Technology Boutique for the Life Sciences industry. With more 400+ consultants, we operate out of eight countries: US, Switzerland, Germany, UK, Portugal, Poland, Japan, and India. 16 of the top 20 Life Sciences companies worldwide already rely on Tenthpin, trusting our independent, unbiased advice and services. Why Tenthpin technical consulting ? Life Sciences are in our DNA and technical delivery in Life Sciences GxP is a specialist skillset and includes working on leading SAP innovations; we value technical members as part of one consulting team; and we are not a factory - we have an approach, an opinion, and pride ourselves on our expertise. We offer a competitive salary and benefits package. Plus, a collaborative work environment that encourages professional growth and development. Are you passionate about digitally transforming Life Sciences companies? Do you want to create an impact with leading brands and deliver real value? Enjoy working in an entrepreneurial and collaborative team? Then we look forward to hearing from you Tenthpin is an equal opportunities employer.

Product Owner, Chennai ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We re looking for a Product Owner who thrives on turning business vision into working products. In this role, you ll be at the core of innovation - leading cross-functional teams, shaping product roadmaps, and delivering solutions that drive revenue, efficiency, and strategic differentiation. What You Will Be Doing: Own the end-to-end product lifecycle, from concept through delivery and continuous improvement Translate business goals into clear, actionable product requirements and prioritize based on value, impact, and effort Partner closely with engineering, design, operations, and commercial teams to align on outcomes and timelines Build and manage product roadmaps that drive growth, efficiency, and new business opportunities Act as the go-to expert for your product domain, internally and externally Champion Agile best practices and keep teams focused on delivering customer and business value Lead feedback loops with customers and stakeholders to iterate quickly based on real-world input Communicate product vision, progress, and results to senior leadership and cross-functional teams Facilitate cross-functional discussions and alignment sessions to accelerate outcomes Deliver high-impact presentations and reports for stakeholders and executives Balance strategic priorities with hands-on execution and shift between big-picture vision and detailed follow-through Your Profile: Bachelor s degree in Computer Science, Information Technology, Business, or a related field (CSPO or similar certification is a plus) 8 to 10 years of overall experience, with 3 to 6 years specifically as a Product Owner or Product Manager in a tech-driven/tech-enabled environment A track record of shipping successful products that solve real business problems and drive measurable results Deep understanding of the product development lifecycle, SDLC, STLC, and Agile or Scrum frameworks Experience managing trade-offs between technical feasibility, business value, and user experience Strong communication and collaboration skills, with the ability to build trust and alignment across diverse teams A bias for action, ownership, and customer-centric thinking; you lead without waiting for permission Experience working in Healthcare or Life Sciences (preferred but not required) What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Product Owner, Chennai We re looking for a Product Owner who thrives on turning business vision into working products. In this role, you ll be at the core of innovation - leading cross-functional teams, shaping product roadmaps, and delivering solutions that drive revenue, efficiency, and strategic differentiation. What You Will Be Doing: Own the end-to-end product lifecycle, from concept through delivery and continuous improvement Translate business goals into clear, actionable product requirements and prioritize based on value, impact, and effort Partner closely with engineering, design, operations, and commercial teams to align on outcomes and timelines Build and manage product roadmaps that drive growth, efficiency, and new business opportunities Act as the go-to expert for your product domain, internally and externally Champion Agile best practices and keep teams focused on delivering customer and business value Lead feedback loops with customers and stakeholders to iterate quickly based on real-world input Communicate product vision, progress, and results to senior leadership and cross-functional teams Facilitate cross-functional discussions and alignment sessions to accelerate outcomes Deliver high-impact presentations and reports for stakeholders and executives Balance strategic priorities with hands-on execution and shift between big-picture vision and detailed follow-through Your Profile: Bachelor s degree in Computer Science, Information Technology, Business, or a related field (CSPO or similar certification is a plus) 8 to 10 years of overall experience, with 3 to 6 years specifically as a Product Owner or Product Manager in a tech-driven/tech-enabled environment A track record of shipping successful products that solve real business problems and drive measurable results Deep understanding of the product development lifecycle, SDLC, STLC, and Agile or Scrum frameworks Experience managing trade-offs between technical feasibility, business value, and user experience Strong communication and collaboration skills, with the ability to build trust and alignment across diverse teams A bias for action, ownership, and customer-centric thinking; you lead without waiting for permission Experience working in Healthcare or Life Sciences (preferred but not required) Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

We are seeking a detail-oriented and technically adept QC Email Analyst - SFMC to join our Marketing Automation team. This role is responsible for ensuring quality assurance of email campaigns and journeys executed through Salesforce Marketing Cloud. You will work closely with campaign managers, developers, and compliance teams to validate that marketing assets are accurate, on-brand, and compliant before launch. Key Responsibilities: Quality Control & Testing Perform detailed QA checks on emails, templates, data extensions, dynamic content, and journeys within SFMC before launch. Validate rendering across various devices, email clients, and browsers using tools like Litmus or Email on Acid. Ensure links, tracking parameters, subject lines, from names, images, and personalization tokens are working as expected. Verify compliance with CAN-SPAM, GDPR, and other regional regulations (e.g., inclusion of unsubscribe, privacy policy links). Data & Segmentation Checks Ensure correct use of audience segmentation and filters. Validate test sends using test data extensions or live preview. Process & Documentation Maintain checklists, QC logs, and documentation for all reviewed campaigns. Support the development of QA best practices, SOPs, and templates for campaign QC. Collaborate with internal teams to triage and resolve issues quickly before deployment. Identify root causes of QA failures and propose process improvements. Required Skills & Qualifications: Bachelor s degree in Marketing, Communications, Computer Science, or related field. 2-4 years of experience in email marketing or digital QA, ideally in healthcare, consumer, or tech sectors. Strong knowledge of Salesforce Marketing Cloud components: Email Studio, Content Builder, Journey Builder, Data Extensions. Hands-on experience with email rendering tools (Litmus, Email on Acid). Understanding of email compliance standards and privacy laws. High attention to detail and a proactive approach to problem-solving. Preferred Qualifications: Experience in regulated industries (e.g., pharma, finance). Knowledge of multi-language or multi-region campaign QC. SFMC certifications (e.g., Email Specialist) are a plus.