129 Life Science Jobs

Role Overview: ZS is a management consulting and technology firm that focuses on transforming ideas into impactful solutions for patients, caregivers, and consumers worldwide. As part of the team, you will collaborate with stakeholders to understand and translate business needs into data requirements, explore innovative data options, manage requests, support research initiatives, and ensure compliance standards are met. Your role will involve mentoring junior team members, driving utilization for data assets, and overseeing day-to-day activities to deliver accurate and timely information. Key Responsibilities: - Develop expertise in the global healthcare data landscape and collaborate with stakeholders to identify data requirements - Engage with data providers to address evolving business needs and explore innovative data options - Present and explain data alternatives, facilitate selection and implementation of optimal solutions, and guide stakeholders through data access processes - Manage and document requests, execute reporting tasks, and collaborate with a global team of diverse skill sets - Support research initiatives, internal projects, and marketing endeavors while ensuring seamless communication - Mentor and coach junior team members, drive utilization for data assets, and ensure adherence to compliance standards Qualifications Required: - Minimum of a Bachelor's degree with a quantitative focus (e.g., Biology, Physics, Business, Analytics) and strong academic performance - 3-4 years of relevant job experience in Data Strategy/management and Life Science preferred - Knowledge of healthcare data and practical applications, experience with RWD/RWE projects, or omics data preferred - Ability to translate unstructured problems into actionable requirements, strong communication skills, and customer service orientation - Self-starter with high motivation, maturity, and personal initiative, ability to plan and organize tasks in an unstructured environment - Capability to multi-task, manage priorities, and work in a fast-paced context Perks & Benefits: ZS offers a comprehensive total rewards package including health and well-being, financial planning, annual leave, personal growth, and professional development. Skills development programs, career progression options, internal mobility paths, and a collaborative culture empower you to thrive as an individual and team member. Additional Company Details: ZS provides a flexible and connected way of working, combining work from home and on-site presence for a balanced approach. The inclusive culture and innovative environment at ZS promote personal growth and professional development. The company values diversity and inclusion, encouraging individuals from varied backgrounds to apply. If you are eager to contribute, grow, and bring your unique self to work, ZS welcomes your application as an equal opportunity employer dedicated to providing advancement opportunities without discrimination. Please ensure to possess or obtain work authorization for the intended country of employment and submit an online application with transcripts for consideration.,

As a Customer Technical Support & Service Coordination Specialist at Cepheid, you will be responsible for providing remote product support to customers requiring assistance with instrumentation, LIS, software, hardware components, and Assays sold and distributed by Cepheid. Your role in the Technical Support Team involves serving as the technical expert in Cepheid's Customer Care experience, providing solutions to customer issues remotely via phone, email, and web. You will also log and maintain all customer queries/complaints in CRM. Additionally, you will support coordination activities to facilitate on-site intervention by Field Service Engineer. In this role, you will have the opportunity to: - Engage customers to collect and compile detailed information about customer complaints. - Conduct data analysis and basic troubleshooting for instruments, hardware, assays, software, and operating systems. - Investigate and resolve first-level customer complaints remotely through phone and email. - Document complaints and resulting investigations in the Complaint Management System. - Adhere to Quality Management System procedures. - Complete all assigned and required training satisfactorily and on time. - Train internal associates and new hires on technical support modules and CRM. - Represent Technical Support on projects and operational teams, communicating findings back to Technical Support. - Coordinate with customers for all service-related activities. - Dispatch Field Service Engineers for service calls as appropriate. - Process purchase orders for billable service activities related to service calls and preventative maintenance events. - Perform additional tasks as assigned by the Technical Support Manager or Supervisor. Qualifications Required: - Bachelor's degree in engineering/electronics or experience working in Biological/Clinical Laboratory Science/Life Science/Medical Device Industry with a minimum of 5+ years of relevant experience (or equivalent). Master's Degree with a minimum of 3+ years of related work experience. - Fluent English (written and oral). - Laboratory or Remote Technical Support Experience in PCR and Microbiology, Molecular Biology Oncology or Virology, patient sample collection practices and workflow, sample preparation practices and methodologies, laboratory analytical diagnostic equipment, medical devices, and software. - Customer-oriented with an understanding of customer expectations and empathy for customer & patient needs. - Knowledge and use of commercial computer application packages (MS Excel), familiarity with SalesForce.com (or similar CRM System) and SAP a plus. - Ability to follow complex procedures and processes, work independently in a structured manner, prioritize critical tasks, build collaborative work relationships with different teams, and thrive in a dynamic and fast-paced environment. Join Cepheid, a Danaher company, and be a part of a global organization committed to empowering associates to push the boundaries of what's possible. Together, we'll accelerate the real-life impact of tomorrow's science and technology, partnering with customers across the globe to architect solutions that bring the power of science to life. For more information, visit www.danaher.com.,

As a Safety Specialist I at Precision, your role will involve performing all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR) for clinical trials and/or post-marketing safety programs. Key Responsibilities: - Process ICSRs following Standard Operating Procedures (SOPs) and project/program-specific safety plans - Triage ICSRs, evaluate data for completeness, accuracy, and regulatory report ability - Enter data into Argus Safety Database - Code events, medical history, concomitant medications, and tests - Draft case narratives - Assess information to be queried and follow up until queries are satisfactorily resolved - Generate timely, consistent, and accurate expedited reports in line with regulatory requirements - Coordinate with data management staff for safety data reconciliation - Ensure distribution of all required individual expedited and periodic reports for clinical and post-marketing projects - Participate in audits/inspections - Submit all relevant documents to Trial Master File (TMF) and Pharmacovigilance System Master File - Maintain understanding and compliance with SOPs, regulations, guidelines, and project plans - Attend department meetings and project-specific teleconferences/meetings - Perform other duties as assigned by management Qualifications: Minimum Required: - Minimum 2 years of clinical trial drug safety experience in the Pharma/CRO industry - Bachelors or first-level Degree in Pharmacy or Nursing preferred - Experience with Oracle Argus Safety Database - Working knowledge of MedDRA, WHODrug, FDA safety regulations, EMA, MHRA, ICH guidelines, and global safety regulations Preferred: - Early phase oncology clinical trial experience Please note that any data provided will be stored as per the company's Privacy Policy. For CA applicants, refer to the CA Privacy Notice. If you require accommodation for the application process, kindly contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.,

Role Overview: As a Senior Clinical Research professional at Ascentrik Research Pvt. Ltd, you will be responsible for leading and managing a research team to curate accurate, timely, insightful, and comprehensive data and intelligence for Beacon Targeted Therapies. You will work closely with UK-based clients, analyze relevant information, and ensure project deliverables are met. Additionally, you will be part of a global network of life science researchers, focusing on dynamic products in cutting-edge life science areas. Key Responsibilities: - Lead and manage a research team to curate accurate, timely, insightful, and comprehensive data and intelligence - Identify and analyze the most relevant information for Beacon and its users - Coordinate with UK-based clients to understand and meet project deliverables - Manage activities towards the launch of a beacon module and provide support post-launch - Perform data management activities efficiently - Generate queries to clarify and improve data quality - Demonstrate a strong understanding of Clinical Trials and preclinical data Qualification Required: - Masters in Pharmacy (except Pharmacognosy)/Biology/Bio-Technology/Bio-Chemistry/Pharm D with minimum 2-3+ years of relevant experience - Bachelors in Pharmacy (except Pharmacognosy)/Biology/Bio-Technology/Bio-Chemistry with at least 4 years of relevant experience - Candidates with additional Clinical research diploma or relevant courses can apply - Basic computer skills, Microsoft Office & detailed Internet Knowledge - One research paper published - Ability to work in a high-pressure, deadline-driven environment - Exceptional communication and reporting skills Additional Company Details: Ascentrik Research Pvt. Ltd is a premier Research & Data Service Provider that serves Top Fortune 500 Companies and multinational companies across various industries. The company specializes in customized Research Services, providing actionable insights and quality data to clients. With offices in Pune, Navi Mumbai, and Noida, Ascentrik Research Pvt. Ltd is committed to growing its workforce and expanding its services further.,

Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we are looking for experienced professionals to join us as we prepare to launch our newest office in Hyderabad, India. This is more than just a job. It's an opportunity to be part of something from the very beginning. You will play a direct role in shaping the culture, building the team, and influencing how we grow in India. Your work from day one will have a meaningful impact across global projects. Joining Medpace in Hyderabad means: - Being a Founding Member: Help establish and lead operations at our newest location. - Making an Immediate Impact: Your experience will directly influence Medpace's growth in the region. - Career Growth: Opportunities for leadership and advancement as the office expands. - Global Reach: Work on cutting-edge clinical trials with international teams and top-tier sponsors. - Strong Culture: Join a company known for stability and commitment to professional development. - Support & Infrastructure: Despite being a new office, you will have the backing of global resources and processes of a well-established CRO. If you are seeking a new challenge and want to be part of building something meaningful while advancing your career with a company that invests in your region, we would love to hear from you. Responsibilities: - Assist in the preparation of Core Lab Data Management documents. - Perform validation on data transfers and edit programs. - Maintain data cleanup via edits, data review, and data changes. - Send data transfers externally. Qualifications: - Bachelor's degree in life science/pharmacy/health-related field with strong attention to detail and working knowledge of Excel and Word. - 1-2 years of experience in a pharmaceutical or CRO setting preferred. Medpace Overview: Medpace is a full-service clinical contract research organization providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Why Medpace People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. Medpace Perks: - Flexible work environment. - Competitive compensation and benefits package. - Competitive PTO packages. - Structured career paths with opportunities for professional growth. - Company-sponsored employee appreciation events. - Employee health and wellness initiatives. Awards: - Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024. - Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility. What To Expect Next: A Medpace team member will review your qualifications, and if interested, you will be contacted with details for the next steps.,

As a Business Design Consultant at EY, you will have the opportunity to be part of business transformation engagements across various functions such as sales, service, marketing, and pricing, all while focusing on enhancing Customer Experience. Your role will involve acting as a trusted advisor by understanding and analyzing the client's business challenges and vision. You will conduct assessments of the current state by engaging with business stakeholders through workshops, questionnaires, and interviews. By analyzing the collected data and artifacts, you will provide valuable insights and recommendations for designing the future state. To excel in this role, you should ideally come from a business consulting background with a strong understanding of key enterprise business processes, customer touchpoints, journey design, design thinking principles, and stakeholder management. Additionally, you will be expected to contribute to practice development, demonstrate thought leadership, and engage in business development activities. In terms of domain expertise, preference will be given to candidates with experience in either sales or service functions. For sales, this includes expertise in B2B/B2C sales strategy, sales planning, lead and funnel management, CRM digital channels, and more. On the other hand, service expertise involves areas such as customer service strategy, channel strategy, customer experience management, and analysis of customer feedback. Proficiency in using Design Collaboration tools like Mural, Miro, PPT, and Visio to create and modify CX Journey flows, Personas, Service Design Flows, and Process Flows is essential for this role. It would also be beneficial to have experience in verticals such as CPG & Retail, Telecom & Media, Advanced Manufacturing, Healthcare, Life Sciences, BFSI, or CX Consulting services. Join EY in building a better working world, where you will be part of a team that leverages data, AI, and advanced technology to shape the future with confidence. EY offers a wide range of services in assurance, consulting, tax, strategy, and transactions across more than 150 countries and territories, supported by sector insights and a globally connected network of professionals.,

Immediate Hiring !! Designation: Medical coder Executive Salary: Upto 20k PM + Incentives Shift : General shift. Skills: Anatomy | Physiology | Pathalogy Eligibility: Life science (UG/PG) Location: Chennai, Hyderabad, Bangalore

As the Chemistry & Immunoassay Marketing Manager at Beckman Coulter Diagnostics, you will play a crucial role in managing and executing product strategies within the HGM segment. Your responsibilities will include gaining a deep understanding of market dynamics, customer needs, and the competitive landscape to drive product success and achieve business objectives. Located within the HGM marketing team, this fully remote position will have you reporting to the Chem/IA/BB Leader HGM. You'll have the opportunity to represent the CC-IA HGM voice in Business Unit and Global Product Marketing meetings, provide projections, priorities, and needs for HGM, and optimize the Clinical Chemistry and Immunoassay portfolio through Product Life Cycle Management strategies. Your role will involve enhancing customer satisfaction, growing margin and revenue, launching new products, and leading growth by applying DBS tools in daily management and problem-solving. Collaboration with local and regional Marketeers, Country Sales leaders, and engaging in Scientific Marketing activities will also be part of your responsibilities. To be successful in this position, you should hold a Bachelor's degree in a technical field with at least 7 years of experience, or a Master's degree with 5+ years of experience. An MBA is preferred, along with a minimum of 5 years of experience in clinical diagnostics, life science, or medical device sales or commercial marketing. Previous experience in product strategy, product management, or product marketing within a life science or scientific software organization is desirable. Travel may be required up to 25% of the time, including overnight stays for client meetings and conferences. A valid driver's license with an acceptable driving record is necessary for travel to client sites or off-site meetings. Additionally, proficiency in Excel, PowerPoint, and Outlook, strong written and oral communication skills, ability to work under tight timelines, and experience working with global time zones are beneficial for this role. At Beckman Coulter Diagnostics, we offer flexible and remote working arrangements for eligible roles, ensuring enriching careers regardless of work arrangement. If you are looking to accelerate the real-life impact of tomorrow's science and technology, join our winning team today and partner with customers globally to solve their most complex challenges. For more information about this role and to explore the opportunities at Beckman Coulter Diagnostics, visit www.danaher.com.,

The Senior Contract Manager plays a critical role in achieving organizational goals by establishing and managing strong relationships with business teams, as well as creating client and vendor contracts. Key responsibilities include negotiating, closing, extending, and renewing contracts, and effectively communicating contractual changes to stakeholders. Essential job functions entail reviewing, drafting, and negotiating various commercial agreements, ensuring compliance with company policies and procedures, informing leadership of contract status, coordinating agreement execution, maintaining contract files and databases, and contributing to the development of contract-related policies and procedures. The role also involves identifying process improvement opportunities and taking proactive steps to enhance efficiency. Minimum qualifications include a Post Secondary Degree or Certificate, along with at least 5 years of relevant experience in drafting, reviewing, and negotiating commercial contracts, preferably in the life science or pharmaceutical industry. Additionally, candidates must possess strong organizational skills, the ability to manage multiple tasks in a fast-paced environment, interpersonal skills, good judgment, and a proactive work style. Proficiency in Microsoft Office programs and fluency in English are also required. Candidates with disabilities requiring accommodations during the application process can reach out for assistance. It is important to note that job offers from the organization involve prior communication with the recruiting team, hiring managers, and a formal interview process to avoid potential fraudulent schemes targeting job seekers.,

As a Counsellor at our organization, you should have a minimum of 1-2 years of experience in a similar role. A graduate degree is required for this position. We are looking for female candidates for this role, and the job locations include Kochi, Ahmedabad, and Thane. Your responsibilities will include having excellent communication and convincing skills. It is essential for you to be aggressive and presentable. You should be comfortable with making calls and handling face-to-face inquiries. Following up on inquiries is a crucial part of your job, along with providing detailed information both over the phone and in person. Cold-calling from a provided database for lead generation and converting inquiries into admissions will be part of your daily tasks. Proper follow-up with interested parents is also expected from you. For the Clinical Research Faculty position, we require candidates with 1-2 years of experience, a Diploma in Clinical Research, and a post-graduation in Life Sciences, Pharmacy, or Medicos. The ideal candidate for this role should be female and willing to work in Kochi, Ahmedabad, or Thane. As a Student Advisor, you should have 1-2 years of counselling experience and a minimum graduate qualification. Female candidates are preferred for this role in Kochi, Ahmedabad, and Thane. Your responsibilities as a Student Advisor will include having good communication and convincing skills, being aggressive and presentable, and handling inquiries both over the phone and in person. Cold-calling from a provided database, converting inquiries into admissions, and following up with interested parents are crucial aspects of this role. If you meet the requirements for either of these positions, please submit your resume to hr@clinomic.in.,

You have an exciting opportunity to join our team at Clinomic as a Clinical Research Faculty or Student Advisor. We are looking for talented individuals who have a passion for teaching and counseling in the clinical or life science field. If you have 1-2 years of experience and hold a Diploma in Clinical Research with a Post Graduation in Life Science/Pharmacy/Medicos, we encourage you to apply. As a Clinical Research Faculty, your responsibilities will include teaching in clinical or life science, demonstrating good communication skills, and possessing strong interpersonal skills. You should be capable of conducting seminars, workshops, and webinars. A minimum of 2 years of experience in the clinical research field is required for this role. The position is open to female candidates and is based in Kochi, Ahmedabad, and Thane. Alternatively, we are also seeking a Student Advisor with 1-2 years of experience as a counselor. As a Student Advisor, you will be responsible for providing guidance to prospective students. The ideal candidate should have a minimum graduate qualification and be proficient in communication and convincing skills. Being aggressive, presentable, and flexible for handling inquiries is essential. You will be required to follow up with inquiries, provide details, and engage in cold-calling for lead generation. The role is open to female candidates and is based in Kochi, Ahmedabad, and Thane. If you believe you are a suitable candidate for either of these positions, please send your resume to hr@clinomic.in. Join us at Clinomic and be a part of our dynamic team dedicated to excellence in education and student support.,

The Senior Contract Manager plays a critical role in achieving organizational goals by establishing and managing strong relationships with business teams, as well as creating client and vendor contracts. Responsibilities include negotiating, closing, extending, and renewing contracts, and effectively communicating contractual changes to stakeholders. Key functions of the role involve reviewing, drafting, and negotiating various commercial agreements, ensuring compliance with company policies and standards, keeping leadership informed about contract status, coordinating agreement execution, maintaining contract files and databases, and contributing to the development of contract-related policies and procedures. The position also involves identifying opportunities for process improvements and taking proactive steps to enhance efficiency. Minimum qualifications include a Post Secondary Degree or Certificate and at least 5 years of relevant experience in drafting, reviewing, and negotiating commercial contracts, preferably within the life science or pharmaceutical industry. Additionally, the ideal candidate should possess strong organizational skills, the ability to manage multiple tasks in a fast-paced environment, excellent interpersonal skills, good judgment, a proactive work style, the capacity to meet deadlines across multiple projects, and the capability to collaborate effectively with colleagues at various organizational levels. Proficiency in Microsoft Office applications and fluency in English are also required. Candidates should be aware that any data shared during the application process will be handled in accordance with the organization's Privacy Policy. Individuals with disabilities requiring accommodations or alternative application methods are encouraged to contact Precision Medicine Group for assistance. Moreover, the company cautions applicants about potential fraudulent activities by unauthorized entities claiming to offer employment opportunities on behalf of the organization. Job offers are only extended following communication with the recruiting team, hiring managers, and a formal interview process.,

You will be responsible for working with business leads to ensure the efficient allocation of resources to client projects at a sub-regional level, business development opportunities, and internal initiatives. This includes developing strong relationships across the wider resource management community and sharing resources across practices to optimize overall productivity and realization. You will partner with business leads to understand, plan for, and meet the resourcing demands of the pipeline, supporting them to achieve realization of utilization and effective skills/grade mix on projects. In this role, you will need to be comfortable with staffing analytics and maintain resource management data integrity in systems supporting resource and project management decisions. You will demonstrate strong commercial awareness, monitor and drive compliance to the financial management system, identify solutions to resolve longer-term patterns related to forecast and actual utilization, monitor and investigate discrepancies between data, and provide insights. Principal Accountabilities: - Work with business leads to ensure efficient resource allocation, business development, and internal initiatives at a sub-regional level. - Develop strong relationships across the wider resource management community for productivity optimization. - Monitor and communicate current and near-term delivery capacity. - Maintain resource management data integrity in systems. - Support reporting of metrics and analytics to business leads. - Demonstrate strong commercial awareness to monitor and drive compliance. We are looking for an individual with the following qualifications: - Bachelor's degree or equivalent. - Proven problem-solving skills with attention to detail. - Strong written and verbal communication skills. - Ability to build strong business relationships. - Excellent team-based interpersonal skills with the ability to work autonomously. - Determination, diplomacy, and resilience. - Proficiency in Microsoft Office applications. - Knowledge of life science is a plus.,

As a Regional Medical Advisor (RMA) specializing in General & Specialty Medicine for the South Region, you will play a crucial role as a key representative for our company. Your primary responsibility will involve engaging with essential stakeholders in the field, with the objective of providing scientific expertise across identified regions, products, and therapy areas to valued customers. Your role will encompass various responsibilities and activities, including developing and maintaining a comprehensive understanding of the company's products, particularly focusing on the cardiovascular therapeutic area. It will be essential to stay updated on the latest medical advancements, clinical guidelines, and treatment protocols to provide accurate information to stakeholders. Building and maintaining relationships with Scientific Leaders (SLs), Key Decision Makers (KDMs), healthcare professionals, and academic institutions will be a key aspect of your role. Engaging in scientific discussions, presenting clinical data, and providing educational support to Key Opinion Leaders (KOLs) regarding the company's products and therapeutic areas will also be part of your responsibilities. Collaboration with the line manager to provide strategic inputs and expertise to product management, delivering scientific and medical education to internal stakeholders, and participating in medical conferences, advisory boards, and scientific meetings are crucial components of your role as an RMA. Interpreting and communicating clinical trial data, real-world evidence, and other scientific information to healthcare professionals and regulators will be part of your responsibilities. Additionally, providing medical support for local studies, collaborating with cross-functional teams, and supporting medical projects aligned with the therapy area will be essential tasks. Your role will also involve addressing medical inquiries, providing timely and accurate responses to healthcare professionals and stakeholders, and ensuring compliance with legal, regulatory, and company policies. Training sales colleagues on assigned therapy areas and assisting in pre-launch and launch training for new products will also be part of your responsibilities. To excel in this role, you must possess a strong academic foundation in life sciences, such as a medical degree (MD) or doctorate (Ph.D.), along with at least 1 year of experience in the pharmaceutical cardiovascular therapy area. Demonstrated knowledge and expertise in the relevant cardiovascular therapeutic area, strong communication skills, analytical abilities, adaptability, and familiarity with regulatory and compliance guidelines are essential requirements for this position. Overall, as an RMA in Medical Affairs, you will act as a scientific expert and liaison between the company and external stakeholders, contributing to building scientific credibility, fostering relationships, and supporting the company's strategic objectives in the healthcare industry. Your focus on excellence and harmonious collaboration with internal and external stakeholders will be key to your success in this role.,

We are seeking dynamic and passionate professionals to join our team at Rapha in various departments of the Company. If you are a Life Science or Science Graduate, an Electrical or Electronics Engineer, a Sales & Marketing Professional, or an HR Professional, we are eager to hear from you. At Rapha, we value individuals who are committed to pursuing their dreams and working hard to turn those dreams into reality. As we continue to grow rapidly, we have numerous opportunities for intelligent and skilled individuals to become part of our team. Location: Factory at Palakkad Qualification & Experience: The ideal candidate will be a graduate in Science with a focus on Chemistry, Biochemistry, Microbiology, or Biotechnology. Preference will be given to candidates with 1-2 years of experience in the production activities of manufacturing kits for In vitro Diagnostics. Freshers are also welcome to apply and be a part of our exciting journey.,

Job Description Position: Medical Coder Ct: HR Shanmugapriya -7358425167 Job Description:Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books. Requirement: knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills No of vacancy: 500 Eligibility: Nursing GNM/DGNM Life science graduates Pharmacy Physician assistant Bio medical Engineers Bio chemistry Bio technology Bio informatics Micro biology Zoology and Advanced zoology Biology Botany Plant biotechnology Genetics Food and Nutrition Paramedical Physiotherapy M.Sc. Clinical Nutrition M.Sc. Human Genetics M.Sc. Medical Laboratory Technology M.Sc. Medical Sociology M.Sc. Epidemiology M.Sc. Molecular Virology M.Sc. Biostatistics M.Sc. Blood Banking Technology M.Sc. Rgnerative Medicine B.Sc. - Accident & Emergency Care Technology B.Sc. - Audiology & speech Language Pathology B.Sc. - Cardiac Technology B.Sc. - Cardio Pulmonary Perfusion Care Technology B.Sc. - Critical Care Technology B.Sc. - Dialysis Technology B.Sc. - Neuro Electrophysiology B.Sc. - M.L.T. B.Sc. - Medical Sociology B.Sc. - Nuclear Medicine Technology B.Sc. - Operation Theatre & Anaesthesia Technology Bachelor of Science in Optometry B.Sc. - Physician Assistant Salary 15K to 17K (fresher) To 50K (experienced) Pm (Incentives && Benefits as per Corporate Standards) 4K fixed hike after six months Other Benefit: 1. Pick Up & Drop Facility 2. Food Facility 3. Day Shift 4. Weekend Off Reach us : HR Shanmugapriya 7358425167

The ideal candidate for this position should have 4 to 6 years of post-qualification experience with a solid understanding of compliance programs and due diligence of contracts. A candidate with knowledge of regulations from various sectors such as Financial Services (FS), Healthcare, Insurance & Life Science (HIL), Service, Utility, Resources and Energy (SURE), Retail, Consumer Goods, Logistics (RCL), and Communication, Media & Technology (CMT) verticals will be preferred. In this role, you will collaborate with ERM, Quality Team, Delivery Leadership, Delivery Risk Management Team, and Sales Account Team to evaluate risks and contribute to the design, development, and implementation of a vertical compliance program. You will review and provide guidance on the design and implementation of Standard Operating Procedures (SOPs) and guidelines in coordination with the aforementioned functions. Additionally, you will be responsible for coordinating between the vertical compliance program team, ERM, Delivery Team, Quality Team, and external SMR for the development and implementation of the compliance framework. You will address and respond to vertical compliance clarifications and queries, conduct risk assessments of downstream processes to ensure compliance conditions are met, and engage in discussions with accounts and delivery teams to gather inputs on vertical compliance questionnaires. Furthermore, your role will involve reviewing customer contracts and relevant documents, identifying contractual obligations for the program, interpreting contractual clauses, laws, and regulations pertinent to specific sectors or verticals. You will act as the legal Single Point of Contact (SPOC) for the vertical compliance program team on compliance framework and governance, assist in designing compliance certification framework, and participate in the learning and development of sectoral compliances through trainings and workshops. You will be required to obtain contract obligations from CTS or associated contract documents, identify applicable regulations for all covered jurisdictions, translate regulatory requirements and industry standards into compliance obligations, map compliance obligations to operational controls, and consolidate compliance obligations to common controls. Additionally, you will provide periodic regulatory updates, obtain approval and sign-off on finalized checklists from the vertical compliance program team, and conduct workshops to support compliance managers for self-assessment and certification.,

As a Senior Insights Associate located in Gurgaon with a hybrid work mode in the Pharma/Life Science industry, your main role is to generate forecast inputs and assumptions for a syndicated drug-level forecast database product in Global Market Insights, reporting to the Manager, Data Analytics. Your responsibilities include building and analyzing country-specific forecast assumptions for multiple indications using secondary sources and your understanding of therapy area, as well as rectifying inconsistencies/gaps in data by utilizing secondary data sources. You will provide manual inputs and assumptions to enhance automated drug-level forecasts, understand and manipulate quantitative data, and ensure the quality and timeliness of input data capture and assumptions. To qualify for this role, you should have a B Pharma/M Pharma/Biotech, MBA in Pharma with experience in pharmaceutical data, along with 2-4 years of relevant work experience. An understanding of the pharmaceutical domain, major economies" pharmaceutical environments, and prior experience in pharmaceutical forecasting and advanced Excel are advantageous. Additionally, you must be diligent in conducting secondary research using search engines and clinical trial websites. Your contribution will support the Manager in maintaining a consistent approach to applying inputs and assumptions across drug classes, countries, and diseases to create standardized outputs that can be segmented by key industry dimensions. Your attention to detail and ability to generate test sets for comparison to automated data outputs will be crucial in this role.,

We are seeking ambitious publishing professionals to join our growing team supporting the peer review process. As a Reviewer Selection Editor, you will be responsible for efficiently managing peer review administration procedures, utilizing tools like Scholar One Manuscripts and PubMed Central to identify international experts suitable for reviewing cutting-edge medical research. Reporting to the Reviewer Selection Lead, you will work alongside a team of Reviewer Selection Editors. The ideal candidate will hold a postgraduate qualification in MTech/M.Sc. in areas such as Electrical and Electronics (ECE, EEE, VLSI, Embedded Systems, Power systems, Communication systems), Life Science (Biotechnology, Biochemistry, Microbiology, Molecular biology), Economics (Business Economics, Financial Economics, Applied Economics), Agriculture, or Horticulture. You should have a solid understanding of the journal peer review process, a keen interest in academic publishing, and knowledge of current market trends. Proficiency in English grammar, experience with process-driven workflows, and a background in customer-facing roles are essential. Your responsibilities will include managing the peer review process for journals, selecting appropriate reviewers through database research, ensuring compliance with ethical publication practices, communicating with reviewers, analyzing data for process improvements, maintaining records, and collaborating with international editorial teams. Strong organizational skills, the ability to handle multiple tasks efficiently, effective communication, and a commitment to excellent customer service are key qualities we are looking for. Flexibility, familiarity with Microsoft Office, and a willingness to adapt to changing work plans are also important. The selection process will involve an online assessment, technical discussion, and final HR-level discussion. This position requires working from our office in Chennai or Puducherry. Prior experience with platforms like Scholar One Manuscripts or Editorial Manager is advantageous but not mandatory, as full training will be provided.,

The Alien Technology Transfer Group leads top-class innovators to success by converting visionary ideas into tangible realities. They support companies with concrete growth ambitions by funding their product development through the Innovation Consulting Line. Additionally, they design, fund, and launch innovative companies through the timely transformation of high-potential concepts into profitable ventures with the support of the Venture Studio. They also deliver unparalleled talent hunting solutions for businesses of all sizes, startups, and SMEs particularly through the Talent Hunting Line. As an Innovation Scout, your role involves sourcing and analyzing the highest quality prospect clients for the business lines among innovative high-tech high-impact start-ups and Small and Medium Enterprises (SMEs) in Europe and the USA. To excel in this position, you must possess a genuine interest in technology and business, an aptitude for quickly understanding complex engineering or medical innovations, be highly analytical and articulate, and have a strong command of English. Being a team player, well-organized, and keen to take on responsibility are key qualities. Demonstrating an entrepreneurial mindset, high self-motivation, and a high degree of stamina to work within an ambitious and goal-driven environment are essential. Your responsibilities will include continuously staying up to date in the technological and business field to recognize business opportunities and industry/market emerging trends effectively. Identifying top-level sources/hubs of potential clients among web platforms, online databases, and events, monitoring current trends in private and public innovative project financing and fund-raising, handling and analyzing databases, preparing regular reports on funding trends, and maintaining internal databases for prospects, clients, and public grant awardees. Job Requirements: - Masters degree in Life Science (Bioengineering, Biomedical, Biotechnology, Neurosciences, Biochemistry, Microbiology, etc.) - Advanced use of Excel and aptitude to master the use of professional industry database - Proficiency in using digital resources (e.g. search engines) to uncover new leads - Self-starting, inquisitive, and pragmatic attitude - Fluent English comprehension, oral and written - Knowledge of Python programming for web scraping/extraction mechanisms is a plus - An added advantage if you have an idea for the creation of web scrapers for extracting startup data from different websites supporting the development of startup Lead Generation. Please note: Due to the high volume of candidates, individual feedback regarding the outcome of every single application cannot be provided.,

As a Same Day Surgery Medical Coder, you will be responsible for handling the day-to-day operations of Same-day Surgery Coding. Your primary tasks will include coding records according to prescribed coding standards such as ICD-9/ICD-10 and CPT, assigning diagnosis and procedure codes for patient charts, and ensuring adherence to the company's Coding Compliance policy/plan. It is essential to have a minimum of two years of Same-day Surgery Coding experience and hold a CPC or COC certification. A graduation in Life Science or medical sciences is also required. Your role will involve working towards service levels to meet productivity and quality requirements. You will be expected to improve performance based on feedback provided by the reporting manager and prepare and maintain status reports. This position is based in Chennai and offers a salary ranging from 4 to 7.5 LPA Max. The work timings are during the day shift with Saturday and Sunday as fixed offs. The ideal candidate for this position must have CCS or CIC certification, with a preference for CPC or COC certification. The job falls under the Healthcare & Life Sciences functional area in the BPO/KPO Call Centre industry. This is a full-time, permanent employment opportunity. If you meet the qualifications and experience required for this role, please share your updated CV with raghu@starworthglobal.com or contact 9176668384 to express your interest.,

As a Medical Writer (Rebuttal) at Vitality, you will play a crucial role in our dynamic and evolving team. We are committed to fostering continuous growth and innovation, and we are looking for individuals who can bring fresh ideas to the table and help us stay ahead in the competitive business landscape. To excel in this role, you should have a background in Pharmacy or life sciences (B.Pharm/B.Sc. Life Science) and possess strong typing skills of minimum 20-25 words per minute with 95% accuracy or above. Proficiency in basic English grammar, medical terminology, and writing skills is essential. Additionally, you should have a solid understanding of tools, methods, and concepts, as well as knowledge of relevant regulatory standards. Excellent communication skills, both verbal and written, are a must for effective collaboration within our team. You should also demonstrate exceptional data collection and analysis abilities, coupled with a keen attention to detail. Before the interview, you will undergo a series of tests to assess your qualifications, including a test of basic medical terms (20 multiple-choice questions), a medical summary writing test, a basic grammar test (20 multiple-choice questions), and a typing test. This full-time position operates during day shifts from 9:00 AM to 6:00 PM, with one working Saturday per week. A one-month training program will be provided, during which a stipend will be paid. The selection criteria include having a background in pharmacy or life sciences (B.Pharm, B.Sc. Life Science), strong typing skills of minimum 20-25 WPM with 95% accuracy or above, proficiency in basic English grammar, medical terminology, and writing skills, as well as successful completion of the pre-interview tests. If you are passionate about healthcare communication and possess the required skills and qualifications, we invite you to send your resume to hr@vitalitybss.com and be a part of our innovative team at Vitality.,

Alien Technology Transfer empowers top-class innovators to transform visionary product concepts into commercial realities. The company helps companies with concrete growth ambitions to secure funding for their product development through their innovation consulting expertise. With a track record of raising more than $500 million for Small and Medium Enterprises (SMEs) across various domains such as agri-tech, artificial intelligence, biotechnology, clean-tech, cyber-security, quantum computing, space, and transport, Alien Technology Transfer is now seeking an Innovation Scout. As an Innovation Scout, you will be responsible for sourcing and analyzing the highest quality prospect clients for the business lines among innovative high-tech high-impact start-ups and SMEs in Europe and the USA. To excel in this role, you must possess a genuine interest in technology and business, quickly understand complex engineering or medical innovations, be highly analytical and articulate, and have a strong command of English. Additionally, being a team player, well-organized, and eager to take on responsibility are key qualities. Demonstrating an entrepreneurial mindset, high self-motivation, and the ability to work in an ambitious and goal-driven environment are also essential. Your duties and responsibilities will include: - Keeping yourself updated in the technological and business field to identify business opportunities and industry/market trends effectively. - Identifying potential clients from web platforms, online databases, and events. - Monitoring innovative project financing and fund-raising trends. - Handling and analyzing databases to deliver appropriate results. - Evaluating information related to innovative technologies and businesses. - Maintaining and enriching internal databases for prospects, clients, and public grant awardees. - Preparing reports on funding trends to define yearly targets. Job requirements include: - A Masters degree in Life Science (Bioengineering, Biomedical, Biotechnology, Neurosciences, Biochemistry, Microbiology, etc.) - Advanced Excel skills and ability to master professional industry databases. - Proficiency in using digital resources to uncover leads. - Self-starting, inquisitive, and pragmatic attitude. - Fluent English communication skills. - Knowledge of Python programming for web scraping/extraction mechanisms is a plus. - Added advantage if you have ideas for creating web scrapers for startup data extraction. Please note that due to the high volume of applications, individual feedback on application outcomes cannot be provided.,

You are invited to attend a WALK-IN INTERVIEW at eNoah iSolution India Pvt Ltd. The dates for the interview are 24th & 25th July 2025 and 28th & 29th July. The interview timings are from 11 AM to 6 PM on the specified dates. To be eligible for the interview, you should hold a UG/PG degree in Pharmacy, Life Science, Microbiology, or any Medical Degree. The work hours for this position are from 8:30 AM to 5 PM with a 5-day working week (Saturday & Sunday Off). The interview will take place at NRK Business Park, No. 603-B, 6th Floor, Vijay Nagar, Behind Mangal City Mall, Indore. For more details or queries, you can contact Rashmeet at 7200902979 or Krishna at 9522220247. Make sure to bring your updated resume with you to the interview. This is a great opportunity that you wouldn't want to miss!,

At Tenthpin, we are looking for talented, client-facing, and collaborative SAP Quality Management (QM)/ Production Planning (PP) Consultants to be part of our fast-growing team. If you are passionate about delivering innovative solutions that bring substantial value to clients and want to contribute to our success story in the Management Consulting Industry, we are excited to hear from you. As an SAP QM/PP Consultant at Tenthpin, you will play a key role in aligning technology with business objectives. Your responsibilities will include collaborating closely with clients, providing valuable assistance in implementing cutting-edge SAP systems, executing build, testing, and deployment phases, emphasizing Life Science best practices, and thriving in a diverse environment working within multi-language, multicultural, and multi-disciplinary teams. Additionally, you will have the exceptional opportunity to further your training through our R&D functions, creating Co-Innovations with leading Lifesciences Organizations to develop Industry Leading Products. You will also actively contribute to the Tenthpin Community, working with a passionate group of consultants dedicated to staying at the forefront of the industry. We offer an environment that eliminates traditional red tape in Consulting, allowing you more time to focus on your workload, deliver to top-tier clients, and advance your career in a positive and empowering setting. To be successful in this role, you must be a genuine Management Consultant with exceptional communication skills, the ability to see the bigger picture, and a collaborative approach to creating exceptional solutions. You should have 7 to 14 years of relevant experience, at least 2 full project lifecycles as an SAP QM/PP Consultant, and significant experience in S/4HANA. Moreover, you should have a strong understanding of manufacturing, quality management, and production planning processes in SAP QM, including integration with PP module, proficiency in SAP template design, functional configuration & customization, and adept at providing business consulting services for SAP QM and SAP PP modules. Experience in Life Sciences or process manufacturing industries would be advantageous. Tenthpin is a Global Consulting and Technology Boutique for the Life Sciences industry, operating out of 8 countries. We offer a competitive salary and benefits package, as well as a collaborative work environment that fosters professional growth and development. If you are passionate about digitally transforming Life Sciences companies and want to make an impact with leading brands, we encourage you to join our entrepreneurial and innovative team. Tenthpin is an equal opportunities employer.,