2068 Biotechnology Jobs - Page 49

A leading KPO/ BPO / ITES sector company servicing international clients for several decades requires # BScs / M.Scs / BPharm / BTech in Bioinformatics, Biotechnology & Biochemistry and other Life Sciences. # Graduates/Post Graduates in Chemistry / Chemical technology Work respectively involve data capture, extracting, document summary and analysis, data analytics etc Part Time / Freelance / External working and Work From Home WFH for selected areas of work. Freshers can also apply. Attractive remuneration for part time / freelancers / external and work from home Job Types: Full-time, Part-time, Permanent, Fresher, Freelance Pay: ₹12,000.00 - ₹15,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person Expected Start Date: 04/10/2025

Join Amgen's Mission to Serve Patients If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and deliver ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Associate Data Analytics Live What You Will Do Let’s do this. Let’s change the world. We are seeking a detail-oriented and proactive Data Steward to support our pharmaceutical data governance initiatives. The ideal candidate will ensure the quality, consistency, integrity, and security of data across our systems, particularly within commercial, regulatory, R&D, and supply chain functions. You will play a key role in managing master data, supporting compliance (e.g., GxP, GDPR), and facilitating data-driven decision-making across the organization. Maintain and monitor master data for key domains (e.g., customer, product, vendor, material) Identify, investigate, and remediate data issues using profiling tools and dashboards. Define and enforce data definitions, naming conventions, and standard operating procedures Identify and correct data quality issues and anomalies using established data validation protocols. Implement data cleansing and enrichment processes Support company-wide data governance policies and frameworks. Ensure data complies with internal standards and external regulations (e.g., FDA, EMA, GDPR). Work closely with regulatory and quality teams to ensure alignment with compliance standards. Use statistical tools and modeling techniques to interpret trends, patterns, and correlations maintain data pipelines and manage data cleaning processes. Help identify data gaps and recommend solutions for improvement. ensure data accuracy, consistency, and integrity across systems Analyze large and complex datasets from internal and external sources (e.g., clinical trials, sales, market data). Serve as a liaison between business units (e.g., marketing, regulatory, supply chain) and IT. Collaborate with data owners and SMEs to define and enforce data standards. Provide training and support to end-users on data management best practices. Maintain the accuracy and completeness of master data in key systems (e.g., SAP, Veeva, Oracle). Support data migration and integration projects, ensuring clean and standardized data input. Assist in data extraction, reporting, and analytics to support business operations and decision-making. Generate periodic data quality reports and metrics Basic Qualifications: Degree in computer science, Data Management, or related field & engineering preferred with 2-5 years of software development experience 2–5 years of experience in a Data Steward, Data Analyst, or related role in the pharmaceutical industry Experience with data systems such as SAP, Veeva, Salesforce, Oracle, or Informatica is a plus. Excellent communication and collaboration skills. Preferred Qualifications: Experience with global data governance or enterprise data management initiative Knowledge of GxP, FDA/EMA guidelines, and industry-specific data compliance. Proficiency in SQL and at least one programming language (e.g., Python, R). Strong skills in data visualization tools (Power BI, Tableau, Qlik, etc.). Strong skills Postgres SQL /Mongo DB SQL database, vector database for large language models, Databricks or RDS, S3 Buckets Excellent communication skills, with the ability to present complex data in a simple, understandable way Good To Have Skills Postgres SQL /Mongo DB SQL database, vector database for large language models, Databricks or RDS, S3 Buckets design patterns, data structures, data modelling, data algorithms Soft Skills: Excellent analytical and troubleshooting skills. Strong verbal and written communication skills. Ability to work effectively with global, remote teams. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented, with a focus on achieving team goals. Strong presentation and public speaking skills. Thrive What You Can Expect From Us As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us. careers.amgen.com Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Show more Show less

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. " Job Description We are seeking a dynamic and strategic Business Development Partner to join our Biologics team in Hyderabad, Indi a. In this pivotal role, you will be responsible for driving licensing initiatives for our portfolio, identifying potential partners, and negotiating favorable agreements to maximize the value of our intellectual property portfolio. Develop and implement licensing strategies aligned with the company's overall business objectives Identify and evaluate potential licensing opportunities for the company's products and technologies Conduct market analysis to assess commercial potential of own products for out-licensing Lead negotiations & due diligence with current and potential partners, ensuring favorable terms and conditions for licensing agreements Lead term sheet / agreement sign-off, ensuring adherence to BD guidelines, contract development & sign off through collaboration with cross-functional teams, including commercial/ alliance, country teams, legal, finance, portfolio, regulatory, SCM, IPM, clinical, operations, etc. to support deal diligence and out-licensing activities Manage and maintain relationships with existing licensees and partners and drive new BD opportunities with existing and potential customers Evaluate proposals from external manufacturing partners to de-risk internal assets through Contract Manufacturing proposals Monitor industry trends and competitor activities to inform out-licensing strategies Prepare and present business cases, financial models, and reports to senior management Ensure compliance with regulatory requirements and company policies in all out-licensing activities BD Process Management and Digitization: create work flows to digitize Business Development process; assign ownerships to tasks across stakeholders and use BD tools/ automated solution to facilitate measurement, tracking and business process improvement Qualifications Bachelor's degree in Business, Life Sciences, or related field; MBA or advanced degree preferred 2-3 years post MBA (overall 5-6 years preferred) of experience in business development or licensing within the pharmaceutical or biotechnology industry Prior Exposure/Experience in: Strategic management / Business Development / Partnering / Alliance Management/ Management Consulting for Life Sciences Strong understanding of the drug development and commercialization process Proven track record in successfully negotiating and closing out licensing deals Demonstrated ability to analyze market trends and competitive landscapes; relate macro-economic developments with impact on local market, understand & track competitors Understanding of internal processes, people & organization Strong financial acumen and experience with financial modeling Exceptional articulation, communication and presentation skills Ability to build and maintain relationships with internal and external stakeholders Willingness to travel as required for business development activities Additional Information " Skills & attributes: Business Case development/ analysis Partner management/ alliance management Fundamental awareness of the Biologics/ Bio-pharma industry Financial Analysis/ P&L analysis Good knowledge of recent trends & Market Intelligence and business dynamics Behavioral Skills Excellent communication, negotiation, and interpersonal skills Strong analytical and problem-solving abilities with a keen eye for detail Ability to work collaboratively in a cross-functional team environment Strong Networking skills and quick learning ability Benefits Offered At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. " Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ " Show more Show less

At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good. Your impact Your Impact The world needs innovators and problem solvers who turn challenges into greater opportunities. At Jacobs, we push the limits of what’s possible to make the world smarter, more connected and more sustainable. In our life sciences work, that means designing spaces that foster innovation, cultivate collaboration and drive the next great discovery for humanity. Bring your expertise, collaborative spirit to team and we will help you to grow, pursue & fulfill what drives you. As the largest professional services provider to the pharmaceutical and biotechnology industries, we are recognized expert in clean manufacturing, specialized manufacturing, research and development laboratories and data centers. We provide end-to-end client solutions for highly specialized facilities around the world. Our technical knowledge allows us to meet the challenging demands our clients face to deliver products that make people’s lives better. Here’s What You Need Planning / guiding a team of Revit modelers in developing BIM model meeting LOD 100 to 350 requirements during various phases of the projects Reviewing the model / ensuring quality control on the model / guiding the modelers in extracting layouts from the 3D model like HVAC equipment layout / ducting layouts Preparation of site works tender Preparation of cost estimation for the HVAC part of the project Procurement assistance like providing technical clarifications, participating pre bid / post bid meeting / technical bid analysis / preparation or order specification Vendor drawing review Providing clarification to request for information from site during construction Visiting sites for residual engineering / resolving site queries Coordination with various stake holders like Client / various internal disciplines like projects / electrical / mechanical / architect / civil / vendors for effective engineering management Ensuring HVAC engineering execution within the budget / on time / meeting the quality set for the project and to the satisfaction of all the stake holders Providing Management Information for the HVAC engineering part of the project Providing information for & Attending Project review meeting / Internal review meetings / Management review meetings Preparation of HVAC engineering effort estimation Knowledge of HSD system We value collaboration and believe that in-person interactions are crucial for both our culture and client delivery. We empower employees with our hybrid working policy, allowing them to split their work week between Jacobs offices/projects and remote locations enabling them to deliver their best work. Here's what you'll need Minimum Job Requirements BE Mechanical Engineer – Specialization in HVAC Design Experience. Minimum 14 years of experience out of which at least 5 years in HVAC Engineering of Data Centre/ Industrial /Pharma/ FMCG projects is preferred Jacobs. A world where you can. From our inclusive employee networks to our positive mental health champions – we’re committed to driving a culture of caring where you can be you. Joining Jacobs not only connects you locally but globally - and together, our diverse perspectives and unique backgrounds power our collective strength. We collaborate and share! By supporting one another, we all succeed. With safety and flexibility always top of mind, we’ve gone beyond traditional ways of working so you have the support, means and space to maximize your potential. You’ll uncover flexible working arrangements, benefits and opportunities to do good too – from participating in our global giving and volunteering program, to exploring new and inventive ways to help our clients make the world a better place. No matter what drives you, you’ll discover how you can cultivate, nurture and achieve your goals – all at a single global company. Show more Show less

Biocon Biologics is a fully integrated ‘pure play’ biosimilars organization globally committed towards transforming patient lives through innovative and inclusive healthcare solutions. It is engaged in developing high-quality, affordable biosimilars aimed at expanding patient access to cutting-edge class of therapies across the world. Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led-global biopharmaceuticals company and India's first publicly listed biotech enterprise. Biocon Biologics has one of the largest biosimilars portfolios, a wide global footprint, state-of-the-art manufacturing facilities, world-class R&D ecosystem, and high quality & compliance standards, enabling it to fulfil unmet needs of patients across the globe. Job Description. 1. Handling of OOS and OOL Investigation related to Environmental excursions and ensure closure of report on time and before batch release as applicable (report preparation, report review and closure). 2. Initiation of CAPA related to OOS and OOL for Environmental excursions and ensure its closure. 3. Keeping online tracking sheet for OOS/OOL. 4. Training of manufacturing personnel on relevantSOP's.5. Ensuring audit Compliance for Fill Finish Production. 5. Ensure the microbial events related to product (Deviations, OOS/OOTs), and microbial water excursion (OOS) investigations are timely conducted, and root cause analysis is identified out and appropriate CAPAs are identified to avoid repeat occurrence. 6. Timely assess the impact due to microbial excursion on the ongoing batches and subsequent batches and propose recommendation to the site. 7. Review of Investigation reports for data furnished for correctness of statements, evidence-based review and ensure no errors in the data and conclusions derived. 8. Involve in management review meetings to present the microbial excursions and status of closures. 9. Provide inputs during trending of microbial related deviations, OOS and propose recommendations and aseptic practise review. 10. Ensure oversight on microbial related investigations, to ensure consistency of global standards, harmonization, sharing of best practice. 11. Drive continuous improvement in microbial investigations to meet and sustain compliance with internal and external regulatory requirements. Qualifications and Experience BSc/MSc Microbiology or biotechnology or equivalent experience. 13 + Years Relevant Experience. Microsoft Office (Outlook, Excel, Word, PowerPoint, etc.) Organized Strong leadership skill Show more Show less

Job Overview Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may include safety data collected from clinical trials and/or post marketing settings (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the client and/or the regulatory agencies (if required) within the agreed/stated timelines. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. Responsible to provide all clients, both internal and external, with the appropriate quality of service in a safe and costeffective manner. The role will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Perform case intake and triage of the incoming safety information or reports from various sources either spontaneously or from a clinical trial. Assist with processing of the adverse events, including but not limited to: Data entry of safety data onto adverse event tracking systems. Write patient narratives and code adverse events accurately using MedDRA (for Marketed products, if applicable). Assist in the listedness assessment against appropriate label (for Marketed products, if applicable). Assist in generation of queries and collection of missing or discrepant information in consultation with medical staff, if needed. Submission of expedited SAE reports to clients, regulatory authorities, ethics committees, investigators, 3rd party vendors, Partners and Fortrea project personnel, as required within the agreed timelines. Assist with processing and submission of expedited and periodic reports to worldwide regulatory agencies or other recipients (Clients, Regulatory Authorities, Ethics Committees, investigators and Fortrea project personnel etc.), and prioritize the reports for processing and submission within the regulatory and/or study specific applicable timelines. Assist in the reconciliation of databases, as applicable. Work within the Quality Management System framework, including but not limited to Standard Operating Procedure (SOP), departmental Work Instructions (WIs) etc. as appropriate. Assist in the maintenance of supporting files/ documentation regarding adverse event reporting requirements in all countries, if applicable. Support upload/archival of case/study/project documentation, as appropriate. Build and maintain good PSS relationships across functional units. Support compliance of operations with governing regulatory requirements. All other duties as needed or assigned. Qualifications (Minimum Required) Healthcare professionals with 0 to 6 months relevant experience. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. To be used in lieu of experience, Degree required to be in one or more of the following disciplines: Pharmacy, Nursing, Medical Sciences, Life Sciences, or related area *Safety experience includes actual experience of processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions. ** Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, working in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitoring, Regulatory Affairs, or Quality Assurance. Experience (Minimum Required) Attention to detail. Team player. Solid written and verbal communication skills. Accurate math and spelling skills preferably with an aptitude for handling and proof-reading numerical data. Knowledge of MS office Windows applications beneficial. Ability to operate standard office equipment. Physical Demands/Work Environment Office Environment Learn more about our EEO & Accommodations request here. Show more Show less

Arboreal is an award-winning food ingredients manufacturing and supply company. Arboreal is co-founded by Swati Pandey (IIT, Imperial College London) and Manish Chauhan (BITS Pilani, London Business School) and has won various accolades over time including but not limited to the National Startup Award for Food Processing by Startup India, WTI Award by NITI Ayog and Cartier’s Womens Initiative Awards (adjudged by Mckinsey, INSEAD Business School & Cartier) as the Top Venture in Asia Pacific. We are looking for a Junior Production Officer, who will play a key role in supporting the smooth, safe, and efficient operation of the production line. Your focus will be on maintaining food safety, ensuring quality standards, optimizing processes, and collaborating across departments to meet production goals. Key Responsibilities: Production Oversight : Monitor daily production activities, ensuring adherence to schedules, safety protocols, and operational standards. Quality & Compliance: Conduct regular quality checks and ensure compliance with food safety regulations (HACCP, GMP). Food Safety & Sanitation: Uphold hygiene standards and maintain a clean, safe work environment. Process Improvement: Identify inefficiencies and support implementation of corrective actions to improve productivity. Team Training: Assist in training and mentoring junior staff to build operational capability and ensure process consistency. Equipment Support: Help with setup, cleaning, basic maintenance, and troubleshooting of machinery and equipment. Documentation & Reporting: Maintain accurate records of production activities and compliance reports. Cross-Functional Collaboration: Coordinate with Quality, Maintenance, and Supply Chain teams to ensure smooth operations. Inventory Support: Assist in raw material inventory checks and stock-level monitoring. The ideal candidate will have; Graduation in Food Technology / Biotechnology 1-2 years’ experience in Quality and Production Understanding of basic food production and equipment operation. Familiarity with food safety standards (e.g., HACCP, GMP). Strong organizational and time management skills. Team player with good communication and interpersonal skills. Attention to detail and ability to follow SOPs. Basic computer literacy for data entry and reporting. What we offer An opportunity to work in a fast scaling award winning startup A meritocracy and performance driven culture Non linear compensation growth Please do not apply if: You do not have relevant experience. You are not based in Lucknow and unwilling to relocate to Lucknow. If you do not hear back from us, within 3 weeks of your application, please assume that your application was unsuccessful in this instance. Show more Show less

Job Type Full-time Description The Operating Room Clinical Specialist plays a vital role in supporting our field sales initiatives and external medical education efforts within the operating room environment. This position is part of the Medical Affairs team and focuses on KOL recruitment and development, while also enhancing peer-to-peer engagement. The Operating Room Clinical Specialist works either from a home office or a Kerecis office and reports directly to the Director of Medical Affairs. Essential Functions Field Sales Support Provide clinical expertise and support to field sales teams within the operating room business unit Assist in training sales personnel on product knowledge, clinical applications, and evidence-based practices related to Kerecis products Conduct product demonstrations and educate healthcare professionals on the benefits and usage of our medical devices Customer Relationship Management Build and maintain strong relationships with key healthcare professionals and stakeholders in the operating room environment Understand their clinical needs, address challenges, and identify opportunities to enhance the adoption of Kerecis products Key Opinion Leader (KOL) Engagement and Development Recruit and cultivate relationships with KOLs and healthcare professionals to support external educational initiatives and clinical research programs Facilitate engagement through organized discussions, workshops, and research collaborations External Medical Education Lead the development and execution of external medical education programs, creating scientific materials, presentations, and training modules Provide clinical support at conferences and educational events, ensuring that healthcare professionals receive comprehensive information about Kerecis products and their applications Cross-functional Collaboration Collaborate with internal teams, including sales, marketing, and clinical affairs, to align and execute on medical education and engagement initiatives Foster cohesive communication and teamwork to support overall business goals Compliance and Regulatory Affairs Ensure that all activities comply with U.S. laws, regulations, and industry standards Assist in the preparation and submission of regulatory documents pertinent to medical education initiatives Data Analysis and Communication Demonstrate an aptitude for digesting clinical research and effectively communicate key insights to internal stakeholders and external partners Prepare reports and presentations that succinctly summarize important findings and implications for clinical practice Requirements Education & Experience Bachelor's degree from an accredited college or university in life sciences, medical sciences, or a related field; advanced degree preferred Minimum of 5 years of experience in medical education or related roles within the biotechnology or medical device industry Competencies & Attributes Strong project management skills with the ability to deliver results on time Excellent communication and interpersonal skills for effective collaboration with various stakeholders Knowledge of medical device regulations, compliance requirements, and industry guidelines Familiarity with clinical research processes Proficiency in data analysis and scientific documentation Exceptional attention to detail and organizational capabilities Anticipated travel: 75-80% This job description is not intended to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this role. Duties and responsibilities may change at any time. Kerecis is an equal opportunity employer. Show more Show less

About Clarivate Clarivate provides innovative data and analytical solutions to the largest biopharmaceutical and medical technology companies in the world. Clarivate’s Medtech Data team harnesses real-world healthcare data and identifies meaningful insights from large data and metadata sources to help medical device companies make some of their most important business decisions. Who are you? You are passionate about data and have at least 2 years of hands-on experience wrangling through large data using SQL/ Python. You are also an effective communicator who can explain complex ideas using clear and concise language, including through written communication. You are comfortable collaborating with a diverse group of internal colleagues, including subject matter experts, product managers, sales leaders, technical experts, and other client-facing analysts. You are solution-oriented and understand the importance of timely execution while juggling multiple priorities. What will you do? Understand the worldview and pain points of Clarivate customers, working closely with the stake holders as a problem-solver. Effectively build, mine, and manage multiple datasets, which will be required for market modelling and analysis. Maintain existing Medtech product catalogs. Research and understand novel device markets, including major competitors, uses, and product segmentation. Evaluate data outputs for market trends and draw insights; correct any potential errors and issues. Identify opportunities and issues for data analysis and experiments, with bias towards driving customer delight. Work with clients to understand the business requirements and provide data driven insights. Contribute your vision; influence the evolution of our products, data models, and data usage strategy. What do you know? You have strong quantitative foundations, as evidenced by your educational and professional background. You are more than proficient with Excel, SQL and want to continue to improve your skills. You have a background and/or interest in Life Sciences and are keen to learn a lot more about medical devices and supplies in Latin American region. You know how to deliver an effective presentation. Requirements Expertise in understanding data variables and connecting the dots in various datasets. Expertise in handling and manipulating large datasets. Proficiency with written and oral communications and must be able to communicate complex quantitative ideas to internal and external stakeholders. Should have handled short/long term projects end to end. Skills Expertise in MS SQL. Strong MS Office and Excel skills is mandatory. Analytical Skills Ability to do secondary research and synthesize the findings. Problem solving ability. Education Any graduate/ Post-graduate, B.E or M.Sc. in the disciplines of Biotechnology, Medical Electronics, Pharmacy preferred. Preferred (Good To Have) Skills Understanding of Medtech data and Healthcare in the Latin American countries Exposure to Medtech or Claims/Pharmacy data. Experience working with data from data vendors. Expertise in anyone (or more) of the data analysis tools/languages such as – R/Python is a plus. Work Mode: Hybrid, Monday to Friday 12:00 pm to 8:00 pm At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations. Show more Show less

Immediate Hiring !! Designation: Medical Coder . Salary: Upto 20k PM + Incentives. Shift : General, Day. Skills: Anatomy, Physiology, Pathology. Location: Chennai, Coimbatore, Bangalore. Required Candidate profile Eligibility: UG or PG or Diploma ( 3 Years) Specialization: Life Science, Non - Life science , Para-Medical & Medical Studies. Passout: 2020- 2025

Hiring to conduct patent searches, analyze the latest technologies, and create detailed patent reports on inventions. Selected candidates will undergo training with skills in patent analysis, candidates will work as Analyst Required Candidate profile Strong knowledge of biotechnology Proficiency in MS Excel for data analysis and reporting Excellent writing and communication skills Provide a minimum of two references along with their resume.

🔹 Job Title: Freelance Subject Matter Expert (SME) – Pharmacy Subjects 📍 Employment Type: Freelancer 🌐 Location: Work From Home 📢 Open Positions (Subject-wise): Pharmacology Pharmaceutical Chemistry Pharmacognosy Pharmaceutics Allied Subjects (Biochemistry, HAP, Biotechnology, etc.) 🎓 Qualification & Eligibility: Must hold or be in the final year of a B.Pharm degree. Strong command over the selected subject area. 🧠 Experience: 0 to 1 year of relevant experience. Freshers with good knowledge are welcome. 💼 Skill Set Requirements: Basic understanding of Google Suite (Docs, Sheets, Drive, etc.) Clear understanding of quality standards in academic question creation. Must have appeared for Pharmacy entrance/competitive exams like GPAT, NIPER, Drug Inspector, etc. 📌 Roles & Responsibilities: Create high-quality, original, and exam-relevant MCQs and questions for: GPAT NIPER Drug Inspector Exams Ensure academic accuracy, clarity, and relevance of content. Follow the prescribed format and quality benchmarks. 💻 Work Mode: Remote/Freelance – flexible working hours. If you are passionate about pharmacy education and want to contribute to helping aspirants succeed, apply now! Show more Show less

Patent Writing for United States Patent and Trademark Office Kindly provide minimum two references with resume

Patent Writing for United States Patent and Trademark Office Kindly provide minimum two references with resume

Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced professionals to join us as we prepare to launch of 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’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member: Help establish and lead operations at our newest location. Immediate Impact: Your experience will directly influence Medpace’s growth in the region. Career Growth: As the office grows, so will the leadership and advancement opportunities. Global Reach: Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture: Join a company known for its stability and commitment to professional development. Support & Infrastructure: While the Hyderabad office is new, you’ll be backed by the global resources and processes of a well-established CRO. If you’re looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that’s investing in your region — we’d love to hear from you. Help shape the future of Medpace in Hyderabad. Apply today. Responsibilities Compile and maintain project-specific status reports and project timelines associated with Imaging studies; Maintain inventory of imaging supplies for study sites; and Interact with study sites and internal associates. Qualifications Bachelor’s Degree (required), Master's or PhD (preferred) in Biomedical Engineering Prior research related experience is preferred; and Excellent computer, organizational and communication skills. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. 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 next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

Our global activities are growing rapidly, and we are currently seeking a full-time, Pune-based Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Develop, program, validate and maintain clinical trial databases according to company standards; Maintain and contribute to company library of standard CDASH compliant CRFs ; and Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards. Qualifications Bachelor’s degree/Advanced degree in Life Sciences or Computer Science or equivalent; 2-3 years of Rave study build experience in a similar position in Pharma/Healthcare sector; Custom function (C# Programming) experience is preferred; Certified Medidata Rave Study Builders preferred; Excellent verbal and written communication skills; and Meticulous attention to detail. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Hybrid work-from-home options (dependent upon position and level) Competitive PTO packages Company-sponsored employee appreciation events Employee health and wellness initiatives Flexible work schedule Competitive compensation and benefits package Structured career paths with opportunities for professional growth 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 next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

Job ID 75702 Job Title : Associate Account Manager-Romer Lab Ingredients Solution,India Job location : Banagalore Job Type: Hybrid The Sales Manager is responsible for managing business development activities with a primary focus on prospecting new opportunities in Food Safety products with a specific focus on Mycotoxin, Allergen, Food Pathogen, GMO, Sampling and Hygiene products. Defining and driving strategies and ensuring the achievement of sales, lead generation and pipeline growth is a key objective, the Sales manager will be responsible for revenue target for South india and will have a strong role in contributing to India region overall success. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your Key Responsibilities Provide new sales opportunities and drives technical validations in Regulatory Departments, Global Key Accounts and Regional Key Accounts across South India region will be primary objective of this position and will involve working closely with cross functional teams within Romer Labs India Strategic Business Unit Partners with APAC Regional Business and Application Teams on customer visits to provide strong commercial support, and assist in the promotion of Mycotoxin, Allergen, Food Pathogen, GMO and Hygiene products (CytoQuant) at all marketing events and activities Work closely with Distributors, Channel Partners and India Management Team will also be part of a daily routine Responsible for salesforce.com processes such as provide quotation to distributors for special cases or projects and closing orders Manage Global Key Account at regional level and responsible for achieving the Global Key Account sales and targets attainment in South India Responsible for forecasting and sales tracking, and to achieve the revenue and profitability targets for Romer Labs products Conduct product demonstrations, global training program, organize workshops and seminars regionally in South China Responsible to support customers on-site validations and execute experimental protocols to gain qualifications and order success Assist and collaborate with regional marketing team in the development of sales support materials and marketing campaigns Drives brand awareness of products, conduct training and seminars for clients, channel partners and sales team Maintains contacts with local business and technical associations and network with industry key opinion leaders in South India to expand sales opportunities Responsible for daily salesforce.com engagement to support opportunities tracking You Bring Bachelor’s degree in Food Technology, Biotechnology, Microbiology, Biomedical Science, or related field, with 6–8 years of experience in sales and business development. Proven sales leadership with a successful track record in driving results and developing talent, including channel partner management. Strong closing skills and preferably trained in Customer Focus Selling; prior experience in food safety diagnostic kits is a plus. Excellent communication, presentation, and interpersonal skills. Highly motivated, goal-oriented, and passionate about the food safety industry with strong networking abilities. Willingness to travel frequently based on business requirements. We Bring Opportunity to participate in the most important national and international fairs and industry events Great products; Exciting and challenging tasks in well-established, developing and new markets You are part of an international team which operates globally A team of diverse employees who aren’t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. The application process Interested in this position? Please apply on-line by uploading your resume in English via our career portal. Equal Opportunities Commitment dsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress. We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate: there's a place for everyone at dsm-firmenich. dsm-firmenich is an Equal Opportunity and Affirmative Action Employer. dsm-firmenich people are as diverse as our customers. For us that includes a commitment to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. About Dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world's growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than €12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life™ every day, everywhere, for billions of people Show more Show less

Are you a Business Development Manager passionate about e.g. driving sales for innovative healthcare products? If so, this opportunity could be for you! Join us in at B. Braun in India, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare! As a Business Development Manager at B. Braun Group you will play a vital role maintaining efficient production processes for the manufacturing of our high-quality medical products. Key Responsibilities Manages sales activities for a range of products Responsible for executing the sales strategy to achieve the sales targets by cascading and amalgamating Marketing Strategy and focus with Field Effort Strategy. To manage the sales force (as per organization structure, if any) to meet the company’s sales goals To Train team members regularly KRAs & Specific Roles Customer management Develop strong Key Opinion Leader (KOL) base Understanding the market, the customer and the competition To Establish & monitor strong distribution network in the territory Manage client relationship effectively Collecting customer feedback regularly & take necessary actions Maintains and expands customer base & identifies new customer opportunities To ensure market development and brand establishment To monitor Receivables as per divisional guidelines Target achievement Achieving sales as per targets in terms of value & units assigned Achieving desired market shares in defined area Develop new accounts Timely submission of tenders & relevant information to Sales admin Reports Sales Forecast to be submitted every month Submission of sales reports on a monthly basis Monthly review of sales targets of self & team Matrix working CO ordinate with teams to develop & grow sales Creating a sales plan Making joint calls with TSE/TSMs Conducts one-on-one and group sales presentations Create awareness of products, conduct training and seminars for clients and sales team Guiding and mentoring the teams Develop Strong KOL relationship Create strong user base for consumables What You Will Bring To The Team Show Trust, Value Diversity, Be Accountable to performance delivery. Initiative and execution towards active learning in order to be competitive and effective. Ability to plan logically and conduct numerical analysis. Innovativeness and ability to drive ideas and change and include different perspectives. Positive influencing and negotiating skills and ability to act with customer focus for effective Customer Management. Excellent written, communication & listening skills and empathy. Demonstrate performance and result orientation and utmost integrity , equity. Educational Qualification And Experience Graduation in Science in a must. Graduation in Pharmaceuticals,Biotechnology, Biomedical engineering would be an added advantage. Masters in Bachelor of science/Pharmacy/. Post graduation in Management is preferred. Experience: 10-13 years of total sales experience of which 4 years of managerial experience (Most Preferred - medical device / equipment industry , Preferred - Health care and Pharmacy/ desirable) Experience in Sutures and Bio-Surgicals would be preferable. Should be willing to travel 100% of the work time. What sets B. Braun apart? B. Braun is one of the world's leading medical technology companies headquartered in Germany. We are proud to say that since the inception of our India operations in 1984, we have made significant strides in the Indian healthcare market. We supply more than 5,000 products and 120,000 articles in areas like anaesthetics, intensive care medicine, cardiology, extracorporeal blood treatment and surgery. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision – to protect and improve the health of people around the world. What can we offer you? Exciting sales incentives Mediclaim & life insurance Recognition & rewards to celebrate your efforts. Learning programs & skill development to accelerate your growth. Global exposure to broaden your horizons. Paternity & birthday leave for life’s special moments. Mental wellness support with counselling and mindfulness sessions. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on Social Media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube Show more Show less

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Medical Writer to join our Core Labs in Mumbai office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. Responsibilities Generate, revise, and maintain clinical documents; Coordinate quality control of documents and maintain audit trail of reviews and changes; Provide input on data analysis planning and its impact on clinical document outcome ; and Performs other duties and responsibilities as assigned. Qualifications Master’s degree in a health or science-related field; Possess strong communication skills (oral and written); Intermediate knowledge of medical terminology and clinical patient management; Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. 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 next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

Hiring to conduct patent searches, analyze the latest technologies, and create detailed patent reports on inventions. Selected candidates will undergo training with skills in patent analysis, candidates will work as Analyst Required Candidate profile Strong knowledge of biotechnology Proficiency in MS Excel for data analysis and reporting Excellent writing and communication skills Provide a minimum of two references along with their resume.

Hiring to conduct patent searches, analyze the latest technologies, and create detailed patent reports on inventions. Selected candidates will undergo training with skills in patent analysis, candidates will work as Analyst Required Candidate profile Strong knowledge of biotechnology Proficiency in MS Excel for data analysis and reporting Excellent writing and communication skills Provide a minimum of two references along with their resume.

Job Description: Applications are invited for the post of Project Research Scientist – I (Non-Medical) for the ICMR New Extramural (First in the World Challenge) grant in the Centre for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT). (No. EM/Dev/FIW/00252/2024 (E-Office-227016)). Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have First class post graduate degrees with PhD degree in relevance to nano technology, nano-delivery, biological therapeutics, pharmaceutical sciences, Biotechnology, Desirable experience: PhD thesis submitted or having Research fellow experience or having previous experience in nano/liposomal formulation, stability and characterization. Stipend: Rs. 56,000 + 10% HRA (Rs. 61,600) per month, stipend will be as per Institute norms. Sponsoring Agency: ICMR, New Delhi Duration: 3 years Principal Investigator: Dr. Natarajan Chandrasekaran, Professor, Higher Academic Grade, Centre for Nanobiotechnology (CNBT), Vellore Institute of Technology (VIT) Vellore – 632 014, Tamil Nadu Co-Principal Investigator: Dr. George Priya Doss C, Professor Grade 1, Department of Integrative Biology School of Bio Sciences and Technology Vellore Institute of Technology (VIT) Vellore – 632 014, Tamil Nadu Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (10/06/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

A leading KPO/ BPO / ITES sector company servicing international clients for several decades requires # BScs / M.Scs / BPharm / BTech in Bioinformatics, Biotechnology & Biochemistry and other Life Sciences. # Graduates/Post Graduates in Chemistry / Chemical technology Work respectively involve data capture, extracting, document summary and analysis, data analytics etc Part Time / Freelance / External working and Work From Home WFH for selected areas of work. Freshers can also apply. Attractive remuneration for part time / freelancers / external and work from home Job Types: Full-time, Part-time, Permanent, Fresher, Freelance Pay: ₹12,000.00 - ₹15,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person Expected Start Date: 04/10/2025

FICCI Research & Analysis Centre is hiring for the position of Quality Assurance Executive 📍 Location: Dwarka Sector-8, New Delhi 🕒 Employment Type: Full-time 🔍 Role Summary: We are looking for a dedicated and detail-oriented Quality Assurance Executive to support and strengthen our lab's Quality Management System (QMS). This role plays a key part in ensuring consistent compliance with ISO 17025:2017 and maintaining the lab’s accreditation readiness. As a QA Executive, you will contribute to internal audits, management review meetings (MRMs), and implementation of QMS protocols. This is an excellent opportunity for someone with 1–4 years of experience who is passionate about quality, documentation, and regulatory compliance in a laboratory environment. Success in this position means proactively maintaining quality standards, supporting audit processes, and driving continuous improvement. You will play a critical role in upholding our lab’s reputation for excellence. 🛠️ Responsibilities: Assist in the implementation and maintenance of the laboratory QMS in accordance with ISO 17025:2017. Coordinate and participate in internal audits, identify non-conformities, and ensure timely corrective actions. Support the planning and execution of Management Review Meetings (MRM) and maintain records. Prepare and maintain controlled documents, SOPs, and quality records. Assist in audit preparation and participate in external audits including NABL assessments. Promote awareness of quality standards and best practices among lab staff. ✅ Qualifications: Master’s degree in Science or Technology disciplines (Chemistry, Biotechnology, Environmental Science, etc.). 1 to 4 years of experience in a quality assurance role within a laboratory or testing facility. Solid understanding of ISO 17025:2017 and its application. Experience in QMS implementation, document control, and compliance. Hands-on experience in conducting or assisting with internal audits. Familiarity with NABL audits and accreditation processes. Strong analytical thinking, attention to detail, and communication skills. 📩 Are you committed to quality and compliance? Join a team that values precision and integrity. Apply today or refer someone who might be a perfect fit! Share your CVs at hr1@fraclabs.org or bawna@fraclabs.org hashtag #Hiring hashtag #QualityAssurance hashtag #QAExecutive hashtag #ISO17025 hashtag #QMS hashtag #InternalAudit hashtag #NABL hashtag #LabCompliance hashtag #QualityManagement hashtag #ScienceJobs hashtag #JoinOurTeam Show more Show less

Role & responsibilities: Killed Vaccine production as per planning. Operate and clean production equipment (CIP/SIP) and maintain logs as per cGMP guidelines. Coordinate with QC department regarding results Prepare and maintain Batch Manufacturing Records (BMRs) and deviation reports Collaborate with QA/QC, Engineering, and Validation teams during audits and batch reviews Support scale-up and technology transfer activities for killed vaccine processes. Education: B.Sc & M.Sc (Microbiologist / Biotechnology) Experience: 2 to 4 years in vaccine production Salary Range: 2 to 4.5 Lac Job Location: Kadi, Gujarat (Bus transport facility available from Ahmedabad, Kalol & Kadi) Interested candidate can share their resume on careers@hester.in Show more Show less