71 Bioengineering Jobs - Page 3

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Role: Bioproduction Group, Purification and Pharma Analytics division is seeking a motivated and dedicated protein purification Field Application scientist to support Poros and CaptureSelect (CS) resin design in, optimization and troubleshooting at Downstream purification and process development primarily for novel therapeutic monoclonal antibody products including bispecifics, Vaccines and general bioprocessing throughout all stages of clinical trials at key bioprocessing customer sites in India. Responsibility Conduct routine Knowledge culture seminars to highlight Poros and CS resin technology and application at key customer sites Initiate and support customer evaluation of resins with SOP and guidance on process development / evaluations Work closely with BPG cell culture team and map ongoing molecule / process development ay key customer sites to ensure technical engagement and awareness of resin solution Support customer with high-throughput protein purification process development using Poros and CaptureSelect resin Support and guide customers in downstream process development, optimization, and scale-up manufacturing, including column packing support and CIP Map customer problems and develop solutions needed optimization of process on Poros and CaptureSelect resins Champion Poros, CS technology and applications and present data at Key conferences and events Empower customers on to new technology and NPI solutions Meet country specific design in and process development targets Education And Experience Master’s degree or Doctoral degree (Ph.D.) in biochemistry, bioengineering, biology, chemistry or related fields, preferably with some relevant industry experiences with 3 to 5 years of demonstrated ability in downstream process development or manufacturing Knowledge, Skills and Abilities: Good knowledge in protein chemistry and bioprocessing Previous Field based application support experience. Good knowledge and hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology; TFF Experiences in using AKTA line of purification instruments Experiences in using ultrafiltration/diafiltration instrument for buffer exchange, product concentration, and formulation Experiences in protein analysis such as HPLC, CGE, ELISA, etc. is a plus Good verbal and written communication skills, organized, coordinated, independent, meticulous Ability to multitask on different projects and work with multiple customers locally, regionally & globally Able to perform successfully under pressure while prioritizing and handling multiple projects or activities Ability to travel extensively and provide sustained customer support Benefits We offer attractive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Apply today http://jobs.thermofisher.com. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

ADVERTISEMENT Department of Biological Sciences and Bioengineering Advertisement Number: P.Rect./R&D/2025/122 Applications are invited for the post of Deputy Project Manager under the guidance of Dr. Amitabha Bandyopadhyay, Department of Biological Science and Bioengineering, Indian Institute of Technology, Kanpur. This Post is purely temporary and contractual basis. Designation: Deputy Project Manager Number of positions: One Minimum Qualification: Master’s degree (MA/M.Sc./MBA) with a minimum of 6 years of experience of working in an experimental developmental biology laboratory or other department. Tally & CCC certification & Diploma in office management is necessary. Desirable : Experience in purchase procedures both Import and local purchase, maintaining the stock registers, Vendor management, and bill processing for purchases, Audit and Stock Verification, Administrative and managerial skills, Handling Recruitment Process and Administration, Knowledge of Office Procedures and knowledge of computer i.e., MS Office suite. Duration : Initially for one year and extendable on the basis of performance. Salary : In the range Rs. 23,000 – 2,000 – 59,000/- per month (Consolidated). Last date for receipt of application: 14 th July 2025 , till 5:30 PM. Application Process: Instructions for Candidates : All candidates are requested to duly fill Form 303 (Download link provided below), self-attest all supporting documents, and submit the complete application through the Google Form. Please ensure the following steps are completed: Download and fill Form 303 – https://www.iitk.ac.in/dord/data/303.pdf Self-attest all supporting documents. Fill the Google Form https://forms.gle/Sw7zZKw14adxypRq9 and upload all required documents, including the completed Form 303. Note: Submission of the application is to be done only through the Google Form. No physical copies or email submissions will be accepted. Selection Procedure: The selection will be based on offline interview at IIT Kanpur. Short listed candidate will be informed with an email about the date and time of the interview. Dr. Amitabha Bandyopadhyay Department of Biological Sciences and Bioengineering Indian Institute of Technology Kanpur 208016

ADVERTISEMENT Department of Biological Sciences and Bioengineering Advertisement Number: P.Rect./R&D/2025/109 Applications are invited for the post of Project Multi Skilled Worker (L- 3) under the guidance of Dr. Amitabha Bandyopadhyay, Department of Biological Science and Bioengineering, Indian Institute of Technology, Kanpur. This Post is purely temporary and contractual basis. Designation: Project Multi Skilled Worker (L-3) Number of positions: One Minimum Qualification: 8 th class with a minimum of 15 years of experience of working in an experimental developmental biology laboratory or other department . Desirable : Preference will be given to the candidate having at least 15 years of experience in handling biological laboratory such as autoclaving, media preparation, washing, cleaning and maintenance of machines. Duration : Initially for one year and extendable on the basis of performance. Salary : In the range Rs. 12000-600-36000/- per month (Consolidated). Application Process: Instructions for Candidates : All candidates are requested to duly fill Form 303 (Download link provided below), self-attest all supporting documents, and submit the complete application through the Google Form. Please ensure the following steps are completed: Download and fill Form 303 – https://www.iitk.ac.in/dord/data/303.pdf Self-attest all supporting documents. Fill the Google Form https://forms.gle/Sw7zZKw14adxypRq9 and upload all required documents, including the completed Form 303. Note: Submission of the application is to be done only through the Google Form. No physical copies or email submissions will be accepted. Last date for receipt of application: 14 th July 2025, till 5:30 PM. Selection Procedure: The selection will be based on offline interview at IIT Kanpur. Short listed candidate will be informed with an email about the date and time of the interview. Dr. Amitabha Bandyopadhyay Department of Biological Sciences and Bioengineering Indian Institute of Technology Kanpur 208016

NHS Greater Glasgow and Clyde is one of the largest healthcare systems in the UK employing around 40,000 staff in a wide range of clinical and non-clinical professions and job roles. We deliver acute hospital, primary, community and mental health care services to a population of over 1.15 million and a wider population of 2.2 million when our regional and national services are included. The shift pattern for this post is Monday to Friday. This is a highly rewarding role that provides opportunities for varied and challenging work as the Head of Electronic Engineering for the Medical Devices Unit (MDU), a multi-disciplinary clinical engineering team supporting innovation projects to improve patient diagnosis, treatment and care. MDU staff also provide equipment repair, maintenance and calibration services. The successful candidate will lead a small team of electronic engineers delivering a range of services in support of the wider objectives of the MDU. You will manage the design and development of medical electronic systems to deliver innovative and cost-effective healthcare solutions as part of a wider initiative which focuses on translational research and the development of collaborative projects between NHS Greater Glasgow & Clyde, academia and industry. You will ensure that medical device technical documentation complies with the MDU’s ISO 13485 certified Quality Management System (QMS). You will also manage a calibration service for medical test and diagnostic equipment in compliance with an ISO 55001 certified QMS and will explore service improvement opportunities including UKAS accreditation and service expansion. As the lead for electronic engineering in the Department of Clinical Physics and Bioengineering (DCPB), you will provide expert advice and guidance to clinical and technical staff and will regularly update your technical and regulatory knowledge as it applies to electronic systems with healthcare applications. You will be involved in the strategic development of the MDU and will also take a leading role in the development of its services and systems. You will be a committed, energetic and self-motivated person with good team-working skills and excellent communication and presentation skills. You will be able to demonstrate the following essential attributes: Strong analytical and problem-solving skills; an excellent grasp of state of the art analogue and digital electronics techniques and their application; sound knowledge of electronic design, prototyping and production using industry standard tools; experience of working under Quality Management Systems in a safety critical environment; practical, in-depth experience of a broad range of complex electronic instrumentation; project management of complex electronic design and development projects; and training of technical and scientific staff. Ideally you will have experience of medical equipment and instrumentation and related regulations and standards. You will have an MSc/MEng in Electrical and Electronic Engineering, or other appropriate discipline from a recognised University; or BSc/BEng with profile of knowledge and training equivalent to MSc/MEng. Preferably, you will be a Chartered Engineer, registered with a professional industry body and the Engineering Council. You will normally work 37 hours a week, Monday to Friday. Occasional travel may be required to attend off-site meetings and events. This is a permanent position with a competitive salary and generous holiday entitlement. Informal Contact: Robin Sayer, Head of Mechanical Engineering at Robin.Sayer2@nhs.scot or 0141 211 0091. Details on how to contact the Recruitment Service can be found within the Candidate Information Packs NHS Greater Glasgow and Clyde encourages applications from all sections of the community. We promote a culture of inclusion across the organisation and are proud of the diverse workforce we have. By signing the Armed Forces Covenant, NHSGGC has pledged its commitment to being a Forces Friendly Employer. We support applications from across the Armed Forces Community, recognising military skills, experience and qualifications during the recruitment and selection process. Candidates should provide original and authentic responses to all questions within the application form. The use of artificial intelligence (AI), automated tools, or other third-party assistance to generate, draft, or significantly modify responses is strongly discouraged. By submitting your application, you confirm that all answers are your own work, reflect your personal knowledge, skills and experience, and have not been solely produced or altered by AI or similar technologies. Failure to comply with this requirement may result in your application being withdrawn from the application process. For application portal/log-in issues, please contact Jobtrain support hub in the first instance.

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . The Data Scientist II will play a crucial role in supporting operational analytics across GPS to ensure products continue to serve most pressing GPS analytics needs, with potential opportunities to build new advanced analytics capabilities such as predictive modelling, simulation, and optimization. The Data Scientist II should have a strong interest in solving business problems, and an eagerness to work on all parts of the analytics value chain, from partnering with IT on data pipelines to operationalizing predictive models in the service of our patients around the world. Roles & Responsibilities Conduct analysis and interpretation of complex data sets to derive meaningful insights and recommendations based on an understanding of GPS priorities, critical issues, and value levers. Collaborate with stakeholders to identify business problems, goals, and KPIs to to design, establish and maintain data pipelines, models and business facing reports and dashboards. Design, develop, and implement a broad array of GPS analytics that solve complex problems in a computationally efficient and statistically valid manner. Identify and implement enhancement and automation of high-value analytics while ensuring they continue to function efficiently. Collaborate proactively with IT teams to develop and enhance data infrastructure, data pipelines, and analytical tools for efficient data collection, processing, and analysis. Prepare reports, dashboards, and presentations to communicate analyses to stakeholders at various levels of the organization. Follow technical best practices in building, maintaining, and enhancing analytics output with scalable solutions, including code version control, pipeline management, deployment, and documentation. Provide training, guidance, and mentorship to junior analysts and team members when required. Work hours that provide sufficient overlap with standard east coast US working hours. Skills and competencies Strong analytical thinking and problem-solving skills with the ability to analyse complex data sets and draw meaningful conclusions. Agile problem-solving ability and desire to learn new things and continuously improve. Proficiency in statistical analysis techniques and methodologies. Strong project management skills and the ability to work independently or as part of a team. Solid understanding of digital analytics tools and platforms and version control. Strong communication skills with the ability to present complex information to non-technical stakeholders in a clear manner. Strong business acumen and strategic thinking, with the ability to translate analytical findings into actionable insights and recommendations. Experience Bachelor's degree in operations research / industrial engineering / supply chain/chemical engineering/bioengineering. Advanced degree (Masters/PHD is a plus). Proven experience (typically 3-5 years) in a hands-on working environment in operation research, supply chain, data analytics and data integration Knowledge and expertise of analytical models such as linear programming, network optimization, goal programming, multiple objective optimizations, decision analysis Markov decision processes Experience working with large datasets, data visualization tools, statistical software packages and platforms (specifically R, Python, advanced SQL, Domino, AWS, GitHub, dbt, Tableau) Experience with simulation software (SIMIO, Arena, etc.) or DES libraries (simmer, simpy) Experience with biotech product development, manufacturing operations, supply chain, and quality control is a significant plus. Experience in the biopharma industry a plus. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About LH2 Holdings LH2Holdings is an AI Operating System to scale digital content brands and creators. We buy or partner with great digital content brands (web platforms, YouTube channels, apps, podcasts, newsletters, etc) and scale them. LH2 is being built by second-time founders, who have scaled tech platforms with hundreds of millions of users in their previous ventures. Our vision is to enable digital creators to scale with the speed and sophistication of large media conglomerates. About The Role We’re seeking a Senior Science Writer who can tell stories that bridge rigorous scientific research and public understanding. You will be responsible for authoring accessible, engaging, and authoritative content across fields like climate science, evolutionary biology, genetics, ecology, conservation, and emerging technologies. This is not just about summarizing studies; it’s about translating them with accuracy, empathy, and impact. If you’re passionate about science and storytelling and love simplifying complexity without diluting meaning, we’d love to meet you. Responsibilities Write 2 high-quality, compelling science articles per day (800–1,200 words each) Break down peer-reviewed research into engaging, accurate, and well-structured content Pitch weekly article ideas drawn from emerging research, science news, and recent academic publications. Interview scientists or researchers when needed and include expert insights in articles Collaborate with editors on tone, structure, and reader engagement strategies Stay current with trends in environmental science, genetics, climate, and sustainability Required Qualifications 3–7 years of professional experience in science journalism, environmental reporting, or academic communication Bachelor’s or Master’s degree in a scientific field (Biology, Environmental Science, Bioengineering, Earth Sciences, or related) Demonstrated ability to write about complex topics in an engaging, accessible way Strong portfolio of science or environmental content Ability to analyze and accurately summarize peer-reviewed research Strong research skills and attention to detail, particularly in interpreting scientific findings Strong editorial instincts with a reader-first mindset Comfortable switching between technical precision and narrative flair Familiarity with academic publishing, citation formats, and scientific terminology Experience working with content management systems and newsroom workflows What We Offer Competitive compensation Remote working options A collaborative editorial team that values clarity, curiosity, and credibility A platform to reach millions of science-curious readers monthly Skills:- Content Writing

As a Consultant, you will be required to address the following: Collaborate in the fulfillment of consulting projects with a special focus on global markets. This will require working closely with other consultants and project managers located in any of our global offices Conduct primary research with healthcare professionals, industry players as well as industry associations, and national agencies Conduct secondary research on large data sets from various data sources Collaborate in the analysis of quantitative and qualitative data for the development of financial models (i.e. eNPV), market models, economic impact models, health-economic models, as well as product adoption and acceptance models Clean, transform, and standardize complex datasets from multiple sources—including EMR, medical and pharmacy claims, and large prescription and healthcare datasets—to ensure consistency and reliability in analysis Design and develop interactive dashboards and reports using Excel and visualization tools (e.g., Power BI, Tableau) to communicate actionable insights to cross-functional team Develop market landscape presentations, market entry strategies, product positioning strategies, and others Work to solve complex business problems Participate in meetings and presentations to clients across the globe Engage in regular global training modules and required Pharmacovigilance training (internal and client-specific) Qualifications A minimum of 2-3 years of demonstrable experience within the healthcare industry in roles related to market insights/analytics, product management, strategy consulting or related roles Education: Master’s degree in Biotechnology, Pharmacy (MPharm), Bioengineering/Biomedical Engineering, Business Administration, or a related field Marketing, management consulting and/or market research, and reimbursement/pricing expertise are a plus Flexibility to work within a multicultural interdisciplinary team across various time zones Fluent in English and preferably speak other foreign languages. Self-motivated with exceptional organizational skills Advanced degree (PhD) a plus

Senior Regulatory Affairs Manager The Senior Regulatory Affairs Manager will be responsible for supporting international regulatory affairs registrations of medical devices across the globe. Job Description This position involves the creation, identification, collection, and entry of regulatory affairs information related to medical devices. The role includes supporting international regulatory submissions, managing country registration requests, and ensuring compliance with global regulatory requirements. The position requires strong organizational skills, effective communication, and the ability to manage multiple tasks efficiently . Essential Responsibilities Create, submit, and maintain product registration requests for submission. Develop, submit, and manage EU MDR, MDSAP, and EN ISO 13485 documents for regulatory compliance. Review and approve submission documents to ensure compliance with regulatory standards. Maintain up-to-date metrics with product registration requests and submission schedules. Track and monitor regulations applicable to medical devices in designated countries. Manage and update internal regulatory databases, including licenses and registration records . Qualifications Educational Background B.S. degree or higher in a technical discipline, preferably in Computer Science, Engineering, Bioengineering, Biology, or Chemistry . Professional Experience 3-7 years of Regulatory Affairs experience in the medical device industry , including international product registrations and new product development. Knowledge and Skills Knowledge: Working knowledge of 510(k) submissions, EU MDR 2017/745, MDSAP, EN ISO 13485, and 21 CFR 820 - Quality System. Skills: Proficient in Microsoft Word, Excel, and PowerPoint. Strong communication skills (oral and written) in English. Excellent project management skills. Ability to manage multiple tasks with strong attention to detail. Self-motivated and comfortable working remotely with international teams. Organized and analytical thinker with problem-solving abilities.  Primary Work Location: Valsad, Gujarat

University: INRAE (French National Research Institute for Agriculture, Food, and Environment) / University of Paris-Saclay Country: France Deadline: 10/06/2025 Fields: Synthetic Biology, Biotechnology, Molecular Biology, Bioengineering, Computational Biology The French National Research Institute for Agriculture, Food, and Environment (INRAE), in partnership with AgroParisTech and the University of Paris-Saclay, invites applications for a PhD position focused on the design of cross- and multi-species genetic circuits. The successful candidate will join the Micalis unit, a collaborative research environment dedicated to advancing bioengineering solutions for agriculture, food, and environmental challenges. This doctoral project aims to develop innovative tools and strategies to facilitate the implementation of genetic circuits in non-model organisms and multi-species communities. The research will support the rapid deployment of synthetic genetic and metabolic circuits in diverse biotechnology applications. Requirements – Master’s degree or Engineering degree in a relevant field – Experience in experimental synthetic biology, including microbiology and molecular/cell biology techniques – Background in programming, bioinformatics, or computational modelling is an asset – Strong communication skills – Willingness to work collaboratively with an interdisciplinary team – Recruitment is subject to validation by the Ministry due to the unit’s status as a Restricted Zone Application Information For further details and to apply, please visit: https://jobs.inrae.fr/en/ot-25811 Remuneration: 2,200€ gross per month Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register

University: INRAE (French National Research Institute for Agriculture, Food, and Environment) / University of Paris-Saclay Country: France Deadline: 10/06/2025 Fields: Synthetic Biology, Biotechnology, Molecular Biology, Bioengineering, Computational Biology The French National Research Institute for Agriculture, Food, and Environment (INRAE), in partnership with AgroParisTech and the University of Paris-Saclay, invites applications for a PhD position focused on the design of cross- and multi-species genetic circuits. The successful candidate will join the Micalis unit, a collaborative research environment dedicated to advancing bioengineering solutions for agriculture, food, and environmental challenges. This doctoral project aims to develop innovative tools and strategies to facilitate the implementation of genetic circuits in non-model organisms and multi-species communities. The research will support the rapid deployment of synthetic genetic and metabolic circuits in diverse biotechnology applications. Requirements – Master’s degree or Engineering degree in a relevant field – Experience in experimental synthetic biology, including microbiology and molecular/cell biology techniques – Background in programming, bioinformatics, or computational modelling is an asset – Strong communication skills – Willingness to work collaboratively with an interdisciplinary team – Recruitment is subject to validation by the Ministry due to the unit’s status as a Restricted Zone Application Information For further details and to apply, please visit: https://jobs.inrae.fr/en/ot-25811 Remuneration: 2,200€ gross per month Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register Show more Show less

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Senior R&D Scientist Analytics , Fast Trak Process Design and Validation Services will be responsible for planning and executing the technical portion of R&D development or improvement projects for any service in the R&D strategic plan. This will include services and/or products associated with analytical methods used in our process development and validation services. Working from early phase (definition of specs) through concept and design and then into testing and validation. Supervision of facility setup and documentation to support launch of the service to the market. This position reports to the Senior Manager R&D Fast Trak and is part of the Process Design and Validation Services team located in Bangalore and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you’ll do: Be a technical lead on innovation projects. Collaborate closely the R&D project managers and other departments to ensure seamless execution of deliverables in new service/product development projects. Define technical requirements to support new service/product designs to meet marketing defined customer needs. Plan, risk assess, execute and report on technical studies at various stages of a project. Design and conduct verification/validation studies to demonstrate compliance of new product/service designs with technical and marketing requirements. Provide support to ensure laboratory compliance to Environment, Health & Safety regulations. Who you are: Bachelor's, Master's or PhD degree in molecular / biology / biochemistry / bioengineering (or related fields) 5+ years strong experience leading and delivering technical projects. Highly motivated, with a creative and forward-thinking attitude to problem-solving and troubleshooting. Able to work autonomously to achieve results. Agility to work across multiple and varied projects simultaneously. Good reporting and presentation skills; able to adjust to different audiences. It would be a plus if you also possess previous experience in: Aseptic laboratory methods and techniques Knowledge of Good Laboratory Practice (GLP) and scientific methods Upstream or downstream biotechnology unit operations Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

Job Summary Responsible for managing a portfolio of key accounts. Being the primary contact and buildlong-term relationships with customers. Develop a trusted advisor relationship with key accounts, customer stakeholders and executive sponsor. Iidentifying and actively seeking for new opportunities in line with the market and segment strategies Duties and Responsibilities: - Define and implement key strategic biopharma/pharma account plans to achieve sales targets, foster account growth and identify new business opportunities. Conduct regular business reviews with key accounts to assess their needs, address concerns and provide solutions that meet their objectives. Collaborate with cross-functional teams, such as product management, BD, customer service to ensure seamless delivery of products/services and exceptional customer experience. Identify upselling and cross-selling opportunities within existing accounts to maximize revenue generation. Stay updated on industry trends, market conditions, and competitor activities to proactively identify potential threats and opportunities. Prepare and present reports on account performance, sales forecasts, and market insights to internal stakeholders. Manage contract negotiations, renewals, and pricing discussions in collaboration with the sales team. Provide exceptional customer service by promptly addressing customer inquiries, resolving issues, and coordinating with internal teams to deliver timely solutions. Collaborate with product development teams to provide feedback and insights from clients, contributing to the development of new products/services. Job Requirement/Specification: - Education: Bachelor’s Degree in Pharmaceutical Technologies, Bioengineering. Experience: Minimum 12 years of proven track record in Biopharma/Pharma Key Account Management roles Experience in Biopharma market Others: Good business acumen and communication skills to build long-standing and successful relationships with customers. Strategic thinking and problem-solving abilities to identify client challenges, propose innovative solutions, and drive business growth. Strong negotiation and influencing skills to navigate complex client relationships and achieve mutually beneficial outcomes. Adapt & develop solutions as per customer needs with clear & decisive communication. Analytical mindset with the ability to interpret data, extract insights, and make Data driven decisions. Exceptional organizational and time management skills to effectively prioritize tasks, manage multiple projects and meet deadlines. Good understanding with CRM software and other relevant ales tools Ability to travel to customer as needed. Strong Collaboration, negotiation, persuasion skills Certification or training in sales, account management or customer relationship management is a plus. High competency working with Microsoft office. Work independently with minimum supervision Self-motivated and disciplined approach is essential. Proficiency in English is essential, fluent in any SEA language is an added advantage. Brenntag TA Team Show more Show less

Ref Number B04-06194 Professional Expertise Research and Research Support Department UCL BEAMS (B04) Location UCL East Working Pattern Full time Salary £43,374 £51,860 Contract Type Fixed-term Working Type Hybrid Available for Secondment No Closing Date 02-Jul-2025 About Us At the Programmable Biomaterials Lab (PBL), our goal is to solve some of the major challenges facing large-scale bioproduction via innovative 3D light-assisted programming of biological matter. We envision a future where objects are produced, mechanisms triggered and materials handled purely by photons. Nature achieves much if not all of its evolution through the interactions of light and matter. Operations as complex as food production, life and evolution itself. We're here to perfect our engineering and scientific prowess in harnessing this massive potential. Further information about PBL can be found https://iomats.com/ Established in 2014 as part of the Mathematical and Physical Sciences (MAPS) Faculty, the UCL Institute for Materials Discovery (IMD) acts as a focal point of materials research at UCL across all departments. The IMD strives to be at the forefront of advanced materials research and teaching. We run state-of-the-art experimental and computational facilities and offer vibrant MSc programs aross UCL’s Bloomsbury and UCL East campuses. We are pioneering novel data-driven approaches for materials discovery, understanding fundamental materials behaviour, developing innovative sustainable materials for new innovative applications and boosting enterprise (i.e., industry) oriented materials research. About The Role We are seeking a talented postdoctoral researcher to work on the exciting UKRI project "SPARK 3D” at UCL. You will design and explore synthesis, caging and release of various caged compounds and growth factor molecules which will instruct the spatiotemporal evolution of cellular systems in 3D microenvironments. Your caged compounds alongside functionalised photoactive biomaterials matrices (codeveloped with you) will be used towards building an in vitro model of the physiological tissue. The tissue sites of interest are micro- and macro-vasculature and neuro-vasculature for the purposes of understanding the growth patterns of these complex structures under external stimulation with released chemical and biological growth factors. You will work with leading experts in both academic and industrial sectors. This is a full-time appointment for a period of two years continuously, available immediately. Requirements and person specifications of the role as well as your responsibilities and benefits are included in the following. Ample networking and collaboration opportunities within UCL including Biology, Medicine, Chemistry, Physics and Engineering departments as well as with the emerging UCL East campus in London and with leading international researchers and industry are offered. About You We seek a motivated Postdoctoral fellow interested in combining biochemical, photochemistry and optobiology skills. You will contribute to the development and utilization of biomodulation and biostimulation systems which will be used to trigger and control the growth and organization of bioprinted tissue constructs in vitro. The successful candidate will have a PhD in Chemistry/Biochemistry/Bioengineering/Biology/Materials Science or Engineering, or relevant related discipline. A full job description and person specification can be found at the bottom of this page. As part of your application please include a short cover letter and a CV with a list of major research achievements to date and a publications list. References to online profiles are welcome if applicable (but not necessary). Informal enquiries should be made to Dr Hossein Heidari h.heidari@ucl.ac.uk What we offer As well as the exciting opportunities this role presents, we also off er great benefits. Please visit: https://www.ucl.ac.uk/work-at-ucl/rewards-and-benefits to find out more. Our commitment to Equality, Diversity and Inclusion As London’s Global University, we know diversity fosters creativity and innovation, and we want our community to represent the diversity of the world’s talent. We are committed to equality of opportunity, to being fair and inclusive, and to being a place where we all belong. We therefore particularly encourage applications from candidates who are likely to be underrepresented in UCL’s workforce. These include people from Black, Asian and ethnic minority backgrounds; disabled people; LGBTQI+ people; and for our Grade 9 and 10 roles, women. You can read more about our commitment to Equality, Diversity and Inclusion here : https://www.ucl.ac.uk/equality-diversity-inclusion/. Available documents Attached documents are available under links. Clicking a document link will initialize its download. download: Job description - FLF Post Doc Research Fellow.pdf Show more Show less

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Senior R&D Scientist Downstream , Fast Trak Process Design and Validation Services will be responsible for planning and executing the technical portion of R&D development or improvement projects for any service in the R&D strategic plan. This will include services and/or products associated with our portfolio downstream process development services. Working from early phase (definition of specs) through concept and design and then into testing and validation. Supervision of facility setup and documentation to support launch of the service to the market. What you’ll do: Be a technical lead on innovation projects. Collaborate closely the R&D project managers and other departments to ensure seamless execution of deliverables in new service/product development projects. Define technical requirements to support new service/product designs to meet marketing defined customer needs. Plan, risk assess, execute and report on technical studies at various stages of a project. Design and conduct verification/validation studies to demonstrate compliance of new product/service designs with technical and marketing requirements. Provide support to ensure laboratory compliance to Environment, Health & Safety regulations. Who you are: Bachelor's, Master's or PhD degree in molecular / biology / biochemistry / bioengineering (or related fields) 5+ years strong experience leading and delivering technical projects. Highly motivated, with a creative and forward-thinking attitude to problem-solving and troubleshooting. Able to work autonomously to achieve results. Agility to work across multiple and varied projects simultaneously. Good reporting and presentation skills; able to adjust to different audiences. It would be a plus if you also possess previous experience in: Aseptic laboratory methods and techniques Knowledge of Good Laboratory Practice (GLP) and scientific methods Upstream or downstream biotechnology unit operations Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The R&D Scientist Validation , Fast Trak Process Design and Validation Services will be responsible to support planning and executing the technical portion of R&D development or improvement projects for any service in the R&D strategic plan. This will include services and/or products associated with our portfolio validation services. Working from early phase (definition of specs) through concept and design and then into testing and validation. Support supervision of facility setup and documentation to support launch of the service to the market. What you’ll do: Be a technical support on innovation projects. Collaborate closely the R&D project managers and other departments to ensure seamless execution of deliverables in new service/product development projects. Help defining technical requirements to support new service/product designs to meet marketing defined customer needs. Help planning, risk assess, execute and report on technical studies at various stages of a project. Design and conduct verification/validation studies to demonstrate compliance of new product/service designs with technical and marketing requirements. Provide support to ensure laboratory compliance to Environment, Health & Safety regulations. Who you are: Bachelor's, Master's or PhD degree in molecular / biology / biochemistry / bioengineering (or related fields) 3+ years strong experience in supporting and/ or leading technical projects. Highly motivated, with a creative and forward-thinking attitude to problem-solving and troubleshooting. Able to work autonomously to achieve results. Agility to work across multiple and varied projects simultaneously. Good reporting and presentation skills; able to adjust to different audiences. It would be a plus if you also possess previous experience in: Aseptic laboratory methods and techniques Knowledge of Good Laboratory Practice (GLP) and scientific methods Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

As a Consultant, you will be required to address the following: Collaborate in the fulfillment of consulting projects with a special focus on global markets. This will require working closely with other consultants and project managers located in any of our global offices Conduct primary research with healthcare professionals, industry players as well as industry associations, and national agencies Conduct secondary research on large data sets from various data sources Collaborate in the analysis of quantitative and qualitative data for the development of financial models (i.e. eNPV), market models, economic impact models, health-economic models, as well as product adoption and acceptance models Clean, transform, and standardize complex datasets from multiple sources—including EMR, medical and pharmacy claims, and large prescription and healthcare datasets—to ensure consistency and reliability in analysis Design and develop interactive dashboards and reports using Excel and visualization tools (e.g., Power BI, Tableau) to communicate actionable insights to cross-functional team Develop market landscape presentations, market entry strategies, product positioning strategies, and others Work to solve complex business problems Participate in meetings and presentations to clients across the globe Engage in regular global training modules and required Pharmacovigilance training (internal and client-specific) Qualifications A minimum of 2-3 years of demonstrable experience within the healthcare industry in roles related to market insights/analytics, product management, strategy consulting or related roles Education: Master’s degree in Biotechnology, Pharmacy (MPharm), Bioengineering/Biomedical Engineering, Business Administration, or a related field Marketing, management consulting and/or market research, and reimbursement/pricing expertise are a plus Flexibility to work within a multicultural interdisciplinary team across various time zones Fluent in English and preferably speak other foreign languages. Self-motivated with exceptional organizational skills Advanced degree (PhD) a plus Show more Show less

Program Management Team/Bioinformatics BU (Full Time Employment) Excelra is looking for highly skilled and motivated members for the Program Management Team with technical experience across multiple domains (AI/ML,NGS/human genetics/statistics, software development, project management, agile methodology) in bioinformatics to join the Bioinformatics team. The successful candidate will be expected to demonstrate the following competencies: 1. Project management as well as program management across different projects in key client accounts. 2. Liaison the relationship between client and Excelra 3. Contribute to efforts to increase operational efficiency among projects. 4. Collaboration with delivery for successful delivery of projects 5. Interact with the technical stakeholders of clients to identify new business opportunities. Qualifications: • PhD with 2-3 years of industrial experience or M.Sc/M.Tech with 5+ years’ experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology, or related field. • Strong track record of omics (NGS) data analysis, scRNA-Seq analysis or ML/AI and downstream systematic interpretation are must. • Expertise in one or more programming/scripting languages such as R, Python, shell-script for complex data analysis. • Experience in image analysis, knowledge graphs, deep learning and/or LLM’s is an advantage. • Some experience in data engineering techniques, full-stack development is expected. • Understanding of current best practices in computational biology data-management (NGS/Transcriptiomics/Microarray/Proteomics/Clinical-trials/Text-mining, etc.) is an added advantage. • Experience with Docker, Linux environment or cloud computing (AWS/GCP) is a plus. • Experience with Relational database such as Postgres, MySQL, or Oracle, is a plus. • Experience with version control systems such as GitHub, is a plus. • Ability to generate in-silico experimental workflows and in-depth knowledge in proprietary and public biological databases, methods, and tools. • Ability to generate scientific hypothesis along with good scientific/technical communication skills would be preferred. Show more Show less

Senior Bioinformatics Engineer Medicine moves too slow. At Velsera, we are changing that. Velsera was formed in 2023 through the shared vision of Seven Bridges and Pierian, with a mission to accelerate the discovery, development, and delivery of life-changing insights. Velsera provides software and professional services for: AI-powered multimodal data harmonization and analytics for drug discovery and development IVD development, validation, and regulatory approval Clinical NGS interpretation, reporting, and adoption With our headquarters in Boston, MA, we are growing and expanding our teams located in different countries! What will you do? ● Design, develop and maintain various Bioinformatics solutions for analyzing and managing Biological data as per our best practices and quality standards. ● Collaborate with Product Management and Software Engineers, to build bioinformatics solutions. ● Produce high quality and detailed documentation for all projects. ● Provide consultation and technical solutions to cross functional bioinformatics projects. ● Identify and/or conceive novel approaches to better and more efficiently analyze client and public datasets. ● Participate in defining the high-level application architecture for future roadmap requirements and features. ● Coach other team members by sharing domain and technical knowledge and code reviews. ● Participate in activities such hiring and onboarding. ● Work with cross-functional teams to ensure quality throughout the bioinformatics software and analytical pipelines development lifecycle. ● Ensure compliance with our SDLC process during product development. ● Stay up-to-date on technology to deliver quality at each phase of the product life-cycle. You take leadership in evangelizing technical excellence within the team. What do you bring to the table? ● Ph.D. degree with 3-5+ years of postdoc or industrial experience or Masters Degree with 5-8+ years of industrial experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology or related field ● Excellent programming skills in Python and Shell scripting ● Experience with Relational database such as PostgreSQL, mySQL or Oracle ● Experience with version control systems such as GitHub. ● Experience with Linux/UNIX/Mac OS X based systems ● Experience with high-performance Linux cluster and cloud computing (AWS is preferred). ● Deep understanding of analytical approaches and tools for genomic data analysis along with familiarity with genomic databases. Candidates with proven expertise in the analysis of NGS data generated on sequencing platforms such as Illumina, Oxford Nanopore, or Thermo will be prioritized. ● Experience with open source bioinformatics tools and publicly available variant databases. ● Ability to manage moderately complex projects and initiatives. ● Exceptionally strong communication, data presentation and visualization skills. ● Personal initiative and ability to work effectively with in a cross functional team. ● Excellent communication skills and ability to learn and work independently when necessary. ● High energy and inquisitive and strong attention to detail Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry. Show more Show less

Job Title: Assistant Professor / Associate Professor – Department of Bio-Engineering Location: School of Engineering & Technology, MIT World Peace University, Pune MIT World Peace University (MIT-WPU) invites applications for the position of Assistant Professor / Associate Professor in the Department of Bio-Engineering . We are looking for passionate educators and researchers committed to fostering academic excellence, innovation, and research in the rapidly evolving field of Bio-Engineering. Specializations Required: Immunology Genetics Biochemistry Bioinformatics Eligibility Criteria: Ph.D. from IITs, Top 50 NIRF-ranked institutions, or reputed overseas universities B.Tech in a relevant field | M.Tech in BioEngineering or allied areas Strong academic background with a proven record of research and publications in relevant fields Responsibilities: Deliver high-quality lectures and academic content Supervise and mentor students in their academic and research endeavors Contribute to the development of the department’s curriculum Engage in research and scholarly activities, including publishing in reputed journals Collaborate with other departments and external research institutions Application Process: Interested candidates are invited to send their CV along with relevant documents to: 📧 jidnyasa.jain.ve@mitwpu.edu.in Join MIT-WPU and be part of a vibrant academic ecosystem where innovation meets purpose, and every opportunity is an avenue for growth! Show more Show less

Alien Technology Transfer empowers top-class innovators to transform visionary product concepts into commercial realities. We do this by helping companies with concrete growth ambitions to secure funding for their product development through our innovation consulting expertise. To date, we have raised more than $500 million for our clients - Small and Medium Enterprises (SMEs) - across many domains including agri-tech, artificial intelligence, biotechnology, clean-tech, cyber-security, quantum computing, space, and transport. We are looking for a Innovation Scout able to source and analyse the highest quality prospect clients for our business lines amongst the most innovative high-tech high-impact start-ups and Small and Medium Enterprises (SMEs) in Europe and the USA. To join the team you have to possess a genuine interest in technology and business, an aptitude in quickly understanding complex engineering or medical innovations, be highly analytical and articulate, and have a strong command of English. You must be a team player, well organized, and also keen to take on responsibility. Key qualities include being able to demonstrate an entrepreneurial mindset, being highly self-motivated, and having a high degree of stamina to work within an ambitious and goal-driven environment. The role will see you undertake the responsibility of scouting potential clients, mainly by leveraging digital resources and channels (search engines, industry websites, and events), and by analyzing various databases (implying also some software programming tasks). DUTIES AND RESPONSIBILITIES Keeping yourself continuously up to date in the technological and business field to quickly and effectively recognize business opportunities and industry/market emerging trends Continuously identifying top-level sources/hubs of potential clients among web platforms, online databases, and events (trade fairs, conferences, pitches, start-up competitions, etc) Monitoring current trends in private and public innovative project financing and fund-raising Handling and analyzing databases, including any applicable customized filtering option to deliver the most appropriate results Analyzing and critically evaluating information resulting from any search related to innovative technologies and businesses Maintaining and enriching internal databases for prospects, clients, and public grant awardees. Preparing regular reports on funding trends, requiring quantitative skills, which help define the company’s yearly targets. JOB REQUIREMENTS Must have at least a Master’s 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 has an idea for the creation of web scrapers for extracting startup data from different websites supporting the development of a startup Lead Generation. Please note: Due to the high volume of candidates we are unfortunately not able to provide individual feedback regarding the outcome of every single application. Show more Show less

Plaksha University Location Plaksha University, Mohali, Punjab Open Date Sep 13, 2022 Description The Plaksha Research Fellowship (PRF) aims to recruit brilliant fellows in the filed of engineering, applied sciences, and social sciences, who are interested in building a research career at the cutting edge of technology and associated interdisciplinary areas. Research Fellows will be exposed to emerging challenges in research which will lead to the evolution of their research leadership at an international level. They will work under the mentorship of a team of reputed faculty within Plaksha as an integral member of a research lab while collaborating with peers in partner institutions including universities, research laboratories, and industry. Research Fellows will be selected based on their research interests, talent for innovation, and drive to make an impact. We are looking for candidates who are keen to take up intellectual challenges with an eye toward building novel artefacts, devices, and systems, investigating the interface between technology and society, and solving real-life problems. The candidates will get a stipend competitive with the industry, along with an annual grant to attend international conferences/workshops. We expect the Research Fellows to evolve and be an integral part of globally reputed research programs within a short time. We will also strive to offer a suitable environment for the growth of entrepreneurial skills and vision. Responsibilities In the capacity of PRF, you will be required to assist your faculty supervisor in conducting research as well as teaching-related activities. This will include, but is not limited to, the following tasks: Undertaking research in respective areas Writing research and conference papers under the assistance of the faculty. Set up and manage laboratory and project work Assisting faculty in conducting research projects that may involve fabrication, prototyping or programming activities. Interaction with vendors, suppliers, research institutions and related entities on academics and research-related matters Assisting faculty in teaching courses, which may involve 20 hours of work every week. This will involve working with faculty to plan and administer lectures, conducting tutorial and laboratory classes, developing homework problems, performing student assessments, and evaluating quizzes and examination sheets. Compensation and benefits Consolidated monthly stipend of INR 50,000 Medical insurance coverage of INR 5 lac. Travel/conference allowance of up to INR 40,000 per year for attending conferences/workshops. An on-campus residence facility may be provided subject to availability and at cost Contract duration - 6 months or a One-year contract Renewal of contract - The contract can be renewed once upon successful completion of the first term Additional career benefits Priority consideration for admission to the Ph.D. programs at Plaksha based on an excellent performance. Priority consideration for full-time research engineer positions at Plaksha’s research centres based on an excellent performance. Mentorship and guidance in future career trajectories in academia and industry. Qualifications Eligibility criteria Open to brilliant individuals desirous of starting their career in academia. The fellowship is very selective and only those who have a genuine interest in pursuing research and building a career in technological leadership will be selected. Requirements include: Master's degree or equivalent in computer science/ engineering, electrical and electronics engineering, mechanical engineering, bioengineering, mathematics, physics, biology and natural sciences, engineering education, humanities and liberal arts or related areas. Exceptional candidates with only a Bachelor's degree may be considered Research interests should preferably align with our thrust areas such as machine learning, artificial intelligence, data science, robotics and cyber-physical systems, sensors, IoT, biological systems, bioinformatics, engineering ethics, genetic engineering, applied mathematics and humanities among others. For more details and specific areas of faculty research interests, please click here. The candidate should be below 30 years of age. Application Instructions Applications can be submitted by filling out the online form. Along with the form, applicants should send their: (1) CV (2) Statement of Interest (3) Passport size photograph (4) Copy of academic records, work experience (if any) and identity proof Those applicants who meet the eligibility criteria and are found relevant for the PRF position will have to appear for an online written admission test. Applicants shortlisted after the test will be called for an interview. For more information or questions, contact us via email at phd.academics@plaksha.edu.in