As an Automation Expert in the Product Development department based in Chennai, you will be responsible for leveraging automation to drive innovation in healthcare and pharmaceutical products. Your primary focus will be designing and implementing automated systems to enhance the development process, ensuring efficiency, precision, and compliance with industry standards. Your expertise in automation, particularly in biotechnological or medical environments, will play a crucial role in accelerating the creation of impactful solutions. Your key responsibilities will include proficiency in designing and implementing automation solutions, knowledge of process control principles, experience with robotics and instrumentation, understanding of bioprocessing techniques, and familiarity with regulatory standards relevant to bioprocess environments. Additionally, you will research and recommend automation technologies tailored to biotechnology and medical product development needs, collaborate with cross-functional teams, ensure regulatory compliance, and provide training and support to enhance productivity across the product development lifecycle. To qualify for this role, you should hold a Bachelor's degree in engineering, computer science, or a related field, with an advanced degree being a plus. You are expected to have at least 4 years of experience in automation engineering or a related role, preferably in healthcare and medical devices. Proficiency in programming languages such as Python, C++, or Java, experience with software platforms like LabVIEW and MATLAB, and familiarity with automation software are essential technical knowledge requirements. Strong problem-solving skills, hands-on experience in designing automated systems, and the ability to work effectively in multidisciplinary teams are key skills needed for this position. Preferred qualifications include experience with biotechnology/medical-specific automation and familiarity with regulatory standards and quality systems. Key competencies for this role include innovative thinking, attention to regulatory detail, adaptability, and a collaborative and proactive approach. If you are ready to take on this exciting opportunity, please send your resume to hr@cellbios.com.,
You will be responsible for driving international sales growth for Single Use Bioprocessing solutions. Your role will involve providing sales support and coordination for global sales teams, conducting market research, and tracking industry trends. Developing and maintaining strong client relationships in key international markets will be crucial, along with identifying and qualifying international sales leads. You will also assist in pricing strategies, proposals, and RFP responses, while maintaining accurate CRM records and managing the sales pipeline. Collaboration with regional sales teams to align market strategies and preparing reports on sales performance, market trends, and customer feedback will be part of your responsibilities. Additionally, you will support participation in international trade shows, events, and conferences. To qualify for this position, you should possess a Bachelors/Masters degree in Business, Biotechnology, or Life Sciences, along with 2-5 years of experience in international sales and business development. An understanding of Single Use Bioprocessing solutions is essential, as well as strong negotiation and communication skills. You should also be willing to travel internationally. If you meet the qualifications and are interested in this opportunity, please send your resume to hr@cellbios.com.,
The selected candidates will be responsible for drafting and designing various products using SolidWorks, specifically for medical device manufacturing. In this role, you will engage in all phases of new development, prototyping, design evaluation, and transfer to production activities. You will also be involved in product testing, evaluation, and creating test reports to support design selection. Organizing projects, maintaining Design History Files, completing design drawings, and developing component specifications will be key aspects of the job. Additionally, you will introduce new equipment, materials, and technologies, manage project tasks, and contribute to innovation within the team by filing disclosures and patents. Qualifications for this position include experience in SolidWorks (Solid Modelling, Surface Modelling, Assembly, Flow analysis & Simulation), a degree in Mechanical Engineering or Biomedical Engineering, and knowledge of DMR/DHF. Understanding of quality and regulatory requirements for medical devices classification is essential. Interpersonal skills to handle clients, result-oriented approach, and self-driven attitude are also required. The job is in the Medical Device Manufacturing industry and is a Full-Time, Permanent position. Freshers as well as candidates with up to 2 years of experience are welcome to apply. If you meet the qualifications and are interested in this opportunity, please send your resume to legoan@cellbios.com / hr@cellbios.com.,