Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Job Summary

• Job Title – Technical Leader - Drug Products and Sciences

• Location – Whitefield, Bangalore

• Shift – General

 Job Responsibilities and Skills:

• As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front
• Lead multi-functional project team for effective collaboration and deliverables
• Prior experience of managing diverse and cross functional teams at a global front
• Understanding of regulatory, process development, quality management systems, QbD tools, drug modelling and design of experiments in the field of drugs and medical devices
• Good knowledge of product development stages, Bio design process  and life cycle management in the area of drugs and medical devices
• Prior experience with the new  product and process development in the area  of drugs, medical devices and combination drug/device systems
• Prior track record of translating new  ideas to workable and commercially feasible products in the area of drugs and medical devices
• Being able to anticipate risks/challenges and willingness to deal with ambiguity
• Sound understanding of invention disclosures and patent filing processes
• Coordinate and ensure follow-up of technical activities in collaboration with key stakeholders, with respect of project commitment, quality procedures and business needs
• Propose options and develop action plans for problem-solving, product and process inventions and improvements
• Establish, maintain and update technical & Design documentation according to Good Documentation Practices
• Fluent with Technical Writing, Documentation and reports generation
• Influential leadership and ability to flex as the role demands while interacting with internal and external stakeholders
• Out of the box and critical thinking ability

   Qualifications

• Ph.D/Masters in Pharmaceutics, Chemical Engineering, Biology, Biosciences and Biomedical engineering
• Minimum of 10  years of diverse industrial experience post  Ph.D and about 15 years post Masters in the given  technical domains of interest
• Desired if the  incumbent had more than one jobs/roles  and has interacted with many different global  stakeholders in a given role
• Clear and effective communication (written, oral) and presentation skills.
• Good stakeholder management (local and global)
• A proven track record of effectiveness in a fast-paced environment.
• Proven ability to create results within budget, timeline, and product/project deliverables

    Skills

• Demonstrate strong project management and people leadership skills
• Ability to work independently
• Can effectively communicate with internal and external customers
• Demonstrates flexibility and the ability to shift gears between projects comfortably
• Fluency in English
• Good knowledge of Design Control documentation and medical writing
• Sound  knowledge of international/regional/national regulations and standards for drugs and medical devices
• Acquire business acumen with time
• Experience with Statistics and Six Sigma tools
• Solid computer skills: email, documentation and collaboration tools: e.g. WebEx, Teams, Microsoft Office products, etc.

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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