Career

Medical Writers

  • Qualification : A science or engineering graduate or post-graduate
  • Key Skills : minimum of 2 years of demonstrable experience in one or more of the following areas: clinical trial protocol and associated documents, clinical study reports, clinical evaluation reports, performance evaluation reports. Knowledge of global medical device regulations would be an added advantage. A keen sense of language and grammar with a passion for reading and writing
  • Experience : 2 year
  • Location : Vadodara (remote working possible for experienced and deserving candidates)
  • Openings : multiple
  • Description : We are looking for medical writers to work on clinical evaluation and performance evaluation reports, clinical trial protocols and study reports of a wide range of medical and IVD devices.
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Marketing Professionals

  • Qualification : BBA or MBA with additional qualification in engineering or sciences
  • Key Skills : minimum 2 years of demonstrable experience of B2B services marketing. Experience in a consulting firm or certification body preferred. Good analytical and communication skills, both verbal and written. Ability to efficiently work on presentations.
  • Experience : 2
  • Location : Vadodara (remote working possible on a case-to-case basis)
  • Openings : multiple
  • Description : We are looking for experienced individuals to manage marketing and customer communication. The job involves conducting market research, brand building and communicating effectively with customers to take the business to the next level.
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Regulatory and QA professionals

  • Qualification : science or engineering graduate or postgraduate
  • Key Skills : minimum of 2 years of experience in medical device and IVD device regulatory, QA or medical writing areas would be preferred.
  • Experience : 2 Years
  • Location : Vadodara (remote working possible for experienced and deserving candidates)
  • Openings : multiple
  • Description : minimum of 2 years of experience in medical device and IVD device regulatory, QA or medical writing areas would be preferred. However, we are also open to exceptional freshers.
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Regulatory Affairs Specialists

  • Qualification : pharmacy, microbiology, biomedical engineering
  • Key Skills : minimum 2-3 years of experience of working in medical device sector, preferably in regulatory or QA departments.
  • Experience : 2+ Years
  • Location : Vadodara (remote working possible for experienced and deserving candidates)
  • Openings : multiple
  • Description : minimum 2-3 years of experience of working in medical device sector, preferably in regulatory or QA departments.
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Clinical Affairs Specialist

  • Qualification : pharmacy, microbiology, biomedical engineering
  • Key Skills : minimum 2-3 years of experience of working in medical device sector, preferably in regulatory, QA or clinical departments.
  • Experience : 2+ Years
  • Location : Vadodara (remote working possible for experienced and deserving candidates)
  • Openings : multiple
  • Description : minimum 2-3 years of experience of working in medical device sector, preferably in regulatory, QA or clinical departments. Ability to write clinical trial protocols and reports.
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QMS Specialist

  • Qualification : pharmacy, microbiology, biomedical engineering
  • Key Skills : minimum 2-3 years if experience of working in medical device sector, preferably in regulatory or QA departments.
  • Experience : 2+ Years
  • Location : Vadodara (remote working possible for experienced and deserving candidates)
  • Openings : multiple
  • Description : minimum 2-3 years if experience of working in medical device sector, preferably in regulatory or QA departments.
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Toxicological Specialist

  • Qualification : zoology, biochemistry or equivalent
  • Key Skills : minimum 2-3 years of working in a CRO or lab handling animal studies or similar experience.
  • Experience : 2+ Years
  • Location : Vadodara (remote working possible for experienced and deserving candidates)
  • Openings : multiple
  • Description : minimum 2-3 years of working in a CRO or lab handling animal studies or similar experience. Ability to write biological evaluation plans and reports, review of biocompatibility protocols and reports.
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