Medical Writer (Tata Elxsi Ltd)

  • Medical Writer
  • Full time
  • 1 week ago
  • Mumbai

Job Information

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    Salary Not Disclosed Not Disclosed / Monthly
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    Shift Round
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    No. of Openings 10 openings
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    Job Level : Senior
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    Job Experience : 2 - 7 Years
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    Job Qualifications bachelors or above

Job Description

Company Name: Tata Elxsi Ltd

Designation: Medical Writer

Location: Mumbai, Pune, Bangalore/Bengaluru

Experience: 2 – 7 years
Qualification: UG :Any Graduate

Job Description: Roles and Responsibilities

Job description

Tata Elxsi works with leading medical device OEMs and technology companies for market research and human factor engineering, hardware and software engineering, verification & validation, regulatory standards & compliance requirements along with technologies such as artificial intelligence, cloud and IoT.

Tata Elxsi’s Medical Device and Healthcare practice is ISO 13485 certified.

Job Summary

This position requires an excellent resource that does development of Clinical Evaluation Plans/Reports (CERs) and Post Marketing Reports with future additional for development of other clinical evidence documents as part of the Medical Device Regulation and Medical Device Directive. This is an excellent opportunity to grow your career and improve quality of life for people around you.

Principal duties and Responsibilities

Author and conduct medical and technical writing of clinical evaluation reports (CERs) in support of compliance to EU MDR- Med Dev 2.7, rev 4 for devices across therapeutic areas

Author and review post-market clinical follow up (PMCF) plan and PMCF reports

Summarize post-marketing surveillance and risk management data for the target device

Work cross-functionally to ensure adherence to submission and company-driven deadlines

Collaborate with stakeholders and participate in client calls and supporting work stream leaders

Providing product guidance and expertise to conduct literature searches on products/product families.

Review the literature and interpret and summarize risks, alternate therapies and device specific benefits from literature; collect and summarize primary data to support risk assessment.

Conduct proofreading, editing, document formatting, review comment integration and document completion/approval activities

Support senior writers to prepare regulatory documents that meet client expectations in terms of content, quality, and presentation

Expected areas of competence (i.e., knowledge, skills and abilities)

Exemplary knowledge of clinical research processes and medical device development

Ability to understand and interpret complex clinical trial data

Strong, concise scientific style of writing with a high level of attention to detail

Demonstrated strong writing and communication skills

Ability to function well as a member of the team and build relationships between Clinical Affairs and other areas of the organization

Proven analytical and negotiation skills

Intermediate computer skills, including Microsoft Office Suite

Ability to lead a team and influence others

Proficient knowledge of EU regulations (MDR/MDD) and regulations outside of the EU

Education/Experience Requirements

Masters or Bachelors degree in Biomedical, Medical, life sciences or related field preferred. Alternate degrees may be considered

Has authored CER, PMCF plan, PMCF reports and has hands on experience with addressing Notified body comments

A minimum of 2-10 years of experience in Clinical Affairs/Medical Writing (e.g. biomedical research, medical/regulatory/scientific writing, clinical trial management) required

Job location: Pune/Mumbai/Bangalore

Job code: 1145

Qualification: BE/B.Tech in Biomedical Engineering/B.Pharm/MPharm/MBBS/BHMS/BAMS/BDS/ Life Science background

Salary: Not Disclosed


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