Freshers Hiring Medical Writer Jobs in Ahmedabad 2026 | Zydus Medtech Recruitment

Apply for Medical Writer Jobs at Zydus Medtech Ahmedabad. Check MBBS, BHMS, Pharm D eligibility, experience, skills, responsibilities and application details.

Zydus Medtech Private Limited is hiring for the position of Medical Writer at its MedTech Office in Ahmedabad, Gujarat. This opportunity is suitable for medical and scientific professionals with 0–3 years of experience in medical device medical writing or clinical affairs.

The Medical Writer will be responsible for authoring, reviewing, and maintaining clinical and regulatory documents related to medical devices while supporting clinical evidence generation and regulatory compliance throughout the product lifecycle.

Medical Writer Job Details

Job DetailsInformation
CompanyZydus Medtech Private Limited
Job TitleMedical Writer
DepartmentMedTech Office
Experience0–3 Years
Job TypeFull-Time
LocationAhmedabad, Gujarat, India
Work AreaMedical Device Medical Writing / Clinical Affairs
EducationMBBS or BHMS
Other Eligible QualificationExceptional Pharm D candidates with medical device exposure may be considered

Job Overview

The Medical Writer will work on clinical and regulatory documentation for medical devices. The role involves preparing, reviewing, updating, and maintaining documents required for clinical evidence generation, regulatory submissions, and ongoing product lifecycle activities.

The selected candidate will collaborate with Regulatory Affairs, Quality, and R&D teams to ensure clinical data supports the required safety and performance objectives.

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Key Responsibilities

Medical Device Medical Writing

The Medical Writer will be responsible for authoring, updating, and reviewing medical device-focused clinical and regulatory documents, including:

  • Clinical Evaluation Plans (CEP)
  • Clinical Evaluation Reports (CER)
  • Post-Market Clinical Follow-Up (PMCF) Plans and Reports
  • Clinical Investigation Plans (CIP)
  • Clinical Study Protocols
  • Clinical Study Reports (CSRs)
  • Summaries of Safety and Clinical Performance (SSCP)
  • Informed Consent Documents (ICD)
  • Investigator’s Brochures (IB)
  • Periodic Safety Update Reports (PSUR)
  • Publications and White Papers
  • Health Hazard Analysis (HHA)
  • Health Hazard Evaluation (HHE)
  • Public Health Threat Analysis (PHTA)
  • Other relevant clinical and regulatory documents

Literature Search and Clinical Evidence

The role will also involve literature-based clinical evidence activities, including:

  • Developing literature search protocols and strategies.
  • Conducting systematic literature searches to identify relevant clinical data.
  • Evaluating and extracting clinical evidence for inclusion in reports.
  • Preparing literature summary reports.
  • Preparing literature-based documents such as State-of-the-Art (SotA) reports.
  • Interpreting and summarizing relevant clinical information.

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Regulatory Compliance

The Medical Writer will ensure that clinical and regulatory documents comply with applicable requirements, including:

  • India Medical Device Rules (MDR)
  • EU Medical Device Regulation (EU MDR)
  • ISO 13485
  • Company SOPs
  • Other applicable regulatory requirements

Collaboration

The selected candidate will work closely with internal teams, including:

  • Regulatory Affairs
  • Quality
  • Research & Development (R&D)
  • Clinical Affairs

The role requires effective collaboration to align clinical evidence and documentation with medical device safety and performance requirements.

Eligibility Criteria

Educational Qualification

Only candidates with the following qualifications are eligible to apply:

  • MBBS
  • BHMS

Exceptionally strong Pharm D candidates with relevant exposure to and understanding of medical devices may also be considered.

Experience

Candidates should have 0–3 years of experience in:

  • Medical Device Medical Writing
  • Clinical Affairs
  • Related clinical or regulatory documentation roles

Required Skills

Candidates should have the following skills and knowledge:

  • Strong understanding of medical device medical writing
  • Knowledge of EU MDR requirements
  • Understanding of literature search methodologies
  • Clinical data interpretation skills
  • Excellent writing and editing abilities
  • Strong English communication skills
  • High attention to detail
  • Strong analytical thinking
  • Proficiency in MS Word and Excel
  • Ability to work collaboratively with cross-functional teams

Knowledge of French or Portuguese will be considered an added advantage.

Who Can Apply?

This position is particularly suitable for MBBS and BHMS graduates interested in medical device medical writing, clinical affairs, clinical evidence generation, and regulatory documentation.

Exceptional Pharm D candidates with relevant medical device exposure and a good understanding of the medical device industry may also be considered.

Job Location

The Medical Writer position is based at:

Zydus Medtech Private Limited
MedTech Office, Ahmedabad, Gujarat, India

How to Apply for Medical Writer Job?

Interested and eligible candidates should apply through the official Zydus Medtech recruitment portal. Candidates should review the complete job requirements and ensure that their educational qualification and experience match the eligibility criteria before submitting their application.

Apply Online

Frequently Asked Questions

What is the job title?

The position is for Medical Writer at Zydus Medtech Private Limited.

What is the required experience?

The required experience is 0–3 years in medical device medical writing or clinical affairs.

What qualifications are accepted?

MBBS and BHMS candidates may apply. Exceptionally good Pharm D candidates with relevant medical device exposure may also be considered.

Where is the job located?

The position is based in Ahmedabad, Gujarat, India.

What will the Medical Writer do?

The Medical Writer will prepare, review, and maintain clinical and regulatory documents for medical devices, conduct literature searches, interpret clinical evidence, and support regulatory compliance.

Is knowledge of EU MDR required?

Yes. A strong understanding of EU MDR requirements is listed among the required knowledge for this position.

Is knowledge of French or Portuguese mandatory?

No. Knowledge of French or Portuguese is an added advantage, not a mandatory requirement mentioned in the job description.

Important Note

Candidates should verify the latest vacancy status, eligibility requirements, application procedure, and other recruitment details through the employer’s official career portal before applying. Job requirements and vacancy availability may change.

Source: Zydus Medtech Private Limited Official Recruitment Portal


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Founder & Editor

Ranjeet K is the Founder and Editor of LatestPharmaJobs.in, sharing verified pharma and life sciences job opportunities across India. for freshers and experienced professionals.

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