Stryker Hiring Medical Writer

Stryker Hiring Medical Writer | Life Sciences | Gurugram

Healthcare and medical device professionals seeking careers in medical writing, clinical evaluation reporting, regulatory affairs, and medical device compliance have an exciting opportunity with Stryker. The company is currently hiring for the position of Medical Writer at its Gurugram location.

This role is ideal for candidates with experience in clinical documentation, regulatory medical writing, clinical evaluation reports (CERs), EU MDR submissions, and scientific writing within the healthcare products or medical device industry. Professionals looking to advance their careers in regulatory writing, clinical affairs, medical device compliance, and healthcare documentation can explore this opportunity with a globally recognized medical technology company.

Company Overview

Stryker is a global leader in medical technologies, delivering innovative products and services across MedSurg, Neurotechnology, and Orthopaedics. The company works closely with healthcare providers worldwide to improve patient outcomes and enhance healthcare delivery.

Serving millions of patients annually, Stryker continues to invest in innovation, clinical research, regulatory excellence, and product development. The organization offers professionals the opportunity to work on global healthcare projects while contributing to medical device safety, compliance, and clinical evidence generation.

Job Role & Responsibilities

Position: Medical Writer

The Medical Writer will collaborate with Regulatory Affairs, Clinical, Quality, Marketing, and Research teams to prepare high-quality clinical and regulatory documentation supporting medical device registrations and compliance activities.

Key Responsibilities

• Prepare Clinical Evaluation Reports (CERs) for medical devices.
• Develop Post Market Clinical Follow-up (PMCF) documents.
• Prepare Summary of Safety and Clinical Performance (SSCP) documentation.
• Support preparation of Clinical Study documents and reports.
• Compile and evaluate clinical evidence from clinical trials, literature reviews, post-market surveillance data, and safety information.
• Support EU MDR submissions and annual clinical evaluation updates.
• Conduct gap assessments and update existing clinical evaluation documentation.
• Perform literature searches and analyze scientific publications for regulatory submissions.
• Interpret clinical and scientific data and present findings in clear regulatory documents.
• Coordinate document review cycles with cross-functional stakeholders.
• Resolve document review comments and ensure timely approvals.
• Support development of internal templates, procedures, and style guides.
• Participate in clinical documentation strategy discussions.
• Identify project risks and recommend solutions for resource or timeline challenges.
• Serve as a subject matter expert within the medical writing function.

Eligibility / Qualifications

Educational Qualification

• Bachelor’s Degree in a Scientific Discipline
• Master’s Degree in Life Sciences or Scientific Discipline (Preferred)

Relevant Courses

B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Biomedical Sciences, Clinical Research, Pharmacology, Medical Writing, Regulatory Affairs, Biological Sciences, Healthcare Sciences.

Experience Required

• 2–5 Years of Experience
• Minimum 2 years of experience in healthcare products or medical devices
• Minimum 1 year of medical writing experience in healthcare products or medical device industry

Required Skills

• Medical Writing
• Clinical Evaluation Reports (CER)
• EU MDR Documentation
• Clinical Research Documentation
• Scientific Writing
• Regulatory Affairs
• Literature Review
• Clinical Data Analysis
• Medical Device Regulations
• Clinical Evaluation Strategy
• Technical Documentation
• Regulatory Submission Support

Preferred Skills

• MEDDEV 2.7/1 Rev. 4
• EU Medical Device Regulation 2017/745 (MDR)
• Clinical Operations Knowledge
• Risk Management
• FDA Guidelines
• ISO Standards
• Regulatory Submission Experience

Location & Salary

Location: Gurugram, Haryana

Salary: ₹10 LPA – ₹18 LPA (Approximate)

Application Process

Interested candidates can apply through the official Stryker careers portal.

Apply Here: https://careers.stryker.com/medical-writer/job/F6D02BB5EB2EB5FF315CF2BD8C71B07A

Job Information

• Company: Stryker
• Position: Medical Writer
• Job ID: R566664
• Location: Gurugram, Haryana
• Work Mode: Hybrid
• Experience: 2–5 Years
• Travel Requirement: Up to 10%

Frequently Asked Questions (FAQs)

1. What qualification is required for the Stryker Medical Writer role?

Candidates with a Bachelor’s Degree in a scientific discipline are eligible. A Master’s Degree is preferred.

2. How much experience is required?

Applicants should have 2–5 years of experience, including medical writing experience in healthcare products or medical devices.

3. What documents will the Medical Writer prepare?

The role involves preparing Clinical Evaluation Reports (CERs), PMCF documents, SSCPs, clinical study reports, and regulatory clinical documentation.

4. Is medical device industry experience mandatory?

Yes. Candidates should have prior experience in healthcare products or the medical device industry.

5. Is knowledge of EU MDR important for this role?

Yes. Experience with EU MDR and MEDDEV guidelines is highly preferred.

6. What is the work model for this position?

The role follows a hybrid work model based in Gurugram.

Summary Table

Company	Stryker
Department Vacancies	Medical Writer
Qualification	B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry
Experience	2–5 Years
Location	Gurugram

Tagged as: Pharma Jobs in Gurgaon