Regulatory Medical Writer
Regulatory Medical Writer
Eurofins
Job description
Do you want to have a career in scientific writing and technical communication? Check out the Technical Documentation Specialist role at Eurofins, Bengaluru, India.
Company Description
Eurofins Scientific is a global life sciences company that offers an extensive suite of testing services to a broad range of sectors. Its areas of expertise include food, environmental, pharmaceutical and cosmetics testing and agroscience contract research, genomics, forensics, advanced materials and clinical research support. The company also provides specialty clinical diagnostic tests and laboratory services in global markets.
Job Summary
This is a full-time post located in Bengaluru, Karnataka, with concentration on scientific documentation coordination, technical communication and document life cycle management. The scientific writer will manage the input of authors and subject matter experts, monitor documents through review and approval, and examine their completeness and consistency. As a regulatory medical writer, you will also manage documentation issue resolution, and collaboration with scientific, quality, regulatory and client-facing teams to ensure that deliverables satisfy applicable standards.
Key Responsibilities
Integrate scientific knowledge and input from numerous authors, reviewers and subject matter experts.
Track papers through drafting, review and approval process to ensure that each stage is completed on time.
Ensure uniform use of scientific vocabulary, format, and communication throughout the material.
Review documents for clarity, completeness, adherence to client expectations, and applicable regulatory requirements.
Identify missing information, conflicting information, and unresolved reviewer comments and coordinate resolution.
Act as a liaison between scientific, quality assurance, regulatory and client-facing groups.
Support transition between content writers, reviewers, and documentation coordinators.
Inform relevant stakeholders of document progress, deadlines, outstanding actions and expectations.
Help integrate and control scientific documents to ensure they are accurate, consistent and ready for review or audit.
Educational Qualification
A Master’s degree in a science-related discipline is necessary.
Preferred background in a scientific or technological field.
Previous experience managing scientific or technical documentation is necessary.
Experience in regulated contexts (GMP, GxP, clinical research) is preferred.
Experience with contract research organizations (CROs), GMP laboratories or other controlled scientific environments is highly desirable.
Skills Required
Committed to quality, ethics and customer service.
Ability to juggle opposing priorities and perform under work-related strain.
Accuracy and precision in processing scientific and technological information.
Ability to perform a job that may entail extended durations of sitting.
Salary Structure
The average salary of a Regulatory Medical Writer in India is ₹7 Lakhs to ₹8 Lakhs per year.
Career Development
This role, as a scientific writer, is perfect for those people who want to enhance their skills in scientific writing, regulatory quality, project management, and technical writing. This experience as a regulatory medical writer, in a controlled scientific setting might be a springboard into careers in documentation management, scientific project coordination, regulatory documentation or technical communications.
How to Apply
Go to our employment portal and look for Regulatory Medical Writer.
Click the link to get the full job description and eligibility requirements.
Upload your updated resume and enter the required fields.
Submit your application.
Education
Postgraduate Degree (Master's/PhD)
Key Skills
Market insights & trends
Salary Insights
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Hiring Trends
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