
Editor and Proofreader
4 weeks ago
Reporting To: Lead Global Branding and Creatives
Business Area: Global Marketing Communications
Job Description: The Editor & Proofreader will be responsible for ensuring the accuracy, consistency, and clarity of all marketing and communication materials developed by GMC.
This role will involve reviewing content across corporate, product, and medico-marketing materials to ensure they meet Biocon Biologics' brand voice, compliance standards, and industry best practices.
Key Responsibilities of the position: Content Editing & Proofreading:
• Review and refine corporate, product, and medicomarketing content for clarity, consistency, and grammatical accuracy.
• Ensure all materials align with Biocon Biologics' brand tone, messaging, and regulatory requirements.
• Edit scientific and promotional content for readability without altering medical accuracy.
• Conduct final quality checks before content distribution across digital and print channels. Brand & Compliance Alignment:
• Ensure content adheres to Biocon Biologics' global brand identity, Sphaera, and meets internal compliance guidelines.
• Work closely with Medical, Legal, and Regulatory teams to ensure content accuracy and compliance with industry regulations.
• Maintain a standardized editorial style guide for GMC to ensure uniformity across all communications.
Collaboration & Content Optimization:
• Work with GMC's Brand Communications & Creatives, Medico-Marketing and Regional Marketing teams to enhance content effectiveness.
• Provide feedback to content creators to improve messaging impact and clarity.
• Assist in developing high-quality marketing and training materials that support global branding efforts.
Candidate Pre-Requisites
• Experience: 3-5 years in editing, proofreading, or content review, preferably in pharmaceuticals, healthcare, or life sciences.
• Education: Bachelor's/Master's in English, Journalism, Communications, or Life Sciences.
• Strong command of English and attention to detail in scientific and marketing content.
• Experience working with regulatory-compliant content in the pharmaceutical industry is a plus.
• Ability to manage multiple projects and meet tight deadlines
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