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Content Writer Pharma Job in Quascenta

Published on

Quascenta

B.Pharm, M.Pharm, Msc, BSc, Lifesciences, B.Tech, M.tech (Pharmaceuticals Biotech MedTech Regulatory Affairs / Quality / Validation)

Chennai

0โ€“3 years

Verified Job

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Are you passionate about transforming complex pharmaceutical and regulatory concepts into engaging, high-impact content? Quascenta is hiring a Content Writer โ€“ Pharma Manufacturing in Chennai, offering a unique opportunity to work at the intersection of pharma, validation, and B2B SaaS content strategy.

This role is ideal for candidates with exposure to GxP, validation, regulatory affairs, or quality systems, who want to build authority-driven content for pharma and biotech manufacturing professionals.


๐Ÿ” Job Overview

  • Role: Content Writer โ€“ Pharma Manufacturing
  • Company: Quascenta
  • Location: Chennai
  • Job Type: Full-time, On-site
  • Experience Level: 0โ€“3 years (with portfolio preferred)
  • Industry: Pharma, Biotech, SaaS, Validation

โœ๏ธ Key Responsibilities

  • Write 2โ€“4 long-form blog articles/month (1000โ€“1800 words) focused on:
    • Pharma manufacturing quality
    • Validation lifecycle management
    • Digital systems (e.g., eLogBook, eProcess)
  • Create LinkedIn content (thought leadership posts, summaries, carousel copy)
  • Translate complex GxP, validation, and regulatory concepts into clear, structured content
  • Repurpose internal documents into publication-ready articles
  • Conduct basic research on regulatory trends and terminology
  • Implement SEO best practices (keywords, meta tags, readability)
  • Collaborate with leadership (Validation Head/founder) for content briefs

๐ŸŽ“ Qualifications & Skills

  • Strong command of professional English writing
  • Experience in long-form blog writing + social media content
  • Ability to convert technical inputs into compelling narratives
  • Background in:
    • Pharmaceuticals
    • Biotech
    • MedTech
    • Regulatory Affairs / Quality / Validation
  • Understanding of GxP, validation lifecycle, or QMS concepts (highly preferred)
  • Portfolio with 3โ€“5 writing samples

๐Ÿ’ผ Why Join Quascenta?

  • Work with industry experts in validation and compliance software
  • Exposure to pharma SaaS products like:
    • eResiduePro
    • eProcessPro
    • eLogBook
  • Opportunity to build authority in B2B pharma content writing
  • Direct mentorship from domain experts
  • High ownership and fast feedback loops

๐Ÿš€ How to Apply

Application Link

Content Writer Pharma Job in Quascenta
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