Are you a pharma-savvy writer with a passion for transforming deep scientific and regulatory knowledge into clear, engaging content? Pharmabharat is excited to announce an immediate hire for a Pharma Content Writer / Internal SME who can act as our in-house subject matter expert (SME). In this role, you will produce high-quality, scientifically accurate, SEO-optimized content—blogs, white papers, web pages, product dossiers—for healthcare professionals, pharma stakeholders, regulatory bodies, and marketing audiences. If you have experience writing in the pharmaceutical and life science domain, a strong grasp of FDA / GMP / cGMP / ICH, and the ability to simplify complex concepts without losing rigor, we want to hear from you.
Key Responsibilities
- Serve as the internal Pharma SME / Subject Matter Expert, ensuring scientific credibility and regulatory accuracy across all content deliverables
- Develop, write, review, and edit pharma domain content: blogs, white papers, articles, web pages, product descriptions, marketing collateral, and educational material
- Create scientifically accurate, compliant, and audience-specific content aligned with industry standards and regulations (FDA, cGMP, GMP, GLP, ICH, etc.)
- Collaborate with internal SMEs, regulatory teams, marketing, and external stakeholders to ensure technical accuracy, brand consistency, and regulatory alignment
- Translate and simplify complex scientific, clinical, and regulatory concepts into clear, concise, and engaging content for varied audiences (HCPs, regulatory bodies, business audiences)
- Ensure all content follows SEO best practices, content strategy guidelines, readability, and digital marketing standards
- Uphold consistency in tone, style, voice, and brand guidelines across all deliverables
- Manage multiple writing assignments and projects under tight deadlines, ensuring review cycles and quality checks
- Stay updated with evolving regulatory guidelines, pharma industry trends, and scientific advances to ensure content freshness and compliance
Required Skills & Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Chemistry, or related discipline
- Minimum 2 years’ experience in pharmaceutical or life sciences content writing or medical / regulatory writing
- Strong understanding of U.S. pharma market, drug development lifecycle, manufacturing processes (e.g. API manufacturing, formulation, QC, validation), and regulatory compliance (FDA, GMP, ICH, GLP)
- Excellent written and verbal communication skills in English
- Robust research skills: ability to interpret scientific literature, regulatory documents, guidelines, clinical study reports
- Familiarity with SEO, content marketing strategy, digital publishing tools (e.g. WordPress, SEMrush, Grammarly)
- Ability to juggle multiple projects, meet tight deadlines, and incorporate feedback from multiple stakeholders
- Highly detail-oriented, with strong editing and fact-checking ability
Preferred / Nice to Have
- Experience working with pharma marketing agencies, CDMOs, CROs, or life science consulting
- Exposure to medical writing, regulatory writing, or scientific communication
- Experience in B2B pharma content creation, global/regional audiences, and cross-border regulatory environments
- Familiarity with publication norms (e.g. journal articles, clinical study reports), medical communication formats
What We Offer
- Competitive compensation package (INR range provided below)
- Work with leading pharmaceutical, biotech, and healthcare brands
- Flexible working environment and remote / hybrid opportunities
- Professional growth and learning opportunities in pharma and regulatory content
- Collaborative, knowledge-sharing, innovation-oriented culture
- Exposure to high-impact projects in drug development, medical communications, regulatory strategy
Application Instructions
Interested candidates should email careers@aaythamconsulting.com
