Quascenta is hiring a Pharmaceutical QA Blog Content Writer in Chennai, Tamil Nadu for its PQMS Software Suite for Pharma Manufacturing. This is a full-time, on-site opportunity for professionals with expertise in pharmaceutical quality assurance (QA), GMP compliance, QMS systems, and regulatory documentation who are passionate about technical content writing and SEO.
If you have a strong background in pharma QA systems, validation, regulatory compliance, and digital transformation in pharma manufacturing, this role offers an opportunity to work at the intersection of quality management systems (QMS) and content strategy.
📌 Job Overview
- Position: Pharmaceutical QA Blog Content Writer
- Company: Quascenta
- Location: Chennai, Tamil Nadu, India
- Work Mode: On-site
- Employment Type: Full-time
- Industry Focus: Pharma Manufacturing, PQMS Software, Quality Management Systems
📝 Key Responsibilities
As a Pharmaceutical QA Content Writer, you will:
- Write authoritative blog posts, whitepapers, and case studies on:
- Pharmaceutical Quality Assurance (QA)
- GMP compliance
- Validation processes (IQ/OQ/PQ)
- Quality Management Systems (QMS)
- Digital transformation in pharma manufacturing
- Create SEO-optimized content targeting pharma QA keywords and regulatory topics.
- Collaborate with product, QA, and marketing teams to translate technical PQMS workflows into engaging content.
- Develop thought leadership content on regulatory compliance and validation frameworks.
- Suggest content strategies based on pharma industry trends and user search behavior.
This role requires the ability to simplify complex pharmaceutical regulatory workflows and QA systems into high-quality digital content.
🎓 Qualifications & Skills
Essential Requirements:
- Excellent written and spoken English.
- Proven experience in content writing or technical writing.
- Strong understanding of SEO principles and keyword optimization tools.
- Experience in pharma, biotech, or life sciences domain writing.
Preferred (Strong Advantage):
- Familiarity with:
- Quality Management Systems (QMS)
- GMP documentation
- Validation lifecycle
- Regulatory compliance workflows
- PQMS software platforms
- Experience writing content for pharmaceutical software products.
💼 Why This Role Matters
With increasing regulatory scrutiny and digital transformation across pharma manufacturing, PQMS software and pharma QA systems are critical for compliance and operational excellence. This Pharmaceutical QA Content Writer role enables professionals to contribute to:
- Regulatory awareness
- GMP best practices
- Digital QA adoption
- Thought leadership in pharma compliance technology
💰 Salary (Estimated Market Range – Chennai)
Based on similar pharma technical content roles in India:
₹4,00,000 – ₹8,50,000 per annum (CTC)
(Final compensation depends on experience and domain expertise.)
📩 How to Apply
