Looking for a Technical Writer Pharma QA job in Chennai? Quascenta is hiring an experienced Technical Writer – Pharmaceutical Quality Assurance to create high-quality content on sterile injectables, validation lifecycle management, quality systems, and regulatory compliance.
This full-time, on-site opportunity in Chennai is ideal for professionals with a background in pharmaceutical manufacturing, quality assurance (QA), validation, or regulatory affairs who have strong scientific writing skills.
About Quascenta
Quascenta develops advanced validation lifecycle management software solutions for the pharmaceutical manufacturing industry. Its flagship products—eResiduePro, eProcessPro, and eLogBook—help pharma companies streamline product, process, and cleaning lifecycle management while ensuring regulatory compliance and operational excellence.
The company works closely with pharmaceutical QA, validation, and regulatory teams to enhance compliance with global standards such as EU GMP Annex 1 and 21 CFR Part 210/211.
Job Overview: Technical Writer – Pharmaceutical Quality Assurance
As a Technical Writer (Pharma QA), you will develop in-depth, research-driven content including:
- Blog articles
- Whitepapers
- Regulatory explainers
- Checklists and how-to guides
- Validation lifecycle knowledge series
This role focuses on translating complex topics like aseptic processing, cleaning validation, data integrity, QMS, and process validation into structured, clear, and engaging content for pharma professionals.
Key Responsibilities
- Research and write articles on pharmaceutical manufacturing, validation, and quality systems
- Create explainers on topics like:
- Aseptic processing
- Cleaning validation
- Data integrity compliance
- Annex 1 updates
- 21 CFR Part 210/211 requirements
- Interview internal SMEs (QA, Production, Validation, Regulatory Affairs)
- Develop structured content outlines and editorial calendars
- Ensure regulatory accuracy and technical correctness
- Optimize content for digital publishing (SEO, headings, summaries, internal links)
- Maintain terminology consistency and version control
- Stay updated with global pharma regulatory developments
This pharma technical writing job in Chennai requires precision, regulatory awareness, and strong domain understanding.
Qualifications & Requirements
- Educational background in Pharmacy, Life Sciences, Biotech, or related field
- Demonstrated experience in:
- Pharmaceutical technical writing
- Regulatory documentation
- QA/Validation documentation
- Strong knowledge of:
- EU GMP Annex 1
- 21 CFR Part 210/211
- Cleaning validation & hold time studies
- Process validation lifecycle (Stage 1–3)
- Data integrity principles
- Excellent written English and structured writing ability
- Strong research and analytical skills
- High attention to detail and regulatory terminology accuracy
- Portfolio or writing samples required
Professionals from QA, Validation, Regulatory Affairs, or Medical Writing backgrounds are strongly encouraged to apply.
Salary & Benefits
- Estimated Salary Range: ₹5,00,000 – ₹8,00,000 per annum (based on experience)
- Full-time on-site role in Chennai
- Opportunity to work at the intersection of pharma compliance and technology
- Exposure to advanced validation lifecycle management software
- Collaborative work with subject matter experts
- Career growth in pharmaceutical knowledge leadership
Location
📍 Chennai, Tamil Nadu, India
(On-site, Full-Time)
Why This Role Is Valuable for Pharma Professionals
This Technical Writer Pharma QA job offers a unique opportunity to build subject matter authority in:
- Validation lifecycle management
- Cleaning validation strategy
- Aseptic processing compliance
- Data integrity frameworks
- Pharmaceutical quality systems
It is especially suitable for professionals transitioning from QA/Validation to technical or regulatory writing careers.
How to Apply
