What you will do Write blogs, articles and long-form pieces on pharma quality topics: validation, data integrity, audits, supplier qualification, document control. Own the content calendar and keep it moving.

Write the shorter things too: Linked In posts, email copy, landing page text, case studies. Build and run Linked In ad campaigns in Campaign Manager: audience setup, ad copy, A/B tests, budget pacing, weekly reporting.

Qualifications Excellent written English. This is the single most key thing we are hiring for. Clear, correct, readable, and in your own voice. A bachelor's degree in Biotechnology/ Pharmacy (BPharm); prior experience in the pharmaceutical manufacturing industry is an advantage Basic knowledge of how to use Claude How we will assess you Go through our website .

Research either electronic logbook or Equipment Qualification. Send us by email a short write-up (200-300 words)on one of the 2 topics.



Use AI to research if you like, but the article you send us has to be yours.

Send the sample to hr@ Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including e Residue Pro, e Process Pro, and e Log Book, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles.

With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations.

📌 Biotech/bpharm/science Graduates - Chennai - Content Writing
🏢 Quascenta
📍 Chennai