Technical Writer - Pharmaceutical

Technical Writer / Document Control Specialist (Pharma) – India → U.S. Support

Mumbai, India | Full-Time | On-site | U.S. Overlap

Turn complex manufacturing and quality work into clear, compliant, releasable records. Hubot, Inc. (CDMO) is hiring a pharma Technical Writer / Document Control Specialist to support our U.S. operations—authoring and QA-grade reviewing BMR / BPR, Specifications, SOP / WI, APR / PQR, and Product Release packages inside a validated eQMS.

Why Join Hubot?

25–30% YoY growth with momentum through 2030

4.8 Glassdoor | 4.7 Indeed | 95% recommend | Wellbeing 79

Impact that counts : Your documents enable batch release and audit readiness in the U.S.

Global collaboration : Daily partnership with U.S. QA / Manufacturing / Validation / Regulatory

Career path : Senior Writer → Documentation Lead → Quality Systems / Regulatory Docs

What You’ll Do

• Draft, edit, and review BMR / BPR and packaging records to GDP standards
• Create / maintain raw / pack / FG specifications; manage redlines and version control
• Compile release packages; verify vs. specs, CoA / CoC, deviations / CAPA; sign off as authorized
• Build APR / PQR trend reports (OOS / OOT, deviations, complaints, stability, yields)
• Author / revise SOPs / WIs / forms / process flows; route via eQMS / DMS with full change control
• Support audit / inspection readiness and rapid document retrieval

Who You Are (Pharma-first)

Success Metrics

Ready to write the records that release the products? Apply or message us directly.

For a more detailed brief, visit www.hubot.us.

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