• US Citizen

• Green Card

• EAD (OPT/CPT/GC/H4)

• H1B Work Permit

• Corp-Corp

• W2-Permanent

• W2-Contract

• 1099-Contract

• Contract to Hire

• Consulting/Contract

• UG :- - Not Required

• PG :- - Not Required

• No of position :- ( 1 )

• Post :- 5th May 2026

·         7+ years of technical writing experience, with a strong focus on regulated industries such as medical devices, pharmaceuticals, or biotechnology

·         Extensive experience working with FDA and ISO 13485:2016 standards, with a proven track record of delivering high-quality, compliant technical documentation

·         Strong understanding of Good Manufacturing Practices (GMP) and experience in Quality Management Systems (QMS)

·         Demonstrated ability to lead complex documentation projects, manage multiple priorities, and meet tight deadlines

·         Excellent written and verbal communication skills, with the ability to present complex technical information clearly and concisely to various audiences

·         Highly detail-oriented with a commitment to producing error-free documentation

·         Strong leadership skills, with the ability to collaborate effectively within cross-functional teams and mentor junior staff

·         Familiarity with electronic document management systems and change control processes in a regulated environment