Technical reputed company - QA (Life Sciences)
Details:
We are looking for a Technical reputed company with experience in reputed company Assurance reputed company the Life Sciences industry. The candidate will be responsible for creating, reviewing, and maintaining QA documentation in compliance with regulatory standards.
Key Responsibilities:
• Write and review SOPs, validation documents, deviations, CAPA, and change controls
• Ensure compliance with FDA, GMP, and ISO standards
• Support QA audits and documentation control
• Work closely with QA and cross-functional teams
Requirements:
• 4–6+ years of Technical Writing experience in Life Sciences
• Strong knowledge of QA documentation in regulated environments
• Experience with document management systems
• Good communication and attention to detail
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