Job title: Technical writing specialist
Company: Golden Opportunities Private Limited
Job description: Description Ability to author and review technical process documents with specific attention to detail and consistency Create, maintain and update policies, , training materials, and other technical materials in accordance with applicable laws and co
Description Ability to author and review technical process documents with specific attention to detail and consistency Create, maintain and update policies, , training materials, and other technical materials in accordance with applicable laws and company/site standards. Gather inputs and collaborate with the team Works closely with the project lead(s) and ensures that all assigned documents are proceeding to stated operational commitments with minimal guidance Coordinate and collaborate with cross-functional teams. Secure stakeholders buy-in on timing and process for completing agreed-upon procedural changes. Conducts issue resolution, supports communications with clients (internal) and their functional areas to ensure that all issues are resolved in a compliant manner Perform basic document management tasks including file transfer, storage, tracking, and archival Contribute to the completion of projects and milestones. Assist in technical training of staff, as needed. Other duties as assigned Job Requirements: Bachelors degree in Science (Chemistry, Biology, or related science) 5+ years of experience in a technical writing role in the pharmaceutical industry environment is required. Strong writing and communication skills Excellent communication skills Ability to interact and build relationships with individuals at all levels Adept at translating technical and scientific information Strong knowledge of Microsoft office software and browser-based platform Experience with writing Standard Operating Procedures Prior experience in Operations and life Sciences industry Experience working both independently and, in a team,-oriented, collaborative environment is essential. Additional preferred Qualifications: Understanding of regulations and standards governing digital and electronic recordkeeping and e-signatures, and how these standards impact our customers compliance with GCP, GMP, GVP, MDR and other regulations governing pharma, medical device, biologics and other Life Sciences companies. Excellent presentation, technical writing and editing skills, with focus on distilling and explaining completed documents to stakeholders Proficiency in additional languages a plus
Expected salary:
Location: Ernakulam, Kerala
Job date: Fri, 18 Feb 2022 23:31:57 GMT
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