Documentation Specialist

job
  • Planet Pharma
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Job Summary
Location
Woburn ,MA
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
03 Feb 2025
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Job Description

Onsite 2 days per week

Woburn, MA

$30 - $40 per hr

4- 5 month extendable CONTRACT (may convert permanent but not guaranteed)


*MUST HAVE Pharma, biotech, or medical device experience*


Job description

Key Responsibilities:

  • Document Analysis and Assessment:
  • Review existing manufacturing and engineering documentation from the acquired company.
  • Assess documents for relevance, accuracy, completeness, and compliance with industry standards.
  • Content Transfer and Standardization:
  • Convert legacy documentation into the acquiring company’s formats and templates.
  • Ensure content adheres to corporate branding and formatting guidelines.
  • Restructure technical content to align with the acquiring company’s processes and workflows.
  • Collaboration and Communication:
  • Work closely with engineering, manufacturing, and quality assurance teams to ensure accuracy and completeness of documentation.
  • Liaise with subject matter experts (SMEs) to clarify technical details and resolve discrepancies.
  • Version Control and Organization:
  • Maintain proper version control during the document transfer and update process.
  • Organize and archive transferred documents in the company’s document management system.
  • Quality Assurance:
  • Conduct thorough reviews and audits of transferred documentation to ensure high-quality standards.
  • Identify and rectify errors or inconsistencies in technical content.
  • Process Improvement:
  • Provide recommendations for improving documentation processes and workflows.
  • Assist in developing guidelines and best practices for future documentation integration projects.


Qualifications

  • Bachelor’s degree in any subject or 5+ years in Technical Writing, Engineering, OR a related field (or equivalent experience).
  • 3+ years of experience editing documentation or managing corporate documentation in the pharma, biotech or medical device industry - required
  • Past experience working with a Quality Management System (QMS)
  • Proficiency in using document management systems and tools such as Microsoft Office, Adobe Acrobat, and (specific tools, e.g., SharePoint, Confluence, or others as relevant).
  • Excellent written communication skills.
  • Exceptional attention to detail and organizational skills.
  • Ability to manage multiple tasks and deadlines effectively.

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