- Education: Bachelor's degree in Engineering or Biological Sciences with 1-3 years of relevant industry experience
- Experience in a GMP environment
- Understanding of GMP documentation requirements
- Ability to work autonomously and within a team
- Prior involvement in the production of large molecule substances like vaccines or biologics
- Familiarity with SAP system is beneficial
- Knowledge of electronic document management systems, including Veeva Vault. Strong technical writing skills (in a GMP setting)
- Effective organizational and communication abilities
- Managing project timelines and schedules efficiently
- Proficiency in MS Word, and working knowledge of MS Office (Excel, PowerPoint)
- Creating and updating SOPs following Good Documentation Practices (GDP) to aid in the upcoming business system implementation in the large molecule manufacturing domain
- Collaborating with subject matter experts from different business areas to incorporate functional and technical needs from manufacturing and other supporting units into SOPs for compliance with the new business system implementation
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Technical Writer - West Point, United States - IMS People
Description
Job Description
Job Title: Technical Document Writer
Duration: 1 Year Contract
Location: ONSITE - 770 Sumneytown Pike, West Point, PA 19486
Hours: Monday to Friday, 8:00 am - 4:30 pm
Compensation: $40.17 per hour (38% Markup)
Qualifications:
Required Skills and Experience:
Desired Skills and Experience:
Responsibilities:
Candidate will engage in various tasks such as: