Technical writer (cGMP/FDA regulated)

100% Onsite Role in Bothell, Washington

Job Title: Technical Writer
TOP SKILLS:

• Minimum of 1 year of relevant document management in a cGMP/FDA regulated environment.
• 1-2 years of MS Office 365
• 1 years working in quality systems or project work

Experience Basic Qualifications:

• Minimum of 1 year of relevant document management in a cGMP/FDA regulated environment.
• Strong communication and customer service skills.
• Some technical writing skill set including the ability to critically review documents while effectively inputting and expressing Quality principles.
• Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System)
• Must demonstrate the following behaviors consistently: Innovative, proactive, and resourceful; committed to quality and continuous improvement.
• Able to prioritize, manage time well, multi-task, and troubleshoot effectively.
• Ability to work effectively and collaboratively at a fast pace with cross functional departments to finalize time-sensitive deliverables.
• Possess project management skills.
• Experience interacting with FDA or other regulatory agencies preferred.
• Knowledge of cGMPs and regulatory requirements.
• Knowledge of manufacturing quality (manufacturing, packaging, facilities, critical systems, validation, etc.).
• Must complete tasks independently, notify manager of decisions outside of established processes and the ability to build an internal network.

Job Types: Full-time, Contract

Pay: $49.97 - $53.17 per hour

Schedule:

• 10 hour shift
• 12 hour shift
• 8 hour shift
• Monday to Friday

Experience:

• Microsoft Powerpoint: 1 year (Preferred)

Ability to Commute:

• Bothell, WA 98021 (Required)

Ability to Relocate:

• Bothell, WA 98021: Relocate before starting work (Required)

Work Location: In person

Salary : $50 - $53