Associate Technical Writing

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com.

Duration: 36+ Months (Possible Of Extension)

Location: Thousand Oaks, CA

Technical Writing:
1. Initiate, revise, and approve manufacturing procedures using quality systems.
2. Work with subject matter experts to ensure procedures reflect current operations.
3. Draft and edit documents to produce clear, consistent and accurate procedures.
4. Format documents to established standards.
5. Assess document accuracy by observation of floor operations.
6. Assist in generation and revision of training materials.
7. Interact with functional groups to respond to comments during document revision and drive to resolution.

Project Management:
1. Update document schedules for revisions and product introductions.
2. Manage revision workflows so that document revisions meet the established target effective dates.

Projects and Initiatives:
1. Participate on the assessment or implementation of special projects or initiatives.

Education/ Licenses:
• Bachelors Degree or
• Associates Degree with 4 years related experience, or
• High School diploma/GED with 6 years related experience

Basic Qualifications:
Technical writing experience for documents in a regulated environment

Preferred Qualifications:
• Experience working with documents in a regulated industry
• Understanding of GMP requirements
• Ability to perform routine functions using established standards and procedures
• Ability to work independently and on teams
• Able to prioritize and manage multiple tasks
• Ability to work in a fast paced environment
• Organizational and presentation skills.
• Basic project management skills.

Education/ Licenses:
• Bachelors Degree or
• Associates Degree with 4 years related experience, or
• High School diploma/GED with 6 years related experience

Basic Qualifications:
Technical writing experience for documents in a regulated environment

Preferred Qualifications:
• Experience working with documents in a regulated industry
• Understanding of GMP requirements
• Ability to perform routine functions using established standards and procedures
• Ability to work independently and on teams
• Able to prioritize and manage multiple tasks
• Ability to work in a fast paced environment
• Organizational and presentation skills.
• Basic project management skills.