Job Summary

A consulting and talent solutions company has an open position for a Remote Senior Technical Writer.

Candidates will be responsible for the following:

• Validation activities in a cGMP /CBER regulated medical device manufacturing environment
• Preparation of validation documents such as protocols, final reports and plans

Qualifications Include:

• 1-3 years experience in manufacturing, preferably in a biotech or diagnostic equipment industry, required
• Demonstrates potential for technical proficiency
• Demonstrated troubleshooting and problem solving skills
• Strong teamwork and communication skills
• Bachelor’s degree in science, engineering or related field