Principal Technical Writer

Summary

Hiring: Engineering Technical Writer – Medical Device

Location: North Haven, CT (Preferred) | Lafayette, CO | Mounds View, MN

Work Model: Onsite 4 days/week, Remote 1 day/week

Duration: 12 Months

Employment Type: W2 Contract

Key Skills Required:

5–10 years of experience in Technical Writing, preferably in the Medical Device industry.

Strong written/verbal communication and cross-functional collaboration skills.

Experience with medical device labeling and Instructions for Use (IFU) documentation.

Proficiency with authoring tools such as Adobe InDesign, FrameMaker, and XML tools.

Knowledge of regulatory compliance, quality management systems, CAPA, and Engineering Change Orders (ECO).

Experience coordinating translations, reviewing labeling proofs, and supporting product launches.

Key Responsibilities:

Develop and update medical device labeling and IFU documentation.

Coordinate document approvals, translations, and labeling deliverables.

Collaborate with cross-functional teams to ensure regulatory compliance and support product launches.

Important: Candidates must be able to work onsite 4 days per week. North Haven, CT, is the preferred location, but candidates in Lafayette, CO, and Mounds View, MN, will also be considered.

Job Description

Hiring: Engineering Technical Writer – Medical Device

Location: North Haven, CT (Preferred) | Lafayette, CO | Mounds View, MN

Work Model: Onsite 4 days/week, Remote 1 day/week

Duration: 12 Months

Employment Type: W2 Contract

Key Skills Required:

5–10 years of experience in Technical Writing, preferably in the Medical Device industry.

Strong written/verbal communication and cross-functional collaboration skills.

Experience with medical device labeling and Instructions for Use (IFU) documentation.

Proficiency with authoring tools such as Adobe InDesign, FrameMaker, and XML tools.

Knowledge of regulatory compliance, quality management systems, CAPA, and Engineering Change Orders (ECO).

Experience coordinating translations, reviewing labeling proofs, and supporting product launches.

Key Responsibilities:

Develop and update medical device labeling and IFU documentation.

Coordinate document approvals, translations, and labeling deliverables.

Collaborate with cross-functional teams to ensure regulatory compliance and support product launches.

Important: Candidates must be able to work onsite 4 days per week. North Haven, CT, is the preferred location, but candidates in Lafayette, CO, and Mounds View, MN, will also be considered.