Principal Technical Writer
Grove Technical Resources · North Haven, Connecticut, United States
FULL TIMEpermanent
Job Description
Hiring: Engineering Technical Writer – Medical DeviceLocation: North Haven, CT (Preferred) | Lafayette, CO | Mounds View, MNWork Model: Onsite 4 days/week, Remote 1 day/weekDuration: 12 MonthsEmployment Type: W2 Contract
Scroll down the page to see all associated job requirements, and any responsibilities successful candidates can expect.
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. xzbcwsv North Haven, CT, is the preferred location, but candidates in Lafayette, CO, and Mounds View, MN, will also be considered.
Scroll down the page to see all associated job requirements, and any responsibilities successful candidates can expect.
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. xzbcwsv North Haven, CT, is the preferred location, but candidates in Lafayette, CO, and Mounds View, MN, will also be considered.
Details
| Company | Grove Technical Resources |
| Location | North Haven, Connecticut, United States |
| Type | FULL TIME |
| Niche | hr |
| Experience | permanent |