Technical Writer - Danvers, United States - Johnson & Johnson

Johnson & Johnson

Verified Company

Danvers, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Johnson & Johnson is currently seeking a Technical Writer to join our Quality department located in Danvers, MA. This role is open to a hybrid schedule.

Abiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives.

Abiomed's "Patients First" culture drives our skilled workforce and strong relationships with clinicians.

Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.

Founded in 1981, Abiomed has a proven track record for growth, integrity and innovation.

Principle Du ti
es and Responsibili ti
es:

Develop and update process documentation including assembly procedures, test procedures, routers, travelers, BOMs, process flows, and process FMEAs.
Work with the training team to develop short videos that can supplement hands on training.
Ability to work in crossfunctional teams that span global operations. Proficient in English verbal and written communication. Ability to translate WI and JIBs to and from to German or work with a translator is necessary.
Must enjoy team approach over individual contributions. Ability to be a liaison with manufacturing assemblers and engineering teams to develop and edit work instructions and assembly documentation.
Support and implement company goals and objectives, policies and procedures, Good Manufacturing Practices, Good Documentation Practices, FDA QSR and ISO regulations. Knowledge of FDA QSR and ISO regulations required.
Regularly report on project status, schedule progress and key project metrics through scorecard presentations
Assist engineering team to qualify and optimize processes and tooling via documentation for IQ/OQ/PQ, preventive maintenance, Gage R&R Studies, Process Capability Studies and Designs of Experiments.
Participate in the implementation of internal corrective actions and audit findings
Maintain accurate documentation of concepts, designs, and processes while maintaining current knowledge of medical, technical, and biomedical developments related to company products.

Qualifications:

Bachelors required in life sciences and/or writing, medical device experience preferred.
2+ years of technical documentation experience
Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) within the internal project team
Must be proficient in Microsoft Office Suite. Working knowledge of QMS desired.
Willing & able to travel internationally (~5%)

Preferred Quali fi
ca ti
ons: