Position Summary:
Technical Writer prepares/writes Design Verification reports for submission to KEMA and the FDA. This person is responsible for working closely with the engineering staff in preparing, reviewing and editing documents for proper use of terminology, style, direction, content, grammar, punctuation, and clarity along with ensuring uniformity and formatting of documents.
Duties & Responsibilities:
• Consults with the engineering team to write design verification reports for submission to KEMA and the FDA.
• Reviews and coordinates the preparation of reports.
• Reviews and edits technical writing.
• Provides consultation, makes recommendations, gives appropriate advise, and/or facilitates decisions regarding technical document format.
• Review and/or edit documents for accuracy and completeness
• Provide technical writing assistance to others
• Responsible for coordinating the display of graphics and the production of the document.
• Perform other task as assigned.
Qualification:
• Bachelor’s degree in related area preferred.
• 3 years experience in the field or related area.
• Knowledge of commonly used concepts, practices and procedures within the FDA regulated medical device development/manufacturing field preferred
• Be able to work effectively with engineering team.
• Ability to follow instructions and pre-established guidelines to perform functions of the position
• Exceptional knowledge and us of MS Word.
• Able to communicate information and ideas clearly and concisely, both in oral and written form.
• Able to read and understand information presented in writing.
• Able to evaluate information against a set of standards.
• Must speak clearly, concisely, and effective; must listen to, and understand information and ideas as presented verbally.
Email: job-796773029@craigslist.org
* Location: San Clemente
* Compensation: $35-40/hr
Duration: 3-6 months contract
Technical Writer prepares/writes Design Verification reports for submission to KEMA and the FDA. This person is responsible for working closely with the engineering staff in preparing, reviewing and editing documents for proper use of terminology, style, direction, content, grammar, punctuation, and clarity along with ensuring uniformity and formatting of documents.
Duties & Responsibilities:
• Consults with the engineering team to write design verification reports for submission to KEMA and the FDA.
• Reviews and coordinates the preparation of reports.
• Reviews and edits technical writing.
• Provides consultation, makes recommendations, gives appropriate advise, and/or facilitates decisions regarding technical document format.
• Review and/or edit documents for accuracy and completeness
• Provide technical writing assistance to others
• Responsible for coordinating the display of graphics and the production of the document.
• Perform other task as assigned.
Qualification:
• Bachelor’s degree in related area preferred.
• 3 years experience in the field or related area.
• Knowledge of commonly used concepts, practices and procedures within the FDA regulated medical device development/manufacturing field preferred
• Be able to work effectively with engineering team.
• Ability to follow instructions and pre-established guidelines to perform functions of the position
• Exceptional knowledge and us of MS Word.
• Able to communicate information and ideas clearly and concisely, both in oral and written form.
• Able to read and understand information presented in writing.
• Able to evaluate information against a set of standards.
• Must speak clearly, concisely, and effective; must listen to, and understand information and ideas as presented verbally.
Email: job-796773029@craigslist.org
* Location: San Clemente
* Compensation: $35-40/hr
Duration: 3-6 months contract
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