Top 12 Technical writers Jobs in Canton, Ga

Deviation Writer
Osmotica Pharmaceutical —Marietta, GA
- From $1 an hour
- Full-time
- Mid-level
- Microsoft Office
- 3 years
Quick Apply
14d
Technical Writer II
Yamaha Motor US —Kennesaw, GA
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Profit sharing
- Wellness program
Publications Technical Senior Editor
Honda —Alpharetta, GA
- $72,100 - $90,100 a year
- Full-time
- 5 years
- Office
- Ability to lift 50 pounds
- Paid holidays
- Loan repayment program
Technical Writer
Landis+Gyr —Alpharetta, GA
- $76,400 - $92,000 a year
- Microsoft Outlook
- English
- Mid-level
- Paid holidays
- Health insurance
6d
Senior Technical Writer
Fiserv —Alpharetta, GA
- $60,000 - $105,600 a year
- Full-time
- Computer Science
- Research
- 3 years
9d
Deviation Writer - Osmotica Pharmaceuticals
Osmotica —Marietta, GA
- Mid-level
- Microsoft Office
- 3 years
Quick Apply
Deviation Writer - Osmotica Pharmaceuticals
Alora Pharmaceuticals —Marietta, GA
- Mid-level
- Microsoft Office
- 3 years

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To succeed in this role, you must have a solid foundation in UX and technical writing practices and be able to connect content decisions to user needs, product…
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8d

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Technical Writer - Raymond Ohio
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Bachelor's degree in communications or appropriate comparable discipline or 3 + years technical writing experience.
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technical writers jobs near canton, ga

Deviation Writer

Osmotica Pharmaceutical -
Marietta, GA

Quick Apply

Job Details

Full-time
From $1 an hour
14 days ago

Qualifications

Report writing
Content creation for technical audiences
Technical documentation
Technical writing experience within manufacturing
GMP
Manufacturing facility experience
Bachelor's degree
Technical writing
Pharmaceutical manufacturing facility experience

Full Job Description

POSITION OVERVIEW

Conduct and write formal investigation of process deviations for Manufacturing with the assistance of site personnel. This position will also perform initial and final impact risk assessment as well as assist in root cause determination and plan appropriate corrective action and preventative action. The incumbent will also assist in the tracking and trending of historical data and assure timely closure.

DUTIES AND RESPONSIBILITIES

Ensure compliance with relevant SOP’s while gathering, analyzing and applying information from

internal and external sources in order to perform a risk assessment of the impact each process

deviation and complaint has on the product, process and patient health and safety.

As part of the investigation, gather information from all necessary internal and external sources

in order to evaluate the impact of the deviation on previously manufacturing product, as well

as the risk to future operations.

Leads and support investigations across Manufacturing, Packing and other departments to ensure

timely closure for each investigation and follow-up activities.

Works with the functional areas to identify the most probably root cause(s) and determine

appropriate preventative and corrective actions.

Trend and analyze product compliant investigation data and address appropriate as well as

liaison with production and quality.

Work independently to comply with procedure driven guidelines relating to deviation and complaint investigations.
Conduct interviews with site personnel to gather data for the deviation report.
Perform as the lead in root cause problem-solving sessions.

EXPERIENCE AND QUALIFICATIONS

Bachelor’s degree (Biology, Microbiology, Chemistry, Pharmacy or similar)
3-5 years related experience in a cGMP facility
3-5 years of deviation, investigative writer experience or equivalent technical writing experience
Advanced writing skills
Strong critical thinking and deductive reasoning skills
Excellent interpersonal and communication (written and verbal) skills
Strong MS Office skills
Understanding of QA practices and standards is preferred

Job Type: Full-time

Pay: From $1.00 per hour

Education:

Bachelor's (Required)

Experience:

Technical writing: 3 years (Required)
working in a cGMP facility: 3 years (Required)
deviation investigative writer: 3 years (Required)

Work Location: In person

Quick Apply

Refine Your Search

technical writers jobs in canton, ga

Deviation Writer

Technical Writer II

Publications Technical Senior Editor

Technical Writer

Senior Technical Writer

Deviation Writer - Osmotica Pharmaceuticals

Deviation Writer - Osmotica Pharmaceuticals

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