Technical Writer

2 days ago

Athens, United States Source One Technical Solutions Full time

Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturer in Athens, GA. This role will require you to be onsite 100%


Title: Specialist 3 - Technical Writing

w2 hourly rate: $34.23

Contract Duration: 12 months, with likely extension


General Summary:

***Must have pharmaceutical, biotech life science experience. Will be working in a GMP / regulatory environment


Produces complex technical written communications used for projects assigned to department. Projects may include marketing tools, technical manuals, and presentations.

May participate in special projects. Duties & Responsibilities: Prepares work to be accomplished by reviewing delivery schedules and prioritizing work, gathering, organizing and analyzing technical information from various relevant sources. Verifies facts and clarifies information as needed. Develops, writes, edits and proofs complex assignments for various internal customers. Ensures Company publications meet established standards of style and format. Reviews photographs, drawings, sketches, diagrams, and charts selected for specific publications to ensure relevance to content.

Generates and reviews text for nontechnical documents upon request. Serves as editing consultant to other staff. Suggests format, layout and graphics for materials reviewed. Reviews published materials and recommends revisions or changes in scope, format, and content.

Produces rough draft of revised versions. Mentors less experienced employees by providing guidance and input on work assignments. Reviews drafts for adherence to business standards. Investigates and resolves customer complaints and concerns. Responds to complicated inquiries. Participates in or leads projects as assigned.

Provides input into project parameters and timelines. Makes recommendations on method and materials for optimum results.


Work Experience: Generally Requires 4-6 Years

Education Required: University/Bachelor’s Degree or Equivalent


Additional Notes

Role is 100% ONSITE:

- Bachelors degree in technical area

- At least 2+ years of exp of technical writing

- Will be working in a GMP / regulatory environment

- Must be able to work with minimal information/direction to get tasks done

- There will be data sorting and decision making

- Working with a team of Engineers

- Must have exp with Chemical Engineering or Industrial Engineering

- Must be detail oriented

- Will write validations and protocols (they use templates)


Please Note: This position is W2 hourly. Will not respond to C2C, 3rd party agencies, or candidates not authorized to work in the United States.

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