REF#BIG20334



Hours:

• 8a.m.-5p.m. - Monday-Friday, Onsite

Scope:

Create VWIs, LOTO, SOP, SOS, PM documents in support of Pharmaceutical Technologies. Experience with cGMP and or EtQ a plus.

 

• Creates, develops, plans, writes, and edits operational, instructional, maintenance or test procedures for paper, multimedia or web-based publication.


• Conducts interviews with various users and technical staff to gather data for documentation.


• Researches and translates technical information into manuals and/or web-based documents for nontechnical users.


• May document engineering processes and specifications.


• Recommends formats responsive to technical and customer requirements.


• Produces products that conform to the company documentation and quality assurance standards.


• Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.


• Exercises judgment within defined procedures and practices to determine appropriate action.


• Has internal and some external contacts.

• Location: USA - NY - Big Flats 


• Duration of contract: 7 Months


• Education/ Experience: AS, 3+ Years