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Technical Writer (Need local)
San Francisco, CA
San Francisco
CA
94188
Date
: Apr-25-19
2019-04-25
2020-04-24
Technical Writer (Need local)
San Francisco, CA
Apr-25-19
Work Authorization
US Citizen
GC
H1B
OPT EAD, GC EAD, L2 EAD, H4 EAD
Preferred Employment
Corp-Corp
W2-Permanent
W2-Contract
1099-Contract
Contract to Hire
Job Details
Experience
:
Architect, Senior, Midlevel, Junior
Rate/Salary ($)
:
Market
Duration
:
9 months
Sp. Area
:
JS, Front End, UI, UX, Web, CMS
Sp. Skills
:
Technical/Content Writer
Consulting / Contract
CONTRACTOR
Required Skills
:
Technical Writer
Preferred Skills
:
Domain
:
Work Authorization
US Citizen
GC
OPT EAD, GC EAD, L2 EAD, H4 EAD
H1B
Preferred Employment
Corp-Corp
W2-Permanent
W2-Contract
1099-Contract
Contract to Hire
Job Details
Experience
:
Architect, Senior, Midlevel, Junior
Rate/Salary ($)
:
Market
Duration
:
9 months
Sp. Area
:
JS, Front End, UI, UX, Web, CMS
Sp. Skills
:
Technical/Content Writer
Consulting / Contract
CONTRACTOR
Required Skills
:
Technical Writer
Preferred Skills
:
Domain
:
Xchange Softwares
Parlin, NJ
Post Resume to
View Contact Details &
Apply for Job
Job Description
:
This is a nine month assignment in South San Francisco, CA, with potential for extension based on performance.
9 Months
Need local only
Overview:
Work with an up and coming company who is focused on developing and commercializing novel therapies in the field of Oncology.
The company is currently in the process of completing multiple clinical trials, and they need additional support due to an ramp up in clinical trials.
The primary responsibility of the Technical Writer will be to write and/or revise the written content of Standard Operating Procedures (SOP’s) to be used by the client''s Manufacturing and Global Supply Chain department.
Primary Responsibilities:
Create new or revise existing content for SOPs with a high degree of quality in accordance with cGMP requirements and corporate guidelines
Work collaboratively with project team members including Manufacturing, Analytical Development, Global Supply Chain, Quality and other subject-matter experts to solidify content.
Ensure SOPs are completed on schedule.
Technical Must Haves:
BS Degree in Science/Life science
3+ years related experience in technical writing
Experience in a Quality environment, and knowledge of GMP and/or ISO standards.
Experience writing SOPs from scratch in pharmaceutical and/or biotech manufacturing environment an asset.
Ability to work well with others and translate verbally received technical information and details into written SOPs.
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