*Hi Friends,*

*Need Technical Writer w/ Pharma Validation*

*Please send me the related resumes to [email protected] *

Location : Groton, CT

Duration : 7 months

*Phone interview*

* *

*MANAGER WILL PREFER CANDIDATES THAT SUPPLY writing samples of things like
requirements documents. *

* *

*PLEASE PUT IN RESUME, OR EMBED ATTACHMENT(S) WITHIN RESUME.

**PHARMA VALIDATION** EXPERIENCE IS A MUST!***

The* *Technical Writer* *will be expected to:

a)         Develop and implement document standards consistent with the ELC
across the program and associated work streams

b)        Author required program and work stream documentation as agreed to
and outlined in the Deliverable Signature Matrix

c)         Manage the document review/approval cycle process to ensure all
appropriate team members are involved and a timely approval is achieved

d)        As required, attend work stream meetings, product information
demonstrations, workshops, and technical meetings for initial information
gathering

e)         Contribute to and participate in any testing activities that are
identified by the work stream team

f)          Thoroughly understand and apply the ELC to contribute to work
stream compliance with all requirements

g)        Support the Project Manager at ELC checkpoints by ensuring that
all documentation prerequisites are met and electronic copies are posted to
the document repository within the specified timeframe

h)        Maintain the work stream Deliverable Signature Matrix

i)          Manage the document repository contents for assigned work
stream(s)

j)           Maintain open communication and conduct peer review within the
Technical Writer group to ensure standardization and quality deliverables
across the program

k)        Co-ordinate activities to ensure efficient use of Colleagues’ time
and initiate corrective action where necessary


-- 
Thanks & Regards
James
Astoline Inc
Phone : 732-658-9252
E-mail : [email protected]
www.astoline.com
please make a note of my new email ID [email protected]

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