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GMP Online Consultancy is seeking to appoint independent professional writers to author
GMP documents and templates (e.g. standard operating procedures or validation plans) for our
online document portfolio.
Applicants should have in-depth knowledge of the pharmaceutical industry and, in particular,
GxP regulations in one of the following areas:
- Drug products
- Active pharmaceutical ingredients (drug substances)
- Biologics
- Devices
Applicants must also have experience in writing GMP documents and should be able to work
independently and provide final drafts of documents in line with a set format provided by
GMP Online Consultancy. Applicants should also be able to submit proposals for additional
documents that could enhance our portfolio.
Remuneration will be negotiated on an individual basis and will be determined by the quality
and quantity of submitted documents.
Applicants should send a resume and covering letter to
info@gmp-online-consultancy.com
with up to three sample documents attached.
In the covering letter, you should explain why you are the best person to write GMP documents
for our online service and provide an approximate figure for the number of documents you will
be able to submit.
Please do not contact us by phone. Successful applicants will be contacted and invited to
submit a proposal for further consideration. We regret that we may be unable to reply to all
applicants on an individual basis.
We look forward to receiving your application.
Your GMP Online Consultancy team
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