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In this position the Quality Assurance Associate will be responsible
for the creation and editing of cGMP standard operating procedures,
test instructions, batch records, and protocols. Incumbent will ensure
that all documents are consistent and contain the proper GMP elements
before review and approval. Will apply detail writing skills and acute
proof reading skills in creation of technical documents and review
of other employees documents respectively.
Human Resources, jobs@Vyteris.com
Tel: 201 703 2406
Fax: 201 703 2295
13-01 Pollitt Drive, Fair Lawn, NJ 07410
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