Technical Writer (NJ) (FullTime)

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Provide technical writing support to Eyetech personnel (users) in the manufacturing, quality and regulatory departments. Create and revise protocols, reports, SOPs, test methods, specifications, batch records, forms, etc., as required by the users based on user input obtained through draft documents, flow charts, meetings, etc. Will also create documents with only minimal user input through reading company, contractor, supplier, regulatory or pharmacopoeial documents and observing facilities, utilities, equipment, manufacturing and laboratory activities as necessary. Ensures documents are written and formatted according to company procedures and GMPs.

Qualifications

• A college degree in a scientific or technical discipline is required. A degree in chemistry is preferred.
• Experienced in writing technical documents combined with excellent writing skills.
• A minimum of 2-3 years experience working in the pharmaceutical or allied industry. Experienced in writing technical documents combined with excellent writing skills.
• Past experience working in a laboratory and/or manufacturing environment is preferred.
• Strong interpersonal skills, an attention to detail, computer proficiency including MS office and a good working knowledge of cGMPs are required.