Job Description
Summary: In search of a Manufacturing Technical Writer with expertise in sterile drug manufacturing for authoring, revising and managing technical documentation.
Job Requirements:
Bachelor's degree or equivalent work experience
A minimum of three years of related professional experience
Strong command over English language including grammar and composition
Demonstrated understanding of GMP / cGMP regulations
Preferred Skills:
Experience in sterile drug manufacturing
Familiarity with reactor and cyclotron derived new products
Job Responsibilities:
Use technical writing strategies to create clear, concise, and complete documentation
Author and revise technical documents such as facility and equipment SOPs, batch records, specifications, training documents etc.
Author and manage change controls to implement new procedures as well as revisions to existing documents to facilitate the launch of new products
Participate in process and equipment testing to understand the systems being documented.
Pay Details: $24.00 to $31.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
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The Company will consider qualified applicants with arrest and conviction records subject to federal contractor requirements and/or security clearance requirements.