Seeking a Technical Writer with 2+ years of experience in pharmaceutical or regulated environments, or 5+ years with an AS in Communications or related field.
Responsibilities include creating, reviewing, and revising SOPs, forms, job aids, and training materials, ensuring accuracy, clarity, and compliance with cGMP and safety standards.
Must be skilled in editing, formatting, and document control systems, with strong English language proficiency and excellent grammar.
Ability to interpret technical information, adapt to shifting priorities, and collaborate effectively is essential.
Qualifications include knowledge of pharmaceutical processes, document management, and regulations, along with strong organizational and communication skills.
Ideal candidates are detail-oriented, capable of working efficiently under pressure, and committed to maintaining high-quality documentation standards.