Technical Writer

Integrated Resources Inc.; Sanford (NC); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in workforce solutions is seeking a Technical Writer in North Carolina. The successful applicant will be responsible for creating and reviewing essential documents while adhering to regulatory standards. Ideal candidates will have extensive experience in technical writing, particularly within the pharmaceutical industry, and must demonstrate superior editing skills and attention to detail. This role emphasizes collaboration with various departments and requires a proven track record in managing documents in compliance with cGMP guidelines.

Qualifications

• At least 5 years of technical writing experience.
• Experience in regulated environments preferred.
• Familiarity with cGMP and safety regulations.

Responsibilities

• Assist in creating and revising documents for the manufacturing department.
• Edit and format incoming document requests and maintain document control.
• Collaborate with departments to ensure content accuracy and compliance.

Skills

Editing

Technical Writing

Document Control

Proofreading

Communication Skills

Education

Bachelor's in Science, Communications, or English

AS in Communications or related field

Job description

IRI believes in commitment, integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with decades of industry experience. We deliver strategic workforce solutions to help manage talent and business efficiently. Since 1996, IRI has attracted and retained experts in various fields, expanding into new sectors and growing steadily.

We focus on finding qualified professionals in our specialty areas. Our partner-employers trust us to match their needs with top-tier candidates. By exceeding expectations, we've built successful partnerships rooted in performance and integrity.

Our team provides tailored solutions for each client, ensuring the right match between employers and candidates. We value long-term partnerships that align skills and cultures. At IRI, our success is linked to our clients' success.

Job Description

• Assist in creating, reviewing, and revising documents such as SOPs, forms, job aids, and training materials for the manufacturing department.

• Collaborate with co-workers and supervisors to understand document objectives, ensuring content accuracy and completeness.

• Organize information for clarity, accuracy, and proper formatting, maintaining high standards of grammar and spelling.

• Perform duties in accordance with site and corporate cGMP, safety, environmental, and HR policies.

• Prioritize primary responsibilities critical to the role, focusing on accountability and judgment rather than task listing.

• Edit and format incoming document requests, track revisions through approval workflows.

• Assist in developing new and revised documents, suggesting terminology, content, and format improvements in line with policies.

• Participate in bi-annual reviews of SOPs and related documents.

• Complete assigned commitments to support Corrective and Preventative Actions.

• Maintain document control, ensuring accurate history and revision records.

Organizational Relationships

• Interact regularly with site departments such as Supply Chain, Manufacturing, Quality, Compliance, and Technical Operations.

• Engage with network customers as needed.

Resources Managed

• Responsible for financial accountability, including budget or revenue management.

• Manage or coordinate resources, including direct or indirect reports, and possibly contingent workers.

Qualifications

• Bachelor's in Science, Communications, or English with at least 2 years of technical writing experience, preferably in pharmaceuticals.

• AS in Communications or related field with a minimum of 5 years in technical writing in regulated environments.

• At least 5 years of technical writing experience.

Technical Skills

• Efficiently edit documents, incorporate revisions, and develop standardized formats.

• Navigate document control and E-Systems for routing and approval.

• Proofread for content accuracy and clarity.

• Write clearly with excellent grammar and sentence structure.

• Translate verbal instructions into precise operating procedures.

• Adhere to document formats while maintaining technical content.

• Adapt to shifting priorities and manage stress effectively.

• Incorporate feedback and insights from others.

• Understand pharmaceutical processes and SOP design.

• Comply with cGMP and safety regulations.

• Demonstrate strong organizational and communication skills, with a collaborative approach to problem-solving.