KKR Consulting · 18 hours ago
Technical Writer
North Carolina, United States
Contract
Onsite
Entry, Mid Level
2+ years expKKR Consulting partners with businesses to solve challenges, streamline processes, and achieve lasting success. The Technical Writer is responsible for creating, reviewing, and maintaining controlled documentation in support of pharmaceutical manufacturing, quality, and validation activities.
Staffing & Recruiting
Hiring Manager
Dyutipriya Sarkar
Responsibilities
Author, edit, and format GMP documentation including SOPs, work instructions, protocols, reports, and technical manuals
Collaborate with subject matter experts to gather and clarify technical content
Ensure documentation complies with FDA, EU GMP, and internal quality standards
Maintain document control, versioning, and archival practices
Support validation, qualification, and quality documentation efforts
Review documents for clarity, consistency, and data integrity
Support audits, inspections, and documentation remediation activities
Qualification
Required
Bachelor's degree in Life Sciences, Technical Communication, Engineering, or related field
2–5 years of experience as a Technical Writer in the pharmaceutical or regulated life sciences industry
Strong knowledge of GMP documentation practices
Experience authoring controlled documents within a quality management system
Excellent written and verbal communication skills
High attention to detail and organizational skills
Benefits
Medical insurance
Vision insurance
Dental insurance
401(k)
Company
KKR Consulting
At KKR Consulting, we collaborate with businesses across a wide range of industries to tackle complex challenges, fuel sustainable growth, and connect them with exceptional talent.
11-50 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase