Quality Technical Writer (Contract)

KymanoxMorrisville, NC
Onsite

About The Position

The Technical Writer – General QMS (Contract) will perform technical writing and client support on a site readiness project authoring a range of engineering, compliance, and commercialization Standard Operating Procedures (SOPs).

Requirements

  • A minimum of 3 to 5 years of experience in development and/or manufacturing in the pharmaceutical, biotechnology, combination product, and/or medical device sectors is required.
  • Bachelor’s degree in any Engineering discipline (prefer Biomedical, Mechanical, or Chemical engineering) or other STEM discipline (Biology, Chemistry, other) from an accredited institution or equivalent.
  • Resourceful
  • Extremely detail oriented
  • Ability to work effectively with remote team members
  • Highly organized
  • Self-directing, self-pacing
  • Excellent written and oral English communication skills
  • Understanding of own limitations
  • Ability to solicit and utilize subject matter expert input
  • Fast learner
  • Pleasant and positive communication style
  • Strong customer-service aptitude
  • Ability to motivate self, team members, and direct reports
  • High energy level
  • Excellent problem-solving skills
  • Seasoned soft skills (i.e., high EQ)
  • Team player

Nice To Haves

  • Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired.

Responsibilities

  • Technical writing may include any of the following focus areas: Manufacturing equipment and processes, Quality Control Laboratory instruments and methods, Utility systems, Facilities and maintenance equipment, Logistics and warehousing processes, Quality Assurance processes, Environment, Health, and Safety processes, Warehouse and Supply Chain, Information Technology, Training content.

Benefits

  • Hourly rate is commensurate with experience, qualifications, and other intangibles evident during the interview process – as well as market conditions.
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