Quality Technical Writer (Contract)
About the role
As a Technical Writer – General QMS (Contract), you will perform technical writing and client support on a site readiness project, authoring a range of engineering, compliance, and commercialization Standard Operating Procedures (SOPs).
Responsibilities
- Technical writing for manufacturing equipment and processes
- Technical writing for Quality Control Laboratory instruments and methods
- Technical writing for utility systems
- Technical writing for facilities and maintenance equipment
- Technical writing for logistics and warehousing processes
- Technical writing for Quality Assurance processes
- Technical writing for Environment, Health, and Safety processes
- Technical writing for Warehouse and Supply Chain
- Technical writing for Information Technology
- Technical writing for training content
Requirements
- Bachelor’s degree in any Engineering discipline (preferably Biomedical, Mechanical, or Chemical engineering) or other STEM discipline (Biology, Chemistry, etc.) from an accredited institution or equivalent
- Minimum of 3 to 5 years of experience in development and/or manufacturing in the pharmaceutical, biotechnology, combination product, and/or medical device sectors
- Senior-level candidates with 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries are desired
Skills
- Resourceful
- Extremely detail-oriented
- Ability to work effectively with remote team members
- Highly organized
- Self-directing and 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
About Kymanox
Kymanox is a life sciences professional services company dedicated to helping a broad range of life science products get to market more quickly, affordably, and with the highest quality and safety standards. We have successfully delivered over 4,000 projects across 20+ countries in the biotechnology, pharmaceutical, medical device, and combination product industries.
With a reputation for providing unparalleled professional services, our highly collaborative team of engineering, compliance, and project management experts offers outstanding opportunities for learning and career advancement. Kymanox encourages team members, especially new graduates and young professionals, to work on a variety of projects to gain increased knowledge in our service offerings and the life science industry as a whole.
Founded in 2004 and headquartered in Research Triangle Park, NC, Kymanox serves clients ranging from Fortune 100 companies to virtual start-ups. We are looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market.