(Contract) Quality, Veeva Document Admin

Kymanox • Morrisville, NC

5d

About The Position

The Contract Quality, Veeva Document Admin will provide technical writing and client support for a site readiness project. The role involves authoring a range of engineering, compliance, and commercialization Standard Operating Procedures (SOPs). Technical writing may cover manufacturing equipment and processes; Quality Control laboratory instruments and methods; utility systems; facilities and maintenance equipment; logistics and warehousing processes; Quality Assurance; Environment, Health, and Safety; warehouse and supply chain; Information Technology; and training content. Travel may be necessary to support client work.

Kymanox is a life sciences professional services company that provides engineering, compliance, and project management services to clients ranging from Fortune 100 companies to virtual start-ups. Its work supports life science products reaching the market more quickly and affordably, while meeting high quality and safety standards. Kymanox describes its team as collaborative and offers opportunities for learning and career advancement.

Requirements

• A bachelor’s degree in an Engineering discipline, preferably Biomedical, Mechanical, or Chemical Engineering, or another STEM discipline such as Biology or Chemistry, from an accredited institution or equivalent.
• 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.
• Resourcefulness and strong attention to detail.
• Ability to work effectively with remote team members; strong organization; and ability to work independently and at a self-directed pace.
• Excellent written and oral English communication skills.
• Ability to understand personal limitations and solicit and use subject matter expert input.
• Ability to learn quickly and communicate pleasantly and positively.
• Strong customer-service aptitude and problem-solving skills.
• Ability to motivate oneself, team members, and direct reports.
• High energy, seasoned interpersonal skills (including high EQ), and a collaborative team orientation.

Nice To Haves

• 8 to 15 years of technical writing experience in the pharmaceutical, medical device, or biotechnology industries is desired.

Responsibilities

• Perform technical writing and client support on a site readiness project.
• Author engineering, compliance, and commercialization Standard Operating Procedures (SOPs).
• Develop technical content that may cover manufacturing equipment and processes; Quality Control laboratory instruments and methods; utility systems; facilities and maintenance equipment; logistics and warehousing processes; Quality Assurance; Environment, Health, and Safety; warehouse and supply chain; Information Technology; and training.
• Travel as necessary to support client work.

What This Job Offers

• Career Level: Mid Level