[Hiring] Quality, Veeva Document Admin @Kymanox

Role Description

The Contract Quality, Veeva Document Admin 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 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

Qualifications

• 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.

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

Desired Aptitude and Skill Set

• 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

Compensation

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

Travel

Travel may be necessary to support client work.

Company Description

Join Kymanox – a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today’s biotechnology, pharmaceutical, medical device, and combination product industries.

• Kymanox provides an outstanding opportunity 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 learnings in Kymanox’s service offerings and the life science industry as a whole.
• Kymanox is 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.
• Kymanox provides professional services related to engineering, compliance, and project management.
• We service clients ranging from Fortune 100 companies to virtual start-up companies.
• The company was founded in 2004 and has been growing steadily since its inception.
• Our corporate HQ is based in Research Triangle Park, NC.