(Contract) Quality, Veeva Document Admin
Kymanox
Summary
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).
Job description
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
Educational Background
The ideal candidate will have a 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.
Experience
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
Travel
Travel may be necessary to support client work.
Requirements
- Bachelor's degree in an Engineering discipline (prefer Biomedical, Mechanical, or Chemical engineering) or other STEM discipline (Biology, Chemistry, other) 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 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired
- Excellent written and oral English communication skills
- Ability to work effectively with remote team members
- Extremely detail oriented
- Highly organized
- Self-directing, self-pacing
- Excellent problem-solving skills
- Strong customer-service aptitude
- Team player
Company overview
Kymanox is a professional services company specializing in the life sciences industry, providing comprehensive solutions to support pharmaceutical, biotechnology, and medical device companies. The company offers a range of technical and operational services designed to accelerate product development and commercialization processes. Kymanox focuses on delivering expertise in areas such as process development, quality assurance, regulatory compliance, and technical operations. Their services are tailored to help clients navigate complex challenges in bringing innovative therapies and medical products to market. With a commitment to quality and efficiency, Kymanox serves as a strategic partner for life science organizations seeking to optimize their development pipelines and ensure successful product launches. The company's professional services model enables clients to access specialized expertise without the need for extensive internal infrastructure investments.