Associate Scientist II: Stability & Documentation

Lancesoft; Kansas City (MO); On-site; USD 65,000 - 90,000; Full time

Job summary

Lancesoft is seeking an Associate Scientist II to support a regulated laboratory environment in the Kansas City area under general supervision. The role emphasizes document control, stability program planning, and adherence to cGMP and site SOPs.

The successful candidate will maintain high-quality documentation, draft labs and stability reports, and collaborate with team members to meet project milestones while ensuring regulatory compliance and timely delivery.

Qualifications

• Bachelor's degree required in Life Sciences or Physical Science; no work experience required.
• Proficiency in MS Office; maintain documentation per regulatory guidance.
• Strong written and verbal communication; ability to learn and retain technical information.
• Ability to multitask and work under deadlines.

Responsibilities

• Labeling, organizing and tracking the flow of documents, including spreadsheets, reports, protocols etc.
• Authors documents, such as stability protocols, text reports, certificates of analysis, and operating procedures
• Performs parallel review of documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance.
• Develop and execute stability work plans/schedules independently, using customer milestones and Division/site performance standards and metrics.
• Review technical documents for accuracy, thoroughness and regulatory compliance
• Identifies opportunities for improvement projects.
• Perform activities under cGMP as appropriate.
• All other duties as assigned.

Skills

Documentation

Regulatory knowledge

Communication

Time management

Multitasking

Team collaboration

Education

Bachelor's Degree in Life Sciences or Physical Science

Tools

Microsoft Office Suite

Word

Excel

Outlook

Job description

Lancesoft is seeking an Associate Scientist II to support a regulated laboratory environment in the Kansas City area under general supervision. The role emphasizes document control, stability program planning, and adherence to cGMP and site SOPs.

The successful candidate will maintain high-quality documentation, draft labs and stability reports, and collaborate with team members to meet project milestones while ensuring regulatory compliance and timely delivery.