Stability Coordination Scientist II – Documentation

Planet Pharma; Kansas City (MO); On-site; USD 28,000 - 36,000; Full time

Job summary

Planet Pharma in Kansas City, MO is seeking a motivated candidate for a document control role supporting compliance with cGMP standards. The role involves labeling, organizing, and tracking documents, and authoring stability protocols and reports under supervision.

The ideal candidate has a Bachelor’s Degree in Life or Physical Sciences and strong MS Office skills. No work experience is required, and training will emphasize regulatory documentation accuracy and timely, precise communication.

Qualifications

• Bachelor’s Degree in Life Sciences or Physical Science field; no work experience required.
• Proficiency in Microsoft Office with strong documentation standards.

Responsibilities

• Label, organize, and track the flow of documents.
• Author stability protocols, text reports and operating procedures.
• Review documents for accuracy and regulatory compliance.
• Develop and execute stability work plans using milestones and standards.
• Identify opportunities for process improvements.
• Perform activities under cGMP.

Skills

MS Office

Documentation

Regulatory compliance

Written communication

Time management

Attention to detail

Learning quickly

Teamwork

Education

Bachelor’s Degree in Life Sciences or Physical Science

Tools

Excel

Word

Outlook

Job description

Planet Pharma in Kansas City, MO is seeking a motivated candidate for a document control role supporting compliance with cGMP standards. The role involves labeling, organizing, and tracking documents, and authoring stability protocols and reports under supervision.

The ideal candidate has a Bachelor’s Degree in Life or Physical Sciences and strong MS Office skills. No work experience is required, and training will emphasize regulatory documentation accuracy and timely, precise communication.