Associate Scientist II - Stability Coordination

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

Pay range: 20-26/hr

depending on experience

Essential Functions

• 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.

Education And Experience

Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required

Knowledge/Skills Requirements

• High Proficiency in Microsoft Office, Word, Excel, Outlook
• Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs.
• Ability to learn and retain technical information.
• Proactively address work issues at both an individual level and a team level.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Mathematical and scientific reasoning ability.
• Excellent written and verbal communications skills with internal and external customers.
• Lead by example according to values and culture.
• Strategy is focused on personal time management and efficiency.
• Well organized with ability to multitask.
• Ability to work effectively under pressure to meet deadlines.