Associate Scientist II – Stability Coordination

ALLTECH CONSULTING SVC INC; Kansas City (MO); Vor Ort; USD 50.000 - 70.000; Vollzeit

Zusammenfassung

A biotechnology firm located in Kansas City is looking for an Associate Scientist II to perform varied tasks under supervision. Responsibilities include organizing documentation, authoring reports, and developing stability work plans. The ideal candidate will have a Bachelor’s Degree in a relevant field and strong proficiency in Microsoft Office tools. This position is suitable for motivated individuals eager to learn and develop their skills in a regulatory environment.

Qualifikationen

• No work experience required.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

Aufgaben

• Labeling, organizing and tracking the flow of documents.
• Authors documents such as stability protocols and certificates of analysis.
• Develop and execute stability work plans independently.
• Review technical documents for accuracy and compliance.
• Identify opportunities for improvement projects.

Kenntnisse

High Proficiency in Microsoft Office

Excellent written and verbal communications skills

Ability to learn and retain technical information

Mathematical and scientific reasoning ability

Well organized with ability to multitask

Ausbildung

Bachelor’s Degree in Life Sciences or Physical Science

Jobbeschreibung

Job Description:

Position Overview

Associate Scientist II under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians / assistants. Comply with divisional and site Environmental Health and Safety requirements.

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.

Position Requirements

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 Company’s 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.