What are the responsibilities and job description for the Scientist position at BCforward?
Job Title: Associate Scientist II - Stability Coordination
Location: Kansas City, MO
Duration: Contract to hire - 6 months
Shift: Monday – Friday, 8:00 AM – 4:00 PM
Work Setting: Onsite
Job ID: 372059
Job Description
We are seeking an Associate Scientist II to join our stability coordination team. The successful candidate will demonstrate strong experience in documentation management, cGMP practices, and Microsoft Office tools, and a proven ability to develop and execute stability work plans that meet customer milestones and compliance standards.
Responsibilities:
- Label, organize, and track documents, including spreadsheets, reports, and protocols.
- Author stability protocols, text reports, certificates of analysis, and operating procedures.
- Perform parallel review of documentation and qualify to perform technical reviews for accuracy, completeness, and regulatory compliance.
- Develop and execute stability work plans and schedules independently using customer milestones and site performance standards.
- Identify opportunities for process and documentation improvements.
- Perform activities under cGMP as appropriate and comply with Environmental Health and Safety requirements.
- Execute other duties as assigned.
Required Skills & Qualifications:
- Bachelor’s degree in Life Sciences or a Physical Science field.
- High proficiency in Microsoft Word, Excel, and Outlook.
- Ability to maintain high-quality documentation per regulatory guidance and site SOPs.
- Ability to learn and retain technical information and apply mathematical and scientific reasoning.
- Ability to interpret written, oral, diagram, or schedule instructions.
- Strong written and verbal communication with internal and external stakeholders.
- Effective personal time management and efficiency with the ability to multitask and meet deadlines under pressure.
Preferred Skills:
- Experience authoring or reviewing stability protocols and certificates of analysis in a cGMP environment.
- Experience with process improvement or documentation optimization initiatives.