Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Job Description

Location/Division Specific Information

The Bend, Oregon Thermo Fisher Scientific site consists of approximately 90 highly motivated employees focused on contract early phase clinical drug product development and manufacture. The site is a part of global network which encompasses manufacture of drug substance, scale up, clinical distribution, and commercial drug product launch. Bend, Oregon is al community of around 95,000 people commonly known as 'the outdoor playground of the West' because of the myriad of available outdoor activities and desirable living conditions.

• Work in a fast-paced environment supporting and organizing processes for scientists.
• Draft stability tables, COAs, specifications, protocols, reports, and data packages.
• Support sample retrieval, inventory management, and Laboratory Information Management System (LIMS).
• Perform stability set downs and pulls.
• Coordinate shipments to vendors.
• Issue, review, and maintain laboratory notebooks, logbooks, and other documentation in accordance with good documentation practices (GDP).
• Support scheduling and status updates.
• May support laboratory kitting (preparation of glassware, solutions, etc.).
• Lead initiatives to improve laboratory operations.
• Maintain a clean and organized laboratory workspace consistent with management expectations.
• Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintain the necessary compliance status required by company and facility standards.

• High School Diploma or GED. Associate's degree in business, science or related field preferred.
• At least 3 years experience with document control, data entry, report generation, quality assurance, or other relevant background.
• GMP experience preferred.
• Equivalent combinations of education, training, and relevant work experience may be considered.

• Proficiency in Microsoft Office Suite (Word, Excel, Outlook, and PowerPoint).
• Excellent organizational skills.
• Good critical and logical thinking skills.
• Ability to read, analyze, and interpret technical procedures and governmental regulations.
• Effective written and interpersonal skills.
• Ability to work on multiple projects simultaneously.