Document and Data Management Contingent Associate
Pay rate: $23-$27 (based on experience)
Summary:
Prepare and review Finished Product Specifications (MLPs) for Commercial Operations and Pharmaceutical Development Services groups.
Essential Functions:
- Master documents can include Raw Material Specifications, Package Material Specifications, Finished Product Specifications. The initial assignment will be transferring current Finished Product Specifications from sequel LIMS (Laboratory Information Management System) to a new Sample Manager LIMS.
- Example of Job Challenges:
- Interpreting current Finished Product Specifications and transferring data into Sample Manager LIMS.
Education:
• Bachelor’s in Chemistry, Biology, Microbiology, or related discipline.
Experience:
- Must have basic scientific background.
- High level of attention to detail.
- Knowledge of Good Manufacturing Practices, GLP, EU Good Manufacturing Practices, Pharmacopial requirements and FDA and the ability to recognize non-compliance with these regulations.
- Strong writing skills.
- Good organization skills.
Equivalency:
• Equivalent combinations of education, training, and relevant work experience may be considered.
Physical Requirements:
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.