Job Description
Chesterfield, MO, United States (On-site)
Contract (12 months 19 days)
Published 4 months ago
CLOSED
Summary
This position resides within the Pharmaceutical Research and Development department at Pfizer. The position involves working within a multidisciplinary team providing laboratory support for all required medical device and combination product (MDCP) development programs. This will include hands‑on testing, troubleshooting and method/testing investigations as well as recording of data in accordance with SOPs and analysis of data to input back into the project team.
Responsibilities
Carries out hands‑on testing of devices to generate data on the selected parameters, in accordance with the agreed protocols and methods. The testing will often involve the execution of specialized techniques using Instron force measurement systems, balances, and other gauges/tools related to the specific drug delivery device functional attribute
Operating laboratory equipment according to SOPs, Manuals, Methods, and Risk Assessments
Maintains accurate records of results, analysis, and interpretation of experimental data in laboratory notebooks in a timely manner and according to accepted good practices
Uses tools to analyse, interpret, and record data to quantify the functional performance characteristics of a device and control parameters for its consistent performance
Prepares scientific reports of experiments, data analysis, and data verification in accordance with approved procedures and practices
Qualifications
Bachelor's Degree or higher in appropriate Science & Engineering disciplines, e.g. Chemistry, Biochemistry; Biomedical, Mechanical, Materials, Chemical Engineering; or other related discipline
A minimum of 3+ years of experience in a related role
Knowledge and/or interest in parenteral packaging, components and component testing equipment, e.g. Instron, Computrac, plunger movement chamber, Wilco vacuum decay, etc.
Experience with lab‑based testing
Mechanical aptitude
Knowledge of Good Manufacturing Practices (GMP)
Knowledge of packaging related regulatory standards and guidance
Capable of working independently with minimal supervision
High level of attention to technical details and accuracy
Being able to prioritize multiple responsibilities and to work on multiple tasks simultaneously
Demonstrated ability to work collaboratively in cross functional teams
Excellent communication (e.g. oral, written, presentation) and interpersonal relationship skills
Proficiency in general computer software such as word processing, spreadsheets, presentations
Please note contractors are engaged to provide services to Pfizer temporarily in connection with a specific assignment. Contractors are hired and employed through Atrium, our third‑party payrolling partner.
This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits, and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on several factors, including skills, competencies, experience, location and/or being pursued, and other job‑related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
Pay Rate Range
Min Pay Rate $47
Max Pay Rate $57
Currency USD
Unit hourly
Benefits Information
Comprehensive Benefits Package available based on eligibility
Short‑Term Disability (STD)
Long‑Term Disability (LTD)
Supplemental and Voluntary Life Insurance
#J-18808-Ljbffr Pfizer
Job Tags
Hourly pay, Contract work, Temporary work, For contractors