Packaging Engineer
Listed on 2025-11-27
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Engineering
Quality Engineering
Chesterfield, MO, United States (On-site)
Contract (12 months 19 days)
Published 4 months ago
CLOSED
SummaryThis position resides within the Pharmaceutical Research and Development department 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
- 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 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.
Min Pay Rate $47
Max Pay Rate $57
Currency USD
Unit hourly
Benefits InformationComprehensive Benefits Package available based on eligibility
- Short‑Term Disability (STD)
- Long‑Term Disability (LTD)
- Supplemental and Voluntary Life Insurance
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