Packaging Engineer (contract) at Pfizer
Chesterfield, Missouri, USA -
Full Time


Start Date

Immediate

Expiry Date

14 Oct, 25

Salary

57.0

Posted On

16 Jul, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Word Processing, Materials, Biochemistry, Presentations, Spreadsheets, Regulatory Standards, Components, Engineering Disciplines, Chemical Engineering, Gmp

Industry

Pharmaceuticals

Description

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.

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
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
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