Polymer Engineer Santa Clarita - CA - California

Santa Clarita, CA, US • Posted 1 day ago • Updated 1 day ago
Contract Corp To Corp
Contract W2
12 Months
On-site
$50 - $50/hr
Fitment

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Job Details

Skills

  • Chemical
  • Medical

Summary

Role Descriptions: Must Have TechnicalFunctional Skills

Hands-on wet lab experience in chemicals and polymer synthesis Ability to work independently in a fast-paced lab

environment and support various projects

Experience working with hazardous chemicals and lab safety protocols Isocyanate chemistry experience preferred but not

required.

Preparation and handling of chemical formulations, resins, and solutions Strong experimental design and problem-

solving capability

Familiar with test method development and variety of chemical characterization methods such as titration, FTIR, DSC,

polymer structure-property testing etc.

Troubleshooting of reaction, formulation, or material performance issues

Authoring of protocols, reports, and technical documentation

Data analysis and interpretation with clear technical conclusions

Nice to Have Skill

Understanding of GMP and regulated lab environments (medical devicepharma preferred)

Experience supporting IQOQPQ for lab equipment or processes

Documentation practices aligned with audit-ready and traceable systems Lab management experience

Roles & Responsibilities

Conduct wet lab experiments involving chemical and polymer synthesis to support R&D projects.

Prepare, handle, and manage chemical formulations, resins, and laboratory solutions.

Design experiments and apply problem-solving techniques to achieve project objectives.

Ensure strict adherence to lab safety protocols while working with hazardous chemicals.

Perform chemical characterization using techniques like FTIR, DSC, and titration methods.

Analyze experimental data and derive meaningful technical conclusions.

Troubleshoot reactions, formulations, and material performance issues effectively. Develop, document, and maintain test

methods, protocols, and technical reports.

Support compliance with GMP and maintain documentation aligned with audit-ready standards.

Assist in lab equipmentprocess validation activities (IQOQPQ) and overall lab operations.

Generic Managerial Skills, If any

Strong communication skills, with proficiency in reading, writing, and speaking English.

Ability to multitask, understand customer requirements, and respond promptly and accurately.

Capability to prioritize and manage multiple tasks in a fastpaced environment.

Ability to understand and follow complex written procedures.

Ability to work effectively in a team environment and contribute to team goals.

Strong decisionmaking and problemsolving abilities with sound situational judgment.

Essential Skills: EIS : Medical Device & Regulations

Desirable Skills:

Keyword:

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 90911958
  • Position Id: 9050834
  • Posted 1 day ago
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