Randstad Lab Technician in Deland, Florida

Lab Technician


Deland, FL

Date Posted:

Thursday, October 13, 2016

Job Type:


Reference #:



Randstad Life Sciences

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Job Title: Lab Technician l

Position Description

  • The technician supports the activities related to chemical and material characterization of materials and/or devices for the biomaterials group. These chemical characterization activities support biocompatibility studies for devices and materials for regulatory submissions and toxicological assessments. With supervision and direction from the study directors and scientists, this position will assist study directors in the execution of chemical/material characterization projects

Position Responsibilities


  • Material Characterization for Biocompatibility and Toxicological Assessments

o Prepares samples for extraction and leachable testing per ISO 10993.

o Sets up extraction and completes sample analysis form.

o Performs the extraction and collection of subsequent extract solutions.

o Complete the nonvolatile gravimetric residue analysis.

o Send out sample extracts to secondary lab for analysis if needed (ICP-MS).

o Train and follow all laboratory SOPs and Work Instructions (WI).

  • Biological Testing

o Perform sample preparation for ELISA and other biological analysis.

o Train and follow all laboratory SOPs and Work Instructions (WI).

Other responsibilities include:

  • Regulations

o Under the guidance of the study director, reviews Preclinical study data intended for regulatory submissions for compliance to Good Laboratories Practices, and interfaces with quality assurance, regulatory committees (e.g. IACUC), and Regulatory Affairs regarding requirements and results of the study.

o Reviews submissions to regulatory bodies for correlation and traceability to preclinical data, and compliance to the FDA Good Laboratories Practices for Non-clinical Studies.

Position Requirements

EDUCATION REQUIRED: (No equivalencies)

Two year degree or Bachelor s degree in biological sciences or related medical/scientific field.

  • Experience working in a preclinical clinical, or regulated environment.

  • Familiarity with ISO 10993 standards, biocompatibility, and/or regulatory submissions

SPECIALIZED KNOWLEDGE REQUIRED (Needs to be objective, relevant, and non-comparative)

  • Demonstrated ability to effectively support a cross-functional team when necessary.

  • Advanced written and oral communications skills.

  • Able to manage multiple tasks.

  • Proficiently broad knowledge of medical terminology and scientific principles.

  • Functional knowledge of GLP and regulatory compliance guidelines, and the regulatory environment.


  • Medical, Dental, and Vision Insurance

  • 401K Plan with Company Match

  • Life and AD&D Insurance

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