Job Description
The Toxicologist will ensure that Toxicology Risk Assessments and Biocompatibility validations are conducted in line with all quality system and regulatory requirements.
Responsibilities
Demonstrate a primary commitment to patient safety and product quality.
Understands and complies with all the regulations governing the quality systems.
Performs or coordinates a wide variety Toxicological Risk Assessments which are performed in accordance with approved protocols and summarises the results in a final report or qualification.
Validates new and existing products to ensure compliance with current biocompatibility regulatory standards.
Participates in product development teams to ensure validation of products to agreed timelines. Assists in the documentation of validations for regulatory submissions.
Other duties as assigned, such as approval of test report.
Decision-making ability coupled with the ability to work on one?s own initiative, and with the minimum of supervision is required. Good interpersonal and communication (written and verbal) skills are required.
Good administrative/organisational ability is required.
To build quality into all aspects of work by maintaining compliance to all quality requirements
Supervises specialists and graduates, as required
Designee for Principal Biocompatibility specialist
Approves biocompatibility documentation in PDM
Qualifications and Requirements:
BS, MSc, or PhD in the field of Toxicology, Pharmacology, Chemistry or related field of science. (Min HETAC level 8)
5-8 years post grad experience in a relevant area.
People management experience highly desirable
For further information on this Biocompatibility Specialist -Toxicologist
position please contact Laurentina Kennedy at The RFT Group on 01 2302400 Check out all our open jobs on our Recruitment website: www.rftgroup.ie
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