Medical Device Toxicologist II

HERO

Job Detail

Location Galway
Salary Negotiable
Posted
Role Type Permanent
Contact Mark Wilson
email talent@hero.ie

Medical Device Toxicologist II

Apply Now

Job ID: JOB-12126

Medical Device Toxicologist II

A leading medical device company in Galway are seeking a Toxicologist to join their team on a permanent baisis. The primary purpose of this role is to provide support for the biocompatibility and toxicology processes, new product development, regulatory submissions, and manufacturing and engineering changes to meet business objectives.

Key Responsibilities

  • Provides support for biocompatibility processes initiated by department management and ensure biocompatibility and toxicology related information and data are accurate, reliable, and support business objectives as consistent with Global Preclinical objectives and Quality Management System requirements.
  • Demonstrates a primary commitment to patient safety and product quality.
  • Under direction and mentorship of more senior staff author Chemical Safety Assessments and toxicology memos as necessary to support divisional objectives.
  • Completes biocompatibility test plans, organize testing at external test laboratories, and assessing test data. Review and completion of Biocompatibility Assessments and Reports and reports as necessary to support business objectives, including authoring such reports.
  • Provides input on the regulatory requirements related to medical device submissions. on procedures, techniques, concepts and approaches used at divisional levels for biocompatibility and toxicology programs
  • Serves as a resource for biocompatibility and toxicology information for medical devices and pharmaceutical materials, which may include issues related to materials of animal origin, colorant additives, exposure assessments of chemicals, and other chemical toxicities as assigned.
  • Communicates with internal customers on biocompatibility and toxicology issues and  supports problem solving and resolution related to chemical risk assessments and biocompatibility assessments as assigned.
  • Provides input on biocompatibility, chemistry and toxicology testing related to new investigational and strategic device development programs during Technology and Product development programs (TDP/PDP)
  • Participates in a Biocompatibility Training Program for all functional groups of device development teams based on standards and regulatory requirements.
  • Plans, organises, and prioritises own daily work routine to meet established schedule with guidance from manager.
  • Receives general supervision.  Makes recommendations which may be reviewed by manager.  May exercise authority within limits.  May seek guidance in resolving problems.
  • Begins establishing and cultivating internal business relationships to facilitate completion of tasks. May participate in project teams.
  • Participates in the completion of departmental projects and goals. Errors in judgment or failure to achieve results would normally require an expenditure of resources to rectify.

Key Requirements

  • BSc in a Science related discipline e.g. Toxicology, Chemistry or Biomedical Sciences.
  • 1-3 years’ experience in medical device, pharmaceutical or related industry.
  • General knowledge and application of technical and business concepts, procedures, and practices. Interprets company policies and procedures to resolve issues. Beginning knowledge of industry practices and standards. Knowledge of 10993 and advantage.
  • Experience applying professional concepts and company policies and procedures, analyses data or situations, and exercises judgment to recommend solutions to solve problems. Follows standard practices and procedures in analysing situations or data from which answers can be obtained.
  • Excellent attention-to-detail. 
  • Demonstrates business writing, proofreading and editing skills.
  • Knowledge of internal company and occasional external contacts. Uses discretion, diplomacy and tact in interactions.
  • Strong communication  and influencing skills.

For further information on this role in please contact Mark Wilson on 0860449473 or email talent@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given.  You have supplied us with your personal data in the process of applying for a position.  Our client company may have personnel outside of the EEA who will review you data.  We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Mark Wilson

JOB-12126

Apply Now

Medical Device Toxicologist II

Mark Wilson

Role Type Permanent
Contact Mark Wilson
email talent@hero.ie
mobile +353 86 044 94 73
linkedIn profile click here

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