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Principal Toxicology Associate – Global Medical Devices company – Yorkshire (hybrid working) - £competitive salary, bonus, pension, healthcare, 25 days holiday + BH

Bonus-schemeFree-parkingHybrid-workingSustainable-business-practicesOption-to-start-immediatelyPrivate-medical-insurance

The Company

A market leading, global medical devices company focusing on multiple therapy areas. Their highlights include;

  • Global medical devices company
  • Distribute a range of devices from Class I-III across multiple therapy areas
  • Award winning company
  • Excellent training and development opportunities
  • Idyllic location with plenty of onsite parking

 

The Role

Your responsibilities will include (but not limited to) the following;

  • Creating, maintaining and updating biological evaluation plans (BEPs) and biological evaluation reports (BERs) for Class I to III devices
  • Reviewing and assessing of scientific and toxicological data
  • Creating, maintaining and updating TRA’s
  • Performing literature searches and interpreting data
  • Scheduling, managing and reviewing biocompatibility and toxicological testing protocols and reports
  • Ensuring compliance with regulations and guidance
  • Reviewing and providing input as necessary into technical files, clinical documentation, risk management and instructions for use with regards to biocompatibility
  • Reviewing material safety datasheets and providing feedback and evaluation of such documents

 

You

Ideally you will have experience in the following;

  • Experience in biocompatibility within medical devices (3+ years)
  • Experience of writing BEPs & BERs with (ideally) qualifications for BEP and BER writing per ISO 10993
  • Experience with reviewing toxicological data and writing toxicological risk assessments
  • Experience of reviewing material data sheets, biocompatibility testing data, extractable and leachable data, toxicological risk assessments, material literature
  • Working knowledge of the MDR, MDD, FDA regulations, and related ISO standards
  • Experience with current ISO 10993, MEDDEV and MDCG guidance, and ISO 14971.

 

What should you do next?

This Principal Toxicology Associate role is one not to be missed; it encompasses the opportunity to work with a global medical devices client, who are going from strength to strength. To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.

Apply Now!

Job Consultant

Hayley Shayestehroo

Regulatory Affairs & QA UK

Senior Consultant

hayley@carrotrecruitment.com

+44 (0)1625 361072

+1 (984) 444 9907

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