* Job Title: Scientist 2 – Physical Testing
* Contract: 12 months
* Location: Deeside
SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care.
Please make an application promptly if you are a good match for this role due to high levels of interest.
We are seeking a Scientist to join their Deeside team.
Duties and Responsibilities:
* Working within a controlled ISO13485 and ISO9001 Laboratory quality system and in accordance with GLP/GMP procedures.
* Design, plan and execute physical testing in support of New Product Development activities in accordance with applicable procedures and guidelines.
* Development and Validation of new Physical Testing Methods.
* Author validation protocols, reports and technical documents for medical devices / pharmaceutical products.
* Effective organisation of assigned workload; ensures integrity of all data generated and timely/accurate provision of results to GLP standards.
* Accurate recording and analysis of laboratory data in accordance with good documentation practices.
* Perform detailed laboratory investigations to determine the root cause of atypical and out of specification results, apply corrective and preventative actions and author concise investigation reports.
* Assist in laboratory test method/procedural revisions.
* Responsible for standard laboratory routines, equipment calibration, maintenance replenishment etc.
* Ensures lab compliances with applicable cGMP regulations and SOPs/TD’s
* Involvement in change control activities and associated actions.
Education/Qualifications:
* Bachelor’s Degree in a relevant science related discipline
* 2-3 years’ experience in a working laboratory environment, within Medical Devices / Pharmaceutical industry is preferred.
* Working knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO13485:2016, ISO9001:2000, FDA 21 CFR part 820) and G