Carbon
Scientist 1 - Physical Testing
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Scientist I - Physical Testing
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.
Location - Deeside
Fully on site
Pay rate - £122.62 per day
Contract Length - 12 months
A Scientist I in the physical Testing Department supports the product development process for medical devices. Scientist I's should have a good understanding of the importance of physical testing in ensuring the safety, efficacy, and quality of medical devices. Scientists are responsible for conducting various tests and experiments to assess the physical properties of medical devices. Scientists will generate, document, and analyse data in compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). Scientist I's should also be able to use their knowledge and experience to develop test methods based on recognised industry standards and bespoke test methods that satisfy the requirements of our products. Scientists should be detail-oriented, able to work on multiple projects and adapt to changes, with good problem-solving skills and strong communication skills essential.
Key Responsibilities
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- Working within a controlled ISO 13485 and ISO 9001 laboratory quality system and in accordance with GxP procedures.
- Design, plan and execute Physical Testing in support of R&D activities and base business projects in accordance with applicable procedures and guidelines.
- Development and validation of new Physical Testing methods.
- Estimating the resources and time required to conduct an experiment and monitoring performance to ensure targets are met.
- Author validation protocols, reports, and technical documents for medical devices/pharmaceutical products.
- Independently analyse and interpret data through statistical analysis.
- Prepare and present internal presentations to present findings of the laboratory.
- 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 analysis of atypical and out-of-specification results, apply corrective and preventative actions, and author concise investigation reports.
- Assist in laboratory test method/procedural revisions.
- Ensures laboratory compliance with cGMP regulations and SOP's/TDs.
- Involvement in change control activities and associated actions.
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Skills & Experience
- 1-2 years' experience in a working laboratory environment, with Medical Devices/Pharmaceutical Industry preferred.
- Good written and verbal communication skills.
- Broad understanding of physical testing.
- Good working knowledge of Microsoft Office, specifically Word and Excel.
- Familiarity with safe working in a laboratory environment. 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 GMP Guidelines and Regulation.
- A detailed understanding of common statistical analysis and experience with MiniTab desirable.
Qualifications/Education
- Bachelor's Degree in a relevant science-related discipline, i.e., biological sciences.
Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy
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