Scientist
at Mast Group Limited
Deeside CH5 2UA, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 22 Apr, 2025 | Not Specified | 23 Jan, 2025 | N/A | Good communication skills | No | No |
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Description:
LABORATORY SCIENTIST
Mast Group Ltd. are a world class manufacturer and supplier of diagnostic products for clinical, industrial and veterinary testing. As an independent company, since 1959, our commitment to maintaining integrityand customer satisfaction, combined with innovation in in-vitro diagnostics, has resulted in improved clinical decisions and pathways.
We are looking to recruit highly skilled and conscientious Scientist, on a 12-month fixed-term basis, to join the team based short term in Bootle, long term at our Deeside site. The job holder will be an integral part of the team, ensuring development, evaluation and registration of products for diagnostic microbiology, in line with regulatory requirements. The successful candidate should be willing to actively engage and contribute their technical knowledge, to aid the progression of portfolio development, bringing relevant products to successful manufacture and commercialisation.
Responsibilities:
· Responsible for carrying out existing and new product development activities as agreed under the general supervision of the line manager. All activities are to be conducted to the agreed scientific and regulatory standard or directives e.g. European IVDD and IVDR of the department and promptly reporting deviations from stated targets of performance.
· Responsible, with minimum supervision, for conducting reviews of literature related to investigations being undertaken, conducting and, where necessary, enhancing experimental design, carrying out research studies, analysis of experimental data, reporting of studies in the form of a written report as per laboratory standards and ensuring raw materials are available as required for investigative studies,
· Responsible for performing scientific and documentary activities related to regulatory requirements e.g. European IVDD and IVDR, to the agreed scientific and regulatory standards and promptly reporting deviations.
· Responsible for the collation of reference information relevant to all investigations and for the correct maintenance and updating of technical records in appropriate project files for allocated projects.
· To participate in laboratory project meetings where technical matters affecting current projects and present results are discussed and to provide assistance to senior staff in technical training for Sales and Marketing and laboratory personnel.
· To provide cover for the team, as agreed between the Quality Control and R&D Managers when necessary.
· Prepare and present written reports and documents as directed, including the preparation and updating of Standard Operating Procedures, technical dossiers demonstrating product compliance with regulatory standards or directives, reports and documents for company policy and other meetings. Such reports should usually be presented in an appropriate electronic format (e.g. Microsoft Word).
In addition to the specified duties the Scientist is expected to perform additional tasks that the company may require.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Deeside CH5 2UA, United Kingdom