Technical Operations Scientist in Caernarfon, Gwynedd, United Kingdom
Caernarfon, Gwynedd, United Kingdom |
GBP £14.35 per hour |
Contract
Mane are recruiting for a Technical Operations Scientist to work on a 3 month contract in Llanberis. As a Technical Operations Scientist you will be involved in the effective resolution of product performance issues and improvements. You will focus on obtaining, collating, and analysing technical information to accomplish complex tasks and project managing technical investigations for the site.
Key Responsibilities
*Design, direct, organise and implement actions required to resolve allocated product troubleshooting and improvements.
*Design analytical experiments to run, either internally or in collaboration with key stakeholders, with the aim of identifying the root cause of product performance issues and optimisation of processes.
*Review, assess and, where required, perform suitable statistical analysis, on data generated as a consequence of, or in relation to, a technical investigation.
*Interpret, summarise and present results to the required standard.
*Awareness of priorities and deadlines, and to ensure work assignment and organisation to maximise efficiency according to these priorities.
*Write and circulate technical reports for all assigned investigations. Also generate reports and participate in meetings to support the relevant processes.
*Involvement in risk assessment activities as required.
*To communicate effectively with all levels of staff within and outside of the department in a timely manner in regards investigation status.
*Demonstrate a positive and professional attitude toward workplace, co-workers and company policies and procedures.
*To comply with all company Health and Safety policies and procedures. To highlight any real or potential Health and Safety issues to management in a timely manner and assist in actioning their decisions.
*To comply at all times with the relevant Quality and Environmental Standards e.g. BS EN ISO 13485, and ENI46001, US FDA Quality System Regulations (QSR 21 CFR Part 820) and relevant European Directives as documented within our company Quality Management Systems.
What do I need to qualify for this role?
* A proven scientific background ideally gained in a laboratory or R&D environment.
*A scientific degree (or equivalent) is highly desirable.
*Strong trouble shooting and analytical skills with a high level of competency in Excel.
*Experience with Minitab - desirable.
*Knowledge of immunoassay data desirable.
*Adept at running good scientific investigations.
*Experience of designing experiments is highly desirable
*Experience of working in a regulated industry
*GMP experience is highly desirable.
The successful candidate will be adept at report writing and confident presenting findings. If you feel you have the relevant experience please apply to this advert.
Key Responsibilities
*Design, direct, organise and implement actions required to resolve allocated product troubleshooting and improvements.
*Design analytical experiments to run, either internally or in collaboration with key stakeholders, with the aim of identifying the root cause of product performance issues and optimisation of processes.
*Review, assess and, where required, perform suitable statistical analysis, on data generated as a consequence of, or in relation to, a technical investigation.
*Interpret, summarise and present results to the required standard.
*Awareness of priorities and deadlines, and to ensure work assignment and organisation to maximise efficiency according to these priorities.
*Write and circulate technical reports for all assigned investigations. Also generate reports and participate in meetings to support the relevant processes.
*Involvement in risk assessment activities as required.
*To communicate effectively with all levels of staff within and outside of the department in a timely manner in regards investigation status.
*Demonstrate a positive and professional attitude toward workplace, co-workers and company policies and procedures.
*To comply with all company Health and Safety policies and procedures. To highlight any real or potential Health and Safety issues to management in a timely manner and assist in actioning their decisions.
*To comply at all times with the relevant Quality and Environmental Standards e.g. BS EN ISO 13485, and ENI46001, US FDA Quality System Regulations (QSR 21 CFR Part 820) and relevant European Directives as documented within our company Quality Management Systems.
What do I need to qualify for this role?
* A proven scientific background ideally gained in a laboratory or R&D environment.
*A scientific degree (or equivalent) is highly desirable.
*Strong trouble shooting and analytical skills with a high level of competency in Excel.
*Experience with Minitab - desirable.
*Knowledge of immunoassay data desirable.
*Adept at running good scientific investigations.
*Experience of designing experiments is highly desirable
*Experience of working in a regulated industry
*GMP experience is highly desirable.
The successful candidate will be adept at report writing and confident presenting findings. If you feel you have the relevant experience please apply to this advert.
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