Main characteristics
- Location
- Plymouth, Devon
- Company
- Randstad Inhouse Services
- Salary
- £10000/month
- Employment type
- Temporary
- Category
- Medical / Pharmaceutical / Scientific
Job summary
Do you have a keen eye for detail, excellent problem-solving skills, and a passion for maintaining quality control processes?If yes, we want to hear from you.
Our client is a renowned global leader in the healthcare industry, specializing in medical technology, devices, and solutions that enhance patient care and improve clinical outcomes.
Job title: Quality Technician
Job type: Temporary - Ongoing
Location: Plymouth, PL6
Pay rate: £25,400 + 33% Shift Premium
Working days: Monday to Sunday
Shift pattern: 3 days on 3 days off
Shift timings: 11:00-23:00
Reporting to: Quality Engineer
Start date: Immediate
Role: You will be responsible for supporting the day to day activities within the manufacturing departments to ensure that the quality levels are maintained and nonconforming product is dealt with appropriately.
Benefits:
Free car parking on site
A great choice of lunch refreshments
Monday-Friday work pattern
Ongoing assignments, Temp to Perm opportunities
Randstad benefit app - discounts at many high-street and online retailersJob Responsibilities:
Raising Quality Notifications in accordance with standardised practices and ensuring that the nonconforming product is segregated and identified in accordance with the relevant procedures including the investigation into the root cause of the non-conformance.
Device History Record auditing to ensure that all records are complete and comply with GMP requirements.
Product inspections as required by the process control plans which may include moulding product dimensional checks, functional checks and any others that require Quality support.
Support of Validation / trial runs in manufacturing ensuring product is controlled appropriately.
Provide support for internal audits, third party regulatory audits and customer complaints as required.
Providing a source of advice / knowledge on shift to manufacturing / technical associates on all matters relating to Quality.
Supporting the Quality Engineering team on reasonable requests as they may arise.
Conducting regular cycle counts of hold work as required.
Supporting operational CI initiatives as required including documentation improvements.
Individuals have the authority to execute all responsibilities detailed within their job description and any procedures or processes in C2C or otherwise.Education and Experience:
Ideally GCSE Maths and English qualifications.
Experience in a quality role within a high volume medical device-manufacturing controlled environment.
Basic knowledge of Six Sigma and Lean Manufacturing principles.Knowledge and Skills:
Good numeracy and literacy skills.
Working knowledge of MS Office and MinitabIf this interests you, please apply with your up-to-date CV to be considered for the role and our team will contact you to discuss further