Quality Inspector
| Posting date: | 15 April 2024 |
|---|---|
| Salary: | £23,000 per year |
| Hours: | Full time |
| Closing date: | 15 May 2024 |
| Location: | Worcester, WOR, WR4 0HD |
| Company: | Workforce Recruitment and Training |
| Job type: | Permanent |
| Job reference: | 113015 |
Summary
**Quality Inspector**
**£23k **
**Monday to Friday **
**Duties to include **
****
* Inspect, record, and release all parts with an inspection status against their current specification sheets or physical samples. Reporting quality issues or outdated/incorrect specifications to the relevant personnel.
* Inspect, record and process returned goods and materials.
* Monitor the temperature of the UK locations
* Prepare different glue and disinfectant formulations which are used in a cleanroom manufacturing environment.
* Review and recording of product rejections from production.
* Inspect product returns for viability options.
* Carry out necessary calibration for all relevant measuring equipment to conform with the quality requirements as outlined in the calibration schedule.
* Raise purchase orders for quality consumables, spares, and services.
* Manage Quarantine area and inventory. Communicate quarantined and expired stock via a monthly report.
* Reconcile all batch reports to ensure complete batches have been processed and certified sterile retaining records for the required retention period (including PSP packs).
* Prepare, review, and sign the documentation required to produce pharmaceutical packs.
* Prepare and sign certificates of conformance for Requested client manufactured products.
* Review and File including but not limited to Certificates of conformance sent by suppliers.
* Review and sign completed check sheets for clean room pressures and cleaning.
* Organise the disposal of products where necessary.
* Undertake periodic training as required to perform duties, including health and safety, environmental and regulatory requirements.
* Follow the companys documented processes related to the assigned duties and inform of deviations, impracticalities, or absence of such documented processes.
* Co-ordinate with other team members to cover and be covered during holiday absences.
* Maintain an up-to-date multi-site filing system for all superseded technical drawings adhering to the required retention periods.
* Liaise with suppliers to obtain certification to support approved suppliers list and obtain technical information on components purchased to support colleagues
* Co-ordinate and promote continuous improvement.
****
**Alternative Duties to Be Performed As Required **
****
* Understand and apply quality assurance procedures in line with Medical Device Directive 93/42EC, Regulation (EU) 745/2017 on Medical Devices, ISO13485, ISO14001 and health and safety standards.
* Carry out Process and Internal Audits.
* Raise CAPAs, Non-Conformities, complete investigations of root causes.
* Assist the technical department with product testing when required.
* Carry out duties in line with Good Distribution Practices (GDP)and Good Manufacturing Practices (GMP) where required and to keep the companys Responsible Person(s) informed of all relevant developments.
Other duties as necessary to support the operations of the Quality and Regulatory department.
* ** Qualifications required for the Job (minimum requirement) **
* GCSE standard including mathematics/sciences/English language.
* Computer Literate
* Full UK Driving Licence
* ** Experience required to do the job (minimum requirement)**
* Previous experience in a Quality environment preferred.
* Knowledge of Medical Devices
* Knowledge of Auditing preferred.
* ** Skills and abilities including key competencies**
****
* Microsoft Office
* Measuring and Analysis equipment (preferred)
* Physical Effort (Pump Trucks, Box Lifting)
* Teamwork
* Communication
* Excellent interpersonal skills
* Ability to organise own work
95% Warehouse & Shop Floor, 5% Office. Main locations are Bromsgrove and Worcester.
**£23k **
**Monday to Friday **
**Duties to include **
****
* Inspect, record, and release all parts with an inspection status against their current specification sheets or physical samples. Reporting quality issues or outdated/incorrect specifications to the relevant personnel.
* Inspect, record and process returned goods and materials.
* Monitor the temperature of the UK locations
* Prepare different glue and disinfectant formulations which are used in a cleanroom manufacturing environment.
* Review and recording of product rejections from production.
* Inspect product returns for viability options.
* Carry out necessary calibration for all relevant measuring equipment to conform with the quality requirements as outlined in the calibration schedule.
* Raise purchase orders for quality consumables, spares, and services.
* Manage Quarantine area and inventory. Communicate quarantined and expired stock via a monthly report.
* Reconcile all batch reports to ensure complete batches have been processed and certified sterile retaining records for the required retention period (including PSP packs).
* Prepare, review, and sign the documentation required to produce pharmaceutical packs.
* Prepare and sign certificates of conformance for Requested client manufactured products.
* Review and File including but not limited to Certificates of conformance sent by suppliers.
* Review and sign completed check sheets for clean room pressures and cleaning.
* Organise the disposal of products where necessary.
* Undertake periodic training as required to perform duties, including health and safety, environmental and regulatory requirements.
* Follow the companys documented processes related to the assigned duties and inform of deviations, impracticalities, or absence of such documented processes.
* Co-ordinate with other team members to cover and be covered during holiday absences.
* Maintain an up-to-date multi-site filing system for all superseded technical drawings adhering to the required retention periods.
* Liaise with suppliers to obtain certification to support approved suppliers list and obtain technical information on components purchased to support colleagues
* Co-ordinate and promote continuous improvement.
****
**Alternative Duties to Be Performed As Required **
****
* Understand and apply quality assurance procedures in line with Medical Device Directive 93/42EC, Regulation (EU) 745/2017 on Medical Devices, ISO13485, ISO14001 and health and safety standards.
* Carry out Process and Internal Audits.
* Raise CAPAs, Non-Conformities, complete investigations of root causes.
* Assist the technical department with product testing when required.
* Carry out duties in line with Good Distribution Practices (GDP)and Good Manufacturing Practices (GMP) where required and to keep the companys Responsible Person(s) informed of all relevant developments.
Other duties as necessary to support the operations of the Quality and Regulatory department.
* ** Qualifications required for the Job (minimum requirement) **
* GCSE standard including mathematics/sciences/English language.
* Computer Literate
* Full UK Driving Licence
* ** Experience required to do the job (minimum requirement)**
* Previous experience in a Quality environment preferred.
* Knowledge of Medical Devices
* Knowledge of Auditing preferred.
* ** Skills and abilities including key competencies**
****
* Microsoft Office
* Measuring and Analysis equipment (preferred)
* Physical Effort (Pump Trucks, Box Lifting)
* Teamwork
* Communication
* Excellent interpersonal skills
* Ability to organise own work
95% Warehouse & Shop Floor, 5% Office. Main locations are Bromsgrove and Worcester.