Quality Engineer - Onsite
at Sartorius
Cambridge, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Apr, 2025 | Not Specified | 31 Jan, 2025 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Come and join our Quality Operations Department as a Quality Engineer at our Royston site.
We are looking for a Quality Engineer for the Quality Operations department at Sartorius. In this role, you will be responsible for ensuring compliance to ISO9001, managing the quality management system including internal audits. Additional audit activities will also include customer audits, managing deviations and CAPA activities.
Contributing and driving improvement of quality processes. Key supporting task will require the supervision, development and coaching of QC resources to meet production demands for small scale equipment systems and consumable products.
You will be joining a small team of quality professionals and will be integral to shaping the future site quality dynamic.
This position is full time permanent role and site based at Royston, Hertfordshire. The operating site is 15 minutes’ walk from the train station, just off of A505 with easy access.
Responsibilities:
- On a daily basis you will be responsible for providing day to day quality support to production, support raising deviations, carry out investigations and support of the QMS
- Drafting new and revising SOPs, writing investigations reports, support change control activities.
- Maintain quality documentation including quality process maps, work instructions, testing protocols and testing evidence traceability and adhering to compliance
- Driving continuous improvement to improve site product quality and customer experience including root cause analysis and solving customer complaints.
- Raising CAPAS to ensure production quality and customer satisfaction
- Manage internal and customer audits and ensure compliance for ISO9001
- Supervise QC resources to ensure smooth running of production operation
- Collaborating and working directly with production engineering, product development and manufacture, supply chain and distribution teams.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Proficient
1
Cambridge, United Kingdom