Quality Engineer - Onsite

at  Sartorius

Cambridge, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate30 Apr, 2025Not Specified31 Jan, 2025N/AGood communication skillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – 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