Quality Assurance Auditor

at  Greencore Group

Boston PE21, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate11 Oct, 2024Not Specified11 Jul, 2024N/AReport Writing,Technical Standards,Project Work,Adherence,It,Working Environment,Legal RequirementsNoNo
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:

Responsibilities:

WHAT YOU’LL BE DOING

In the role of QA, the key focus will be to assist in the production of safe food, which meets customer specification and legal requirements by ensuring the effective operations of agreed procedures through regular auditing.

  • Sample, test, audit and monitor to verify that all processes, procedures and products are being manufactured in a safe and compliant manner.
  • Conduct verification checks to ensure equipment is suitably calibrated to comply with required standards.
  • Complete all necessary documentation ensuring that it is kept accurate and ready for internal and external audits and highlighting when non-conformance requires corrective action.
  • Maintain on going communication with the team and other relevant functions ensuring they are fully aware of quality assurance results.
  • Collect all relevant samples (products, swabs, water samples etc.), with adherence to procedures and protocols, to ensure quality, safety and legality of products sampled.
  • Provide technical support & advice to operational staff and other teams to ensure compliance with all relevant technical standards, seeking guidance and advice from QA Area Leaders / Technical Manager where necessary.
  • Ensure that a safe working environment exists for all employees and that as a minimum the department meets the standards set out in the safety, health and environment policy.
  • Test traceability of finished product for legal compliance audits, customer complaint and out of specification micro investigations.
  • Communicate effectively between the team, shifts and all other functions
  • Incident report writing, collection and presentation of data
  • Undertaking project work as part of the technical team


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Boston PE21, United Kingdom