QA Officer

at  Clinical Professionals

Maidenhead, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate08 Jul, 2024GBP 16 Hourly09 Apr, 2024N/AGood communication skillsNoNo
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Description:

REFERENCE NUMBER: JO-2404-532804

QA Officer
Rate: Negotiable
Job Type: Contract
Location: Hurley, Maidenhead
Quality Assurance Officer
Batch Release
Hurley, hybrid 2/3 days on site
23 month contract
£16.63 per hour
We are currently recruiting for one of the largest global pharmaceutical companies, recruiting for a Quality Assurance Officer to support with the day to day QA activities of batch release. This role will work alongside the QA Manager and QP ensuring all duties in regards to batch disposition, supply chain and documentation meet GMP/ GDP regulations.

Main responsibilities;

  • To compile & review batch document sets for completeness & compliance to EU GMP, internal requirements and regulatory dossier submissions.
  • To resolve manufacturing, testing, packaging, and supply chain issues to support batch disposition.
  • To complete all relevant documentation to support the QP in the release of drug products, and to assist the certifying QP in the release of the drug product within internal systems
  • To assist in maintenance of quality systems including complaint handling, deviations/exception reporting, change control, supply agreements, document control, complaint handling, quality metrics reporting, temperature excursion resolution, document control and retention systems

Experience;

  • Previous QA experience within the pharma industry
  • GMP experience

For more information please contact Amy.goddard@cpl.com

Responsibilities:

  • To compile & review batch document sets for completeness & compliance to EU GMP, internal requirements and regulatory dossier submissions.
  • To resolve manufacturing, testing, packaging, and supply chain issues to support batch disposition.
  • To complete all relevant documentation to support the QP in the release of drug products, and to assist the certifying QP in the release of the drug product within internal systems
  • To assist in maintenance of quality systems including complaint handling, deviations/exception reporting, change control, supply agreements, document control, complaint handling, quality metrics reporting, temperature excursion resolution, document control and retention system


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Software Testing, Clinical Pharmacy

Graduate

Proficient

1

Maidenhead, United Kingdom