Senior QA Officer

☞ Just Life Sciences

View: 101

Update day: 13-05-2024

Location: Bridgend Wales

Category: Pharmaceutical / Chemical / Biotech

Industry:

Job type: Full-time

Salary: £28,000 a year

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Job content

  • Reference:JLS SQA1
  • Location:Bridgend
  • Salary:£28k
  • Type:Full time
  • Start:ASAP

Just Life Sciences are working with a hugely successful and expanding Global Healthcare Business, who through internal promotion are seeking a Senior Quality Assurance Officer on a permanent basis


Qualifications, Skills and Experience

  • Specific Job Responsibilities:
    • To ensure that all work carried out is in compliance with company, cGMP, cGLP’s, SOP’s, regulatory, H&S and environmental requirements.
    • To provide support for Quality Incident root cause analysis, risk assessments and approval as required.
    • Handling customer questionnaires and complaints from receipt, through to investigation and reply to the customer.
    • Handling and approval of deviations and CAPAs.
    • Review and approval of change controls and related documentation for compliance with regulatory and GMP requirements.
    • To conduct internal audits and participation in the external audit programme.
    • To support Regulatory and Customer Audits.
    • To support the Technical Manager in the approval of suppliers and starting materials.
    • To participate in continuous improvement activities concerning the Quality Management System including preparation, issuing and distribution of SOPs.
    • Any other reasonable duties as identified by management.
  • Relevant Skills, Education and Experience:Essential:
    • Sound written and verbal communication skills
    • Decisive thinker able to work within agreed timescales
    • Degree Qualification in a Science Discipline.
    • Technical report writing skills
    • Excellent computer skills, experience with Microsoft office essential
    • Excellent planning and organisational skills to ensure workload prioritisation and schedule adherence
  • Desirable:
    • Knowledge of BRC, MHRA FDA Guidelines
    • Knowledge and understanding of interpretation of cGMPs and regulatory requirements, experience of regulatory inspections and customer audits.
    • Auditing skills and / or lead auditor trained.
    • Experience of QC/QA related activities within a food or pharmaceutical manufacturing business
  • If you have the experience or are looking for your next position please email your CV through to justyn at justlifesciences dot com

  • Just Life Sciences

    • 2a Foster Drive,
      Cardiff,
      CF23 9BZ
    • Mobile 07968 551450
    • Email justyn.withey@justlifesciences.com
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Deadline: 27-06-2024

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