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Operational Quality Officer

gsk

New
Onsite Junior 🇬🇧 English
GMP cGMP GLP SOPs Batch records Validation EHS Excel Word

Job description

About the role

GSK is hiring an Operational Quality Officer who ensures adherence to GMP standards and procedures through independent oversight of GMP processes. The role supports a proactive quality culture, provides first-line support to operations and maintains inspection readiness through independent checks. It is fully on site and follows a shift-based schedule.

Key responsibilities

  • Ensure GMP processes and personnel follow current procedures, covering oversight shifts and keeping areas ready for inspection
  • Take part in key quality decisions, including initial impact assessments for deviations, and conduct spot checks in production, warehouse, utilities and laboratory areas
  • Follow the Quality Oversight program and ALCOA+ documentation principles, and escalate housekeeping deviations promptly
  • Manage rework and reprocessing within the site as required by the QMS
  • Review and approve quality documents (SOPs, master batch records, BOMs) and check batch documentation before product release
  • Ensure proper sampling of retained finished product batches and oversee OQ measures during routine and validation batches and engineering changes
  • Act as QA reviewer in deviations, handle customer complaint investigations and follow up on incidents seen during routine production
  • Deliver Stop for Quality training, coach staff and foster a quality-first culture
  • Give quality input to management monitoring and quality systems (CCRs, deviations, customer complaints) and support EHS and GPS implementation

Required profile

  • University degree in Pharmacy
  • At least one year of experience in the pharma industry
  • Fluent in Arabic and English, written and spoken
  • Experience managing diverse teams and controlling budgets against agreed targets

Required skills

  • Current knowledge of GMP, EDA regulatory requirements and the GSK QMS system
  • Validation knowledge and strong experience in cGMP/GLP compliance
  • Good documentation and report writing skills; Word and Excel
  • Excellent verbal and written communication, self-motivation and organisation

Questions fréquentes

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Source : ats:workday

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Published 13 hours ago

Expires 1 month from now

8 views · 0 interested

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