Alvotech

Alvotech

·11 days ago

Principal specialist - qa engineering

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Location

onsite, Reykjavik, 1, Iceland

Commitment

Full Time

Level

Senior (5+ years)

Required skills

Quality Assurance OversightQualification and ValidationFacilities and UtilitiesEquipment QualificationComputerized System ValidationGxP Regulatory ComplianceGAMP 5Change ControlDeviation ManagementCAPAInvestigation and Corrective ActionsMaintenance and Calibration ReviewData IntegrityAudit and Inspection SupportContinuous ImprovementCross-Functional Collaboration

Job Description

Key Responsibilities

  • Provide QA oversight and collaborate with cross-functional teams in planning maintenance, qualification, and validation activities for facilities, utilities, equipment, and computer systems (CSV).
  • Serve as a Quality representative and a subject matter expert (SME) in selection, design and build of new technologies and new facilities within Alvotech.
  • Support and provide QA oversight with review and approval of qualification documents for facility, utility, equipment and computerized systems as applicable.
  • Contribute to investigations into discrepancies arising during qualification / validation activities and subsequent approval of appropriate corrective actions.
  • Review of planned and unplanned work orders for maintenance, preventive maintenance, calibrations and other Engineering related activities.
  • Reviews and approve change controls, deviations, CAPAs, effectiveness checks for facilities, utilities, and equipment, computer systems.
  • Stay current on applicable external requirements and industry standards and drive continuous improvement on Engineering and CSV processes and tools.
  • Advice on quality matters, and assistance for closing compliance gaps found in audits and inspections.
  • Escalation of any data integrity or critical quality issues to the supervisor and Quality Management of Alvotech.
  • Responsible for ensuring all facilities, utilities, equipment, computer systems are appropriately validated and qualification in line with current EU and US legislation for parenteral/biologics.

Minimum Education and Experience Required

  • A bachelor’s degree within relevant area, or other relevant business experience.
  • Minimum 5 years of experience within the Pharmaceutical or Medical Device Industry (preferably in parenteral/biologics formulations).
  • Experience working with regulatory requirements in GxP required (Preferably FDA and EU regulations).
  • Good understanding of GAMP 5 guide required.
  • Knowledge of and experience with validation and qualification specifically within facility, utility, and equipment/computer systems.

Ready to join the team?

Apply now