About the RoleThe QA Manufacturing Inspector ensures the final product release of all manufactured products, oversees Operator Certification, conducts Compliance Audits and QA Surveillance Audits, and maintains quality system compliance.ResponsibilitiesRelease products and review DHR for completeness.Administer certification tests and review reject samples and cosmetic rejects.Maintain a clean and orderly area and equipment.Observe and report deviations from Good Manufacturing Practices during compliance audits.Conduct surveillance audits and walkthroughs of production areas.Identify and issue non conformities, investigate root causes, and provide corrective/preventive actions.Track and trend data, evaluate sampling plans, and recommend reductions based on statistical analysis.Maintain accurate documentation for DHR/BHRs and QA projects.Update procedures and specifications and keep SOPs and Inspection Plans current.Support validation and process improvement work; perform laboratory testing duties as needed.Train area personnel on applicable SOPs and Inspection Plans.Ensure continual QS compliance by adhering to evolving regulatory and Alcon QS requirements.Use root cause analysis tools when leading NCE investigations.QualificationsMinimum: Leaving Cert or equivalent.Preferred: Certificate or Diploma in a quality related field.Minimum: 1 year in Quality/Technical or Manufacturing role.Preferred: 2 years in medical device or pharmaceutical industry.Strong organizational skills, attention to detail, ability to work quickly and efficiently.Adaptable and flexible, able to move quickly between tasks.BenefitsA competitive salary package with fixed salary, bonus, pension, and health insurance. A flexible work environment with competent and committed colleagues. Opportunities for growth and development.
#J-18808-Ljbffr