Allergan Work Values

Daily Duties at Allergan:

Led internal quality audits to ensure compliance with 21 CFR 820, CMDR, and MDD regulations as well as ISO 13485 requirements. Conducted quality audits of over forty raw material suppliers, API manufacturers, testing laboratories, and distributors to assess compliance with ISO 9001 or 13485 requirements. Verified the effectiveness of CAPAs implemented to address internal and supplier audit nonconformities. Conducted QSR and ISO training for all employees.

What they like about Allergan:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

Quality Engineer, Supplier Quality Engineer, Quality Supervisor, Documentation Supervisor, Regulatory Compliance, Pharmaceuticals, Medical Devices, In Vitro Diagnostics, Clinical Products, Commercial products, Training, FDA, Health Canada, Notified Bodies, SOPs, Test Methods, Stability Testing, Product Complaints, Calibration, ISO 13485: Lead Auditor, Reliability Engineer, Risk Management, Six Sigma, CAPA, Regulatory Affairs Certified, Nonconforming Product, Quality Auditor, Biomedical Auditor, Internal Audits, Supplier Audits, Validation

Skills

Quality Audits, Corrective and preventive actions, FDA Pharmaceutical and Medical Device Regulations, Providing GMP, QSR, and ISO Training, Risk management, Communicating with all levels of personnel, Conducting management review meetings, Logistics, Product transfer, Supplier Quality Management

These are some of the questions we asked our climbers about their experiences with Allergan: