Abbott Laboratories Work Values

Daily Duties at Abbott Laboratories:

Coordinated support of global supply chain for 7-product portfolio (including sterile fill, tablets, capsules, and medical devices), partnering with stakeholders in supply chain management, manufacturing, and regulatory sectors. Built and maintained key relationships across all third-party operators and global supply chain, managing QA for 5 TPM sites that supplied 15 domestic and international products. Steered critical change and process optimization initiatives, approving process change controls and validation protocols, conducting deviation investigations, and generating CAPAs. Conducted strategic analysis looking at CAPA effectiveness, and track GMP audits for intermediate and final CMO products, initiating adjustments as needed. Managed all deviation investigations and resulting CAPA quality improvement programs. Maintained and monitored quality agreements with all outside contractor manufacturing operations.

What they like about Abbott Laboratories:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

Tags

North Carolina, South Carolina, Florida, Texas, Missouri, Chicago, Atlanta, Associate Director of Quality Assurance, Quality Assurance Manager, Sr. Compliance QA Manager, Associate Director of Validation, Validation Director, CAPA Management, Supplier QA Manager, Director of Supplier Assurance, CMO QA Manager, Pharmaceutical QA Manager, Medical Device QA Manager, Corporate QA Auditor, CAPA Manager, API Manufacturer, Sterile Fill Pharmaceutical Manufacturer, Medical Device Manufacturer, Sr. Quality Engineer, Oklahoma, Illinois, Milwaukee WI, Validation Manager, Internal QA Auditor

Skills

GMP CAPA assessments, GMP MFG Audits / Supplier Audits, Change Management, Process Change Controls, Process Optimization, Pharmaceutical and Medical Device Operations, Risk Management, Validation Management, Validation Master Plans, Validation Protocol Development, Risk Management, Project Management, Facility / Equipment Qualifications, Problem Solving, Deviation / CAPA Remediation, Team Leadership, Training Programs, Regulatory Compliance, Supplier Quality Management, Supplier Quality Agreements

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