Aaipharma/Cambridge Major Laboratories Work Values

Daily Duties at Aaipharma/Cambridge Major Laboratories:

Steered development and management of new validation department for API manufacturing operation at Cambridge Major Laboratories, overseeing team of 12 and up to $900K operating budget. Designed and developed all policies and procedures for new validation department, and set up system to ensure that all cGMP requirements were met for equipment, facility, utility, and process qualification for approved API products. Conducted employee performance reviews. Maintained validation master plans throughout tenure, ensuring all equipment reviews were performed on schedule. Trained QA staff to ensure high quality performances met cGMP requirements. Provided key support for all internal/external audits, and developed CAPA plans for audit observations. Coordinated SOP development and associated trainings to support implementation of deviation/CAPA program for Master Control Software and Change Management systems. Conducted quality audits.

What they like about Aaipharma/Cambridge Major Laboratories:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

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 Aaipharma/Cambridge Major Laboratories: