Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world.
Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives every day.
Allergan is a company that will inspire you to aim high with your ambition. Where you can build bridges all over the world. Where you can power ideas that drive change. And where you will act fast and drive results for customers and patients. Power your future & join our bold team.
Serves as an investigator and technical writer with responsibilities in operations, production, process, and equipment at the Waco facility.
Main Areas of Responsibilities
Investigation of significant events within the production process relating to process, equipment, and product quality.
Technical writing of investigations reports and risk assessments
Work with the Operation / Engineering stakeholders and Quality Assurance to determine effective corrective and preventative actions.
Assist with the implementation of certain corrective and preventive actions.
Outline and implement process improvements to increase quality, efficiency, and compliance.
Tracking and providing appropriate updates on status.
Perform other duties as assigned.
Incumbent has full authority to make decisions and/or take actions required to carry out job duties. Allergan internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements, and objectives. The incumbent must be willing to take temporary assignments as required.
The following listed requirements need to be met at a minimum level to be considered for the job:
Bachelor's degree in Industrial Engineering/Operations Management, the Sciences or related field.
Three (3) years' experience with a minimum of one (1) year working in relevant areas such as Operations, Engineering, or Quality Assurance.
Proficient in Microsoft Office
Familiarity with Trackwise system (or similar system) a plus.
Experience working in a GMP regulated environment preferred.
Experience working in an Aseptic Production environment preferred.
Demonstrated ability in technical writing and problem solving.
Strong detail orientation
Broad understanding of manufacturing environments.
Ability to obtain gowning access to the controlled area.