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. ? Position Overview ? Ensuring that all inspections are conducted within the allowed release time as scheduled and that the areas are properly staffed.? Incumbent will have the ability to perform all Incoming and Final QA inspections of products and components. This position is essential to the operation to Production/Manufacturing and Quality Assurance.? ? ? ? Main Areas of Responsibilities: ? Coordinates the daily activities of Incoming/Final Inspections by directing staff in sampling, inspecting, and releasing components and chemicals per pre-established procedures, verifying and approving all final QA inspections.? Verifying log book entries and performs required preventative maintenance relating equipment used in the area. Responsible for handling all special requests originating from various Allergan, Inc., locations.? Responsible for coordinating the incoming ?hot? list at a minimum of two times a week, ensuring that all personnel are prioritizing off the ?hot? list. Prepares and routes component deviations.? Demonstrates proficient knowledge of and performance in all functional areas of Incoming and Final QA.? Provides matrixes for inspection release time on a weekly basis. Ensures and conducts the manual release of products in SAP when required.? Responsible for converting part numbers in SAP and updating SAP. Responsible for conducting SOP revisions and verifications.? Reviews and revises procedures as needed or as directed by the supervisor.? Assists in the training of Incoming and Final QA employees to comply with all Allergan SOPs, cGMPs , and safety guidelines.? Provides input and assists in problem solving and analysis with continuous improvement. Preferred Skills/Qualification's Ability to work effectively with peers and supervisors. Good problem solving skills and be detailed oriented. Detail oriented; thorough in thought process and following directions. Good math skills; must be able to work and or calculate percentages.? Experience working in an Aseptic Production environment preferred. ? Requirements: ? Able to lift up to 35 pounds (women), 40 pounds (men).? Must exhibit good written and verbal communication skills.? The ability to read, write and comprehend English and follow instructions in order to perform the responsibilities described above. Ability to work under pressure and with general direction to meet deadlines, and concentrate on details and following instructions. ?Three (3) to seven (7) years? experience in a Quality Assurance manufacturing environment. Working knowledge of cGMPs with hands-on knowledge experience. Thorough knowledge of SAP and AQL Inspectors rule. Experience working in a GMP regulated environment preferred. Education and Experience: High School education or GED equivalent.
Associated topics: dietician, drug, healthcare, medical, microbiology, nephrology, physiologist, physiology, therapy, transfection