- $31,750.00 -48,930.00/year*
912 Regimental Dr
Back to our career areas United States
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people s exceptional skills with those of people from all over the globe.
The Technician, Inspection is a direct labor position reporting to a Process Execution Team Process Facilitator on the Manufacturing floor, which supports operations. This position will require working in various Controlled/Non-Classified areas. The Technician operates equipment, performs in- process monitoring, line clearances, OEE data collection, cosmetic inspection and completes batch record entries in accordance with cGMPs. Perform cleaning and housekeeping activities for assigned areas as required to maintain a cGMP environment. Perform 5S activities and maintain organization of operating areas. Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety procedures in accordance with OSHA requirements and guidelines. Be familiar with Material Safety Data Sheets for area chemicals. Perform batch record and GMP documentation entries. Maintain records and/or logs as required in performance of job responsibilities. This will include mathematical computation where needed. Knowledge of product security controls including controlled substance handling. Responsible for outgoing quality level. Some overtime will be required with prior notice to support business needs. Be able to start up and make minor adjustments to machinery. Computer on-line may require some data input. This includes SCADA and HMI entries. Perform the duties of operating assigned machinery consisting of servicing machines with materials, removing finished materials from machine tables, and assuring smooth flow of product. Perform visual and physical checks of in-process and finished materials as requested. Be familiar with job related hazards. Report all discrepancies to process facilitator. Perform all other duties with minimal supervision under the direction of the process facilitator or designee. Knowledge of light material handling equipment (non-motorized lifts). Perform inventory control and reconciliation activities, which may require use of SAP in a limited role. Work with various printing devices including printing mats, ink-jet, etc. OEE data collection either by manual method or knowledge of automated collection system. Certified OJT trainer activities on the team, as needed. Flexibility in cross training between packaging functions. Responsible for assembling, disassembling and sanitizing various packaging equipment. Familiarity with chemical handling and spill control procedures in connection with hazardous waste pick-up duties. Assist mechanical staff with preventive maintenance procedures, as required. High school graduate or GED. 1 Year of experience in a pharmaceutical or GMP regulated environment. Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language. Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations. Prior production experience. Experience working in a LEAN manufacturing environment. Knowledge of cGMPs and FDA policies/procedures. PET staff Ability to work effectively in a team environment. Candidate should possess the ability to work in a changing/demanding environment.
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Associated topics: aseptic, clinical, drug, drug discovery, histology, immunology, medicine, microbiology, physiologist, therapeutic
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.
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