We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals. Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products. Transforming Delivery of high quality products Why Patients Need You Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action. What You Will Achieve Working with Pfizer’s dynamic engineering team, you will play a critical part in providing technical or business support to engineers on a variety of technical tasks. Your documentation skills will come in handy to prepare engineering documentation, reports and drawings. You will be conducting preliminary analysis of trajectory adequacy data, model dimensional consistency and quantitative judgments concerning technical data. You will also support the team by conducting tests and recording data to assist engineering evaluations. You will be a team member who is relied upon to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team’s success by sharing your previously acquired knowledge. The essential duties for this position include but are not limited to: Performs all tasks as outlined in the Batch Card, SOPs, and/or Job Aids. Effectively demonstrates and understands the SOPs and Job Aids pertinent to all assigned tasks. Inspects filled syringes to established criteria and sorts defects into the appropriate receptacle for reconciliation. Performs manual packaging operations as assigned by the supervisor according to the appropriate SOP or Job Aid. Observes all SOPs and Safety and Health Regulations. Re-stocks packaging supplies from line stock as required to maintain packaging operation. Notifies supervisor, PMO and/or Quality Specialist of unusual or recurring defects in syringe products or packaging materials. Maintains work area in a clean and orderly manner. Assists in training new colleagues as required. If required, verifies packaging supplies and product against product board or Batch Card to assure correctness. Signs pertinent forms as required. Participates in all required training programs to maintain required level of cGMP compliance. Performs off-line inspection of product, such as media reading, as required. Performs other miscellaneous duties as assigned by supervisor. How You Will Achieve It Accountable for own results and prioritizes workflow based on needs. Coordinate with maintenance to complete repairs and develop solutions to equipment issues. Perform all tasks as outlined in batch records, procedures, and job aids. Assemble, operate, clean and troubleshoot micronizing, formulation and aseptic filling equipment. Manage own time and professional development. Qualifications Must-Have High School Diploma or GED 2 years of experience Understands basic problem-solving methods. Mathematics and reading skills required for SOP, Good Manufacturing Practices {also cGMP} and Batch Record comprehension Physical/Mental Requirements This position is in a Penicillin Facility. The candidate cannot be allergic to Penicillin, and will be required to undergo Penicillin allergy testing. This department requires the SMO to bend, reach, lift and stand for extended periods of time. The SMO must be able to grasp from 4 – 5 filled syringes at a time in one hand while manipulating them with the other hand for overall evaluation for defects. All SMOs must have corrected 20/20 vision and must be able to pass a routine inspection test using seeded syringes. Good skills in communication and leadership Ability to contribute to department success in a team environment Performs tasks at a productive level under demanding conditions is mandatory Non-Standard Work Schedule, Travel, or Environment Requirements The Penicillin Inspection/Packaging department is currently operating on a one-shift basis, five days per week. However, SMOs must be available for extended hours and six to seven day operations, if required in order to maintain the required delivery schedule, overtime may be required. This is a Collective Bargaining Agreement (Union) position, Union Hourly Rate: $25.79. The work schedule is 7am to 3:30pm with overtime as needed. Other job details Last day to apply: September 30, 2024 Eligible for employee referral bonus: Yes. LI-PFE Work Location Assignment: On Premise J-18808-Ljbffr