Kalamazoo, MI, United States
Engineering, Manufacturing, Chemistry
Analyzes / designs sequence of operations and work flow to improve the company's production facilities within regulations and GMP guidelines. Activities may include process monitoring, safety and environmental improvements, troubleshooting, process reliability improvements, validation, and technology transfers. May establish or assist in establishing accident prevention measures and may train personnel concerning all phases of production operations. Conducts studies pertaining to cost control, cost reduction, inventory control, and production record systems. On the basis of these studies, develops and implements plans and programs for facility modifications and revisions to operating methods. May assist project managers or engineers in the planning and design of facilities.ROLE RESPONSIBILITIESFunctional/Technical Knowledge: Knowledge of basic discipline. Limited knowledge of industry practices and standards. Focus is on overseeing defined processes.Problem Solving and Innovation: Develop solutions to routine problems following established Pfizer policies and procedures.Discretion, Latitude, Level of Independence: Closely supervised. Follows specific instructions.Impact and Organizational Contribution: Contribute to the completion of routine tasks.Teamwork/Influence: Contacts are primarily within immediate work group or within normal process-related work flow.Time Span of Work: Daily tasks and deliverables. Results can usually be measured on daily or weekly basis.BASIC QUALIFICATIONSEducation: 2 years of related experience and BS/BA in Chemical Engineering/Chemistry/related filed or 1 years of related experience and MS Chemical Engineering/Chemistry/related filedLanguage Skills: Effective written and oral communication.Computer Skills: Microsoft Applications.Physical Demands: Frequent time in the manufacturing area around equipment with moving parts, stair climbing, roof access.PHYSICAL/MENTAL REQUIREMENTS• Physical Demands: Frequent time in both manufacturing and office environments. The manufacturing environment includes equipment with moving parts. Must be able to perform gowning requirements for entry in the manufacturing areas.Requires lifting, sitting, standing, walking, stair climbing and roof access. Must be available to support 24/7 – 365 operation.• Work Environment: Office environment, with frequent time in the manufacturing areas. Possible exposure to high noise environments, solvents, and pharmaceutical ingredients. Use of hearing and eye protection is required. Must be available to support 24/7 – 365 operation.NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTSRole supports a 24 hour production environment. Primary responsibilities occur M-F during normal working hours. Some off hour and holiday coverage may be required.Sunshine ActPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are
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Good health is vital to all of us, and finding sustainable solutions to the most pressing health care challenges of our world cannot wait. That's why we at Pfizer are committed to applying science and our global resources to improve health and well-being at every stage of life. We strive to provide access to safe, effective and affordable medicines and related health care services to the people who need them.