Use Your Power for Purpose
At Pfizer, our mission is to cultivate a best-in-class culture of continuous improvement and project management, empowering colleagues and streamlining effective processes. Your contributions help foster an environment where breakthroughs are not just possible but inevitable, ensuring that our work consistently meets the highest standards of excellence and impact.
What You Will Achieve
In this role, you will:
As a Continuous Improvement (CI) Specialist you will play a crucial role in enhancing organizational efficiency and effectiveness. You will be responsible for identifying areas for improvement within processes, systems, and workflows. By analyzing data and performance metrics, you will develop strategies to optimize operations, reduce waste, and increase productivity. You will collaborate across the Focus Factory to implement changes within your operations and monitor progress, ensuring that improvements are sustainable and aligned with the organization's goals. You will focus on fostering a culture of continuous improvement within the team. You will support colleagues by encouraging them to adopt best practices and innovative approaches. By promoting a mindset of ongoing development, you will help the organization stay competitive and adapt to changing market conditions. Your expertise in problem-solving and project management is essential for driving long-term success and achieving operational excellence. The CI Specialist will report into the Sr. Manager of Operations within the Focus Factory. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
ROLE RESPONSIBILITIES
Lead, support and coach data analysis by using and fostering the adequate operational excellence tool.
Identify, analyze, prioritize and execute business solutions through development of largest sources of loss analysis.
Own and manage the Tier 1 CI loop · Support/perform root cause analysis for elimination of repeat performance issues/occurrences.
Contribute to the completion of moderately complex projects.
Manage own time to meet agreed targets, develops plans for activities on own projects.
Collaborate with the site’s OPEx team to progress and monitor delivery of performance and goals.
Work with engineers to learn and implement techniques to continuously improve packaging equipment reliability and efficiency.
Develop proposals for improving process technology from a quality, cost and capacity optimization perspective.
Inspire a culture of continuous improvement by partnering effectively with personnel involved in the investigation process.
Ensure that (Current) Good Manufacturing Practices (part of GxP) and regulatory compliance is incorporated into all CI projects in the CI loop as part of projects scope, design and execution.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelor's degree with at least 2 years of
experience; OR a master's degree with more than 0+ years of experience;
OR an associate's degree with 6 years of experience; OR a high school
diploma (or equivalent) and 8 years of relevant experience.
Solid understanding of Process Monitoring systems, including knowledge of PLC/computer systems
Ability to work effectively with site colleagues through the change process
Strong verbal and written English communication capabilities
Functional knowledge of Microsoft SharePoint and Office applications, particularly Excel
Ability to organize data and plan for the future
Experience in fostering a Continuous Improvement Culture
PREFERRED QUALIFICATIONS
Master's degree
Relevant pharmaceutical experience, or experience working in a regulated environment
Demonstrated ability to effectively coach and mentor colleagues and manage diverse relationships
Lean exposure and capability
Bonus Points If You Have (Preferred Requirements)
Relevant pharmaceutical experience
Demonstrated ability to effectively coach and mentor colleagues
Strong problem-solving skills
Ability to lead and influence cross-functional teams
Experience with Six Sigma methodologies
Ability to manage multiple projects simultaneously and meet deadlines
PHYSICAL/MENTAL REQUIREMENTS
Must be able to climb flights of stairs and standing for ~1-2 hours at a time.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Occasional off-shift and weekend requirements
Work Location Assignment: On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer 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 a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
Continuous Imprv and Proj Mgmt