Use Your Power for PurposeEverything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.  Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.What You Will AchieveYou will help us with the investigations of our equipment quality issues in manufacturing and quality laboratories. You will investigate deviations and equipment out-of-specification results and atypical result investigations. Your problem-solving skills will help to identify root cause and suggest appropriate corrective action plans. Your attention to detail will help us ensure that the reports are aligned to regulatory requirements and company policies and procedures.As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team.  Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams.It is your hard work and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve It<ul><li>Contribute to the completion of complex projects and manage own time to meet agreed targets.</li><li>Develop plans for work activities on own projects within a team.</li><li>Perform, lead and review deviation investigation reports, change control and validation/qualification.</li><li>Provide direct input or coaching support for other functional groups in investigations.</li><li>Manage investigations and apply relevant and necessary actions/ systems to ensure appropriate levels of compliance.</li></ul>Here Is What You Need (Minimum Requirements) <ul><li>Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience</li><li>Proven record of problem-solving decision-making skills and application of process improvement tools</li><li>Experience in the pharmaceutical industry</li><li>Strong background and knowledge in manufacturing, compliance and technology investigations, processes and systems</li><li>Experience with Method 1 (yellow belt), DMAIC process, Fishbone diagrams, and/or 5 Whys</li><li>Technical writing experience such as authoring SOPs, technical reports, and/or investigations</li><li>Must be comfortable working both independently and collaboratively</li><li>Must be comfortable with working on multiple projects simultaneously</li><li>Effective communication skills are required, both written and verbal</li><li>Computer literate, with superior skills in managing eQMS</li></ul>Bonus Points If You Have (Preferred Requirements) <ul><li>Experience with investigations, including conducting and writing investigations, using current industry methodology</li></ul>  PHYSICAL/MENTAL REQUIREMENTSPosition requirements are typical for an office-based work environment with some shop floor exposure.  There are no unusual physical or mental requirements for this position.NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Schedule is primarily day shift (M-F, 8 hrs.) but may require off-shift work on occasions.  The position may require working on the floor in manufacturing or utility areas at times which will require a focus on safety. Aseptic gowning could be required. OTHER JOB DETAILSLast Date to Apply for Job: October 1st, 2025.Referral Bonus Eligibility: YESEligible for Relocation Package: NO Work Location Assignment: OnsiteThe annual base salary for this position ranges from $80 300,00 to $133 900,00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10,0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.Relocation assistance may be available based on business needs and/or eligibility.<div><div><div><div><div><div><div><div>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 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.</div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><div>EEO &amp; Employment EligibilityPfizer 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 <a href="#" rel="noopener noreferrer" target="_blank">www.pfizer.com/careers</a> 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 <a href="#" rel="noopener noreferrer" target="_blank">disabilityrecruitment@pfizer.com</a>. 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.</div></div></div></div></div></div></div></div>Quality Assurance and Control

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Pfizer

Pfizer is a global pharmaceutical leader focused on quality and innovation. We seek a full-time Engineering Excellence Sr. Associate with a relevant degree and pharmaceutical experience. You will investigate equipment quality issues, lead deviation reports, and support compliance. We offer competitive salary, bonus, 401(k) with match, paid leave, health benefits, and onsite work.

Engineering Excellence Sr. Associate

Summary