Why Patients Need You

Everything 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 Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies.

As a Manager, your breadth of knowledge on internal or external business challenges will help us improve our products, processes and services. Your will guide projects by meeting objectives and preparing forecasts for resource requirements. Your risk-taking ability will help us advance new concepts and methodologies. You will provide technical guidance and oversight to team members and help in problem solving.

How You Will Achieve It

• Manage and provide guidance and coaching to Quality Operations team and provide direction or approval of activities and decisions.
• Manage multiple projects and ongoing work activities within the division typically involving cross-functional representatives.
• Manage the specific Inspection preparation plan for key Good Manufacturing Practices {also cGMP} elements etc.
• Take independent actions and decisions and motivate key stakeholders to deliver quality outcomes for business requirements.
• Provide Quality Assurance expertise to colleagues On and off the Manufacturing floor as required.
• Identify continuous improvement opportunities based on metrics and drive consistency through the process to align with Pfizer's standard processes and quality systems.
• Assist in key site quality behavior establishment, set clear company policies and behavior expectation for team member.
• Manage and conduct regular Production areas walkthroughs (Area product clarences, GMP and compliance walkthroughs)
• Assist Quality Operations Deviations and Product Floor Support for all planned and unplanned manufacturing deviations.
• Investigate, document Quality Assurance related deviations and escalate issues as appropriate to the Quality Assurance Lead in a timely manner.
• Maintain regulatory compliance in accordance with current Good Manufacturing Practices.
• Accurately communicate Supply/Operational needs/perspectives as well as Quality Operations (QO) perspectives.
• Review and approval of validation documents Process, cleaning & method validation.
• Manage and conduct On floor QA review of executed batch records and Logbooks to assure compliance with regulatory standards and regulatory filing.
• Quality Assurance approval of SOPs, Campaigns start up Form and QA validation protocols and reports.
• Prepare departmental budgets and control the departmental cost within the budgets.
• Interface with Regulatory Agencies in audits.

Qualifications

Must-Have

• Applicant must have a High School Diploma (or Equivalent) and 10 years of relevant experience OR an associates degree with 8 years of experience OR a bachelors with at least 5 years of experience OR Masters Degree with more than 3 years of experience, OR a PhD with 0+ years of experience.
• Working knowledge of current Good Manufacturing Practices {cGMP} for a pharmaceutical industry
• Extensive knowledge of corporate quality systems that are applicable to the quality unit and the production operations serviced
• Strong collaboration, relationship management, and interpersonal skills
• Strong people management experience
• Excellent written and oral communication skills
• Strong computer proficiency skills in MS Office, Word, Excel, Access, Project, Trackwise or equivalent

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Ability to work Monday to Friday 2nd Shift Schedule.

Work Location Assignment: On Premise

OTHER JOB DETAILS

• Last Date to Apply for Job: December 1, 2023
• Referral Bonus Eligibility: YES
• Eligible for Relocation Package: NO

The annual base salary for this position ranges from $96,900.00 to $161,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. 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.

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