QC Systems Laboratory Specialist

Use Your Power for Purpose
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the needs of those we serve. By being part of our team, you play a crucial role in maintaining this high standard and making a difference in the lives of patients.
What You Will Achieve
You will be a member of Pfizer's dedicated and highly effective Quality Assurance and Control team. You will support commercial manufacturing and QC testing labs by managing sample lifecycle including bulk sample receipt, aliquot, labeling, delivery, and storage of QC test samples. Sample types may include release test, backups, retains, reference material, assay controls, and stability.
As a member of the QC team, your knowledge will make you an active team member who influences the success of the team.
Your contribution to the Quality Control Sample Operations team will help Pfizer provide safe drugs to patients. It is your knowledge and skills
that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
In this role, you will:

• Contribute to achievement of goals at the work group/ project team level as a full team participant.
• Aliquot of laboratory samples to support site and global requirements
• Coordinate receipt and delivery of samples from designated sample ports to QC laboratories or QC cGMP areas and maintain
  the inventory for retain samples, backup samples and reference material.
• Perform tasks associated with maintaining {Current} Good Manufacturing Practices {part of GxP} compliant Quality Control
  laboratories.
• Serve on cross functional teams to represent Quality Control and facilitate communications and activities between Quality
  Control and site departments.
• Assist Lab leadership in determining scheduling priorities and workload distribution to ensure customer needs are met.
• Train junior colleagues, develop training plans, and oversee training activities for groups.
• Responsible for contributing to laboratory investigations.
• Perform laboratory support functions and maintain work area in a neat and orderly manner.
• Participate in continuous improvement culture within laboratories utilizing continuous improvement tools.
• Create and revise sample plans for Quality Control Sampling Operations to support aliquoting programs.
• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work
  activities on own projects within a team.
• Procure equipment, consumables, and miscellaneous items to support QC operation.
• Support change controls, CAPA, and investigations.
• Follow procedures with general instructions, maintaining compliance with regulatory standards and working under moderate supervision.
• Perform work consistent with Pfizer Values of Courage, Excellence, Equity, and Joy.

Here Is What You Need (Minimum Requirements)

• Applicant must have a Bachelor's Degree with 3+ years of relevant experience working in a GMP Laboratory environment.
• Knowledge of basic laboratory techniques including processing in a Biological Safety Cabinet, pipetting, aseptic technique, and
  basic laboratory safety practices.
• Experience in Quality Operations in biopharmaceutical industry,
• Experience with cGMPs, regulatory guidance and audits.
• Proficiency with computer systems: Microsoft Office: Excel spreadsheets utilizing detailed scheduling parameters and electronic laboratory information management systems such as LIMS.
• Demonstrates written and verbal communication skills, as well as interpersonal abilities, with experience liaising with
  stakeholders to identify opportunities for enhanced QCSO support.
• Knowledge of aseptic practices.
• The ability to understand manufacturing flow and concepts.
• Strong technical writing skills, including investigations.
• Experience with originating and revising Standard Operating Procedures (SOPs) in a GMP environment.
• Qualified Trainer or experience training others on GMP procedures or tasks.

Bonus Points If You Have (Preferred Requirements)

• Project management skills.
• Experience with continuous improvement tools including standard work, visual management, and DMAIC.
• Ariba application experience.
• 5S implementation and continuous support experience.
• Experience with deviations and investigations including CAPA's, and Impact Assessments.
• Experience in a GMP purification manufacturing environment.
• Experience with GMP Electronic Document Management System application.

Physical/Mental Requirements

• Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office and on the floor (laboratory, suites, etc.).
• Self-motivated and able to adapt to rapidly changing project priorities.
• Demonstrated leadership skills in decision making, planning, and prioritization with a focus on team success in meeting
  defined metrics and timelines.
• Strong problem-solving skills and attention to detail.
• Ability to receive feedback and take accountability for actions and personal development.

Non-Standard Work Schedule, Travel, or Environment Requirements

• This role is second shift, Wednesday through Saturday or Sunday through Wednesday 12:00PM to10:30PM. Some off-hour (night/weekend/holiday) support may be required to support staff and operations.

Other Job Details:

• Last Date to Apply for Job: August 19th, 2025
• Referral Bonus Eligibility: YES
• Eligible for Relocation Package: NO

The annual base salary for this position ranges from $66 500,00 to $110 900,00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7,5% 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.
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 [email protected] . 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.
Quality Assurance and Control