DSRD Global Pathology Quality Control Scientist

Pfizer; United States; In loco; USD 79.000 - 132.000; Tempo pieno

Vantaggi offerti da questo lavoro

401(k) plan with Pfizer matching

Bonus target 7.5%

Relocation assistance

Health benefits

Descrizione del lavoro

Pfizer seeks a Global Pathology Quality Control Scientist to independently perform QC of anatomic and/or clinical pathology data, specimens and reports. The role may flex to necropsy/histology support for regulatory studies while developing and validating high‑complexity methods.

Minimum requirements include a biology bachelor’s with 6+ years or a Master’s with 4+ years in a GLP environment, plus strong communication and training abilities. On-site US location with comprehensive benefits.

Competenze

• Bachelor's degree in biology or related field with equivalent experience; 6+ years
• Master's degree with 4+ years in GLP environment is acceptable
• Experience in quality control and regulatory compliance is required

Mansioni

• Perform Quality Control of anatomic and/or clinical pathology data, specimens and reports
• Maintain compliance with Good Laboratory Practices and animal welfare regulations
• Interact with and train staff, support necropsy and histology procedures as needed
• Develop, validate and document new methods for high-complexity assays
• Ensure study report timelines and data integrity for publications

Conoscenze

GLP environment

Quality control

Regulatory compliance

Communication skills

Training others

Formazione

Bachelor's degree in biology or related field

Master's degree (preferred)

Strumenti

TEAMS

Word

PowerPoint

Spreadsheets

Descrizione del lavoro

Use Your Power for Purpose

Pfizer's purpose is to deliver breakthroughs that change patients' lives. At the core of this mission is Research and Development, where we strive to transform advanced science and technologies into the most impactful therapies and vaccines. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, you will leverage cutting‑edge design and process development capabilities to accelerate and deliver top‑tier medicines to patients globally.

Through their expert knowledge in anatomic and/or clinical pathology techniques and processes, the Global Pathology Quality Control Scientist will primarily and independently conduct all aspects of Quality Control of anatomic and/or clinical pathology data, specimens and reports.

Based on their qualification, they may also flex to independently perform all aspects of rodent and non-rodent routine necropsy and/or histology procedures to support investigative, exploratory, and regulatory studies of high complexity.

They will independently support, develop, trouble‑shoot and validate new procedures and technologies of high complexity in the field of anatomic and/or clinical pathology.

What You Will Achieve

In this role, you will:

• Perform all regulatory responsibilities in compliance with applicable regulatory standards including Good Laboratory Practices and animal welfare regulations.
• Perform Quality Control of anatomic and/or clinical pathology data, specimens and reports independently
• Adheres to all study report timelines
• Based on their qualifications, may flex to support necropsy, histology of exploratory, regulatory and investigative studies
• Contribute to laboratory procedures and Controlled Documents
• Contribute to DSRD publication data integrity Quality Control
• Interact with and train individuals
• Contribute to pathology scheduling tasks
• Independently develop, refine, document methods/processes/reporting for assays of high complexity in the field of anatomic and/or clinical pathology (e.g. new sampling methods, non-standard endpoints) based on their scientific knowledge

Here Is What You Need (Minimum Requirements)

• Bachelor's Degree biology or a related field with at least 6 years of experience or a Master's Degree with at least 4 years of experience
• ≥ 3 years in GLP environment
• ≥ 2 years relevant experience in quality control
• Exceptional communication skills
• Strong organizational change management abilities
• Proficiency in Word, TEAMS, spreadsheets, PowerPoint, and relevant scientific software

Bonus Points If You Have (Preferred Requirements)

• HT (ASCP) certification
• Master's degree (MS) with over 4 years of relevant experience
• Strong understanding and adherence to regulatory guidelines
• Proficiency in VBA, .NET, SAS, SQL Server, Oracle, and MS Access
• Scripting capabilities
• Experience in a research laboratory setting
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

PHYSICAL/MENTAL REQUIREMENTS

sitting, standing, walking, ability to lift 20 lbs.

Work Location Assignment: On Premise

The annual base salary for this position ranges from $79,400.00 to $132,400.00. 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.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

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 st