Global Pathology QC Scientist | Data & Specimen Integrity

Regulatory Jobs; Groton (CT); On-site; USD 79,000 - 132,000; Full time

Benefits offered by this job

401(k) plan with Pfizer Matching

Paid vacation

Holiday and personal days

Parental and medical leave

Health benefits (medical, dental, visо

Job summary

Pfizer is seeking a Global Pathology Quality Control Scientist to independently conduct quality control of anatomical and/or clinical pathology data, specimens and reports. Based on qualification, you may flex to perform necropsy and histology for regulatory studies.

You will develop and validate high-complexity procedures and contribute to data integrity and publication-quality datasets. The role requires GLP experience, strong communication, and the ability to train others, with on-premises

Qualifications

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

Responsibilities

• Perform regulatory responsibilities in compliance with GLP and animal welfare regulations
• Quality Control of anatomic and/or clinical pathology data, specimens and reports
• Adhere to study report timelines
• Support necropsy, histology for various studies as qualified
• Develop, validate, and document new procedures and methods for high-complexity pathology assays
• Interact with and train staff and contribute to scheduling and data integrity

Skills

Communication skills

Organizational change management

Proficiency in MS Office

Scientific software

Independent work

Education

Bachelor’s degree in biology or related field

Master’s degree

Tools

Word

Excel

PowerPoint

TEAMS

Job description

Pfizer is seeking a Global Pathology Quality Control Scientist to independently conduct quality control of anatomical and/or clinical pathology data, specimens and reports. Based on qualification, you may flex to perform necropsy and histology for regulatory studies.

You will develop and validate high-complexity procedures and contribute to data integrity and publication-quality datasets. The role requires GLP experience, strong communication, and the ability to train others, with on-premises