QC Scientist I: cGMP Microbiology & Quality Impact

Pfizer Inc.; Massachusetts; On-site; USD 60,000 - 100,000; Full time

Job summary

Pfizer Inc. is seeking a Quality Control/Quality Assurance lab professional to maintain cGMP-compliant QC and stability testing in a biotech/pharma environment.

You will perform routine testing, data review, and sample reconciliation, and support product dispositions while following HR policies and safety guidelines. The role requires a BA/BS with biotech or pharmaceutical manufacturing experience, strong analytical skills, and proficiency with Word and Excel.

Qualifications

• Minimum BA/BS with any years of experience in biotech/pharma manufacturing or quality
• Fundamental understanding of laboratory instrumentation and analytical method troubleshooting
• Excellent oral, written, and interpersonal communication skills
• Knowledge of Microsoft Office applications, specifically Word and Excel
• Ability to perform complex mathematical problems and data analysis

Responsibilities

• Perform tasks associated with maintaining cGMP compliant Quality Control and Stability laboratories
• Follow Environment Health and Safety requirements for site and QC laboratories
• Perform bioburden and endotoxin testing of routine in-process and drug substance product samples
• Support product dispositions through sample review and reconciliation
• Support lab activities with routine inventory checks and adhoc requests
• Write Standard Operating Procedures (SOPs), technical reports, project plans, etc

Skills

cGMP knowledge

QC lab experience

Biotech/pharma experience

Analytical method troubleshooting

Strong communication

Data analysis

Education

BA/BS degree

Tools

Microsoft Word

Microsoft Excel

Job description

Pfizer Inc. is seeking a Quality Control/Quality Assurance lab professional to maintain cGMP-compliant QC and stability testing in a biotech/pharma environment.

You will perform routine testing, data review, and sample reconciliation, and support product dispositions while following HR policies and safety guidelines. The role requires a BA/BS with biotech or pharmaceutical manufacturing experience, strong analytical skills, and proficiency with Word and Excel.