Use Your Power for Purpose
Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.
What You Will Achieve

In this role, you will:

• Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.
• Support environmental monitoring and water collection in the QC Microbiology laboratory.
• Follow Environment Health and Safety requirements for site and QC laboratories.
• Write cleaning validation protocols and reports, and perform complex mathematical problems and data analysis.
• Support product transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation.
• Operate within established HR policies and basic colleague relations guidelines.
• Write Standard Operating Procedures (SOPs), technical reports, project plans, etc.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelor’s degree with 0+ years of experience; OR an associate’s degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience.
• Demonstrated experience in manufacturing quality or engineering experience in the biotech or pharmaceutical industry
• Fundamental understanding of laboratory instrumentation function 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

Bonus Points If You Have (Preferred Requirements)

• A deep understanding of Microbiology testing and experience in defending laboratory practices during regulatory audits
• Proficiency in both viable and non-viable environmental monitoring within pharmaceutical manufacturing
• Solid grasp of aseptic techniques
• Strong problem-solving skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks simultaneously

PHYSICAL/MENTAL REQUIREMENTS

Ability to lift 30lbs, stand for 2 to 3 hours at a time, site for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.

• Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.
• Support environmental monitoring and water collection in the QC Microbiology laboratory.
• Follow Environment Health and Safety requirements for site and QC laboratories.
• Write cleaning validation protocols and reports, and perform complex mathematical problems and data analysis.
• Support product transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation.
• Operate within established HR policies and basic colleague relations guidelines.
• Write Standard Operating Procedures (SOPs), technical reports, project plans, etc