QC Senior Associate Scientist, Stability

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

In this role, you will:

• Perform tasks associated with maintaining cGMP compliant Stability and Stability area/equipment
• Complete activities to implement Stability protocols, gLIMS studies for new products, and annual stability studies for commercial products
• Perform stability pulls and coordination of subsequent aliquoting
• Responsible for requesting detailed gLIMS builds and gLIMS master data changes
• Forecasting of expected Stability pulls for QC and Contract labs
• Complete actions for end of studies and sample disposal
• Metric tracking and reporting
• Maintenance and continuous improvement of Stability procedures and process
• Serve on cross functional teams to represent QC and facilitate communications and activities/projects between QC and other site departments

Here Is What You Need (Minimum Requirements)

• BA/BS with at least 3 years of experience or MBA/MS with any years of experience
• Demonstrated experience in manufacturing, quality, or engineering within the biotech or pharmaceutical industry
• Experienced and proficient with laboratory practices, Good Manufacturing Practices (cGMP), and compliance requirements for Quality Control Laboratories
• Ability to establish strong relationships within business lines
• Excellent written and verbal communication and interpersonal skills
• Proficiency in laboratory information management systems and data analysis software
• Strong problem-solving skills and attention to detail

Bonus Points If You Have (Preferred Requirements)

• Experience in Quality Operations
• Experience with gLIMS and eQMS
• Ability to work independently and as part of a team
• Strong organizational and time management skills
• Ability to adapt to changing priorities and work in a fast-paced environment
• 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

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

Other Job Details:

• Last day to apply: October 22nd, 2026.
• Working hours: Flexible - 1st shift.
  
  

The annual base salary for this position ranges from $68,600.00 to $114,300.00. 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.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Quality Assurance and Control

About Us

A career at Pfizer offers opportunity, ownership and impact.

All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the bio pharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.