Sr. Associate Scientist - Bioanalytical
PfizerAbout the role
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.
Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records.
Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories.
Support ELISA, plate-based, along with other relevant analytical testing and conduct QC Analytical related investigations.
Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data.
Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues.
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
Strong technical skills in method validation and QC testing
Experience in QC analytical testing preferably in ELISA and plate-based testing
Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations
Detail-oriented with robust knowledge of quality systems
Familiarity with research unit clinical and analytical laboratory environments
Bonus Points If You Have (Preferred Requirements)
Relevant pharmaceutical experience
Strong understanding of computer system hardware, infrastructure, and networks
Experience with Laboratory Information Management Systems (LIMS)
Proficiency in data analysis and interpretation
Knowledge of regulatory requirements and guidelines
Ability to mentor and train junior colleagues
Physical/Mental Requirements:
Ability to lift 30 lbs, stand for 3 to 4 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
Intellectual capability to perform complex mathematical problems and perform complex data analysis.
Effective written and verbal communication, as well as interpersonal skills
Strong problem-solving abilities
Effective time management and organizational skills
Non-Standard Work Schedule, Travel, or Environment Requirements
Work schedule is first shift (8:00 am to 4:30 pm) but can include weekdays and/or weekend days as appropriate for assigned tasks/activities. Minimal flexibility in work schedule to cover business needs. Minimal off-shift work to ensure business needs are met.
Other Job Details:
Last day to Apply: November 7th, 2025
Eligible for Relocation Assistance: No
Work Location Assignment: On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state tr
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