Sr. Associate Scientist - Bioanalytical
PfizerAbout the role
Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.
What You Will Achieve
In this role, you will:
- 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 Bioanalytical testing including ELISA and plate-based assay and conduct investigations as needed.
- 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)
- High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
- Strong technical skills in method validation and testing
- Experience in bioanalytical 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
- Effective written and verbal communication, as well as interpersonal skills
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
- Strong problem-solving abilities
- Effective time management and organizational skills
- Ability to mentor and train junior colleagues
PHYSICAL/MENTAL REQUIREMENTS
Ability to lift 30 lbs, stand for 2 to 3 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.
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.
Non-existent to minimal travel.
Must be able to wear appropriate PPE (e.g., lab coat, safety glasses, non-porous shoes, gloves, etc.)
Work Location Assignment: On Premise
OTHER JOB DETAILS
- Last Date to Apply for Job: July 11th, 2025
- Referral Bonus Eligibility: YES
- Eligible for Relocation Package: NO
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