QC IM Lab Analyst III

Pfizer • Rocky Mount, NC

2d • Onsite

About The Position

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our flexible, innovative, and customer-oriented quality culture is rooted in science and risk-based compliance. 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 highest standards, making a meaningful difference in the lives of those we serve. Join us in our mission to improve patient outcomes through excellence in every aspect of our work.

Requirements

• HS Diploma or GED and 8 years of relevant experience; OR an Associate's degree with 6 years of experience; OR a Bachelor's degree (preferably in Chemistry or other related Science) with 4 years of relevant experience
• Certifications in the relevant areas, if applicable
• Ability to write clear technical documents
• Good organizational and time management skills
• Proficiency in Microsoft Office
• Experience with laboratory equipment and procedures
• Knowledge of Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP)
• Permanent work authorization in the United States.

Nice To Haves

• Bachelor's Degree
• Incoming Material inspection experience with components.
• AQL Inspection; Defect Recognition
• Effective problem-solving skills
• Strong analytical skills
• Strong attention to detail
• Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

Responsibilities

• Serve as a key resource and potentially lead lower-level team members within your area of expertise.
• Manage personal time and professional development, taking accountability for your results and prioritizing workflow.
• Contribute to project and departmental tasks, providing direction and training to team members, and may act as a lead worker.
• Be recognized as a "LEAD" or "Subject Matter Expert" in your field.
• Proactively identify and resolve basic complexity problems, considering wider implications.
• Complete assignments independently, selecting appropriate methods, and ensuring team assignments are completed.
• Review non-standard work for technical soundness and may review others' work.
• Adhere to Pfizer standards, guidelines, and values, influencing teams, and contributing to the development of departmental standards and guidelines.
• Provide input for performance assessments, ensure timely and compliant documentation, and develop processes to enhance cGMP standards.
• Maintain high standards of safety and housekeeping, participate in Continuous Improvement projects, and ensure adherence to all policies and procedures, while providing training and conducting peer reviews.

Benefits

• Eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies.
• 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
• Health benefits to include medical, prescription drug, dental and vision coverage.
• Relocation assistance may be available based on business needs and/or eligibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level