QC IM Lab Analyst III
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 and Associate's degree with 6 years of experience; OR an 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)
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
- 401(k) plan with Pfizer Matching Contributions
- 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
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
