Senior QC Coordinator
About The Position
Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients. What You Will Achieve You will be a member of Pfizer’s dedicated and highly effective quality control laboratory support team. You will be responsible for the equipment sanitization, pipette maintenance programs, glass washing/autoclaving, and reagent entry/ordering. You will participate in process improvement and collaborating with others by sharing experiences. Your skill and knowledge will help in making decisions that require choosing among limited options. You will be proactive in leveraging your team’ knowledge to learn and develop your own work products. It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Manage own time and professional development, accountable for own results and prioritize workflow. Follow Good Manufacturing Practices and documentation practices. Work is completed following routine laboratory procedures and established SOPs utilizing LIMS system Perform other duties related to the Quality Control department or special projects as assigned by management for increased productivity within department.
Requirements
- High School Diploma or GED with 2+ years' experience in a cGMP environment
- Experience working with cGMP Quality Systems
- Effective interpersonal and communication skills
- Working knowledge of Microsoft Office applications
Nice To Haves
- Experience with LIMS
- Experience working with controlled temperature chambers, including cleaning, defrosting and sanitization.
- Experience working with industrial glasswashers and autoclaves
- Experience writing Investigations and Corrective and Preventive Actions (CAPA)
- Revising GMP Standard Operating Procedures
Responsibilities
- Manage own time and professional development, accountable for own results and prioritize workflow.
- Follow Good Manufacturing Practices and documentation practices.
- Work is completed following routine laboratory procedures and established SOPs utilizing LIMS system
- Perform other duties related to the Quality Control department or special projects as assigned by management for increased productivity within department.
Benefits
- this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies.
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees
