McPherson, KS
Full-time

Full Job Description
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 assurance team. You will be responsible for evaluation, review and approval of validation master plan, protocols and reports. Your methodological approach will help us ensure compliance of our quality systems with company standards and government regulatory requirements. Your problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct statistical analysis of testing results and process anomalies. Your documentation skills will guide the writing, review and approval of for validation process documents and technical reports related to equipment, products and processes.
You will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations. You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients.
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
Qualifications
Must-Have

High School Diploma Required- Some college preferred
2 years of Advanced computer skills
Trained/experience with technical writing
Ability to effectively communicate with all levels of site colleagues
Strong communication skills (both written and verbal)
Ability to understand and follow standard practice and oral instruction
Ability to work effectively both independently and as part of a team


Nice-to-Have
Bachelor's Degree
2 years of experience in a Pharmaceutical Industry


PHYSICAL/MENTAL REQUIREMENTS
Must be able to read and understand required documentation. Satisfactory performance and attendance are required.
NON-STANDARD WORK SCHEDULE, TRAVEL, OR ENVIRONMENT REQUIREMENTS

Ability to work assigned shift
Some overtime required as necessary per supervisor/manager/site request
Eligible for Shift Differential

Job Details:
Last Date to Apply for Job: August 5, 2022
Eligible for Employee Referral Bonus: Yes
Schedule: Day Shift