Quality Control Analyst II (1st Shift)

Use Your Power for Purpose
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. 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 real 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.
What You Will Achieve
Performs lab support activities and participates in basic routine and non-routine testing and general QC laboratory work for the in-process support, release and/or stability of clinical development and/or commercial products in a GMP testing environment. Monday-Friday shift. Must be able to work, off-shifts, and overtime as required. Must be willing and able to work reliably on a flexible schedule.
How You Will Achieve It

• Applying the principles of good manufacturing practices (GMP) on a daily basis
• Performing sample testing using basic test methods such as bioburden, endotoxin, TOC and conductivity and growth promotion testing for facility utilities, in process and release product samples
• Performing environmental monitoring and collecting critical utility samples of the facility.
• Performing maintenance of QC lab equipment, procedures and systems
• Creating and revising standard operating procedures (SOP's) and other documents as needed
• Identifying and participating in continuous improvement projects
• Maintain training to current standards and procedures on all assigned curriculums
• Fully comply with company health and safety procedures and practices

Here Is What You Need (Minimum Requirements)

• High School Diploma or GED with 4+ years of experience OR Associates/Bachelor's degree in a relevant field with 2 years of experience working in a GMP laboratory
• Broad experience with Microsoft Office products
• Highly organized with an attention to detail
• Knowledge of biological and/or chemical handling

Bonus Points If You Have (Preferred Requirements):

• Experience in parenteral drug product pharmaceutical manufacturing
• 2 years of experience QC Microbiology.
• Demonstrated proficiency in computerized systems
• Ability to train and mentor less-experienced colleagues
• Commitment to continuous improvement and professional development
• Environmental Monitoring testing, clean utility gas testing, bioburden testing, conductivity testing, total organic carbon testing, endotoxin testing

PHYSICAL/MENTAL REQUIREMENTS
Job will include standing, walking, sitting, bending and occasional lifting is required. document review and ability to perform mathematical calculations and complex data analysis.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Monday- Friday shift. Evening, weekend, holidays and/or on-call work may be required.
Work Location Assignment: On Premise
The salary for this position ranges from $29.26 to $48.77 per hour. In addition, 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. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Washington - Bothell location.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected] . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
Quality Assurance and Control