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Quality Control Lab Analyst I

Company

Pfizer

Address , Rocky Mount, Nc
Employment type FULL_TIME
Salary
Expires 2023-06-24
Posted at 1 year ago
Job Description
Why Patients Need You
Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
What You Will Achieve
As part of the Technical Operations team, your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
  • Participate in functions involving teams which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
  • Report testing results through computerized systems, or through standard laboratory paper-based documentation.
  • Prioritize own workflow and assist in prioritizing the work flow of less-experienced colleagues.
  • Consistently adhere to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.
  • Compare laboratory results with specifications for acceptability and determine if repetition or Out of Stock is required.
  • Complete all testing including special project/ protocol testing in a timely and appropriate manner.
  • Manage own time, professional development, and accountable for own results.
  • Generate valid data and reports results in appropriate database.
  • Calculate results and compares to specification limits.
  • Follow procedures at all times, adopting {Current} Good Manufacturing Practices {part of GxP} and cGDP practices.
Qualifications
Must-Have
  • Ability to proficiently enter computerized data
  • Certification in assigned area, if applicable
  • Demonstrated analytical laboratory experience in a Good Manufacturing Practices {also cGMP} regulated environment
  • Demonstrated ability to troubleshoot analytical methods
  • Handles multiple tasks concurrently and in a timely fashion
  • Ability to work with simple scientific equipment
  • High School Diploma or GED
  • Self-motivated and work with minimal direction
  • 4+ years of experience
Nice-to-Have
  • Bachelor's Degree
  • Demonstrated proficiency in computerized systems (Experience and use of Laboratory Information Management System)

PHYSICAL/MENTAL REQUIREMENTS
Use computer terminal 2 hours per shift, work with chemicals, work with biological materials, wear PPE (safety shoes/glasses, etc.), work with lasers, work with potent drug powders. Standing up to 3-4 hours, sitting for up to 5-6 hours, twisting at waist 2 times per hour, regularly lift up to 10 pounds per activity 10 times per shift, occasionally lift a maximum of 50 pounds per activity 2 times per shift.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
This position is eight hours day shift. Overtime is required as needed. Safe work practices are a requirement and expectation.

Work Location Assignment: On Premise
OTHER JOB DETAILS
Last Date to Apply for Job: April 27th, 2023
Eligible for Relocation Package: NO
Eligible for Employee Referral Bonus: YES
Relocation assistance may be available based on the business needs and/or eligibility.
Relocation assistance may be available based on business needs and/or eligibility.
Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.
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.
Research and Development
#LI-PFE