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CQ Lab Analyst

Employer
Pfizer
Location
Lake Forest, Illinois
Salary
Competitive
Closing date
May 24, 2022

View more

Discipline
Other, Other
Position Type
Full Time
Organization Type
All Industry, Pharma
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

  • Manage own time, professional development, and accountable for own results.
  • Prioritize own workflow and assist in prioritizing the work flow of less-experienced colleagues.
  • Participate in functions involving teams which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
  • Compare laboratory results with specifications for acceptability and determine if repetition or Out of Stock is required.
  • Follow procedures at all times, adopting {Current} Good Manufacturing Practices {part of GxP} and cGDP practices.
  • Consistently adhere to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.
  • Generate valid data and reports results in appropriate database.
  • Calculate results and compares to specification limits.
  • Complete all testing including special project/ protocol testing in a timely and appropriate manner.
  • Report testing results through computerized systems, or through standard laboratory paper-based documentation.


Qualifications

Must-Have
  • Bachelor's degree in science discipline (preferably Chemistry, Biochemistry, or Biology).
  • 0-1 years experience in a Quality Control or R&D laboratory.
  • Demonstrated analytical laboratory experience in a Good Manufacturing Practices {also cGMP} regulated environment
  • Demonstrated ability to troubleshoot analytical methods
  • Ability to proficiently enter computerized data
  • Ability to work with simple scientific equipment
  • Handles multiple tasks concurrently and in a timely fashion
  • Self-motivated and work with minimal direction
  • Knowledge of cGMPs and pharmaceutical regulations, LIMS, Empower, and Microsoft Office is desired.


Nice-to-Have
  • Experience with a wide variety of analytical techniques (e.g. HPLC, GC, AA, UV-VIS, etc.) is desired.
  • Demonstrated proficiency in computerized systems (Experience and use of Laboratory Information Management System)



Physical / Mental requirements

  • This individual will be expected to work in the laboratory performing testing as well as desk work when documenting or calculating data.
  • This will involve standing for long periods, handling of hazardous and non-hazardous chemicals, wearing of personal protective equipment (lab coat, safety glasses, closed toe shoes, gloves, and potentially respirator).
  • This individual will be expected to lift approximately 20 lbs. on an occasional basis.
  • This individual will need to follow written procedures and perform mathematical calculations


Non-Standard wor schedule, travel or environment requirements

  • This position is a Monday to Friday first shift position.
  • There is no travel associated with the position.
  • Overtime can be utilized as needed based on workload and business needs.


Other job details

  • Last day to apply: 5/23/2022
  • Employee Referral Bonus eligible


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

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