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Lab Analyst III

Company: Pfizer Inc.
Location: Rocky Mount
Posted on: December 5, 2019

Job Description:

ROLE SUMMARY

The Lab Analyst III performs basic analysis for raw materials, in process, finished products, and/or TSR/validation/investigational testing in a safe, compliant, and efficient manner. The job responsibilities include:

  • Performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality.
  • Reports testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required.
  • Provides technical support as necessary to the assigned laboratory. Investigates, analyzes, problem solves, and communicates technical information to internal and external customers. Other related duties essential to these operations or special assignments as required.
  • Trains and supports inexperienced analysts, working as a Certified Fellow Employee and mentor to aid in their development as analysts.
    ROLE RESPONSIBILITIES
    • Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.
    • Follows procedures at all times, adopting current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP).
    • Able to function independently, but asks questions as necessary; follows supervisor directions at all times.
    • Accepts dynamic work sequences.
    • Must be self-motivated and work with minimal direction.
    • Must have strong technical and/or leadership skills.
    • Routinely participates in daily Shift Handover and/or Chemical Quality (CQ) Performance huddles, including discussions on improving planning communication, and teamwork efforts in the CQ laboratory (where applicable for function).
    • Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed.
    • Works with supervision and management to identify opportunities to improve testing efficiencies and actively participates in subsequent related projects.
    • Consistently communicates work sequence status to supervisor in a timely manner.
    • Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement and actively works on efforts to recover adherence gaps.
    • Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals.
    • When faced with roadblocks and issues, routinely offers suggestions for improvements and actively participates in associated improvement activities wherever possible
    • Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift and across shifts wherever possible.
    • Maintains on-time training.
      BASIC QUALIFICATIONS
      • Bachelor's Degree in Chemistry or related Science field required.
      • 4+ years analytical laboratory experience in a GMP regulated environment OR 3 years analytical laboratory experience with a Masters Degree/PhD in a related field required.
      • Successful hands-on analytical testing experience in a GMP environment.
      • Must have strong organizational skills and an ability to multi-task across projects and activities.
      • Demonstrated proficiency in computerized systems.
      • Demonstrated ability to troubleshoot analytical methods
      • Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Auto-titrations, UV-Vis, Polarimeter as wells as more advanced techniques, i.e. GC, HPLC, AA, FTIR, etc.
        PREFERRED QUALIFICATIONS
        • Experience in parenteral drug product pharmaceutical manufacturing is plus.
        • Certified Fellow Employee trained/Control Drug Agent status is preferred.
        • Experience and use of LIMS, Empower are preferred.
          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.

          Other Job Details:
          • Last Date to Apply for Job: 09 DECEMBER 2019
          • Eligible for Employee Referral Bonus
          • #LI-PFE

            Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

            Quality Assurance and Control

Keywords: Pfizer Inc., Rocky Mount , Lab Analyst III, Healthcare , Rocky Mount, North Carolina

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