QC Lab Analyst II

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

The CQ Lab Analyst II, will perform basic analysis for Validation of new and existing products on manufacturing lines in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of multiple sample sites across the manufacturing process to demonstrate that our process is able to meet the high standards of quality for patient use.

Report testing results through computerized systems, or through standard laboratory paper-based documentation.  Other related duties essential to these operations or special assignments as required.

How You Will Achieve It

• 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 cGMP, cGDP practices.
• Follows supervisor directions at all times.
• Able to function independently but asks questions as necessary.
• Accepts dynamic work sequences.
• Must be self-motivated and work with minimal direction.
• Demonstrate proficiency in computerized systems (Experience and use of LIMS, Empower are plus).
• Demonstrated ability to troubleshoot analytical methods.
• Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve RFT and achieve schedule adherence as needed.
• Works with supervision and management to identify opportunities to improve testing efficiencies.
• 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.
• Demonstrates engagement in helping to achieve QC 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.
• Has proficiency of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Auto titrations, UV-Vis, Polarimeter as well as more advanced techniques, i.e. HPLC and UPLC etc.

Qualifications

Must-Have

• High School Diploma or GED.
•  4+ years' experience.
• Certification in assigned area, if applicable.
• Successful hands-on analytical testing experience in a Good Manufacturing Practices {also cGMP} environment.
• Technical Skills- Knowledge of laboratory equipment, testing and technique.
• Basic math skills and computer skills, such as data entry, along with a high level of attention to detail.
• Strong organizational skills and ability to multi-task across projects and activities.
• Must be self-motivated and work with minimal direction.
• Ability to read, communicate understanding and follow written procedures.

Nice-to-Have

• Bachelor’s degree in chemistry.
• Demonstrate proficiency in computerized systems, such as Laboratory Information Management System.

  

PHYSICAL/MENTAL REQUIREMENTS

• Stand up for up to 8 hours, sit for up to 8 hours, walking, climbing stairs, responding to visual warning indicators.
• Respond to audible warning indicators, respond to color or special visual indicators.
• Wear specialized protective clothing (lab coat, safety glasses, gloves, face shield/goggles, apron), repetitive use of upper extremities.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• There are not out of the ordinary travel or shift requirements associated with the position.   Individuals will be expected to work nonstandard schedule as needed to support the business objectives.
• Work Location Assignment: On Premise colleagues work in a Pfizer site because they’re needed to get their job done.
• 2nd Shift Weekdays 15:00 to 23:30

Work Location Assignment: On Premise

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