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QC Supervisor - Weekend Shift

Job in Rocky Mount, Nash County, North Carolina, 27815, USA
Listing for: Pfizer, S.A. de C.V
Full Time position
Listed on 2026-02-05
Job specializations:
  • Healthcare
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 82700 USD Yearly USD 82700.00 YEAR
Job Description & How to Apply Below

Overview

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals. Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

What You Will Achieve

Under the general guidance and functional direction of the CQ Laboratory Manager, the QC Supervisor is responsible for supervision of analysts performing chemical testing in a safe, compliant and efficient manner of raw materials, in process, and finished product samples. This position will evaluate analytical data to determine compliance with established specifications. The QC Supervisor is expected to resolve daily analytical and quality problems, generally without any additional high level technical assistance other than the chemical quality manager/director.

In this role, you will:

  • 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.

  • Supervision of QC Chem change control

  • Schedule work sequences for documentation personnel and track progress of work sequences and provide feedback and coaching as required

  • Participate in daily and weekly planning discussions with team offering suggestions to improve efficiency and schedule adherence.

  • Resolve daily problems, generally without any additional high level technical assistance other than the chemical quality manager.

  • Review and provide feedback on SOP’s, Investigations, and Reports as needed in the absence of Management.

  • Spearhead special projects such as Continuous Improvement initiatives or process flow improvements

  • Act as Liaison between lab analyst, data review, change control and investigations were appropriate

  • Demonstrated strong technical and leadership skills

  • Ability to serve as primary CQ representative on multidisciplinary project teams

  • Act as Department representative for Internal and External Business tours and Audits

Minimum Requirements
  • Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with more than 0+ years of experience; OR an associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience.

  • Strong written and verbal communication skills.

  • High level of organizational skills and independence.

  • Strong judgment and decision making ability.

  • Must be familiar with cGMP and cGLP for a pharmaceutical industry.

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 no out of the ordinary travel or shift requirements associated with the position. Individual will be expected to work nonstandard schedule as needed to support the business objectives

  • Shift: Weekends, Friday - Monday, 10 hour first shift

Last day to apply: January 30, 2026

Work Location Assignment:
On Premise

The annual base salary for this position ranges from $82,700.00 to $. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. 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,…

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