QC IM Lab Analyst III

Pfizer, S.A. de C.V; Rocky Mount (NC); Hybrid; USD 36,000 - 59,000; Full time

Benefits offered by this job

401(k) matching

Health benefits

Paid time off

Job summary

Pfizer is seeking a skilled professional for on-site work in Rocky Mount, NC. The role involves leading a small team, ensuring rigorous documentation, and applying cGMP/GLP standards to sustain quality manufacturing processes.

You will participate in process improvements, training, and safety initiatives while aligning with Pfizer's commitment to patient outcomes. Candidates should have relevant science education and substantial experience, with strong written communication and organizational

Qualifications

• HS Diploma or GED with extensive relevant experience, or higher education with progressive related experience.
• Ability to write clear technical documents and maintain organized records.
• Knowledge of cGMP and GLP practices in a laboratory or manufacturing setting.
• Proficiency with Microsoft Office and basic data handling.

Responsibilities

• Serve as a key resource and may lead lower-level team members in your area of expertise.
• Manage personal time and professional development, prioritizing workflow and accountability.
• Contribute to project tasks, provide direction and training to team members, and act as a lead worker when needed.
• Be recognized as a LEAD or Subject Matter Expert and drive technical review for non-standard work.
• Adhere to Pfizer standards and help develop departmental guidelines while maintaining safety and quality.

Skills

Attention to detail

Time management

Written communication

Education

HS Diploma or GED + 8 years experience

Associate's degree + 6 years experience

Bachelor's degree in Chemistry or related Science + 4 years experience

Tools

MS Office

Laboratory equipment

Job description

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.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our flexible, innovative, and customer-oriented quality culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve. Join us in our mission to improve patient outcomes through excellence in every aspect of our work.

What You Will Achieve

Serve as a key resource and potentially lead lower-level team members within your area of expertise.

Manage personal time and professional development, taking accountability for your results and prioritizing workflow.

Contribute to project and departmental tasks, providing direction and training to team members, and may act as a lead worker.

Be recognized as a "LEAD" or "Subject Matter Expert" in your field.

Proactively identify and resolve basic complexity problems, considering wider implications.

Complete assignments independently, selecting appropriate methods, and ensuring team assignments are completed.

Review non-standard work for technical soundness and may review others' work.

Adhere to Pfizer standards, guidelines, and values, influencing teams, and contributing to the development of departmental standards and guidelines.

Provide input for performance assessments, ensure timely and compliant documentation, and develop processes to enhance cGMP standards.

Maintain high standards of safety and housekeeping, participate in Continuous Improvement projects, and ensure adherence to all policies and procedures, while providing training and conducting peer reviews.

What You Will Achieve

• Serve as a key resource and potentially lead lower-level team members within your area of expertise.

• Manage personal time and professional development, taking accountability for your results and prioritizing workflow.

• Contribute to project and departmental tasks, providing direction and training to team members, and may act as a lead worker.

• Be recognized as a "LEAD" or "Subject Matter Expert" in your field.

• Proactively identify and resolve basic complexity problems, considering wider implications.

• Complete assignments independently, selecting appropriate methods, and ensuring team assignments are completed.

• Review non-standard work for technical soundness and may review others' work.

• Adhere to Pfizer standards, guidelines, and values, influencing teams, and contributing to the development of departmental standards and guidelines.

• Provide input for performance assessments, ensure timely and compliant documentation, and develop processes to enhance cGMP standards.

• Maintain high standards of safety and housekeeping, participate in Continuous Improvement projects, and ensure adherence to all policies and procedures, while providing training and conducting peer reviews.

Here Is What You Need (Minimum Requirements)

• Applicant must have HS Diploma or GED and 8 years of relevant experience; OR and Associate's degree with 6 years of experience; OR an Bachelor's degree (preferably in Chemistry or other related Science) with 4 years of relevant experience

• Certifications in the relevant areas, if applicable

• Ability to write clear technical documents

• Good organizational and time management skills

• Proficiency in Microsoft Office

• Experience with laboratory equipment and procedures

• Knowledge of Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP)

Bonus Points If You Have (Preferred Requirements)

• Bachelor's Degree

• Incoming Material inspection experience with components. AQL Inspection; Defect Recognition

• Effective problem-solving skills

• Strong analytical skills

• Strong attention to detail

• Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

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. May have to lift objects approximately 10 pounds.

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

Work Location Assignment:On Premise

OTHER JOB DETAILS

Last Date to Apply for Job August 28th, 2026

The salary for this position ranges from $25.88 to $43.14 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. 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, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - North Carolina - Rocky Mount location.

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

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. This position requires permanent work authorization in the United States.

Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [e-mail] . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .

Quality Assurance and Control