Use Your Power for Purpose

At Pfizer, every day is an opportunity to make a difference in patients' lives. Your contributions will directly impact patient care, as you work within a flexible, innovative, and customer-oriented culture rooted in science and risk-based compliance. By joining our team, you will help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.

The resource will work on-site at the Pfizer, Sanford, North Carolina facility and will be a member of Pfizer’s Quality Control Portfolio Management team to support multiple quality programs. resource will be able to analyze chemical, or biological or microbiological products.
 

What You Will Achieve

In this role, you will:

Demonstrate comprehensive and specialized knowledge and skills in procedures, techniques, tools, materials and/or equipment needed for the positionDemonstrate a comprehensive understanding of technical skills and operational knowledgeContribute to the completion of project/work group/department tasksAct as a lead on icIEF and CE-SDS, HPLC and UPLC techniques, coordinating the work of others ⎯ but is not a supervisor (""SME"")Develop or adapts new processes and procedures for work area to improve performance and increase efficiency, consciously balancing the risk and reward trade-offNon-standard work is periodically reviewed with a focus on soundness of technical judgment.May be responsible for reviewing the work of others within the work groupDemonstrate deep knowledge of varied aspects or a specialized aspect of a disciplineRecognized as a technical expert with growing scientific contributionsMay use or develop novel processes or hypotheses;  applies ingenuity; new ideas and knowledge are used frequentlyMake decisions that require choosing or developing new options to solve moderately complex problemsUse own scientific judgment to apply and adapt standard methods and techniques with increased independence by applying prior work experienceWork independently on assignments using knowledge and work experienceIndependently plan and execute laboratory experiments.Collaborate with trainers, colleagues and subject matter experts to perform the assays in the laboratories, including the use of computational predictive tools, modeling software, and data visualization tools as necessary.Assist teams in completing the assays required for the validation and transfer of methods.Engage with the method development team and participate in both in-process and final product sample analyses.Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes.Prepare technical reports, critically review data as second analyst for the validations, and evaluate new instrumentation and analytical techniques as required.Independently analyze experimental data and provide conclusive insights.Mentor associate and senior and associate scientists and offer technical guidance when required.

Here Is What You Need (Minimum Requirements)

Applicant must have a Bachelor's degree with at least 2 years of experience; OR a Master's degree with 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

Demonstrated Subject Matter Expert level technical expertise on icIEF and CE- SDS techniques.

Proven track record of independently accomplishing complex analytical method validation.

Experience with troubleshooting assays and improving method performance.

Basic computer skills, including data entry with a high level of attention to detail

Bonus Points If You Have (Preferred Requirements)

Master's degree with over 4 years of relevant experience

Strong background in leading continuous improvement projects

Demonstrated expertise in defending laboratory practices during regulatory audits

Proficient in organic chemistry, particularly in understanding the degradation mechanisms of pharmaceutical active ingredients and products

Experience in environmental testing, utility monitoring, analytical testing, microbial identification, and sterility testing

Expertise in Quality Control instruments and meeting accuracy specifications against established standards.

Ability to set requirements for the transfer of methodology from R&D

Experience with method validation and method transfer skills to manufacturing site.Experience with bio-process downstream development

Physical/Mental Requirements

Resource is expected to be self-motivated and driven and able to manage day to day work activities with minimum direction.Should have a positive and teamwork mindset.Should be an analytical thinker and use their skills to troubleshoot the daily challenges faced at the workbenches, in data reviewing and documentation.Should be able to lift or handle up to 25 lbs containers

Excellent written and verbal communication skills

Strong interpersonal abilities

Non-Standard Work Schedule, Travel, or Environment Requirements

This role is standard day Monday through Friday work shift: 8-5PM Onsite.Occasional OT and weekend work might be expected to support continuous business activities.  

Other Job Details:

Last day to Apply: September 2nd, 2025Eligible for Relocation Assistance: NoWork Location Assignment: On Premise.

The annual base salary for this position ranges from $80 300,00 to $133 900,00. 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, 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 does not apply to Tampa, FL or any location outside of the United States.

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

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 disabilityrecruitment@pfizer.com. 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.

Quality Assurance and Control