New Products Quality Support Tech Transfer Job at Pfizer, S.A. de C.V, Sanford, NC

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  • Pfizer, S.A. de C.V
  • Sanford, NC

Job Description

New Products Quality Support Tech Transfer
  • United States - North Carolina - Sanford
Were in relentless pursuit of breakthroughs that change patients lives. We innovate every day to make the world a healthier place.

To fully realize Pfizers 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, Pfizers unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

  • Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications.
  • Conduct rigorous sampling and statistical process control procedures to identify deviations from standards.
  • Approve investigations and change control activities to maintain compliance with configuration management policies.
  • Contribute to moderately complex projects, managing time effectively and developing short-term work plans.
  • Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts.
  • Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed.
  • Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards.

Here Is What You Need (Minimum Requirements)

  • High school diploma (or equivalent) with 8+ years of experience or associates degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
  • Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards
  • Strong critical thinking skills
  • Ability to facilitate learning for adults by applying teaching theories and practices.
  • Ability to work effectively within own team and interdepartmental teams
  • Good working knowledge of Microsoft Excel and Word
  • Proactive approach to problem-solving

Bonus Points If You Have (Preferred Requirements)

  • An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements.
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.
  • Proven ability to manage multiple priorities and work independently with minimal supervision.
  • Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements.
  • Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.
  • Ability to build and nurture strong and positive relationships.
  • The ability to work in a team environment and interact with all levels of the organization

OTHER JOB DETAILS

Last Date to Apply for Job: 8/6/25

Use Your Power for Purpose

Every day, Pfizers unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

  • Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications.
  • Conduct rigorous sampling and statistical process control procedures to identify deviations from standards.
  • Approve investigations and change control activities to maintain compliance with configuration management policies.
  • Contribute to moderately complex projects, managing time effectively and developing short-term work plans.
  • Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts.
  • Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed.
  • Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards.

Here Is What You Need (Minimum Requirements)

  • High school diploma (or equivalent) with 8+ years of experience or associates degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
  • Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards
  • Strong critical thinking skills
  • Ability to facilitate learning for adults by applying teaching theories and practices.
  • Ability to work effectively within own team and interdepartmental teams
  • Good working knowledge of Microsoft Excel and Word
  • Proactive approach to problem-solving

Bonus Points If You Have (Preferred Requirements)

  • An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements.
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.
  • Proven ability to manage multiple priorities and work independently with minimal supervision.
  • Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements.
  • Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.
  • Ability to build and nurture strong and positive relationships.
  • The ability to work in a team environment and interact with all levels of the organization

OTHER JOB DETAILS

Last Date to Apply for Job: 8/6/25

Work Location Assignment:On Premise

The annual base salary for this position ranges from $80300,00 to $133900,00. In addition, this position is eligible for participation in Pfizers 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 lifes 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 providers 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.

Quality Assurance and Control#LI-PFE
Breakthroughs that change patients lives

Research confirms what intuition tells us: that purpose-driven companies perform better, are more innovative, attract and retain the best people, and know how to unleash the power of those people. Pfizers purposeBreakthroughs that change patients' livesfuels everything we do and reflects our passion for building on our legacy as one of the greatest contributors of good to the world.

Each word in our purpose has meaning and reflects the value we strive to bring to patients and society:

Breakthroughs - These are the innovations, scientific and commercial, that we seek to deliver every day. All colleagues, regardless of role, level or location, strive for breakthroughs every day.

Change - We want to do more than simply improve patients medical conditions; we want to dramatically change their lives for the better.

Patients lives - We consider not only patients, but everyone they touchincluding their families, caregivers, and friendsand everything they love to do. Its an intentionally holistic view.

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Every decision we make and every action we take is done with the patient in mindand to nurture an environment where breakthroughs can thrive.

Our Values

To fully realize Pfizers purpose, 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.

The how is represented by four simple, powerful valuescourage, excellence, equity, and joythat define our company and our culture.

Courage: Breakthroughs start by challenging convention, especially in the face of uncertainty or adversity. This happens when we think big, speak up, and are decisive.

Excellence: We can only change patients lives when we perform at our best together. This happens when we focus on what matters, agree who does what, and measure our outcomes.

Equity: We believe that every person deserves to be seen, heard, and cared for. This happens when we are inclusive, act with integrity, and reduce healthcare disparities.

Joy: We give ourselves to our work, but it also gives to us. We find joy when we take pride, recognize one another, and have fun.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

With an unwavering commitment to ensuring the availability and accessibility of these life-saving medications, we play a pivotal role in reaching patients, healthcare professionals, and markets across the globe.

Our network of state-of-the-art manufacturing facilities, strategically located distribution centers , and streamlined logistics systems enables us to deliver Pfizer's medicines with utmost efficiency and reliability, making a tangible difference in patients' lives worldwide.

Benefits at Pfizer

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. Our Pay for Performance Philosophy and Practices reward colleagues based on the contributions they make to our business.

Our Competitive Benefits Programs help our colleagues by:

  • Promoting Health and Wellness to help colleagues maintain and improve their physical and mental wellbeing . Pfizer offerings include health and disability insurance, preventative health programs, medical screenings, free or reduced-cost vaccinations, discounts on Pfizer products, mental health support, nutrition and fitness counseling and more.
  • Strengthening Colleagues Financial Security by providing company contributions to retirement plans, life insurance and financial planning education to help colleagues achieve their financial goals.
  • Providing Benefits and Time off for the Moments that Matter to ensure Pfizer colleagues have the time away from the office to recharge, recover and return to work as the best version of themselves. Vacation, Holiday time and Sick time are just the beginning, with a 12 week parental leave policy for both parents of a new born, 10 day of caregiver leave for those times when your family needs you whether its a child, spouse or parent, bereavement leave, and additional country-specific programs.
  • And so much more , depending on your country and site, Pfizer offers childcare facilities or discount programs, on-site health and/or fitness centers , movement and mindfulness solutions, Log in for your Day work flexibility and so much more.
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Job Tags

Permanent employment, Temporary work, Work at office, Local area, Worldwide, Relocation package, Flexible hours,

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