Principal Validation Engineer

Posted Yesterday
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Andover, MA, USA
Hybrid
124K-207K Annually
Senior level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Owns Pfizer’s Andover site validation program and master plan for biologics manufacturing, testing, storage, and transport. Establishes validation philosophies, governance, and program health practices; operates the validation lifecycle project PMO; oversees third-party technical service providers; plans capital and departmental expenses; and leads validation activities for complex assets and capital projects. Requires biopharmaceutical industry experience, complex project leadership, and cross-functional collaboration. Occasional domestic and international travel and off-hours support are required.
Summary Generated by Built In
Use Your Power for Purpose
The Principal Validation Engineer under Andover Site Technical Services (STS) is the principal owner of the Pfizer (PGS) Andover site validation program and master plan. The incumbent is responsible for delivering overall site validation program effectiveness and compliance in partnership with validation program owners across Andover site functions and the Pfizer network
What You Will Achieve
In this role, you will:
  • Establish and maintain overall Andover site validation philosophy and master plan in partnership with local validation program owners, technical subject matter experts, and relevant Pfizer global/network/site quality system principals applicable to biologics drug substance/drug substance intermediate production, testing, storage, and transport
  • Operate PMO for Validation Program Lifecycle Projects
  • Establish and maintain site governances necessary to interpret validation philosophies and polices, implement and improve uniform validation practices and approaches, as well as to measure and maintain site validation program health
  • Maintain STS departmental infrastructure, and provide planning support for third party services utilized in validation and other technical services; oversee third party service provider service level and quality of service
  • Program owner and expert for select technical/validation disciplines
  • STS capital project portfolio and expense planning
  • Lead site validation planning and management of validation activities for large capital or complex asset lifecycle projects

Here Is What You Need (Minimum Requirements)
  • BA/BS degree in Science or Engineering with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience
  • Experience in pharmaceutical, biopharmaceutical or biotechnology industry
  • Experience or broad knowledge in biopharmaceutical development, manufacturing, and lifecycle management
  • Experience in project management and leading complex projects
  • Effective written and verbal communication skills
  • Strong interpersonal skills and the ability to work collaboratively in a team environment across various business functions

Bonus Points If You Have (Preferred Requirements)
  • Experience developing philosophies/approaches for or managing validation programs applicable to the manufacture of biopharmaceutical drug substance, drug product, or medical device
  • Active participation in industrial/professional organization focused on advancing biopharmaceutical development, manufacturing, regulatory practices
  • Demonstrated ability to lead or build teams for complex technical projects involving risk management
  • Demonstrated leadership in a matrix organization

Physical / Mental requirements
  • Ability to perform mathematical calculations, scientific computation, complex data analysis, verbal communication, written communication

Non-Standard work schedule, travel or environment requirements
  • Occasional domestic and international travels
  • Occasional off-hour support to address time-sensitive production and business-related issues

Other job details
  • Last day to apply: July 17th, 2026
  • Work Location Assignment: Hybrid

The annual base salary for this position ranges from $124,400.00 to $207,400.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. 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.
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 [email protected] . 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 .
Engineering
#BI-Hybrid

Skills Required

  • BA/BS degree in Science or Engineering with 6+ years of experience
  • MBA/MS degree with 5+ years of experience
  • PhD/JD with 1+ year of experience
  • MD/DVM with relevant experience
  • Experience in the pharmaceutical, biopharmaceutical, or biotechnology industry
  • Broad knowledge of biopharmaceutical development, manufacturing, and lifecycle management
  • Experience in project management and leading complex projects
  • Effective written and verbal communication skills
  • Strong interpersonal skills and ability to collaborate across business functions
  • Experience developing validation philosophies or managing validation programs for biopharmaceutical drug substance, drug product, or medical device manufacturing
  • Active participation in an industrial or professional organization focused on biopharmaceutical development, manufacturing, or regulatory practices
  • Ability to lead or build teams for complex technical projects involving risk management
  • Demonstrated leadership in a matrix organization

What the Team is Saying

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Esteban
Pfizer

Pfizer Compensation & Benefits Highlights

  • Healthcare Strength — Healthcare coverage is described as comprehensive, with multiple plan options, dental and vision, mental-health services, telehealth, and eligible Pfizer medications at no cost. Family-building benefits such as infertility treatment, adoption, and surrogacy support further reinforce the offering.
  • Retirement Support — Retirement support includes a 401(k) with employer matching plus an additional company retirement contribution, alongside access to financial-planning resources. This combination is positioned as a meaningful part of total rewards.
  • Leave & Time Off Breadth — Paid time off includes 15 holidays, three to six weeks of vacation depending on service, and the option to purchase additional vacation weeks, plus dedicated caregiver-leave days. Twelve weeks of paid parental leave and backup care resources add flexibility for family needs.

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

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.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Pfizer Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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