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Added 11 mins ago
Information Systems Security Manager
Leidos
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The ISSM is responsible for the management and technical administration of SIPRNET (Secret Internet Protocol Router Network) secure communication infrastructure within the organization. In…
Added 11 mins ago
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Principal Validation Engineer
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- $124,400 to $207,400 USD / year
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Added 12 mins ago
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2027 Surveillance & Navigation Architecture Performance Technical Engineer
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Added 51 mins ago
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Added 51 mins ago
Global Clinical Supplies Sr Project Coordinator
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Greenville, NC · Wilmington, NC
As a GCS Senior Project Coordinator, you will provide administrative and technical support to Study Supply Project Team including planning, organizing and coordinating responsibilities of…

Pfizer

Principal Validation Engineer

Andover, MA, United States

$124,400 to $207,400 USD / year

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Job details

Pay: $124,400 to $207,400 USD / year
Posting language: English
Posted: Aug 1, 2026

Original job description

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 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.

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

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Jobs in the United States