Process Validation Manager (Secondment 6 Months)

Pfizer

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profile Job Location:

Sanford, FL - USA

profile Monthly Salary: Not Disclosed
Posted on: 02-11-2025
Vacancies: 1 Vacancy
The job posting is outdated and position may be filled

Job Summary

WHY PATIENTS NEED YOU

At Pfizer everything we do every day is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture rooted in science and risk-based compliance is both flexible and innovative always putting the customer first. Whether your role involves development maintenance compliance or analysis through research programs your contributions will be instrumental in ensuring that our products meet the highest standards of quality and safety.

WHAT YOU WILL ACHIEVE

In this role you will:

  • Lead or co-lead moderately complex projects managing time and resources effectively while providing guidance.

  • Apply skills and discipline knowledge to contribute to departmental work and make decisions to resolve moderately complex problems.

  • Operate independently in ambiguous situations determining objectives of assignments and seeking directional review when necessary.

  • Review your own work and potentially mentor others exercising judgment and becoming a resource for colleagues.

  • Establish and implement validation strategies for equipment computer systems process verification and cleaning ensuring compliance with corporate policies.

  • Guide operational teams in project management resource forecasting and identifying areas for improvement in products processes or services.

  • Facilitate agreements between teams to achieve project goals and coordinate validation/qualification work including plans strategies and risk assessments.

  • Review and approve change controls ensuring validation impact assessments and appropriate testing to maintain validated states.

  • Collaborate with Operations Quality Technical groups and other site/network groups to meet business and compliance requirements.

  • Provide technical support participate in change control implementations deliver validation training and ensure compliance with company policies and government regulations.

QUALIFICATIONS

Must-Have

  • Applicant must have a bachelors degree with at least 5 years ofexperience; OR a masters degree with at least 3 years of experience; ORa PhD with 0 years of experience; OR as associates degree with 8 yearsof experience; OR a high school diploma (or equivalent) and 10 years ofrelevant experience.

  • Strong understanding of validation principles and practices.

  • Experience with regulatory requirements and guidelines for validation.

  • Proficiency in project management and resource planning.

  • Ability to work independently and make decisions in ambiguous situations.

  • Excellent communication and interpersonal skills.

  • Proficiency in computerized systems and software applications.

Nice-to-Have

  • Pharmaceutical experience.

  • Comprehensive knowledge of GMP regulations and guidance including 21 CFR Parts 11 210 & 211 EC Annex 15 and ICH 7.

  • Strong background in problem-solving negotiations and data integrity principles.

  • Experience in project management/support within a matrixed reporting environment.

  • Good understanding of risk management methodologies and their application to Bio-pharmaceutical operations.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Occasional evening or weekend work may be required.


OTHER JOB DETAILS

  • Last Date to Apply for Job:November 7 2025

  • Additional Location Information:NO

  • Eligible for Relocation Package NO

  • Secondment 6 months

  • If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

  • There will be no change to your current work location.

  • Note: This secondment offers a valuable opportunity for professional growth. It will need to be funded by the secondees home market.

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.

Pfizer endeavors to make 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. 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


Required Experience:

Manager

WHY PATIENTS NEED YOUAt Pfizer everything we do every day is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture rooted in science and risk-based compliance is both flexible and innovative always putting the customer first. Whether your role ...
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