Manufacturing Manager (Day shift)
- United States - North Carolina - Sanford
Use Your Power for Purpose
Our breakthroughs would not reach patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand their crucial role in Pfizer's mission. Patients need colleagues like you who take pride in their work and strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to necessary medicines. Your role will involve determining manufacturing methods, procedures, and tooling requirements, as well as designing tools and planning production sequences in line with continuous improvement, Six Sigma, Lean, and other Good Manufacturing Principles (GMP). Your contributions will support Pfizer's mission to prioritize innovation, creativity, and respect for patients, colleagues, and society.
What You Will Achieve
In this role, you will:
Serve as a technical resource and departmental liaison with primary support groups.
Provide on-floor oversight for at least 75% of operations, ensuring a consistently safe and compliant work environment.
Deliver training and technical guidance to bioprocessing technicians and team leads, fostering skill development and operational excellence.
Support internal and external audits, ensuring regulatory adherence and successful audit outcomes.
Lead, guide, and develop production teams to maintain the highest standards of regulatory compliance.
Champion continuous improvement initiatives and facilitate cross-functional projects to drive operational efficiency.
Exercise sound judgment in investigations, escalating critical issues as appropriate to ensure timely resolution.
Promote effective interdepartmental collaboration to achieve organizational goals.
Mentor direct reports through comprehensive performance management, including goal setting, coaching, and ongoing professional development.
Share expertise across teams to encourage knowledge exchange and innovation within operations.
Assist with operational planning, scheduling, and preventive maintenance strategies to optimize resource utilization.
Lead the adoption and implementation of Six Sigma, Lean, and other GMP methodologies to drive innovative and compliant practices.
Supervise hourly and exempt staff, motivating personnel by setting high standards and encouraging teamwork through clear, effective communication.
Review completed batch records, develop training materials, update curricula, address training gaps, and support the onboarding of new supervisors.
Provide input on the development and revision of cGMP-related documents to ensure compliance and operational integrity.
Clearly articulate challenges and solutions to both technical and non-technical audiences, including department management.
Serve as a technical resource and departmental liaison with primary support groups.
Here Is What You Need (Minimum Requirements)
Applicant must have a PhD with 0 years of experience OR Master’s degree in Engineering, Business or Scienc with more than 2 years of experience and 1+ years demonstrated leadership capability in a pharmaceutical and/or manufacturing environment OR Bachelor’s degreein Engineering, Business or Science with at least 4 years of experience and 3+ years demonstrated leadership capability in a pharmaceutical and/or manufacturing environment OR Associate’s degree with 8 years of experience and 5+ years demonstrated leadership capability in a pharmaceutical OR High School Diploma (or Equivalent) and 10 years of relevant experience and 7+ years demonstrated leadership capability in a pharmaceutical
People management experience.
Skilled in administrative, managerial, and technical reporting.
Knowledge of GMP, regulatory requirements, and audit management.
Strong project management, leadership, and decision-making skills.
Excellent interpersonal and communication abilities.
Advanced understanding of industry practices and business operations.
Team motivation and development experience.
Physical / Mental requirements
Requires the moving of heavy equipment and the ability to lift ~40 pounds.
Moderate repetitive standing, sitting, bending, and ladder climbing on a daily basis.
The incumbent needs to take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
Demonstrates leadership, fosters innovation, and influences teams across different functions.
Communicates and presents ideas effectively.
Excels at persuasion and building consensus.
Skilled in strategic planning and managing risks.
Non-Standard work schedule, travel or enironment requirements
Supports a 24/7 facility.
Hiring for 12 hour 2-2-3 schedule
Other job details
Last day to apply: december 24th, 2025
Work Location Assignment: On Premise
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.