Number of Applicants
:000+
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WHY PATIENTS NEED YOU
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need when they need them.
WHAT YOU WILL ACHIEVE
As a member of the Pfizer Drug Substance team, you will work with others to be accountable for activities involved in the production of many of Pfizer's products. In your work, you will help to determine the manufacturing methods, procedures, and tooling requirements for products, as well as designing the tools and planning production sequences in accordance with continuous improvement, Six Sigma, Lean and other Good Manufacturing Principles (GMP). Your work will help Pfizer in its mission to focus on innovation, creativity and respect for patients, colleagues, and society.
As a Process Centric Team (PCT) Lead of a manufacturing suite, your breadth of knowledge on internal challenges will help in overseeing the process stream and driving continuous improvement to improve our products, processes, and services. You will guide us to lead projects by meeting objectives and collaborating in a matrix organization. Your risk-taking ability will help us advance new concepts and methodologies. You will provide technical guidance and oversight to team members and help in problem solving.
It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
HOW YOU WILL ACHIEVE IT
Maintain and continually improve business standards (IMEx) to create an environment that is change agile, culture of continuous improvement, and learning at all levels.
Work in partnership with team members and accountable for performance in the dimensions of safety, quality, supply, financials, and people.
Coaches and supports team in business process (IMEx).
Manages and provides leadership for the Continuous Improvement (CI) Specialist.
Manages the escalation and cascade process between the tiered levels and shifts.
Manage multiple projects and ongoing work activities in the department including cross-functional representatives to ensure delivery of CI goals.
Actively share knowledge with others across assets through existing knowledge sharing processes/systems.
Identify and makes improvements to existing work processes/products within and across assets.
Make decisions with autonomy and escalates decisions when there is significant impact on department.
Solve more complex problems within area of expertise or cross-functional teams outside immediate area of expertise.
Encourage the participation and perspectives of all team members. Effectively listen to and explains difficult issues to reach shared understanding and building alignment. Build alignment across manufacturing assets.
Articulate challenges and solutions to technical and non-technical peers and to department management.
Provide technical guidance and act as a departmental liaison with primary support groups.
Motivate direct and indirect reports to ensure the function works cross-functionally across shifts.
QUALIFICATIONS
Must-Have
Applicant must have a bachelor's degree with at least 5 years of experience; OR a master's degree with at least 3+ years of experience; OR a PhD with 0+ years of experience; OR as associate's degree with 8+ years of experience; OR a high school diploma (or equivalent) and 10+ years of relevant experience.
High performing People Leader.
Strong understanding of industry knowledge of a regulated manufacturing operations.
Working knowledge of lean six sigma principles and an ability to translate them into practical solutions to help drive CI.
Administrative skills, managerial skills, technical writing, computer, and presentation skills.
Effective written and oral communication skills.
Excellent leadership, influencing, communication and interpersonal skills.
Strong coaching and decision- making capability.
Nice-to-Have
Continuous Improvement or Project Management Certifications.
Knowledge of Local Environmental, Health and Safety standards.
Knowledge of GMP and regulatory requirements.
Ability to lead change and build a culture of positive engagement.
PHYSICAL/MENTAL REQUIREMENTS
Job will include standing, walking and sitting.
Manufacturing suite, gowning and PPE.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Occasional weekend/evening support may be required to support continuous improvement activities.
Occasional travel may be required for specific projects or training
OTHER JOB DETAILS
Last Date to Apply for Job: June 9, 2026
Additional Location Information: NA
Eligible for Relocation Package – NO
Secondment 9-12 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 for 12 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.
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.
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