Pfizer CentreOne (PC1) - Program Manager
Pfizer CentreOne (PC1) - Program Manager
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$ 80300 - 133900
1 Vacancy
Job Description
Why Patients Need You
Pfizer CentreOne (PC1) is a Contract Manufacturing Organization (CMO) for therapies that define legacies. As an award-winning CMO we help maximize customer products potential and reach patients faster. Powered by Pfizers proven technical expertise and extensive global network we provide premium contract manufacturing to help ensure the lightspeed delivery of life changing therapies to patients waiting. We specialize in commercial manufacturing for oral solids sterile injectables and biologic drug products. With seamless process optimization scalable production rigorous IP protection and regulatory excellence giving confidence at every stage of the customer journey.
What You Will Achieve
As the PC1 Program Mgr. you will be responsible for coordinating site activities related to the launch of new products and/or managing existing product portfolio key commercial accounts. You will interface with all facets of site operations to execute program deliverables as defined in technical transfer or scope of work documentation. Your position plays a vital communication role for the site in assuring that all stakeholders (Corporate/Site Cross-Functional team members Third Party customers Regulatory Authorities Suppliers etc.) are versed in advancing the objective forward.
You will also assist in the preparation of Abbreviated New Drug Application (ANDA) New Drug Application (NDA) and Supplemental New Drug Application (SNDA) submissions and any required registration batches. Your role will play a key part in monitoring IMEx related metrics to achieve business unit goals. This includes driving the release of products manufactured for PC1 and coordinating deviation batch record and validation documentation review. Your role also requires participation in regulatory audits/inspections including tours leading Business Quality Reviews between all parties (Customer and Corporate PC1) and managing necessary activities driven by confidential customer Supply and/or Quality Agreements.
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Contribute to the completion of projects and manage own time to meet agreed targets.
Understand the fundamental business drivers for Pfizer and make decisions within organizations guidelines and policies.
Actively work with customers and stakeholders to understand and address their business needs.
Employ data/text mining tools to extract meaningful information to be presented in clean and crisp messages for customers and stakeholders.
Partner with other analytics group to develop implement and/or maintain analytic tools enabling customers and leadership to continuously monitor the performance and progress of projects.
Serve as an SME for key processes systems or tool and measure performance against established operational targets in line with Pfizers vision and goals.
Ensure cross-functional support from start to finish.
Creates effective lines of communication and coordination.
Integrates information to improve decision making.
Works with core team members to build strong relationships with customer counterparts fostering team accountability ownership and partnership.
Provides formal program management which guarantees continuity throughout the commercial manufacturing process lifecycle.
Here Is What You Need (Basic Requirements)
Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an associates degree with 6 years of experience OR a bachelors with at least 2 years of experience OR Masters with 0 year of experience.
Minimum of 2 years experience with Batch Record documentation Product and Process specifications and SOPs.
Strong written and verbal communication skills and professionalism. Demonstrated ability to write logically and consistently when preparing protocols and reports.
Strong problem solving and organizational skills.
Bonus Points If You Have (Preferred Requirements)
Knowledge of drug and medical device regulations and ability to interface with the FDA during inspections that impact area of responsibility.
Change Request/Control process execution level experience.
Deviation & CAPA investigation process experience.
Efficient with using MS Office suite-related applications (i.e. PowerPoint Excel Word). MS Project or similar software experience is a plus.
Ability to understand commercial strategies and business applications.
Ability to engage with leadership personnel to influence decisions.
Project Management skills.
PHYSICAL/MENTAL REQUIREMENTS
Standard office working environment using a PC with the ability to stand up to 1-2 hours and sit up to 6-8 hours. Works around moving equipment and will be required to wear appropriate PPE and gown where necessary to facilitate business objectives.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
- The position will be performed on a standard MON-FRI schedule (8am-5pm EST) with the ability to work in a hybrid arrangement requiring to be onsite 2.5 days per week.
- Weekend support may be required as dictated by project schedule or customer need.
- 10% travel may be required to support business related meetings.
Work Location Assignment:Hybrid
Last Date To Apply: July 18 2025
The annual base salary for this position ranges from $80300.00 to $133900.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes 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 (). 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.
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.
Required Experience:
Manager
Employment Type
Full-Time
