Manager, Project Management Andover, MA

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Unless specifically stated otherwise this role isOn-Site at the location detailed in the job post.


ROLE SUMMARY

A Project Manager role is available within the Project and Portfolio Management Group in the Pfizer Biotherapeutics Pharmaceutical Sciences Department. The position will report to Director of Portfolio and Project Management in Andover. The successful applicant will join a cross site group to provide project management expertise to the Biotherapeutics Pharmaceutical Sciences organization for both early and late stage product development teams inclusive of CMC regulatory submission support.

ROLE Responsibilities

Apply prior knowledge and experience in project management to manage portfolio projects and improvement initiatives
Support operational teams in managing projects forecasting resource requirements and identifying areas for improvement in products processes or services
Oversee operational aspects of improvement projects acting as a liaison between project teams and line management
Own and review project status budgets and schedules and prepare comprehensive status reports to support programs
Proactively identify and resolve project issues to meet productivity quality and client satisfaction goals
Independently develop project plans for key initiatives interface with partners to drive customer centricity and align continuous improvement opportunities.
Lead or co-lead projects effectively managing time and resources for ones self with consideration of impact on team members
Prepare materials manage application review logistics and lead higher complexity cross-functional projects with input from sponsors and team members.
Apply skills knowledge and discipline to contribute to departmental work and interdepartmental collaborations
Operate independently and determine objectives of assignments
Review your own work and seek directional review from others when necessary
Resolve problems and develop new options guided by policies
Additional Qualifications/Responsibilities
BASIC QUALIFICATIONS

BA/BS with 4 years of experience or MBA/MS with 2 years of relevant experience or PhD/JD with any years of experience
Experience working in the research and development of the pharmaceutical industry
Knowledge of the workings of pharmaceutical manufacturing and associated processes
Demonstrated experience in commercial/customer-facing roles across the business
Familiarity with Pharmaceutical Good Manufacturing Practices (cGMP)
Familiarity with Pharmaceutical Sciences infrastructure
Excellent verbal and written communication skills
Proficiency in MS Project Excel and PowerPoint
PREFERRED QUALIFICATIONS

Masters degree with specific experience in managing pharmaceutical technical or medical device projects and clinical programs
Knowledge and certification in operational excellence methodologies such as Six Sigma and Lean
Strong leadership and team management skills
Ability to work collaboratively in a cross-functional team environment
Ability to work effectively in a fast-paced dynamic environment
Strong analytical and problem-solving skills
Ability to build and maintain strong relationships with stakeholders
High level of adaptability and willingness to learn
PHYSICAL/MENTAL REQUIREMENTS

No restrictions

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Standard work schedule
Some flexibility needed in terms of meeting team deliverables
Up to 10% travel possible
Hybrid work (2.5 days per week on site)
Work Location Assignment: This is a hybrid role requiring you to live within commuting

distance and work on-site an average of 2.5 days per week or more as needed


Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed.

Experience using common AI tools including generative technologies such as ChatGPT or Microsoft Copilot to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices including risk management and ethical use.


The annual base salary for this position ranges from $88500.00 to $147500.00. 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.