Principal Development Engineer Device & Combination Products
Parsippany, NJ - USA
Job Summary
What You Will Achieve
The Device Development Core Team Leader (DD CTL) provides comprehensive project leadership and operational excellence for the execution and delivery of assets/projects from early to late-stage development through launch. The DD CTL serves as an operational leader ensuring all required cross functional deliverables are achieved on or ahead of schedule within budget target and with quality that meets or exceeds business needs. The DD CTL uses leadership and interpersonal skills to motivate and influence team members to high team performance and individual achievement. The DD CTLs responsibilities encompass strategic problem-solving project planning compliance program execution and delivery team effectiveness risk management and communication management.
How You Will Achieve It
Project Execution and Delivery
- Works with key stakeholders in Commercial Launch Excellence GTEL and other partner lines to define the product concept and lead the operational planning for assigned projects
- Provides a single point of accountability for all MDCP aspects of the assigned projects interacting as necessary with stakeholders at all levels of management (inside and outside of PGS) to convey project information/updates and manage expectations.
- Responsible for planning and forecasting team budgets and resources working with Launch Excellence to develop execution plans and then actively managing project budgets plans and forecasts.
- Works with Procurement External Supply and PGS sites as applicable to manage interactions with third party manufacturers and other vendors necessary for the projects
- Negotiates the allocation of resources to support the endorsed strategy and development plan including assessment and communication of any anticipated resource shortfalls to stakeholders
- Facilitates team in appropriate discussions leading to effective decision-making.
- Risk Analysis and Management
- Leads the team in the preparation implementation maintenance communication and management of risk management plans including risk assessment and risk mitigation strategies.
- Partners with team members and line function leadership to identify options to de-risk project plans and capitalize on opportunities.
- Leads or facilitates team discussion and documentation of alternative development options including pros cons and risks.
Risk Analysis and Management
- Leads the team in the preparation implementation maintenance communication and management of risk management plans including risk assessment and risk mitigation strategies.
- Partners with team members and line function leadership to identify options to de-risk project plans and capitalize on opportunities.
Planning and Organization
- Drives creation/maintenance of Device Development project plans.
- Leads development of the program technical critical path. Ensures all functional line leaders understand the strategy key milestones and interdependencies.
Compliance
- Ensure compliance with Pfizer policies and standards and local laws and regulations
Communication Skills
- Ensures effective accurate and timely communication of program information to meet the needs of the asset team and stakeholders
Ability to Influence and Motivate
- Utilizes negotiation facilitation meeting management and conflict resolution skills to enhance team performance.
Here Is What You Need (Basic Requirements)
- Applicant must have a bachelors degree with at least 6 years of
experience; OR a masters degree with at least 5 years of experience; OR
a PhD with 1 years of experience - Mastery of project management skills and product development. Minimum of 7 years in Project Management / Leadership.
- >7 years of experience in developing medical devices combination products and/or pharmaceuticals
- Experience working in multi-disciplinary teams as well as working independently in ambiguous situations/assignments gathering input from colleagues and management to address project-related issues
- Planning experience and fiscal awareness are essential as is a sustained record of satisfactory performance
- Technical abilities should include a sound knowledge of the medical device development process an advanced technical knowledge within the applicants own discipline as well as a strong knowledge of other related disciplines
- Demonstrated skills in planning scheduling forecasting including the use of relevant IT tools together with the ability to use a high level of scientific / business judgement to adapt or create systems and processes by applying the breadth of knowledge and prior work experience.
- Demonstrated influencing and negotiating skills; and proven skills in developing others within own functional area. Ability to identify and develop options to support short to mid-term goals and set direction for team. High awareness of personal limits and a willingness to proactively consult others to ensure quality of judgement
Bonus Points If You Have (Preferred Requirements)
- Advanced degree (PhD PharmD MS) desirable.
- Strong understanding of and experience in combination product development (drug plus device) highly preferred.
- Medical device development/design control experience preferred.
- Strong track record of performance on cross-functional teams and results through effective implementation of project management methodology tools and techniques.
- Strong leadership negotiation interpersonal communication and meeting facilitation skills.
- Experience with stakeholder management governance management and communicating key messages to senior-level stakeholders.
- Demonstrated ability to utilize project management tools and techniques (such as developing integrated project plans critical path management project change control project risk management and decision analysis).
- Extensive hands-on experience using Microsoft Project or equivalent project planning system to create and manage project timelines
- Track record for delivery against challenging personal and team goals.
- Proven ability to succeed in a fast-paced challenging and complex matrix team environment.
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers develop and coach others oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
PHYSICAL/MENTAL REQUIREMENTS
The successful candidate will be capable of independent problem solving and working with minimal direction under most circumstances. Applicants should demonstrate strongly collaborative behaviors and teamwork and demonstrate expertise in most or all of the following: team dynamics coaching negotiation motivating and other soft skills necessary to foster team effectiveness in a matrixed environment. The successful candidate will also possess strong oral and written communication skills. Strong analytical and computer skills are required.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
Typically less than 10%. May be higher dependent on project and timing within project.
Work Location Assignment:Hybrid
Last Date To Apply: May 29 2026
The annual base salary for this position ranges from $124400.00 to $207400.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. 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.
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 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.
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Required Experience:
Staff IC
About Company
Erfahren Sie mehr über uns als forschendes und produzierendes Pharmaunternehmen: Von unserem Beitrag zum medizinischen Fortschritt bis zur nachhaltigen Produktion.