$177K – $294KExecutiveFull Time
ROLE SUMMARY:
The Active Pharmaceutical Ingredient (API) Analytics group is working diligently to bring new cutting-edge medicines to patients around the world. Our team members use the latest science and technology to characterize and develop new drug candidates from the early phases of development through to commercial launch.
As a Director in our group, you will lead a team of analytical scientists to assess the chemical and physical properties of Pfizer’s newest drug candidates and evaluate their suitability for progression into clinical studies and ultimately to commercialization. You will have a strong passion for developing early career scientists and be skilled at guiding them to solve difficult technical problems. You will also be constantly looking for ways to improve the speed and efficiency of scientific and business processes used in the development of Pfizer medicines.
A deep knowledge of pharmaceutical development, analytical measurements, control strategies, formulation & process development, as well as relevant computational skills are desirable for this leadership position. In addition, experience of working successfully as part of a multidisciplinary organization is vital for your success. You will be responsible for the continuous enhancement of technical skills, scientific knowledge, and personal growth of colleagues. You will also have the opportunity to grow your skills as a people leader and your influence within global analytical research and development at Pfizer.
The successful candidate will have a proven track record in pharmaceutical development and extensive experience in regulatory filing requirements and strategies, as well as being comfortable leading multiple teams inside and outside the Pfizer network to meet milestones and deliverables. An ability to respond well to change, thrive in a dynamic environment, support and champion technology and innovation are also needed to thrive in this role.
As a Director in the API Analytics team, you will work in an environment where you will:
-Lead a team of analytical chemists with responsibilities for the progression of analytical methodology throughout all stages of development.
-Coach and develop analytical chemists to drive towards mastery, to ensure your team is appropriately supported, and to develop meaningful growth plans.
-Partner with Chemical Research and Development to successfully deliver new medicines.
-Define and drive the control strategy in partnership with Chemical Research and Development, and other CMC associated functions (Formulation Development, Clinical and Commercial Supply Chains, Nonclinical and Clinical Development, Quality Assurance, Regulatory Affairs, Pfizer Global Supply for Commercial Manufacturing)
- Have overall accountability for the project management of the analytical activities and associated strategy in the field of Chemistry, Manufacturing and Controls (CMC) Development for defined therapeutic development projects
-- Plan, track, drive all project related analytical activities and expenditures.
- Drive the decision-making process in a multidisciplinary matrix organization.
- Be a leader across Analytical Research and Development (ARD) and contribute to departmental operational and strategic teams.
- Ensure fit for purpose and robust analytical deliverables with respect to the project timelines and costs.
As an API Analytics Director you will contribute with the following activities:
- Being accountable for the analytical development strategy and contribute to the high-level milestone plan (CMC Plan) in alignment with the overall ARD development strategy
- Defining the timelines, budget and resources and to coordinate all analytical activities to meet the overall project timelines and deliverables
- Fostering effective collaboration with the other lines in order to ensure high-quality fit-for-purpose analytical deliverables.
- Monitoring progress against project plans and report progress updates to co-development project team and governance bodies.
- Ensuring effective communication with all other involved CMC and associated functions as well as with external partners
- Participating in continuous improvement initiatives as required to ensure best in class project management
- Being a champion for novel ways of working, including digital efforts, modeling, simulation and integrated online efforts.
QUALIFICATIONS
- PhD in Analytical Chemistry, Organic Chemistry, Chemical Engineering, or related discipline with 10+ years relevant experience in small molecule drug substance / drug product development, or BS/MS in Analytical Chemistry, Chemical Engineering, or related discipline with a minimum of 25+ years relevant pharmaceutical industry experience.
- Extensive practical experience working within cross-disciplinary project teams and achieving results in a matrix environment.
- Demonstrated track record of delivering and defending full analytical control strategies as part of regulatory submissions, preferably across multiple modalities (e.g. small molecule, peptides, drug linkers, etc)
- Experience in actively developing and advancing scientific initiatives and external collaborations.
- Proven track record of mentoring and coaching early and mid-career scientists.
- A passion for leadership and the ability to guide the work of other colleagues to achieve meaningful outcomes and create business impact.
- Excellent organizational and communication (oral and written) skills.
- Ability to work independently, as well as thrive as part of a team. Interchange roles imperceptibly.
- Possess a passion for coaching and mentoring a new generation of leaders and scientists.
- 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.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- Occasional travel may be required for in-person meetings, conferences, or project support. Less than 10% travel is anticipated for this role.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- Occasional travel may be required for in-person meetings, conferences, or project support. Less than 10% travel is anticipated for this role.
Relocation support availableRelocation 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
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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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Research and Development
