Director Analytical Chemistry
$176.6k - $294.3kPfizer, S.A. de C.V
Overview We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals. Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life‑changing medicines to the world. Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. 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 the 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 while continuously improving 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, and relevant computational skills are desirable for this leadership position. Experience working successfully as part of a multidisciplinary organization is vital. You will be responsible for the continuous enhancement of technical skills, scientific knowledge, and personal growth of colleagues, and have the opportunity to grow your skills as a people leader and influence within global analytical research and development at Pfizer. Responsibilities Lead a team of analytical chemists responsible for the progression of analytical methodology throughout all stages of development. Coach and develop analytical chemists to drive mastery, ensuring the team is appropriately supported and has 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, including planning, tracking, driving all project‑related analytical activities and expenditures, and driving decision‑making 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. Additional Director Activities Accountable for the analytical development strategy and contribution to the high‑level milestone plan (CMC Plan) aligned with the overall ARD development strategy. Define timelines, budget, and resources; coordinate all analytical activities to meet overall project timelines and deliverables. Foster effective collaboration with other lines to ensure high‑quality fit‑for‑purpose analytical deliverables. Monitor progress against project plans and report updates to co‑development project teams and governance bodies. Ensure effective communication with all other involved CMC and associated functions as well as with external partners. Participate in continuous improvement initiatives to ensure best‑in‑class project management. Champion 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 of 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 (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 colleagues to achieve meaningful outcomes and create business impact. Excellent organizational and communication (oral and written) skills. Ability to work independently and thrive as part of a team. Possess a passion for coaching and mentoring a new generation of leaders and scientists. Demonstrated breadth of diverse leadership experiences and capabilities, including influencing and collaborating with peers, developing and coaching others, and guiding the work of 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. Benefits and Compensation Annual base salary range: $176,600.00 to $294,300.00. Bonus target: 20.0% of the base salary as part of Pfizer’s Global Performance Plan. Equity: Eligibility to participate in Pfizer’s share‑based long‑term incentive program. Retirement: 401(k) plan with Pfizer matching contributions and an additional Pfizer retirement savings contribution. Paid time off: Paid vacation, holiday and personal days, paid caregiver/parental and medical leave. Health benefits: Medical, prescription drug, dental and vision coverage. Relocation support: Relocation assistance may be available based on business needs and/or eligibility. Work location assignment: On Premise. 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. Accessibility Pfizer endeavors to make 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 View email address on click.appcast.io . 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. #J-18808-Ljbffr
$176.6k - $294.3k
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