Senior Scientist - Pfizer
Groton, CT
About the Job
ROLE SUMMARY
Pfizer’s Drug Product Design group is seeking formulation team members with a desire to bring new, cutting edge medicines to patients around the world. Our team members use science and technology to design, characterize and develop drug product formulations from candidate selection to commercial launch.
You will be able to leverage your existing scientific knowledge, as well as develop in new areas, to evaluate the chemical & physical stability, bio-performance and manufacturability of the drug product across a diverse range of therapeutic areas.
You will be responsible for formulation and manufacturing process design of pharmaceutical oral dosage forms for new drug candidates and product enhancement programs. You will participate in multi-disciplinary teams during the formulation development, process scale up, and technology transfer of conventional and continuous processing technologies including immediate release, modified release, pediatric and other specialized technologies to our clinical and commercial manufacturing sites in the Pfizer Global Supply organization.
You will be an active contributor on matrix project teams and must be a strong team player with excellent communication skills working in a complex cross-functional matrix.
This position also offers the opportunity for cross-training and growth in multiple technical areas to encourage a flexible working environment. Enjoy the entrepreneurial mindset and infrastructure to develop new technologies and processes for drug delivery and dosage form manufacture while having access to the resources of a larger company.
The role requires general knowledge of pharmaceutical science, materials science, chemistry and engineering principles as applied to the design of solid oral dosage forms and advancement of drug delivery platforms for immediate and modified release including pediatric design.
As member of the Drug Product Design group you will interact closely with other Pharm Sci partner lines (e.g. Analytical R&D, Chemical R&D, Global CMC, Pharm Sci Operations, Drug Product Supply, Quality Assurance) and other lines involved in developing drug assets such as Clinical Pharmacology, Clinical Sciences, Pharmacology & Drug Metabolism and Pfizer Global Supply.
Finally, this position will challenge you to pursue scientific excellence and creativity, in collaboration with industry-leading experts across multiple scientific disciplines.
Role Responsibilities
Leverages advanced technical knowledge understanding of chemistry, pharmaceutics, engineering and/or materials science fundamentals to the design and development of immediate and modified release formulations and manufacturing process understanding.
Designs and executes laboratory and computational experiments to support novel solid oral drug delivery platforms, initiatives, and portfolio-driven projects. Operates and maintains laboratory equipment to produce and characterize formulated drug products.
Uses his/her/their scientific judgment to apply or adapt standard methods, technical concepts, and prior work experience to make project decisions.
Utilizes predictive models and computational approaches to understand mechanical and physico-chemical characteristics of pharmaceutical compounds and formulations to assess drug product performance and drive team decisions.
Applies results from biopharmaceutics modeling tools, physicochemical (solubility, precipitation, & dissolution) and biological (passive, transporter mediated, efflux) transport phenomena, and pre-clinical and clinical pharmacokinetic studies to influence drug product development.
Collaborates with cross-disciplinary teams.
Authors regulatory documents supporting drug product development, including relevant drug product sections of IND submissions and CTD applications and associated queries to regulatory agencies.
Effectively mentors other scientists in their area of expertise.
Strives to grow scientifically. Collaborates with others on departmental technology initiatives, and contributes to current scientific literature
Minimum Qualifications
BA or BS + 8 years experience, MS + 5 years experience, or PhD with 0 to 4 years of experience in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or allied discipline.
Preferred Qualifications
Extensive practical experience working within department and/or cross-disciplinary project teams and achieving results in a matrix environment.
Experience in actively developing and advancing scientific initiatives and external collaborations.
Excellent organizational and communication (oral and written) skills.
Ability to work independently, as well as collaboratively.
A strong interest and motivation to learn and implement new technologies and concepts
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- Occasional travel may be required for in-person meetings, conferences, or program support
- This position will interact closely with other Pharm Sci partner lines (e.g. Analytical R&D, Global CMC, Pharm Sci Operations, Drug Product Supply, Quality Assurance), in addition to other lines involved in developing drug assets such as and Pfizer Global Supply (Technical Support and Manufacturing Sites)
Work Location Assignment: On Premise
The annual base salary for this position ranges from $88,300.00 to $147,100.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% 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 life’s 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 | (uscandidates.mypfizerbenefits.com). 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 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.
Research and Development
