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Senior Scientist, Formulation

Employer
Pfizer
Location
Andover, Massachusetts
Salary
Competitive
Closing date
Oct 23, 2021

View more

Discipline
Physical Sciences, Chemistry
Position Type
Full Time
Job Type
Senior Scientist
Organization Type
All Industry, Pharma
Role Description

Sr. Scientist- Formulation Development, is a position within the Pharmaceutical Research & Development (PhRD) department in Pfizer's Biotherapeutics Pharmaceutical Sciences organization. This scientific leadership role will be responsible for formulation development and investigating physico-chemical characterization methods of Pfizer's biotherapeutics portfolio molecule formulations in a dynamic and highly interdisciplinary environment to support pre-clinical, clinical, and commercial development. In addition, the candidate should be able to contribute formulation selection and characterization source documentation to support regulatory submissions. This position requires exceptional time management and communications skills with strong attention to detail. A breadth of knowledge of analytical tools and techniques applied to materials science, colloidal structure and stability, nanotechnologies for formulation design, nucleic acid drug delivery, and general pharmaceutical R&D is required.

Responsibilities

The incumbent candidate will be responsible for conducting experiments in support of developing, evaluating, and characterizing formulations/processes, components, and supporting delivery technologies for diverse therapeutic modalities including (but not limited to) mammalian and microbial fermentation-derived candidate molecules, vaccines, plasmids, RNA-based medicines, peptides, and targeted delivery strategies. This individual functions cooperatively with other members of the team to achieve the project goals. The incumbent displays technical awareness in various aspects of drug discovery and development, a strong drive in learning new techniques and scientific commitment, and impactful scientific and technical contributions within the PhRD team and the respective project teams. Specific responsibilities include:

Role Responsibilities
  • Design, execute and analyze experiments for existing and novel modalities.
  • Define the appropriate parenteral dosage form, formulation, process design, scale-up approaches, identify critical parameters, and define the design space
  • Support development of novel characterization techniques to characterize formulations to support process development and formulation design.
  • Lead experiments to confirm robust process performance across the control space. Compile experimental and analytical results, perform data interpretation, summarize, and report on data with conclusions and recommended next steps
  • Provide technical representation and subject matter expertise (SME) in cross functional formulation, process and analytical investigations for commercial production processes
  • Collect and share relevant academic literature, leverage external consultants/SMEs, and establish new collaborations with internal groups. Optimize current processes to ensure robust manufacturing of Pfizer's biotherapeutic portfolio
  • Interface extensively in a matrixed environment with process and analytical development teams for process investigation support, assess new analytical technologies, support on-going process characterization and post-approval changes.
  • Maintain accountability for project success and results delivery.
  • Communicate research and development findings internally and externally.


Educational Background

Minimum : B.S. or M.S in Pharmacy, Chemistry, Biomedical Eng, Chemical Eng, Biochemistry, Biotechnology, Virology, Biology or equivalent scientific field, with 5 - 8 (B.S) or 3-6 (M.S.) years of industrial experience

Desirable : PhD in Pharmaceutical Sciences, Analytical Chemistry, Biophysics, Biomedical Eng, Chemical Eng, Biochemistry, Biotechnology, or equivalent scientific field with 0 - 3 years industrial experience preferably in in biotherapeutic formulation development and scale up and/or nanoparticle-based modalities.

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Requirements

Minimum :
  • Solid foundation in Formulation, analytical, chemistry, material science, and/or nano-particle technologies.
  • Experience in formulation development, pharmaceutics, pharmacy or drug product manufacturing or scale-up of biotherapeutics modalities.
  • Effective communication skills and the ability to write detailed technical reports
  • Experience with various biophysical and light scattering techniques (DLS, NTA, Coulter Counter, etc.)
  • Experience with regulatory filings and submissions.
  • Exceptional organizational, communication, and critical thinking skills, and the ability to thrive in an interdependent and idea-rich environment
  • Strong work ethic and attention to detail


Desirable :
  • Expert understanding and leadership of technical areas necessary for biotherapeutic molecule formulation development.
  • Experience in designing parenteral dosage forms for biotherapeutics modalities including protein-based, gene therapy, vaccines or nanoparticle delivery systems
  • Experience in nucleic acid drug development (DNA, RNA, oligonucleotides)
  • Excellent leadership skills
  • Experience in scale-up and technology transfer of aseptic processes to pilot/commercial-scale manufacturing facilities
  • Solid understanding of thermodynamics and kinetics
  • Working knowledge of GLP/GMP requirements.
  • Experience in authoring regulatory submissions (IND, IMPD, BLA, MAA)
  • Solid understanding of QbD concept in design, execution, and interpretation of formulation and process development experiments.
  • Ability to demonstrate autonomy in representing functional area.


Additional Posting Information
  • Last Date to Apply for Job: October 28 , 2021
  • Eligible for Employee Referral Bonus
  • Eligible for Relocation Package
  • #LI-PFE


Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.

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.

Research and Development

#LI-PFE

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