Senior Scientist, Formulation Development
- Employer
- Pfizer
- Location
- St. Louis, Missouri
- Start date
- Aug 29, 2021
View more
- Discipline
- Science/R&D, Biotechnology
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Best Places to Work
Why Patients Need You
Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
What You Will Achieve
As a Senior Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. This colleague will be part of the Pharmaceutical Research and Development team. In this role, you will lead the development, scale-up and transfer of parenteral formulations and manufacturing processes for various biologics modalities such as gene therapies, monoclonal antibodies, antibody drug conjugates, proteins and vaccines. This is a project-based position performing formulation and process development activities for biotherapeutic molecules from pre-clinical and Ph I clinical trials through manufacturing process performance qualification, license application and commercialization.
It is your dedication that will make Pfizer ready to achieve new milestones and help patients across the globe
How You Will Achieve It
The Senior Scientist is responsible for
Developing parenteral formulations, alternate drug delivery systems, and tech transfer manufacturing processes to enable the successful development of biotherapeutic drug products including gene therapies, prophylactic and therapeutic vaccines and protein-based modalities
Lead a technical project team inside and outside the lab that will apply characterization and stability information to develop an appropriate dosage form to meet clinical and commercial needs
Lead the formulation and development activities from pre-clinical and Ph I clinical trials through commercialization
Executing new technologies and procedures to accelerate the biotherapeutic development process across projects
Qualifications
Must-Have
BS in Degree in in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology, Biomedical engineering and 9+ years of industry or equivalent experience
MS degree in the disciplines above and 7+ or PhD and 1+ years of industry or equivalent experience
Nice-to-Have
Demonstrated industry experience in parenteral formulation and process development of biotherapeutic
Demonstrated understanding and leadership of technical area necessary for biotherapeutic molecule formulation development
Experience in scale-up and technology transfer of aseptic processes to pilot/commercial scale manufacturing facilities
Solid understanding of thermodynamics and kinetics as well as QbD concept in design, execution, and interpretation of formulation and process development experiments
Working knowledge of GLP/GMP requirements
Experience in authoring regulatory submissions (IND, IMPD, BLA, MAA)
Ability to demonstrate autonomy in representing functional area
Other Job Details
Eligible for Employee Referral Bonus
#LI-PFE
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