Formulation Scientist
Listed on 2026-01-12
-
Research/Development
Research Scientist, Clinical Research -
Healthcare
Clinical Research
Job title:
Scientist I
Location:
West point PA
Duration:12 months
Pay rate: $36/hr.
DescriptionVaccine Drug Product Development, a part of ***’s Research Laboratories in West Point, PA, is seeking a Contract Scientist or Engineer to join our department for one year. The selected candidate will work as part of a team responsible for the design and development of vaccine drug products from preclinical through Phase III with a line of sight to commercialization. The successful candidate will work hands-on in a fast-paced laboratory and collaborate closely with cross‑functional teams to develop the next generation of vaccine drug products.
Responsibilities- Design and perform hypothesis‑driven formulation and process development experiments for sterile vaccine drug products (buffers, stabilizers, antigen/adjuvant, vials, syringes) across multiple vaccine modalities (subunit, conjugate, live‑attenuated, etc.).
- Prepare formulations and fill vials/syringes for characterization & animal studies using aseptic technique and Good Laboratory Practices (GLP); support transfer to GMP manufacturing.
- Conduct stability and forced‑degradation studies; analyze data, summarize findings, and author technical reports and electronic notebook entries.
- Operate and troubleshoot benchtop unit operations (mixing, filtration, pumping, lyophilization), common lab instruments (pH, scales, pipettes), and analytical tools (DLS, SLS, KF, DSC, DSF).
- Collaborate with cross‑functional teams (discovery, analytical, manufacturing, regulatory) to meet project timelines and deliverables.
- Continuously learn and apply current literature, methods, and technologies to improve formulations and processes.
- Support selected analytical studies on formulated products such as osmolality, viscosity, pH, and dynamic light scattering.
- Follow safe laboratory practices and maintain the work area in a clean, orderly and safe manner.
- Draft, review and execute protocols for batch manufacture.
Minimum
Education Requirements:
B.S. in Chemical/Biochemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, Immunology, Materials Science, or related field with 1-3 years of relevant experience.
- Hands‑on laboratory experience (academic or industry) with basic sterile technique, buffer preparation, and sample handling.
- Strong written and verbal communication skills; experience documenting experiments in electronic or paper lab notebooks.
- Basic data analysis skills and ability to summarize and visualize experimental results.
- Scientific and mechanical aptitude and experience maintaining, designing, and/or operating scientific equipment and machinery.
- Ability to follow safe laboratory practices and maintain work area in a clean, orderly, and safe manner.
- Team‑oriented, motivated to learn, and able to manage multiple priorities under technical supervision.
- Comfortable working in a face‑paced environment and adapting to change.
- Familiarity with biophysical/biochemical analytical methods (e.g., DLS, HPLC, SDS‑PAGE, UV/Vis).
- Understanding of aseptic/formulation processes in a non‑GMP or GMP environment.
- Familiarity with statistical/design‑of‑experiments tools (JMP, Minitab) or numerical software (Matlab).
- A desire to develop complex pharmaceutical products and continuously learn.
- A passion to contribute to the development of pharmaceutical products with a significant potential to impact global human health.
Preferred candidates will have experience in drug product development techniques (e.g. formulation, filtration, analytical/biochemical/biophysical characterization, and process development).
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).