Scientist - I (Assistant) - PA/NJ Only Scientist - I (Assistant) - PA/NJ Only

TALENT Software Services; West Point (PA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical company in West Point, PA is seeking a Contract Scientist or Engineer for a full-time role focused on the development of vaccine drug products. The successful candidate will work hands-on in a laboratory and collaborate with various teams to design and develop formulations. The ideal candidate should have a B.S. in a related field and relevant lab experience. This position is 100% lab-based onsite.

Qualifications

• 1-2 years of relevant experience preferred.
• Experience with basic sterile technique and sample handling.
• Ability to document experiments effectively.

Responsibilities

• Design and perform development experiments for vaccine products.
• Conduct stability studies and analyze data.
• Collaborate with cross-functional teams to meet timelines.

Skills

Hands-on laboratory experience

Strong written and verbal communication skills

Basic data analysis skills

Scientific and mechanical aptitude

Team-oriented and motivated to learn

Comfortable in fast-paced environments

Education

B.S. in Chemical/Biochemical/Biomedical Engineering

Tools

DLS

HPLC

SDS-PAGE

UV/Vis

Job description

Overview

Vaccine 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 and 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.

Qualifications

Minimum Education Requirements:
B.S. in Chemical/Biochemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, Immunology, Materials Science, or related field with 1-2 years of relevant experience.

• Required Skills and 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 fast-paced environment and adapting to change.

Preferred Skills and Experience

• 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.

Note: Positions available: 2. 100% lab based onsite role.

Other

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Other
• Industries: IT Services and IT Consulting