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Net2Source (N2S)

Scientist – Vaccine Drug Product Development

Net2Source (N2S), Lansdale, Pennsylvania, United States

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This range is provided by Net2Source (N2S). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range $30.00/hr - $36.00/hr

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Location: West Point, PA, 19486

100% onsite

Duration: 12 months Contract

Position Summary

The Vaccine Drug Product Development team within Client's Research Laboratories is seeking a Contract Scientist/Engineer to join their department for one year. The selected candidate will contribute to the design and development of vaccine drug products from preclinical through Phase III stages, with a clear path toward commercialization. The role is hands-on, working in a fast-paced laboratory and collaborating with cross-functional teams to advance 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 techniques and GLP standards; support technology transfer to GMP manufacturing

Conduct stability and forced-degradation studies; analyze data, summarize results, and document findings in electronic lab notebooks and technical reports

Operate and troubleshoot benchtop equipment (mixing, filtration, lyophilization), instruments (pH, balances, pipettes), and analytical tools (DLS, SLS, KF, DSC, DSF)

Collaborate with discovery, analytical, manufacturing, and regulatory teams to achieve project deliverables

Continuously learn and apply emerging literature, methods, and technologies to optimize formulations and processes

Support analytical characterization (osmolality, viscosity, pH, dynamic light scattering) of formulated products

Maintain a clean, safe laboratory environment and adhere to safety protocols

Draft, review, and execute batch manufacturing protocols

Qualifications

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

Hands-on laboratory experience (academic or industry) with sterile technique, buffer preparation, and sample handling

Strong written and verbal communication skills with experience maintaining laboratory documentation

Data analysis and visualization skills to summarize experimental results

Mechanical aptitude for maintaining and operating lab equipment

Strong teamwork, adaptability, and ability to manage multiple priorities

Comfortable working in a fast-paced environment with changing priorities

Preferred Skills

Familiarity with biophysical/biochemical analytical techniques (e.g., DLS, HPLC, SDS-PAGE, UV/Vis)

Understanding of aseptic/formulation processes in non-GMP or GMP environments

Experience with statistical/design-of-experiments tools (JMP, Minitab) or numerical software (Matlab)

Prior experience in formulation, filtration, analytical/biochemical/biophysical characterization, or process development

Passion for pharmaceutical innovation and improving global health outcomes

Seniority level:

Associate

Employment type:

Contract

Job function:

Manufacturing and Science

Industries:

Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research

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