Scientist / Associate Scientist - Peptide Formulation

Scientist / Associate Scientist•Peptide Formulation in Newark, California Overview Scientist / Associate Scientist•Peptide Formulation W2

Contract Pay Rate:

$55•$65 per hour

Location:

Newark, CA•

Onsite Role Job Summary:

We are seeking a highly motivated formulation scientist to support our clinical programs. The ideal candidate will have experience designing and developing early-stage clinical formulations and process development across multiple delivery routes, particularly oral and parenteral. Peptide experience is preferred, though relevant biologics or small molecule formulation experience will also be considered. This role requires independent laboratory work, cross-functional collaboration, and knowledge of preclinical and clinical formulation preparation.

Duties and Responsibilities:

Develop solid oral dosage forms for early•and late-stage clinical trials. Conduct pre-formulation, formulation development, process selection, and scale-up. Oversee GMP drug product manufacturing and comply with global regulatory CMC requirements (INDs, IMPDs, NDAs). Design and execute laboratory experiments to optimize clinical formulations. Provide formulation guidance to chemistry and biology teams to integrate formulation early into the discovery process. Utilize modern delivery technologies to enhance the bioavailability of small molecules or peptides. Generate and interpret pre-formulation data (e.g., logP, thermal analysis, moisture content, particle size, stability). Apply laboratory techniques such as sterile technique, pH measurement, dissolution testing, lyophilization, and spray drying. Oversee formulation screening studies in preclinical animal models. Collaborate with internal and external quality control, quality assurance, and regulatory personnel to resolve technical or procedural issues. Represent pharmaceutical sciences in cross-functional meetings and present data and conclusions. Travel domestically or internationally as needed for manufacturing oversight at CDMOs.

Requirements and Qualifications:

Hands-on experience in solid oral dosage form formulation and process development. Knowledge of gastrointestinal site-specific drug delivery is a plus. Proficient with analytical techniques such as HPLC/MS, UV, DSC, TGA, XRPD, FTIR, and DLS. Understanding of pharmacokinetic data generation and interpretation. Strong organizational, critical thinking, and problem-solving skills. Excellent written and verbal communication skills. BS in Chemistry, Pharmaceutics, Engineering, or related scientific discipline with 8+ years of formulation experience MS in a related field with 5-8 years of experience Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s