Scientist, Drug Product Development - Lexington, MA 02421 (4 days​/week onsite

Position: Scientist, Drug Product Development -  Lexington, MA  02421 (4 days/week onsite)
Title:

Scientist, Drug Product Development    

Location:

Lexington, MA 02421 (4 days/week onsite)
Duration: 12 months

The Contract Scientist will support parenteral drug product development activities with a focus on hands-on in-use compatibility and stability studies, oversight support of drug product manufacturing, and management of technical documentation. The role is intended to provide dedicated technical and operational capacity across mid-stage and late-stage development programs, ensuring studies are executed on schedule, manufacturing activities are appropriately supported, and program documentation is complete and accurate.

The successful candidate will work cross-functionally with formulation, analytical, manufacturing, quality, and clinical operations teams to advance drug product deliverables.

ACCOUNTABILITIES :
Design and execute in-use studies for parenteral (injectable/infusion) drug products, including dose preparation, dilution, compatibility, hold-time, filter
and infusion-set compatibility, and simulated clinical-administration assessments.

• Test in-use study samples using relevant physicochemical and analytical methods, including micro-flow imaging (MFI) for subvisible particles, pH, osmolality, protein concentration, and size-exclusion chromatography (SEC); generate, review, and trend the resulting data.

• Author study protocols, plans, and reports for in-use and related drug product studies (potentially including formulation and process development studies); interpret analytical results and summarize conclusions to support clinical use instructions and regulatory filings.

• Coordinate and support sample management and testing logistics with analytical and quality laboratories, including stability pull schedules and data
tracking.

• Organize, review, and maintain electronic technical documentation, ensuring documents are current, accurately versioned, appropriately filed in electronic
document management and data systems, and inspection-ready.

• Ensure all work is performed in compliance with applicable GMP, GDP, safety, and data-integrity requirements, as well as internal procedures and quality
standards.

• Present study updates and findings to project teams and contribute to cross- functional development discussions.

Education and Experience:

• Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, Biology, or a related scientific discipline with 6+
years of relevant pharmaceutical/biopharmaceutical industry experience; OR Master's degree with 4+ years; OR Ph.D. with 0–2 years of relevant experience.

• Demonstrated experience in parenteral / sterile drug product development, formulation, or manufacturing support.

• Hands-on experience with in-use, compatibility, and/or stability studies for injectable or infusion products strongly preferred.

• Working knowledge of drug product manufacturing operations (e.g., compounding, filtration, filling, lyophilization) in a development or GMP environment.

• Experience authoring technical documents (protocols, reports, batch records) and working within electronic document management systems (e.g., Veeva,
Documentum, or equivalent).

• Familiarity with GMP, GDP, ICH, and data-integrity expectations in a regulated environment.

Knowledge and

Skills:

• Strong technical understanding of parenteral drug product formulation, physicochemical stability, and compatibility principles.

• Solid laboratory skills and familiarity with analytical techniques used to characterize protein/biologic or small-molecule drug products (e.g., appearance, particulates, concentration, aggregation, pH, osmolality).

• Excellent scientific/technical writing skills, with the ability to produce clear, accurate, and well-organized protocols and reports.

• Strong organizational and documentation-management skills, with meticulous attention to detail and version control.

• Effective cross-functional collaboration and communication, able to interface with formulation, manufacturing, analytical, and quality partners.

• Comfortable working on-site in laboratory and adhering to associated gowning and safety requirements.

• Proficiency with standard productivity and data tools (e.g., Microsoft Office; electronic lab notebook and document systems)

Benefits:
We offer a competitive compensation package that includes:
• [Pay Rate]: $70 - $75 per [Hour/Year]
o

Note:

Pay rate will be commensurate with experience.

• Medical for full time employees

• Dental, and Vision Insurance

• Life Insurance, Short-Term Disability, Long-Term Disability, etc.