Engineer, Parenteral Drug Product Process Development, Testing & TT (JP14749)
3 Key ConsultingThousand Oaks, California, United States
Posted November 12, 2025
72000 - 82000 USD year
Full Time
About the Company
3 Key Consulting is a specialized staffing and consulting firm with 12 years of experience placing business and IT professionals in the life sciences and healthcare sectors. Leveraging a broad network of industry experts and partnerships with leading academic institutions, the firm offers a full suite of talent acquisition services—including PEO, compliance, and niche domain staffing in biomedical, pharma, medical devices, and business intelligence. Its core focus on people, process, and technology enables faster, cost‑effective solutions that improve workforce productivity and market efficiencies. 3 Key’s collaborative culture and commitment to delivering better, faster, and more efficient staffing and consulting services distinguish it as a trusted partner for organizations seeking high‑quality talent and operational excellence.
Job Description
We are seeking a skilled Process Development Engineer to support technical projects with expertise in laboratory testing, drug product fill finish processing, holistic drug product process knowledge, technical transfer, and drug product manufacturing.
Requirements
- Author, data verify, and review guideline documents, technical protocols, reports, product impact assessments.
- Execute laboratory analytical testing such as: viscosity, protein concentration, pH, osmolality.
- Execute laboratory experiments such as pipetting, formulation, filtration.
- Provide technical support for drug product process development, including formulation, filtration, and filling (vials/syringes/devices) of parenteral products.
- Assist in the development and characterization of drug product processes and the transfer of new technologies to commercial sterile fill/finish sites.
- Support process development for commercial drug product processing in areas such as sterile processing, process characterization, tech transfer, and validation.
- Collaborate with manufacturing and support functions to provide coordinated support for commercial drug product manufacturing operations and technology transfer.
- Participate in global cross-functional teams, working effectively in a highly matrixed team environment to drive efficiency and foster strong relationships.
- Troubleshoot issues with drug product processing technologies and equipment, utilizing data-driven analyses and visualizations to determine true root causes.