Engineer, Biopharma Process Development – Onsite/Hybrid (JP10834)
3 Key ConsultingThousand Oaks, California, United States
Posted September 20, 2022
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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 hiring an Engineer for a consulting engagement with a leading global biopharmaceutical company. The candidate will support senior staff in developing and characterizing drug product technologies and manufacturing capabilities.
Requirements
- Master's degree OR Bachelor's Degree and 2 years of relevant experience
- Educational background in Chemical Engineering, Biomedical Engineering, Biotechnology correlated technical field of study in biotechnology, life sciences or related discipline
- Knowledge in scientific principles of freeze/thaw, formulation/mixing, filtration, filling, lyophilization, capping, and visual inspection
- Ability to work on multiple projects simultaneously, learn new techniques, keep accurate records, follow SOP’s and instructions in compliance with company policies
- Ability to independently design and execute characterization studies, author characterization protocols, process transfer documents, application notes and technical reports
- Proficiency in technical problem solving, critical thinking, and delivery of technical solutions with some oversight
- Strong knowledge of Quality systems and Drug Product Manufacturing (GMP)
- Demonstrated ability to use interpersonal skills to build strong technical relationships
- Self-motivation, adaptability, and a positive attitude
- Excellent communication skills, both oral and written