- Strong HPLC experience
- Experience in analytical method development and separation technologies including multiple modes such as HPLC, capillary electrophoresis, AUC and mass spectrometric in analyses of biologics
- Prior AAV or Antivirus characterization
- Develop assays for GMP release of gene therapy products
- Develop assays for product characterization of gene therapy products
- Develop assays for AAV/protein/DNA to assist in evaluation of process change, formulation and stability study
- Report project status (development plans, timelines, and results) to supervisor and technical teams.
- Write tech transfer and development reports.
- Keep current with all regulatory guidelines, compendia requirements, and technical innovations.
- Maintain accurate, error-free records of all analytical development activities timely
- Bachelor of Science with 3+ years, or Masters of Science with 1+ years' experience in biopharma industry with proven expertise of a range of physicochemical methodologies for quantifying purity/quality of proteins, viruses, and viral vectors Extensive experience and knowledge in operating HPLC applied to DNA/RNA, protein and/or viral vectors.
- Positive, professional self-starter with a passion for science, innovative technical and analytical skills required to perform at the highest level
- Highly motivated and independent yet has successfully worked in a group setting with efficient, flexible and self-motivated work ethic; to be utilized in work planning, executing, and data analyzing.
- Excellent clear and concise writing skills for technical reports and documents along with strong verbal
- communication skills
- Proven ability to work in cross-functional teams as a strong team player as well as independently.
- Successful history and the ability to handle several fast-paced projects concurrently.
- Excellent communication, writing and presentation skills to technical and non-technical audiences.
- Proficient working in Microsoft Office Suite
- 5+ years of HPLC usage and troubleshooting
- Experience in analytical method development and separation technologies including multiple modes such as HPLC, capillary electrophoresis, AUC and mass spectrometric in analyses of biologics
- Prior AAV or Antivirus characterization
- Experience in statistical analysis using JMP or other software
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Research Associate
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Sr. Research Associate - Frederick, United States - SPECTRAFORCE
Description
Job Title: Sr. Research Associate
Location: South San Francisco, CA 94080
Duration: 12 Months
Pay Range: $38- $40/hr on W2
Top Skills:
The Sr. Research Associate will be responsible for developing assays for the GMP release of drug substances and drug products, using HPLC, Capillary Electrophoresis, AUC and Mass Spectrometry. Maintain a well- documented record of activities in ELN and reports. Summarize and present experimental results in meetings and participate in report and SOP writing. The position level will be commensurate with education and experience level. This role will be at our South San Francisco R&D facility.
Responsibilities
Required Qualifications:
Preferred
