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Randstad US sr. research associate, analytical development in south san francisco, California

sr. research associate, analytical development.

  • south san francisco , california

  • posted may 28, 2024

job details

summary

  • $30 - $39.34 per hour

  • contract

  • bachelor degree

  • category life, physical, and social science occupations

  • reference48199

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now!

location: South San Francisco, California

job type: Contract

salary: $30.00 - 39.34 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

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.

  • 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

qualifications:

Required

  • 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

Preferred

  • 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

skills: HPLC, Assay Development, Assay Method, Assay Verification, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

Applications accepted on ongoing basis until filled.

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

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