- Company is seeking to fill a temporary contracting role on the Process and Analytical Development team at its viral vector CDMO facility in Carlsbad, CA. The candidate will be responsible for the execution and development of analytical assays in support of process development activities for innovative viral vector therapeutics.
location: Carlsbad, California
job type: Contract
salary: $60.00 - 72.29 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Perform analytical testing using Thermo Vanquish UHPLC, Sciex CE system BioPhase 8800, Wyatt SEC-MALS and FFF-MALS.
- Develop methods using Thermo Vanquish UHPLC system.
- Generate worksheets, summary reports, and method transfer documents.
- Interface effectively with both internal and external partners to communicate technical guidance and updates.
- Investigate, create, and develop new methods and technology to achieve technical objectives and advancement.
- Independently design, plan, and execute experiments.
- Independently analyze complex data and interpret results.
- Able to contribute to and execute technical transfers of analytical methods from and/or to internal and external partners.
qualifications:
Minimum Qualifications:
- Bachelors degree in chemistry, biochemistry, or related life science studies.
- 7+ years of relevant experience in biopharmaceutical industry.
- Masters degree in chemistry, biochemistry, or related life science studies.
- 5+ years of relevant experience in biopharmaceutical industry.
- Ph.D. in chemistry, biochemistry, or related life science studies.
- 3+ years of relevant experience in biopharmaceutical industry.
- Knowledge and technical expertise in biologics analytical techniques and method development with a focus on HPLC and CE.
- Highly experienced in using Thermo Vanquish UHPLC system and proficient in using Thermo Chromeleon software.
- Experience in using Sciex CE system BioPhase 8800 or PA 800 Plus.
- Experience in using Wyatt SEC-MALS and FFF-MALS.
- Highly detail oriented.
- Helpful to have academic and/or industry-based background in virology
- Critical and analytical thinking skills to effectively solve problems and improve outcomes.
- Effective communicator of scientific results
- Knowledge of quality systems within an FDA-regulated environment
- Knowledge of ICH quality guidelines
skills: Chemistry, High Pressure Liquid Chromatography (HPLC), Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), International Council for Harmonization (ICH)
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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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.
