Job Description

Our client who is a leader in biopharmaceuticals located in Pasadena CA is currently seeking a Compliance Scientist.
$41-48/hr W2
The Opportunity
We have an exciting opportunity available for a to join the Research and Clinical Bioanalytics (RCB) Department in Pasadena, CA. In this role, you will ensure appropriate compliance and quality standards are set, applied and maintained in the planning, organization, co-ordination and day-to-day operation of the research, development and validation of regulatory compliant bioassays and biomarkers to support R&D projects from Stage Gate 1 (SG1) through to all stages of Clinical Development.

The successful incumbent will:

• Support RCB's growing compliant laboratory operations and documentation processes to enable delivery of appropriately compliant bioassays and biomarkers with associated reagents to measure the pharmacokinetics (PK), pharmacodynamics (PD) and immunogenicity of biologic therapies in research, GLP toxicology and clinical development studies
• Ensure that work is conducted according to the specific requirements of GCP/GCLP standard
• Be trained in the conduct of the assays, to both enable better appreciation of the compliance requirements of the processes involved and to allow participation in assay campaigns when required

Skills and Experience Required:

• A MS/PhD in a scientific/medical/(bio)pharmaceutical discipline
• At least 3 years' experience in pre-clinical and clinical development of biopharmaceuticals or equivalent related experience in industry and/or academic environments
• Experience in writing SOPs, Forms, Scientific/Validation protocols and reports
• Experience of working in a compliant Laboratory environment
• Relevant and demonstrated expertise in the following:
• In vitro assays (e.g. ELISA, electrochemiluminescence [ECL], multiplex assays [MSD, Olink], flow cytometry [cell phenotyping and receptor binding/occupancy]), and the associated instrumentation and software
• Experience in molecular biology [dd/qPCR, primer design,...] is a plus
• Proficient in Microsoft Office and graphics programs (e.g. GraphPad Prism, Visio)
• Very good communication and networking skills. The ability to work successfully in a cross-functional, multidisciplinary and multinational team environment.

Benefits:
We put our Ambassadors first. When it comes down to it, we know we can't fulfill our Promise to our business customers without your commitment. You represent our organization while on assignment. In return, we do our best to show our commitment to you. Our Ambassador Benefits package includes: Medical, dental and vision coverage. It also includes 401k, sick time, holiday and much more. We are an equal opportunity employer.
 

We are an equal opportunity employer and make hiring decisions based on merit. Recruitment, hiring, training, and job assignments are made without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, or any other protected classification. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.
To apply please email your resume to lfulayter@rothstaffing.com

Job Snapshot

• Employee Type:Full-Time
• Location:Pasadena, CA
• Job Type:Biotech, Pharmaceutical, QA - Quality Control, Research, Science
• Experience:Not Specified
• Education:Not Specified
• Date Posted:9/19/2023
• Contact: Laura Fulayter (480) 966-0090
• Pay Range: $41.00 - $48.00 Hourly

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