Immediate Openings
Los Angeles, CA
Validation Engineer/Specialist - Materials Qualification: We are immediately seeking a qualified candidate with experience to support the qualification of resin materials used for chromatography processes by our client in the greater Los Angeles area.
This position may be either full time permanent or contract and is expected to last for 3 – 6 months.
In this position, you will:
- Develop documents, execution of tests and prepare final reports
- Analyze data, determining results and the presentation of conclusions and recommendations to clients, ensuring that projects are implemented in accordance with the agreed scope time lines, policies and procedures
- Provide technical leadership and support within the client organization and in VTI
- Organize, schedule and track validation projects in order to meet client requirements and agreed timelines
Requirements
- Previous experience with materials qualification, process development, or technology transfer in a cGMP regulated environment
- Bachelors Degree or higher in an applicable technical area, such as Process Engineering, Chemistry, Biochemistry, Microbiology, or related degree
- At least 3 years of experience in a biotechnology or pharmaceutical Quality Control, Development or Manufacturing environment
- Knowledge of cGMP requirements
- Knowledge of Microsoft Windows, Word and Excel are mandatory
- Experience in writing technical documents, including validation documents, protocols, and reports
- Excellent written and oral communication skills in English
- The ability to work effectively with team members and work under minimal supervision
- Able and willing to work flexible hours
- Strong organizational skills and demonstrated ability to manage projects to completion
OR
E-Mail resume and cover letter to hr@validation.org or fax to (858) 673-3677