Validation Tech I Job

VALIDATION TECHG I needed for a CONTRACT opportunity with Yoh's client located in SOUTH SAN FRANCISCO, CA.

THE BIG PICTURE - TOP SKILLS YOU SHOULD POSSESS:

- Minimum of five (5) years experience
- GMP documentation
- quality computer systems (ie Trackwise, SAP)

WHAT YOU'LL BE DOING:

- Identify, troubleshoot, and propose resolution to technical problems.
- Identify gaps in and potential improvements to systems and procedures
- Receive and provide training
- Provide input to and participate in assay transfer and assay validation
- Perform equipment qualification/maintenance
- Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures
- Support the maintenance and compliance of operational areas.

WHAT YOU NEED TO BRING TO THE TABLE:

- Minimum of five (5) years post college experience in equipment validation and computer validation.
- Recent Pharma experience preferred
- Participate in and/or lead group and project teamwork; project and process improvements
- Write protocols and reports under limited supervision
- Operate within the relevant quality computer systems (ie Trackwise, SAP) ensuring implementation in line with quality and timeliness objectives
- Communication-both verbal and written with diverse teams and for GMP documentation
- Understanding and interpretation of Policies, Process, Procedures
- Ability to work with cross functional teams

BONUS POINTS! OTHERWISE KNOWN AS PREFERRED QUALIFICATIONS:

- A B.S or higher in Chemical, Biochemical or Mechanical Engineering or Science discipline

RECRUITER: Mary Nguyen

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

J2W: CLINICAL

TAX TERM: CON_W2

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