Senior Associate Quality Complaints Job

SR ASSOCIATE QUALITY COMPLAINTS needed for a CONTRACT opportunity with Yoh's client located in THOUSAND OAKS, CA.

THE BIG PICTURE - TOP SKILLS YOU SHOULD POSSESS:

- Related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry.

WHAT YOU'LL BE DOING:

- History of managing product complaints (other examples of ideal experience similar to complaint management includes management of investigations, non-conformances, corrective actions, etc.) would be ideal.
- Ability to manage small projects (Data Trending and Metrics Reporting).
- Great time management skills.
- Ability to write short documents for GMP compliance.
- Ability to follow written procedures.

WHAT YOU NEED TO BRING TO THE TABLE:

- Typically two (2) plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry.
- Evaluate documentation and operation and documentation according to company guidelines.
- Be self motivated, attentive to details and able to prioritize and meet deadlines.
- Basic statistical mathematical skills including the ability to trend data.
- Basic project management skills.
- Independently understand, follow and implement instructions.
- Strong word processing, database and spreadsheet (excel) application skills.
- Strong organizational skills with the ability to manage multiple projects or assignments.

BONUS POINTS! OTHERWISE KNOWN AS PREFERRED QUALIFICATIONS:

- Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience.

RECRUITER:Mary Nguyen

Yoh, a DayJ2W: CLINICAL; MONJOB

TAX TERM: CON_W2 J2WBRLA

Ref:

SFSF: LS