Associate QA Job

ASSOCIATE QA needed for a CONTRACT opportunity with Yoh's client located in WEST GREENWICH, RI

THE BIG PICTURE - TOP SKILLS YOU SHOULD POSSESS:

- GMP experience one (1+) years.
- Quality one (1+) years of experience.
- Technical Writing one (1+) years of experience.

WHAT YOU'LL BE DOING:

- Support the Corporate Product Quality department through the verification, review, tracking, and archiving of technical data.
- Required skills include knowledge of GMP, five (5) years operational experience in pharmaceutical or regulated industry; data entry; data verification; clerical and/or administrative experience; proficient in MS Excel, Word, PowerPoint, MS Project.

WHAT YOU NEED TO BRING TO THE TABLE:

- Perform transcriptional data verification of technical reports and other documents, following corporate Standard Operating Procedures.
- Enter documents into corporate quality databases, checking for completion and correctness.
- Gather documents and materials, collates, distributes and/or files.
- Enter and distribute documents and forms.
- Data processing support to include maintaining database for all documentation.
- Audit reports and files for discrepancies.
- May compile information and metrics from various documents or databases.
- Provide guidance or refer staff members to appropriate contacts.
- Coordinate or manage multiple documents and team members through the document review and approval process following corporate SOPs.
- Communicate via telephone, instant message, voice-mail, meetings, teleconferences, and/or e-mail.

RECRUITER:Mary Nguyen

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

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