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Quality Control Analyst II Job

Eingestellt von Yoh

Gesuchte Skills: Support, Client

Projektbeschreibung

QUALITY CONTROL ANALYST II needed for a CONTRACT opportunity with Yoh's client located in San Carlos, CA.

THE BIG PICTURE:

- Our client located in San Carlos is seeking a Quality Assurance Batch Record Reviewer/Person-In-Plant to support Quality oversight of manufacturing operations.
- This is a night shift position

WHAT YOU'LL BE DOING:

- Responsible for on-the-floor, timely and effective GMP review and production close-out of batch record documentation in order to maintain a continuous flow of batch records
- Conducts QA Person-In-Plant activities including, Area Approval, Line Clearance Approval, Batch Record Review, Deviation triage and preliminary investigation, etc.
- Ensures all GMP's, SOP's and protocols are followed.
- Single point of contact in the plant during the assigned Manufacturing shift for the Batch Record Review Process and Quality matters.
- Operates on a 12-hour shift to support 24x7 Operations Night shift
- Responsibilities include approval and issuance of batch records, approving records; issue resolution; batch record review.
- Reviews batch documentation for accuracy and completeness according to cGMP's to ensure timely release.
- Assists with Deviation investigations, Compliance investigations, and Customer complaint investigations.
- Supports implementation of CAPAs, SOP revisions, Quality improvement initiatives, Operational Excellence projects, etc.
- Adheres to internal/external Guidelines, Specifications and Regulatory requirements while reviewing batch documentation.
- Positively interacts with internal associates to quickly and effectively resolve issues.
- Addresses deficiencies and ensures completion of follow-up actions, specifically those that target process fixes to maintain consistent resolutions to batch review issues according to GMP standards and Novartis objectives.

WHAT YOU NEED TO BRING TO THE TABLE:

- Two to five (2-5) years of related manufacturing or quality experience.
- Demonstrated cGMP knowledge and experience.
- Strong interpersonal, written, communication and problem solving skills.
- Must be well organized, flexible and able work with minimal supervision.

BONUS POINTS! OTHERWISE KNOWN AS PREFERRED QUALIFICATIONS:

- BS degree in Science in preferred.
- Prior experience with Quality Assurance Batch Record Review and/or Person-In-Plant is preferred.
- Strong background and skills in Quality, Manufacturing, communication and computer related systems are preferred.
- Experience with Deviation Investigations and Root Cause Analysis is a plus.
- Experience with Microsoft Word/Excel, SAP and TrackWise is a plus.

WHAT ARE YOU WAITING FOR? APPLY NOW!

RECRUITER: Joan Lowery

Yoh, a DayJ2W: CLINICAL

MONJOBJ2WPACNW

Ref:

SFSF: LS

Projektdetails

  • Einsatzort:

    San Carlos, Vereinigte Staaten

  • Projektbeginn:

    asap

  • Projektdauer:

    Keine Angabe

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Yoh