QC Analyst

Job Title: QC Analyst III
Location: 1000 New Horizons way, Vacaville. CA - 95688
Duration: 12+ months contract (with possibility for extension or FTE conversion)
Shift: Monday - Friday 8 Hours shift 8:00 am to 4:30 pm
Payrate: $16.97 - $27.93 per hr. on W2 paid weekly, along with Vision, Dental and Medical Benefits.

Job Description:
Today, *** is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Job Summary
The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw materials, and stability lots for customers. Their primary role will be to participate in quality reagent preparation and inventory management for all testing in order to achieve on-time, high quality results to meet ***’s manufacturing demands. Responsibilities (e.g., testing, review) can expand to all other functional areas of QC as needed. A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are both routine and semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.

Key Responsibilities
Preparing reagents to support testing for in-process, lot release and stability studies.
Manage and improve the laboratory inventory processes to enable all laboratory operations
Reviewing GMP documentation
Writing quality records (Deviations, CAPA, Change Control) and test methods.
Performs other duties as assigned
Use of Microsoft Suites (e.g., Word, Excel, PowerPoint).
Use of Laboratory computer systems.
Works on assignments that are semi-routine in nature where the ability to recognize deviation from accepted practice is required.
Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Apply Data Integrity principles in all aspects of work, in compliance with *** DI policies, guidelines and procedures.

Key Requirements
Bachelor's degree preferred.
Relevant QC work experience preferred, such as:
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Potential previous use of GMP Quality Systems such as: TrackWise, LIMS.
Solid ability to speak publicly.
Solid ability to interpret data.
Perform assigned, complex and/or varied tasks with guidance from Supervisor.
Prioritization and problem solving.
Comprehend and follow instructions.
Direct, control and plan tasks/projects.
Brainstorming.

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