Quality Assurance Associate Job

QUALITY ASSURANCE ASSOCIATE needed for a contract opportunity with Yoh's client located in Thousand Oaks, CA.

The Big Picture - Top Skills You Should Possess:
- Perform sampling of chemical containers.
- Perform operations per GMP regulations.
- Perform Appearance and ID testing.

What You'll Be Doing:
- Perform sampling and inspection of incoming materials used in the production of pharmaceutical products.
- Assess physical attributes of material such as visual characteristics, dimensions, and label print accuracy to ensure conformance with specifications, procedures, and regulations.
- Perform sampling of chemical containers to obtain samples for laboratory analysis.
- Perform Appearance and ID testing during sampling process (ie NIR, Raman technology).
- Perform operations per GMP regulations including following detailed SOPs, maintaining training, maintain accurate inventory management, deviation reporting, and good documentation practices.
- Will work in multiple databases and will require experience with query and documentation using electronic database systems.
- Expected to communicate effectively, work well in teams, and demonstrate a science based approach and ability to focus on results.

WHAT YOU NEED TO BRING TO THE TABLE:
- Bachelor's Degree in Biochemistry, Biology, Chemistry or related science field and two (2) years of experience in GMP operations or similarly regulated industry.
- Demonstrated ability to use computer databases for query of data, managing batch status, and input of data and documentation.
- Ability to focus on detail and ensure accuracy of execution tasks, documentation per GMP standards.
- Must be able to lift and carry containers and boxes up to 25lbs.
- Effective verbal and written communication skills, strong interpersonal skills.

Bonus Points! Otherwise Known As Preferred Qualifications:
- Three (3+) years of experience performing incoming material receipt and approval in a GMP/GLP function.
- Previous experience in quality systems (SAP, LIMS, CCMS, Trackwise, EDMQ).
- Experience in supporting GMP functions such as QC, supplier quality management, material dispensing, manufacturing.
- Experience in supporting Analytical Testing such as NIR, FTIR, Ramman ID testing process.
- Strong technical writing skills, demonstrated experience creating procedures, deviation reports, specifications, technical assessments or equivalent.
- Need three (3+) years of experience performing incoming material receipt, sampling and inspection processes in a GMP/GLP function.

WHAT ARE YOU WAITING FOR? APPLY NOW!

RECRUITER: Salima Hakim

Yoh, a DayJ2W: CLINICAL

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