Associate Quality Assurance III Job

Yoh has a contract opportunity for ASSOCIATE QUALITY ASSURANCE III to join our client in Thousand Oaks, CA.

JOB RESPONSIBILITIES:

- Primary job duties are to author new/revised raw material specifications that comply with regulatory requirements.
- Depending on the knowledge, experience, and team resources, the individual may perform any combination of the following duties as a member of the Clinical Supplier Quality team:
- Work on projects to support continuous improvement activities for raw materials processes
- Revise raw material specifications to meet current requirements.

JOB QUALIFICATIONS:

- Demonstrated ability to perform GMP operations including following detailed SOPs, maintaining training, and good documentation practices.
- Educated in a science field with five (5) years of experience in GMP/GCP operations or similarly regulated industry.
- Bachelor's degree and two (2) years of directly related experience OR
- Associate's degree and six (6) years of directly related experience OR
- High school diploma/GED and eight (8) years of directly related experience.
- Bachelor's Degree in Biochemistry, Biology, Chemistry or related science field.
- One (1) or more years of experience in a Quality Assurance or related role, (ie. supporting GMP functions such as Demonstrated science based approach and ability to deliver results).
- Experience working in multiple GMP databases.
- This position requires effective communication, ability to work well in teams, demonstrated science based approach and ability to deliver results.
- The successful candidate will have experience working in a GMP role.
- Ability to focus on detail and ensure accuracy of execution tasks, documentation per GMP standards.
- Effective verbal and written communication skills, strong interpersonal skills.
- Ability to complete tasks autonomously, provide updates to area manager, and identify potential issues.
- Demonstrated ability to perform GMP operations including following detailed SOPs, maintaining training, and good documentation practices.
- Experience in Change Control records and with specifications.
- Demonstrated ability to use computer databases for query of data, managing status, and input of data and documentation.
- Previous experience in quality systems (SAP, LIMS, Change Control (CCMS), Trackwise, EDMQ) is a plus.
- Ability to focus on detail and ensure accuracy of execution tasks, documentation per GMP standards.
- Effective verbal and technical written communication skills, strong interpersonal skills to articulate quality requirements and rationale to others.
- Strong team player.

DISCOVER ALL THAT'S POSSIBLE WITH YOH. APPLY NOW.

RECRUITER: Salima Hakim

Yoh is a professional staffing provider with over 70 years of experience in the short- and long-term staffing services industry.

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

J2W: SCIENTIFIC; J2W: CLINICAL

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