QA Associate | Quality Assurance Associate | GMP Quality Specialist

QA Associate | Quality Assurance Associate | GMP Quality Specialist

Immediate need for a talented QA Associate | Quality Assurance Associate | GMP Quality Specialist. This is a 06+ Months Contract opportunity with long-term potential and is located in Los Angeles, CA (Onsite).

Job
-25732 Pay Range: $40 - $44/hour. Traveler benefits as per agency package. (Benefits vary by vendor and assignment.).

Key Responsibilities:

• Provide QA oversight and approval of Deviations, OOS investigations, and Change Controls.
• Review quality records to ensure investigations are thorough, properly documented, and completed within required timelines.
• Provide QA oversight for CAPA and Effectiveness Verification (EV) records.
• Ensure quality events are appropriately escalated according to established procedures.
• Support investigations involving manufacturing processes, in-process products, final products, environmental conditions, facilities, equipment, and materials.
• Partner with Manufacturing and QC teams to identify root causes and implement appropriate corrective and preventive actions.
• Review and approve quality documentation in accordance with GMP requirements and site procedures.
• Identify opportunities to improve the efficiency and effectiveness of Deviation and CAPA processes while maintaining compliance.
• Support continuous improvement and quality system initiatives.
• Communicate effectively with cross-functional teams regarding quality risks, investigations, and required actions.
• Manage multiple quality activities and changing priorities in a fast-paced manufacturing environment.
• Perform additional QA duties as assigned.

Key Requirements and Technology

Experience:

• Master's degree in Biological Sciences or related field; OR
• Bachelor's degree in Biological Sciences or related field with 2+ years of relevant experience; OR
• Associate's degree with 4+ years of relevant experience; OR
• High School Diploma/GED with 5+ years of relevant experience.
• Required Experience
• Experience working in a GMP/cGMP regulated environment.
• Experience with one or more of the following:
• Deviations
• OOS / Out-of-Specification investigations
• CAPA
• Change Control
• Quality investigations
• Manufacturing quality support
• Strong understanding of GMP compliance and documentation.
• Ability to work effectively with cross-functional teams.
• Preferred Experience
• Biopharmaceutical, pharmaceutical, biotechnology, biologics, or cell/gene therapy experience.
• Quality Control experience in:
• Microbiology
• Virology
• Analytical testing
• Experience with U.S. and/or EU GMP requirements.
• Experience with manufacturing investigations and quality systems.
• Experience with root-cause analysis and corrective/preventive actions.
• Experience supporting environmental, facility, equipment, or material-related quality investigations.
• Strong proficiency with Microsoft Word, Excel, and PowerPoint.
• Excellent written and verbal communication skills.
• Strong organization and time-management abilities.

Our client is a leading IT Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.