Randstad Life Sciences US
Quality Assurance (QA) Senior Associate
Randstad Life Sciences US, Thousand Oaks, California, United States, 91362
Overview
Quality Assurance (QA) Senior Associate role at Randstad Life Sciences US. Provides daily compliance oversight on the manufacturing floor, ensuring adherence to GMP standards. Duties include purposeful presence on the floor, electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations. Responsibilities include evaluation of compliance issues, providing recommendations, and ensuring progress of quality records to completion. Responsibilities
Maintain a purposeful and visible presence on the manufacturing floor to support real-time quality oversight, including inspection support, ASP, and QA assessments. Conduct electronic batch record reviews and provide QA approval for SOP revisions. Approve work orders and job plans within the Maximo System. Provide timely quality support and approval for minor deviations and CAPAs. Review and approve Manufacturing Execution System (MES) changes. Identify and evaluate compliance issues; provide recommendations and monitor progress of quality records to closure. Represent Plant QA in cross-functional team projects to achieve departmental operational goals. Partner effectively in a team matrix environment with manufacturing operators, engineers, and leadership to ensure best practices in quality culture and GMP compliance. Qualifications
Bachelor's Degree (BS) in Biochemistry, Biology, Chemistry, or related science field. 1-2+ years of hands-on experience in a regulated GMP environment, preferably within the pharmaceutical, biotech, or food industries. Demonstrated ability to perform GMP operations including following detailed SOPs, maintaining training, and good documentation practices. Ability to make quality-based decisions to ensure compliance. Experience managing projects through to completion and meeting timelines. Evaluating documentation and operations according to company procedures. Experience working with Quality Systems. Strong organizational skills and ability to manage multiple tasks. Effective communication skills (both written and verbal). Demonstrated ability to work as both a team player and independently. Display leadership attributes and drive improvement initiatives. Preferred
Manufacturing floor experience in a GMP environment. Location: Newbury Park, California | Job type: Contract | Salary: $30.00 - $37.44 per hour | Work hours: 9 to 5 | Education: Bachelors Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. Randstad provides accommodations on request to applicants with disabilities. For accommodations, contact HRsupport@randstadusa.com. #J-18808-Ljbffr
Quality Assurance (QA) Senior Associate role at Randstad Life Sciences US. Provides daily compliance oversight on the manufacturing floor, ensuring adherence to GMP standards. Duties include purposeful presence on the floor, electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations. Responsibilities include evaluation of compliance issues, providing recommendations, and ensuring progress of quality records to completion. Responsibilities
Maintain a purposeful and visible presence on the manufacturing floor to support real-time quality oversight, including inspection support, ASP, and QA assessments. Conduct electronic batch record reviews and provide QA approval for SOP revisions. Approve work orders and job plans within the Maximo System. Provide timely quality support and approval for minor deviations and CAPAs. Review and approve Manufacturing Execution System (MES) changes. Identify and evaluate compliance issues; provide recommendations and monitor progress of quality records to closure. Represent Plant QA in cross-functional team projects to achieve departmental operational goals. Partner effectively in a team matrix environment with manufacturing operators, engineers, and leadership to ensure best practices in quality culture and GMP compliance. Qualifications
Bachelor's Degree (BS) in Biochemistry, Biology, Chemistry, or related science field. 1-2+ years of hands-on experience in a regulated GMP environment, preferably within the pharmaceutical, biotech, or food industries. Demonstrated ability to perform GMP operations including following detailed SOPs, maintaining training, and good documentation practices. Ability to make quality-based decisions to ensure compliance. Experience managing projects through to completion and meeting timelines. Evaluating documentation and operations according to company procedures. Experience working with Quality Systems. Strong organizational skills and ability to manage multiple tasks. Effective communication skills (both written and verbal). Demonstrated ability to work as both a team player and independently. Display leadership attributes and drive improvement initiatives. Preferred
Manufacturing floor experience in a GMP environment. Location: Newbury Park, California | Job type: Contract | Salary: $30.00 - $37.44 per hour | Work hours: 9 to 5 | Education: Bachelors Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. Randstad provides accommodations on request to applicants with disabilities. For accommodations, contact HRsupport@randstadusa.com. #J-18808-Ljbffr