Quality Assurance Systems Specialist

Creative Solutions Services, LLC; Houston (TX); On-site; USD 28,000 - 41,000; Full time

Benefits offered by this job

Weekly pay

Medical insurance

Dental insurance

Vision insurance

Job summary

Creative Solutions Services, LLC is seeking a Quality Assurance Systems Specialist onsite in Houston to support deviation investigations and CAPA activities. You will gather data from multiple sources, perform root cause analyses, assess impact to SISQP, trend results, and lead corrective actions to prevent recurrence.

The role involves coordinating with cross-functional teams on the manufacturing floor, facilitating meetings, and delivering status updates to leadership while under a six‑month

Responsibilities

• Gather data from on-site sources, perform RCA to identify deviation root cause and assess impact to SISQP; trend analysis; identify CAPAs.
• Manage multiple projects/timelines concurrently; adhere to schedules and escalate actions; participate in Daily Management meetings to update leaders.
• Interact with customers; prepare PowerPoint status updates; lead alignment meetings; discuss CAPAs and resolve comments.
• Work on the manufacturing floor to gather data, observe processes, and interview associates.
• Facilitate meetings with cross-functional teams; resolve complex conflicts; lead deviation review board meetings.

Job description

Quality Assurance Systems Specialist

Location: 14905 Kirby Drive HoustonTexas77047

Contract Duration:6 Months (Potential for Extension or Full-Time Conversion)

Pay Rate:$25/hr (W2)

Benefits:Weekly Pay, Medical, Dental, and Vision Insurance

Working Model-Fully Onsite

Summary: The Deviation Investigator/Initiator Level II is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.

JOB DESCRIPTION

• Gathering Data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation, assessment of event for impact to Safety Identity Strength Quality Purity (SISQP), perform trending analysis, identification of Corrective and Preventative Actions to reduce deviation recurrence, performance of Risk Assessments, Causing Mapping, Interviewing.
• Management of multiple projects and timelines concurrently. Ability to adhere to standard timeline, and elevate actions appropriately for resolution in a timely manner. Participation in the Daily Management meetings to update leadership or current deviation statuses.
• Routine interaction with the customer, including compilation of Power Points to communicate investigational current status, Alignment meetings, facilitated reviews, CAPA discussions, Comments resolution.
• Work on the manufacturing floor for data gathering, observing of processes for investigations, and performance of associate interviews.
• Meeting Facilitation and participation, aligning internal review team and area subject matter experts on an agreed to investigational path forward. Complex Conflict resolution, problem solving in a cross functional setting, and ability to keep the meeting on track to achieve objectives of varying difficulty. Attendance and occasional leadership of the daily management system, and participating/leading the deviation review board.

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