VIVOS Professional Services, LLC · 16 hours ago
Quality Technician - Intermediate
Port Allen, LA
Contract
Onsite
Mid Level
$22/hr - $25/hrVIVOS Professional Services, LLC is seeking a Quality Technician - Intermediate to ensure compliance with Good Manufacturing Practices (cGMPs) in the manufacturing and processing of pharmaceutical ingredients and medical devices. The role involves performing inspections, monitoring manufacturing processes, and supporting quality audit functions to maintain product quality and integrity.
Staffing & Recruiting
Hiring Manager
Praduman J.
Responsibilities
Perform area/line clearances, in-process inspections, and inspection/disposition of incoming material
Monitor manufacturing process performance as it relates to SPC/SQC, compliance of manufacturing/warehouse areas, and proper control of components, products, or equipment not in compliance
Prepare and attach material quality status labels
Verify all labels after final printing
Execute assigned activities according to production schedules and participate in schedule planning as needed
Assist in developing, implementing, and maintaining site quality procedures, standards, and controls
Support quality audit functions, occasionally conducting investigations of nonconformances/deviations and assisting with CAPAs
Perform tasks ensuring products meet established standards for quality and efficacy
Complete special projects assigned by supervisor to meet company and departmental goals
Perform chemical analysis of raw materials, in-process materials, finished drug products, stability samples, validation samples, and R&D samples in accordance with OSHA, EPA, FDA, cGMP, and other regulatory requirements
Collect, handle, and document raw materials, reagents, laboratory standards, and sample vessels (including handling compressed gas cylinders)
Calibrate and perform preventive maintenance on analytical instruments per regulatory requirements
Review work completed by other analysts
Perform routine housekeeping; create and submit HOLD alerts, work orders, etc., as needed
Perform special projects assigned by supervisor to support departmental and company goals
Qualification
Required
Associate's Degree in a technical or scientific field required
Understanding of drug cGMPs, OSHA, EPA, and FDA regulations related to drug and medical device manufacturing
Proficiency in Microsoft Word and Excel
Strong mathematical skills
Mechanical aptitude
Excellent oral, written, interpersonal, and organizational communication skills
Detail-oriented with strong team ethics
Collaborative and tactful; able to communicate across organizational levels
Assertive in enforcing regulations, policies, and procedures
Basic knowledge of laboratory analyzers and inspection equipment used for chemical analyses and component inspections
Preferred
Bachelor's Degree (preferably in a science-related field) preferred
Experience in a regulated environment preferred
Quality certification (ASQ CQE, CQA, etc.) preferred
Company
VIVOS Professional Services, LLC
VIVOS Professional Services (a Kellton Company) is a premier professional workforce solutions firm.
Founded in 1999
1001-5000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase