Medgene Labs has a single mission: To be a world-class Immunological Services Provider™ for leading livestock producers and their veterinarians. POSITION SUMMARY Medgene Labs seeks a Quality Assurance Technician, who is responsible for Quality Assurance functions for a veterinary vaccine production company.
The successful candidate will be responsible for developing, improving, and adhering to quality assurance goals and systems, including prioritization, and providing quality oversight for a manufacturing facility. This position will report to the Quality Assurance Manager. Professional and experienced in handling a wide range of Quality Assurance responsibilities. Able to work independently
with little or no supervision. JOB DUTIES The Quality Assurance Technician, as a member of the Compliance Team, is responsible for ensuring quality assurance by ensuring processes and personnel activities are compliant with company policy and governing regulations.
Operations Provide document support to team members who produce batches and serials releases. Perform production batch and serial releases. Generation and quality approval of deviation investigation and auditing records Review of regulatory documentation such as Outlines of Production, Special Outlines, and labels. Communicate between departments to ensure projects are started, executed, and finished according to regulations
and company policies. Coordinate with Regulations regarding facility documentation and equipment to ensure compliance.
Support the document management system related to manufacturing. Auditing functions of facilities, processes, and inventories as prescribed Review of internal Master Documents Process improvement Management of the internal training program Management and internal release of raw materials Assist in internal and external audits. Organization Manage regulated labels including production and inventory. Support Manufacturing in the movement of products through computer systems Provide support in Quality Assurance activities such as Change Controls, Deviations, and Document Management Develop and implement workflows and processes.
Manage the internal inventory system of inputs and final products. Review end-user records for the accuracy of implemented operations Training and Support Conduct a review of the adequacy and effectiveness of the Quality Management System Support and encourage a Quality Culture. Create, monitor, and train internal processes. Perform additional duties as required. MINIMUM QUALIFICATIONS: Knowledge of: Interest in vaccine licensing practices and procedures Interest in science and biotechnology Proven office management, administrative, or assistant experience Knowledge of office management responsibilities, systems, and procedures Excellent time management skills and ability to multi-task and prioritize work.
Attention to detail and problem-solving skills. Excellent written and verbal communication skills Strong organizational and planning skills Proficient in MS Office Knowledge of data and administrative management practices and procedures Knowledge of clerical practices and procedures Ability to: Follow detailed directions and instructions. Communicate information clearly and concisely. Establish and maintain effective relationships with coworkers. Job Posted by Applicant Pro
