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Medgene
Brookings, SD | Full Time
$84k-101k (estimate)
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Medgene Labs
Brookings, SD | Full Time
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Quality Assurance Technician
Medgene Brookings, SD
$84k-101k (estimate)
Full Time 1 Week Ago
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Medgene is Hiring a Quality Assurance Technician Near Brookings, SD

Company DescriptionMedgene Labs helps veterinarians and producers protect livestock with precisely constructed immunological products and services. Applying a strategy of continual diagnostic surveillance and data analytics to the practice of immunology, creating vaccines for the disease at hand quicker and more precisely than previously possible. Medgene Labs has a single mission: To be a world-class Immunological Services Providerâ„¢ for leading livestock producers and their veterinarians.
Position SummaryMedgene 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 DutiesThe 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 QualificationsKnowledge 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 ApplicantPro

Job Summary

JOB TYPE

Full Time

SALARY

$84k-101k (estimate)

POST DATE

05/23/2024

EXPIRATION DATE

06/08/2024

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