What are the responsibilities and job description for the Animal Genetics Specialist position at Genus PLC?
Company Overview
pioneering animal genetic improvement to help nourish the world.
Our vision is clear: we aim to be a worldwide leader in porcine and bovine animal genetics, partnering with farmers to transform how we nourish the world for a sustainable future.
Job Description
The role involves reviewing and approving QMS-related activities such as SOP review and revision, staff training, document control, and creation of required reporting. You will also collaborate with R&D and product development teams to develop, maintain, and enhance compliance capabilities and relationships to support Genus product pipeline.
Key responsibilities include conducting periodic facility inspections and record audits of regulated analytical laboratories and production barns, determining compliance, and serving as the primary point of contact and representative of the Company for FDA-CVM audits and facility inspections.
You will provide solutions and guidance on implementation of solutions for out-of-scope operational defects, drawing from established principles and direction of business. You will also discern and communicate quality standards and parameters to R&D team, product development team, and other appropriate staff.
Requirements
You must have demonstrated experience in project management and compliance with regulations, excellent organizational and interpersonal skills, and the ability to work both autonomously and collaborate across teams and functional areas.
You should be able to work in and maintain performance expectations in diverse cultural contexts and fast-paced environments, with continual attention to detail and the ability to establish priorities and meet deadlines.
Benefits
pioneering animal genetic improvement to help nourish the world.
Our vision is clear: we aim to be a worldwide leader in porcine and bovine animal genetics, partnering with farmers to transform how we nourish the world for a sustainable future.
Job Description
The role involves reviewing and approving QMS-related activities such as SOP review and revision, staff training, document control, and creation of required reporting. You will also collaborate with R&D and product development teams to develop, maintain, and enhance compliance capabilities and relationships to support Genus product pipeline.
Key responsibilities include conducting periodic facility inspections and record audits of regulated analytical laboratories and production barns, determining compliance, and serving as the primary point of contact and representative of the Company for FDA-CVM audits and facility inspections.
You will provide solutions and guidance on implementation of solutions for out-of-scope operational defects, drawing from established principles and direction of business. You will also discern and communicate quality standards and parameters to R&D team, product development team, and other appropriate staff.
Requirements
You must have demonstrated experience in project management and compliance with regulations, excellent organizational and interpersonal skills, and the ability to work both autonomously and collaborate across teams and functional areas.
You should be able to work in and maintain performance expectations in diverse cultural contexts and fast-paced environments, with continual attention to detail and the ability to establish priorities and meet deadlines.
Benefits
