• To implement the Client's Regulatory Compliance Program designed to assure the adherence of facilities, operations, studies, reports and practices to regulations (e.g. FDA, EMEA, NRC, DEA USDA) as well as to the Client's Standard Operating Procedures (SOPs), Client policies, regulatory guidelines and good scientific and documentation practices.
• To inform the Client's Management of deviations from the cGMP, GLP, other Regulations observed during audits/inspections, to recommend appropriate corrective action when necessary and to verify that appropriate corrective actions have been implemented that adequately address any deviations reported during inspections.
• As an employee of the Client, you will actively contribute to the discovery, development and delivery of our products to our patients and customers.
• Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people.
• We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance.

Duties & Responsibilities:

• Review procedures for compliance to GxP requirements and Company standards.
• Conduct audits to support GLP studies (e.g. protocol, amendment, study data, Principal Investigator reports such as Toxicokinetic reports, etc.).
• Issue electronic audit reports and perform follow-up actions.
• Scan study records to facilitate audit requests.
• Monitor and update electronic system with new audit requests.
• Update the GLP Master Schedule as needed.
• Conduct internal facility audits as needed.
• Provide support during corporate audit and regulatory inspections as needed.