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Regulatory Affairs Specialist | Regulatory Affairs Specialist in Other Job Job at Monster in Saint1

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Regulatory Affairs Specialist

Location:
Saint Paul, MN
Description:

Hemostasis, LLC designs, develops, manufactures, and markets advanced hemostat, wound healing technologies, and advanced medical devices for use in the healthcare industry. We are currently seeking a Regulatory Affairs Specialist that will be able to ensure compliance with regulations. Responsibilities Include: Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, and clarification/follow-up of submissions under review. Provide technical review of data or reports that will be incorporated into regulatory submissions. Analyze validation test data to determine whether systems or processes have met validation criteria. Study product characteristics or customer requirements and confer with management to determine validation objectives and standards. Identify deviations from established product or process standards and provide recommendations for resolving deviations. Develop validation master plans, process flow diagrams, test cases, and standard operating procedures. Create, populate and maintain the database for tracking validation activities, test results and validation systems. Prepare, maintain, and review validation and compliance documentation such as engineering change notices, schematics, and technical files to obtain and sustain product approval. Conduct audits of validation or performance qualification processes to ensure compliance with internal or regulatory requirements. Prepare additional information or responses as requested by regulatory agencies. Research and interpret regulatory rules or rule changes and ensure they are communicated through company procedures. Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents. Recommend changes to company procedures in response to changes in regulations or standards. Advise team members on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues. Qualifications Master's degree in Regulatory Affairs and Services. Excellent written and oral communication skills. Demonstrate proactive and strategic thinking and be able to handle change and ambiguity. Competitive industry compensation based on experience 401K, Dental, Life, Medical, Disability Full-time in-office Hemostasis, LLC believes in the synergy of teamwork while maintaining an entrepreneurial spirit, providing an environment in which our associates develop and accomplish professional objectives. We offer a competitive salary and benefits package including health, life, retirement and related benefits.Apply today!PDN-9b7262e7-c7bc-4f19-a049-97361b3b6b7f
Company:
Monster
Industry:
Other
Posted:
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