The QA Associate supports Quality aspects and activities within their area of responsibility, helping to ensure and support overall GxP conformity and Compliance with the Telix Quality Management Systems for the Angleton manufacturing site with a focus on operational activities.
Responsibilities
Understand and adhere to GMP Policies
Prepare, review, and maintain quality documents within the QMS (MasterControl), including document control and lifecycle support
Support training management, ensuring training matrices and records are accurate and up to date in the QMS
Support internal and external audits, supplier quality activities, and CMO oversight, including document reviews, audits participation, and quality agreements
Assist functional areas with achieving timely and compliant final product dispositions of the product being manufactured
Requirements
Bachelor's degree in Life Sciences, Quality Management, or related field
The Regulatory Coordinator supports the implementation and maintenance of regulatory activities and programs within the Flight and Ambulance Services team, ensuring adherence to regulatory standards, internal policies, and best practices.
Compensation
The hourly range for this position is listed below. Actual hourly rate dependent upon experience. $25.39 - $40.00
Responsibilities
Support for state and federal licensing, credentialing and primary-source verification, regulatory and accreditation activities, audits, regulatory documentation and reporting, data integrity, education, and continuous readiness.
Collaborate with internal and external stakeholders to address regulatory requirements and maintain accurate, complete, and audit-ready records.
Identify and track documentation or regulatory discrepancies and trends to support correction, education, process improvement, and appropriate escalation.
Support regulatory education and training for caregivers, leaders, and other stakeholders based on assigned functions.
Collaborate on quality improvement and education initiatives.
Requirements
Associate’s degree or relevant professional licensure or certification
Nice to have: Medical Transport related role
Nice to have: Experience in reading and interpreting governmental statutes and regulations
Nice to have: Knowledge of Intermountain structure, operations, policies, and procedures
Nice to have: Leadership or supervisory experience in a healthcare setting
Medical Science Liaison – Oncology GU responsible for scientific engagement, relationship building, and support within the Tennessee & Arkansas territory.
Locations (2)
Nashville, Tennessee, United States
Arkansas, United States
Responsibilities
Develop and implement a scientific engagement plan for the territory
Cultivate strong professional relationships with community and academic opinion leaders
Engage in high quality, two‑way scientific exchange
Provide product and technical assistance and educational training to physicians
Leverage AI tools and insights to enhance decision making
Requirements
Doctorate level degree (PharmD, PhD, MD, Advanced Practice Providers)
Serves as the overall account lead for numerous accounts in an assigned geographic territory; focuses on driving value for the client while maximizing revenue and margin for the company.
Compensation
The expected salary/wage range for this position is provided below. Actual offer may vary from this range based upon geographic location, work experience, education/training, and/or skill level.
– United States of America: Annual Salary USD 198,000 - 465,500 in Washington
Responsibilities
Builds growth opportunities using the account planning process; actively manages planning process through scheduled reviews and updates.
Extensive time working with and leveraging external partners to deliver solution sale.
Significant percentage of time spent directly with customer; interfaces with all levels, including highest within customer organization.
Develops business plan in conjunction with customer.
Applies consultative-selling techniques to identify and advance opportunities that result in ongoing profitable revenue growth for the company.
Ensure that the product quality and site standards are maintained at all times and that the product meets the customer’s expectations and is legally compliant in all aspects.
Compensation
£15.45 p/h
Responsibilities
Ensure that intake checks are completed on all raw materials
Complete relevant paperwork, record and logs for Quality procedures
Conduct relevant audits
Regularly work with SOP’s
Shelf life analysis and NPD product testing as required
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