QA Operations Lead

Telix Pharmaceuticals (AMER)•Angleton, TX

1d•Hybrid

About The Position

The QA Operations Lead is responsible for managing quality-related activities and projects within their area of responsibility, with a primary focus on manufacturing operations at the Angleton site. This role ensures GxP compliance and alignment with IsoTherapeutics’ Quality Management Systems, while supporting overall quality oversight of operational activities. The position partners closely with site operations to maintain compliance, support day‑to‑day execution, and uphold regulatory and quality standards across radiopharmaceutical manufacturing activities.

Requirements

Bachelor’s degree in Life Sciences, Quality Management, or related field
5+ years of experience in quality assurance role
Experience in GxP manufacturing operations is requested
Cross functional collaboration is a requirement for the position
Ability to work in a team environment and communicate effectively with diverse groups.
Willingness to work with radioactive materials and follow strict safety protocols is required.
Technical understanding of manufacturing, quality and regulatory requirements,
Previous experience writing and reviewing with understanding SOPs and specifications,

Nice To Haves

Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

Responsibilities

Provide manufacturing quality oversight of all production, quality control, and supply chain departments to monitor all work according to requirements under ITG quality system.
Review and evaluate all standard operating procedures, batch records and quality control results to ensure compliance with ITG quality and regulatory.
Perform live review of manufacturing batch records in preparation for batch release and escalate any exceptions immediately as requested by the quality system of the site.
Assist functional areas with achieving timely and compliant final product dispositions of the product being manufactured.
Participate in writing, implementing and approving Deviations, Investigations, CAPA Change Control and complaint reports.
Ensure compliance of site personnel and application of aseptic techniques and full compliance to sterile manufacturing regulations.
Participate in the management of supplier, vendor assurance activities and supplier quality agreements.
Lead FDA/Regulatory interactions for the Angleton site activities and products to ensure successful regulatory submissions and inspections.
Lead QA Operations as a valued business partner, with a culture of safety, quality, delivery to patients, cost, compliance and data integrity.
Provide support to cross-functional team and Assist other departments exception management for compliance and timely closure of exceptions.