Full-Time
Quality Control Specialist
Updated on 9/12/2026
Telix Pharmaceuticals
1,001-5,000 employees
Develops targeted radiation diagnostics and therapies
No salary listed
Angleton, TX, USA
Hybrid
Bachelor's
 Biology & Biotech (1) |
|---|
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- A minimum of a Bachelor's degree in chemistry, biochemistry, biology, or a related field is required.
- At least 3 years of experience in a laboratory role within a good manufacturing practice environment is required.
- Experience in good practice manufacturing operations is preferred.
- Experience performing proper aseptic technique in controlled areas is preferred.
- Willingness to work with radioactive materials and follow strict safety protocols is required.
- Cross-functional collaboration is required.
- Ability to work in a team environment and communicate effectively with diverse groups is required.
- Execute analytical and biological testing in support of good manufacturing practice manufacturing operations at the radiopharmaceutical facility.
- Execute laboratory operations in compliance with good manufacturing practice principles, data integrity, and applicable good laboratory practices.
- Escalate all quality events and investigations to management in a timely manner.
- Perform quality control testing on radioactive material.
- Identify areas of improvement for laboratory and testing processes.
- Complete routine documentation in compliance with good documentation practices.
- Execute method validation activities, including method development and qualification.
- Review quality control testing data for accuracy to support the batch release process for monoclonal antibodies and small molecules.
- Participate in and perform laboratory investigations, including out-of-specification investigations and deviations, manage change control, and implement associated corrective and preventive actions.
- Manage quality control materials, including consumables and chemicals.
- Manage laboratory equipment, including maintenance, calibration, qualification, requalification, and installation.
- Write and update Quality Control procedures.
- Ensure site personnel comply with aseptic techniques and good manufacturing practice principles.
- Support Food and Drug Administration and regulatory interactions for Angleton site activities and products to support regulatory submissions and inspections.
- Assist Quality Assurance and other departments with investigations and timely investigation closure.
- Understand and adhere to good manufacturing practice policies and procedures.
- Experience in good practice manufacturing operations.
- Experience performing proper aseptic technique in controlled areas.
Telix Pharmaceuticals develops and commercializes diagnostic and therapeutic products that use targeted radiation to diagnose and treat cancer and rare diseases. Its pipeline covers urologic oncology (prostate and kidney cancers), neuro-oncology (glioma), musculoskeletal oncology (sarcoma), and bone marrow conditioning. The treatments work by delivering targeted radiation to diseased tissues, enabling more precise decisions for treatment and allowing for personalized therapy. The company differentiates itself through a global, robust supply chain and a focus on integrating diagnostic and therapeutic options to address unmet medical needs, along with strong commitments to patient care, ethical practices, and environmental responsibility. Telix’s goal is to improve quality of life and outcomes for patients by providing targeted, clinically meaningful diagnostic and therapeutic solutions that support better treatment decisions and personalized care.
Company Size
1,001-5,000
Company Stage
IPO
Headquarters
Melbourne, Australia
Founded
2015
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Simplify's Take
What believers are saying
- Telix reported US$477 million first-half 2026 revenue, up 22%, and raised R&D spending.
- Pixclara’s resubmitted NDA was accepted in April 2026, creating a near-term brain-cancer catalyst.
- Regeneron paid US$40 million upfront, validating Telix’s radiopharmaceutical platform and partnership appeal.
What critics are saying
- Zircaix received FDA CMC rejection in 2026; manufacturing fixes gate any kidney-cancer launch.
- Telix faces securities litigation over SEC subpoenas and alleged manufacturing misstatements from 2025.
- Pixclara’s September 11, 2026 PDUFA is existential; another rejection damages credibility and financing.
What makes Telix Pharmaceuticals unique
- Illuccix and Gozellix anchor a two-product PSMA imaging franchise across 22 countries.
- Telix pairs diagnostics and therapies, creating patient-selection moats in radiopharmaceutical oncology.
- ProstACT SELECT publication strengthened TLX591-Tx’s theranostic positioning before ProstACT Global readouts.
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Benefits
Annual Performance Bonus
Equity-Based Incentive Program
Paid Vacation
Paid Wellness Days
Hybrid Work Options
Remote Work Options
Growth & Insights and Company News
6 month growth
↑ 0%1 year growth
↑ 16%2 year growth
↑ 2%The End Brain Cancer Initiative partners with Telix Pharmaceuticals for TLX101-Px (pixclara(r) and PDUFA awareness. September 03, 2026, 14:00 GMT SEATTLE, WA, UNITED STATES, September 3, 2026 / EINPresswire.com / - The FDA has set a Prescription Drug User Fee Act (PDUFA) review goal date of September 11, 2026, for TLX101-Px (Pixclara (R)), an investigational PET imaging agent developed by Telix Pharmaceuticals to help doctors evaluate brain cancer. The End Brain Cancer Initiative (EBCI) has partnered with Telix Pharmaceuticals to develop and provide patient disease education around TLX101-Px (Pixclara (R)), what a PDUFA date is, and why it matters to patients. A PDUFA date is the target date established by the U.S. Food and Drug Administration (FDA) for completing its review of a new drug or medical product application and determining whether it can be approved for use in the United States. PDUFA stands for the Prescription Drug User Fee Act, which helps provide the FDA with resources to review new drug applications within established timelines. By the PDUFA target date of September 11th, the FDA is expected to complete its review and may approve TELIX's application, request additional information or requirements before approval, or take another regulatory action that affects the review timeline. A PDUFA date is therefore not a guaranteed approval date, but it is an important milestone for everyone following the development of a potentially meaningful new option for people affected, in this case, by brain cancer. Patients, caregivers, healthcare providers, and the general public who would like more information about TLX101-Px (Pixclara (R)) or PDUFA should visit https://endbraincancer.org/telix/. People can also directly contact EBCI's Clinical Research Coordinator and Patient Navigator, Shreya Prakash, at [email protected] or at 425-436-8688. About Telix Pharmaceuticals Telix Pharmaceuticals uses a radioactive isotope as a payload, attached to a targeting agent, such as a small molecule or antibody, with an affinity for targeted biomarkers on the surface of cancerous or diseased cells. Depending on the choice of radioisotope payload, either imaging or therapy can be delivered. This specificity of the targeting agent is designed to concentrate radiation at the tumor sites and to limit off-target tissue exposure. For more information, visit the company's website at https://telixpharma.com/. About the End Brain Cancer Initiative To support/donate to the End Brain Cancer Initiative's increased access and health delivery for patients, mission, services and programs, please visit EndBrainCancer.org and make a donation today. The End Brain Cancer Initiative (EBCI) is a 501(c)3 non-profit patient advocacy organization focused on disease education, awareness, outreach, increasing patient access and improving Standard of Care. The End Brain Cancer Initiative, formerly known as the Chris Elliott Fund (CEF), is dedicated to ensuring that all patients diagnosed with brain cancer, a brain tumor, or metastatic disease to the brain have equal access to advanced diagnostics, treatments, specialists, and clinical trial participation. We believe that IMMEDIATE ACCESS to these options provides this patient community with the best HOPE for survival and sustained quality of life. We partner with industry, patients, researchers, advocacy groups, medical teams, hospital networks and others to educate patients and their caregivers so they can have empowered conversations with their medical teams. Learn more about the End Brain Cancer Initiative or how to sponsor this annual campaign at EndBrainCancer.org. Dellann Elliott Mydland, End Brain Cancer Initiative, 425-785-8489, [email protected] Dellann Elliott Mydland End Brain Cancer Initiative +1 425-785-8489 email us here Visit us on social media: LinkedIn Instagram Facebook YouTube X Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above. You just read: September 03, 2026, 14:00 GMT EIN Presswire's priority is author transparency. We do our best to weed out false and misleading content. The content above is the sole responsibility of the author who makes it available. If you have any complaints, kindly contact the author above. Dellann Elliott Mydland End Brain Cancer Initiative +1 425-785-8489
The End Brain Cancer Initiative partners with Telix Pharmaceuticals for TLX101-Px (pixclara(r) and PDUFA awareness. SEATTLE, WA, UNITED STATES, September 3, 2026 / EINPresswire.com / - The FDA has set a Prescription Drug User Fee Act (PDUFA) review goal date of September 11, 2026, for TLX101-Px (Pixclara (R)), an investigational PET imaging agent developed by Telix Pharmaceuticals to help doctors evaluate brain cancer. The End Brain Cancer Initiative (EBCI) has partnered with Telix Pharmaceuticals to develop and provide patient disease education around TLX101-Px (Pixclara (R)), what a PDUFA date is, and why it matters to patients. A PDUFA date is the target date established by the U.S. Food and Drug Administration (FDA) for completing its review of a new drug or medical product application and determining whether it can be approved for use in the United States. PDUFA stands for the Prescription Drug User Fee Act, which helps provide the FDA with resources to review new drug applications within established timelines. By the PDUFA target date of September 11th, the FDA is expected to complete its review and may approve TELIX's application, request additional information or requirements before approval, or take another regulatory action that affects the review timeline. A PDUFA date is therefore not a guaranteed approval date, but it is an important milestone for everyone following the development of a potentially meaningful new option for people affected, in this case, by brain cancer. Patients, caregivers, healthcare providers, and the general public who would like more information about TLX101-Px (Pixclara (R)) or PDUFA should visit https://endbraincancer.org/telix/. People can also directly contact EBCI's Clinical Research Coordinator and Patient Navigator, Shreya Prakash, at [email protected] or at 425-436-8688. About Telix Pharmaceuticals Telix Pharmaceuticals uses a radioactive isotope as a payload, attached to a targeting agent, such as a small molecule or antibody, with an affinity for targeted biomarkers on the surface of cancerous or diseased cells. Depending on the choice of radioisotope payload, either imaging or therapy can be delivered. This specificity of the targeting agent is designed to concentrate radiation at the tumor sites and to limit off-target tissue exposure. For more information, visit the company's website at https://telixpharma.com/. About the End Brain Cancer Initiative To support/donate to the End Brain Cancer Initiative's increased access and health delivery for patients, mission, services and programs, please visit EndBrainCancer.org and make a donation today. The End Brain Cancer Initiative (EBCI) is a 501(c)3 non-profit patient advocacy organization focused on disease education, awareness, outreach, increasing patient access and improving Standard of Care. The End Brain Cancer Initiative, formerly known as the Chris Elliott Fund (CEF), is dedicated to ensuring that all patients diagnosed with brain cancer, a brain tumor, or metastatic disease to the brain have equal access to advanced diagnostics, treatments, specialists, and clinical trial participation. Healthcare Industry Today believe that IMMEDIATE ACCESS to these options provides this patient community with the best HOPE for survival and sustained quality of life. Healthcare Industry Today partner with industry, patients, researchers, advocacy groups, medical teams, hospital networks and others to educate patients and their caregivers so they can have empowered conversations with their medical teams. Learn more about the End Brain Cancer Initiative or how to sponsor this annual campaign at EndBrainCancer.org. Dellann Elliott Mydland, End Brain Cancer Initiative, 425-785-8489, [email protected] Dellann Elliott Mydland End Brain Cancer Initiative +1 425-785-8489 email Healthcare Industry Today here Visit Healthcare Industry Today on social media: LinkedIn Instagram Facebook YouTube X Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. Healthcare Industry Today do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.
Telix Appoints David Gill as Chair TMCnet News [August 31, 2026] | / | Telix Appoints David Gill as Chair * David Gill appointed Chair of the Telix Board, effective immediately. * Mr. Gill joined Telix as a Non-Executive Director in May 2026, with the intention that he would become Chair. * Dr. Mark Nelson will continue to serve on the Board as a Non-Executive Director, having served as interim Chair. MELBOURNE, Australia and INDIANAPOLIS, Sept. 01, 2026 (GLOBE NEWSWIRE) - Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, "Telix" or the "Company") today announces that David Gill has been appointed Chair of the Board, effective immediately. Mr. Gill joined Telix as a Non-Executive Director in May 2026 as part of the Company's Board expansion and succession planning[1], with the intention that he would be appointed Chair in due course. He succeeds Dr. Mark Nelson, who has served as interim Chair and will remain on the Board as a Non-Executive Director. Mr. Gill is a life sciences executive with over 35 years' experience in senior general management and financial leadership roles across commercial and clinical-stage biopharmaceutical (including radiopharmaceutical development, manufacturing and supply chain) and medical device companies. He currently serves on the boards of Evolus, Inc. (NASDAQ: EOLS), Allucent LLC, Bridge to Life Ltd, RapidPulse Inc., and huMannity Medtec. Mr. Gill brings deep expertise in capital markets, scaling businesses, governance and corporate turnaround strategy and has served as Chief Financial Officer or President of multiple publicly traded companies, including EndoChoice Holdings, Inc. (acquired by Boston Scientific), INC Research (now Syneos Health), and CTI Molecular Imaging (acquired by Siemens). He holds a B.S. in Accounting from Wake Forest University and an MBA from Emory University. Telix Managing Director and Group CEO, Dr. Christian Behrenbruch, said, "I am delighted to welcome David as Chair of Telix. His global life sciences leadership - including extensive experience in radiopharmaceuticals - along with financial and capital markets expertise, will be invaluable as Telix continues to scale. I would also like to thank Mark for his leadership as interim Chair and look forward to his continued contribution as a Non-Executive Director." About Telix Pharmaceuticals Limited Telix Pharmaceuticals (ASX: TLX, NASDAQ: TLX) is a commercial-stage global radiopharmaceutical company, advancing targeted theranostics to improve outcomes for people with cancer across the patient journey. Theranostics pairs a precision diagnostic with a targeted therapy to both diagnose and treat disease. Telix's commercial franchise is anchored by its prostate cancer imaging portfolio: Illuccix(R)(kit for the preparation of gallium-68 gozetotide injection), commercially available in 22 countries including the U.S. and Gozellix(R)(kit for the preparation of gallium-68 gozetotide injection), approved by the U.S. Food and Drug Administration (FDA). The Company's late-stage therapeutic pipeline includes three investigational assets in pivotal-stage trials: TLX591-Tx (lutetium-177 ([177] Lu) rosopatamab tetraxetan) in prostate cancer, TLX101-Tx ([131] I-iodofalan) in recurrent glioblastoma, and TLX250-Tx (lutetium ([177] Lu) girentuximab tetraxetan) in kidney cancer, additionally complemented by a deep pipeline of next generation candidates. Telix is headquartered in Melbourne, Australia, with operations across North America, Europe, Latin America and Asia-Pacific. For more information, visit www.telixpharma.com or follow Telix on LinkedIn, X and Facebook. Investor Relations Annie Kasparian [email protected] Charlene Jaw [email protected] This announcement has been authorized for release by the Telix Pharmaceuticals Limited Disclosure Committee on behalf of the Board. Legal Notices Cautionary Statement Regarding Forward-Looking Statements. You should read this announcement together with its risk factors, as disclosed in its most recently filed reports with the Australian Securities Exchange (ASX), U.S. Securities and Exchange Commission (SEC), including its Annual Report on Form 20-F filed with the SEC, or on its website. The information contained in this announcement is not intended to be an offer for subscription, invitation or recommendation with respect to securities of Telix Pharmaceuticals Limited (Telix) in any jurisdiction, including the United States. The information and opinions contained in this announcement are subject to change without notification. ?To the maximum extent permitted by law, Telix disclaims any obligation or undertaking to update or revise any information or opinions contained in this announcement, including any forward-looking statements (as referred to below), whether as a result of new information, future developments, a change in expectations or assumptions, or otherwise. No representation or warranty, express or implied, is made in relation to the accuracy or completeness of the information contained or opinions expressed in the course of this announcement. This announcement may contain forward-looking statements, including within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that relate to anticipated future events, financial performance, plans, strategies or business developments. Forward-looking statements can generally be identified by the use of words such as "may", "expect", "intend", "plan", "estimate", "anticipate", "believe", "outlook", "forecast" and "guidance", or the negative of these words or other similar terms or expressions. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause its actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. Forward-looking statements are based on Telix's good-faith assumptions as to the financial, market, regulatory and other risks and considerations that exist and affect Telix's business and operations in the future and there can be no assurance that any of the assumptions will prove to be correct. In the context of Telix's business, forward-looking statements may include, but are not limited to, statements about: the initiation, timing, progress, completion and results of Telix's preclinical and clinical trials, and Telix's research and development programs; Telix's ability to advance product candidates into, enroll and successfully complete, clinical studies, including multi-national clinical trials; the timing or likelihood of regulatory filings and approvals for Telix's product candidates, manufacturing activities and product marketing activities; Telix's sales, marketing and distribution and manufacturing capabilities and strategies; the commercialization of Telix's product candidates, if or when they have been approved; Telix's ability to obtain an adequate supply of raw materials at reasonable costs for its products and product candidates; estimates of Telix's expenses, future revenues and capital requirements; Telix's financial performance; developments relating to Telix's competitors and industry; the anticipated impact of U.S. and foreign tariffs and other macroeconomic conditions on Telix's business, including as a result of war or other geopolitical conflicts; and the pricing and reimbursement of Telix's product candidates, if and after they have been approved. Telix's actual results, performance or achievements may be materially different from those which may be expressed or implied by such statements, and the differences may be adverse. Accordingly, you should not place undue reliance on these forward-looking statements. Trademarks and Trade Names. All trademarks and trade names referenced in this press release are the property of Telix Pharmaceuticals Limited (Telix) or, where applicable, the property of their respective owners. For convenience, trademarks and trade names may appear without the(R) or(TM) symbols. Such omissions are not intended to indicate any waiver of rights by Telix or the respective owners. Trademark registration status may vary from country to country. Telix does not intend the use or display of any third-party trademarks or trade names to imply any affiliation with, endorsement by, or sponsorship from those third parties. (C) 2026 Telix Pharmaceuticals Limited. All rights reserved. _____________________________ [1] [Telix ASX disclosure April 2, 2026.] [ Back To TMCnet.com's Homepage] |
Telix Pharmaceuticals is among three fast-growing companies with high insider ownership identified in a recent screen. The Australian radiopharmaceutical firm develops and sells products for cancer imaging and treatment, including TLX591 for advanced prostate cancer. Telix generated US$704.7 million in revenue from its Precision Medicine division and US$277.1 million from Manufacturing Solutions. The company has a market capitalisation of approximately A$5.3 billion. The screen identified 102 companies with strong growth prospects and significant insider ownership. Investors are increasingly focused on businesses that can convert AI-related demand into actual revenue, particularly those where management teams demonstrate confidence through meaningful share ownership. Other companies highlighted include PDI Gold, a West Africa-focused gold developer with a market cap of A$4.4 billion.
Telix Pharmaceuticals reported 22% year-on-year revenue growth to $477 million in the first half of 2026, driven by strong demand for Illuccix and the launch of Gozellix. The company maintained full-year revenue guidance of $950 million to $970 million, expecting results at the upper end of the range. Management increased R&D guidance to $230 million–$270 million to accelerate Phase III therapeutic candidates and the Regeneron collaboration. The company is preparing for the US launch of Pixclara following the 11 September regulatory decision date, targeting brain metastases. Telix successfully refinanced convertible bonds, increasing its cash balance to $252 million. The company plans to resubmit its Zircaix application within the next one to two months, addressing manufacturing deficiencies identified by the FDA.