Our Frederick Manufacturing Center (FMC) creates life-changing medicines for people around the world and has been recognized by our local community as being a Top 50’ Business in Frederick and awarded Frederick County’s ‘Best Place to Work’. This distinctive biologic manufacturing facility, with over 800 employees, makes a direct contribution to treating people with cancer, respiratory and autoimmune conditions across the globe. We work hard to deliver life-changing medicines to patients, and we take time to have fun and celebrate our accomplishments. From catered site festivities to competitive events, community outreach activities, environmental and wellness showcases and team-building functions, we take time to recognize our achievements and celebrate our diversity. We are dedicated to creating a culture of inclusion and collaboration and are committed to continuous learning by offering ongoing skill building and training for our staff. Fueled by our aspiration to deliver accelerated growth for our company and to make people’s lives better, there’s never been a more exciting time to join the team and shape the future of AstraZeneca Operations.
Are you ready to break new ground and leave a collective legacy? As a Production Technician I/II/III at AstraZeneca, you will have the opportunity to play a pivotal role in evolving our Supply Chain. You will be operating downstream processing equipment according to established SOPs. This is your chance to be part of a team that's reimagining how we do things and creating a collective legacy.
This role is a 12 hour rotating day shift, 6AM to 6:30PM
Accountabilities:
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected.
Essential Skills/Experience: Production Tech I
- 0-1 yrs experience with High School Diploma
- Ability to work independently or in collaboration with others on assigned tasks
- Ability to comply with cGMP standards
- Must possess computer skills
- Ability to follow instruction and directions
Essential Skills/Experience: Production Tech II
- 0-1 years experience with Bachelors, >1 year with Associates, >2 years with High School Diploma
- Ability to work independently or in collaboration with others on assigned tasks
- Ability to follow cGMP standards
- Must possess computer skills
- Ability to follow instruction and directions
- Prior experience with aseptic/cGMP standards
-Prior experience in Bioprocessing work environment/systems/equipment operation
Essential Skills/Experience: Production Tech III
-1-2 years experience with Bachelors, >2 year with Associates, >3 years with High School Diploma
- Ability to work independently or in collaboration with others on assigned tasks
- Ability to follow cGMP standards
- Possess computer skills
- Ability to follow instruction and directions
- Ability to perform job responsibilities with minimal oversight
- Prior experience with aseptic/cGMP standards
- Advanced prior experience in Bioprocessing work environment/systems/equipment operation • BS/BA degree preferred
Desirable Skills/Experience:
• BS/BA degree preferred
• Degree in STEM field
• Prior experience or exposure with aseptic/cGMP standards and environment
At AstraZeneca, we are driven by the challenge to stay ahead in rapidly changing markets. We continuously seek new and better ways to deliver medicines all the way to our patients. Our resilience helps us thrive as we innovate and evolve. We foster a safe and positive space where ideas are welcomed and rewarded. If you are self-driven, thrive at pace, continuously learning, and proactively taking on more, then this is the place for you.
Ready to make an impact? Join our Operations team today and contribute to life-changing medicines. Apply now!
The annual base pay (or hourly rate of compensation) for this position ranges from $56,0720.00 to $84,108.00 Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
22-Oct-2026Closing Date
05-Nov-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
AstraZeneca develops and markets prescription medicines and vaccines for global health, focusing on oncology, cardiovascular/metabolic, respiratory, and infectious diseases. Its products work by targeting specific biological pathways or cells to treat diseases or prevent infections, using small-molecule drugs, biologics, and vaccines. The company differentiates itself through its dual heritage from Sweden and the UK, a broad pipeline, and strong R&D with collaborations to move from discovery to patient access across multiple therapeutic areas. Its goal is to improve people’s health by discovering, developing, and delivering medicines and vaccines worldwide.
Company Size
10,001+
Company Stage
IPO
Headquarters
Cambridge, United Kingdom
Founded
1913
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AstraZeneca has launched Zegfrovy (sunvozertinib) in the US, a daily oral pill for adults with advanced or metastatic non-small cell lung cancer (NSCLC) that carries EGFR exon 20 insertion mutations. The drug is for patients whose disease has progressed on or after platinum-based chemotherapy. AstraZeneca shares rose 2% on Thursday. The US Food and Drug Administration (FDA) granted accelerated approval based on the WU-KONG1B trial. Among 85 patients, the confirmed overall response rate was 46%. The median response lasted 11.1 months, and 72% of responders had responses of at least six months. AstraZeneca has applied for first-line use in the US and China. Both regulators granted Breakthrough Therapy Designation, but the applications are pending.
China slams US ban on DeepSeek AI over security concerns. by Politixia about 4 hours ago 121 Views Announcement Pharmaceutical giant AstraZeneca is teaming up with tech powerhouse Oracle to use artificial intelligence to identify patients for clinical trials and monitor potential safety risks, in a move aimed at speeding up drug development and improving medical research. The partnership will combine AstraZeneca's drug development expertise with Oracle's AI technology and healthcare data capabilities to help researchers match patients with clinical trials and identify potential safety concerns. The collaboration will initially focus on cancer, cardiovascular and respiratory diseases, immunology and rare diseases, with the technology potentially helping doctors diagnose serious illnesses earlier. AstraZeneca CEO Pascal Soriot said the partnership could help researchers and healthcare providers improve patient care through AI-driven technology. "We can help clinicians identify patients sooner, optimize clinical trials, and generate evidence continuously across the lifecycle of a medicine," Soriot said in a statement. The first project will focus on hypertension research in Abu Dhabi, in partnership with UAE-based healthcare company M42. Announcement Patient recruitment remains a major obstacle in clinical research, with enrollment delays often extending trial timelines and driving up development costs. AstraZeneca has also faced clinical trial setbacks, including delays involving a breast cancer treatment and the failure of a nerve disorder drug, raising concerns about its drug development efforts, according to Reuters. The companies have signed a non-binding agreement and have not disclosed financial terms. The partnership comes as AstraZeneca seeks to expand its drug portfolio and reach more than $80 billion in annual revenue by 2030. Announcement Reuters contributed to this report. Announcement
Ambrose Healthcare fortifies rare disease pipeline on AM-Pharma takeover. Ambrose will now enter the race to debut a new medicine on the HPP market as the only approved therapy edges closer to key patent expiries. Ambrose Healthcare has acquired 100% of Dutch pharma company AM-Pharma's shares, absorbing the company and fortifying its pipeline with a rare bone disease drug that's could be set to take on AstraZeneca's blockbuster therapy, Strensiq (asfotase alfa). At the core of this deal is ilofotase alfa, an investigational, Phase II-ready enzyme replacement therapy (ERT) and anti-inflammatory currently in development for an inherited condition called hypophosphatasia (HPP). This rare disease, which impacts approximately one in 100,000 people globally, is characterised by the softening of patients' bones and teeth due to low activity of alkaline phosphatase (ALP) - an enzyme involved in normal skeletal development. Thus far, ilofotase alfa has shown early promise in Phase Ib clinical trials, with the drug having demonstrated its positive safety profile and dose-dependent effect on key biomarkers of disease in HPP across adult patients. On top of securing access to ilofotase alfa, Ambrose's AM-Pharma takeover will also expand the British company's footprint into new territories, as it will now have an established base in the Netherlands - specifically in the central city of Utrecht. According to Toby Wilson Waterworth, CEO of Ambrose, the takeover will also secure the company access to AM's regulatory quality and scientific infrastructure in Europe, offering what he calls "a strong base" from which it can develop the rest of its pipeline. This includes two other acquisition-derived rare disease drugs - namely Val401, a Phase II palliative care and cachexia-targeting medicine for pancreatic cancer, and renzapride, a mid-stage candidate in development to treat gastrointestinal symptoms of cystic fibrosis. Through this acquisition, AM-Pharma's shareholders receive up to €161m (approx. $180m) in upfront and potential milestone payments tied to ilofotase alfa's commercialisation, as well as royalties on potential future sales of the drug. New drugs inch closer to the HPP market. Ambrose's bet on AM-Pharma is the latest in a string of pharma activity in HPP, as companies look to challenge AstraZeneca-owned Alexion Pharmaceuticals' monopoly on the market stemming from ERT, Strensiq, which will start to lose its market exclusivity in 2027. One of the key current players in this race is AstraZeneca itself, which is eyeing a potential place on the HPP market for efzimfotase alfa, despite the drug missing its primary endpoints in the Phase III HICKORY study (NCT06079281). Meanwhile, BioMarin has also hedged its bets on HPP through a $490m acquisition of rare disease drug developer, Alesta Therapeutics - opting to keep only its HPP drug, ALE1. Currently, Strensiq is a blockbuster seller for AstraZeneca, as the drug pulled in more than $1.6bn in sales during 2025. Looking ahead, GlobalData analysts forecast the therapy's sales will peak at $2.1bn in 2027, before taking a hit due to a loss of market exclusivity until the end of the forecast period in 2032. GlobalData is the parent company of Pharmaceutical Technology. Give your business an edge with its leading industry insights.
Health AI Chronicle - October 20, 2026. Hook of the day. 270 European clinical sites are now standardizing AI performance metrics for cancer detection and cardiovascular risk prediction - yet 69% of cancer patients using AI chatbots never tell their doctors about it. Executive summary. October 2026 marks Europe's transition from AI pilot networks to operational infrastructure: 270+ clinical sites across 29 EU nations are integrating standardized AI validation protocols, while €80M in EU Chips funding accelerates supercomputing capacity for health-data AI factories. Simultaneously, patient behavior reveals a critical disconnect - those using AI-enabled digital health tools often hide this from clinicians, despite reporting high trust in physician judgment and preference for physician-recommended AI use. Summary section A: practical AI in healthcare. Summary: European healthcare infrastructure is shifting from isolated pilots to continent-wide, standardized AI validation networks. The EU Screening Network's 270+ sites represent the largest coordinated effort to test cancer detection and cardiovascular risk algorithms in real clinical environments, with a November 2026 implementation summit signaling imminent operational deployment. EU Screening Network launches 270+ site Network with November implementation summit. The EU Screening Network has assembled 270+ clinical sites across 29 EU Member States to standardize performance metrics and validation protocols for AI triage, oncological imaging, and cardiovascular risk prediction systems. This federated approach enables real-world testing while maintaining data sovereignty - raw clinical data stays within national borders using federated EHDS registries. A November 2026 implementation summit will establish operational protocols, creating the continent's first standardized pathway for AI clinical validation at scale. This infrastructure directly addresses the "deployment-to-validation gap" that has slowed European AI adoption compared to other regions. AstraZeneca-insitro partnership launches virtual Human platform - $1.46B milestone deal. AstraZeneca and insitro announced a landmark partnership deploying "Virtual Human" machine learning platforms to identify rare disease sub-phenotypes for metabolic dysfunction-associated fatty liver disease (MASH) and cardiomyopathy. The $40M upfront commitment with up to $1.46B in development milestones represents AI's shift toward precision phenotyping at scale. Virtual Human models integrate patient genomics, clinical data, and real-world outcomes to predict treatment responses before trial enrollment - dramatically accelerating target validation and reducing drug development timelines. This model exemplifies how AI tackles one of healthcare's largest administrative and financial burdens: unnecessary clinical trial failures and extended development cycles. Can AI help healthcare move from treatment to prevention? Governance gaps emerge as adoption surges. European healthcare leaders are asking a critical question: How can AI shift medicine from reactive treatment to proactive prevention? The challenge isn't technological - it's systemic. Healthcare incentive structures reward treatment volume over prevention success, and most European nations (only 1 in 12) have implemented AI governance strategies despite widespread adoption. Healthcare informaticist Ricardo Baptista Leite warns that "retrofitting AI into an inefficient system makes you very efficient at being inefficient." The path forward requires three interventions: (1) regulatory frameworks that maintain oversight post-deployment, not just at launch; (2) incentive restructuring to reward prevention outcomes; and (3) governance bodies with authority to audit active AI systems in clinical use. Without these, scaling AI to population health will amplify existing system inefficiencies rather than transform them. Summary section B: reducing administrative burden. Summary: Administrative infrastructure is accelerating across Europe through federated data registries and €80M in EU Chips funding. These complementary initiatives move healthcare IT from organizational silos to continent-wide, coordinated research ecosystems while maintaining data privacy and national sovereignty. EHDS federated registries and €80M EU Chips funding establish data infrastructure across 29 nations. The European Health Data Space is operationalizing through federated registries that enable data sharing without raw data crossing borders - a breakthrough for privacy-preserving research at continental scale. Simultaneously, €80M in EU Chips Act funding supports construction of AI supercomputing facilities and "health-data AI factories" positioned regionally across Europe. These complementary initiatives address a core administrative burden: duplicative infrastructure and incompatible data systems that force researchers to negotiate bilateral agreements for each cross-border collaboration. The federated approach also reduces compliance overhead - organizations apply standardized HealthDCAT-AP metadata standards once, then participate in multiple research networks without re-certifying for each one. This infrastructure-as-commons model shifts healthcare IT from organizational silos to continent-wide, coordinated research ecosystems. Ireland's EU Presidency advances EHDS implementation through "Data in Motion" Conference. During Ireland's EU Presidency, the "Data in Motion" EHDS conference convened European health leaders (October 13-14, 2026) to accelerate implementation of cross-border health data infrastructure. Central discussions focused on establishing Health Data Access Bodies and Digital Health Authorities - the operational governance structures that will enforce EHDS regulations in practice. Health Minister Jennifer Carroll MacNeill emphasized the goal of delivering health information "when and where it is needed" while maintaining privacy and trust. Sessions covered data quality standards, interoperability protocols, and real-world impact on clinicians, researchers, and patients. This phase - moving from regulatory text to operational governance - directly reduces administrative friction for healthcare organizations by establishing clear, consistent standards across all EU Member States rather than requiring organization-by-organization compliance negotiations. Summary section C: how patients use AI (#patientsuseai). Summary: Patient behavior reveals a critical paradox: those using AI-enabled digital health tools often hide this from clinicians, despite reporting high trust in physicians. Understanding this disconnect is essential for healthcare organizations aiming to safely integrate AI into patient care pathways. Cancer patients silently use AI chatbots, don't disclose to doctors - yet trust physicians' judgment. A Supportive Care in Cancer journal study of 400 cancer patients and caregivers at a Turkish tertiary oncology center revealed a striking paradox: 75% of patients knew about AI-enabled health tools, but only 24% used them - and 69% of those users never told their physicians. The secrecy wasn't driven by distrust of physicians (no patient reported decreased trust from using AI) but by fear of judgment. However, the same cohort showed strong conditional acceptance: 73% would openly use AI if their physician verified and recommended it. The study identified key predictors of AI adoption: university-level education (4.47x odds), age under 55 (2.64x odds), and recent diagnosis (2.16x odds). The clinical implication is clear: oncologists and healthcare providers who non-judgmentally inquire about AI use can identify misinformation, correct knowledge gaps, and guide patients toward reliable tools rather than allowing silent, unvalidated AI use to persist. European Open Science Cloud launches 13 regional nodes with standardized AI training pipelines. The European Open Science Cloud has activated 13 regional nodes across Europe, each equipped with standardized AI training pipelines for health data research. This infrastructure enables patients and research participants to understand how their health data is being used in AI model development - increasing transparency and supporting informed consent. The standardized pipelines also reduce barriers for patient-led research initiatives and citizen science projects that use AI for personal health tracking or community health advocacy. By decentralizing AI infrastructure to regional hubs rather than centralizing in single institutions, the EOSC approach distributes both technical capacity and governance responsibility - empowering healthcare organizations and patient communities to participate in AI development, not just consume it as end-users. So what for you? If you lead patient education, clinical workflows, or healthcare administration: How would you differently guide patients toward trusted AI tools if you knew 69% of them are already quietly using digital health AI without telling you? Daily Health AI Chronicle - Edition 13 October 20, 2026 Curated AI healthcare news focused on Europe, patient perspectives, and reducing administrative burden Book Lucien for your next event. Keynotes, masterclasses, panels and board-room sessions.
Sferical One: Ericsson and partners make AI supercomputing a reality in Sweden. Oct 16, 2026 * Ericsson is among several major Swedish companies who have started to utilise a new sovereign AI supercomputer in Sweden, called Sferical One, officially launched today by the Sferical AI initiative. As a founding member of Sferical AI - alongside AstraZeneca, Saab, SEB and Wallenberg Investments, with SKF as a strategic partner - Ericsson gains access to secure, sovereign Swedish computing capacity to develop, deliver, and deploy advanced AI solutions alongside the partner companies. The initiative aims to deliver direct societal benefits to Sweden as AI use case momentum gathers pace. Shared use of investment, capacity and expertise under the Sferical AI initiative means the partners can scale AI development faster. Ericsson will contribute telecom expertise, drive AI use cases, and jointly develop a secure, sovereign AI platform, while simultaneously using the platform to further develop Ericsson's own network and automation capabilities. The system is an NVIDIA DGX SuperPOD built on NVIDIA DGX GB300 systems. The system has been running since late summer 2026. Sferical AI will also build services based on NVIDIA Nemotron open multimodal AI models. Today's event was attended by senior executives from Sferical AI, the Swedish partner companies, including Ericsson President and CEO, Per Narvinger, and Nvidia founder and CEO, Jensen Huang. Ericsson CTO, Erik Ekudden, who led Ericsson's co-development of Sferical from inception, says: "I envision the future as a 6G/AI intelligent fabric - a universal framework which enables different AI systems to work together securely and with reliable performance, no matter where they are or who built them. Ensuring a robust and secure infrastructure requires best in class AI models. To build those, we need the best compute infrastructure. Through our cooperation with Sferical we get access to sovereign infrastructure for model training and refinement." Addressing the partner companies at the Sferical One launch, Jensen Huang predicted an exciting future. "You have done the hardest part... you have started," he said. Ericsson's Sferical One engagement to date relates to ensuring secure and reliable networks through AI-based network operations. Jenny Nordlöw, CEO, Sferical AI, says: "Sferical One enables the companies to train and run AI models at a larger scale on a sovereign platform. What makes Sferical unique isn't just the technology, but that several of Sweden's largest companies share the same infrastructure, develop solutions together and share knowledge across industries." Marcus Wallenberg, Chair of Wallenberg Investments, says: "AI will be a critical component of Swedish industry's future competitiveness. Sferical One will help some of Sweden's leading companies stay at the forefront of that development. It is a long-term investment in the capabilities and expertise we will need to compete in the future."