Injective jobs

Lead Formulation Technician (12hr nights, D shift, 2-2-3 rotation) Greenville, North Carolina, United States of America Embrace the opportunity to become a Lead Formulation Technician and play a vital role in producing life-saving sterile injectable drugs. Oversee complex formulation processes, mentor team members, and ensure top-quality standards in a GMP-compliant environment. Grow your career with us and make a global impact in pharmaceutical manufacturing.

Phlebotomist -Kissimmee-PRN Kissimmee FL posted: Posted 15 Days Ago

Lead Formulation Technician (12hr days, 2-2-3 rotation) Greenville, North Carolina, United States of America Embrace the role of a Lead Formulation Technician and play a vital role in ensuring the quality and safety of sterile injectable drug products. Leverage your expertise in aseptic techniques, cGMP compliance, and team leadership to drive process improvements and support life-saving pharmaceutical manufacturing. Grow your career with Thermo Fisher Scientific in a dynamic, mission-driven environment.

Health Representative - IM (GP) Malaysia - Johor posted: Posted 30+ Days Ago

Sr. Formulation Technician (12hr nights, D shift, 2-2-3 rotation) Greenville, North Carolina, United States of America Join our team as a Senior Formulation Technician and play a vital role in sterile injectable drug manufacturing. Utilize your expertise in cGMP compliance, aseptic techniques, and process optimization to ensure quality and safety. Collaborate with cross-functional teams and contribute to life-saving pharmaceutical solutions in a dynamic, fast-paced environment.

Quality Assurance Area Specialist III (QA for Warehouse & Logistics) Job Posting Country United States | Job Posting State/Province North Carolina (NC) | Job Posting City Clayton About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At PS AM, you'll join a global network of manufacturing professionals who are passionate about what they do. What we offer you: Leading pay and annual performance bonus for all positions All employees enjoy generous paid time off including 14 paid holidays Health Insurance, Dental Insurance, Vision Insurance - effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave Free access to Novo Nordisk-marketed pharmaceutical products Tuition Assistance Life & Disability Insurance Employee Referral Awards At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential?

Entry Level Phlebotomy USA - AZ - Glendale posted: Posted 30+ Days Ago

Quality Assurance Area Specialist III - QC Operational Readiness Job Posting Country United States | Job Posting State/Province North Carolina (NC) | Job Posting City Clayton About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At PS AM, you'll join a global network of manufacturing professionals who are passionate about what they do. What we offer you: Leading pay and annual performance bonus for all positions All employees enjoy generous paid time off including 14 paid holidays Health Insurance, Dental Insurance, Vision Insurance - effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave Free access to Novo Nordisk-marketed pharmaceutical products Tuition Assistance Life & Disability Insurance Employee Referral Awards At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join

Director, Therapeutic Area Strategy, Immunology 2 Locations posted: Posted 30+ Days Ago

Offensive Security Researcher, SEAR Cupertino, United States of America Apple's Security Engineering & Architecture (SEAR) organization is responsible for the security of all Apple products. Passionate about safeguarding our users, we lead with offence proactively uncovering and eliminating vulnerabilities before attackers ever get the chance. As AI systems become deeply integrated into operating systems, developer tools, and user experiences, they introduce entirely new attack surfaces vulnerable to prompt injection, agentic privilege escalation, data exfiltration, and AI-assisted exploitation at unprecedented scale. Think you have the creativity and determination to break these systems? Join us and help secure the next generation of intelligent platforms used by billions of people. In this role, you will identify and exploit vulnerabilities in AI-powered features and agentic systems across Apple platforms. The AI systems themselves are the attack surface. You will help to build offensive capabilities against autonomous systems and anticipate how adversaries may exploit AI enabled systems in the wild. You will join a team working with world-class offensive security researchers. The work is critical directly shapes the security posture of Apple. You will conduct offensive research into AI-specific attack classes, including prompt injection, agentic data exfiltration and lateral movement, persistence mechanisms in AI workflows, AI-assisted vulnerability discovery and exploitation. Minimum Qualifications: Solid grounding in common vulnerability classes (memory corruption, logic flaws, auth bypass) Proven experience in security research, vulnerability discovery, or offensive security (e.g., browsers, 0-click, messaging systems, distributed systems, or AI platforms) Strong understanding of modern AI/LLM systems and their failure modes (e.g.,

Registered Nurse*Float RN* 01908 - Hialeah Artificial Kidney Cent posted: Posted 7 Days Ago

Alternance - Assistant(e) Stratégie de Services Onco-Hématologie H/F France - Paris posted: Posted Today

Account Specialist, Chronic Migraine - Manhattan North, NY Remote | New York, NY, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Account Specialist role promotes a product to community practices and health systems. Customer accounts may include community/private practices, community-based hospitals, academic medical centers, and government accounts (military treatment facilities and/or Veteran's Affairs Medical Centers). The Account Specialist develops and maintains relationships with various accounts/departments such as neurology, pain medicine, physical medicine and rehabilitation, primary care, and pharmacy. Or in Urology, specialists such as urology, urogynecology, obstetrics and gynecology, female pelvic medicine, ambulatory surgical centers, and reconstructive surgery. Responsibilities Promote a product to meet/exceed sales goals in community/private practices as well as hospitals/health systems Comply with all company policies, required reports, requests and promotional compliance and effectively manages AbbVie field assets. Identify/uncover customer needs (training, clinical, operational, reimbursement) and address with appropriate AbbVie resources. Expert delivery of anatomical/procedural information and training, including the appropriate use of anatomical terminology to train injection paradigms/postures while highlighting various anatomical and injection insights and considerations. Provide education

Responsable Technique F/H Montpellier posted: Posted 30+ Days Ago

Senior Quality Specialist (Contract) Emeryville, California Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY 4DMT is hiring a Sr. Quality Specialist, Document & Records Management. Reporting to the Senior Manager, Quality Document & Records Management, the Sr. Quality Specialist will be responsible for ensuring 4DMT's Quality Document & Records Management is designed and executed in an efficient, compliant, and inspection ready manner. This individual will support the

Rédacteur Médical Principal - Senior Medical Writer 3 Locations posted: Posted 3 Days Ago

Principal Medical Writer Remote, United States Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY: The Principal Medical Writer will support 4D‑150, a gene therapy in late-stage development for retinal vascular diseases, including nAMD and DME, and associated BLA‑enabling activities as well as clinical stage work within the lung program. This role is responsible for the planning, development, and delivery of high‑quality clinical and regulatory documents across late‑stage

Specialist Bid & Proposal Vascular - Portuguese (Located in Madrid) Spain - Madrid posted: Posted 30+ Days Ago

Clinical Supply Specialist (Contract) Emeryville, California; Remote, United States Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY: Reporting to the Director, Supply Chain, this role is expected to work closely within the Supply Chain team, as well as cross-functional groups such as Clinical Operations and Quality. This is a remote or hybrid position. RESPONSIBILITIES: - Supports the development and execution of Clinical Supply strategies for all 4DMT's

Emerging Talent Acquisition Trainee (f/m/div) Porto (Maia) (Portugal)

Director, Clinical Operations (Lung Program) Remote, United States Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY: Provide strategic and operational leadership for global clinical trial execution across the 4DMT lung portfolio. This role is responsible for delivering clinical programs aligned with corporate timelines, budget, quality, and regulatory expectations while building scalable operational infrastructure appropriate for a fast-paced biotechnology environment. The Director, Clinical Operations will lead internal Clinical

Inženir tehničnih storitev (m/f/d) Ljubljana posted: Posted 29 Days Ago

Research, Mid-Training San Francisco | OnSite WHO WE ARE We are an applied AI lab building end-to-end software agents. We're the team behind Devin, the first AI software engineer, and Windsurf, an AI-native IDE. These products represent our vision for AI that doesn't just assist engineers, but works alongside them as a genuine teammate. Our team is small and talent-dense: world-class competitive programmers, former founders, and researchers from the frontier of AI, including Scale AI, Palantir, Cursor, Google DeepMind, and others. ROLE MISSION Mid-training sits at the seam between pre-training and post-training and is one of the highest-leverage points in the entire model pipeline. This is where raw base model capability is sharpened into something that can reason deeply, generalize reliably, and serve as the foundation that post-training builds on. You will own the late-stage training decisions that determine what our models are fundamentally capable of: data mix and quality uplift, annealing schedules, context length extension, capability injection across coding, math, and reasoning, and the synthetic data strategies that make all of it scale. This role does cross-cutting work across what is classically considered both pre-training and post-training. We don't distinguish between research and engineering; we expect both. WHAT YOU'LL ACCOMPLISH - Data Mix and Quality Uplift: Design and iterate on high-quality data mixtures for late-stage and annealing training runs. Develop principled methods for sourcing, filtering, and weighting data to sharpen model capabilities without degrading general performance. - Capability Injection: Drive targeted improvements in coding, mathematics, and long-horizon reasoning through

Medical Affairs Manager (m/w/d) Amyloidosis Germany - Hamburg posted: Posted Yesterday