26 therapist jobs found

  Shift: Nights, 12-Hour Rotating Schedule (Including Weekends & Holidays) Join a World-Class Manufacturing Team Are you detail-oriented, mechanically inclined, and passionate about quality? We are looking for a Diagnostic Technician to join our manufacturing team and play a critical role in ensuring product quality, operational excellence, and continuous production performance. In this hands-on position, you will monitor manufacturing equipment, perform quality inspections, troubleshoot production issues, and help maintain the highest standards of safety and compliance. This is an excellent opportunity for individuals who enjoy working in a fast-paced environment where precision and teamwork are highly valued. What You'll Be Doing Monitor manufacturing equipment to ensure continuous operation and product quality Perform in-process quality inspections and make product disposition decisions following established procedures Measure, verify, and record...

  Quality Assurance Manager, Operations Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–4:30 PM EST. What you will get: Below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge. What you will do: We are seeking an experienced Quality Assurance Manager, Operations to lead a team supporting GMP compliance and quality oversight across site operations. This role is responsible for ensuring quality objectives are achieved, supporting cross-functional teams, and promoting a strong culture of quality and continuous...

Overview Our Pharmacology team is seeking a highly motivated and detail-oriented Research Associate IV / Scientist I contractor. The ideal candidate will contribute to the development and evaluation of new anti-infective agents, focusing on understanding their mechanism(s) of action and efficacy against various pathogens. Detailed Description Key Responsibilities Experimental Design and Execution: Assist in the design, conduct, and analysis of experiments to assess the activity of anti-infective compounds against bacterial and fungal pathogens, including in vitro microbiological and pharmacological assays and in vivo studies. Studies in Animal systems: Utilize appropriate animal models to evaluate the pharmacokinetics, pharmacodynamics, and therapeutic efficacy of anti-infective agents. Data Analysis: Utilize statistical software to analyze experimental data and interpret results, ensuring accuracy and reproducibility. Literature Review: Conduct literature reviews to...

  Shift: Nights, 12-Hour Rotating Schedule (Including Weekends & Holidays) Join a World-Class Manufacturing Team Are you detail-oriented, mechanically inclined, and passionate about quality? We are looking for a Diagnostic Technician to join our manufacturing team and play a critical role in ensuring product quality, operational excellence, and continuous production performance. In this hands-on position, you will monitor manufacturing equipment, perform quality inspections, troubleshoot production issues, and help maintain the highest standards of safety and compliance. This is an excellent opportunity for individuals who enjoy working in a fast-paced environment where precision and teamwork are highly valued. What You'll Be Doing Monitor manufacturing equipment to ensure continuous operation and product quality Perform in-process quality inspections and make product disposition decisions following established procedures Measure, verify, and record...

  Product Development Manager GMP Operations Tampa, FL, USA The actual location of this job is in Tampa, FL. Relocation assistance is available for eligible candidates and their families, if needed.   The Manager, Product Development GMP Operations is a site‑based leadership role supporting early‑phase clinical trial drug product manufacturing and packaging. This position offers the opportunity to design and lead GMP capabilities, guide multidisciplinary teams, and directly contribute to bringing innovative therapies into the clinic. What you will get An agile career with opportunities for growth in a dynamic Product Development environment A collaborative, inclusive, and ethical workplace culture Compensation programs that recognize high performance and leadership impact Competitive medical, dental, and vision insurance coverage Access to Lonza’s learning, development, and leadership programs What you will do: Lead and develop Product Development GMP...

Post Doctoral.Post Doctoral.Associate Med-Neurological Surgery - Pennsylvania-Pittsburgh - ( 26004846 ) The Department of Neurological Surgery at the University of Pittsburgh, The Laboratory for NeuroControl and Monitoring ( https://www.huangneurolab.org/ ), led by Dr. Zhimin Huang, Assistant Professor in the Department of Neurological Surgery at the University of Pittsburgh, is seeking a highly motivated Postdoctoral Fellow to join our growing research team. The Huang Lab integrates focused ultrasound, gene therapy, protein engineering, synthetic biology, exosome engineering, and computational biology to develop next-generation tools for targeted drug delivery, molecular sensing, and precision therapeutics. Our long-term goal is to enable safe, noninvasive, and programmable therapies for neurological disorders and cancer. Located within the University of Pittsburgh School of Medicine, the lab collaborates extensively with researchers...

Dana-Farber Cancer Institute is seeking an experienced PhD-level scientist to join the antibody discovery and antibody-based therapeutics development-focused Lab for Antibody and Nanobody Phage Display and Discovery (LAUNCHPAD). A pre-clinical strategic center, LAUNCHPAD’s mission is to streamline “discovery to translation” of antibody-based immunotherapies for cancer. The role also offers the possibility to work closely with faculty in DFCI's Data Science department for ongoing computational professional development and collaboration. The LAUNCHPAD team works closely with academic partners to design experimental strategies to identify promising antibody ‘hits’ as well as engineering hits to generate potential therapeutics, e.g. bispecific and CAR T-cell immunotherapies. The candidate should be an exceptionally motivated individual with a passion for working in multidisciplinary teams to model, design, screen and engineer immunotherapy candidates and advance next-generation...

  Quality Assurance Specialist II - Viral Vector Location: Houston, Texas – Onsite Shift: Monday through Friday, 7:30 AM – 4:0 0 PM As a Quality Assurance Specialist II - Viral Vector , you will serve as a key representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector and advanced therapy manufacturing operations. This role provides the opportunity to partner closely with Manufacturing, Quality Control, Engineering, and other support functions to support production activities, maintain cGMP compliance, and help deliver life-changing therapies to patients. What you will get: A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related...

  Quality Assurance Specialist III - Viral Vector Location: Houston, Texas – Onsite Shift: Tuesday through Saturday, 11:00 PM – 8:00 AM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a comprehensive...

Job Description: Company Overview Founded over a decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY ®  (exagamglogene autotemcel (exa-cel)), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics is advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its...

Job Description: Company Overview Founded over a decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel (exa-cel)), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics is advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact, CRISPR...

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Siemens Healthineers is looking for a Mechanical Engineer to join our Interventional Oncology (IO) development team. The individual will be a member of our growing embolics team that is focused on treating cancers by delivery internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by developing new intravascular therapy products and mechanical devices for administering intravascular therapy. The ideal candidate would be a self-driven individual with a passion for medical device development and a desire to work on products that change people's lives....

  QC Scientist – Compendial & Analytical Quality Bend, OR The actual location of this job is in Bend, Oregon (USA) . Relocation assistance is available for eligible candidates and their families, if needed. Lonza is looking for a QC Scientist – Compendial & Analytical Quality to join our Quality team in beautiful Bend, Oregon. This role will be responsible for reviewing and updating internal documentation based on compendial changes and ensuring QC is in compliance with official pharmacopeial monographs. Additionally, this role will be responsible for coordinating all testing activities performed at external contract laboratories and ensuring that all outsourced analytical data meets strict regulatory standards and Lonza quality requirements. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What...

  Quality Assurance Specialist III - Viral Vector (Second Shift) Location: Houston, Texas – Onsite Shift: Monday through Friday, 3:00 PM – 11:30 PM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a...

  Quality Assurance Specialist III - Viral Vector Location: Houston, Texas – Onsite Shift: Sunday through Thursday, 11:00 PM – 8:00 AM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a comprehensive...

  Location:   Portsmouth, NH, USA. Schedule:   Monday – Friday, 8:00 AM – 5:00 PM (Standard Business Hours).   Note: Flexibility to adjust schedules to support shifting campaign timelines or floor demands may be required. We are seeking a proactive and highly organized technical professional to join our team in Portsmouth, NH, as a Biotechnologist II. This specialized role is designed for a candidate with a traditional cGMP biomanufacturing background who wants to focus on the operational staging, material lifecycle management, and equipment readiness that makes production possible. Operating under general supervision, you will ensure that the production suites have a flawless, continuous supply of materials—including single-use bioreactors, specialized raw materials, and processing consumables. While your primary mandate is logistical readiness and material flow, you will maintain the technical baseline necessary to jump onto the manufacturing floor and support...

Theradex is an Equal Opportunity Employer. US-NJ-Princeton ID 2026-1447 Category Information Technology Type Full Time Celebrating 40+ years! Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials. As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will work to support our sponsors in the development of these therapies. Theradex Oncology is an environment...

  Associate Director, Process & Analytical Development Location: This position is currently remote. A future transition to an on-site location on the U.S. East-Coast/Mid-West is anticipated as the project progresses, with an expected timeline in 2027. This is a full-time role with a Monday–Friday schedule from 8:00 a.m. to 5:00 p.m. What you will get: The full-time base annual salary for this position is expected to range between $155,700 to $181,650. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge. What will you do: The Associate Director, Process &...

  Director, Process & Analytical Development Location: This position is currently remote. A future transition to an on-site location on the U.S. East-Coast/Mid-West is anticipated as the project progresses, with an expected timeline in 2027. This is a full-time role with a Monday–Friday schedule from 8:00 a.m. to 5:00 p.m. What you will get: The full-time base annual salary for this position is expected to range between $196,700 to $232,650. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge. What will you do: The Director, Process & Analytical Development...

  Director, Operational Excellence & Production Systems Location: This position is currently remote. A future transition to an on-site location on the U.S. East-Coast/Mid-West is anticipated as the project progresses, with an expected timeline in 2027. This is a full-time role with a Monday–Friday schedule from 8:00 a.m. to 5:00 p.m. What you will get: The full-time base annual salary for this position is expected to range between $196,700 to $232,650. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge. What will you do: The Director, Operational Excellence...