Today's Pharma & Biotech Jobs

About the role Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a plasma donor screener and perform phlebotomy to support plasma center operations. How you will contribute · You will answer phones, and greet and focus on our donors, while ensuring the safety of donors and our team. · You will screen new and repeat donors and take and record donor vital signs and finger stick results. ·...

Location Lake County, IL (AbbVie Headquarters) and open to other AbbVie office locations in the US. Purpose Medical Device Safety Physician leads the safety oversight relevant to her/his assigned products to determine and advise the course of action necessary to meet the safety goals and objectives of specific products and projects. Works in close collaboration with cross-functional teams and counterparts in quality systems, regulatory affairs, medical writing, clinical development, clinical operations, manufacturing, epidemiology, marketing and other functional areas to identify, evaluate, and communicate safety issues. May contribute relevant clinical safety input to new product design teams as needed. The Medical...

The Non-clinical Statistics Project Lead of the TED (Translational and Early Development) team supports Vaccine R&D under the supervision of the head of Non-Clinical Statistics Team and/or the TED Global head who are all part of the Global Biostatistical Sciences (GBS) team. As a core objective, the Project Lead responsibilities include provideing statistical support in R&D for pre-clinical work, bioassay and biomarker research and/or CMC, biological assay, and biomarker research, as well as working in close collaboration with the scientists and/or project managers. The Project Lead will assume responsibility for methodological and statistical aspects of non-clinical studies, with general direction...

IQA Inspector This position works out of our Westfield, Indiana location for our Structural Heart business. Our purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. What You’ll Work On As the IQA Inspector, you will be responsible for the inspection of incoming components (i.e. plastics, metals, extrusions, and tubing), raw material, information for use (IFUs), package, and labeling. Perform and process first article inspections as directed by IQA Supervisor. Correlate supplier’s first article inspection report with AVI first article inspection results. Inspect incoming, R&D...

IQA Inspector This position works out of our Westfield, Indiana location for our Structural Heart business. Our purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. What You’ll Work On As the IQA Inspector, you will be responsible for the inspection of incoming components (i.e. plastics, metals, extrusions, and tubing), raw material, information for use (IFUs), package, and labeling. Perform and process first article inspections as directed by IQA Supervisor. Correlate supplier’s first article inspection report with AVI first article inspection results. Inspect incoming, R&D...

IQA Inspector This position works out of our Westfield, Indiana location for our Structural Heart business. Our purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. What You’ll Work On As the IQA Inspector, you will be responsible for the inspection of incoming components (i.e. plastics, metals, extrusions, and tubing), raw material, information for use (IFUs), package, and labeling. Perform and process first article inspections as directed by IQA Supervisor. Correlate supplier’s first article inspection report with AVI first article inspection results. Inspect incoming, R&D...

IQA Inspector This position works out of our Westfield, Indiana location for our Structural Heart business. Our purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. What You’ll Work On As the IQA Inspector, you will be responsible for the inspection of incoming components (i.e. plastics, metals, extrusions, and tubing), raw material, information for use (IFUs), package, and labeling. Perform and process first article inspections as directed by IQA Supervisor. Correlate supplier’s first article inspection report with AVI first article inspection results. Inspect incoming, R&D...

IQA Inspector This position works out of our Westfield, Indiana location for our Structural Heart business. Our purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. What You’ll Work On As the IQA Inspector, you will be responsible for the inspection of incoming components (i.e. plastics, metals, extrusions, and tubing), raw material, information for use (IFUs), package, and labeling. Perform and process first article inspections as directed by IQA Supervisor. Correlate supplier’s first article inspection report with AVI first article inspection results. Inspect incoming, R&D...

Translational Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of clinical development at our company's Research Laboratories. Translational Molecular Biomarkers laboratories leverage a diverse array of technologies to develop biomarker assays to help confirm engagement of therapeutic targets and understand mechanisms of drug action and patient response. The Molecular Pathology group within the Translational Molecular Biomarkers organization is seeking a highly motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist (Director) to join our innovative team. This position will play a crucial role in the supporting...

ROLE SUMMARY The leader in this role will provide strategic leadership and drive innovation in medical study orchestration and design, including integrated evidence planning, research design, and implementation to ensure end-to-end evidence generation activities are strategically aligned, methodologically rigorous, and operationally efficient by harmonizing study design and delivery approaches, thereby strengthening the organization’s ability to support regulatory, clinical, payer, and patient-centered decision-making globally. ROLE RESPONSIBILITIES Oversee cross-functional teams specializing in Integrated Evidence Planning (IEP), RWE/epidemiology study design, patient-centered research design and execution, and RWE/epidemiology methods development and innovation Set strategic direction for study design and orchestration, ensuring alignment with portfolio...

Purpose * This role requires four 10-hour shifts. Sets up equipment for routine processes. Operates complex equipment and monitors manufacturing processes. Conversant with overall functionality of departmental processes. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Operates all certified jobs and maintains operating conditions within the desired range with minimal supervision. Sets up equipment to accommodate minor processing changes. Is knowledgeable on work processes to assist with identifying and implementing work improvements. Responsibilities Knowledgeable of jobs in assigned...

Purpose * This role requires four 10-hour shifts. Sets up equipment for routine processes. Operates complex equipment and monitors manufacturing processes. Conversant with overall functionality of departmental processes. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Operates all certified jobs and maintains operating conditions within the desired range with minimal supervision. Sets up equipment to accommodate minor processing changes. Is knowledgeable on work processes to assist with identifying and implementing work improvements. Responsibilities Prepared to take on leadership...

Careers That Change Lives This posting is intended for candidates attending the 2025 National SWE Convention in New Orleans, Louisiana . The possibilities at the intersection of medicine and technology are endless, which means endless opportunities to make your mark on the world. Our interns do real work within experienced engineering teams to improve lives of millions. We are hiring for Engineering (Software, R&D, Operations, Quality) interns for Summer 2026. You have learned a lot to get here — we want you to keep growing. With our expanding portfolio of innovative products and services, Medtronic is the global leader in...

The Manufacturing Associate, Manufacturing Operations manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. Start and end times are subject to change based on business demands. Shift Available TBD Responsibilities Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation. Aseptic...