11 equipment associate jobs found

Merck Job Description This position is in our organization's Device Development & Technology (DD&T) group in our Research division. Our organization's DD&T group is responsible for the development of devices, combination products, processes, testing and assembly equipment from conception through product launch. Products include autoinjectors, inhalers, implants, infusion pumps, vaginal rings and connected devices/apps. The person in this position contributes to high impact, complex, cross-functional, and cross-divisional teams, initiatives and will provide input to achieve project goals. Effective collaboration with teams is essential to meet our company's goals/objectives. The group also plays a key role in supporting commercially launched products. Our company's DD&T Team is seeking a hands-on medical device product manufacturing and assembly engineer. This position will be responsible for hands-on factory floor work and collaboration, via interfacing...

Merck Job Description PDMB provides data-driven operations and automation support to regulated bioanalytical laboratories. We combine laboratory domain knowledge, robotic work cells, and modern data platforms to ensure reliable, compliant, and continuously improving lab operations. You'll join a multidisciplinary team partnering with lab scientists, automation engineers, IT, Clinical, and QA, to turn operational and scientific data into trusted insights. The PDMB Regulated Bioanalytics Department is seeking a Data Management Associate to join our LIMS & Data Management group.This role will support work across groups within the Regulated Bioanalytics Department, including work at our Company's new state-of-the-art GxP lab facility in West Point, PA. At this new facility, we will combine the power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated...

Biogen This role operates on a 2 2 3 schedule for Day Shift- 6a-6p. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations - each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including - Large Scale Cell Culture MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You'll Do Execute daily manufacturing activities, to include operating process equipment and executing validation protocols according to cGMP Standard Operating Procedures (SOPs) Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation like batch records,...

Biogen Job Description This role operates on a 2 2 3 schedule for Red Day Shift- 6a-6p. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations - each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including - Large Scale Cell Culture MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You'll Do Execute daily manufacturing activities, to include operating process equipment and executing validation protocols according to cGMP Standard Operating Procedures (SOPs) Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation...

Merck Job Description Summary of Position: Our Company's Industrial Hygiene Laboratory (IHL) group within the Safety Center of Excellence (COE) is seeking a highly motivated individual for an Associate Chemist position. The Associate Chemist will be responsible for performing routine industrial hygiene (IH) sample analysis using LC/UPLC, MS, and ELISA techniques. Using precise analytical skills and understanding of chemical principles, the successful candidate will perform analysis of air and surface samples for a variety of active pharmaceutical ingredients (APIs) both small and large molecules using approved analytical methods. Must have the ability to work independently using laboratory instrumentation and computer systems. The successful candidate will maintain accurate records and comply with laboratory operation and safety SOPs. Working within the requirements of ISO 17025 is expected. The IHL Associate Chemist will demonstrate analytical proficiency on a...

Biogen This position follows a traditional 2-2-3 format from 6a-6P ( Red Day Shift) About This Role: The Manufacturing Lead performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents, ensuring compliance to cGMP, as well as maintaining equipment and facilities. This position works closely with shift Supervisor to coordinate critical activities collaboratively and utilizes resources efficiently. This is a key preparatory role for the Manufacturing Supervisor position. The Manufacturing Lead responsibilities include but are not limited to: Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record, SLR and control system. Coordinates and/or leads process steps as required, serving as a process step(s) expert. In coordination with Supervisor, schedules tasks for a given shift and...

Biogen About This Role The Translational Pathology group at Biogen, part of Biomarkers and Systems Biology in Research, is seeking a highly motivated and talented scientist to join a dynamic pathology team engaged in human disease translational research and drug development. The scientist will employ cutting-edge histopathologic techniques to develop innovative multiplexed assays for the analysis of human tissues and translational models. As part of a collaborative scientific Team, the scientist will validate/discover molecular targets/pathways. We are looking for an individual that has demonstrated forward-thinking, creativity and a passion to develop novel therapeutics. What You'll Do Utilize advanced automation for multiplex assay development and troubleshooting across immunohistochemistry and in situ hybridization platforms Support histologic aspects of spatial omics studies Seek out new techniques and technologies to support clinical and non-clinical studies...

Biogen This onsite, 1st shift role runs Monday to Friday, with some weekend and off-shift support as needed About This Role We are seeking a highly experienced and motivated Biochemistry Senior Associate II to join the Biochemistry team at our RTP biologics drug substance manufacturing facility. The role will support advancing biochemistry laboratory activities, including method execution, troubleshooting, instrument validation, data interpretation, and participation in project teams. This role primarily works independently with minimal supervision as needed, consults with management on key decisions. What You'll Do Act as the primary team lead and represent the team in absence of Manager Conduct laboratory investigations (i.e. invalids, OOS, and atypical) and deviations Reviews tests, approves release data, and issues certificates Authors and review protocols, change control requests, and SOPs Serve as a technical resource for the workgroup or project...

Biogen Schedule: This onsite position operates on 10-hour shifts from Sunday through Wednesday during the first shift (8AM-6PM), with some occasional support required outside of those hours. About This Role We are seeking a highly motivated QC Microbiology Sr Associate I to support microbiological testing of in-process and raw materials, and environmental/utilities monitoring at RTP drug substance manufacturing facility. The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory. The Sr. Associate I performs and trains other team members on the microbial testing of all in-process drug substance, EM/UM, and raw materials samples. Additionally this role is responsible for method qualification and projects as assigned. What You'll Do Review test data in LIMS Prepare quarterly EM/UM reports Supports testing for all qualification and study directed testing Troubleshoot complex assays Perform microbiology testing...

Biogen About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. Biogen Manufacturing Engineering at the RTP Pharma site supports two sterile filling lines and an Automated Visual Inspection Machine at the Parenteral Facility and a small-scale filling line, Oligonucleotide Synthesis Manufacturing Area, and an Oral Solid Dose Manufacturing Area in Building 35. Manufacturing Engineering helps with design, installation, modification, troubleshooting and qualification of new and existing equipment. Manufacturing Engineering also provides technical support for Manufacturing and other Engineering Departments. What You'll Do: Detailed description of role including but not limited to: Protocol and report creation for validation of equipment Support continuous improvement projects Example projects may include: Job shadowing during equipment troubleshooting Equipment commissioning and...

Biogen About This Role This position is on a 12-hour rotation, Night shift on a 2, 2, 3 schedule This position is responsible for the supervision of manufacturing of clinical and commercial products under GMP conditions on our Large Scale Manufacturing Purification Team . The incumbent will supervise Manufacturing Associates on a Night shift; schedules shift tasks; ensures GMP compliance and safety; drafts and reviews manufacturing documents; troubleshoots; and coordinates with other departments. What You'll Do Supervises Manufacturing Associates - observing/instructing, coaching, leading and developing staff. Identifies technical/non-technical development gaps and implements applicable plans/objectives. Performs manufacturing activities per cGMPs, ensuring that reports are fully trained on a given activity prior to performing the activity. Schedules and directs daily manufacturing activities, timely communicating scheduling changes/issues to staff and...