- AUROBINDO (Dayton, OH)
- …- Skills & RequirementsBachelor's degree in Engineering, Engineering Technology, or related field (or equivalent combination of education and experience)Strong ... Division OverviewAurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the… more
- Life Dental Spec - Spring (Manchester, NH)
- Overview We are a state-of-the-art practice looking for a Periodontic Associate . The practice is experiencing tremendous growth and is supported by a top notch ... best patient care possible, we want to meet you. Responsibilities As a Periodontist Associate at our practice, you will play a crucial role in providing specialized… more
- Cipla (Hauppauge, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate (Reviewer) Location: 7 Oser Avenue Hauppauge, NY (Onsite) Employment Type: ... benefits. Shift: Second Shift - 3:00pm - 11:30pm Job Overview: The QA Associate (Reviewer) is responsible for review of batch production records, ensuring that all… more
- Eisai, Inc (Baltimore, MD)
- …maintenances schedules, new equipment/instrument installations, daily production activities, documentation generation, and special projects. This position will ... projects. They ensure all appropriate documents are completed per Good Documentation Practices and enter appropriate information into electronic databases. This… more
- Insmed Incorporated (San Diego, CA)
- …we're in. Are you?About the Role:Insmed is seeking a Senior Research Associate - Lab Technician with specialized expertise in supporting preclinical and ... complex laboratory procedures with autonomy, generate high-quality data, maintain accurate documentation , and contribute to the design and execution of research… more
- Jazz Pharmaceuticals (Menlo Park, CA)
- …serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information. The Associate Director, AI Data Scientist will be responsible for leading ... and implementation of GenAI applications for automated clinical trial documentation generation including such areas medical reports, clinical study reports,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Operations Associate , 1st Shift as part of the Technical Operations team based in ... production data and information in a clear, concise, format according to Good Documentation Practices (GDP).Perform tasks on time in a manner consistent with quality… more
- Cipla (Central Islip, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate II AQA FLSA Classification: Professional, Exempt Work Location: Central Islip, NY ... but are not limited to the following: Scope: The Analytical Quality Assurance (AQA) associate II O III position is an team or individual contributor role and reports… more
- Merck & Co. (Rahway, NJ)
- …DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is ... Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and has… more
- Aequor (Thousand Oaks, CA)
- …onsite approximately dependent on business needs Job Title: GCO LP, Associate (Learning Enablement & Operations) Reporting to: Manager, Training and Development ... Job Summary The Training and Development Associate on the GCO Global Learning and Performance Learning...existing files to ensure audit readiness Assist in providing documentation for inspections/audits. Adhere to processes and standards and… more
- Insmed Incorporated (San Diego, CA)
- …of science, we're in. Are you?About the Role:Insmed is seeking an associate scientist with significant experience with droplet digital PCR (ddPCR). This scientist ... for analysisWestern Blotting (traditional Western Blotting and automated quantitative Western) Documentation of results in appropriate formats provided by supervisorWho… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Scientist will work with a multidisciplinary team of research scientists to investigate ... PowerPoint presentations to communicate key data and findings.Maintain proper documentation of experimental procedures and results via an electronic laboratory… more
- Merck & Co. (Durham, NC)
- Job DescriptionQuality Assurance Associate SpecialistOur Quality Assurance group ensures every single material inside our products is manufactured, processed, ... on time, every time, across the globe.The Quality Assurance Associate Specialist provides Quality support to manufacturing operations. The successful-candidate… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... analytical test method technology transfer process.Skilled in laboratory good documentation practices and electronic documentation systems.Self-motivated with… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate MES Engineer as part of the Manufacturing Excellence team based in ... Raritan, NJ. Role OverviewThe Associate MES Engineer will be part of MSAT team...Plans (CTP), Installation/Operational Qualification (IOQ).Support updates to standardizations and documentation (eg SOPs, WIs, Technical & Design Specifications, and… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and ... to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible providing… more
- Merck & Co. (Rahway, NJ)
- …operations, process development activities, compliance investigations/change management, authoring of GMP documentation , and lead other staff in the pilot plant as ... readiness and execution activities. Prepare, review, and/or approve GMP Documentation as appropriate. Author/Approve Standard Operating Guidelines and Procedures.… more
- Jazz Pharmaceuticals (Redwood City, CA)
- …of day-to-day issue management, communication, and escalation, CAPA resolution, documentation and timely communication to stakeholders and health authorities as ... appropriate. Manage and/or Advise on deviations and change control management process. Partner with Quality, Regulatory Affairs, Regulatory Operations and CMC and Labeling organizations in inspection readiness forums. Assist with all inspection management… more
- Merck & Co. (Durham, NC)
- …Manufacturing Technical Operations, Validation, and New Product Technical Transfer Departments.The Associate Specialist - Process Engineer will support one of these ... ensure a reliable supply of Durham manufactured vaccines-Author technical documentation Position Qualifications: Education Minimum Requirement: Bachelor's Degree or… more
- Merck & Co. (Lower Gwynedd, PA)
- …trusted insights.- The PDMB Regulated Bioanalytics Department is seeking a Data Management Associate to join our LIMS & Data Management group. This role will support ... Analysis, Data Visualization, Detail-Oriented, Drug Metabolism, Ethical Compliance, GMP Documentation , Good Laboratory Practices (GLPs), Immunoassays, Immunochemistry, Information Technology… more
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