- Aequor (Thousand Oaks, CA)
- …EHSS, cGMPs, and other applicable regulatory requirements. Adhere to good documentation practices. Complete all required training before starting any tasks. Work ... lab, checking to ensure removal of expired media performed, archiving documentation , preliminary plate readings etc. Support Microbiology lab with analytical… more
- Aequor (Thousand Oaks, CA)
- …skills (ie documentation systems, databases and spreadsheets). Bachelor's degree OR Associate 's degree and 4 years of directly related experience OR High school ... or GED and two years of relevant work or military experience, though an associate 's degree with six months of experience is also acceptable. A bachelor's degree is… more
- Aequor (West Greenwich, RI)
- …routine laboratory procedures. 3. Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks. 4. Operate and ... preferred.Basic Qualifications: Science related background, lab experience Bachelor's degree OR Associate 's degree and 4 years of experience OR High school diploma… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOverviewThe Associate Director of Federal Tax Audit plays a crucial role in supporting the audit function within the Tax Department, reporting ... Company to ensure compliance and effective audit execution.The Federal Tax Audit Associate Director will be responsible for preparing responses to Internal Revenue… more
- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of authorship agreements, financial disclosures and author approvals- Ensure documentation of compliance with authorship and publication guidelines as stipulated ... by the International Committee of Medical Journal Editors (ICMJE) and Good Publication Practice for Communicating Company-Sponsored Medical Research (GPP)- Work with and oversee publication vendors to ensure deliverables are of high quality, delivered in a… more
- Merck & Co. (Rahway, NJ)
- …date: -As soon as possible.Job Description: Seeking a full-time Business System Associate for the Labeling Operations area within the GRACS Regulatory Innovation & ... IT Business Partners including activities relating to Requirements Gathering, Documentation , Testing, Implementation, Deployment and Hypercare phases.Facilitate and oversee… more
- Repligen (Hopkinton, IA)
- OverviewWe are seeking a Document Control/QA Associate I to join our growing Quality Department team in Hopkinton, MA for 1st shift operations (M-F) from 8 am EST - ... 4:30 pm EST.The Document Control/QA Associate I will report directly to the QA/QC Director.This...responsible for assisting the document control department in processing documentation requests. They will work closely with cross-functional teams… more
- Aequor (Pearl River, LA)
- …preparation areas of the cGMP commercial manufacturing facility. Requires good documentation skills and attention to detail. Duties will include the operation, ... issues, troubleshoot, propose solutions, and keep management informed. Ensure good documentation practices (GDP) in execution and reviews of production records.… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist/ Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... foster collaboration and innovation.Document Excellence: Author regulatory and technical documentation , ensuring all processes align with our company's expectations.Mentor… more
- Twist BioScience (South San Francisco, CA)
- …our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate , will perform basic molecular biology workflows in a highly automated, ... DNA quantitation, purification and cloning. Maintain thorough, accurate and detailed documentation of all work performed using existing document templates and… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist/Sr Principal ... of global regulatory CMC requirements and critical evaluation of supporting documentation to confirm acceptability and identification of potential risks.Lead the… more
- Aequor (Thousand Oaks, CA)
- …recommendations, and assuring progress of quality records to completion. The Sr. Associate will also represent functional area for the Drug Substance Quality ... GMP operations including following detailed SOPS, maintaining training, and good documentation practices. Also, ability to make Quality based decisions in order… more
- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and ... as supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing scientific… more
- Merck & Co. (Durham, NC)
- …with Microsoft Office (Excel, Word, PowerPoint)Excellent planning, organizational, documentation , presentation and communication skillsAbility to work in ... cross-functional teams and to manage complex projects and tasksProduces/completes various assignments and projects requiring analytical ability, independent judgment, creativity and problem-solving skills.Strong ability to develop, articulate, and build… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Warehouse Operations Associate III as part of the Technical Operations team based in Raritan, NJ. ... a long period of time.Physical dexterity sufficient to use computers and documentation .Ability to accommodate shift work including evenings and weekends as required… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... License:Hazardous Material(s):Required Skills:Business Development, Business Development, Business Management, Clinical Documentation , Clinical Investigations, Clinical Judgment, Clinical Reporting, Clinical Research,… more
- Insmed Incorporated (San Diego, CA)
- …and Best Medium Workplaces™ lists.OverviewInsmed is seeking a Senior Research Associate with significant experience with droplet digital PCR (ddPCR). This individual ... assays to third party contractors. Depending on experience, the Sr Research Associate will expand molecular and product specific assay development working with the… more
- Insmed Incorporated (Los Angeles, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director Medical Science Liaison will develop and maintain professional ... assigned budget parametersIs accountable for the accurate and timely documentation of all activitiesIdentify Medical Experts, consultants, investigators, and… more
- Merck & Co. (Rahway, NJ)
- …audit and assurance services.Position Overview / Function and ResponsibilityThe Associate Director:Leads a small team through financial and compliance audits ... business scenarios following a risk based approach and maintains supporting documentation .Coaches in the skill of detecting, analyzing, quantifying and reporting… more
