- 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
- 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 ... Conduct laboratory-scale and manufacturing-scale studies to support commercial process validation and characterization. You'll design experiments, analyze data, and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls( Associate Director Equivalent) Our company's Device ... with device design, requirement management, FMEA, design verification, design validation , statistical sampling, and control strategyExperience with regulatory fillingsWorking… more
- Insmed Incorporated (San Diego, CA)
- …lead on a PDT as required by the business.ResponsibilitiesThe Analytical Development Operations associate director is responsible for building a team to take care of ... and formulation development processes. Will support method transfer and validation as needed. Support the biotechnology product lifecycle, from early-stage… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …handling, lead the statistical support in safety signal detection, validation , characterization and reporting in collaboration with safety programming team, ... CSPV, and epidemiology for several projects with minimal direction from group head and provide statistical scientific leadership for clinical trial safety data. Lead the statistical support for safety signal monitoring for ongoing trials.Safety analysis… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the ... technical skills in SAS systems and application development and experience. The Associate Director must be a highly specialized individual contributor or functional… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... Under the broad guidance of the DSCS Digital Program Mgmt Lead, the Associate Director, DSCS Digital Project Manager, will be responsible for implementing improved… more
- Merck & Co. (North Wales, PA)
- …lifecycle. Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs ... and good programming practices.Maintain and manage a project plan including resource forecasting.-Coordinate the activities of a global programming team that includes outsource provider staff.Membership on departmental strategic initiative teams Education and… more
- Aequor (Tampa, FL)
- Carries out the practical work in the laboratory including method development, method validation and trouble shooting. Takes over responsibility for the QC part of ... in customer and regulatory audits as area SME. Develops and executes validation protocols for test methods and equipment qualification. Author and review SOPs… more
- Merck & Co. (Rahway, NJ)
- …have 10-15 direct reports composed of experienced, senior and associate scientists.- The successful candidate will effectively partner with Biologics ... / engineering work process and deliverables (eg equipment fabrication, FAT, SAT, Validation etc.)Must be innovative and drive new ideas, but also have pragmatic… more
- Merck & Co. (Durham, NC)
- …tools and calibration equipment)-Assist with execution of calibration, automation, validation and additional testing, as requiredDecisions are guided by policies, ... (during off-hours) and weekend overtime, as needed.Preferred Experience and Skills: Associate Degree in Industrial Systems, Mechanical, Electronics, Electrical or… more
- Merck & Co. (Durham, NC)
- …and assisting process project engineers.Assists with execution of automation, validation and additional testing, as requiredFollows instructions for completion of ... Requirement: High School Diploma or GEDPreferredPreferable: Technical School Diploma or Associate DegreeExperience and Skills: RequiredA minimum of six (6) years of… more
- Merck & Co. (Durham, NC)
- …- 6:30 AM) rotation (2-2-3). -The VMF (Vaccine Manufacturing Facility) Associate Production Technician is an excellent entry-level opportunity for recent university ... through hands on processing activities. Key responsibilities for the Associate Production Technician include the execution of aseptic processing requirements,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager, and Manager.Oversee the hiring, development, and ... scale cGMP manufacturing, operations management, tech transfer, process and equipment validation or quality management; with a preference for Cell/Gene Therapy… more
- Aequor (Devers, TX)
- …is located in Devens, Massachusetts. This role will report to the Devens Associate Director, Cell Therapy Site Procurement Lead and will follow the Client Hybrid ... Update, create, and approve all necessary UAT test scripts. DCT Verification and Validation : Approve Site Procurement Data Load Files in support of simulated to… more
- Novo Nordisk Inc. (Durham, NC)
- …practices, to include increasing awareness of data management standards & validation to create improvements in methods, techniques, approaches etc. for optimization ... a relevant field of study from an accredited university required May consider an Associate 's Degree in Engineering Technology or a relevant field of study from an… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …manufacturing Perform area equipment and process validations in accordance with validation procedures Perform in-process product testing in accordance with standard ... fumes, and dust. Qualifications Education and Certifications: High School diploma or associate 's degree or equivalent with a minimum of three (3) years' experience,… more
- Caterpillar, Inc. (Mossville, IL)
- …green energy solutions for the future. **Job Summary** As a Test & Validation Senior Associate Technologist, you will develop and maintain mechanical standards ... and processes to ensure safe, efficient, and cost-effective facility operations. You'll lead or support projects, provide technical expertise, and ensure compliance with internal and external standards. **What You Will Do** + Develop and optimize mechanical… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Associate Director, Validation & Engineering** Catalent Pharma Solutions is looking to hire a ** Associate Director, Validation & Engineering** to lead ... and will house 8 CGMP manufacturing suites and cold storage warehousing. The ** Associate Director, Validation & Engineering** is responsible for the strategic… more
