- Merck & Co. (Rahway, NJ)
- …plans that are the foundation for meeting a projects strategic-intent .The Associate Specialist , Project Management , is a subject matter expert in scheduling and ... learning agilityExposure to the pharmaceutical/biotechnology industries and discovery or product developmentCoursework/training in project management Preferred Experience… more
- Merck & Co. (Durham, NC)
- …lyophilization, product inspection, and quality control laboratories. The Validation Specialist is responsible for providing technical support to one of the ... Qualification (PQ) for equipment and systems supporting the Drug substance and Drug Product areas. The Validation Specialist will primarily support the drug… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Novo Nordisk's product portfolio across its lifecycle and ensuring central management for the relevant therapy area. This role is responsible for developing and ... loss of exclusivity (LOE). Collaborate with cross-functional teams to refine product positioning, pricing strategies, and lifecycle management tactics Lifecycle… more
- Merck & Co. (Durham, NC)
- …facility will be used to produce the bulk active ingredient, finished product , and laboratory testing for vaccine.The Specialist , Quality Control participates ... Laboratory Specialist performs laboratory testing on a variety of product samples, including bulk vaccine, filled vaccine, and media. The successful candidate… more
- Merck & Co. (Durham, NC)
- … product inspection, and quality control laboratories.The Quality Assurance Specialist will support this expansion. Project activities requiring support include ... Job DescriptionPosition Description: Specialist , Quality Assurance Our Company will construct a...improvements, and manufacturing readiness to initiate production of commercial product .- The focus for the position includes all aspects… more
- Aequor (Seattle, WA)
- …50% onsite PURPOSE AND SCOPE OF POSITION (Position Summary): The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations for ... will support all activities for routine clinical and commercial product release with an emphasis on supporting CMO with...regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and… more
- Merck & Co. (Rahway, NJ)
- … manufactureDirect experience of working with external suppliersProject management experienceNOTICE FOR INTERNAL APPLICANTSIn accordance with Managers' Policy ... and scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench to Good Manufacturing Practice (GMP) manufacturing… more
- Merck & Co. (Rahway, NJ)
- …point of contact with multiple stakeholders including Global Project and Alliance Management , Product Development Team (PDT) Leaders, Alliance Managers, and ... of the Oncology Collaborations Finance Associate Director, the Finance Senior Specialist will:Assist and provide support with assigned external Alliance partners.Act… more
- Aequor (Bothell, WA)
- Job Description: Job Title: Quality Risk Management Specialist Location: Bothell, WA* Hybrid 50%&plus Onsite Top Skills: A minimum of 5 years of relevant Quality ... Management Standard Operating Procedures (SOPs) and associated documents. Ensure product risk management documentation/files are maintained, with good… more
- Merck & Co. (Durham, NC)
- …cause, implement corrective actions, complete trending analysis, and determine product dispositionHelps establish processes that ensure required Safety guidelines ... Experience and Skills: Required:-- Strong planning, scheduling, and time management skillsWorking knowledge of regulatory requirements in accordance with GMP… more
- Merck & Co. (North Wales, PA)
- …membersAssists with end-user training and request fulfillmentParticipates in the management of published literature and conference abstract acquisition and ... in the collaboration with our Company's IT to maintain the Company Product Literature Database to ensure the maximum performance, reliability, data integrity,… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Senior Specialist , Quality Control will be responsible for activities that support cGMP and regulatory compliance during microbiological method ... transfer/qualification and routine product testing to include the following:Microbiology and sterility assay method transfer and qualificationMicrobiology and… more
- Merck & Co. (Durham, NC)
- …technical services support in the areas of equipment and automation systems, validation, deviation management and product franchise. - Travel: 5% of the time - ... Job DescriptionDurham's Technology Transfer Specialist will be an energetic, technical leader with strong interpersonal, communication, and collaboration skills… more
- Merck & Co. (Durham, NC)
- …patients on time, every time, across the globe.-The main functions of the Specialist , Quality Assurance is to assist in the review of records, investigations, ... quality system initiatives and continuous improvements.-Core responsibilities:Supports the deviation management program including the coordination of managing Quality Notifications… more
- Aequor (Seattle, WA)
- …the regional trainings with APAC and EU. Location: Remote/Field The Global Operations Specialist , Scheduling and Cell Logistics will be the primary points of contact ... and logistics partners, both internally and externally over the weekends. The specialist will be responsible for monitoring patient treatment schedules for the… more
- Merck & Co. (Rahway, NJ)
- …a In this role, you will be responsible for acting as a product lead for enterprise systems, collaborating with cross-functional teams, and driving improvements in ... efforts within our organization. - Key Responsibilities: - Act as a product lead for ePas and Cority, ensuring effective implementation and ongoing sustainment… more
- Legend Biotech USA, Inc. (Providence, RI)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Sr. Cell Therapy Account Specialist - Hartford, CT as part of the Commercial team that will be based ... Remotely. Role OverviewThe Sr. Cell Therapy Account Specialist is responsible for representing Legend's products and services to a defined customer base, generating… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role ... OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...simulations of the processes to ensure sterility of the product /process is not compromised.Support material release in SAP for… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Technical Equipment Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewThe Technical Equipment Specialist will be responsible for ensuring equipment/systems required to support an expanding Cell Therapy facility is appropriately… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a CQV Specialist (Contract) as part of the Technical Operations team based in Raritan, ... be responsible in handling day-to-day activities inclusive of execution, protocol management , vendor management , issues, deviations, corrections and remediation… more