- Catalent (Manassas, VA)
- …Quality on scheduling of inbound raw materials needing testing to ensure schedule readiness Lead Ready to Execute process; Participate in training as ... Scheduling ManagerPosition SummaryThe Scheduling Manager will...to schedules as things change, understanding and communicating how schedule modifications affect our financial forecast. This position will… more
- Merck & Co. (Durham, NC)
- …and warehouse.-As the team finishes design and construction of the facility, the Lead Technician will play a critical role in supporting the Global Engineering ... the unique opportunity to give input in the design process, startup their areas, and lead the teams to full production.The ideal candidate for this role will be a… more
- Eisai, Inc (Nutley, NJ)
- …incidents.Conduct annual tests and address vulnerabilities.Analyze threat data and lead hunting efforts.Deploy standards, conduct training, and track KPIs.Define ... critical processes and manage recovery testing.Regularly review adherence to standards.Oversee regional security vendors.Prioritize risk-based reduction… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Lead QC Microbiology Data Reviewer as part of the Quality team based in Raritan, ... New Jersey. Role Overview The Lead QC Microbiology Data Reviewer is an exempt level...the completion of environmental monitoring trend reports. Key Responsibilities Scheduling of daily activities for direct reports. Completion of… more
- Catalent (Philadelphia, PA)
- … schedule for production priorities, working closely with the Scheduling and Production, including coordination of overtime.Responsibility for releasing supplies ... assigning tasks and making adjustments when necessary to meet commitments.Publish daily review /release schedule and completed work report for previous day; Takes… more
- Merck & Co. (Durham, NC)
- …services are of the highest quality, optimal cost, and delivered on schedule . Responsible for supporting departmental vision that will provide for continuous ... MRO systemInterface with other departments, contractors and disciplines on scheduling repairs and maintenance of equipment/utility systems.Assist with execution of… more
- Merck & Co. (North Wales, PA)
- …in applicable system(s) and manage budget, including adherence to invoice and payment schedule .Assist with review and finalization of all Supplier documents such ... activities. This position, under the supervision of a Research Management Team Lead , will execute a variety of research management activities starting from study… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …that audit targets for tactical and strategic GVP audits are in place. Review risk assessment documents stemming from audit outcome to increase compliance within ... areas/process improvement to stakeholders via the QMS scheme (ie, Quality Management Review , Quality Review Board) across the global CSPV organization leaders… more
- Merck & Co. (Durham, NC)
- …time, across the globe.This is a night shift P1 position on the 2/2/3 schedule . The Shop Floor Quality Assurance Associate is responsible for all Quality related ... direct in-line Quality support for all compliance and environmental monitoring matters, review of atypical events including accessing product impact for EM events,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …regulatory activities. The Manager RPM is responsible for supporting the global regulatory lead (GRL), US regulatory lead (USRL) and global regulatory team (GRT) ... focus on quality, reliability, consistency and efficiency.ResponsibilitiesPlan, coordinate, and review US regulatory submissions in collaboration with USRL, Regulatory… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …coordinating sample shipment, and acting as shift or study lead . Activities as lead may include scheduling team work assignments and acting as primary point ... of contact for the study director for a particular shift.QualificationsRequires a high school diploma or equivalent and 3-5 years of related experience in a research, commercial or hospital laboratory or an associate's degree and 2-4years of experience in a… more
- Catalent (St. Petersburg, FL)
- …Senior QA Specialist will assist in organizing and prioritizing the activities and schedule for the QA Specialists. The role is responsible for actively identifying ... escalation for QA Specialists.Assist in organizing and prioritizing the activities and schedule for the QA Specialists.Provides feedback to QA Supervisor and Manager… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …your career. Are you ready to realize your potential? The Position Oversee, schedule and lead day-to-day QC Microbiology activities for routine in-process and ... Performs peer data and report reviews as needed Oversees the scheduling of laboratory work Review and amend test methods and instrumentation SOPs as needed… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …ahead of schedule .- PM/OE Team Management and Development, Vendor Oversight:- Lead and manage a team of Project Managers, providing guidance, coaching, and ... RWD / RWE (CR2) Project Management and Operational Excellence (PM-OE) will lead innovation, coordination, and strategic planning efforts and will be responsible to… more
- Merck & Co. (Durham, NC)
- …as needed.Application of sound project management techniques to meet schedule , budget, benefit realization and other project objectives.Provide technical ... guidance/support including authoring or review and approval of system commissioning and qualification documents, change control, automation incidents, Quality… more
- Aequor (Thousand Oaks, CA)
- …need to make sure they are completing the 8 hours daily with a structured schedule ** **This is a very GMP compliance driven role and environment. We need a candidate ... Details: Owns and Manages Change Control Records. Owns and Manages Deviations, and Lead Root Cause Analysis. Develops, writes, edits, and formats materials such as… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …as deviation and deviation action closure times Facilitate weekly/daily management review of deviation metrics. Create processes to identify response actions and ... map to actionable and effective CAPA that reduce recurrent deviation types Lead and supervise the deviation investigation team, assign deviations based on… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking Quality Systems Lead role as part of the Quality Operations team based in Raritan, New ... Jersey. Role Overview The Quality Systems Lead role is an exempt level position with responsibilities...Support other quality systems activities, as needed. Support drafting, review and approval of standard operating procedures and any… more
- Insmed Incorporated (Bridgewater, NJ)
- …and IP due diligence activities. The role may include a hybrid schedule for the right candidate.ResponsibilitiesProactively work with the research and clinical teams ... identify inventions and to draft invention disclosures.Attends R&D meetings and patent review meetings, serving as a liaison for the IP teamDraft patent… more
- Insmed Incorporated (Bridgewater, NJ)
- …manufacturing process.Responsible for technical support as Insmed's internal SME, technical review of quality documentation, management of schedule /raw material ... for being the Technical Operations liaison to the Insmed research team for lead optimization and early development programs. This position will be the dynamic… more
